CN109689662B - 作为害虫防治剂的稠合双环杂环衍生物 - Google Patents
作为害虫防治剂的稠合双环杂环衍生物 Download PDFInfo
- Publication number
- CN109689662B CN109689662B CN201780054877.0A CN201780054877A CN109689662B CN 109689662 B CN109689662 B CN 109689662B CN 201780054877 A CN201780054877 A CN 201780054877A CN 109689662 B CN109689662 B CN 109689662B
- Authority
- CN
- China
- Prior art keywords
- spp
- formula
- genus
- compounds
- compound
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Expired - Fee Related
Links
- 241000607479 Yersinia pestis Species 0.000 title claims abstract description 58
- 125000002618 bicyclic heterocycle group Chemical group 0.000 title description 6
- 150000001875 compounds Chemical class 0.000 claims abstract description 333
- 238000000034 method Methods 0.000 claims abstract description 152
- 241001465754 Metazoa Species 0.000 claims abstract description 52
- -1 /or Species 0.000 claims description 208
- 239000000203 mixture Substances 0.000 claims description 91
- 238000009472 formulation Methods 0.000 claims description 60
- 239000001257 hydrogen Substances 0.000 claims description 40
- 229910052739 hydrogen Inorganic materials 0.000 claims description 40
- 229910052736 halogen Inorganic materials 0.000 claims description 34
- 150000002367 halogens Chemical class 0.000 claims description 34
- 125000000217 alkyl group Chemical group 0.000 claims description 33
- 125000001424 substituent group Chemical group 0.000 claims description 27
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims description 19
- 125000002023 trifluoromethyl group Chemical group FC(F)(F)* 0.000 claims description 19
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 claims description 17
- 125000001449 isopropyl group Chemical group [H]C([H])([H])C([H])(*)C([H])([H])[H] 0.000 claims description 17
- 125000004093 cyano group Chemical group *C#N 0.000 claims description 15
- 125000001072 heteroaryl group Chemical group 0.000 claims description 14
- PXGOKWXKJXAPGV-UHFFFAOYSA-N Fluorine Chemical compound FF PXGOKWXKJXAPGV-UHFFFAOYSA-N 0.000 claims description 13
- 229910052801 chlorine Inorganic materials 0.000 claims description 13
- 125000001028 difluoromethyl group Chemical group [H]C(F)(F)* 0.000 claims description 13
- 229910052731 fluorine Inorganic materials 0.000 claims description 13
- 239000011737 fluorine Substances 0.000 claims description 13
- 125000004435 hydrogen atom Chemical class [H]* 0.000 claims description 13
- WKBOTKDWSSQWDR-UHFFFAOYSA-N Bromine atom Chemical compound [Br] WKBOTKDWSSQWDR-UHFFFAOYSA-N 0.000 claims description 12
- ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 claims description 11
- GDTBXPJZTBHREO-UHFFFAOYSA-N bromine Substances BrBr GDTBXPJZTBHREO-UHFFFAOYSA-N 0.000 claims description 11
- 229910052794 bromium Inorganic materials 0.000 claims description 11
- 239000000460 chlorine Substances 0.000 claims description 11
- 239000004606 Fillers/Extenders Substances 0.000 claims description 8
- 239000003905 agrochemical Substances 0.000 claims description 7
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical group [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 claims description 6
- 125000004123 n-propyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])* 0.000 claims description 4
- 239000004094 surface-active agent Substances 0.000 claims description 4
- 125000001559 cyclopropyl group Chemical group [H]C1([H])C([H])([H])C1([H])* 0.000 claims description 3
- 238000002405 diagnostic procedure Methods 0.000 claims description 3
- 125000006001 difluoroethyl group Chemical group 0.000 claims description 3
- 125000003784 fluoroethyl group Chemical group [H]C([H])(F)C([H])([H])* 0.000 claims description 3
- 125000006337 tetrafluoro ethyl group Chemical group 0.000 claims description 3
- 125000004205 trifluoroethyl group Chemical group [H]C([H])(*)C(F)(F)F 0.000 claims description 3
- 125000004206 2,2,2-trifluoroethyl group Chemical group [H]C([H])(*)C(F)(F)F 0.000 claims description 2
- 125000004216 fluoromethyl group Chemical group [H]C([H])(F)* 0.000 claims description 2
- 125000006340 pentafluoro ethyl group Chemical group FC(F)(F)C(F)(F)* 0.000 claims description 2
- 239000011814 protection agent Substances 0.000 claims description 2
- 238000002560 therapeutic procedure Methods 0.000 claims 1
- 238000002360 preparation method Methods 0.000 abstract description 29
- 239000002917 insecticide Substances 0.000 abstract description 12
- 230000000895 acaricidal effect Effects 0.000 abstract description 11
- 239000000642 acaricide Substances 0.000 abstract description 9
- 239000013067 intermediate product Substances 0.000 abstract 1
- 241000196324 Embryophyta Species 0.000 description 108
- 239000002904 solvent Substances 0.000 description 78
- 238000006243 chemical reaction Methods 0.000 description 72
- 241001147397 Ostrinia Species 0.000 description 60
- WEVYAHXRMPXWCK-UHFFFAOYSA-N Acetonitrile Chemical compound CC#N WEVYAHXRMPXWCK-UHFFFAOYSA-N 0.000 description 57
- 241000195620 Euglena Species 0.000 description 57
- YMWUJEATGCHHMB-UHFFFAOYSA-N Dichloromethane Chemical compound ClCCl YMWUJEATGCHHMB-UHFFFAOYSA-N 0.000 description 54
- ZMXDDKWLCZADIW-UHFFFAOYSA-N N,N-Dimethylformamide Chemical compound CN(C)C=O ZMXDDKWLCZADIW-UHFFFAOYSA-N 0.000 description 48
- 241000257162 Lucilia <blowfly> Species 0.000 description 46
- 241000256248 Spodoptera Species 0.000 description 43
- 230000002829 reductive effect Effects 0.000 description 43
- 241001414989 Thysanoptera Species 0.000 description 42
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 42
- 241000275067 Phyllotreta Species 0.000 description 41
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 36
- 241000208367 Euonymus Species 0.000 description 35
- QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 description 33
- 241000894007 species Species 0.000 description 33
- 241000238876 Acari Species 0.000 description 31
- 241000758827 Ebenus Species 0.000 description 31
- 239000002585 base Substances 0.000 description 31
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 30
- 230000008569 process Effects 0.000 description 30
- MVPPADPHJFYWMZ-UHFFFAOYSA-N chlorobenzene Chemical compound ClC1=CC=CC=C1 MVPPADPHJFYWMZ-UHFFFAOYSA-N 0.000 description 28
- VZGDMQKNWNREIO-UHFFFAOYSA-N tetrachloromethane Chemical compound ClC(Cl)(Cl)Cl VZGDMQKNWNREIO-UHFFFAOYSA-N 0.000 description 28
- IAZDPXIOMUYVGZ-UHFFFAOYSA-N Dimethylsulphoxide Chemical compound CS(C)=O IAZDPXIOMUYVGZ-UHFFFAOYSA-N 0.000 description 27
- 239000003112 inhibitor Substances 0.000 description 27
- HEDRZPFGACZZDS-UHFFFAOYSA-N Chloroform Chemical compound ClC(Cl)Cl HEDRZPFGACZZDS-UHFFFAOYSA-N 0.000 description 26
- 241000244160 Echinococcus Species 0.000 description 26
- 241000218554 Lyophyllum Species 0.000 description 26
- YFXPPSKYMBTNAV-UHFFFAOYSA-N bensultap Chemical compound C=1C=CC=CC=1S(=O)(=O)SCC(N(C)C)CSS(=O)(=O)C1=CC=CC=C1 YFXPPSKYMBTNAV-UHFFFAOYSA-N 0.000 description 26
- 238000011282 treatment Methods 0.000 description 26
- WYURNTSHIVDZCO-UHFFFAOYSA-N Tetrahydrofuran Chemical compound C1CCOC1 WYURNTSHIVDZCO-UHFFFAOYSA-N 0.000 description 24
- 239000003795 chemical substances by application Substances 0.000 description 24
- 241000255925 Diptera Species 0.000 description 23
- 239000000575 pesticide Substances 0.000 description 23
- MHAJPDPJQMAIIY-UHFFFAOYSA-N Hydrogen peroxide Chemical compound OO MHAJPDPJQMAIIY-UHFFFAOYSA-N 0.000 description 22
- 241001516577 Phylloxera Species 0.000 description 22
- 240000002791 Brassica napus Species 0.000 description 20
- 241000489975 Diabrotica Species 0.000 description 20
- 150000002431 hydrogen Chemical class 0.000 description 20
- BWHMMNNQKKPAPP-UHFFFAOYSA-L potassium carbonate Chemical compound [K+].[K+].[O-]C([O-])=O BWHMMNNQKKPAPP-UHFFFAOYSA-L 0.000 description 20
- 150000003839 salts Chemical class 0.000 description 20
- 241001124076 Aphididae Species 0.000 description 19
- 230000003647 oxidation Effects 0.000 description 19
- 238000007254 oxidation reaction Methods 0.000 description 19
- 239000000126 substance Substances 0.000 description 19
- CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 18
- 241001600407 Aphis <genus> Species 0.000 description 18
- 241000254173 Coleoptera Species 0.000 description 18
- 241000209020 Cornus Species 0.000 description 18
- XEKOWRVHYACXOJ-UHFFFAOYSA-N Ethyl acetate Chemical compound CCOC(C)=O XEKOWRVHYACXOJ-UHFFFAOYSA-N 0.000 description 18
- 241001568860 Coccinia Species 0.000 description 17
- BDAGIHXWWSANSR-UHFFFAOYSA-N methanoic acid Natural products OC=O BDAGIHXWWSANSR-UHFFFAOYSA-N 0.000 description 17
- 241000244206 Nematoda Species 0.000 description 16
- 125000004414 alkyl thio group Chemical group 0.000 description 16
- XBDQKXXYIPTUBI-UHFFFAOYSA-N dimethylselenoniopropionate Natural products CCC(O)=O XBDQKXXYIPTUBI-UHFFFAOYSA-N 0.000 description 16
- 239000000047 product Substances 0.000 description 16
- 235000011293 Brassica napus Nutrition 0.000 description 15
- 241000238631 Hexapoda Species 0.000 description 15
- ZMANZCXQSJIPKH-UHFFFAOYSA-N Triethylamine Chemical compound CCN(CC)CC ZMANZCXQSJIPKH-UHFFFAOYSA-N 0.000 description 15
- 150000003254 radicals Chemical class 0.000 description 15
- 241001414826 Lygus Species 0.000 description 14
- 241000517325 Pediculus Species 0.000 description 14
- JUJWROOIHBZHMG-UHFFFAOYSA-N Pyridine Chemical compound C1=CC=NC=C1 JUJWROOIHBZHMG-UHFFFAOYSA-N 0.000 description 14
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 description 14
- 239000005944 Chlorpyrifos Substances 0.000 description 13
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 13
- 239000005531 Flufenacet Substances 0.000 description 13
- 240000007594 Oryza sativa Species 0.000 description 13
- 235000007164 Oryza sativa Nutrition 0.000 description 13
- 239000002671 adjuvant Substances 0.000 description 13
- SBPBAQFWLVIOKP-UHFFFAOYSA-N chlorpyrifos Chemical compound CCOP(=S)(OCC)OC1=NC(Cl)=C(Cl)C=C1Cl SBPBAQFWLVIOKP-UHFFFAOYSA-N 0.000 description 13
- IANUJLZYFUDJIH-UHFFFAOYSA-N flufenacet Chemical compound C=1C=C(F)C=CC=1N(C(C)C)C(=O)COC1=NN=C(C(F)(F)F)S1 IANUJLZYFUDJIH-UHFFFAOYSA-N 0.000 description 13
- 150000008282 halocarbons Chemical class 0.000 description 13
- 125000000623 heterocyclic group Chemical group 0.000 description 13
- 108090000623 proteins and genes Proteins 0.000 description 13
- WSLDOOZREJYCGB-UHFFFAOYSA-N 1,2-Dichloroethane Chemical compound ClCCCl WSLDOOZREJYCGB-UHFFFAOYSA-N 0.000 description 12
- KXDAEFPNCMNJSK-UHFFFAOYSA-N Benzamide Chemical compound NC(=O)C1=CC=CC=C1 KXDAEFPNCMNJSK-UHFFFAOYSA-N 0.000 description 12
- XTHFKEDIFFGKHM-UHFFFAOYSA-N Dimethoxyethane Chemical compound COCCOC XTHFKEDIFFGKHM-UHFFFAOYSA-N 0.000 description 12
- 240000008042 Zea mays Species 0.000 description 12
- 235000002017 Zea mays subsp mays Nutrition 0.000 description 12
- 150000001298 alcohols Chemical class 0.000 description 12
- 125000003118 aryl group Chemical group 0.000 description 12
- 150000002170 ethers Chemical class 0.000 description 12
- 235000009566 rice Nutrition 0.000 description 12
- YLQBMQCUIZJEEH-UHFFFAOYSA-N tetrahydrofuran Natural products C=1C=COC=1 YLQBMQCUIZJEEH-UHFFFAOYSA-N 0.000 description 12
- 230000009261 transgenic effect Effects 0.000 description 12
- 238000005160 1H NMR spectroscopy Methods 0.000 description 11
- 241001674044 Blattodea Species 0.000 description 11
- 241000545593 Scolytinae Species 0.000 description 11
- 241001454294 Tetranychus Species 0.000 description 11
- 241000256618 Trichogramma Species 0.000 description 11
- 235000011054 acetic acid Nutrition 0.000 description 11
- 125000003282 alkyl amino group Chemical group 0.000 description 11
- 125000004966 cyanoalkyl group Chemical group 0.000 description 11
- 239000007788 liquid Substances 0.000 description 11
- FPQQSJJWHUJYPU-UHFFFAOYSA-N 3-(dimethylamino)propyliminomethylidene-ethylazanium;chloride Chemical compound Cl.CCN=C=NCCCN(C)C FPQQSJJWHUJYPU-UHFFFAOYSA-N 0.000 description 10
- 241000239223 Arachnida Species 0.000 description 10
- 108050006807 Nicotinic acetylcholine receptors Proteins 0.000 description 10
- 239000002253 acid Substances 0.000 description 10
- 239000003995 emulsifying agent Substances 0.000 description 10
- 230000036541 health Effects 0.000 description 10
- 239000000463 material Substances 0.000 description 10
- 239000007800 oxidant agent Substances 0.000 description 10
- 229910000027 potassium carbonate Inorganic materials 0.000 description 10
- 235000011181 potassium carbonates Nutrition 0.000 description 10
- RYHBNJHYFVUHQT-UHFFFAOYSA-N 1,4-Dioxane Chemical compound C1COCCO1 RYHBNJHYFVUHQT-UHFFFAOYSA-N 0.000 description 9
- NHQDETIJWKXCTC-UHFFFAOYSA-N 3-chloroperbenzoic acid Chemical compound OOC(=O)C1=CC=CC(Cl)=C1 NHQDETIJWKXCTC-UHFFFAOYSA-N 0.000 description 9
- 241000193388 Bacillus thuringiensis Species 0.000 description 9
- 241000894006 Bacteria Species 0.000 description 9
- RWSOTUBLDIXVET-UHFFFAOYSA-N Dihydrogen sulfide Chemical compound S RWSOTUBLDIXVET-UHFFFAOYSA-N 0.000 description 9
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 description 9
- 241001143352 Meloidogyne Species 0.000 description 9
- 241000721621 Myzus persicae Species 0.000 description 9
- 244000061176 Nicotiana tabacum Species 0.000 description 9
- 241000223259 Trichoderma Species 0.000 description 9
- 150000004945 aromatic hydrocarbons Chemical class 0.000 description 9
- 229940097012 bacillus thuringiensis Drugs 0.000 description 9
- 150000001735 carboxylic acids Chemical class 0.000 description 9
- 239000002270 dispersing agent Substances 0.000 description 9
- 235000013399 edible fruits Nutrition 0.000 description 9
- 235000019253 formic acid Nutrition 0.000 description 9
- 239000008187 granular material Substances 0.000 description 9
- 150000007529 inorganic bases Chemical class 0.000 description 9
- 244000045947 parasite Species 0.000 description 9
- 239000012071 phase Substances 0.000 description 9
- 239000002798 polar solvent Substances 0.000 description 9
- 238000012360 testing method Methods 0.000 description 9
- 239000013598 vector Substances 0.000 description 9
- OSWFIVFLDKOXQC-UHFFFAOYSA-N 4-(3-methoxyphenyl)aniline Chemical compound COC1=CC=CC(C=2C=CC(N)=CC=2)=C1 OSWFIVFLDKOXQC-UHFFFAOYSA-N 0.000 description 8
- 241000256111 Aedes <genus> Species 0.000 description 8
- 229920000742 Cotton Polymers 0.000 description 8
- 241000995023 Empoasca Species 0.000 description 8
- 241000237858 Gastropoda Species 0.000 description 8
- 241000219146 Gossypium Species 0.000 description 8
- 241000721623 Myzus Species 0.000 description 8
- 238000005481 NMR spectroscopy Methods 0.000 description 8
- 235000002637 Nicotiana tabacum Nutrition 0.000 description 8
- 102000019315 Nicotinic acetylcholine receptors Human genes 0.000 description 8
- CTQNGGLPUBDAKN-UHFFFAOYSA-N O-Xylene Chemical compound CC1=CC=CC=C1C CTQNGGLPUBDAKN-UHFFFAOYSA-N 0.000 description 8
- 241000665010 Phylloptera Species 0.000 description 8
- CDBYLPFSWZWCQE-UHFFFAOYSA-L Sodium Carbonate Chemical compound [Na+].[Na+].[O-]C([O-])=O CDBYLPFSWZWCQE-UHFFFAOYSA-L 0.000 description 8
- 241000985245 Spodoptera litura Species 0.000 description 8
- 241000244174 Strongyloides Species 0.000 description 8
- 241000700605 Viruses Species 0.000 description 8
- 230000000853 biopesticidal effect Effects 0.000 description 8
- 239000000969 carrier Substances 0.000 description 8
- 201000010099 disease Diseases 0.000 description 8
- 208000037265 diseases, disorders, signs and symptoms Diseases 0.000 description 8
- 239000000975 dye Substances 0.000 description 8
- DNJIEGIFACGWOD-UHFFFAOYSA-N ethanethiol Chemical compound CCS DNJIEGIFACGWOD-UHFFFAOYSA-N 0.000 description 8
- DDNRNCSGIYDEMC-UHFFFAOYSA-N ethanol;formic acid Chemical compound CCO.OC=O DDNRNCSGIYDEMC-UHFFFAOYSA-N 0.000 description 8
- 150000002825 nitriles Chemical class 0.000 description 8
- 235000019260 propionic acid Nutrition 0.000 description 8
- IUVKMZGDUIUOCP-BTNSXGMBSA-N quinbolone Chemical compound O([C@H]1CC[C@H]2[C@H]3[C@@H]([C@]4(C=CC(=O)C=C4CC3)C)CC[C@@]21C)C1=CCCC1 IUVKMZGDUIUOCP-BTNSXGMBSA-N 0.000 description 8
- RIOQSEWOXXDEQQ-UHFFFAOYSA-N triphenylphosphine Chemical compound C1=CC=CC=C1P(C=1C=CC=CC=1)C1=CC=CC=C1 RIOQSEWOXXDEQQ-UHFFFAOYSA-N 0.000 description 8
- LWIHDJKSTIGBAC-UHFFFAOYSA-K tripotassium phosphate Chemical compound [K+].[K+].[K+].[O-]P([O-])([O-])=O LWIHDJKSTIGBAC-UHFFFAOYSA-K 0.000 description 8
- 235000013311 vegetables Nutrition 0.000 description 8
- 239000008096 xylene Substances 0.000 description 8
- 240000002234 Allium sativum Species 0.000 description 7
- 241000219198 Brassica Species 0.000 description 7
- 241000098277 Cnaphalocrocis Species 0.000 description 7
- 241001255091 Criconema Species 0.000 description 7
- 206010018498 Goitre Diseases 0.000 description 7
- SECXISVLQFMRJM-UHFFFAOYSA-N N-Methylpyrrolidone Chemical compound CN1CCCC1=O SECXISVLQFMRJM-UHFFFAOYSA-N 0.000 description 7
- 241001147398 Ostrinia nubilalis Species 0.000 description 7
- 229910019142 PO4 Inorganic materials 0.000 description 7
- 239000005822 Propiconazole Substances 0.000 description 7
- 235000016383 Zea mays subsp huehuetenangensis Nutrition 0.000 description 7
- 230000002378 acidificating effect Effects 0.000 description 7
- 230000009471 action Effects 0.000 description 7
- 229910052784 alkaline earth metal Inorganic materials 0.000 description 7
- 125000004397 aminosulfonyl group Chemical group NS(=O)(=O)* 0.000 description 7
- 230000015572 biosynthetic process Effects 0.000 description 7
- OEBRKCOSUFCWJD-UHFFFAOYSA-N dichlorvos Chemical compound COP(=O)(OC)OC=C(Cl)Cl OEBRKCOSUFCWJD-UHFFFAOYSA-N 0.000 description 7
- KQYPMOAGWMNYDC-UHFFFAOYSA-N dihydroxy-propan-2-yloxy-sulfanylidene-$l^{5}-phosphane Chemical compound CC(C)OP(O)(O)=S KQYPMOAGWMNYDC-UHFFFAOYSA-N 0.000 description 7
- 235000004611 garlic Nutrition 0.000 description 7
- 201000003872 goiter Diseases 0.000 description 7
- 235000009973 maize Nutrition 0.000 description 7
- ZLBGSRMUSVULIE-GSMJGMFJSA-N milbemycin A3 Chemical class O1[C@H](C)[C@@H](C)CC[C@@]11O[C@H](C\C=C(C)\C[C@@H](C)\C=C\C=C/2[C@]3([C@H](C(=O)O4)C=C(C)[C@@H](O)[C@H]3OC\2)O)C[C@H]4C1 ZLBGSRMUSVULIE-GSMJGMFJSA-N 0.000 description 7
- 230000002438 mitochondrial effect Effects 0.000 description 7
- 235000021317 phosphate Nutrition 0.000 description 7
- 239000000843 powder Substances 0.000 description 7
- STJLVHWMYQXCPB-UHFFFAOYSA-N propiconazole Chemical compound O1C(CCC)COC1(C=1C(=CC(Cl)=CC=1)Cl)CN1N=CN=C1 STJLVHWMYQXCPB-UHFFFAOYSA-N 0.000 description 7
- FVSKHRXBFJPNKK-UHFFFAOYSA-N propionitrile Chemical compound CCC#N FVSKHRXBFJPNKK-UHFFFAOYSA-N 0.000 description 7
- UMJSCPRVCHMLSP-UHFFFAOYSA-N pyridine Natural products COC1=CC=CN=C1 UMJSCPRVCHMLSP-UHFFFAOYSA-N 0.000 description 7
- 229910052717 sulfur Inorganic materials 0.000 description 7
- 230000032258 transport Effects 0.000 description 7
- ZCVAOQKBXKSDMS-PVAVHDDUSA-N (+)-trans-(S)-allethrin Chemical compound CC1(C)[C@H](C=C(C)C)[C@H]1C(=O)O[C@@H]1C(C)=C(CC=C)C(=O)C1 ZCVAOQKBXKSDMS-PVAVHDDUSA-N 0.000 description 6
- 125000004215 2,4-difluorophenyl group Chemical group [H]C1=C([H])C(*)=C(F)C([H])=C1F 0.000 description 6
- OISVCGZHLKNMSJ-UHFFFAOYSA-N 2,6-dimethylpyridine Chemical compound CC1=CC=CC(C)=N1 OISVCGZHLKNMSJ-UHFFFAOYSA-N 0.000 description 6
- ZWEHNKRNPOVVGH-UHFFFAOYSA-N 2-Butanone Chemical compound CCC(C)=O ZWEHNKRNPOVVGH-UHFFFAOYSA-N 0.000 description 6
- 125000004182 2-chlorophenyl group Chemical group [H]C1=C([H])C(Cl)=C(*)C([H])=C1[H] 0.000 description 6
- WFDIJRYMOXRFFG-UHFFFAOYSA-N Acetic anhydride Chemical compound CC(=O)OC(C)=O WFDIJRYMOXRFFG-UHFFFAOYSA-N 0.000 description 6
- 241000256186 Anopheles <genus> Species 0.000 description 6
- 241000219194 Arabidopsis Species 0.000 description 6
- 241000238421 Arthropoda Species 0.000 description 6
- 235000011331 Brassica Nutrition 0.000 description 6
- 235000006008 Brassica napus var napus Nutrition 0.000 description 6
- 240000007124 Brassica oleracea Species 0.000 description 6
- FGUUSXIOTUKUDN-IBGZPJMESA-N C1(=CC=CC=C1)N1C2=C(NC([C@H](C1)NC=1OC(=NN=1)C1=CC=CC=C1)=O)C=CC=C2 Chemical compound C1(=CC=CC=C1)N1C2=C(NC([C@H](C1)NC=1OC(=NN=1)C1=CC=CC=C1)=O)C=CC=C2 FGUUSXIOTUKUDN-IBGZPJMESA-N 0.000 description 6
- CURLTUGMZLYLDI-UHFFFAOYSA-N Carbon dioxide Chemical compound O=C=O CURLTUGMZLYLDI-UHFFFAOYSA-N 0.000 description 6
- 241001635274 Cydia pomonella Species 0.000 description 6
- ZAFNJMIOTHYJRJ-UHFFFAOYSA-N Diisopropyl ether Chemical compound CC(C)OC(C)C ZAFNJMIOTHYJRJ-UHFFFAOYSA-N 0.000 description 6
- LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 description 6
- 241000189565 Frankliniella Species 0.000 description 6
- 235000010469 Glycine max Nutrition 0.000 description 6
- 244000068988 Glycine max Species 0.000 description 6
- 241001480224 Heterodera Species 0.000 description 6
- LSDPWZHWYPCBBB-UHFFFAOYSA-N Methanethiol Chemical compound SC LSDPWZHWYPCBBB-UHFFFAOYSA-N 0.000 description 6
- 241000257229 Musca <genus> Species 0.000 description 6
- JGFZNNIVVJXRND-UHFFFAOYSA-N N,N-Diisopropylethylamine (DIPEA) Chemical compound CCN(C(C)C)C(C)C JGFZNNIVVJXRND-UHFFFAOYSA-N 0.000 description 6
- 241000238814 Orthoptera Species 0.000 description 6
- KDLHZDBZIXYQEI-UHFFFAOYSA-N Palladium Chemical compound [Pd] KDLHZDBZIXYQEI-UHFFFAOYSA-N 0.000 description 6
- 235000010717 Phyllostachys nigra Nutrition 0.000 description 6
- 240000005827 Phyllostachys nigra Species 0.000 description 6
- 241000589180 Rhizobium Species 0.000 description 6
- 241000258242 Siphonaptera Species 0.000 description 6
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 6
- 235000002595 Solanum tuberosum Nutrition 0.000 description 6
- 244000061456 Solanum tuberosum Species 0.000 description 6
- 241000256251 Spodoptera frugiperda Species 0.000 description 6
- 150000007513 acids Chemical class 0.000 description 6
- VEMKTZHHVJILDY-UXHICEINSA-N bioresmethrin Chemical compound CC1(C)[C@H](C=C(C)C)[C@H]1C(=O)OCC1=COC(CC=2C=CC=CC=2)=C1 VEMKTZHHVJILDY-UXHICEINSA-N 0.000 description 6
- FJDQFPXHSGXQBY-UHFFFAOYSA-L caesium carbonate Chemical compound [Cs+].[Cs+].[O-]C([O-])=O FJDQFPXHSGXQBY-UHFFFAOYSA-L 0.000 description 6
- 229910000024 caesium carbonate Inorganic materials 0.000 description 6
- 244000038559 crop plants Species 0.000 description 6
- 125000004122 cyclic group Chemical group 0.000 description 6
- JHIVVAPYMSGYDF-UHFFFAOYSA-N cyclohexanone Chemical compound O=C1CCCCC1 JHIVVAPYMSGYDF-UHFFFAOYSA-N 0.000 description 6
- GCKZANITAMOIAR-XWVCPFKXSA-N dsstox_cid_14566 Chemical compound [O-]C(=O)C1=CC=CC=C1.C1=C[C@H](C)[C@@H]([C@@H](C)CC)O[C@]11O[C@H](C\C=C(C)\[C@@H](O[C@@H]2O[C@@H](C)[C@H](O[C@@H]3O[C@@H](C)[C@H]([NH2+]C)[C@@H](OC)C3)[C@@H](OC)C2)[C@@H](C)\C=C\C=C/2[C@]3([C@H](C(=O)O4)C=C(C)[C@@H](O)[C@H]3OC\2)O)C[C@H]4C1 GCKZANITAMOIAR-XWVCPFKXSA-N 0.000 description 6
- YYJNOYZRYGDPNH-MFKUBSTISA-N fenpyroximate Chemical compound C=1C=C(C(=O)OC(C)(C)C)C=CC=1CO/N=C/C=1C(C)=NN(C)C=1OC1=CC=CC=C1 YYJNOYZRYGDPNH-MFKUBSTISA-N 0.000 description 6
- NYPJDWWKZLNGGM-UHFFFAOYSA-N fenvalerate Aalpha Natural products C=1C=C(Cl)C=CC=1C(C(C)C)C(=O)OC(C#N)C(C=1)=CC=CC=1OC1=CC=CC=C1 NYPJDWWKZLNGGM-UHFFFAOYSA-N 0.000 description 6
- 239000003337 fertilizer Substances 0.000 description 6
- 239000000417 fungicide Substances 0.000 description 6
- 230000000749 insecticidal effect Effects 0.000 description 6
- 125000004269 oxiran-2-yl group Chemical group [H]C1([H])OC1([H])* 0.000 description 6
- 229910052760 oxygen Inorganic materials 0.000 description 6
- XHXFXVLFKHQFAL-UHFFFAOYSA-N phosphoryl trichloride Chemical group ClP(Cl)(Cl)=O XHXFXVLFKHQFAL-UHFFFAOYSA-N 0.000 description 6
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N silicon dioxide Inorganic materials O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 6
- JQWHASGSAFIOCM-UHFFFAOYSA-M sodium periodate Chemical compound [Na+].[O-]I(=O)(=O)=O JQWHASGSAFIOCM-UHFFFAOYSA-M 0.000 description 6
- 239000002689 soil Substances 0.000 description 6
- 239000007787 solid Substances 0.000 description 6
- CXBMCYHAMVGWJQ-CABCVRRESA-N (1,3-dioxo-4,5,6,7-tetrahydroisoindol-2-yl)methyl (1r,3r)-2,2-dimethyl-3-(2-methylprop-1-enyl)cyclopropane-1-carboxylate Chemical compound CC1(C)[C@H](C=C(C)C)[C@H]1C(=O)OCN1C(=O)C(CCCC2)=C2C1=O CXBMCYHAMVGWJQ-CABCVRRESA-N 0.000 description 5
- LMDZBCPBFSXMTL-UHFFFAOYSA-N 1-Ethyl-3-(3-dimethylaminopropyl)carbodiimide Substances CCN=C=NCCCN(C)C LMDZBCPBFSXMTL-UHFFFAOYSA-N 0.000 description 5
- 239000005660 Abamectin Substances 0.000 description 5
- QGZKDVFQNNGYKY-UHFFFAOYSA-N Ammonia Chemical compound N QGZKDVFQNNGYKY-UHFFFAOYSA-N 0.000 description 5
- 241000271857 Aphis citricidus Species 0.000 description 5
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 5
- 235000007319 Avena orientalis Nutrition 0.000 description 5
- 244000075850 Avena orientalis Species 0.000 description 5
- 241000271566 Aves Species 0.000 description 5
- 241000219310 Beta vulgaris subsp. vulgaris Species 0.000 description 5
- 229920002101 Chitin Polymers 0.000 description 5
- 241000233866 Fungi Species 0.000 description 5
- 235000007340 Hordeum vulgare Nutrition 0.000 description 5
- 240000005979 Hordeum vulgare Species 0.000 description 5
- 241000256602 Isoptera Species 0.000 description 5
- 241000406668 Loxodonta cyclotis Species 0.000 description 5
- 239000005951 Methiocarb Substances 0.000 description 5
- 241000157886 Monopterus Species 0.000 description 5
- 241000729876 Niveus Species 0.000 description 5
- 241000935974 Paralichthys dentatus Species 0.000 description 5
- 241000238661 Periplaneta Species 0.000 description 5
- 241001674048 Phthiraptera Species 0.000 description 5
- 241000224016 Plasmodium Species 0.000 description 5
- 241000500437 Plutella xylostella Species 0.000 description 5
- 240000000111 Saccharum officinarum Species 0.000 description 5
- 235000007201 Saccharum officinarum Nutrition 0.000 description 5
- 235000007238 Secale cereale Nutrition 0.000 description 5
- 244000082988 Secale cereale Species 0.000 description 5
- KEAYESYHFKHZAL-UHFFFAOYSA-N Sodium Chemical compound [Na] KEAYESYHFKHZAL-UHFFFAOYSA-N 0.000 description 5
- 241000256247 Spodoptera exigua Species 0.000 description 5
- 235000021536 Sugar beet Nutrition 0.000 description 5
- 241000255626 Tabanus <genus> Species 0.000 description 5
- 241001494489 Thielavia Species 0.000 description 5
- 235000005824 Zea mays ssp. parviglumis Nutrition 0.000 description 5
- 125000004453 alkoxycarbonyl group Chemical group 0.000 description 5
- 150000001412 amines Chemical class 0.000 description 5
- FTNJWQUOZFUQQJ-NDAWSKJSSA-N azadirachtin A Chemical compound C([C@@H]([C@]1(C=CO[C@H]1O1)O)[C@]2(C)O3)[C@H]1[C@]23[C@]1(C)[C@H](O)[C@H](OC[C@@]2([C@@H](C[C@@H]3OC(=O)C(\C)=C\C)OC(C)=O)C(=O)OC)[C@@H]2[C@]32CO[C@@](C(=O)OC)(O)[C@@H]12 FTNJWQUOZFUQQJ-NDAWSKJSSA-N 0.000 description 5
- 201000008680 babesiosis Diseases 0.000 description 5
- 125000003917 carbamoyl group Chemical group [H]N([H])C(*)=O 0.000 description 5
- 150000001732 carboxylic acid derivatives Chemical class 0.000 description 5
- 235000013339 cereals Nutrition 0.000 description 5
- 235000005822 corn Nutrition 0.000 description 5
- 229960001591 cyfluthrin Drugs 0.000 description 5
- 239000003814 drug Substances 0.000 description 5
- 244000078703 ectoparasite Species 0.000 description 5
- 244000079386 endoparasite Species 0.000 description 5
- 150000002148 esters Chemical class 0.000 description 5
- IXORZMNAPKEEDV-OBDJNFEBSA-N gibberellin A3 Chemical class C([C@@]1(O)C(=C)C[C@@]2(C1)[C@H]1C(O)=O)C[C@H]2[C@]2(C=C[C@@H]3O)[C@H]1[C@]3(C)C(=O)O2 IXORZMNAPKEEDV-OBDJNFEBSA-N 0.000 description 5
- 238000003306 harvesting Methods 0.000 description 5
- 238000004128 high performance liquid chromatography Methods 0.000 description 5
- 208000015181 infectious disease Diseases 0.000 description 5
- 239000000543 intermediate Substances 0.000 description 5
- 230000014759 maintenance of location Effects 0.000 description 5
- YFBPRJGDJKVWAH-UHFFFAOYSA-N methiocarb Chemical compound CNC(=O)OC1=CC(C)=C(SC)C(C)=C1 YFBPRJGDJKVWAH-UHFFFAOYSA-N 0.000 description 5
- FXWHFKOXMBTCMP-WMEDONTMSA-N milbemycin Natural products COC1C2OCC3=C/C=C/C(C)CC(=CCC4CC(CC5(O4)OC(C)C(C)C(OC(=O)C(C)CC(C)C)C5O)OC(=O)C(C=C1C)C23O)C FXWHFKOXMBTCMP-WMEDONTMSA-N 0.000 description 5
- 210000000056 organ Anatomy 0.000 description 5
- 244000052769 pathogen Species 0.000 description 5
- 150000003013 phosphoric acid derivatives Chemical class 0.000 description 5
- 229920000151 polyglycol Polymers 0.000 description 5
- 239000010695 polyglycol Substances 0.000 description 5
- 102000004169 proteins and genes Human genes 0.000 description 5
- 239000012312 sodium hydride Substances 0.000 description 5
- 229910000104 sodium hydride Inorganic materials 0.000 description 5
- 239000000243 solution Substances 0.000 description 5
- 238000003860 storage Methods 0.000 description 5
- 239000011593 sulfur Substances 0.000 description 5
- 238000003786 synthesis reaction Methods 0.000 description 5
- 229960005199 tetramethrin Drugs 0.000 description 5
- 239000004308 thiabendazole Substances 0.000 description 5
- 229960004546 thiabendazole Drugs 0.000 description 5
- 235000010296 thiabendazole Nutrition 0.000 description 5
- WJCNZQLZVWNLKY-UHFFFAOYSA-N thiabendazole Chemical compound S1C=NC(C=2NC3=CC=CC=C3N=2)=C1 WJCNZQLZVWNLKY-UHFFFAOYSA-N 0.000 description 5
- JLIDBLDQVAYHNE-YKALOCIXSA-N (+)-Abscisic acid Chemical compound OC(=O)/C=C(/C)\C=C\[C@@]1(O)C(C)=CC(=O)CC1(C)C JLIDBLDQVAYHNE-YKALOCIXSA-N 0.000 description 4
- FLBAYUMRQUHISI-UHFFFAOYSA-N 1,8-naphthyridine Chemical compound N1=CC=CC2=CC=CN=C21 FLBAYUMRQUHISI-UHFFFAOYSA-N 0.000 description 4
- GNFTZDOKVXKIBK-UHFFFAOYSA-N 3-(2-methoxyethoxy)benzohydrazide Chemical compound COCCOC1=CC=CC(C(=O)NN)=C1 GNFTZDOKVXKIBK-UHFFFAOYSA-N 0.000 description 4
- XTDZGXBTXBEZDN-UHFFFAOYSA-N 3-(difluoromethyl)-N-(9-isopropyl-1,2,3,4-tetrahydro-1,4-methanonaphthalen-5-yl)-1-methylpyrazole-4-carboxamide Chemical compound CC(C)C1C2CCC1C1=C2C=CC=C1NC(=O)C1=CN(C)N=C1C(F)F XTDZGXBTXBEZDN-UHFFFAOYSA-N 0.000 description 4
- 125000003349 3-pyridyl group Chemical group N1=C([H])C([*])=C([H])C([H])=C1[H] 0.000 description 4
- IBSREHMXUMOFBB-JFUDTMANSA-N 5u8924t11h Chemical compound O1[C@@H](C)[C@H](O)[C@@H](OC)C[C@@H]1O[C@@H]1[C@@H](OC)C[C@H](O[C@@H]2C(=C/C[C@@H]3C[C@@H](C[C@@]4(O3)C=C[C@H](C)[C@@H](C(C)C)O4)OC(=O)[C@@H]3C=C(C)[C@@H](O)[C@H]4OC\C([C@@]34O)=C/C=C/[C@@H]2C)/C)O[C@H]1C.C1=C[C@H](C)[C@@H]([C@@H](C)CC)O[C@]11O[C@H](C\C=C(C)\[C@@H](O[C@@H]2O[C@@H](C)[C@H](O[C@@H]3O[C@@H](C)[C@H](O)[C@@H](OC)C3)[C@@H](OC)C2)[C@@H](C)\C=C\C=C/2[C@]3([C@H](C(=O)O4)C=C(C)[C@@H](O)[C@H]3OC\2)O)C[C@H]4C1 IBSREHMXUMOFBB-JFUDTMANSA-N 0.000 description 4
- YVKXOVXFRDNISU-UHFFFAOYSA-N 7-ethylsulfanyl-6-[3-methyl-6-(trifluoromethyl)imidazo[4,5-b]pyridin-2-yl]-[1,3]thiazolo[4,5-c]pyridine Chemical compound CCSc1c(ncc2ncsc12)-c1nc2cc(cnc2n1C)C(F)(F)F YVKXOVXFRDNISU-UHFFFAOYSA-N 0.000 description 4
- 102000012440 Acetylcholinesterase Human genes 0.000 description 4
- 108010022752 Acetylcholinesterase Proteins 0.000 description 4
- 241000218473 Agrotis Species 0.000 description 4
- 241000399940 Anguina tritici Species 0.000 description 4
- 239000005878 Azadirachtin Substances 0.000 description 4
- 241000223836 Babesia Species 0.000 description 4
- 241000223846 Babesia canis Species 0.000 description 4
- 235000011303 Brassica alboglabra Nutrition 0.000 description 4
- 235000011302 Brassica oleracea Nutrition 0.000 description 4
- 235000010149 Brassica rapa subsp chinensis Nutrition 0.000 description 4
- 235000000536 Brassica rapa subsp pekinensis Nutrition 0.000 description 4
- 241000499436 Brassica rapa subsp. pekinensis Species 0.000 description 4
- 241001246270 Calophyllum Species 0.000 description 4
- 241000784792 Ceratocarpus Species 0.000 description 4
- 241000195585 Chlamydomonas Species 0.000 description 4
- 241001414836 Cimex Species 0.000 description 4
- 240000007154 Coffea arabica Species 0.000 description 4
- 241000258922 Ctenocephalides Species 0.000 description 4
- XDTMQSROBMDMFD-UHFFFAOYSA-N Cyclohexane Chemical compound C1CCCCC1 XDTMQSROBMDMFD-UHFFFAOYSA-N 0.000 description 4
- 239000005946 Cypermethrin Substances 0.000 description 4
- 241001124144 Dermaptera Species 0.000 description 4
- QOSSAOTZNIDXMA-UHFFFAOYSA-N Dicylcohexylcarbodiimide Chemical compound C1CCCCC1N=C=NC1CCCCC1 QOSSAOTZNIDXMA-UHFFFAOYSA-N 0.000 description 4
- 241001517923 Douglasiidae Species 0.000 description 4
- 241000255581 Drosophila <fruit fly, genus> Species 0.000 description 4
- 241000258955 Echinodermata Species 0.000 description 4
- 241000223924 Eimeria Species 0.000 description 4
- 229930191978 Gibberellin Natural products 0.000 description 4
- 108050006905 Glutamate-Gated Chloride Channel Proteins 0.000 description 4
- 241000282412 Homo Species 0.000 description 4
- DGAQECJNVWCQMB-PUAWFVPOSA-M Ilexoside XXIX Chemical compound C[C@@H]1CC[C@@]2(CC[C@@]3(C(=CC[C@H]4[C@]3(CC[C@@H]5[C@@]4(CC[C@@H](C5(C)C)OS(=O)(=O)[O-])C)C)[C@@H]2[C@]1(C)O)C)C(=O)O[C@H]6[C@@H]([C@H]([C@@H]([C@H](O6)CO)O)O)O.[Na+] DGAQECJNVWCQMB-PUAWFVPOSA-M 0.000 description 4
- XEEYBQQBJWHFJM-UHFFFAOYSA-N Iron Chemical compound [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 description 4
- 239000005799 Isopyrazam Substances 0.000 description 4
- 241000255777 Lepidoptera Species 0.000 description 4
- HLFSDGLLUJUHTE-SNVBAGLBSA-N Levamisole Chemical compound C1([C@H]2CN3CCSC3=N2)=CC=CC=C1 HLFSDGLLUJUHTE-SNVBAGLBSA-N 0.000 description 4
- BZLVMXJERCGZMT-UHFFFAOYSA-N Methyl tert-butyl ether Chemical compound COC(C)(C)C BZLVMXJERCGZMT-UHFFFAOYSA-N 0.000 description 4
- 239000005918 Milbemectin Substances 0.000 description 4
- 241000257159 Musca domestica Species 0.000 description 4
- LRHPLDYGYMQRHN-UHFFFAOYSA-N N-Butanol Chemical compound CCCCO LRHPLDYGYMQRHN-UHFFFAOYSA-N 0.000 description 4
- 239000005950 Oxamyl Substances 0.000 description 4
- 241000606860 Pasteurella Species 0.000 description 4
- 241000562493 Pegomya Species 0.000 description 4
- 235000010627 Phaseolus vulgaris Nutrition 0.000 description 4
- 244000046052 Phaseolus vulgaris Species 0.000 description 4
- 241000745988 Phyllostachys Species 0.000 description 4
- GLUUGHFHXGJENI-UHFFFAOYSA-N Piperazine Chemical compound C1CNCCN1 GLUUGHFHXGJENI-UHFFFAOYSA-N 0.000 description 4
- 241000219000 Populus Species 0.000 description 4
- 241000208422 Rhododendron Species 0.000 description 4
- 240000008301 Rhynchosia minima Species 0.000 description 4
- 241000257190 Sarcophaga <genus> Species 0.000 description 4
- 241000243774 Trichinella Species 0.000 description 4
- 241000255985 Trichoplusia Species 0.000 description 4
- 241000209140 Triticum Species 0.000 description 4
- 235000021307 Triticum Nutrition 0.000 description 4
- 241000219095 Vitis Species 0.000 description 4
- 235000009392 Vitis Nutrition 0.000 description 4
- 229950008167 abamectin Drugs 0.000 description 4
- WEVYAHXRMPXWCK-FIBGUPNXSA-N acetonitrile-d3 Chemical compound [2H]C([2H])([2H])C#N WEVYAHXRMPXWCK-FIBGUPNXSA-N 0.000 description 4
- 125000002777 acetyl group Chemical group [H]C([H])([H])C(*)=O 0.000 description 4
- 229940022698 acetylcholinesterase Drugs 0.000 description 4
- 239000000654 additive Substances 0.000 description 4
- 150000001338 aliphatic hydrocarbons Chemical class 0.000 description 4
- FPIPGXGPPPQFEQ-OVSJKPMPSA-N all-trans-retinol Chemical compound OC\C=C(/C)\C=C\C=C(/C)\C=C\C1=C(C)CCCC1(C)C FPIPGXGPPPQFEQ-OVSJKPMPSA-N 0.000 description 4
- 230000003281 allosteric effect Effects 0.000 description 4
- AVKUERGKIZMTKX-NJBDSQKTSA-N ampicillin Chemical compound C1([C@@H](N)C(=O)N[C@H]2[C@H]3SC([C@@H](N3C2=O)C(O)=O)(C)C)=CC=CC=C1 AVKUERGKIZMTKX-NJBDSQKTSA-N 0.000 description 4
- 125000000129 anionic group Chemical group 0.000 description 4
- 230000000507 anthelmentic effect Effects 0.000 description 4
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 description 4
- VEHPJKVTJQSSKL-UHFFFAOYSA-N azadirachtin Natural products O1C2(C)C(C3(C=COC3O3)O)CC3C21C1(C)C(O)C(OCC2(OC(C)=O)C(CC3OC(=O)C(C)=CC)OC(C)=O)C2C32COC(C(=O)OC)(O)C12 VEHPJKVTJQSSKL-UHFFFAOYSA-N 0.000 description 4
- FTNJWQUOZFUQQJ-IRYYUVNJSA-N azadirachtin A Natural products C([C@@H]([C@]1(C=CO[C@H]1O1)O)[C@]2(C)O3)[C@H]1[C@]23[C@]1(C)[C@H](O)[C@H](OC[C@@]2([C@@H](C[C@@H]3OC(=O)C(\C)=C/C)OC(C)=O)C(=O)OC)[C@@H]2[C@]32CO[C@@](C(=O)OC)(O)[C@@H]12 FTNJWQUOZFUQQJ-IRYYUVNJSA-N 0.000 description 4
- 238000009395 breeding Methods 0.000 description 4
- TWFZGCMQGLPBSX-UHFFFAOYSA-N carbendazim Chemical compound C1=CC=C2NC(NC(=O)OC)=NC2=C1 TWFZGCMQGLPBSX-UHFFFAOYSA-N 0.000 description 4
- 150000001718 carbodiimides Chemical class 0.000 description 4
- 150000004649 carbonic acid derivatives Chemical class 0.000 description 4
- 239000003054 catalyst Substances 0.000 description 4
- 239000012320 chlorinating reagent Substances 0.000 description 4
- 238000000576 coating method Methods 0.000 description 4
- 235000016213 coffee Nutrition 0.000 description 4
- 235000013353 coffee beverage Nutrition 0.000 description 4
- 238000004891 communication Methods 0.000 description 4
- QQODLKZGRKWIFG-QSFXBCCZSA-N cyfluthrin Chemical compound CC1(C)[C@@H](C=C(Cl)Cl)[C@H]1C(=O)O[C@@H](C#N)C1=CC=C(F)C(OC=2C=CC=CC=2)=C1 QQODLKZGRKWIFG-QSFXBCCZSA-N 0.000 description 4
- ZXQYGBMAQZUVMI-UNOMPAQXSA-N cyhalothrin Chemical compound CC1(C)C(\C=C(/Cl)C(F)(F)F)C1C(=O)OC(C#N)C1=CC=CC(OC=2C=CC=CC=2)=C1 ZXQYGBMAQZUVMI-UNOMPAQXSA-N 0.000 description 4
- 229960005424 cypermethrin Drugs 0.000 description 4
- 229950001327 dichlorvos Drugs 0.000 description 4
- 235000014113 dietary fatty acids Nutrition 0.000 description 4
- QLFZZSKTJWDQOS-YDBLARSUSA-N doramectin Chemical compound O1[C@@H](C)[C@H](O)[C@@H](OC)C[C@@H]1O[C@@H]1[C@@H](OC)C[C@H](O[C@@H]2C(=C/C[C@@H]3C[C@@H](C[C@@]4(O3)C=C[C@H](C)[C@@H](C3CCCCC3)O4)OC(=O)[C@@H]3C=C(C)[C@@H](O)[C@H]4OC\C([C@@]34O)=C/C=C/[C@@H]2C)/C)O[C@H]1C QLFZZSKTJWDQOS-YDBLARSUSA-N 0.000 description 4
- 229960003997 doramectin Drugs 0.000 description 4
- 239000012039 electrophile Substances 0.000 description 4
- 238000010931 ester hydrolysis Methods 0.000 description 4
- 239000000194 fatty acid Substances 0.000 description 4
- 229930195729 fatty acid Natural products 0.000 description 4
- 230000035784 germination Effects 0.000 description 4
- 239000003448 gibberellin Substances 0.000 description 4
- 230000026030 halogenation Effects 0.000 description 4
- 238000005658 halogenation reaction Methods 0.000 description 4
- 244000000013 helminth Species 0.000 description 4
- 238000007327 hydrogenolysis reaction Methods 0.000 description 4
- HICUREFSAIZXFQ-JOWPUVSESA-N i9z29i000j Chemical compound C1C[C@H](C)[C@@H](CC)O[C@@]21O[C@H](C\C=C(C)\[C@H](OC(=O)C(=N/OC)\C=1C=CC=CC=1)[C@@H](C)\C=C\C=C/1[C@]3([C@H](C(=O)O4)C=C(C)[C@@H](O)[C@H]3OC\1)O)C[C@H]4C2 HICUREFSAIZXFQ-JOWPUVSESA-N 0.000 description 4
- 150000002576 ketones Chemical class 0.000 description 4
- 229950000961 latidectin Drugs 0.000 description 4
- 229960001614 levamisole Drugs 0.000 description 4
- ZCSHNCUQKCANBX-UHFFFAOYSA-N lithium diisopropylamide Chemical compound [Li+].CC(C)[N-]C(C)C ZCSHNCUQKCANBX-UHFFFAOYSA-N 0.000 description 4
- 229910052751 metal Inorganic materials 0.000 description 4
- 239000002184 metal Substances 0.000 description 4
- 150000004702 methyl esters Chemical class 0.000 description 4
- 244000005700 microbiome Species 0.000 description 4
- 239000002480 mineral oil Substances 0.000 description 4
- 238000002156 mixing Methods 0.000 description 4
- YZBLFMPOMVTDJY-CBYMMZEQSA-N moxidectin Chemical compound O1[C@H](C(\C)=C\C(C)C)[C@@H](C)C(=N/OC)\C[C@@]11O[C@H](C\C=C(C)\C[C@@H](C)\C=C\C=C/2[C@]3([C@H](C(=O)O4)C=C(C)[C@@H](O)[C@H]3OC\2)O)C[C@H]4C1 YZBLFMPOMVTDJY-CBYMMZEQSA-N 0.000 description 4
- 229960004816 moxidectin Drugs 0.000 description 4
- YNFMRVVYUVPIAN-AQUURSMBSA-N nemadectin Chemical compound C1[C@H](O)[C@H](C)[C@@H](C(/C)=C/C(C)C)O[C@]11O[C@H](C\C=C(C)\C[C@@H](C)\C=C\C=C/2[C@]3([C@H](C(=O)O4)C=C(C)[C@@H](O)[C@H]3OC\2)O)C[C@H]4C1 YNFMRVVYUVPIAN-AQUURSMBSA-N 0.000 description 4
- 229950009729 nemadectin Drugs 0.000 description 4
- YNFMRVVYUVPIAN-UHFFFAOYSA-N nemadectin alpha Natural products C1C(O)C(C)C(C(C)=CC(C)C)OC11OC(CC=C(C)CC(C)C=CC=C2C3(C(C(=O)O4)C=C(C)C(O)C3OC2)O)CC4C1 YNFMRVVYUVPIAN-UHFFFAOYSA-N 0.000 description 4
- 230000001069 nematicidal effect Effects 0.000 description 4
- 239000005645 nematicide Substances 0.000 description 4
- QJGQUHMNIGDVPM-UHFFFAOYSA-N nitrogen group Chemical group [N] QJGQUHMNIGDVPM-UHFFFAOYSA-N 0.000 description 4
- 230000008520 organization Effects 0.000 description 4
- KZAUOCCYDRDERY-UHFFFAOYSA-N oxamyl Chemical compound CNC(=O)ON=C(SC)C(=O)N(C)C KZAUOCCYDRDERY-UHFFFAOYSA-N 0.000 description 4
- 239000001301 oxygen Substances 0.000 description 4
- LCCNCVORNKJIRZ-UHFFFAOYSA-N parathion Chemical compound CCOP(=S)(OCC)OC1=CC=C([N+]([O-])=O)C=C1 LCCNCVORNKJIRZ-UHFFFAOYSA-N 0.000 description 4
- 229960000490 permethrin Drugs 0.000 description 4
- 239000000546 pharmaceutical excipient Substances 0.000 description 4
- 229910000160 potassium phosphate Inorganic materials 0.000 description 4
- 235000011009 potassium phosphates Nutrition 0.000 description 4
- 229940044601 receptor agonist Drugs 0.000 description 4
- 239000000018 receptor agonist Substances 0.000 description 4
- AFJYYKSVHJGXSN-KAJWKRCWSA-N selamectin Chemical compound O1[C@@H](C)[C@H](O)[C@@H](OC)C[C@@H]1O[C@@H]1C(/C)=C/C[C@@H](O[C@]2(O[C@@H]([C@@H](C)CC2)C2CCCCC2)C2)C[C@@H]2OC(=O)[C@@H]([C@]23O)C=C(C)C(=N\O)/[C@H]3OC\C2=C/C=C/[C@@H]1C AFJYYKSVHJGXSN-KAJWKRCWSA-N 0.000 description 4
- 229960002245 selamectin Drugs 0.000 description 4
- 239000011734 sodium Substances 0.000 description 4
- 229910052708 sodium Inorganic materials 0.000 description 4
- 229910000029 sodium carbonate Inorganic materials 0.000 description 4
- 238000005507 spraying Methods 0.000 description 4
- 230000007480 spreading Effects 0.000 description 4
- 238000003892 spreading Methods 0.000 description 4
- XLNZEKHULJKQBA-UHFFFAOYSA-N terbufos Chemical compound CCOP(=S)(OCC)SCSC(C)(C)C XLNZEKHULJKQBA-UHFFFAOYSA-N 0.000 description 4
- 230000001225 therapeutic effect Effects 0.000 description 4
- 239000002562 thickening agent Substances 0.000 description 4
- MGSRCZKZVOBKFT-UHFFFAOYSA-N thymol Chemical compound CC(C)C1=CC=C(C)C=C1O MGSRCZKZVOBKFT-UHFFFAOYSA-N 0.000 description 4
- JOXIMZWYDAKGHI-UHFFFAOYSA-N toluene-4-sulfonic acid Chemical compound CC1=CC=C(S(O)(=O)=O)C=C1 JOXIMZWYDAKGHI-UHFFFAOYSA-N 0.000 description 4
- AMFGTOFWMRQMEM-UHFFFAOYSA-N triazophos Chemical compound N1=C(OP(=S)(OCC)OCC)N=CN1C1=CC=CC=C1 AMFGTOFWMRQMEM-UHFFFAOYSA-N 0.000 description 4
- NFACJZMKEDPNKN-UHFFFAOYSA-N trichlorfon Chemical compound COP(=O)(OC)C(O)C(Cl)(Cl)Cl NFACJZMKEDPNKN-UHFFFAOYSA-N 0.000 description 4
- WJKHJLXJJJATHN-UHFFFAOYSA-N triflic anhydride Chemical compound FC(F)(F)S(=O)(=O)OS(=O)(=O)C(F)(F)F WJKHJLXJJJATHN-UHFFFAOYSA-N 0.000 description 4
- QAEDZJGFFMLHHQ-UHFFFAOYSA-N trifluoroacetic anhydride Chemical compound FC(F)(F)C(=O)OC(=O)C(F)(F)F QAEDZJGFFMLHHQ-UHFFFAOYSA-N 0.000 description 4
- 235000015112 vegetable and seed oil Nutrition 0.000 description 4
- 239000008158 vegetable oil Substances 0.000 description 4
- 239000000080 wetting agent Substances 0.000 description 4
- 239000002023 wood Substances 0.000 description 4
- HIXDQWDOVZUNNA-UHFFFAOYSA-N 2-(3,4-dimethoxyphenyl)-5-hydroxy-7-methoxychromen-4-one Chemical compound C=1C(OC)=CC(O)=C(C(C=2)=O)C=1OC=2C1=CC=C(OC)C(OC)=C1 HIXDQWDOVZUNNA-UHFFFAOYSA-N 0.000 description 3
- AZSNMRSAGSSBNP-UHFFFAOYSA-N 22,23-dihydroavermectin B1a Natural products C1CC(C)C(C(C)CC)OC21OC(CC=C(C)C(OC1OC(C)C(OC3OC(C)C(O)C(OC)C3)C(OC)C1)C(C)C=CC=C1C3(C(C(=O)O4)C=C(C)C(O)C3OC1)O)CC4C2 AZSNMRSAGSSBNP-UHFFFAOYSA-N 0.000 description 3
- 125000004211 3,5-difluorophenyl group Chemical group [H]C1=C(F)C([H])=C(*)C([H])=C1F 0.000 description 3
- SPBDXSGPUHCETR-JFUDTMANSA-N 8883yp2r6d Chemical compound O1[C@@H](C)[C@H](O)[C@@H](OC)C[C@@H]1O[C@@H]1[C@@H](OC)C[C@H](O[C@@H]2C(=C/C[C@@H]3C[C@@H](C[C@@]4(O[C@@H]([C@@H](C)CC4)C(C)C)O3)OC(=O)[C@@H]3C=C(C)[C@@H](O)[C@H]4OC\C([C@@]34O)=C/C=C/[C@@H]2C)/C)O[C@H]1C.C1C[C@H](C)[C@@H]([C@@H](C)CC)O[C@@]21O[C@H](C\C=C(C)\[C@@H](O[C@@H]1O[C@@H](C)[C@H](O[C@@H]3O[C@@H](C)[C@H](O)[C@@H](OC)C3)[C@@H](OC)C1)[C@@H](C)\C=C\C=C/1[C@]3([C@H](C(=O)O4)C=C(C)[C@@H](O)[C@H]3OC\1)O)C[C@H]4C2 SPBDXSGPUHCETR-JFUDTMANSA-N 0.000 description 3
- 241000934067 Acarus Species 0.000 description 3
- 241000526180 Acizzia Species 0.000 description 3
- 241000234282 Allium Species 0.000 description 3
- QGZKDVFQNNGYKY-UHFFFAOYSA-O Ammonium Chemical compound [NH4+] QGZKDVFQNNGYKY-UHFFFAOYSA-O 0.000 description 3
- 241000722809 Armadillidium vulgare Species 0.000 description 3
- 241000193830 Bacillus <bacterium> Species 0.000 description 3
- 244000063299 Bacillus subtilis Species 0.000 description 3
- 235000014469 Bacillus subtilis Nutrition 0.000 description 3
- 241001147758 Bacillus thuringiensis serovar kurstaki Species 0.000 description 3
- 239000005734 Benalaxyl Substances 0.000 description 3
- WVDDGKGOMKODPV-UHFFFAOYSA-N Benzyl alcohol Chemical compound OCC1=CC=CC=C1 WVDDGKGOMKODPV-UHFFFAOYSA-N 0.000 description 3
- 241000283690 Bos taurus Species 0.000 description 3
- 240000000385 Brassica napus var. napus Species 0.000 description 3
- 235000004977 Brassica sinapistrum Nutrition 0.000 description 3
- 241000186312 Brevibacterium sp. Species 0.000 description 3
- 241001350371 Capua Species 0.000 description 3
- 241000533754 Cayaponia americana Species 0.000 description 3
- 241001098608 Ceratophyllus Species 0.000 description 3
- 241000258920 Chilopoda Species 0.000 description 3
- 241001414720 Cicadellidae Species 0.000 description 3
- 241000223782 Ciliophora Species 0.000 description 3
- 241001266001 Cordyceps confragosa Species 0.000 description 3
- 108010002156 Depsipeptides Proteins 0.000 description 3
- 241000238710 Dermatophagoides Species 0.000 description 3
- 241000299419 Echinodera Species 0.000 description 3
- 102000015782 Electron Transport Complex III Human genes 0.000 description 3
- 108010024882 Electron Transport Complex III Proteins 0.000 description 3
- 239000005894 Emamectin Substances 0.000 description 3
- 241000630736 Ephestia Species 0.000 description 3
- 206010014979 Epidemic typhus Diseases 0.000 description 3
- IAYPIBMASNFSPL-UHFFFAOYSA-N Ethylene oxide Chemical compound C1CO1 IAYPIBMASNFSPL-UHFFFAOYSA-N 0.000 description 3
- 241000735527 Eupatorium Species 0.000 description 3
- 241001034433 Eutetranychus Species 0.000 description 3
- 239000005657 Fenpyroximate Substances 0.000 description 3
- PNVJTZOFSHSLTO-UHFFFAOYSA-N Fenthion Chemical compound COP(=S)(OC)OC1=CC=C(SC)C(C)=C1 PNVJTZOFSHSLTO-UHFFFAOYSA-N 0.000 description 3
- 201000006353 Filariasis Diseases 0.000 description 3
- 239000005781 Fludioxonil Substances 0.000 description 3
- 235000016623 Fragaria vesca Nutrition 0.000 description 3
- 240000009088 Fragaria x ananassa Species 0.000 description 3
- 235000011363 Fragaria x ananassa Nutrition 0.000 description 3
- 241000896533 Gliocladium Species 0.000 description 3
- PEDCQBHIVMGVHV-UHFFFAOYSA-N Glycerine Chemical compound OCC(O)CO PEDCQBHIVMGVHV-UHFFFAOYSA-N 0.000 description 3
- 241000606790 Haemophilus Species 0.000 description 3
- 235000003222 Helianthus annuus Nutrition 0.000 description 3
- 241000255967 Helicoverpa zea Species 0.000 description 3
- 241000256257 Heliothis Species 0.000 description 3
- 241000258937 Hemiptera Species 0.000 description 3
- 241001466007 Heteroptera Species 0.000 description 3
- 101000610640 Homo sapiens U4/U6 small nuclear ribonucleoprotein Prp3 Proteins 0.000 description 3
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 3
- 241000257303 Hymenoptera Species 0.000 description 3
- 241001149911 Isopoda Species 0.000 description 3
- 241001447252 Leptospora Species 0.000 description 3
- WMFOQBRAJBCJND-UHFFFAOYSA-M Lithium hydroxide Chemical compound [Li+].[OH-] WMFOQBRAJBCJND-UHFFFAOYSA-M 0.000 description 3
- 241000227653 Lycopersicon Species 0.000 description 3
- 235000007688 Lycopersicon esculentum Nutrition 0.000 description 3
- 241000220225 Malus Species 0.000 description 3
- 241000124008 Mammalia Species 0.000 description 3
- 239000005807 Metalaxyl Substances 0.000 description 3
- 241000237852 Mollusca Species 0.000 description 3
- 241001147660 Neospora Species 0.000 description 3
- JCXJVPUVTGWSNB-UHFFFAOYSA-N Nitrogen dioxide Chemical compound O=[N]=O JCXJVPUVTGWSNB-UHFFFAOYSA-N 0.000 description 3
- 241000488557 Oligonychus Species 0.000 description 3
- 241000238887 Ornithodoros Species 0.000 description 3
- MUBZPKHOEPUJKR-UHFFFAOYSA-N Oxalic acid Chemical compound OC(=O)C(O)=O MUBZPKHOEPUJKR-UHFFFAOYSA-N 0.000 description 3
- 239000004100 Oxytetracycline Substances 0.000 description 3
- 208000030852 Parasitic disease Diseases 0.000 description 3
- 241000238675 Periplaneta americana Species 0.000 description 3
- 241000219833 Phaseolus Species 0.000 description 3
- 241000222395 Phlebia Species 0.000 description 3
- 241000219843 Pisum Species 0.000 description 3
- 235000005805 Prunus cerasus Nutrition 0.000 description 3
- 240000002878 Prunus cerasus Species 0.000 description 3
- 241000589516 Pseudomonas Species 0.000 description 3
- 241000220324 Pyrus Species 0.000 description 3
- 244000184734 Pyrus japonica Species 0.000 description 3
- 235000019484 Rapeseed oil Nutrition 0.000 description 3
- 241001509970 Reticulitermes <genus> Species 0.000 description 3
- 241001481703 Rhipicephalus <genus> Species 0.000 description 3
- 241000235527 Rhizopus Species 0.000 description 3
- ISRUGXGCCGIOQO-UHFFFAOYSA-N Rhoden Chemical compound CNC(=O)OC1=CC=CC=C1OC(C)C ISRUGXGCCGIOQO-UHFFFAOYSA-N 0.000 description 3
- 241000125162 Rhopalosiphum Species 0.000 description 3
- 101001110823 Saccharomyces cerevisiae (strain ATCC 204508 / S288c) 60S ribosomal protein L6-A Proteins 0.000 description 3
- 101000712176 Saccharomyces cerevisiae (strain ATCC 204508 / S288c) 60S ribosomal protein L6-B Proteins 0.000 description 3
- 241000256250 Spodoptera littoralis Species 0.000 description 3
- 241000760908 Stenoptera Species 0.000 description 3
- 239000005934 Sulfoxaflor Substances 0.000 description 3
- 239000004098 Tetracycline Substances 0.000 description 3
- 208000004006 Tick-borne encephalitis Diseases 0.000 description 3
- 241000131345 Tipula <genus> Species 0.000 description 3
- 241000255901 Tortricidae Species 0.000 description 3
- 241000223996 Toxoplasma Species 0.000 description 3
- 235000019714 Triticale Nutrition 0.000 description 3
- 240000000359 Triticum dicoccon Species 0.000 description 3
- 102100040374 U4/U6 small nuclear ribonucleoprotein Prp3 Human genes 0.000 description 3
- 241000895647 Varroa Species 0.000 description 3
- 240000006365 Vitis vinifera Species 0.000 description 3
- 235000014787 Vitis vinifera Nutrition 0.000 description 3
- ZVQOOHYFBIDMTQ-UHFFFAOYSA-N [methyl(oxido){1-[6-(trifluoromethyl)pyridin-3-yl]ethyl}-lambda(6)-sulfanylidene]cyanamide Chemical compound N#CN=S(C)(=O)C(C)C1=CC=C(C(F)(F)F)N=C1 ZVQOOHYFBIDMTQ-UHFFFAOYSA-N 0.000 description 3
- 239000000853 adhesive Substances 0.000 description 3
- 230000001070 adhesive effect Effects 0.000 description 3
- 239000003513 alkali Substances 0.000 description 3
- 229910052783 alkali metal Inorganic materials 0.000 description 3
- 150000001340 alkali metals Chemical class 0.000 description 3
- 125000003545 alkoxy group Chemical group 0.000 description 3
- 125000002877 alkyl aryl group Chemical group 0.000 description 3
- 125000004682 aminothiocarbonyl group Chemical group NC(=S)* 0.000 description 3
- 235000011130 ammonium sulphate Nutrition 0.000 description 3
- 150000008064 anhydrides Chemical class 0.000 description 3
- 238000003975 animal breeding Methods 0.000 description 3
- 239000003904 antiprotozoal agent Substances 0.000 description 3
- 230000008901 benefit Effects 0.000 description 3
- FYZBOYWSHKHDMT-UHFFFAOYSA-N benfuracarb Chemical compound CCOC(=O)CCN(C(C)C)SN(C)C(=O)OC1=CC=CC2=C1OC(C)(C)C2 FYZBOYWSHKHDMT-UHFFFAOYSA-N 0.000 description 3
- 125000002619 bicyclic group Chemical group 0.000 description 3
- 239000011230 binding agent Substances 0.000 description 3
- 229960001901 bioallethrin Drugs 0.000 description 3
- 230000005540 biological transmission Effects 0.000 description 3
- 230000001488 breeding effect Effects 0.000 description 3
- KXRPCFINVWWFHQ-UHFFFAOYSA-N cadusafos Chemical compound CCC(C)SP(=O)(OCC)SC(C)CC KXRPCFINVWWFHQ-UHFFFAOYSA-N 0.000 description 3
- DUEPRVBVGDRKAG-UHFFFAOYSA-N carbofuran Chemical compound CNC(=O)OC1=CC=CC2=C1OC(C)(C)C2 DUEPRVBVGDRKAG-UHFFFAOYSA-N 0.000 description 3
- 239000001569 carbon dioxide Substances 0.000 description 3
- 229910002092 carbon dioxide Inorganic materials 0.000 description 3
- CWFOCCVIPCEQCK-UHFFFAOYSA-N chlorfenapyr Chemical compound BrC1=C(C(F)(F)F)N(COCC)C(C=2C=CC(Cl)=CC=2)=C1C#N CWFOCCVIPCEQCK-UHFFFAOYSA-N 0.000 description 3
- 235000020971 citrus fruits Nutrition 0.000 description 3
- ICJSJAJWTWPSBD-UHFFFAOYSA-N cloquintocet Chemical compound C1=CN=C2C(OCC(=O)O)=CC=C(Cl)C2=C1 ICJSJAJWTWPSBD-UHFFFAOYSA-N 0.000 description 3
- 239000011248 coating agent Substances 0.000 description 3
- 238000004440 column chromatography Methods 0.000 description 3
- 239000012141 concentrate Substances 0.000 description 3
- 235000008504 concentrate Nutrition 0.000 description 3
- BXNANOICGRISHX-UHFFFAOYSA-N coumaphos Chemical compound CC1=C(Cl)C(=O)OC2=CC(OP(=S)(OCC)OCC)=CC=C21 BXNANOICGRISHX-UHFFFAOYSA-N 0.000 description 3
- 229910001610 cryolite Inorganic materials 0.000 description 3
- SCKHCCSZFPSHGR-UHFFFAOYSA-N cyanophos Chemical compound COP(=S)(OC)OC1=CC=C(C#N)C=C1 SCKHCCSZFPSHGR-UHFFFAOYSA-N 0.000 description 3
- 125000000753 cycloalkyl group Chemical group 0.000 description 3
- KAATUXNTWXVJKI-UHFFFAOYSA-N cypermethrin Chemical compound CC1(C)C(C=C(Cl)Cl)C1C(=O)OC(C#N)C1=CC=CC(OC=2C=CC=CC=2)=C1 KAATUXNTWXVJKI-UHFFFAOYSA-N 0.000 description 3
- OAWUUPVZMNKZRY-UHFFFAOYSA-N cyprosulfamide Chemical compound COC1=CC=CC=C1C(=O)NS(=O)(=O)C1=CC=C(C(=O)NC2CC2)C=C1 OAWUUPVZMNKZRY-UHFFFAOYSA-N 0.000 description 3
- 230000006378 damage Effects 0.000 description 3
- 238000011161 development Methods 0.000 description 3
- 230000018109 developmental process Effects 0.000 description 3
- UOAMTSKGCBMZTC-UHFFFAOYSA-N dicofol Chemical compound C=1C=C(Cl)C=CC=1C(C(Cl)(Cl)Cl)(O)C1=CC=C(Cl)C=C1 UOAMTSKGCBMZTC-UHFFFAOYSA-N 0.000 description 3
- 238000010790 dilution Methods 0.000 description 3
- 239000012895 dilution Substances 0.000 description 3
- 229960002125 enilconazole Drugs 0.000 description 3
- 208000028104 epidemic louse-borne typhus Diseases 0.000 description 3
- WPNHOHPRXXCPRA-TVXIRPTOSA-N eprinomectin Chemical compound O1[C@@H](C)[C@@H](NC(C)=O)[C@H](OC)C[C@@H]1O[C@H]1[C@@H](OC)C[C@H](O[C@@H]2C(=C/C[C@@H]3C[C@@H](C[C@@]4(O3)C=C[C@H](C)[C@@H](C(C)C)O4)OC(=O)[C@@H]3C=C(C)[C@@H](O)[C@H]4OC\C([C@@]34O)=C\C=C/[C@@H]2C)\C)O[C@H]1C WPNHOHPRXXCPRA-TVXIRPTOSA-N 0.000 description 3
- 229960002346 eprinomectin Drugs 0.000 description 3
- RTZKZFJDLAIYFH-UHFFFAOYSA-N ether Substances CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 3
- 125000001301 ethoxy group Chemical group [H]C([H])([H])C([H])([H])O* 0.000 description 3
- 238000001704 evaporation Methods 0.000 description 3
- MUJOIMFVNIBMKC-UHFFFAOYSA-N fludioxonil Chemical compound C=12OC(F)(F)OC2=CC=CC=1C1=CNC=C1C#N MUJOIMFVNIBMKC-UHFFFAOYSA-N 0.000 description 3
- 239000006260 foam Substances 0.000 description 3
- 125000000524 functional group Chemical group 0.000 description 3
- JLYXXMFPNIAWKQ-UHFFFAOYSA-N gamma-hexachlorocyclohexane Natural products ClC1C(Cl)C(Cl)C(Cl)C(Cl)C1Cl JLYXXMFPNIAWKQ-UHFFFAOYSA-N 0.000 description 3
- 239000000499 gel Substances 0.000 description 3
- 238000010353 genetic engineering Methods 0.000 description 3
- 238000003898 horticulture Methods 0.000 description 3
- 239000012535 impurity Substances 0.000 description 3
- 239000012770 industrial material Substances 0.000 description 3
- PNDPGZBMCMUPRI-UHFFFAOYSA-N iodine Chemical compound II PNDPGZBMCMUPRI-UHFFFAOYSA-N 0.000 description 3
- INQOMBQAUSQDDS-UHFFFAOYSA-N iodomethane Chemical compound IC INQOMBQAUSQDDS-UHFFFAOYSA-N 0.000 description 3
- 229960002418 ivermectin Drugs 0.000 description 3
- 229930014550 juvenile hormone Natural products 0.000 description 3
- 239000002949 juvenile hormone Substances 0.000 description 3
- 150000003633 juvenile hormone derivatives Chemical class 0.000 description 3
- 239000003120 macrolide antibiotic agent Substances 0.000 description 3
- 229940041033 macrolides Drugs 0.000 description 3
- 238000004519 manufacturing process Methods 0.000 description 3
- ZQEIXNIJLIKNTD-UHFFFAOYSA-N methyl N-(2,6-dimethylphenyl)-N-(methoxyacetyl)alaninate Chemical compound COCC(=O)N(C(C)C(=O)OC)C1=C(C)C=CC=C1C ZQEIXNIJLIKNTD-UHFFFAOYSA-N 0.000 description 3
- CJPQIRJHIZUAQP-UHFFFAOYSA-N methyl N-(2,6-dimethylphenyl)-N-(phenylacetyl)alaninate Chemical compound CC=1C=CC=C(C)C=1N(C(C)C(=O)OC)C(=O)CC1=CC=CC=C1 CJPQIRJHIZUAQP-UHFFFAOYSA-N 0.000 description 3
- 229960001952 metrifonate Drugs 0.000 description 3
- 230000000813 microbial effect Effects 0.000 description 3
- NJPPVKZQTLUDBO-UHFFFAOYSA-N novaluron Chemical compound C1=C(Cl)C(OC(F)(F)C(OC(F)(F)F)F)=CC=C1NC(=O)NC(=O)C1=C(F)C=CC=C1F NJPPVKZQTLUDBO-UHFFFAOYSA-N 0.000 description 3
- 238000000655 nuclear magnetic resonance spectrum Methods 0.000 description 3
- IWVCMVBTMGNXQD-PXOLEDIWSA-N oxytetracycline Chemical compound C1=CC=C2[C@](O)(C)[C@H]3[C@H](O)[C@H]4[C@H](N(C)C)C(O)=C(C(N)=O)C(=O)[C@@]4(O)C(O)=C3C(=O)C2=C1O IWVCMVBTMGNXQD-PXOLEDIWSA-N 0.000 description 3
- 229960000625 oxytetracycline Drugs 0.000 description 3
- 235000019366 oxytetracycline Nutrition 0.000 description 3
- 229910052763 palladium Inorganic materials 0.000 description 3
- RLBIQVVOMOPOHC-UHFFFAOYSA-N parathion-methyl Chemical compound COP(=S)(OC)OC1=CC=C([N+]([O-])=O)C=C1 RLBIQVVOMOPOHC-UHFFFAOYSA-N 0.000 description 3
- 230000001717 pathogenic effect Effects 0.000 description 3
- RLLPVAHGXHCWKJ-UHFFFAOYSA-N permethrin Chemical compound CC1(C)C(C=C(Cl)Cl)C1C(=O)OCC1=CC=CC(OC=2C=CC=CC=2)=C1 RLLPVAHGXHCWKJ-UHFFFAOYSA-N 0.000 description 3
- 239000003208 petroleum Substances 0.000 description 3
- 150000002989 phenols Chemical class 0.000 description 3
- 230000008635 plant growth Effects 0.000 description 3
- 229920003023 plastic Polymers 0.000 description 3
- 239000004033 plastic Substances 0.000 description 3
- 239000003880 polar aprotic solvent Substances 0.000 description 3
- 229920000642 polymer Polymers 0.000 description 3
- 239000003755 preservative agent Substances 0.000 description 3
- 125000002924 primary amino group Chemical group [H]N([H])* 0.000 description 3
- KJRCEJOSASVSRA-UHFFFAOYSA-N propane-2-thiol Chemical compound CC(C)S KJRCEJOSASVSRA-UHFFFAOYSA-N 0.000 description 3
- CXJSOEPQXUCJSA-UHFFFAOYSA-N pyridaphenthion Chemical compound N1=C(OP(=S)(OCC)OCC)C=CC(=O)N1C1=CC=CC=C1 CXJSOEPQXUCJSA-UHFFFAOYSA-N 0.000 description 3
- 229940108410 resmethrin Drugs 0.000 description 3
- VEMKTZHHVJILDY-FIWHBWSRSA-N resmethrin Chemical compound CC1(C)[C@H](C=C(C)C)C1C(=O)OCC1=COC(CC=2C=CC=CC=2)=C1 VEMKTZHHVJILDY-FIWHBWSRSA-N 0.000 description 3
- 239000011435 rock Substances 0.000 description 3
- JUVIOZPCNVVQFO-UHFFFAOYSA-N rotenone Natural products O1C2=C3CC(C(C)=C)OC3=CC=C2C(=O)C2C1COC1=C2C=C(OC)C(OC)=C1 JUVIOZPCNVVQFO-UHFFFAOYSA-N 0.000 description 3
- 238000009331 sowing Methods 0.000 description 3
- 238000001228 spectrum Methods 0.000 description 3
- 239000007921 spray Substances 0.000 description 3
- 239000003381 stabilizer Substances 0.000 description 3
- 239000005936 tau-Fluvalinate Substances 0.000 description 3
- INISTDXBRIBGOC-XMMISQBUSA-N tau-fluvalinate Chemical compound N([C@H](C(C)C)C(=O)OC(C#N)C=1C=C(OC=2C=CC=CC=2)C=CC=1)C1=CC=C(C(F)(F)F)C=C1Cl INISTDXBRIBGOC-XMMISQBUSA-N 0.000 description 3
- IWVCMVBTMGNXQD-UHFFFAOYSA-N terramycin dehydrate Natural products C1=CC=C2C(O)(C)C3C(O)C4C(N(C)C)C(O)=C(C(N)=O)C(=O)C4(O)C(O)=C3C(=O)C2=C1O IWVCMVBTMGNXQD-UHFFFAOYSA-N 0.000 description 3
- 235000019364 tetracycline Nutrition 0.000 description 3
- 150000003522 tetracyclines Chemical class 0.000 description 3
- ZMZDMBWJUHKJPS-UHFFFAOYSA-N thiocyanic acid Chemical compound SC#N ZMZDMBWJUHKJPS-UHFFFAOYSA-N 0.000 description 3
- 150000003573 thiols Chemical class 0.000 description 3
- YFNCATAIYKQPOO-UHFFFAOYSA-N thiophanate Chemical compound CCOC(=O)NC(=S)NC1=CC=CC=C1NC(=S)NC(=O)OCC YFNCATAIYKQPOO-UHFFFAOYSA-N 0.000 description 3
- ITMCEJHCFYSIIV-UHFFFAOYSA-M triflate Chemical compound [O-]S(=O)(=O)C(F)(F)F ITMCEJHCFYSIIV-UHFFFAOYSA-M 0.000 description 3
- 241000701366 unidentified nuclear polyhedrosis viruses Species 0.000 description 3
- 241000228158 x Triticosecale Species 0.000 description 3
- ZCVAOQKBXKSDMS-AQYZNVCMSA-N (+)-trans-allethrin Chemical compound CC1(C)[C@H](C=C(C)C)[C@H]1C(=O)OC1C(C)=C(CC=C)C(=O)C1 ZCVAOQKBXKSDMS-AQYZNVCMSA-N 0.000 description 2
- KAATUXNTWXVJKI-GGPKGHCWSA-N (1R)-trans-(alphaS)-cypermethrin Chemical compound CC1(C)[C@H](C=C(Cl)Cl)[C@H]1C(=O)O[C@H](C#N)C1=CC=CC(OC=2C=CC=CC=2)=C1 KAATUXNTWXVJKI-GGPKGHCWSA-N 0.000 description 2
- FJDPATXIBIBRIM-QFMSAKRMSA-N (1R)-trans-cyphenothrin Chemical compound CC1(C)[C@H](C=C(C)C)[C@H]1C(=O)OC(C#N)C1=CC=CC(OC=2C=CC=CC=2)=C1 FJDPATXIBIBRIM-QFMSAKRMSA-N 0.000 description 2
- ZXQYGBMAQZUVMI-RDDWSQKMSA-N (1S)-cis-(alphaR)-cyhalothrin Chemical compound CC1(C)[C@H](\C=C(/Cl)C(F)(F)F)[C@@H]1C(=O)O[C@@H](C#N)C1=CC=CC(OC=2C=CC=CC=2)=C1 ZXQYGBMAQZUVMI-RDDWSQKMSA-N 0.000 description 2
- ZMYFCFLJBGAQRS-IAGOWNOFSA-N (2S,3R)-epoxiconazole Chemical compound C1=CC(F)=CC=C1[C@]1(CN2N=CN=C2)[C@@H](C=2C(=CC=CC=2)Cl)O1 ZMYFCFLJBGAQRS-IAGOWNOFSA-N 0.000 description 2
- RYAUSSKQMZRMAI-ALOPSCKCSA-N (2S,6R)-4-[3-(4-tert-butylphenyl)-2-methylpropyl]-2,6-dimethylmorpholine Chemical compound C=1C=C(C(C)(C)C)C=CC=1CC(C)CN1C[C@H](C)O[C@H](C)C1 RYAUSSKQMZRMAI-ALOPSCKCSA-N 0.000 description 2
- LDVVMCZRFWMZSG-OLQVQODUSA-N (3ar,7as)-2-(trichloromethylsulfanyl)-3a,4,7,7a-tetrahydroisoindole-1,3-dione Chemical compound C1C=CC[C@H]2C(=O)N(SC(Cl)(Cl)Cl)C(=O)[C@H]21 LDVVMCZRFWMZSG-OLQVQODUSA-N 0.000 description 2
- SGKRLCUYIXIAHR-AKNGSSGZSA-N (4s,4ar,5s,5ar,6r,12ar)-4-(dimethylamino)-1,5,10,11,12a-pentahydroxy-6-methyl-3,12-dioxo-4a,5,5a,6-tetrahydro-4h-tetracene-2-carboxamide Chemical compound C1=CC=C2[C@H](C)[C@@H]([C@H](O)[C@@H]3[C@](C(O)=C(C(N)=O)C(=O)[C@H]3N(C)C)(O)C3=O)C3=C(O)C2=C1O SGKRLCUYIXIAHR-AKNGSSGZSA-N 0.000 description 2
- PPDBOQMNKNNODG-NTEUORMPSA-N (5E)-5-(4-chlorobenzylidene)-2,2-dimethyl-1-(1,2,4-triazol-1-ylmethyl)cyclopentanol Chemical compound C1=NC=NN1CC1(O)C(C)(C)CC\C1=C/C1=CC=C(Cl)C=C1 PPDBOQMNKNNODG-NTEUORMPSA-N 0.000 description 2
- 125000000229 (C1-C4)alkoxy group Chemical group 0.000 description 2
- 125000000171 (C1-C6) haloalkyl group Chemical group 0.000 description 2
- 125000006643 (C2-C6) haloalkenyl group Chemical group 0.000 description 2
- 125000005913 (C3-C6) cycloalkyl group Chemical group 0.000 description 2
- WCXDHFDTOYPNIE-RIYZIHGNSA-N (E)-acetamiprid Chemical compound N#C/N=C(\C)N(C)CC1=CC=C(Cl)N=C1 WCXDHFDTOYPNIE-RIYZIHGNSA-N 0.000 description 2
- PGOOBECODWQEAB-UHFFFAOYSA-N (E)-clothianidin Chemical compound [O-][N+](=O)\N=C(/NC)NCC1=CN=C(Cl)S1 PGOOBECODWQEAB-UHFFFAOYSA-N 0.000 description 2
- BKBSMMUEEAWFRX-NBVRZTHBSA-N (E)-flumorph Chemical compound C1=C(OC)C(OC)=CC=C1C(\C=1C=CC(F)=CC=1)=C\C(=O)N1CCOCC1 BKBSMMUEEAWFRX-NBVRZTHBSA-N 0.000 description 2
- CFRPSFYHXJZSBI-DHZHZOJOSA-N (E)-nitenpyram Chemical compound [O-][N+](=O)/C=C(\NC)N(CC)CC1=CC=C(Cl)N=C1 CFRPSFYHXJZSBI-DHZHZOJOSA-N 0.000 description 2
- WHTVZRBIWZFKQO-AWEZNQCLSA-N (S)-chloroquine Chemical compound ClC1=CC=C2C(N[C@@H](C)CCCN(CC)CC)=CC=NC2=C1 WHTVZRBIWZFKQO-AWEZNQCLSA-N 0.000 description 2
- ZFHGXWPMULPQSE-SZGBIDFHSA-N (Z)-(1S)-cis-tefluthrin Chemical compound FC1=C(F)C(C)=C(F)C(F)=C1COC(=O)[C@@H]1C(C)(C)[C@@H]1\C=C(/Cl)C(F)(F)F ZFHGXWPMULPQSE-SZGBIDFHSA-N 0.000 description 2
- HNSDLXPSAYFUHK-UHFFFAOYSA-N 1,4-bis(2-ethylhexyl) sulfosuccinate Chemical compound CCCCC(CC)COC(=O)CC(S(O)(=O)=O)C(=O)OCC(CC)CCCC HNSDLXPSAYFUHK-UHFFFAOYSA-N 0.000 description 2
- PXMNMQRDXWABCY-UHFFFAOYSA-N 1-(4-chlorophenyl)-4,4-dimethyl-3-(1H-1,2,4-triazol-1-ylmethyl)pentan-3-ol Chemical compound C1=NC=NN1CC(O)(C(C)(C)C)CCC1=CC=C(Cl)C=C1 PXMNMQRDXWABCY-UHFFFAOYSA-N 0.000 description 2
- JZWGZVIBYWRECK-RUMWWMSVSA-N 1-[(e)-[2-(4-cyanophenyl)-1-[3-(trifluoromethyl)phenyl]ethylidene]amino]-3-[4-(difluoromethoxy)phenyl]urea Chemical compound C1=CC(OC(F)F)=CC=C1NC(=O)N\N=C(C=1C=C(C=CC=1)C(F)(F)F)/CC1=CC=C(C#N)C=C1 JZWGZVIBYWRECK-RUMWWMSVSA-N 0.000 description 2
- LQDARGUHUSPFNL-UHFFFAOYSA-N 1-[2-(2,4-dichlorophenyl)-3-(1,1,2,2-tetrafluoroethoxy)propyl]1,2,4-triazole Chemical compound C=1C=C(Cl)C=C(Cl)C=1C(COC(F)(F)C(F)F)CN1C=NC=N1 LQDARGUHUSPFNL-UHFFFAOYSA-N 0.000 description 2
- PZBPKYOVPCNPJY-UHFFFAOYSA-N 1-[2-(allyloxy)-2-(2,4-dichlorophenyl)ethyl]imidazole Chemical compound ClC1=CC(Cl)=CC=C1C(OCC=C)CN1C=NC=C1 PZBPKYOVPCNPJY-UHFFFAOYSA-N 0.000 description 2
- MGNFYQILYYYUBS-UHFFFAOYSA-N 1-[3-(4-tert-butylphenyl)-2-methylpropyl]piperidine Chemical compound C=1C=C(C(C)(C)C)C=CC=1CC(C)CN1CCCCC1 MGNFYQILYYYUBS-UHFFFAOYSA-N 0.000 description 2
- 125000006426 1-chlorocyclopropyl group Chemical group [H]C1([H])C([H])([H])C1(Cl)* 0.000 description 2
- NVEPPWDVLBMNMB-SNAWJCMRSA-N 1-methyl-2-[(e)-2-(3-methylthiophen-2-yl)ethenyl]-5,6-dihydro-4h-pyrimidine Chemical compound CN1CCCN=C1\C=C\C1=C(C)C=CS1 NVEPPWDVLBMNMB-SNAWJCMRSA-N 0.000 description 2
- OCINXEZVIIVXFU-UHFFFAOYSA-N 1-methyl-3-[3-methyl-4-[4-(trifluoromethylthio)phenoxy]phenyl]-1,3,5-triazinane-2,4,6-trione Chemical compound CC1=CC(N2C(N(C)C(=O)NC2=O)=O)=CC=C1OC1=CC=C(SC(F)(F)F)C=C1 OCINXEZVIIVXFU-UHFFFAOYSA-N 0.000 description 2
- PFFIDZXUXFLSSR-UHFFFAOYSA-N 1-methyl-N-[2-(4-methylpentan-2-yl)-3-thienyl]-3-(trifluoromethyl)pyrazole-4-carboxamide Chemical compound S1C=CC(NC(=O)C=2C(=NN(C)C=2)C(F)(F)F)=C1C(C)CC(C)C PFFIDZXUXFLSSR-UHFFFAOYSA-N 0.000 description 2
- NFGXHKASABOEEW-UHFFFAOYSA-N 1-methylethyl 11-methoxy-3,7,11-trimethyl-2,4-dodecadienoate Chemical compound COC(C)(C)CCCC(C)CC=CC(C)=CC(=O)OC(C)C NFGXHKASABOEEW-UHFFFAOYSA-N 0.000 description 2
- FMTFEIJHMMQUJI-NJAFHUGGSA-N 102130-98-3 Natural products CC=CCC1=C(C)[C@H](CC1=O)OC(=O)[C@@H]1[C@@H](C=C(C)C)C1(C)C FMTFEIJHMMQUJI-NJAFHUGGSA-N 0.000 description 2
- GQHTUMJGOHRCHB-UHFFFAOYSA-N 2,3,4,6,7,8,9,10-octahydropyrimido[1,2-a]azepine Chemical compound C1CCCCN2CCCN=C21 GQHTUMJGOHRCHB-UHFFFAOYSA-N 0.000 description 2
- 125000004201 2,4-dichlorophenyl group Chemical group [H]C1=C([H])C(*)=C(Cl)C([H])=C1Cl 0.000 description 2
- YTOPFCCWCSOHFV-UHFFFAOYSA-N 2,6-dimethyl-4-tridecylmorpholine Chemical compound CCCCCCCCCCCCCN1CC(C)OC(C)C1 YTOPFCCWCSOHFV-UHFFFAOYSA-N 0.000 description 2
- ZSZFUDFOPOMEET-UHFFFAOYSA-N 2-(4-chlorophenyl)-2-[2,6-dichloro-4-(3,5-dioxo-1,2,4-triazin-2-yl)phenyl]acetonitrile Chemical compound C1=CC(Cl)=CC=C1C(C#N)C1=C(Cl)C=C(N2C(NC(=O)C=N2)=O)C=C1Cl ZSZFUDFOPOMEET-UHFFFAOYSA-N 0.000 description 2
- UFNOUKDBUJZYDE-UHFFFAOYSA-N 2-(4-chlorophenyl)-3-cyclopropyl-1-(1H-1,2,4-triazol-1-yl)butan-2-ol Chemical compound C1=NC=NN1CC(O)(C=1C=CC(Cl)=CC=1)C(C)C1CC1 UFNOUKDBUJZYDE-UHFFFAOYSA-N 0.000 description 2
- XQKYUBTUOHHNDV-UHFFFAOYSA-N 2-[2,6-dichloro-4-(3,5-dioxo-1,2,4-triazin-2-yl)phenyl]-2-(4-fluorophenyl)acetonitrile Chemical compound C1=CC(F)=CC=C1C(C#N)C1=C(Cl)C=C(N2C(NC(=O)C=N2)=O)C=C1Cl XQKYUBTUOHHNDV-UHFFFAOYSA-N 0.000 description 2
- WCBVUETZRWGIJQ-UHFFFAOYSA-N 2-[[(methoxycarbonylamino)-(2-nitro-5-propylsulfanylanilino)methylidene]amino]ethanesulfonic acid Chemical compound CCCSC1=CC=C([N+]([O-])=O)C(NC(NC(=O)OC)=NCCS(O)(=O)=O)=C1 WCBVUETZRWGIJQ-UHFFFAOYSA-N 0.000 description 2
- FSVJFNAIGNNGKK-UHFFFAOYSA-N 2-[cyclohexyl(oxo)methyl]-3,6,7,11b-tetrahydro-1H-pyrazino[2,1-a]isoquinolin-4-one Chemical compound C1C(C2=CC=CC=C2CC2)N2C(=O)CN1C(=O)C1CCCCC1 FSVJFNAIGNNGKK-UHFFFAOYSA-N 0.000 description 2
- GXEUNRBWEAIPCN-UHFFFAOYSA-N 2-chloro-2-(3-chloro-4-cyclohexylphenyl)acetic acid Chemical compound ClC1=CC(C(Cl)C(=O)O)=CC=C1C1CCCCC1 GXEUNRBWEAIPCN-UHFFFAOYSA-N 0.000 description 2
- XWKFPIODWVPXLX-UHFFFAOYSA-N 2-methyl-5-methylpyridine Natural products CC1=CC=C(C)N=C1 XWKFPIODWVPXLX-UHFFFAOYSA-N 0.000 description 2
- BSKHPKMHTQYZBB-UHFFFAOYSA-N 2-methylpyridine Chemical compound CC1=CC=CC=N1 BSKHPKMHTQYZBB-UHFFFAOYSA-N 0.000 description 2
- SOUGWDPPRBKJEX-UHFFFAOYSA-N 3,5-dichloro-N-(1-chloro-3-methyl-2-oxopentan-3-yl)-4-methylbenzamide Chemical compound ClCC(=O)C(C)(CC)NC(=O)C1=CC(Cl)=C(C)C(Cl)=C1 SOUGWDPPRBKJEX-UHFFFAOYSA-N 0.000 description 2
- FSCWZHGZWWDELK-UHFFFAOYSA-N 3-(3,5-dichlorophenyl)-5-ethenyl-5-methyl-2,4-oxazolidinedione Chemical compound O=C1C(C)(C=C)OC(=O)N1C1=CC(Cl)=CC(Cl)=C1 FSCWZHGZWWDELK-UHFFFAOYSA-N 0.000 description 2
- PKTIFYGCWCQRSX-UHFFFAOYSA-N 4,6-diamino-2-(cyclopropylamino)pyrimidine-5-carbonitrile Chemical compound NC1=C(C#N)C(N)=NC(NC2CC2)=N1 PKTIFYGCWCQRSX-UHFFFAOYSA-N 0.000 description 2
- ZXVONLUNISGICL-UHFFFAOYSA-N 4,6-dinitro-o-cresol Chemical compound CC1=CC([N+]([O-])=O)=CC([N+]([O-])=O)=C1O ZXVONLUNISGICL-UHFFFAOYSA-N 0.000 description 2
- UTNPLPXWDUEIJI-UHFFFAOYSA-N 4-[3-[2,6-dichloro-4-(3,3-dichloroprop-2-enoxy)phenoxy]propoxy]-2-methoxy-6-(trifluoromethyl)pyrimidine Chemical compound FC(F)(F)C1=NC(OC)=NC(OCCCOC=2C(=CC(OCC=C(Cl)Cl)=CC=2Cl)Cl)=C1 UTNPLPXWDUEIJI-UHFFFAOYSA-N 0.000 description 2
- IVJKCSCRNVMPNG-OWOJBTEDSA-N 5-[[(E)-3-chloroprop-2-enyl]amino]-1-[2,6-dichloro-4-(trifluoromethyl)phenyl]-4-(trifluoromethylsulfinyl)pyrazole-3-carbonitrile Chemical compound Cl/C=C/CNC1=C(C(=NN1C1=C(C=C(C=C1Cl)C(F)(F)F)Cl)C#N)S(=O)C(F)(F)F IVJKCSCRNVMPNG-OWOJBTEDSA-N 0.000 description 2
- ZOCSXAVNDGMNBV-UHFFFAOYSA-N 5-amino-1-[2,6-dichloro-4-(trifluoromethyl)phenyl]-4-[(trifluoromethyl)sulfinyl]-1H-pyrazole-3-carbonitrile Chemical compound NC1=C(S(=O)C(F)(F)F)C(C#N)=NN1C1=C(Cl)C=C(C(F)(F)F)C=C1Cl ZOCSXAVNDGMNBV-UHFFFAOYSA-N 0.000 description 2
- GOFJDXZZHFNFLV-UHFFFAOYSA-N 5-fluoro-1,3-dimethyl-N-[2-(4-methylpentan-2-yl)phenyl]pyrazole-4-carboxamide Chemical compound CC(C)CC(C)C1=CC=CC=C1NC(=O)C1=C(F)N(C)N=C1C GOFJDXZZHFNFLV-UHFFFAOYSA-N 0.000 description 2
- PCCSBWNGDMYFCW-UHFFFAOYSA-N 5-methyl-5-(4-phenoxyphenyl)-3-(phenylamino)-1,3-oxazolidine-2,4-dione Chemical compound O=C1C(C)(C=2C=CC(OC=3C=CC=CC=3)=CC=2)OC(=O)N1NC1=CC=CC=C1 PCCSBWNGDMYFCW-UHFFFAOYSA-N 0.000 description 2
- VLZKCYMZEMSKHI-UHFFFAOYSA-N 7-ethylsulfanyl-[1,3]thiazolo[4,5-c]pyridine-6-carboxylic acid Chemical compound C(C)SC=1C2=C(C=NC=1C(=O)O)N=CS2 VLZKCYMZEMSKHI-UHFFFAOYSA-N 0.000 description 2
- SSGYGAPSMCXVPJ-UHFFFAOYSA-N 7-ethylsulfinyl-6-[3-methyl-6-(trifluoromethyl)imidazo[4,5-b]pyridin-2-yl]-[1,3]thiazolo[4,5-c]pyridine Chemical compound CCS(=O)c1c(ncc2ncsc12)-c1nc2cc(cnc2n1C)C(F)(F)F SSGYGAPSMCXVPJ-UHFFFAOYSA-N 0.000 description 2
- LTWLQARCXSOXFR-UHFFFAOYSA-N 7-ethylsulfonyl-6-[3-methyl-6-(trifluoromethyl)imidazo[4,5-b]pyridin-2-yl]-[1,3]thiazolo[4,5-c]pyridine Chemical compound CCS(=O)(=O)c1c(ncc2ncsc12)-c1nc2cc(cnc2n1C)C(F)(F)F LTWLQARCXSOXFR-UHFFFAOYSA-N 0.000 description 2
- 241000700606 Acanthocephala Species 0.000 description 2
- 241001558864 Aceria Species 0.000 description 2
- 239000005875 Acetamiprid Substances 0.000 description 2
- 239000005964 Acibenzolar-S-methyl Substances 0.000 description 2
- 241000158748 Acronychia Species 0.000 description 2
- 241000251468 Actinopterygii Species 0.000 description 2
- 241000256173 Aedes albopictus Species 0.000 description 2
- 241000566547 Agrotis ipsilon Species 0.000 description 2
- 241000218475 Agrotis segetum Species 0.000 description 2
- 235000002732 Allium cepa var. cepa Nutrition 0.000 description 2
- 239000005726 Ametoctradin Substances 0.000 description 2
- 241000380490 Anguina Species 0.000 description 2
- 241000256182 Anopheles gambiae Species 0.000 description 2
- 241001626718 Anoplocephala Species 0.000 description 2
- 241000272517 Anseriformes Species 0.000 description 2
- 241000294569 Aphelenchoides Species 0.000 description 2
- 241000952610 Aphis glycines Species 0.000 description 2
- 241001600408 Aphis gossypii Species 0.000 description 2
- 241000256836 Apis Species 0.000 description 2
- 241001048568 Apolygus lucorum Species 0.000 description 2
- 108700040321 Arabidopsis SPP Proteins 0.000 description 2
- 241000402204 Arachnocampa Species 0.000 description 2
- 241000239290 Araneae Species 0.000 description 2
- 241000238888 Argasidae Species 0.000 description 2
- XKRFYHLGVUSROY-UHFFFAOYSA-N Argon Chemical compound [Ar] XKRFYHLGVUSROY-UHFFFAOYSA-N 0.000 description 2
- 235000003097 Artemisia absinthium Nutrition 0.000 description 2
- 240000002877 Artemisia absinthium Species 0.000 description 2
- 241000244186 Ascaris Species 0.000 description 2
- 241000222400 Athelia Species 0.000 description 2
- 239000005730 Azoxystrobin Substances 0.000 description 2
- 241000193744 Bacillus amyloliquefaciens Species 0.000 description 2
- 241000193755 Bacillus cereus Species 0.000 description 2
- 241000193747 Bacillus firmus Species 0.000 description 2
- 241000194103 Bacillus pumilus Species 0.000 description 2
- SPFYMRJSYKOXGV-UHFFFAOYSA-N Baytril Chemical compound C1CN(CC)CCN1C(C(=C1)F)=CC2=C1C(=O)C(C(O)=O)=CN2C1CC1 SPFYMRJSYKOXGV-UHFFFAOYSA-N 0.000 description 2
- 241000751139 Beauveria bassiana Species 0.000 description 2
- 239000005736 Benthiavalicarb Substances 0.000 description 2
- 239000005737 Benzovindiflupyr Substances 0.000 description 2
- 235000016068 Berberis vulgaris Nutrition 0.000 description 2
- 241000335053 Beta vulgaris Species 0.000 description 2
- 239000005884 Beta-Cyfluthrin Substances 0.000 description 2
- BVKZGUZCCUSVTD-UHFFFAOYSA-M Bicarbonate Chemical class OC([O-])=O BVKZGUZCCUSVTD-UHFFFAOYSA-M 0.000 description 2
- 239000005653 Bifenazate Substances 0.000 description 2
- 239000005874 Bifenthrin Substances 0.000 description 2
- 239000005738 Bixafen Substances 0.000 description 2
- 241000238662 Blatta orientalis Species 0.000 description 2
- 235000014698 Brassica juncea var multisecta Nutrition 0.000 description 2
- 235000003899 Brassica oleracea var acephala Nutrition 0.000 description 2
- 235000011301 Brassica oleracea var capitata Nutrition 0.000 description 2
- 235000001169 Brassica oleracea var oleracea Nutrition 0.000 description 2
- 235000006618 Brassica rapa subsp oleifera Nutrition 0.000 description 2
- 241000219193 Brassicaceae Species 0.000 description 2
- 241000244036 Brugia Species 0.000 description 2
- 239000005885 Buprofezin Substances 0.000 description 2
- 241000589513 Burkholderia cepacia Species 0.000 description 2
- 125000000882 C2-C6 alkenyl group Chemical group 0.000 description 2
- 125000003601 C2-C6 alkynyl group Chemical group 0.000 description 2
- JFLRKDZMHNBDQS-UCQUSYKYSA-N CC[C@H]1CCC[C@@H]([C@H](C(=O)C2=C[C@H]3[C@@H]4C[C@@H](C[C@H]4C(=C[C@H]3[C@@H]2CC(=O)O1)C)O[C@H]5[C@@H]([C@@H]([C@H]([C@@H](O5)C)OC)OC)OC)C)O[C@H]6CC[C@@H]([C@H](O6)C)N(C)C.CC[C@H]1CCC[C@@H]([C@H](C(=O)C2=C[C@H]3[C@@H]4C[C@@H](C[C@H]4C=C[C@H]3C2CC(=O)O1)O[C@H]5[C@@H]([C@@H]([C@H]([C@@H](O5)C)OC)OC)OC)C)O[C@H]6CC[C@@H]([C@H](O6)C)N(C)C Chemical compound CC[C@H]1CCC[C@@H]([C@H](C(=O)C2=C[C@H]3[C@@H]4C[C@@H](C[C@H]4C(=C[C@H]3[C@@H]2CC(=O)O1)C)O[C@H]5[C@@H]([C@@H]([C@H]([C@@H](O5)C)OC)OC)OC)C)O[C@H]6CC[C@@H]([C@H](O6)C)N(C)C.CC[C@H]1CCC[C@@H]([C@H](C(=O)C2=C[C@H]3[C@@H]4C[C@@H](C[C@H]4C=C[C@H]3C2CC(=O)O1)O[C@H]5[C@@H]([C@@H]([C@H]([C@@H](O5)C)OC)OC)OC)C)O[C@H]6CC[C@@H]([C@H](O6)C)N(C)C JFLRKDZMHNBDQS-UCQUSYKYSA-N 0.000 description 2
- OYPRJOBELJOOCE-UHFFFAOYSA-N Calcium Chemical compound [Ca] OYPRJOBELJOOCE-UHFFFAOYSA-N 0.000 description 2
- 241001468265 Candidatus Phytoplasma Species 0.000 description 2
- 239000005745 Captan Substances 0.000 description 2
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 2
- 239000005746 Carboxin Substances 0.000 description 2
- 241001347511 Carposina sasakii Species 0.000 description 2
- 241000282985 Cervus Species 0.000 description 2
- 241000242722 Cestoda Species 0.000 description 2
- 241000426499 Chilo Species 0.000 description 2
- 241000426497 Chilo suppressalis Species 0.000 description 2
- 239000005886 Chlorantraniliprole Substances 0.000 description 2
- 108010062745 Chloride Channels Proteins 0.000 description 2
- 102000011045 Chloride Channels Human genes 0.000 description 2
- 239000005887 Chromafenozide Substances 0.000 description 2
- 241000191839 Chrysomya Species 0.000 description 2
- 241001635683 Cimex hemipterus Species 0.000 description 2
- DHQKLWKZSFCKTA-UHFFFAOYSA-N ClC1=CC=C(C=N1)CN1C(C=CC=C1)=NC(C(F)(F)F)=O Chemical compound ClC1=CC=C(C=N1)CN1C(C=CC=C1)=NC(C(F)(F)F)=O DHQKLWKZSFCKTA-UHFFFAOYSA-N 0.000 description 2
- 241001327942 Clonorchis Species 0.000 description 2
- 239000005888 Clothianidin Substances 0.000 description 2
- 241000212948 Cnidium Species 0.000 description 2
- 241000224483 Coccidia Species 0.000 description 2
- 241001465977 Coccoidea Species 0.000 description 2
- 235000013162 Cocos nucifera Nutrition 0.000 description 2
- 244000060011 Cocos nucifera Species 0.000 description 2
- 241000988860 Codia Species 0.000 description 2
- JJLJMEJHUUYSSY-UHFFFAOYSA-L Copper hydroxide Chemical compound [OH-].[OH-].[Cu+2] JJLJMEJHUUYSSY-UHFFFAOYSA-L 0.000 description 2
- 241001509964 Coptotermes Species 0.000 description 2
- 241000186216 Corynebacterium Species 0.000 description 2
- 241001081178 Cryptocarya Species 0.000 description 2
- 241000490513 Ctenocephalides canis Species 0.000 description 2
- 241000258924 Ctenocephalides felis Species 0.000 description 2
- 240000008067 Cucumis sativus Species 0.000 description 2
- 235000010799 Cucumis sativus var sativus Nutrition 0.000 description 2
- 241000256054 Culex <genus> Species 0.000 description 2
- 241000254171 Curculionidae Species 0.000 description 2
- 244000007835 Cyamopsis tetragonoloba Species 0.000 description 2
- 239000005889 Cyantraniliprole Substances 0.000 description 2
- 239000005755 Cyflufenamid Substances 0.000 description 2
- 239000005757 Cyproconazole Substances 0.000 description 2
- 239000005758 Cyprodinil Substances 0.000 description 2
- 239000005644 Dazomet Substances 0.000 description 2
- 239000005892 Deltamethrin Substances 0.000 description 2
- 241001128004 Demodex Species 0.000 description 2
- 241001481694 Dermanyssus Species 0.000 description 2
- YRMLFORXOOIJDR-UHFFFAOYSA-N Dichlormid Chemical compound ClC(Cl)C(=O)N(CC=C)CC=C YRMLFORXOOIJDR-UHFFFAOYSA-N 0.000 description 2
- MDNWOSOZYLHTCG-UHFFFAOYSA-N Dichlorophen Chemical compound OC1=CC=C(Cl)C=C1CC1=CC(Cl)=CC=C1O MDNWOSOZYLHTCG-UHFFFAOYSA-N 0.000 description 2
- 239000005759 Diethofencarb Substances 0.000 description 2
- 239000005760 Difenoconazole Substances 0.000 description 2
- IAZDPXIOMUYVGZ-WFGJKAKNSA-N Dimethyl sulfoxide Chemical compound [2H]C([2H])([2H])S(=O)C([2H])([2H])[2H] IAZDPXIOMUYVGZ-WFGJKAKNSA-N 0.000 description 2
- 241000258963 Diplopoda Species 0.000 description 2
- 241000255601 Drosophila melanogaster Species 0.000 description 2
- 241000241133 Earias Species 0.000 description 2
- 241000223931 Eimeria acervulina Species 0.000 description 2
- 241000499566 Eimeria brunetti Species 0.000 description 2
- 241000223934 Eimeria maxima Species 0.000 description 2
- 241000179199 Eimeria mitis Species 0.000 description 2
- 241000499563 Eimeria necatrix Species 0.000 description 2
- 241000499544 Eimeria praecox Species 0.000 description 2
- 241000223932 Eimeria tenella Species 0.000 description 2
- YUGWDVYLFSETPE-JLHYYAGUSA-N Empenthrin Chemical compound CC\C=C(/C)C(C#C)OC(=O)C1C(C=C(C)C)C1(C)C YUGWDVYLFSETPE-JLHYYAGUSA-N 0.000 description 2
- 241000995027 Empoasca fabae Species 0.000 description 2
- 241000243234 Encephalitozoon Species 0.000 description 2
- 241000195950 Equisetum arvense Species 0.000 description 2
- 239000005768 Equisetum arvense L. Substances 0.000 description 2
- 241001559692 Eriosema Species 0.000 description 2
- ULGZDMOVFRHVEP-RWJQBGPGSA-N Erythromycin Natural products O([C@@H]1[C@@H](C)C(=O)O[C@@H]([C@@]([C@H](O)[C@@H](C)C(=O)[C@H](C)C[C@@](C)(O)[C@H](O[C@H]2[C@@H]([C@H](C[C@@H](C)O2)N(C)C)O)[C@H]1C)(C)O)CC)[C@H]1C[C@@](C)(OC)[C@@H](O)[C@H](C)O1 ULGZDMOVFRHVEP-RWJQBGPGSA-N 0.000 description 2
- 239000005895 Esfenvalerate Substances 0.000 description 2
- FNELVJVBIYMIMC-UHFFFAOYSA-N Ethiprole Chemical compound N1=C(C#N)C(S(=O)CC)=C(N)N1C1=C(Cl)C=C(C(F)(F)F)C=C1Cl FNELVJVBIYMIMC-UHFFFAOYSA-N 0.000 description 2
- 239000005897 Etoxazole Substances 0.000 description 2
- FGIWFCGDPUIBEZ-UHFFFAOYSA-N Etrimfos Chemical compound CCOC1=CC(OP(=S)(OC)OC)=NC(CC)=N1 FGIWFCGDPUIBEZ-UHFFFAOYSA-N 0.000 description 2
- 241001467465 Euglenozoa Species 0.000 description 2
- HMCCXLBXIJMERM-UHFFFAOYSA-N Febantel Chemical compound C1=C(NC(NC(=O)OC)=NC(=O)OC)C(NC(=O)COC)=CC(SC=2C=CC=CC=2)=C1 HMCCXLBXIJMERM-UHFFFAOYSA-N 0.000 description 2
- 239000005656 Fenazaquin Substances 0.000 description 2
- NRFQZTCQAYEXEE-UHFFFAOYSA-N Fenclorim Chemical compound ClC1=CC(Cl)=NC(C=2C=CC=CC=2)=N1 NRFQZTCQAYEXEE-UHFFFAOYSA-N 0.000 description 2
- 239000005777 Fenpropidin Substances 0.000 description 2
- 239000005778 Fenpropimorph Substances 0.000 description 2
- 239000005899 Fipronil Substances 0.000 description 2
- 239000005901 Flubendiamide Substances 0.000 description 2
- 239000005782 Fluopicolide Substances 0.000 description 2
- 239000005783 Fluopyram Substances 0.000 description 2
- 239000005786 Flutolanil Substances 0.000 description 2
- 241000720914 Forficula auricularia Species 0.000 description 2
- 241001466042 Fulgoromorpha Species 0.000 description 2
- 241000248126 Geophilus Species 0.000 description 2
- 241000224466 Giardia Species 0.000 description 2
- 241000235500 Gigaspora Species 0.000 description 2
- 241000235503 Glomus Species 0.000 description 2
- 241001243091 Gryllotalpa Species 0.000 description 2
- 241000224015 Haemosporida Species 0.000 description 2
- 244000020551 Helianthus annuus Species 0.000 description 2
- 241000246627 Heliconema Species 0.000 description 2
- 241000256244 Heliothis virescens Species 0.000 description 2
- 241001058149 Icerya Species 0.000 description 2
- 239000005795 Imazalil Substances 0.000 description 2
- 239000005906 Imidacloprid Substances 0.000 description 2
- 239000005907 Indoxacarb Substances 0.000 description 2
- LFVLUOAHQIVABZ-UHFFFAOYSA-N Iodofenphos Chemical compound COP(=S)(OC)OC1=CC(Cl)=C(I)C=C1Cl LFVLUOAHQIVABZ-UHFFFAOYSA-N 0.000 description 2
- 239000005867 Iprodione Substances 0.000 description 2
- UQSXHKLRYXJYBZ-UHFFFAOYSA-N Iron oxide Chemical compound [Fe]=O UQSXHKLRYXJYBZ-UHFFFAOYSA-N 0.000 description 2
- 241000222342 Irpex Species 0.000 description 2
- 241000188153 Isaria fumosorosea Species 0.000 description 2
- KFZMGEQAYNKOFK-UHFFFAOYSA-N Isopropanol Chemical compound CC(C)O KFZMGEQAYNKOFK-UHFFFAOYSA-N 0.000 description 2
- 241000567229 Isospora Species 0.000 description 2
- 241000238681 Ixodes Species 0.000 description 2
- 241000238889 Ixodidae Species 0.000 description 2
- 235000003228 Lactuca sativa Nutrition 0.000 description 2
- 240000008415 Lactuca sativa Species 0.000 description 2
- 241000222722 Leishmania <genus> Species 0.000 description 2
- 241000589902 Leptospira Species 0.000 description 2
- 241000828880 Leucoptera <angiosperm> Species 0.000 description 2
- 241000244189 Lineus Species 0.000 description 2
- 241000012186 Litura Species 0.000 description 2
- 241000254023 Locusta Species 0.000 description 2
- 241000254022 Locusta migratoria Species 0.000 description 2
- 239000005912 Lufenuron Substances 0.000 description 2
- 241000502639 Lygocoris Species 0.000 description 2
- 241000237354 Lymnaea Species 0.000 description 2
- 239000005949 Malathion Substances 0.000 description 2
- PWHULOQIROXLJO-UHFFFAOYSA-N Manganese Chemical compound [Mn] PWHULOQIROXLJO-UHFFFAOYSA-N 0.000 description 2
- 241001093152 Mangifera Species 0.000 description 2
- 241001599018 Melanogaster Species 0.000 description 2
- 241001415013 Melanoplus Species 0.000 description 2
- 239000005914 Metaflumizone Substances 0.000 description 2
- MIFOMMKAVSCNKQ-HWIUFGAZSA-N Metaflumizone Chemical compound C1=CC(OC(F)(F)F)=CC=C1NC(=O)N\N=C(C=1C=C(C=CC=1)C(F)(F)F)\CC1=CC=C(C#N)C=C1 MIFOMMKAVSCNKQ-HWIUFGAZSA-N 0.000 description 2
- 239000002169 Metam Substances 0.000 description 2
- 241000223250 Metarhizium anisopliae Species 0.000 description 2
- 239000005916 Methomyl Substances 0.000 description 2
- 239000005917 Methoxyfenozide Substances 0.000 description 2
- BAPJBEWLBFYGME-UHFFFAOYSA-N Methyl acrylate Chemical compound COC(=O)C=C BAPJBEWLBFYGME-UHFFFAOYSA-N 0.000 description 2
- NTIZESTWPVYFNL-UHFFFAOYSA-N Methyl isobutyl ketone Chemical compound CC(C)CC(C)=O NTIZESTWPVYFNL-UHFFFAOYSA-N 0.000 description 2
- UIHCLUNTQKBZGK-UHFFFAOYSA-N Methyl isobutyl ketone Natural products CCC(C)C(C)=O UIHCLUNTQKBZGK-UHFFFAOYSA-N 0.000 description 2
- LGDSHSYDSCRFAB-UHFFFAOYSA-N Methyl isothiocyanate Chemical compound CN=C=S LGDSHSYDSCRFAB-UHFFFAOYSA-N 0.000 description 2
- 241000243190 Microsporidia Species 0.000 description 2
- 102000013379 Mitochondrial Proton-Translocating ATPases Human genes 0.000 description 2
- 108010026155 Mitochondrial Proton-Translocating ATPases Proteins 0.000 description 2
- 229930191564 Monensin Natural products 0.000 description 2
- GAOZTHIDHYLHMS-UHFFFAOYSA-N Monensin A Natural products O1C(CC)(C2C(CC(O2)C2C(CC(C)C(O)(CO)O2)C)C)CCC1C(O1)(C)CCC21CC(O)C(C)C(C(C)C(OC)C(C)C(O)=O)O2 GAOZTHIDHYLHMS-UHFFFAOYSA-N 0.000 description 2
- 241001477931 Mythimna unipuncta Species 0.000 description 2
- RAOCRURYZCVHMG-UHFFFAOYSA-N N-(6-propoxy-1H-benzimidazol-2-yl)carbamic acid methyl ester Chemical compound CCCOC1=CC=C2N=C(NC(=O)OC)NC2=C1 RAOCRURYZCVHMG-UHFFFAOYSA-N 0.000 description 2
- CCCGEKHKTPTUHJ-UHFFFAOYSA-N N-[9-(dichloromethylene)-1,2,3,4-tetrahydro-1,4-methanonaphthalen-5-yl]-3-(difluoromethyl)-1-methylpyrazole-4-carboxamide Chemical compound FC(F)C1=NN(C)C=C1C(=O)NC1=CC=CC2=C1C1CCC2C1=C(Cl)Cl CCCGEKHKTPTUHJ-UHFFFAOYSA-N 0.000 description 2
- NQRFDNJEBWAUBL-UHFFFAOYSA-N N-[cyano(2-thienyl)methyl]-4-ethyl-2-(ethylamino)-1,3-thiazole-5-carboxamide Chemical compound S1C(NCC)=NC(CC)=C1C(=O)NC(C#N)C1=CC=CS1 NQRFDNJEBWAUBL-UHFFFAOYSA-N 0.000 description 2
- JMPFSEBWVLAJKM-UHFFFAOYSA-N N-{5-chloro-4-[(4-chlorophenyl)(cyano)methyl]-2-methylphenyl}-2-hydroxy-3,5-diiodobenzamide Chemical compound ClC=1C=C(NC(=O)C=2C(=C(I)C=C(I)C=2)O)C(C)=CC=1C(C#N)C1=CC=C(Cl)C=C1 JMPFSEBWVLAJKM-UHFFFAOYSA-N 0.000 description 2
- VHKXXVVRRDYCIK-CWCPJSEDSA-N Narasin Chemical compound C[C@H]1C[C@H](C)[C@H]([C@@H](CC)C(O)=O)O[C@H]1[C@@H](C)[C@H](O)[C@H](C)C(=O)[C@H](CC)[C@@H]1[C@@H](C)C[C@@H](C)[C@@]2(C=C[C@@H](O)[C@@]3(O[C@@](C)(CC3)[C@@H]3O[C@@H](C)[C@@](O)(CC)CC3)O2)O1 VHKXXVVRRDYCIK-CWCPJSEDSA-N 0.000 description 2
- VHKXXVVRRDYCIK-UHFFFAOYSA-N Narasin Natural products CC1CC(C)C(C(CC)C(O)=O)OC1C(C)C(O)C(C)C(=O)C(CC)C1C(C)CC(C)C2(C=CC(O)C3(OC(C)(CC3)C3OC(C)C(O)(CC)CC3)O2)O1 VHKXXVVRRDYCIK-UHFFFAOYSA-N 0.000 description 2
- ARFHIAQFJWUCFH-IZZDOVSWSA-N Nifurtimox Chemical compound CC1CS(=O)(=O)CCN1\N=C\C1=CC=C([N+]([O-])=O)O1 ARFHIAQFJWUCFH-IZZDOVSWSA-N 0.000 description 2
- 241001126829 Nosema Species 0.000 description 2
- 241000866537 Odontotermes Species 0.000 description 2
- 241001480755 Otobius Species 0.000 description 2
- WFVUIONFJOAYPK-KAMYIIQDSA-N Oxabetrinil Chemical compound C=1C=CC=CC=1C(/C#N)=N\OCC1OCCO1 WFVUIONFJOAYPK-KAMYIIQDSA-N 0.000 description 2
- 241000209117 Panicum Species 0.000 description 2
- 235000006443 Panicum miliaceum subsp. miliaceum Nutrition 0.000 description 2
- 235000009037 Panicum miliaceum subsp. ruderale Nutrition 0.000 description 2
- 241000488585 Panonychus Species 0.000 description 2
- 241001480233 Paragonimus Species 0.000 description 2
- 239000005814 Pencycuron Substances 0.000 description 2
- 239000005815 Penflufen Substances 0.000 description 2
- 241000258972 Pentastomida Species 0.000 description 2
- 239000005816 Penthiopyrad Substances 0.000 description 2
- 241001608567 Phaedon cochleariae Species 0.000 description 2
- 241000722337 Pholiota Species 0.000 description 2
- 239000005921 Phosmet Substances 0.000 description 2
- XYFCBTPGUUZFHI-UHFFFAOYSA-N Phosphine Chemical compound P XYFCBTPGUUZFHI-UHFFFAOYSA-N 0.000 description 2
- NBIIXXVUZAFLBC-UHFFFAOYSA-N Phosphoric acid Chemical compound OP(O)(O)=O NBIIXXVUZAFLBC-UHFFFAOYSA-N 0.000 description 2
- OAICVXFJPJFONN-UHFFFAOYSA-N Phosphorus Chemical compound [P] OAICVXFJPJFONN-UHFFFAOYSA-N 0.000 description 2
- 241000437063 Phyllotreta striolata Species 0.000 description 2
- 241000233614 Phytophthora Species 0.000 description 2
- 241000255972 Pieris <butterfly> Species 0.000 description 2
- 241000907661 Pieris rapae Species 0.000 description 2
- 239000005923 Pirimicarb Substances 0.000 description 2
- 239000005924 Pirimiphos-methyl Substances 0.000 description 2
- 235000010582 Pisum sativum Nutrition 0.000 description 2
- 244000134552 Plantago ovata Species 0.000 description 2
- 235000003421 Plantago ovata Nutrition 0.000 description 2
- 241001363501 Plusia Species 0.000 description 2
- 239000004372 Polyvinyl alcohol Substances 0.000 description 2
- ZLMJMSJWJFRBEC-UHFFFAOYSA-N Potassium Chemical compound [K] ZLMJMSJWJFRBEC-UHFFFAOYSA-N 0.000 description 2
- 239000005821 Propamocarb Substances 0.000 description 2
- MKIMSXGUTQTKJU-UHFFFAOYSA-N Propamocarb hydrochloride Chemical compound [Cl-].CCCOC(=O)NCCC[NH+](C)C MKIMSXGUTQTKJU-UHFFFAOYSA-N 0.000 description 2
- ATUOYWHBWRKTHZ-UHFFFAOYSA-N Propane Chemical compound CCC ATUOYWHBWRKTHZ-UHFFFAOYSA-N 0.000 description 2
- 239000005823 Propineb Substances 0.000 description 2
- 239000005824 Proquinazid Substances 0.000 description 2
- 241000508269 Psidium Species 0.000 description 2
- 241001649229 Psoroptes Species 0.000 description 2
- 239000009223 Psyllium Substances 0.000 description 2
- 244000086363 Pterocarpus indicus Species 0.000 description 2
- 235000009984 Pterocarpus indicus Nutrition 0.000 description 2
- 241000411545 Punargentus Species 0.000 description 2
- 241001083505 Punica Species 0.000 description 2
- 241001465752 Purpureocillium lilacinum Species 0.000 description 2
- 239000005663 Pyridaben Substances 0.000 description 2
- 239000005926 Pyridalyl Substances 0.000 description 2
- 239000005927 Pyriproxyfen Substances 0.000 description 2
- 240000003085 Quassia amara Species 0.000 description 2
- 235000009694 Quassia amara Nutrition 0.000 description 2
- 241000219492 Quercus Species 0.000 description 2
- 241001092473 Quillaja Species 0.000 description 2
- 235000009001 Quillaja saponaria Nutrition 0.000 description 2
- 239000005831 Quinoxyfen Substances 0.000 description 2
- YNQSILKYZQZHFJ-UHFFFAOYSA-N R-29148 Chemical compound CC1CN(C(=O)C(Cl)Cl)C(C)(C)O1 YNQSILKYZQZHFJ-UHFFFAOYSA-N 0.000 description 2
- 241000589194 Rhizobium leguminosarum Species 0.000 description 2
- 241000722251 Rhodnius Species 0.000 description 2
- 241001495449 Robinia pseudoacacia Species 0.000 description 2
- 241000283984 Rodentia Species 0.000 description 2
- 235000004789 Rosa xanthina Nutrition 0.000 description 2
- 241000109329 Rosa xanthina Species 0.000 description 2
- 241000983742 Saccharina Species 0.000 description 2
- 240000004808 Saccharomyces cerevisiae Species 0.000 description 2
- KQXDHUJYNAXLNZ-XQSDOZFQSA-N Salinomycin Chemical compound O1[C@@H]([C@@H](CC)C(O)=O)CC[C@H](C)[C@@H]1[C@@H](C)[C@H](O)[C@H](C)C(=O)[C@H](CC)[C@@H]1[C@@H](C)C[C@@H](C)[C@@]2(C=C[C@@H](O)[C@@]3(O[C@@](C)(CC3)[C@@H]3O[C@@H](C)[C@@](O)(CC)CC3)O2)O1 KQXDHUJYNAXLNZ-XQSDOZFQSA-N 0.000 description 2
- 239000004189 Salinomycin Substances 0.000 description 2
- 241000224003 Sarcocystis Species 0.000 description 2
- 206010039710 Scleroderma Diseases 0.000 description 2
- 241000239226 Scorpiones Species 0.000 description 2
- 241001157779 Scutigera Species 0.000 description 2
- 241000883293 Scutigerella Species 0.000 description 2
- 241000607720 Serratia Species 0.000 description 2
- 235000005775 Setaria Nutrition 0.000 description 2
- 241000232088 Setaria <nematode> Species 0.000 description 2
- 239000005835 Silthiofam Substances 0.000 description 2
- BQCADISMDOOEFD-UHFFFAOYSA-N Silver Chemical compound [Ag] BQCADISMDOOEFD-UHFFFAOYSA-N 0.000 description 2
- 235000011984 Simarouba amara Nutrition 0.000 description 2
- 241000256108 Simulium <genus> Species 0.000 description 2
- 108010052164 Sodium Channels Proteins 0.000 description 2
- 102000018674 Sodium Channels Human genes 0.000 description 2
- VMHLLURERBWHNL-UHFFFAOYSA-M Sodium acetate Chemical compound [Na+].CC([O-])=O VMHLLURERBWHNL-UHFFFAOYSA-M 0.000 description 2
- UIIMBOGNXHQVGW-DEQYMQKBSA-M Sodium bicarbonate-14C Chemical compound [Na+].O[14C]([O-])=O UIIMBOGNXHQVGW-DEQYMQKBSA-M 0.000 description 2
- 244000062793 Sorghum vulgare Species 0.000 description 2
- 239000005929 Spinetoram Substances 0.000 description 2
- GOENIMGKWNZVDA-OAMCMWGQSA-N Spinetoram Chemical compound CO[C@@H]1[C@H](OCC)[C@@H](OC)[C@H](C)O[C@H]1OC1C[C@H]2[C@@H]3C=C4C(=O)[C@H](C)[C@@H](O[C@@H]5O[C@H](C)[C@H](CC5)N(C)C)CCC[C@H](CC)OC(=O)CC4[C@@H]3CC[C@@H]2C1 GOENIMGKWNZVDA-OAMCMWGQSA-N 0.000 description 2
- 239000005930 Spinosad Substances 0.000 description 2
- 241000589973 Spirochaeta Species 0.000 description 2
- 239000005664 Spirodiclofen Substances 0.000 description 2
- 239000005665 Spiromesifen Substances 0.000 description 2
- 239000005931 Spirotetramat Substances 0.000 description 2
- 239000005837 Spiroxamine Substances 0.000 description 2
- 241001494139 Stomoxys Species 0.000 description 2
- 241000958507 Stropharia Species 0.000 description 2
- 241000272534 Struthio camelus Species 0.000 description 2
- QAOWNCQODCNURD-UHFFFAOYSA-N Sulfuric acid Chemical compound OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 description 2
- 241000883295 Symphyla Species 0.000 description 2
- 235000005865 Symphytum officinale Nutrition 0.000 description 2
- 240000002299 Symphytum officinale Species 0.000 description 2
- 239000005839 Tebuconazole Substances 0.000 description 2
- 239000005937 Tebufenozide Substances 0.000 description 2
- 239000005658 Tebufenpyrad Substances 0.000 description 2
- 239000005939 Tefluthrin Substances 0.000 description 2
- 239000005840 Tetraconazole Substances 0.000 description 2
- 241000344246 Tetranychus cinnabarinus Species 0.000 description 2
- 241000916142 Tetranychus turkestani Species 0.000 description 2
- 241001454293 Tetranychus urticae Species 0.000 description 2
- 241000223777 Theileria Species 0.000 description 2
- 239000005941 Thiamethoxam Substances 0.000 description 2
- 239000005842 Thiophanate-methyl Substances 0.000 description 2
- 239000005844 Thymol Substances 0.000 description 2
- 241000018137 Trialeurodes vaporariorum Species 0.000 description 2
- 241001414833 Triatoma Species 0.000 description 2
- 241000894120 Trichoderma atroviride Species 0.000 description 2
- 241000223260 Trichoderma harzianum Species 0.000 description 2
- 241001220308 Trichodorus Species 0.000 description 2
- 241000224526 Trichomonas Species 0.000 description 2
- 241000223238 Trichophyton Species 0.000 description 2
- 241001489151 Trichuris Species 0.000 description 2
- 239000005942 Triflumuron Substances 0.000 description 2
- OKJPEAGHQZHRQV-UHFFFAOYSA-N Triiodomethane Natural products IC(I)I OKJPEAGHQZHRQV-UHFFFAOYSA-N 0.000 description 2
- 241001414858 Trioza Species 0.000 description 2
- 239000005859 Triticonazole Substances 0.000 description 2
- 241001031786 Trochulus Species 0.000 description 2
- 241000208241 Tropaeolum Species 0.000 description 2
- 241000223104 Trypanosoma Species 0.000 description 2
- 241001232874 Tunga Species 0.000 description 2
- XSQUKJJJFZCRTK-UHFFFAOYSA-N Urea Chemical compound NC(N)=O XSQUKJJJFZCRTK-UHFFFAOYSA-N 0.000 description 2
- 244000274883 Urtica dioica Species 0.000 description 2
- 235000009108 Urtica dioica Nutrition 0.000 description 2
- BZHJMEDXRYGGRV-UHFFFAOYSA-N Vinyl chloride Chemical compound ClC=C BZHJMEDXRYGGRV-UHFFFAOYSA-N 0.000 description 2
- 241000219094 Vitaceae Species 0.000 description 2
- 241000353224 Xenopsylla Species 0.000 description 2
- 241000353223 Xenopsylla cheopis Species 0.000 description 2
- 239000005863 Zoxamide Substances 0.000 description 2
- QQODLKZGRKWIFG-RUTXASTPSA-N [(R)-cyano-(4-fluoro-3-phenoxyphenyl)methyl] (1S)-3-(2,2-dichloroethenyl)-2,2-dimethylcyclopropane-1-carboxylate Chemical compound CC1(C)C(C=C(Cl)Cl)[C@@H]1C(=O)O[C@@H](C#N)C1=CC=C(F)C(OC=2C=CC=CC=2)=C1 QQODLKZGRKWIFG-RUTXASTPSA-N 0.000 description 2
- YXWCBRDRVXHABN-JCMHNJIXSA-N [cyano-(4-fluoro-3-phenoxyphenyl)methyl] 3-[(z)-2-chloro-2-(4-chlorophenyl)ethenyl]-2,2-dimethylcyclopropane-1-carboxylate Chemical compound C=1C=C(F)C(OC=2C=CC=CC=2)=CC=1C(C#N)OC(=O)C1C(C)(C)C1\C=C(/Cl)C1=CC=C(Cl)C=C1 YXWCBRDRVXHABN-JCMHNJIXSA-N 0.000 description 2
- YASYVMFAVPKPKE-UHFFFAOYSA-N acephate Chemical compound COP(=O)(SC)NC(C)=O YASYVMFAVPKPKE-UHFFFAOYSA-N 0.000 description 2
- 229960002669 albendazole Drugs 0.000 description 2
- HXHWSAZORRCQMX-UHFFFAOYSA-N albendazole Chemical compound CCCSC1=CC=C2NC(NC(=O)OC)=NC2=C1 HXHWSAZORRCQMX-UHFFFAOYSA-N 0.000 description 2
- VXTGHWHFYNYFFV-UHFFFAOYSA-N albendazole S-oxide Chemical compound CCCS(=O)C1=CC=C2NC(NC(=O)OC)=NC2=C1 VXTGHWHFYNYFFV-UHFFFAOYSA-N 0.000 description 2
- QGLZXHRNAYXIBU-WEVVVXLNSA-N aldicarb Chemical compound CNC(=O)O\N=C\C(C)(C)SC QGLZXHRNAYXIBU-WEVVVXLNSA-N 0.000 description 2
- 229910000102 alkali metal hydride Inorganic materials 0.000 description 2
- 150000008046 alkali metal hydrides Chemical class 0.000 description 2
- 125000005910 alkyl carbonate group Chemical group 0.000 description 2
- 150000001350 alkyl halides Chemical class 0.000 description 2
- 125000000304 alkynyl group Chemical group 0.000 description 2
- 239000011717 all-trans-retinol Substances 0.000 description 2
- 235000019169 all-trans-retinol Nutrition 0.000 description 2
- ZCVAOQKBXKSDMS-UHFFFAOYSA-N allethrin Chemical compound CC1(C)C(C=C(C)C)C1C(=O)OC1C(C)=C(CC=C)C(=O)C1 ZCVAOQKBXKSDMS-UHFFFAOYSA-N 0.000 description 2
- 229940024113 allethrin Drugs 0.000 description 2
- PNEYBMLMFCGWSK-UHFFFAOYSA-N aluminium oxide Inorganic materials [O-2].[O-2].[O-2].[Al+3].[Al+3] PNEYBMLMFCGWSK-UHFFFAOYSA-N 0.000 description 2
- GGKQIOFASHYUJZ-UHFFFAOYSA-N ametoctradin Chemical compound NC1=C(CCCCCCCC)C(CC)=NC2=NC=NN21 GGKQIOFASHYUJZ-UHFFFAOYSA-N 0.000 description 2
- 150000001408 amides Chemical class 0.000 description 2
- 229910021529 ammonia Inorganic materials 0.000 description 2
- BFNBIHQBYMNNAN-UHFFFAOYSA-N ammonium sulfate Chemical compound N.N.OS(O)(=O)=O BFNBIHQBYMNNAN-UHFFFAOYSA-N 0.000 description 2
- 229960003683 amprolium Drugs 0.000 description 2
- 230000000844 anti-bacterial effect Effects 0.000 description 2
- 230000002141 anti-parasite Effects 0.000 description 2
- 230000000842 anti-protozoal effect Effects 0.000 description 2
- 239000002518 antifoaming agent Substances 0.000 description 2
- 239000003096 antiparasitic agent Substances 0.000 description 2
- 235000021016 apples Nutrition 0.000 description 2
- 238000009360 aquaculture Methods 0.000 description 2
- 244000144974 aquaculture Species 0.000 description 2
- 239000001138 artemisia absinthium Substances 0.000 description 2
- VNKBTWQZTQIWDV-UHFFFAOYSA-N azamethiphos Chemical compound C1=C(Cl)C=C2OC(=O)N(CSP(=O)(OC)OC)C2=N1 VNKBTWQZTQIWDV-UHFFFAOYSA-N 0.000 description 2
- WFDXOXNFNRHQEC-GHRIWEEISA-N azoxystrobin Chemical compound CO\C=C(\C(=O)OC)C1=CC=CC=C1OC1=CC(OC=2C(=CC=CC=2)C#N)=NC=N1 WFDXOXNFNRHQEC-GHRIWEEISA-N 0.000 description 2
- 229940005348 bacillus firmus Drugs 0.000 description 2
- 239000003899 bactericide agent Substances 0.000 description 2
- CJPQIRJHIZUAQP-MRXNPFEDSA-N benalaxyl-M Chemical compound CC=1C=CC=C(C)C=1N([C@H](C)C(=O)OC)C(=O)CC1=CC=CC=C1 CJPQIRJHIZUAQP-MRXNPFEDSA-N 0.000 description 2
- XEGGRYVFLWGFHI-UHFFFAOYSA-N bendiocarb Chemical compound CNC(=O)OC1=CC=CC2=C1OC(C)(C)O2 XEGGRYVFLWGFHI-UHFFFAOYSA-N 0.000 description 2
- VVSLYIKSEBPRSN-PELKAZGASA-N benthiavalicarb Chemical compound C1=C(F)C=C2SC([C@@H](C)NC(=O)[C@@H](NC(O)=O)C(C)C)=NC2=C1 VVSLYIKSEBPRSN-PELKAZGASA-N 0.000 description 2
- MKQSWTQPLLCSOB-UHFFFAOYSA-N benzyl 2-chloro-4-(trifluoromethyl)-1,3-thiazole-5-carboxylate Chemical compound N1=C(Cl)SC(C(=O)OCC=2C=CC=CC=2)=C1C(F)(F)F MKQSWTQPLLCSOB-UHFFFAOYSA-N 0.000 description 2
- VHLKTXFWDRXILV-UHFFFAOYSA-N bifenazate Chemical compound C1=C(NNC(=O)OC(C)C)C(OC)=CC=C1C1=CC=CC=C1 VHLKTXFWDRXILV-UHFFFAOYSA-N 0.000 description 2
- OMFRMAHOUUJSGP-IRHGGOMRSA-N bifenthrin Chemical compound C1=CC=C(C=2C=CC=CC=2)C(C)=C1COC(=O)[C@@H]1[C@H](\C=C(/Cl)C(F)(F)F)C1(C)C OMFRMAHOUUJSGP-IRHGGOMRSA-N 0.000 description 2
- 230000004071 biological effect Effects 0.000 description 2
- 229950002373 bioresmethrin Drugs 0.000 description 2
- LLEMOWNGBBNAJR-UHFFFAOYSA-N biphenyl-2-ol Chemical compound OC1=CC=CC=C1C1=CC=CC=C1 LLEMOWNGBBNAJR-UHFFFAOYSA-N 0.000 description 2
- KULDXINYXFTXMO-UHFFFAOYSA-N bis(2-chloroethyl) (3-chloro-4-methyl-2-oxochromen-7-yl) phosphate Chemical compound C1=C(OP(=O)(OCCCl)OCCCl)C=CC2=C1OC(=O)C(Cl)=C2C KULDXINYXFTXMO-UHFFFAOYSA-N 0.000 description 2
- YNHIGQDRGKUECZ-UHFFFAOYSA-L bis(triphenylphosphine)palladium(ii) dichloride Chemical compound [Cl-].[Cl-].[Pd+2].C1=CC=CC=C1P(C=1C=CC=CC=1)C1=CC=CC=C1.C1=CC=CC=C1P(C=1C=CC=CC=1)C1=CC=CC=C1 YNHIGQDRGKUECZ-UHFFFAOYSA-L 0.000 description 2
- LDLMOOXUCMHBMZ-UHFFFAOYSA-N bixafen Chemical compound FC(F)C1=NN(C)C=C1C(=O)NC1=CC=C(F)C=C1C1=CC=C(Cl)C(Cl)=C1 LDLMOOXUCMHBMZ-UHFFFAOYSA-N 0.000 description 2
- 230000000903 blocking effect Effects 0.000 description 2
- 229910021538 borax Inorganic materials 0.000 description 2
- GZUXJHMPEANEGY-UHFFFAOYSA-N bromomethane Chemical compound BrC GZUXJHMPEANEGY-UHFFFAOYSA-N 0.000 description 2
- 229950004965 bunamidine Drugs 0.000 description 2
- PRLVTUNWOQKEAI-VKAVYKQESA-N buprofezin Chemical compound O=C1N(C(C)C)\C(=N\C(C)(C)C)SCN1C1=CC=CC=C1 PRLVTUNWOQKEAI-VKAVYKQESA-N 0.000 description 2
- 239000011575 calcium Substances 0.000 description 2
- 229910052791 calcium Inorganic materials 0.000 description 2
- 229960003475 cambendazole Drugs 0.000 description 2
- 229940117949 captan Drugs 0.000 description 2
- 239000006013 carbendazim Substances 0.000 description 2
- 125000004432 carbon atom Chemical group C* 0.000 description 2
- 125000002915 carbonyl group Chemical group [*:2]C([*:1])=O 0.000 description 2
- 230000006315 carbonylation Effects 0.000 description 2
- 238000005810 carbonylation reaction Methods 0.000 description 2
- JLQUFIHWVLZVTJ-UHFFFAOYSA-N carbosulfan Chemical compound CCCCN(CCCC)SN(C)C(=O)OC1=CC=CC2=C1OC(C)(C)C2 JLQUFIHWVLZVTJ-UHFFFAOYSA-N 0.000 description 2
- GYSSRZJIHXQEHQ-UHFFFAOYSA-N carboxin Chemical compound S1CCOC(C)=C1C(=O)NC1=CC=CC=C1 GYSSRZJIHXQEHQ-UHFFFAOYSA-N 0.000 description 2
- ULDHMXUKGWMISQ-UHFFFAOYSA-N carvone Chemical compound CC(=C)C1CC=C(C)C(=O)C1 ULDHMXUKGWMISQ-UHFFFAOYSA-N 0.000 description 2
- 229920002678 cellulose Polymers 0.000 description 2
- 239000001913 cellulose Substances 0.000 description 2
- 230000003046 cesticidal effect Effects 0.000 description 2
- 239000003153 chemical reaction reagent Substances 0.000 description 2
- PSOVNZZNOMJUBI-UHFFFAOYSA-N chlorantraniliprole Chemical compound CNC(=O)C1=CC(Cl)=CC(C)=C1NC(=O)C1=CC(Br)=NN1C1=NC=CC=C1Cl PSOVNZZNOMJUBI-UHFFFAOYSA-N 0.000 description 2
- UISUNVFOGSJSKD-UHFFFAOYSA-N chlorfluazuron Chemical compound FC1=CC=CC(F)=C1C(=O)NC(=O)NC(C=C1Cl)=CC(Cl)=C1OC1=NC=C(C(F)(F)F)C=C1Cl UISUNVFOGSJSKD-UHFFFAOYSA-N 0.000 description 2
- 125000001309 chloro group Chemical group Cl* 0.000 description 2
- LFHISGNCFUNFFM-UHFFFAOYSA-N chloropicrin Chemical compound [O-][N+](=O)C(Cl)(Cl)Cl LFHISGNCFUNFFM-UHFFFAOYSA-N 0.000 description 2
- WHTVZRBIWZFKQO-UHFFFAOYSA-N chloroquine Natural products ClC1=CC=C2C(NC(C)CCCN(CC)CC)=CC=NC2=C1 WHTVZRBIWZFKQO-UHFFFAOYSA-N 0.000 description 2
- 229960003677 chloroquine Drugs 0.000 description 2
- CYDMQBQPVICBEU-UHFFFAOYSA-N chlorotetracycline Natural products C1=CC(Cl)=C2C(O)(C)C3CC4C(N(C)C)C(O)=C(C(N)=O)C(=O)C4(O)C(O)=C3C(=O)C2=C1O CYDMQBQPVICBEU-UHFFFAOYSA-N 0.000 description 2
- CYDMQBQPVICBEU-XRNKAMNCSA-N chlortetracycline Chemical compound C1=CC(Cl)=C2[C@](O)(C)[C@H]3C[C@H]4[C@H](N(C)C)C(O)=C(C(N)=O)C(=O)[C@@]4(O)C(O)=C3C(=O)C2=C1O CYDMQBQPVICBEU-XRNKAMNCSA-N 0.000 description 2
- HPNSNYBUADCFDR-UHFFFAOYSA-N chromafenozide Chemical compound CC1=CC(C)=CC(C(=O)N(NC(=O)C=2C(=C3CCCOC3=CC=2)C)C(C)(C)C)=C1 HPNSNYBUADCFDR-UHFFFAOYSA-N 0.000 description 2
- OXLKOMYHDYVIDM-UHFFFAOYSA-N ciclobendazole Chemical compound C1=C2NC(NC(=O)OC)=NC2=CC=C1C(=O)C1CC1 OXLKOMYHDYVIDM-UHFFFAOYSA-N 0.000 description 2
- 229960001020 ciclobendazole Drugs 0.000 description 2
- KDLRVYVGXIQJDK-AWPVFWJPSA-N clindamycin Chemical compound CN1C[C@H](CCC)C[C@H]1C(=O)N[C@H]([C@H](C)Cl)[C@@H]1[C@H](O)[C@H](O)[C@@H](O)[C@@H](SC)O1 KDLRVYVGXIQJDK-AWPVFWJPSA-N 0.000 description 2
- 229960002227 clindamycin Drugs 0.000 description 2
- DGBIGWXXNGSACT-UHFFFAOYSA-N clonazepam Chemical compound C12=CC([N+](=O)[O-])=CC=C2NC(=O)CN=C1C1=CC=CC=C1Cl DGBIGWXXNGSACT-UHFFFAOYSA-N 0.000 description 2
- 229960003120 clonazepam Drugs 0.000 description 2
- 229950004178 closantel Drugs 0.000 description 2
- 239000008199 coating composition Substances 0.000 description 2
- 230000002860 competitive effect Effects 0.000 description 2
- 238000009833 condensation Methods 0.000 description 2
- 230000005494 condensation Effects 0.000 description 2
- ARUVKPQLZAKDPS-UHFFFAOYSA-L copper(II) sulfate Chemical compound [Cu+2].[O-][S+2]([O-])([O-])[O-] ARUVKPQLZAKDPS-UHFFFAOYSA-L 0.000 description 2
- CWVRPJSBNHNJSI-XQNSMLJCSA-N coumoxystrobin Chemical compound C1=C2OC(=O)C(CCCC)=C(C)C2=CC=C1OCC1=CC=CC=C1\C(=C/OC)C(=O)OC CWVRPJSBNHNJSI-XQNSMLJCSA-N 0.000 description 2
- 230000008878 coupling Effects 0.000 description 2
- 238000010168 coupling process Methods 0.000 description 2
- 238000005859 coupling reaction Methods 0.000 description 2
- DVBUIBGJRQBEDP-UHFFFAOYSA-N cyantraniliprole Chemical compound CNC(=O)C1=CC(C#N)=CC(C)=C1NC(=O)C1=CC(Br)=NN1C1=NC=CC=C1Cl DVBUIBGJRQBEDP-UHFFFAOYSA-N 0.000 description 2
- 125000006310 cycloalkyl amino group Chemical group 0.000 description 2
- NXQGGXCHGDYOHB-UHFFFAOYSA-L cyclopenta-1,4-dien-1-yl(diphenyl)phosphane;dichloropalladium;iron(2+) Chemical compound [Fe+2].Cl[Pd]Cl.[CH-]1C=CC(P(C=2C=CC=CC=2)C=2C=CC=CC=2)=C1.[CH-]1C=CC(P(C=2C=CC=CC=2)C=2C=CC=CC=2)=C1 NXQGGXCHGDYOHB-UHFFFAOYSA-L 0.000 description 2
- ZSWFCLXCOIISFI-UHFFFAOYSA-N cyclopentadiene Chemical compound C1C=CC=C1 ZSWFCLXCOIISFI-UHFFFAOYSA-N 0.000 description 2
- LPIQUOYDBNQMRZ-UHFFFAOYSA-N cyclopentene Chemical compound C1CC=CC1 LPIQUOYDBNQMRZ-UHFFFAOYSA-N 0.000 description 2
- LSFUGNKKPMBOMG-UHFFFAOYSA-N cycloprothrin Chemical compound ClC1(Cl)CC1(C=1C=CC=CC=1)C(=O)OC(C#N)C1=CC=CC(OC=2C=CC=CC=2)=C1 LSFUGNKKPMBOMG-UHFFFAOYSA-N 0.000 description 2
- ACMXQHFNODYQAT-UHFFFAOYSA-N cyflufenamid Chemical compound FC1=CC=C(C(F)(F)F)C(C(NOCC2CC2)=NC(=O)CC=2C=CC=CC=2)=C1F ACMXQHFNODYQAT-UHFFFAOYSA-N 0.000 description 2
- HAORKNGNJCEJBX-UHFFFAOYSA-N cyprodinil Chemical compound N=1C(C)=CC(C2CC2)=NC=1NC1=CC=CC=C1 HAORKNGNJCEJBX-UHFFFAOYSA-N 0.000 description 2
- 229940008203 d-transallethrin Drugs 0.000 description 2
- QAYICIQNSGETAS-UHFFFAOYSA-N dazomet Chemical compound CN1CSC(=S)N(C)C1 QAYICIQNSGETAS-UHFFFAOYSA-N 0.000 description 2
- 229960002483 decamethrin Drugs 0.000 description 2
- OWZREIFADZCYQD-NSHGMRRFSA-N deltamethrin Chemical compound CC1(C)[C@@H](C=C(Br)Br)[C@H]1C(=O)O[C@H](C#N)C1=CC=CC(OC=2C=CC=CC=2)=C1 OWZREIFADZCYQD-NSHGMRRFSA-N 0.000 description 2
- WEBQKRLKWNIYKK-UHFFFAOYSA-N demeton-S-methyl Chemical compound CCSCCSP(=O)(OC)OC WEBQKRLKWNIYKK-UHFFFAOYSA-N 0.000 description 2
- 230000001419 dependent effect Effects 0.000 description 2
- FCRACOPGPMPSHN-UHFFFAOYSA-N desoxyabscisic acid Natural products OC(=O)C=C(C)C=CC1C(C)=CC(=O)CC1(C)C FCRACOPGPMPSHN-UHFFFAOYSA-N 0.000 description 2
- FHIVAFMUCKRCQO-UHFFFAOYSA-N diazinon Chemical compound CCOP(=S)(OCC)OC1=CC(C)=NC(C(C)C)=N1 FHIVAFMUCKRCQO-UHFFFAOYSA-N 0.000 description 2
- PFBUKDPBVNJDEW-UHFFFAOYSA-N dichlorocarbene Chemical group Cl[C]Cl PFBUKDPBVNJDEW-UHFFFAOYSA-N 0.000 description 2
- 229960003887 dichlorophen Drugs 0.000 description 2
- 229960000248 diclazuril Drugs 0.000 description 2
- LNJNFVJKDJYTEU-UHFFFAOYSA-N diethofencarb Chemical compound CCOC1=CC=C(NC(=O)OC(C)C)C=C1OCC LNJNFVJKDJYTEU-UHFFFAOYSA-N 0.000 description 2
- JXSJBGJIGXNWCI-UHFFFAOYSA-N diethyl 2-[(dimethoxyphosphorothioyl)thio]succinate Chemical compound CCOC(=O)CC(SP(=S)(OC)OC)C(=O)OCC JXSJBGJIGXNWCI-UHFFFAOYSA-N 0.000 description 2
- FAMRKDQNMBBFBR-BQYQJAHWSA-N diethyl azodicarboxylate Substances CCOC(=O)\N=N\C(=O)OCC FAMRKDQNMBBFBR-BQYQJAHWSA-N 0.000 description 2
- BQYJATMQXGBDHF-UHFFFAOYSA-N difenoconazole Chemical compound O1C(C)COC1(C=1C(=CC(OC=2C=CC(Cl)=CC=2)=CC=1)Cl)CN1N=CN=C1 BQYJATMQXGBDHF-UHFFFAOYSA-N 0.000 description 2
- 239000003085 diluting agent Substances 0.000 description 2
- YKBZOVFACRVRJN-UHFFFAOYSA-N dinotefuran Chemical compound [O-][N+](=O)\N=C(/NC)NCC1CCOC1 YKBZOVFACRVRJN-UHFFFAOYSA-N 0.000 description 2
- 238000007598 dipping method Methods 0.000 description 2
- 229960000878 docusate sodium Drugs 0.000 description 2
- 229960003722 doxycycline Drugs 0.000 description 2
- 238000001035 drying Methods 0.000 description 2
- 108010057988 ecdysone receptor Proteins 0.000 description 2
- 239000013057 ectoparasiticide Substances 0.000 description 2
- 239000000839 emulsion Substances 0.000 description 2
- RDYMFSUJUZBWLH-SVWSLYAFSA-N endosulfan Chemical compound C([C@@H]12)OS(=O)OC[C@@H]1[C@]1(Cl)C(Cl)=C(Cl)[C@@]2(Cl)C1(Cl)Cl RDYMFSUJUZBWLH-SVWSLYAFSA-N 0.000 description 2
- 229960000740 enrofloxacin Drugs 0.000 description 2
- 230000007613 environmental effect Effects 0.000 description 2
- 210000002615 epidermis Anatomy 0.000 description 2
- 210000000918 epididymis Anatomy 0.000 description 2
- 201000010063 epididymitis Diseases 0.000 description 2
- NYPJDWWKZLNGGM-RPWUZVMVSA-N esfenvalerate Chemical compound C=1C([C@@H](C#N)OC(=O)[C@@H](C(C)C)C=2C=CC(Cl)=CC=2)=CC=CC=1OC1=CC=CC=C1 NYPJDWWKZLNGGM-RPWUZVMVSA-N 0.000 description 2
- 230000012173 estrus Effects 0.000 description 2
- HEZNVIYQEUHLNI-UHFFFAOYSA-N ethiofencarb Chemical compound CCSCC1=CC=CC=C1OC(=O)NC HEZNVIYQEUHLNI-UHFFFAOYSA-N 0.000 description 2
- NWUJMVBACHKRGC-UHFFFAOYSA-N ethyl 7-(trifluoromethylsulfonyloxy)-[1,3]thiazolo[4,5-c]pyridine-6-carboxylate Chemical compound CCOC(=O)c1ncc2ncsc2c1OS(=O)(=O)C(F)(F)F NWUJMVBACHKRGC-UHFFFAOYSA-N 0.000 description 2
- YIAYLVLZVXWJDQ-UHFFFAOYSA-N ethyl 7-ethylsulfanyl-[1,3]thiazolo[4,5-c]pyridine-6-carboxylate Chemical compound CCOC(=O)c1ncc2ncsc2c1SCC YIAYLVLZVXWJDQ-UHFFFAOYSA-N 0.000 description 2
- QMVNJXAQTPALBB-UHFFFAOYSA-N ethyl 7-hydroxy-[1,3]thiazolo[4,5-c]pyridine-6-carboxylate Chemical compound OC=1C2=C(C=NC=1C(=O)OCC)N=CS2 QMVNJXAQTPALBB-UHFFFAOYSA-N 0.000 description 2
- FAMRKDQNMBBFBR-UHFFFAOYSA-N ethyl n-ethoxycarbonyliminocarbamate Chemical compound CCOC(=O)N=NC(=O)OCC FAMRKDQNMBBFBR-UHFFFAOYSA-N 0.000 description 2
- YREQHYQNNWYQCJ-UHFFFAOYSA-N etofenprox Chemical compound C1=CC(OCC)=CC=C1C(C)(C)COCC1=CC=CC(OC=2C=CC=CC=2)=C1 YREQHYQNNWYQCJ-UHFFFAOYSA-N 0.000 description 2
- IXSZQYVWNJNRAL-UHFFFAOYSA-N etoxazole Chemical compound CCOC1=CC(C(C)(C)C)=CC=C1C1N=C(C=2C(=CC=CC=2F)F)OC1 IXSZQYVWNJNRAL-UHFFFAOYSA-N 0.000 description 2
- 239000000284 extract Substances 0.000 description 2
- 150000004665 fatty acids Chemical class 0.000 description 2
- 229960005282 febantel Drugs 0.000 description 2
- DMYHGDXADUDKCQ-UHFFFAOYSA-N fenazaquin Chemical compound C1=CC(C(C)(C)C)=CC=C1CCOC1=NC=NC2=CC=CC=C12 DMYHGDXADUDKCQ-UHFFFAOYSA-N 0.000 description 2
- 229960005473 fenbendazole Drugs 0.000 description 2
- HDDSHPAODJUKPD-UHFFFAOYSA-N fenbendazole Chemical compound C1=C2NC(NC(=O)OC)=NC2=CC=C1SC1=CC=CC=C1 HDDSHPAODJUKPD-UHFFFAOYSA-N 0.000 description 2
- 229950003537 fenclorac Drugs 0.000 description 2
- VDLGAVXLJYLFDH-UHFFFAOYSA-N fenhexamid Chemical compound C=1C=C(O)C(Cl)=C(Cl)C=1NC(=O)C1(C)CCCCC1 VDLGAVXLJYLFDH-UHFFFAOYSA-N 0.000 description 2
- XQUXKZZNEFRCAW-UHFFFAOYSA-N fenpropathrin Chemical compound CC1(C)C(C)(C)C1C(=O)OC(C#N)C1=CC=CC(OC=2C=CC=CC=2)=C1 XQUXKZZNEFRCAW-UHFFFAOYSA-N 0.000 description 2
- 229940013764 fipronil Drugs 0.000 description 2
- CPEUVMUXAHMANV-UHFFFAOYSA-N flubendazole Chemical compound C1=C2NC(NC(=O)OC)=NC2=CC=C1C(=O)C1=CC=C(F)C=C1 CPEUVMUXAHMANV-UHFFFAOYSA-N 0.000 description 2
- 229960004500 flubendazole Drugs 0.000 description 2
- ZGNITFSDLCMLGI-UHFFFAOYSA-N flubendiamide Chemical compound CC1=CC(C(F)(C(F)(F)F)C(F)(F)F)=CC=C1NC(=O)C1=CC=CC(I)=C1C(=O)NC(C)(C)CS(C)(=O)=O ZGNITFSDLCMLGI-UHFFFAOYSA-N 0.000 description 2
- GBIHOLCMZGAKNG-CGAIIQECSA-N flucythrinate Chemical compound O=C([C@@H](C(C)C)C=1C=CC(OC(F)F)=CC=1)OC(C#N)C(C=1)=CC=CC=1OC1=CC=CC=C1 GBIHOLCMZGAKNG-CGAIIQECSA-N 0.000 description 2
- XRECTZIEBJDKEO-UHFFFAOYSA-N flucytosine Chemical compound NC1=NC(=O)NC=C1F XRECTZIEBJDKEO-UHFFFAOYSA-N 0.000 description 2
- RYLHNOVXKPXDIP-UHFFFAOYSA-N flufenoxuron Chemical compound C=1C=C(NC(=O)NC(=O)C=2C(=CC=CC=2F)F)C(F)=CC=1OC1=CC=C(C(F)(F)F)C=C1Cl RYLHNOVXKPXDIP-UHFFFAOYSA-N 0.000 description 2
- MBHXIQDIVCJZTD-RVDMUPIBSA-N flufenoxystrobin Chemical compound CO\C=C(\C(=O)OC)C1=CC=CC=C1COC1=CC=C(C(F)(F)F)C=C1Cl MBHXIQDIVCJZTD-RVDMUPIBSA-N 0.000 description 2
- GBOYJIHYACSLGN-UHFFFAOYSA-N fluopicolide Chemical compound ClC1=CC(C(F)(F)F)=CN=C1CNC(=O)C1=C(Cl)C=CC=C1Cl GBOYJIHYACSLGN-UHFFFAOYSA-N 0.000 description 2
- KVDJTXBXMWJJEF-UHFFFAOYSA-N fluopyram Chemical compound ClC1=CC(C(F)(F)F)=CN=C1CCNC(=O)C1=CC=CC=C1C(F)(F)F KVDJTXBXMWJJEF-UHFFFAOYSA-N 0.000 description 2
- PTCGDEVVHUXTMP-UHFFFAOYSA-N flutolanil Chemical compound CC(C)OC1=CC=CC(NC(=O)C=2C(=CC=CC=2)C(F)(F)F)=C1 PTCGDEVVHUXTMP-UHFFFAOYSA-N 0.000 description 2
- 238000005187 foaming Methods 0.000 description 2
- 239000004088 foaming agent Substances 0.000 description 2
- 235000013305 food Nutrition 0.000 description 2
- 238000007306 functionalization reaction Methods 0.000 description 2
- 230000000855 fungicidal effect Effects 0.000 description 2
- JLYXXMFPNIAWKQ-GNIYUCBRSA-N gamma-hexachlorocyclohexane Chemical compound Cl[C@H]1[C@H](Cl)[C@@H](Cl)[C@@H](Cl)[C@H](Cl)[C@H]1Cl JLYXXMFPNIAWKQ-GNIYUCBRSA-N 0.000 description 2
- 210000002816 gill Anatomy 0.000 description 2
- 235000021021 grapes Nutrition 0.000 description 2
- 230000012010 growth Effects 0.000 description 2
- 239000003966 growth inhibitor Substances 0.000 description 2
- 125000001188 haloalkyl group Chemical group 0.000 description 2
- 125000004441 haloalkylsulfonyl group Chemical group 0.000 description 2
- CNKHSLKYRMDDNQ-UHFFFAOYSA-N halofenozide Chemical compound C=1C=CC=CC=1C(=O)N(C(C)(C)C)NC(=O)C1=CC=C(Cl)C=C1 CNKHSLKYRMDDNQ-UHFFFAOYSA-N 0.000 description 2
- LVASCWIMLIKXLA-LSDHHAIUSA-N halofuginone Chemical compound O[C@@H]1CCCN[C@H]1CC(=O)CN1C(=O)C2=CC(Cl)=C(Br)C=C2N=C1 LVASCWIMLIKXLA-LSDHHAIUSA-N 0.000 description 2
- 229950010152 halofuginone Drugs 0.000 description 2
- 229950002831 haloxon Drugs 0.000 description 2
- FRCCEHPWNOQAEU-UHFFFAOYSA-N heptachlor Chemical compound ClC1=C(Cl)C2(Cl)C3C=CC(Cl)C3C1(Cl)C2(Cl)Cl FRCCEHPWNOQAEU-UHFFFAOYSA-N 0.000 description 2
- 239000004009 herbicide Substances 0.000 description 2
- ACGUYXCXAPNIKK-UHFFFAOYSA-N hexachlorophene Chemical compound OC1=C(Cl)C=C(Cl)C(Cl)=C1CC1=C(O)C(Cl)=CC(Cl)=C1Cl ACGUYXCXAPNIKK-UHFFFAOYSA-N 0.000 description 2
- 229960004068 hexachlorophene Drugs 0.000 description 2
- RGNPBRKPHBKNKX-UHFFFAOYSA-N hexaflumuron Chemical compound C1=C(Cl)C(OC(F)(F)C(F)F)=C(Cl)C=C1NC(=O)NC(=O)C1=C(F)C=CC=C1F RGNPBRKPHBKNKX-UHFFFAOYSA-N 0.000 description 2
- 238000005984 hydrogenation reaction Methods 0.000 description 2
- PJBQYZZKGNOKNJ-UHFFFAOYSA-M hydron;5-[(2-methylpyridin-1-ium-1-yl)methyl]-2-propylpyrimidin-4-amine;dichloride Chemical compound Cl.[Cl-].NC1=NC(CCC)=NC=C1C[N+]1=CC=CC=C1C PJBQYZZKGNOKNJ-UHFFFAOYSA-M 0.000 description 2
- ZQDWXGKKHFNSQK-UHFFFAOYSA-N hydroxyzine Chemical compound C1CN(CCOCCO)CCN1C(C=1C=CC(Cl)=CC=1)C1=CC=CC=C1 ZQDWXGKKHFNSQK-UHFFFAOYSA-N 0.000 description 2
- 229960000930 hydroxyzine Drugs 0.000 description 2
- 229940056881 imidacloprid Drugs 0.000 description 2
- YWTYJOPNNQFBPC-UHFFFAOYSA-N imidacloprid Chemical compound [O-][N+](=O)\N=C1/NCCN1CC1=CC=C(Cl)N=C1 YWTYJOPNNQFBPC-UHFFFAOYSA-N 0.000 description 2
- 230000001965 increasing effect Effects 0.000 description 2
- VBCVPMMZEGZULK-NRFANRHFSA-N indoxacarb Chemical compound C([C@@]1(OC2)C(=O)OC)C3=CC(Cl)=CC=C3C1=NN2C(=O)N(C(=O)OC)C1=CC=C(OC(F)(F)F)C=C1 VBCVPMMZEGZULK-NRFANRHFSA-N 0.000 description 2
- ONUFESLQCSAYKA-UHFFFAOYSA-N iprodione Chemical compound O=C1N(C(=O)NC(C)C)CC(=O)N1C1=CC(Cl)=CC(Cl)=C1 ONUFESLQCSAYKA-UHFFFAOYSA-N 0.000 description 2
- 229910052742 iron Inorganic materials 0.000 description 2
- QBSJMKIUCUGGNG-UHFFFAOYSA-N isoprocarb Chemical compound CNC(=O)OC1=CC=CC=C1C(C)C QBSJMKIUCUGGNG-UHFFFAOYSA-N 0.000 description 2
- WLPCAERCXQSYLQ-UHFFFAOYSA-N isotianil Chemical compound ClC1=NSC(C(=O)NC=2C(=CC=CC=2)C#N)=C1Cl WLPCAERCXQSYLQ-UHFFFAOYSA-N 0.000 description 2
- PVTHJAPFENJVNC-MHRBZPPQSA-N kasugamycin Chemical compound N[C@H]1C[C@H](NC(=N)C(O)=O)[C@@H](C)O[C@@H]1O[C@H]1[C@H](O)[C@@H](O)[C@@H](O)[C@H](O)[C@@H]1O PVTHJAPFENJVNC-MHRBZPPQSA-N 0.000 description 2
- 244000142813 lacy ambrosia Species 0.000 description 2
- 235000000317 lacy ambrosia Nutrition 0.000 description 2
- 239000005910 lambda-Cyhalothrin Substances 0.000 description 2
- 229950005045 letrazuril Drugs 0.000 description 2
- 229960002809 lindane Drugs 0.000 description 2
- 238000004895 liquid chromatography mass spectrometry Methods 0.000 description 2
- 238000006138 lithiation reaction Methods 0.000 description 2
- 229960000521 lufenuron Drugs 0.000 description 2
- PWPJGUXAGUPAHP-UHFFFAOYSA-N lufenuron Chemical compound C1=C(Cl)C(OC(F)(F)C(C(F)(F)F)F)=CC(Cl)=C1NC(=O)NC(=O)C1=C(F)C=CC=C1F PWPJGUXAGUPAHP-UHFFFAOYSA-N 0.000 description 2
- 206010025135 lupus erythematosus Diseases 0.000 description 2
- RWVUEZAROXKXRT-VQLSFVLHSA-N maduramicin Chemical compound O1[C@@H](C)[C@H](OC)[C@@H](OC)C[C@H]1O[C@@H]1[C@H]([C@@]2(C)O[C@H](CC2)[C@@]2(C)O[C@]3(O[C@@H]([C@H](C)[C@@H](O)C3)[C@@H](C)[C@H]3[C@@H]([C@@H](OC)[C@H](C)[C@@](O)(CC(O)=O)O3)OC)CC2)O[C@@H]([C@@H]2[C@H](C[C@@H](C)[C@@](C)(O)O2)C)C1 RWVUEZAROXKXRT-VQLSFVLHSA-N 0.000 description 2
- 229950006915 maduramicin Drugs 0.000 description 2
- HQKMJHAJHXVSDF-UHFFFAOYSA-L magnesium stearate Chemical compound [Mg+2].CCCCCCCCCCCCCCCCCC([O-])=O.CCCCCCCCCCCCCCCCCC([O-])=O HQKMJHAJHXVSDF-UHFFFAOYSA-L 0.000 description 2
- 229960000453 malathion Drugs 0.000 description 2
- 229910052748 manganese Inorganic materials 0.000 description 2
- 239000011572 manganese Substances 0.000 description 2
- 229960003439 mebendazole Drugs 0.000 description 2
- OPXLLQIJSORQAM-UHFFFAOYSA-N mebendazole Chemical compound C=1C=C2NC(NC(=O)OC)=NC2=CC=1C(=O)C1=CC=CC=C1 OPXLLQIJSORQAM-UHFFFAOYSA-N 0.000 description 2
- ZQEIXNIJLIKNTD-GFCCVEGCSA-N metalaxyl-M Chemical compound COCC(=O)N([C@H](C)C(=O)OC)C1=C(C)C=CC=C1C ZQEIXNIJLIKNTD-GFCCVEGCSA-N 0.000 description 2
- HYVVJDQGXFXBRZ-UHFFFAOYSA-N metam Chemical compound CNC(S)=S HYVVJDQGXFXBRZ-UHFFFAOYSA-N 0.000 description 2
- NNKVPIKMPCQWCG-UHFFFAOYSA-N methamidophos Chemical compound COP(N)(=O)SC NNKVPIKMPCQWCG-UHFFFAOYSA-N 0.000 description 2
- MEBQXILRKZHVCX-UHFFFAOYSA-N methidathion Chemical compound COC1=NN(CSP(=S)(OC)OC)C(=O)S1 MEBQXILRKZHVCX-UHFFFAOYSA-N 0.000 description 2
- UHXUZOCRWCRNSJ-QPJJXVBHSA-N methomyl Chemical compound CNC(=O)O\N=C(/C)SC UHXUZOCRWCRNSJ-QPJJXVBHSA-N 0.000 description 2
- 229930002897 methoprene Natural products 0.000 description 2
- 229950003442 methoprene Drugs 0.000 description 2
- QCAWEPFNJXQPAN-UHFFFAOYSA-N methoxyfenozide Chemical compound COC1=CC=CC(C(=O)NN(C(=O)C=2C=C(C)C=C(C)C=2)C(C)(C)C)=C1C QCAWEPFNJXQPAN-UHFFFAOYSA-N 0.000 description 2
- 229920000609 methyl cellulose Polymers 0.000 description 2
- 239000001923 methylcellulose Substances 0.000 description 2
- 235000010981 methylcellulose Nutrition 0.000 description 2
- CKVMAPHTVCTEMM-ALPQRHTBSA-N milbemycin oxime Chemical compound O1[C@H](C)[C@@H](C)CC[C@@]11O[C@H](C\C=C(C)\C[C@@H](C)\C=C\C=C/2[C@]3([C@H](C(=O)O4)C=C(C)C(=N/O)/[C@H]3OC\2)O)C[C@H]4C1.C1C[C@H](C)[C@@H](CC)O[C@@]21O[C@H](C\C=C(C)\C[C@@H](C)\C=C\C=C/1[C@]3([C@H](C(=O)O4)C=C(C)C(=N/O)/[C@H]3OC\1)O)C[C@H]4C2 CKVMAPHTVCTEMM-ALPQRHTBSA-N 0.000 description 2
- 229940099245 milbemycin oxime Drugs 0.000 description 2
- 229960005358 monensin Drugs 0.000 description 2
- GAOZTHIDHYLHMS-KEOBGNEYSA-N monensin A Chemical compound C([C@@](O1)(C)[C@H]2CC[C@@](O2)(CC)[C@H]2[C@H](C[C@@H](O2)[C@@H]2[C@H](C[C@@H](C)[C@](O)(CO)O2)C)C)C[C@@]21C[C@H](O)[C@@H](C)[C@@H]([C@@H](C)[C@@H](OC)[C@H](C)C(O)=O)O2 GAOZTHIDHYLHMS-KEOBGNEYSA-N 0.000 description 2
- KRTSDMXIXPKRQR-AATRIKPKSA-N monocrotophos Chemical compound CNC(=O)\C=C(/C)OP(=O)(OC)OC KRTSDMXIXPKRQR-AATRIKPKSA-N 0.000 description 2
- 229960005121 morantel Drugs 0.000 description 2
- FGGFIMIICGZCCJ-UHFFFAOYSA-N n,n-dibutyl-4-hexoxynaphthalene-1-carboximidamide Chemical compound C1=CC=C2C(OCCCCCC)=CC=C(C(=N)N(CCCC)CCCC)C2=C1 FGGFIMIICGZCCJ-UHFFFAOYSA-N 0.000 description 2
- LWGJTAZLEJHCPA-UHFFFAOYSA-N n-(2-chloroethyl)-n-nitrosomorpholine-4-carboxamide Chemical compound ClCCN(N=O)C(=O)N1CCOCC1 LWGJTAZLEJHCPA-UHFFFAOYSA-N 0.000 description 2
- DPLHJUQFGXECAS-UHFFFAOYSA-N n-[3-(benzylcarbamoyl)-4-chlorophenyl]-2-methyl-5-(1,1,2,2,2-pentafluoroethyl)-4-(trifluoromethyl)pyrazole-3-carboxamide Chemical compound CN1N=C(C(F)(F)C(F)(F)F)C(C(F)(F)F)=C1C(=O)NC1=CC=C(Cl)C(C(=O)NCC=2C=CC=CC=2)=C1 DPLHJUQFGXECAS-UHFFFAOYSA-N 0.000 description 2
- YNKFZRGTXAPYFD-UHFFFAOYSA-N n-[[2-chloro-3,5-bis(trifluoromethyl)phenyl]carbamoyl]-2,6-difluorobenzamide Chemical compound FC1=CC=CC(F)=C1C(=O)NC(=O)NC1=CC(C(F)(F)F)=CC(C(F)(F)F)=C1Cl YNKFZRGTXAPYFD-UHFFFAOYSA-N 0.000 description 2
- 229960001851 narasin Drugs 0.000 description 2
- 229950006716 netobimin Drugs 0.000 description 2
- 230000007935 neutral effect Effects 0.000 description 2
- 229960002644 nifurtimox Drugs 0.000 description 2
- 229940079888 nitenpyram Drugs 0.000 description 2
- 229910052757 nitrogen Inorganic materials 0.000 description 2
- SGKGVABHDAQAJO-UHFFFAOYSA-N nitroxynil Chemical compound OC1=C(I)C=C(C#N)C=C1[N+]([O-])=O SGKGVABHDAQAJO-UHFFFAOYSA-N 0.000 description 2
- 108010003516 norsynephrine receptor Proteins 0.000 description 2
- 235000015097 nutrients Nutrition 0.000 description 2
- 235000016709 nutrition Nutrition 0.000 description 2
- CKNAQFVBEHDJQV-UHFFFAOYSA-N oltipraz Chemical compound S1SC(=S)C(C)=C1C1=CN=CC=N1 CKNAQFVBEHDJQV-UHFFFAOYSA-N 0.000 description 2
- 229950008687 oltipraz Drugs 0.000 description 2
- PZXOQEXFMJCDPG-UHFFFAOYSA-N omethoate Chemical compound CNC(=O)CSP(=O)(OC)OC PZXOQEXFMJCDPG-UHFFFAOYSA-N 0.000 description 2
- CTSLXHKWHWQRSH-UHFFFAOYSA-N oxalyl chloride Chemical compound ClC(=O)C(Cl)=O CTSLXHKWHWQRSH-UHFFFAOYSA-N 0.000 description 2
- 229960002762 oxibendazole Drugs 0.000 description 2
- 230000010627 oxidative phosphorylation Effects 0.000 description 2
- JYWIYHUXVMAGLG-UHFFFAOYSA-N oxyclozanide Chemical compound OC1=C(Cl)C=C(Cl)C=C1NC(=O)C1=C(O)C(Cl)=CC(Cl)=C1Cl JYWIYHUXVMAGLG-UHFFFAOYSA-N 0.000 description 2
- 229950003126 oxyclozanide Drugs 0.000 description 2
- 238000010422 painting Methods 0.000 description 2
- 229930188716 paraherquamide Natural products 0.000 description 2
- 230000003071 parasitic effect Effects 0.000 description 2
- 239000002245 particle Substances 0.000 description 2
- 235000021017 pears Nutrition 0.000 description 2
- OGYFATSSENRIKG-UHFFFAOYSA-N pencycuron Chemical compound C1=CC(Cl)=CC=C1CN(C(=O)NC=1C=CC=CC=1)C1CCCC1 OGYFATSSENRIKG-UHFFFAOYSA-N 0.000 description 2
- 230000035515 penetration Effects 0.000 description 2
- JGCSKOVQDXEQHI-UHFFFAOYSA-N phenazine-1-carboxylic acid Chemical compound C1=CC=C2N=C3C(C(=O)O)=CC=CC3=NC2=C1 JGCSKOVQDXEQHI-UHFFFAOYSA-N 0.000 description 2
- XAMUDJHXFNRLCY-UHFFFAOYSA-N phenthoate Chemical compound CCOC(=O)C(SP(=S)(OC)OC)C1=CC=CC=C1 XAMUDJHXFNRLCY-UHFFFAOYSA-N 0.000 description 2
- 150000008048 phenylpyrazoles Chemical class 0.000 description 2
- 229920001339 phlorotannin Polymers 0.000 description 2
- LMNZTLDVJIUSHT-UHFFFAOYSA-N phosmet Chemical compound C1=CC=C2C(=O)N(CSP(=S)(OC)OC)C(=O)C2=C1 LMNZTLDVJIUSHT-UHFFFAOYSA-N 0.000 description 2
- RGCLLPNLLBQHPF-HJWRWDBZSA-N phosphamidon Chemical compound CCN(CC)C(=O)C(\Cl)=C(/C)OP(=O)(OC)OC RGCLLPNLLBQHPF-HJWRWDBZSA-N 0.000 description 2
- NBIIXXVUZAFLBC-UHFFFAOYSA-K phosphate Chemical compound [O-]P([O-])([O-])=O NBIIXXVUZAFLBC-UHFFFAOYSA-K 0.000 description 2
- 239000010452 phosphate Substances 0.000 description 2
- 150000004714 phosphonium salts Chemical class 0.000 description 2
- ZJAOAACCNHFJAH-UHFFFAOYSA-N phosphonoformic acid Chemical compound OC(=O)P(O)(O)=O ZJAOAACCNHFJAH-UHFFFAOYSA-N 0.000 description 2
- 239000011574 phosphorus Substances 0.000 description 2
- 229910052698 phosphorus Inorganic materials 0.000 description 2
- ATROHALUCMTWTB-OWBHPGMISA-N phoxim Chemical compound CCOP(=S)(OCC)O\N=C(\C#N)C1=CC=CC=C1 ATROHALUCMTWTB-OWBHPGMISA-N 0.000 description 2
- 229950001664 phoxim Drugs 0.000 description 2
- 239000000049 pigment Substances 0.000 description 2
- YFGYUFNIOHWBOB-UHFFFAOYSA-N pirimicarb Chemical compound CN(C)C(=O)OC1=NC(N(C)C)=NC(C)=C1C YFGYUFNIOHWBOB-UHFFFAOYSA-N 0.000 description 2
- QHOQHJPRIBSPCY-UHFFFAOYSA-N pirimiphos-methyl Chemical group CCN(CC)C1=NC(C)=CC(OP(=S)(OC)OC)=N1 QHOQHJPRIBSPCY-UHFFFAOYSA-N 0.000 description 2
- 239000000419 plant extract Substances 0.000 description 2
- 239000005648 plant growth regulator Substances 0.000 description 2
- 229920000137 polyphosphoric acid Polymers 0.000 description 2
- 229920002689 polyvinyl acetate Polymers 0.000 description 2
- 239000011118 polyvinyl acetate Substances 0.000 description 2
- 229920002451 polyvinyl alcohol Polymers 0.000 description 2
- VBUNOIXRZNJNAD-UHFFFAOYSA-N ponazuril Chemical compound CC1=CC(N2C(N(C)C(=O)NC2=O)=O)=CC=C1OC1=CC=C(S(=O)(=O)C(F)(F)F)C=C1 VBUNOIXRZNJNAD-UHFFFAOYSA-N 0.000 description 2
- 229960003508 ponazuril Drugs 0.000 description 2
- 239000011591 potassium Substances 0.000 description 2
- 229910052700 potassium Inorganic materials 0.000 description 2
- 239000011736 potassium bicarbonate Substances 0.000 description 2
- 229910000028 potassium bicarbonate Inorganic materials 0.000 description 2
- 235000015497 potassium bicarbonate Nutrition 0.000 description 2
- TYJJADVDDVDEDZ-UHFFFAOYSA-M potassium hydrogencarbonate Chemical compound [K+].OC([O-])=O TYJJADVDDVDEDZ-UHFFFAOYSA-M 0.000 description 2
- FGIUAXJPYTZDNR-UHFFFAOYSA-N potassium nitrate Chemical compound [K+].[O-][N+]([O-])=O FGIUAXJPYTZDNR-UHFFFAOYSA-N 0.000 description 2
- 229940096992 potassium oleate Drugs 0.000 description 2
- LPNYRYFBWFDTMA-UHFFFAOYSA-N potassium tert-butoxide Chemical compound [K+].CC(C)(C)[O-] LPNYRYFBWFDTMA-UHFFFAOYSA-N 0.000 description 2
- MLICVSDCCDDWMD-KVVVOXFISA-M potassium;(z)-octadec-9-enoate Chemical compound [K+].CCCCCCCC\C=C/CCCCCCCC([O-])=O MLICVSDCCDDWMD-KVVVOXFISA-M 0.000 description 2
- 244000144977 poultry Species 0.000 description 2
- 235000013594 poultry meat Nutrition 0.000 description 2
- 229960002957 praziquantel Drugs 0.000 description 2
- WHHIPMZEDGBUCC-UHFFFAOYSA-N probenazole Chemical compound C1=CC=C2C(OCC=C)=NS(=O)(=O)C2=C1 WHHIPMZEDGBUCC-UHFFFAOYSA-N 0.000 description 2
- QXJKBPAVAHBARF-BETUJISGSA-N procymidone Chemical compound O=C([C@]1(C)C[C@@]1(C1=O)C)N1C1=CC(Cl)=CC(Cl)=C1 QXJKBPAVAHBARF-BETUJISGSA-N 0.000 description 2
- QYMMJNLHFKGANY-UHFFFAOYSA-N profenofos Chemical compound CCCSP(=O)(OCC)OC1=CC=C(Br)C=C1Cl QYMMJNLHFKGANY-UHFFFAOYSA-N 0.000 description 2
- WZZLDXDUQPOXNW-UHFFFAOYSA-N propamocarb Chemical compound CCCOC(=O)NCCCN(C)C WZZLDXDUQPOXNW-UHFFFAOYSA-N 0.000 description 2
- QZWHWHNCPFEXLL-UHFFFAOYSA-N propan-2-yl n-[2-(1,3-thiazol-4-yl)-3h-benzimidazol-5-yl]carbamate Chemical compound N1C2=CC(NC(=O)OC(C)C)=CC=C2N=C1C1=CSC=N1 QZWHWHNCPFEXLL-UHFFFAOYSA-N 0.000 description 2
- PWYIUEFFPNVCMW-UHFFFAOYSA-N propaphos Chemical compound CCCOP(=O)(OCCC)OC1=CC=C(SC)C=C1 PWYIUEFFPNVCMW-UHFFFAOYSA-N 0.000 description 2
- ZYHMJXZULPZUED-UHFFFAOYSA-N propargite Chemical compound C1=CC(C(C)(C)C)=CC=C1OC1C(OS(=O)OCC#C)CCCC1 ZYHMJXZULPZUED-UHFFFAOYSA-N 0.000 description 2
- 239000003380 propellant Substances 0.000 description 2
- 230000000069 prophylactic effect Effects 0.000 description 2
- KKMLIVYBGSAJPM-UHFFFAOYSA-L propineb Chemical compound [Zn+2].[S-]C(=S)NC(C)CNC([S-])=S KKMLIVYBGSAJPM-UHFFFAOYSA-L 0.000 description 2
- FLVBXVXXXMLMOX-UHFFFAOYSA-N proquinazid Chemical compound C1=C(I)C=C2C(=O)N(CCC)C(OCCC)=NC2=C1 FLVBXVXXXMLMOX-UHFFFAOYSA-N 0.000 description 2
- 235000018102 proteins Nutrition 0.000 description 2
- 229940070687 psyllium Drugs 0.000 description 2
- QHGVXILFMXYDRS-UHFFFAOYSA-N pyraclofos Chemical compound C1=C(OP(=O)(OCC)SCCC)C=NN1C1=CC=C(Cl)C=C1 QHGVXILFMXYDRS-UHFFFAOYSA-N 0.000 description 2
- 229960005134 pyrantel Drugs 0.000 description 2
- YSAUAVHXTIETRK-AATRIKPKSA-N pyrantel Chemical compound CN1CCCN=C1\C=C\C1=CC=CS1 YSAUAVHXTIETRK-AATRIKPKSA-N 0.000 description 2
- HYJYGLGUBUDSLJ-UHFFFAOYSA-N pyrethrin Natural products CCC(=O)OC1CC(=C)C2CC3OC3(C)C2C2OC(=O)C(=C)C12 HYJYGLGUBUDSLJ-UHFFFAOYSA-N 0.000 description 2
- DWFZBUWUXWZWKD-UHFFFAOYSA-N pyridaben Chemical compound C1=CC(C(C)(C)C)=CC=C1CSC1=C(Cl)C(=O)N(C(C)(C)C)N=C1 DWFZBUWUXWZWKD-UHFFFAOYSA-N 0.000 description 2
- AEHJMNVBLRLZKK-UHFFFAOYSA-N pyridalyl Chemical group N1=CC(C(F)(F)F)=CC=C1OCCCOC1=C(Cl)C=C(OCC=C(Cl)Cl)C=C1Cl AEHJMNVBLRLZKK-UHFFFAOYSA-N 0.000 description 2
- WKSAUQYGYAYLPV-UHFFFAOYSA-N pyrimethamine Chemical compound CCC1=NC(N)=NC(N)=C1C1=CC=C(Cl)C=C1 WKSAUQYGYAYLPV-UHFFFAOYSA-N 0.000 description 2
- 229960000611 pyrimethamine Drugs 0.000 description 2
- OYRRZWATULMEPF-UHFFFAOYSA-N pyrimidin-4-amine Chemical compound NC1=CC=NC=N1 OYRRZWATULMEPF-UHFFFAOYSA-N 0.000 description 2
- YYXSCUSVVALMNW-FOWTUZBSSA-N pyriminostrobin Chemical compound CO\C=C(\C(=O)OC)C1=CC=CC=C1COC1=CC(C(F)(F)F)=NC(NC=2C(=CC(Cl)=CC=2)Cl)=N1 YYXSCUSVVALMNW-FOWTUZBSSA-N 0.000 description 2
- BAUQXSYUDSNRHL-UHFFFAOYSA-N pyrimorph Chemical compound C1=CC(C(C)(C)C)=CC=C1C(C=1C=NC(Cl)=CC=1)=CC(=O)N1CCOCC1 BAUQXSYUDSNRHL-UHFFFAOYSA-N 0.000 description 2
- NHDHVHZZCFYRSB-UHFFFAOYSA-N pyriproxyfen Chemical compound C=1C=CC=NC=1OC(C)COC(C=C1)=CC=C1OC1=CC=CC=C1 NHDHVHZZCFYRSB-UHFFFAOYSA-N 0.000 description 2
- JYQUHIFYBATCCY-UHFFFAOYSA-N quinalphos Chemical compound C1=CC=CC2=NC(OP(=S)(OCC)OCC)=CN=C21 JYQUHIFYBATCCY-UHFFFAOYSA-N 0.000 description 2
- FBQQHUGEACOBDN-UHFFFAOYSA-N quinomethionate Chemical compound N1=C2SC(=O)SC2=NC2=CC(C)=CC=C21 FBQQHUGEACOBDN-UHFFFAOYSA-N 0.000 description 2
- WRPIRSINYZBGPK-UHFFFAOYSA-N quinoxyfen Chemical compound C1=CC(F)=CC=C1OC1=CC=NC2=CC(Cl)=CC(Cl)=C12 WRPIRSINYZBGPK-UHFFFAOYSA-N 0.000 description 2
- NEMNPWINWMHUMR-UHFFFAOYSA-N rafoxanide Chemical compound OC1=C(I)C=C(I)C=C1C(=O)NC(C=C1Cl)=CC=C1OC1=CC=C(Cl)C=C1 NEMNPWINWMHUMR-UHFFFAOYSA-N 0.000 description 2
- 229950002980 rafoxanide Drugs 0.000 description 2
- 230000009467 reduction Effects 0.000 description 2
- 230000000246 remedial effect Effects 0.000 description 2
- 239000005871 repellent Substances 0.000 description 2
- 230000002940 repellent Effects 0.000 description 2
- 238000012827 research and development Methods 0.000 description 2
- GHMLBKRAJCXXBS-UHFFFAOYSA-N resorcinol Chemical compound OC1=CC=CC(O)=C1 GHMLBKRAJCXXBS-UHFFFAOYSA-N 0.000 description 2
- 230000035806 respiratory chain Effects 0.000 description 2
- 229940043267 rhodamine b Drugs 0.000 description 2
- 238000007363 ring formation reaction Methods 0.000 description 2
- 229940080817 rotenone Drugs 0.000 description 2
- 102000042094 ryanodine receptor (TC 1.A.3.1) family Human genes 0.000 description 2
- 108091052345 ryanodine receptor (TC 1.A.3.1) family Proteins 0.000 description 2
- 229960001548 salinomycin Drugs 0.000 description 2
- 235000019378 salinomycin Nutrition 0.000 description 2
- 229920006395 saturated elastomer Polymers 0.000 description 2
- 229930000044 secondary metabolite Natural products 0.000 description 2
- 239000003620 semiochemical Substances 0.000 description 2
- 230000011664 signaling Effects 0.000 description 2
- HPYNBECUCCGGPA-UHFFFAOYSA-N silafluofen Chemical compound C1=CC(OCC)=CC=C1[Si](C)(C)CCCC1=CC=C(F)C(OC=2C=CC=CC=2)=C1 HPYNBECUCCGGPA-UHFFFAOYSA-N 0.000 description 2
- 239000000377 silicon dioxide Substances 0.000 description 2
- MXMXHPPIGKYTAR-UHFFFAOYSA-N silthiofam Chemical compound CC=1SC([Si](C)(C)C)=C(C(=O)NCC=C)C=1C MXMXHPPIGKYTAR-UHFFFAOYSA-N 0.000 description 2
- 239000002002 slurry Substances 0.000 description 2
- 239000001632 sodium acetate Substances 0.000 description 2
- 235000017281 sodium acetate Nutrition 0.000 description 2
- 235000017550 sodium carbonate Nutrition 0.000 description 2
- 239000003195 sodium channel blocking agent Substances 0.000 description 2
- 239000001488 sodium phosphate Substances 0.000 description 2
- 229910000162 sodium phosphate Inorganic materials 0.000 description 2
- 235000011008 sodium phosphates Nutrition 0.000 description 2
- 239000004328 sodium tetraborate Substances 0.000 description 2
- 235000010339 sodium tetraborate Nutrition 0.000 description 2
- IYYIUOWKEMQYNV-UHFFFAOYSA-N sodium;ethoxy-oxido-oxophosphanium Chemical compound [Na+].CCO[P+]([O-])=O IYYIUOWKEMQYNV-UHFFFAOYSA-N 0.000 description 2
- 235000012424 soybean oil Nutrition 0.000 description 2
- 239000003549 soybean oil Substances 0.000 description 2
- 229940014213 spinosad Drugs 0.000 description 2
- DTDSAWVUFPGDMX-UHFFFAOYSA-N spirodiclofen Chemical compound CCC(C)(C)C(=O)OC1=C(C=2C(=CC(Cl)=CC=2)Cl)C(=O)OC11CCCCC1 DTDSAWVUFPGDMX-UHFFFAOYSA-N 0.000 description 2
- GOLXNESZZPUPJE-UHFFFAOYSA-N spiromesifen Chemical compound CC1=CC(C)=CC(C)=C1C(C(O1)=O)=C(OC(=O)CC(C)(C)C)C11CCCC1 GOLXNESZZPUPJE-UHFFFAOYSA-N 0.000 description 2
- CLSVJBIHYWPGQY-GGYDESQDSA-N spirotetramat Chemical compound CCOC(=O)OC1=C(C=2C(=CC=C(C)C=2)C)C(=O)N[C@@]11CC[C@H](OC)CC1 CLSVJBIHYWPGQY-GGYDESQDSA-N 0.000 description 2
- PUYXTUJWRLOUCW-UHFFFAOYSA-N spiroxamine Chemical compound O1C(CN(CC)CCC)COC11CCC(C(C)(C)C)CC1 PUYXTUJWRLOUCW-UHFFFAOYSA-N 0.000 description 2
- 150000003455 sulfinic acids Chemical class 0.000 description 2
- CCEKAJIANROZEO-UHFFFAOYSA-N sulfluramid Chemical compound CCNS(=O)(=O)C(F)(F)C(F)(F)C(F)(F)C(F)(F)C(F)(F)C(F)(F)C(F)(F)C(F)(F)F CCEKAJIANROZEO-UHFFFAOYSA-N 0.000 description 2
- 150000003460 sulfonic acids Chemical class 0.000 description 2
- XIUROWKZWPIAIB-UHFFFAOYSA-N sulfotep Chemical compound CCOP(=S)(OCC)OP(=S)(OCC)OCC XIUROWKZWPIAIB-UHFFFAOYSA-N 0.000 description 2
- 230000021918 systemic acquired resistance Effects 0.000 description 2
- QYPNKSZPJQQLRK-UHFFFAOYSA-N tebufenozide Chemical compound C1=CC(CC)=CC=C1C(=O)NN(C(C)(C)C)C(=O)C1=CC(C)=CC(C)=C1 QYPNKSZPJQQLRK-UHFFFAOYSA-N 0.000 description 2
- ZZYSLNWGKKDOML-UHFFFAOYSA-N tebufenpyrad Chemical compound CCC1=NN(C)C(C(=O)NCC=2C=CC(=CC=2)C(C)(C)C)=C1Cl ZZYSLNWGKKDOML-UHFFFAOYSA-N 0.000 description 2
- WWJZWCUNLNYYAU-UHFFFAOYSA-N temephos Chemical compound C1=CC(OP(=S)(OC)OC)=CC=C1SC1=CC=C(OP(=S)(OC)OC)C=C1 WWJZWCUNLNYYAU-UHFFFAOYSA-N 0.000 description 2
- 125000000999 tert-butyl group Chemical group [H]C([H])([H])C(*)(C([H])([H])[H])C([H])([H])[H] 0.000 description 2
- 150000003512 tertiary amines Chemical class 0.000 description 2
- 229960002180 tetracycline Drugs 0.000 description 2
- 229930101283 tetracycline Natural products 0.000 description 2
- CZDYPVPMEAXLPK-UHFFFAOYSA-N tetramethylsilane Chemical compound C[Si](C)(C)C CZDYPVPMEAXLPK-UHFFFAOYSA-N 0.000 description 2
- NWWZPOKUUAIXIW-FLIBITNWSA-N thiamethoxam Chemical compound [O-][N+](=O)\N=C/1N(C)COCN\1CC1=CN=C(Cl)S1 NWWZPOKUUAIXIW-FLIBITNWSA-N 0.000 description 2
- FYSNRJHAOHDILO-UHFFFAOYSA-N thionyl chloride Substances ClS(Cl)=O FYSNRJHAOHDILO-UHFFFAOYSA-N 0.000 description 2
- QGHREAKMXXNCOA-UHFFFAOYSA-N thiophanate-methyl Chemical compound COC(=O)NC(=S)NC1=CC=CC=C1NC(=S)NC(=O)OC QGHREAKMXXNCOA-UHFFFAOYSA-N 0.000 description 2
- 229960000790 thymol Drugs 0.000 description 2
- VJQYLJSMBWXGDV-UHFFFAOYSA-N tiadinil Chemical compound N1=NSC(C(=O)NC=2C=C(Cl)C(C)=CC=2)=C1C VJQYLJSMBWXGDV-UHFFFAOYSA-N 0.000 description 2
- WPALTCMYPARVNV-UHFFFAOYSA-N tolfenpyrad Chemical compound CCC1=NN(C)C(C(=O)NCC=2C=CC(OC=3C=CC(C)=CC=3)=CC=2)=C1Cl WPALTCMYPARVNV-UHFFFAOYSA-N 0.000 description 2
- 229960000898 toltrazuril Drugs 0.000 description 2
- 231100000419 toxicity Toxicity 0.000 description 2
- 230000001988 toxicity Effects 0.000 description 2
- 239000003053 toxin Substances 0.000 description 2
- 231100000765 toxin Toxicity 0.000 description 2
- 108700012359 toxins Proteins 0.000 description 2
- DDVNRFNDOPPVQJ-HQJQHLMTSA-N transfluthrin Chemical compound CC1(C)[C@H](C=C(Cl)Cl)[C@H]1C(=O)OCC1=C(F)C(F)=CC(F)=C1F DDVNRFNDOPPVQJ-HQJQHLMTSA-N 0.000 description 2
- 229910052723 transition metal Inorganic materials 0.000 description 2
- 150000003624 transition metals Chemical class 0.000 description 2
- NKNFWVNSBIXGLL-UHFFFAOYSA-N triazamate Chemical compound CCOC(=O)CSC1=NC(C(C)(C)C)=NN1C(=O)N(C)C NKNFWVNSBIXGLL-UHFFFAOYSA-N 0.000 description 2
- KVSKGMLNBAPGKH-UHFFFAOYSA-N tribromosalicylanilide Chemical compound OC1=C(Br)C=C(Br)C=C1C(=O)NC1=CC=C(Br)C=C1 KVSKGMLNBAPGKH-UHFFFAOYSA-N 0.000 description 2
- ITMCEJHCFYSIIV-UHFFFAOYSA-N triflic acid Chemical compound OS(=O)(=O)C(F)(F)F ITMCEJHCFYSIIV-UHFFFAOYSA-N 0.000 description 2
- XAIPTRIXGHTTNT-UHFFFAOYSA-N triflumuron Chemical compound C1=CC(OC(F)(F)F)=CC=C1NC(=O)NC(=O)C1=CC=CC=C1Cl XAIPTRIXGHTTNT-UHFFFAOYSA-N 0.000 description 2
- 125000000876 trifluoromethoxy group Chemical group FC(F)(F)O* 0.000 description 2
- RYFMWSXOAZQYPI-UHFFFAOYSA-K trisodium phosphate Chemical compound [Na+].[Na+].[Na+].[O-]P([O-])([O-])=O RYFMWSXOAZQYPI-UHFFFAOYSA-K 0.000 description 2
- 230000017260 vegetative to reproductive phase transition of meristem Effects 0.000 description 2
- 230000003612 virological effect Effects 0.000 description 2
- 239000004562 water dispersible granule Substances 0.000 description 2
- AEPMMTRERWOSHG-HULFFUFUSA-N (1E,3E)-dodeca-1,3-dien-1-ol Chemical compound CCCCCCCC\C=C\C=C\O AEPMMTRERWOSHG-HULFFUFUSA-N 0.000 description 1
- SPXBEYPYQKZKGX-USXIJHARSA-N (1R,2S,5S)-2-(chloromethyl)-5-[(4-chlorophenyl)methyl]-2-methyl-1-(1,2,4-triazol-1-ylmethyl)cyclopentan-1-ol Chemical compound C[C@]1(CCl)CC[C@@H](Cc2ccc(Cl)cc2)[C@]1(O)Cn1cncn1 SPXBEYPYQKZKGX-USXIJHARSA-N 0.000 description 1
- CYPYTURSJDMMMP-WVCUSYJESA-N (1e,4e)-1,5-diphenylpenta-1,4-dien-3-one;palladium Chemical compound [Pd].[Pd].C=1C=CC=CC=1\C=C\C(=O)\C=C\C1=CC=CC=C1.C=1C=CC=CC=1\C=C\C(=O)\C=C\C1=CC=CC=C1.C=1C=CC=CC=1\C=C\C(=O)\C=C\C1=CC=CC=C1 CYPYTURSJDMMMP-WVCUSYJESA-N 0.000 description 1
- SPXBEYPYQKZKGX-PVAVHDDUSA-N (1s,2r,5r)-2-(chloromethyl)-5-[(4-chlorophenyl)methyl]-2-methyl-1-(1,2,4-triazol-1-ylmethyl)cyclopentan-1-ol Chemical compound C([C@H]1CC[C@]([C@]1(O)CN1N=CN=C1)(CCl)C)C1=CC=C(Cl)C=C1 SPXBEYPYQKZKGX-PVAVHDDUSA-N 0.000 description 1
- YATDSXRLIUJOQN-SVRRBLITSA-N (2,3,4,5,6-pentafluorophenyl)methyl (1r,3s)-3-(2,2-dichloroethenyl)-2,2-dimethylcyclopropane-1-carboxylate Chemical compound CC1(C)[C@H](C=C(Cl)Cl)[C@H]1C(=O)OCC1=C(F)C(F)=C(F)C(F)=C1F YATDSXRLIUJOQN-SVRRBLITSA-N 0.000 description 1
- WXBHKHTWAPLUSQ-UHFFFAOYSA-N (2-methyl-5-prop-2-ynylfuran-3-yl)methyl 2,2-dimethyl-3-(2-methylprop-1-enyl)cyclopropane-1-carboxylate Chemical compound CC1(C)C(C=C(C)C)C1C(=O)OCC1=C(C)OC(CC#C)=C1 WXBHKHTWAPLUSQ-UHFFFAOYSA-N 0.000 description 1
- HPMOLIHDZUCPIZ-GXSJLCMTSA-N (2R)-2-(1-chlorocyclopropyl)-4-[(1S)-2,2-dichlorocyclopropyl]-1-(1,2,4-triazol-1-yl)butan-2-ol Chemical compound O[C@](CC[C@H]1CC1(Cl)Cl)(Cn1cncn1)C1(Cl)CC1 HPMOLIHDZUCPIZ-GXSJLCMTSA-N 0.000 description 1
- HPMOLIHDZUCPIZ-KOLCDFICSA-N (2S)-2-(1-chlorocyclopropyl)-4-[(1R)-2,2-dichlorocyclopropyl]-1-(1,2,4-triazol-1-yl)butan-2-ol Chemical compound O[C@@](CC[C@@H]1CC1(Cl)Cl)(Cn1cncn1)C1(Cl)CC1 HPMOLIHDZUCPIZ-KOLCDFICSA-N 0.000 description 1
- HPMOLIHDZUCPIZ-ONGXEEELSA-N (2S)-2-(1-chlorocyclopropyl)-4-[(1S)-2,2-dichlorocyclopropyl]-1-(1,2,4-triazol-1-yl)butan-2-ol Chemical compound O[C@@](CC[C@H]1CC1(Cl)Cl)(Cn1cncn1)C1(Cl)CC1 HPMOLIHDZUCPIZ-ONGXEEELSA-N 0.000 description 1
- LZTIMERBDGGAJD-SNAWJCMRSA-N (2e)-2-(nitromethylidene)-1,3-thiazinane Chemical compound [O-][N+](=O)\C=C1/NCCCS1 LZTIMERBDGGAJD-SNAWJCMRSA-N 0.000 description 1
- RDJGLLICXDHJDY-NSHDSACASA-N (2s)-2-(3-phenoxyphenyl)propanoic acid Chemical compound OC(=O)[C@@H](C)C1=CC=CC(OC=2C=CC=CC=2)=C1 RDJGLLICXDHJDY-NSHDSACASA-N 0.000 description 1
- RLLPVAHGXHCWKJ-HKUYNNGSSA-N (3-phenoxyphenyl)methyl (1r,3r)-3-(2,2-dichloroethenyl)-2,2-dimethylcyclopropane-1-carboxylate Chemical compound CC1(C)[C@@H](C=C(Cl)Cl)[C@H]1C(=O)OCC1=CC=CC(OC=2C=CC=CC=2)=C1 RLLPVAHGXHCWKJ-HKUYNNGSSA-N 0.000 description 1
- XUNYDVLIZWUPAW-UHFFFAOYSA-N (4-chlorophenyl) n-(4-methylphenyl)sulfonylcarbamate Chemical compound C1=CC(C)=CC=C1S(=O)(=O)NC(=O)OC1=CC=C(Cl)C=C1 XUNYDVLIZWUPAW-UHFFFAOYSA-N 0.000 description 1
- JONIMGVUGJVFQD-UHFFFAOYSA-N (4-methylphenyl)sulfonylformonitrile Chemical compound CC1=CC=C(S(=O)(=O)C#N)C=C1 JONIMGVUGJVFQD-UHFFFAOYSA-N 0.000 description 1
- YSEUOPNOQRVVDY-OGEJUEGTSA-N (5-benzylfuran-3-yl)methyl (1r,3r)-3-[(e)-3-methoxy-2-methyl-3-oxoprop-1-enyl]-2,2-dimethylcyclopropane-1-carboxylate Chemical compound CC1(C)[C@H](/C=C(\C)C(=O)OC)[C@H]1C(=O)OCC1=COC(CC=2C=CC=CC=2)=C1 YSEUOPNOQRVVDY-OGEJUEGTSA-N 0.000 description 1
- VEMKTZHHVJILDY-WOJBJXKFSA-N (5-benzylfuran-3-yl)methyl (1s,3r)-2,2-dimethyl-3-(2-methylprop-1-enyl)cyclopropane-1-carboxylate Chemical compound CC1(C)[C@H](C=C(C)C)[C@@H]1C(=O)OCC1=COC(CC=2C=CC=CC=2)=C1 VEMKTZHHVJILDY-WOJBJXKFSA-N 0.000 description 1
- 125000004769 (C1-C4) alkylsulfonyl group Chemical group 0.000 description 1
- 125000004767 (C1-C4) haloalkoxy group Chemical group 0.000 description 1
- 125000006656 (C2-C4) alkenyl group Chemical group 0.000 description 1
- FZRBKIRIBLNOAM-UHFFFAOYSA-N (E,E)-2-propynyl 3,7,11-trimethyl-2,4-dodecadienoate Chemical compound CC(C)CCCC(C)CC=CC(C)=CC(=O)OCC#C FZRBKIRIBLNOAM-UHFFFAOYSA-N 0.000 description 1
- PDPWCKVFIFAQIQ-GOSISDBHSA-N (R)-mandestrobin Chemical compound CNC(=O)[C@H](OC)C1=CC=CC=C1COC1=CC(C)=CC=C1C PDPWCKVFIFAQIQ-GOSISDBHSA-N 0.000 description 1
- JERZEQUMJNCPRJ-KRWDZBQOSA-N (R)-mefentrifluconazole Chemical compound C([C@@](O)(C)C=1C(=CC(OC=2C=CC(Cl)=CC=2)=CC=1)C(F)(F)F)N1C=NC=N1 JERZEQUMJNCPRJ-KRWDZBQOSA-N 0.000 description 1
- PDPWCKVFIFAQIQ-SFHVURJKSA-N (S)-mandestrobin Chemical compound CNC(=O)[C@@H](OC)C1=CC=CC=C1COC1=CC(C)=CC=C1C PDPWCKVFIFAQIQ-SFHVURJKSA-N 0.000 description 1
- JERZEQUMJNCPRJ-QGZVFWFLSA-N (S)-mefentrifluconazole Chemical compound C([C@](O)(C)C=1C(=CC(OC=2C=CC(Cl)=CC=2)=CC=1)C(F)(F)F)N1C=NC=N1 JERZEQUMJNCPRJ-QGZVFWFLSA-N 0.000 description 1
- XGWIJUOSCAQSSV-XHDPSFHLSA-N (S,S)-hexythiazox Chemical compound S([C@H]([C@@H]1C)C=2C=CC(Cl)=CC=2)C(=O)N1C(=O)NC1CCCCC1 XGWIJUOSCAQSSV-XHDPSFHLSA-N 0.000 description 1
- QNBTYORWCCMPQP-JXAWBTAJSA-N (Z)-dimethomorph Chemical compound C1=C(OC)C(OC)=CC=C1C(\C=1C=CC(Cl)=CC=1)=C/C(=O)N1CCOCC1 QNBTYORWCCMPQP-JXAWBTAJSA-N 0.000 description 1
- PCKNFPQPGUWFHO-SXBRIOAWSA-N (Z)-flucycloxuron Chemical compound FC1=CC=CC(F)=C1C(=O)NC(=O)NC(C=C1)=CC=C1CO\N=C(C=1C=CC(Cl)=CC=1)\C1CC1 PCKNFPQPGUWFHO-SXBRIOAWSA-N 0.000 description 1
- HOKKPVIRMVDYPB-UVTDQMKNSA-N (Z)-thiacloprid Chemical compound C1=NC(Cl)=CC=C1CN1C(=N/C#N)/SCC1 HOKKPVIRMVDYPB-UVTDQMKNSA-N 0.000 description 1
- QEUOHPLVFSQWME-XDJHFCHBSA-N (e)-3-(4-tert-butylphenyl)-3-(2-chloropyridin-4-yl)-1-morpholin-4-ylprop-2-en-1-one Chemical compound C1=CC(C(C)(C)C)=CC=C1C(\C=1C=C(Cl)N=CC=1)=C/C(=O)N1CCOCC1 QEUOHPLVFSQWME-XDJHFCHBSA-N 0.000 description 1
- DYLIWHYUXAJDOJ-OWOJBTEDSA-N (e)-4-(6-aminopurin-9-yl)but-2-en-1-ol Chemical compound NC1=NC=NC2=C1N=CN2C\C=C\CO DYLIWHYUXAJDOJ-OWOJBTEDSA-N 0.000 description 1
- YDHZUCLRCLIJRL-HXUWFJFHSA-N (r)-[3-(4-chloro-2-fluorophenyl)-5-(2,4-difluorophenyl)-1,2-oxazol-4-yl]-pyridin-3-ylmethanol Chemical compound C=1([C@H](O)C=2C=NC=CC=2)C(C=2C(=CC(Cl)=CC=2)F)=NOC=1C1=CC=C(F)C=C1F YDHZUCLRCLIJRL-HXUWFJFHSA-N 0.000 description 1
- YDHZUCLRCLIJRL-FQEVSTJZSA-N (s)-[3-(4-chloro-2-fluorophenyl)-5-(2,4-difluorophenyl)-1,2-oxazol-4-yl]-pyridin-3-ylmethanol Chemical compound C=1([C@@H](O)C=2C=NC=CC=2)C(C=2C(=CC(Cl)=CC=2)F)=NOC=1C1=CC=C(F)C=C1F YDHZUCLRCLIJRL-FQEVSTJZSA-N 0.000 description 1
- QEUOHPLVFSQWME-CYVLTUHYSA-N (z)-3-(4-tert-butylphenyl)-3-(2-chloropyridin-4-yl)-1-morpholin-4-ylprop-2-en-1-one Chemical compound C1=CC(C(C)(C)C)=CC=C1C(\C=1C=C(Cl)N=CC=1)=C\C(=O)N1CCOCC1 QEUOHPLVFSQWME-CYVLTUHYSA-N 0.000 description 1
- XBCKTJDKWPZLJH-ZUPCBTBPSA-N (z,2e)-5-[1-(4-chlorophenyl)pyrazol-3-yl]oxy-2-methoxyimino-n,3-dimethylpent-3-enamide Chemical compound N1=C(OC\C=C(\C)/C(=N\OC)/C(=O)NC)C=CN1C1=CC=C(Cl)C=C1 XBCKTJDKWPZLJH-ZUPCBTBPSA-N 0.000 description 1
- FNQJDLTXOVEEFB-UHFFFAOYSA-N 1,2,3-benzothiadiazole Chemical compound C1=CC=C2SN=NC2=C1 FNQJDLTXOVEEFB-UHFFFAOYSA-N 0.000 description 1
- TUBQDCKAWGHZPF-UHFFFAOYSA-N 1,3-benzothiazol-2-ylsulfanylmethyl thiocyanate Chemical compound C1=CC=C2SC(SCSC#N)=NC2=C1 TUBQDCKAWGHZPF-UHFFFAOYSA-N 0.000 description 1
- HKELWJONQIFBPO-UHFFFAOYSA-N 1-(2,4-dichlorophenyl)-5-(trichloromethyl)-1,2,4-triazole-3-carboxylic acid Chemical compound N1=C(C(=O)O)N=C(C(Cl)(Cl)Cl)N1C1=CC=C(Cl)C=C1Cl HKELWJONQIFBPO-UHFFFAOYSA-N 0.000 description 1
- JWUCHKBSVLQQCO-UHFFFAOYSA-N 1-(2-fluorophenyl)-1-(4-fluorophenyl)-2-(1H-1,2,4-triazol-1-yl)ethanol Chemical compound C=1C=C(F)C=CC=1C(C=1C(=CC=CC=1)F)(O)CN1C=NC=N1 JWUCHKBSVLQQCO-UHFFFAOYSA-N 0.000 description 1
- IHGSAQHSAGRWNI-UHFFFAOYSA-N 1-(4-bromophenyl)-2,2,2-trifluoroethanone Chemical compound FC(F)(F)C(=O)C1=CC=C(Br)C=C1 IHGSAQHSAGRWNI-UHFFFAOYSA-N 0.000 description 1
- RURQAJURNPMSSK-UHFFFAOYSA-N 1-(4-chlorophenoxy)-3-{[2-(4-ethoxyphenyl)-3,3,3-trifluoropropoxy]methyl}benzene Chemical compound C1=CC(OCC)=CC=C1C(C(F)(F)F)COCC1=CC=CC(OC=2C=CC(Cl)=CC=2)=C1 RURQAJURNPMSSK-UHFFFAOYSA-N 0.000 description 1
- RQTVIKMRXYJTDX-UHFFFAOYSA-N 1-(4-methylphenyl)sulfonyl-4-phenylpiperidine-4-carbonitrile Chemical compound C1=CC(C)=CC=C1S(=O)(=O)N1CCC(C=2C=CC=CC=2)(C#N)CC1 RQTVIKMRXYJTDX-UHFFFAOYSA-N 0.000 description 1
- SIQZJFKTROUNPI-UHFFFAOYSA-N 1-(hydroxymethyl)-5,5-dimethylhydantoin Chemical compound CC1(C)N(CO)C(=O)NC1=O SIQZJFKTROUNPI-UHFFFAOYSA-N 0.000 description 1
- LWWDYSLFWMWORA-BEJOPBHTSA-N 1-[2,6-dichloro-4-(trifluoromethyl)phenyl]-5-[(E)-(4-hydroxy-3-methoxyphenyl)methylideneamino]-4-(trifluoromethylsulfanyl)pyrazole-3-carbonitrile Chemical compound c1cc(O)c(OC)cc1\C=N\c1c(SC(F)(F)F)c(C#N)nn1-c1c(Cl)cc(C(F)(F)F)cc1Cl LWWDYSLFWMWORA-BEJOPBHTSA-N 0.000 description 1
- XVTXMTOYQVRHSK-UHFFFAOYSA-N 1-[2-(2,4-dichlorophenyl)-2-prop-2-enoxyethyl]imidazole;sulfuric acid Chemical compound OS(O)(=O)=O.ClC1=CC(Cl)=CC=C1C(OCC=C)CN1C=NC=C1 XVTXMTOYQVRHSK-UHFFFAOYSA-N 0.000 description 1
- KDMZCYQCANNXSQ-UHFFFAOYSA-N 1-[2-(cyclopropylmethoxy)-4-(trifluoromethyl)phenoxy]-3-[6-(trifluoromethyl)pyridazin-3-yl]-3-azabicyclo[3.2.1]octane Chemical compound C1(CC1)COC1=C(OC23CN(CC(CC2)C3)C=2N=NC(=CC=2)C(F)(F)F)C=CC(=C1)C(F)(F)F KDMZCYQCANNXSQ-UHFFFAOYSA-N 0.000 description 1
- FLEFKKUZMDEUIP-QFIPXVFZSA-N 1-[6-[(5s)-5-(3,5-dichloro-4-fluorophenyl)-5-(trifluoromethyl)-4h-1,2-oxazol-3-yl]spiro[1h-2-benzofuran-3,3'-azetidine]-1'-yl]-2-methylsulfonylethanone Chemical compound C1N(C(=O)CS(=O)(=O)C)CC21C1=CC=C(C=3C[C@](ON=3)(C=3C=C(Cl)C(F)=C(Cl)C=3)C(F)(F)F)C=C1CO2 FLEFKKUZMDEUIP-QFIPXVFZSA-N 0.000 description 1
- 125000004973 1-butenyl group Chemical group C(=CCC)* 0.000 description 1
- REACWASHYHDPSQ-UHFFFAOYSA-N 1-butylpyridin-1-ium Chemical compound CCCC[N+]1=CC=CC=C1 REACWASHYHDPSQ-UHFFFAOYSA-N 0.000 description 1
- BSIMZHVOQZIAOY-SCSAIBSYSA-N 1-carbapenem-3-carboxylic acid Chemical compound OC(=O)C1=CC[C@@H]2CC(=O)N12 BSIMZHVOQZIAOY-SCSAIBSYSA-N 0.000 description 1
- 125000006039 1-hexenyl group Chemical group 0.000 description 1
- AXHRXVXCOMMNLG-UHFFFAOYSA-N 1-hydroxy-10h-anthracen-9-one Chemical compound C1C2=CC=CC=C2C(=O)C2=C1C=CC=C2O AXHRXVXCOMMNLG-UHFFFAOYSA-N 0.000 description 1
- DUWKZHIPEWZXNC-UHFFFAOYSA-N 1-methyl-3-(trifluoromethyl)-n-[2-[2-(trifluoromethyl)phenyl]phenyl]pyrazole-4-carboxamide Chemical compound FC(F)(F)C1=NN(C)C=C1C(=O)NC1=CC=CC=C1C1=CC=CC=C1C(F)(F)F DUWKZHIPEWZXNC-UHFFFAOYSA-N 0.000 description 1
- 125000006023 1-pentenyl group Chemical group 0.000 description 1
- 125000006017 1-propenyl group Chemical group 0.000 description 1
- 125000000530 1-propynyl group Chemical group [H]C([H])([H])C#C* 0.000 description 1
- AVRPFRMDMNDIDH-UHFFFAOYSA-N 1h-quinazolin-2-one Chemical class C1=CC=CC2=NC(O)=NC=C21 AVRPFRMDMNDIDH-UHFFFAOYSA-N 0.000 description 1
- MCUFTOFSZFEQMB-UHFFFAOYSA-N 2,3,4,5,6-pentachlorophenol Chemical compound OC1=C(Cl)C(Cl)=C(Cl)C(Cl)=C1Cl.OC1=C(Cl)C(Cl)=C(Cl)C(Cl)=C1Cl MCUFTOFSZFEQMB-UHFFFAOYSA-N 0.000 description 1
- TVFWYUWNQVRQRG-UHFFFAOYSA-N 2,3,4-tris(2-phenylethenyl)phenol Chemical compound C=1C=CC=CC=1C=CC1=C(C=CC=2C=CC=CC=2)C(O)=CC=C1C=CC1=CC=CC=C1 TVFWYUWNQVRQRG-UHFFFAOYSA-N 0.000 description 1
- LWEAHXKXKDCSIE-UHFFFAOYSA-M 2,3-di(propan-2-yl)naphthalene-1-sulfonate Chemical compound C1=CC=C2C(S([O-])(=O)=O)=C(C(C)C)C(C(C)C)=CC2=C1 LWEAHXKXKDCSIE-UHFFFAOYSA-M 0.000 description 1
- UMPSXRYVXUPCOS-UHFFFAOYSA-N 2,3-dichlorophenol Chemical compound OC1=CC=CC(Cl)=C1Cl UMPSXRYVXUPCOS-UHFFFAOYSA-N 0.000 description 1
- MHKBMNACOMRIAW-UHFFFAOYSA-N 2,3-dinitrophenol Chemical class OC1=CC=CC([N+]([O-])=O)=C1[N+]([O-])=O MHKBMNACOMRIAW-UHFFFAOYSA-N 0.000 description 1
- NIOPZPCMRQGZCE-WEVVVXLNSA-N 2,4-dinitro-6-(octan-2-yl)phenyl (E)-but-2-enoate Chemical compound CCCCCCC(C)C1=CC([N+]([O-])=O)=CC([N+]([O-])=O)=C1OC(=O)\C=C\C NIOPZPCMRQGZCE-WEVVVXLNSA-N 0.000 description 1
- JTHMHWAHAKLCKT-UHFFFAOYSA-N 2,6-difluoro-n-[[4-(trifluoromethyl)phenyl]carbamoyl]benzamide Chemical compound FC1=CC=CC(F)=C1C(=O)NC(=O)NC1=CC=C(C(F)(F)F)C=C1 JTHMHWAHAKLCKT-UHFFFAOYSA-N 0.000 description 1
- KWLVWJPJKJMCSH-UHFFFAOYSA-N 2-(4-chlorophenyl)-N-{2-[3-methoxy-4-(prop-2-yn-1-yloxy)phenyl]ethyl}-2-(prop-2-yn-1-yloxy)acetamide Chemical compound C1=C(OCC#C)C(OC)=CC(CCNC(=O)C(OCC#C)C=2C=CC(Cl)=CC=2)=C1 KWLVWJPJKJMCSH-UHFFFAOYSA-N 0.000 description 1
- AGVACZYQCJRDQE-UHFFFAOYSA-N 2-(6-benzylpyridin-2-yl)quinazoline Chemical compound C=1C=CC(C=2N=C3C=CC=CC3=CN=2)=NC=1CC1=CC=CC=C1 AGVACZYQCJRDQE-UHFFFAOYSA-N 0.000 description 1
- HITWHALOZBMLHY-UHFFFAOYSA-N 2-Butyl-1H-benzimidazole Chemical compound C1=CC=C2NC(CCCC)=NC2=C1 HITWHALOZBMLHY-UHFFFAOYSA-N 0.000 description 1
- NGNBDVOYPDDBFK-UHFFFAOYSA-N 2-[2,4-di(pentan-2-yl)phenoxy]acetyl chloride Chemical compound CCCC(C)C1=CC=C(OCC(Cl)=O)C(C(C)CCC)=C1 NGNBDVOYPDDBFK-UHFFFAOYSA-N 0.000 description 1
- RUUBFCPAVMVRMA-UHFFFAOYSA-N 2-[2-fluoro-4-methyl-5-(2,2,2-trifluoroethylsulfinyl)phenyl]-5-(trifluoromethyl)-1,2,4-triazol-3-amine Chemical compound C1=C(S(=O)CC(F)(F)F)C(C)=CC(F)=C1N1C(N)=NC(C(F)(F)F)=N1 RUUBFCPAVMVRMA-UHFFFAOYSA-N 0.000 description 1
- GJHSCETXAKIWLY-UHFFFAOYSA-N 2-[3,5-bis(difluoromethyl)pyrazol-1-yl]-1-[4-[4-[5-(2-chloro-6-prop-2-ynoxyphenyl)-4,5-dihydro-1,2-oxazol-3-yl]-1,3-thiazol-2-yl]piperidin-1-yl]ethanone Chemical compound N1=C(C(F)F)C=C(C(F)F)N1CC(=O)N1CCC(C=2SC=C(N=2)C=2CC(ON=2)C=2C(=CC=CC=2Cl)OCC#C)CC1 GJHSCETXAKIWLY-UHFFFAOYSA-N 0.000 description 1
- BOTNFCTYKJBUMU-UHFFFAOYSA-N 2-[4-(2-methylpropyl)piperazin-4-ium-1-yl]-2-oxoacetate Chemical compound CC(C)C[NH+]1CCN(C(=O)C([O-])=O)CC1 BOTNFCTYKJBUMU-UHFFFAOYSA-N 0.000 description 1
- JERZEQUMJNCPRJ-UHFFFAOYSA-N 2-[4-(4-chlorophenoxy)-2-(trifluoromethyl)phenyl]-1-(1H-1,2,4-triazol-1-yl)propan-2-ol Chemical compound C=1C=C(OC=2C=CC(Cl)=CC=2)C=C(C(F)(F)F)C=1C(O)(C)CN1C=NC=N1 JERZEQUMJNCPRJ-UHFFFAOYSA-N 0.000 description 1
- YANWOMFJWXJQEF-UHFFFAOYSA-N 2-[6-(3-fluoro-4-methoxyphenyl)-5-methylpyridin-2-yl]quinazoline Chemical compound C1=C(F)C(OC)=CC=C1C1=NC(C=2N=C3C=CC=CC3=CN=2)=CC=C1C YANWOMFJWXJQEF-UHFFFAOYSA-N 0.000 description 1
- PVTHJAPFENJVNC-UHFFFAOYSA-N 2-amino-2-[5-amino-2-methyl-6-(2,3,4,5,6-pentahydroxycyclohexyl)oxyoxan-3-yl]iminoacetic acid Chemical compound NC1CC(N=C(N)C(O)=O)C(C)OC1OC1C(O)C(O)C(O)C(O)C1O PVTHJAPFENJVNC-UHFFFAOYSA-N 0.000 description 1
- 125000004974 2-butenyl group Chemical group C(C=CC)* 0.000 description 1
- QBVBOBWTOSGVEN-UHFFFAOYSA-N 2-chloro-3,4-dinitrophenol Chemical compound OC1=CC=C([N+]([O-])=O)C([N+]([O-])=O)=C1Cl QBVBOBWTOSGVEN-UHFFFAOYSA-N 0.000 description 1
- ZDOOQPFIGYHZFV-UHFFFAOYSA-N 2-ethyl-4-[(4-phenoxyphenoxy)methyl]-1,3-dioxolane Chemical compound O1C(CC)OCC1COC(C=C1)=CC=C1OC1=CC=CC=C1 ZDOOQPFIGYHZFV-UHFFFAOYSA-N 0.000 description 1
- 125000006040 2-hexenyl group Chemical group 0.000 description 1
- KZVMIFXJZQUPKL-UHFFFAOYSA-N 2-methoxy-n-methylpropanamide Chemical compound CNC(=O)C(C)OC KZVMIFXJZQUPKL-UHFFFAOYSA-N 0.000 description 1
- AWSZRJQNBMEZOI-UHFFFAOYSA-N 2-methoxyethyl 2-(4-tert-butylphenyl)-2-cyano-3-oxo-3-[2-(trifluoromethyl)phenyl]propanoate Chemical compound C=1C=C(C(C)(C)C)C=CC=1C(C#N)(C(=O)OCCOC)C(=O)C1=CC=CC=C1C(F)(F)F AWSZRJQNBMEZOI-UHFFFAOYSA-N 0.000 description 1
- NDCIJSKMUFWGRZ-UHFFFAOYSA-N 2-methoxyimino-n-methylpropanamide Chemical compound CNC(=O)C(C)=NOC NDCIJSKMUFWGRZ-UHFFFAOYSA-N 0.000 description 1
- YWDWYOALXURQPZ-CYBMUJFWSA-N 2-methyl-n-[3-[(6s)-2,3,5,6-tetrahydroimidazo[2,1-b][1,3]thiazol-6-yl]phenyl]propanamide Chemical compound CC(C)C(=O)NC1=CC=CC([C@@H]2N=C3SCCN3C2)=C1 YWDWYOALXURQPZ-CYBMUJFWSA-N 0.000 description 1
- IZFZCMFMJKDHJZ-UHFFFAOYSA-N 2-n,3-diphenyl-4-n,5-n-bis(trifluoromethyl)-1,3-thiazolidine-2,4,5-triimine Chemical compound C=1C=CC=CC=1N1C(=NC(F)(F)F)C(=NC(F)(F)F)SC1=NC1=CC=CC=C1 IZFZCMFMJKDHJZ-UHFFFAOYSA-N 0.000 description 1
- RLRUNZFXEAZVIT-UHFFFAOYSA-N 2-n-methyl-5-(trifluoromethyl)pyridine-2,3-diamine Chemical compound CNC1=NC=C(C(F)(F)F)C=C1N RLRUNZFXEAZVIT-UHFFFAOYSA-N 0.000 description 1
- FUBFWTUFPGFHOJ-UHFFFAOYSA-N 2-nitrofuran Chemical class [O-][N+](=O)C1=CC=CO1 FUBFWTUFPGFHOJ-UHFFFAOYSA-N 0.000 description 1
- 125000006024 2-pentenyl group Chemical group 0.000 description 1
- 229940061334 2-phenylphenol Drugs 0.000 description 1
- 125000003903 2-propenyl group Chemical group [H]C([*])([H])C([H])=C([H])[H] 0.000 description 1
- 125000004105 2-pyridyl group Chemical group N1=C([*])C([H])=C([H])C([H])=C1[H] 0.000 description 1
- XUUSYXJGMRQBKQ-UHFFFAOYSA-N 2h-2-benzazepine Chemical compound N1C=CC=C2C=CC=CC2=C1 XUUSYXJGMRQBKQ-UHFFFAOYSA-N 0.000 description 1
- UMZCLZPXPCNKML-UHFFFAOYSA-N 2h-imidazo[4,5-d][1,3]thiazole Chemical class C1=NC2=NCSC2=N1 UMZCLZPXPCNKML-UHFFFAOYSA-N 0.000 description 1
- AUQAUAIUNJIIEP-UHFFFAOYSA-N 3,4,5-trimethylphenyl methylcarbamate Chemical compound CNC(=O)OC1=CC(C)=C(C)C(C)=C1 AUQAUAIUNJIIEP-UHFFFAOYSA-N 0.000 description 1
- BKKBBACGKLNEDT-UHFFFAOYSA-N 3,4-diiodo-2-nitrophenol Chemical compound OC1=CC=C(I)C(I)=C1[N+]([O-])=O BKKBBACGKLNEDT-UHFFFAOYSA-N 0.000 description 1
- CAAMSDWKXXPUJR-UHFFFAOYSA-N 3,5-dihydro-4H-imidazol-4-one Chemical class O=C1CNC=N1 CAAMSDWKXXPUJR-UHFFFAOYSA-N 0.000 description 1
- IRJNJBIOUYJBHG-UHFFFAOYSA-N 3-(1-methylpyrrolidin-2-yl)pyridine Chemical compound CN1CCCC1C1=CC=CN=C1.CN1CCCC1C1=CC=CN=C1 IRJNJBIOUYJBHG-UHFFFAOYSA-N 0.000 description 1
- SWBHWUYHHJCADA-UHFFFAOYSA-N 3-(2-chlorophenyl)-6-(2,6-difluorophenyl)-1,2,4,5-tetrazine Chemical compound FC1=CC=CC(F)=C1C1=NN=C(C=2C(=CC=CC=2)Cl)N=N1 SWBHWUYHHJCADA-UHFFFAOYSA-N 0.000 description 1
- FOGYNLXERPKEGN-UHFFFAOYSA-N 3-(2-hydroxy-3-methoxyphenyl)-2-[2-methoxy-4-(3-sulfopropyl)phenoxy]propane-1-sulfonic acid Chemical class COC1=CC=CC(CC(CS(O)(=O)=O)OC=2C(=CC(CCCS(O)(=O)=O)=CC=2)OC)=C1O FOGYNLXERPKEGN-UHFFFAOYSA-N 0.000 description 1
- OIJVCMGWZZTWJT-UHFFFAOYSA-N 3-(4-chloro-2,6-dimethylphenyl)-4-hydroxy-8-methoxy-1,8-diazaspiro[4.5]dec-3-en-2-one Chemical compound ClC1=CC(=C(C(=C1)C)C=1C(NC2(C=1O)CCN(CC2)OC)=O)C OIJVCMGWZZTWJT-UHFFFAOYSA-N 0.000 description 1
- XCGBHLLWJZOLEM-UHFFFAOYSA-N 3-(difluoromethyl)-N-(7-fluoro-1,1,3-trimethyl-2,3-dihydro-1H-inden-4-yl)-1-methyl-1H-pyrazole-4-carboxamide Chemical compound CC1CC(C)(C)C(C(=CC=2)F)=C1C=2NC(=O)C1=CN(C)N=C1C(F)F XCGBHLLWJZOLEM-UHFFFAOYSA-N 0.000 description 1
- DGOAXBPOVUPPEB-UHFFFAOYSA-N 3-(difluoromethyl)-N-methoxy-1-methyl-N-[1-(2,4,6-trichlorophenyl)propan-2-yl]pyrazole-4-carboxamide Chemical compound C=1N(C)N=C(C(F)F)C=1C(=O)N(OC)C(C)CC1=C(Cl)C=C(Cl)C=C1Cl DGOAXBPOVUPPEB-UHFFFAOYSA-N 0.000 description 1
- 125000004975 3-butenyl group Chemical group C(CC=C)* 0.000 description 1
- 125000000474 3-butynyl group Chemical group [H]C#CC([H])([H])C([H])([H])* 0.000 description 1
- ZNBJSAAROMDHOX-UHFFFAOYSA-N 3-chloro-4-(2,6-difluorophenyl)-6-methyl-5-phenylpyridazine Chemical compound C=1C=CC=CC=1C=1C(C)=NN=C(Cl)C=1C1=C(F)C=CC=C1F ZNBJSAAROMDHOX-UHFFFAOYSA-N 0.000 description 1
- DNDLJUVNJLTMIE-UHFFFAOYSA-N 3-chloro-5-(4-chlorophenyl)-4-(2,6-difluorophenyl)-6-methylpyridazine Chemical compound C=1C=C(Cl)C=CC=1C=1C(C)=NN=C(Cl)C=1C1=C(F)C=CC=C1F DNDLJUVNJLTMIE-UHFFFAOYSA-N 0.000 description 1
- INDMHHREARZNOU-UHFFFAOYSA-N 3-chloro-5-(6-chloropyridin-3-yl)-6-methyl-4-(2,4,6-trifluorophenyl)pyridazine Chemical compound C=1C=C(Cl)N=CC=1C=1C(C)=NN=C(Cl)C=1C1=C(F)C=C(F)C=C1F INDMHHREARZNOU-UHFFFAOYSA-N 0.000 description 1
- 125000006041 3-hexenyl group Chemical group 0.000 description 1
- RUXHWBMJNBBYNL-UHFFFAOYSA-N 3-hydroxy-1,2-dihydropyrrol-5-one Chemical class OC1=CC(=O)NC1 RUXHWBMJNBBYNL-UHFFFAOYSA-N 0.000 description 1
- HDKWFBCPLKNOCK-SFHVURJKSA-N 3-methyl-n-[2-oxo-2-(2,2,2-trifluoroethylamino)ethyl]-5-[(5s)-5-(3,4,5-trichlorophenyl)-5-(trifluoromethyl)-4h-1,2-oxazol-3-yl]thiophene-2-carboxamide Chemical compound S1C(C(=O)NCC(=O)NCC(F)(F)F)=C(C)C=C1C1=NO[C@](C(F)(F)F)(C=2C=C(Cl)C(Cl)=C(Cl)C=2)C1 HDKWFBCPLKNOCK-SFHVURJKSA-N 0.000 description 1
- 125000003542 3-methylbutan-2-yl group Chemical group [H]C([H])([H])C([H])(*)C([H])(C([H])([H])[H])C([H])([H])[H] 0.000 description 1
- SWTPIYGGSMJRTB-UHFFFAOYSA-N 4,4-difluoro-3,3-dimethyl-1-quinolin-3-ylisoquinoline Chemical compound C12=CC=CC=C2C(F)(F)C(C)(C)N=C1C1=CN=C(C=CC=C2)C2=C1 SWTPIYGGSMJRTB-UHFFFAOYSA-N 0.000 description 1
- ODJRGOYSTVDWMP-UHFFFAOYSA-N 4-(2-bromo-4-fluorophenyl)-n-(2,6-difluorophenyl)-2,5-dimethylpyrazol-3-amine Chemical compound C=1C=C(F)C=C(Br)C=1C=1C(C)=NN(C)C=1NC1=C(F)C=CC=C1F ODJRGOYSTVDWMP-UHFFFAOYSA-N 0.000 description 1
- LBGMYUQCXJJLIR-UHFFFAOYSA-N 4-(2-bromo-4-fluorophenyl)-n-(2-chloro-6-fluorophenyl)-2,5-dimethylpyrazol-3-amine Chemical compound C=1C=C(F)C=C(Br)C=1C=1C(C)=NN(C)C=1NC1=C(F)C=CC=C1Cl LBGMYUQCXJJLIR-UHFFFAOYSA-N 0.000 description 1
- FXSRCEOKVUFSGM-UHFFFAOYSA-N 4-(4-chlorophenyl)-5-(2,6-difluorophenyl)-3,6-dimethylpyridazine Chemical compound C=1C=C(Cl)C=CC=1C=1C(C)=NN=C(C)C=1C1=C(F)C=CC=C1F FXSRCEOKVUFSGM-UHFFFAOYSA-N 0.000 description 1
- OXDDDHGGRFRLEE-UHFFFAOYSA-N 4-[5-[3-chloro-5-(trifluoromethyl)phenyl]-5-(trifluoromethyl)-4h-1,2-oxazol-3-yl]-n-[2-oxo-2-(2,2,2-trifluoroethylamino)ethyl]naphthalene-1-carboxamide Chemical compound C12=CC=CC=C2C(C(=O)NCC(=O)NCC(F)(F)F)=CC=C1C(C1)=NOC1(C(F)(F)F)C1=CC(Cl)=CC(C(F)(F)F)=C1 OXDDDHGGRFRLEE-UHFFFAOYSA-N 0.000 description 1
- NHZLNPMOSADWGC-UHFFFAOYSA-N 4-amino-N-(2-quinoxalinyl)benzenesulfonamide Chemical compound C1=CC(N)=CC=C1S(=O)(=O)NC1=CN=C(C=CC=C2)C2=N1 NHZLNPMOSADWGC-UHFFFAOYSA-N 0.000 description 1
- QKLPUVXBJHRFQZ-UHFFFAOYSA-N 4-amino-n-(6-chloropyrazin-2-yl)benzenesulfonamide Chemical compound C1=CC(N)=CC=C1S(=O)(=O)NC1=CN=CC(Cl)=N1 QKLPUVXBJHRFQZ-UHFFFAOYSA-N 0.000 description 1
- WUBBRNOQWQTFEX-UHFFFAOYSA-N 4-aminosalicylic acid Chemical compound NC1=CC=C(C(O)=O)C(O)=C1 WUBBRNOQWQTFEX-UHFFFAOYSA-N 0.000 description 1
- XVSSMEWAXFOWCI-UHFFFAOYSA-N 4-but-2-ynoxy-6-(3,5-dimethylpiperidin-1-yl)-5-fluoropyrimidine Chemical compound CC#CCOC1=NC=NC(N2CC(C)CC(C)C2)=C1F XVSSMEWAXFOWCI-UHFFFAOYSA-N 0.000 description 1
- 125000004801 4-cyanophenyl group Chemical group [H]C1=C([H])C(C#N)=C([H])C([H])=C1* 0.000 description 1
- PGYDGBCATBINCB-UHFFFAOYSA-N 4-diethoxyphosphoryl-n,n-dimethylaniline Chemical compound CCOP(=O)(OCC)C1=CC=C(N(C)C)C=C1 PGYDGBCATBINCB-UHFFFAOYSA-N 0.000 description 1
- BQMRHYBXRAYYQS-UHFFFAOYSA-N 4-dihydroxyphosphinothioyloxy-n,n-diethyl-6-methylpyrimidin-2-amine Chemical compound CCN(CC)C1=NC(C)=CC(OP(O)(O)=S)=N1 BQMRHYBXRAYYQS-UHFFFAOYSA-N 0.000 description 1
- 125000006042 4-hexenyl group Chemical group 0.000 description 1
- ZMYKITJYWFYRFJ-UHFFFAOYSA-N 4-oxo-4-(2-phenylethylamino)butanoic acid Chemical compound OC(=O)CCC(=O)NCCC1=CC=CC=C1 ZMYKITJYWFYRFJ-UHFFFAOYSA-N 0.000 description 1
- VBAVKJPWXSLDSG-UHFFFAOYSA-N 5-amino-1-[2,6-dichloro-4-(trifluoromethyl)phenyl]-4-[2,2-difluoro-1-(trifluoromethyl)cyclopropyl]pyrazole-3-carbonitrile Chemical compound NC1=C(C2(C(C2)(F)F)C(F)(F)F)C(C#N)=NN1C1=C(Cl)C=C(C(F)(F)F)C=C1Cl VBAVKJPWXSLDSG-UHFFFAOYSA-N 0.000 description 1
- GDGIVSREGUOIJZ-UHFFFAOYSA-N 5-amino-3h-1,3,4-thiadiazole-2-thione Chemical compound NC1=NN=C(S)S1 GDGIVSREGUOIJZ-UHFFFAOYSA-N 0.000 description 1
- NRTLIYOWLVMQBO-UHFFFAOYSA-N 5-chloro-1,3-dimethyl-N-(1,1,3-trimethyl-1,3-dihydro-2-benzofuran-4-yl)pyrazole-4-carboxamide Chemical compound C=12C(C)OC(C)(C)C2=CC=CC=1NC(=O)C=1C(C)=NN(C)C=1Cl NRTLIYOWLVMQBO-UHFFFAOYSA-N 0.000 description 1
- 125000006043 5-hexenyl group Chemical group 0.000 description 1
- NQPDXQQQCQDHHW-UHFFFAOYSA-N 6-chloro-5-(2,3-dichlorophenoxy)-2-(methylthio)-1H-benzimidazole Chemical compound ClC=1C=C2NC(SC)=NC2=CC=1OC1=CC=CC(Cl)=C1Cl NQPDXQQQCQDHHW-UHFFFAOYSA-N 0.000 description 1
- VSVKOUBCDZYAQY-UHFFFAOYSA-N 7-chloro-1,2-benzothiazole Chemical compound ClC1=CC=CC2=C1SN=C2 VSVKOUBCDZYAQY-UHFFFAOYSA-N 0.000 description 1
- ZCYVEMRRCGMTRW-UHFFFAOYSA-N 7553-56-2 Chemical compound [I] ZCYVEMRRCGMTRW-UHFFFAOYSA-N 0.000 description 1
- OIGFJDDMHLIREP-UHFFFAOYSA-N 8-[2-(cyclopropylmethoxy)-4-(trifluoromethyl)phenoxy]-3-[6-(trifluoromethyl)pyridazin-3-yl]-3-azabicyclo[3.2.1]octane Chemical compound C1CC1COC1=CC(C(F)(F)F)=CC=C1OC1C(C2)CCC1CN2C1=CC=C(C(F)(F)F)N=N1 OIGFJDDMHLIREP-UHFFFAOYSA-N 0.000 description 1
- HBAQYPYDRFILMT-UHFFFAOYSA-N 8-[3-(1-cyclopropylpyrazol-4-yl)-1H-pyrazolo[4,3-d]pyrimidin-5-yl]-3-methyl-3,8-diazabicyclo[3.2.1]octan-2-one Chemical class C1(CC1)N1N=CC(=C1)C1=NNC2=C1N=C(N=C2)N1C2C(N(CC1CC2)C)=O HBAQYPYDRFILMT-UHFFFAOYSA-N 0.000 description 1
- 230000002407 ATP formation Effects 0.000 description 1
- 241000218642 Abies Species 0.000 description 1
- 241001524388 Abrupta Species 0.000 description 1
- 244000215068 Acacia senegal Species 0.000 description 1
- 240000005020 Acaciella glauca Species 0.000 description 1
- 241000224422 Acanthamoeba Species 0.000 description 1
- 241000224424 Acanthamoeba sp. Species 0.000 description 1
- 241001098072 Acanthocephalus Species 0.000 description 1
- 241001316810 Acanthocephalus dirus Species 0.000 description 1
- 241000178217 Acanthococcus Species 0.000 description 1
- 241001143308 Acanthoscelides Species 0.000 description 1
- 241001580860 Acarapis Species 0.000 description 1
- 241000132121 Acaridae Species 0.000 description 1
- 239000005651 Acequinocyl Substances 0.000 description 1
- IKHGUXGNUITLKF-UHFFFAOYSA-N Acetaldehyde Chemical compound CC=O IKHGUXGNUITLKF-UHFFFAOYSA-N 0.000 description 1
- 102000000452 Acetyl-CoA carboxylase Human genes 0.000 description 1
- 108010016219 Acetyl-CoA carboxylase Proteins 0.000 description 1
- 241000238818 Acheta domesticus Species 0.000 description 1
- 241001351288 Achroia grisella Species 0.000 description 1
- 239000005652 Acrinathrin Substances 0.000 description 1
- 241001614182 Acrogonia Species 0.000 description 1
- 241000908424 Acromyrmex Species 0.000 description 1
- 241001506009 Aculops Species 0.000 description 1
- 241001227264 Adoretus Species 0.000 description 1
- 241001672675 Adoxophyes Species 0.000 description 1
- 241000256118 Aedes aegypti Species 0.000 description 1
- 241000256176 Aedes vexans Species 0.000 description 1
- 241000484419 Aedia Species 0.000 description 1
- 241001103582 Aelia Species 0.000 description 1
- 241000220275 Aethina Species 0.000 description 1
- 241001251200 Agelas Species 0.000 description 1
- 241000589159 Agrobacterium sp. Species 0.000 description 1
- 241000222532 Agrocybe Species 0.000 description 1
- 235000008121 Agrocybe aegerita Nutrition 0.000 description 1
- 244000045069 Agrocybe aegerita Species 0.000 description 1
- RGCKGOZRHPZPFP-UHFFFAOYSA-N Alizarin Natural products C1=CC=C2C(=O)C3=C(O)C(O)=CC=C3C(=O)C2=C1 RGCKGOZRHPZPFP-UHFFFAOYSA-N 0.000 description 1
- 235000005254 Allium ampeloprasum Nutrition 0.000 description 1
- 240000006108 Allium ampeloprasum Species 0.000 description 1
- 239000005995 Aluminium silicate Substances 0.000 description 1
- 241001466460 Alveolata Species 0.000 description 1
- 241000238679 Amblyomma Species 0.000 description 1
- ATRRKUHOCOJYRX-UHFFFAOYSA-N Ammonium bicarbonate Chemical compound [NH4+].OC([O-])=O ATRRKUHOCOJYRX-UHFFFAOYSA-N 0.000 description 1
- 229910000013 Ammonium bicarbonate Inorganic materials 0.000 description 1
- 240000002470 Amphicarpaea bracteata Species 0.000 description 1
- 241000534460 Ampullaria Species 0.000 description 1
- 241000663922 Anasa tristis Species 0.000 description 1
- 241000746375 Andrographis Species 0.000 description 1
- 241000949648 Angulus Species 0.000 description 1
- 241000244023 Anisakis Species 0.000 description 1
- 241000256056 Anopheles arabiensis Species 0.000 description 1
- 241001427556 Anoplura Species 0.000 description 1
- 241001370455 Aphelenchoides arachidis Species 0.000 description 1
- 241001151957 Aphis aurantii Species 0.000 description 1
- 241001425390 Aphis fabae Species 0.000 description 1
- 241000566651 Aphis forbesi Species 0.000 description 1
- 241000660739 Aphis hederae Species 0.000 description 1
- 241001094026 Aphis illinoisensis Species 0.000 description 1
- 241001448479 Aphis nerii Species 0.000 description 1
- 241001095118 Aphis pomi Species 0.000 description 1
- 241000273311 Aphis spiraecola Species 0.000 description 1
- 241000174622 Aphrodisias Species 0.000 description 1
- 241000224482 Apicomplexa Species 0.000 description 1
- 241000208306 Apium Species 0.000 description 1
- 244000105624 Arachis hypogaea Species 0.000 description 1
- 241000872518 Aradus funestus Species 0.000 description 1
- 241000722826 Ardisia Species 0.000 description 1
- 241001480748 Argas Species 0.000 description 1
- 241001340598 Argyresthia conjugella Species 0.000 description 1
- 241000237518 Arion Species 0.000 description 1
- 241001298365 Arion ater Species 0.000 description 1
- 235000011330 Armoracia rusticana Nutrition 0.000 description 1
- 240000003291 Armoracia rusticana Species 0.000 description 1
- 241000319476 Asellus Species 0.000 description 1
- 241001219293 Aspalathus Species 0.000 description 1
- 241001532036 Aspidistra Species 0.000 description 1
- 241000726103 Atta Species 0.000 description 1
- 241000982146 Atylotus Species 0.000 description 1
- 241001367049 Autographa Species 0.000 description 1
- 241000999616 Avitellina Species 0.000 description 1
- 240000005343 Azadirachta indica Species 0.000 description 1
- 241000894008 Azorhizobium Species 0.000 description 1
- 241001478327 Azospirillum sp. Species 0.000 description 1
- 241000099686 Azotobacter sp. Species 0.000 description 1
- 241000414381 Babesia canis rossi Species 0.000 description 1
- 241000193363 Bacillus thuringiensis serovar aizawai Species 0.000 description 1
- 241000193365 Bacillus thuringiensis serovar israelensis Species 0.000 description 1
- 208000035143 Bacterial infection Diseases 0.000 description 1
- 241000218993 Begonia Species 0.000 description 1
- 239000005735 Benalaxyl-M Substances 0.000 description 1
- PFJJMJDEVDLPNE-UHFFFAOYSA-N Benoxacor Chemical compound C1=CC=C2N(C(=O)C(Cl)Cl)C(C)COC2=C1 PFJJMJDEVDLPNE-UHFFFAOYSA-N 0.000 description 1
- 241000997497 Bertella Species 0.000 description 1
- 241001284802 Bertiella <tapeworm> Species 0.000 description 1
- 241000359271 Besnoitia Species 0.000 description 1
- 235000003932 Betula Nutrition 0.000 description 1
- 241000219429 Betula Species 0.000 description 1
- 108010018763 Biotin carboxylase Proteins 0.000 description 1
- 241000237519 Bivalvia Species 0.000 description 1
- 241001573716 Blaniulus guttulatus Species 0.000 description 1
- 241000238657 Blattella germanica Species 0.000 description 1
- 241000929635 Blissus Species 0.000 description 1
- 241001516760 Boisea Species 0.000 description 1
- ZOXJGFHDIHLPTG-UHFFFAOYSA-N Boron Chemical compound [B] ZOXJGFHDIHLPTG-UHFFFAOYSA-N 0.000 description 1
- 241000589968 Borrelia Species 0.000 description 1
- 241000908522 Borreliella Species 0.000 description 1
- 239000005740 Boscalid Substances 0.000 description 1
- 241001323427 Bothridium Species 0.000 description 1
- 241000123650 Botrytis cinerea Species 0.000 description 1
- 241000322475 Bovicola Species 0.000 description 1
- 241001148534 Brachyspira Species 0.000 description 1
- 235000003351 Brassica cretica Nutrition 0.000 description 1
- 235000003343 Brassica rupestris Nutrition 0.000 description 1
- 241001388466 Bruchus rufimanus Species 0.000 description 1
- 241000041029 Bulinus Species 0.000 description 1
- 241001508395 Burkholderia sp. Species 0.000 description 1
- SLZWBCGZQRRUNG-UHFFFAOYSA-N Butacarb Chemical compound CNC(=O)OC1=CC(C(C)(C)C)=CC(C(C)(C)C)=C1 SLZWBCGZQRRUNG-UHFFFAOYSA-N 0.000 description 1
- 241001058840 Buxtonella Species 0.000 description 1
- HHKJNJYJNKVAQV-UHFFFAOYSA-N CCCCC1=CC=CC=C1.OP(O)(O)=O.S Chemical compound CCCCC1=CC=CC=C1.OP(O)(O)=O.S HHKJNJYJNKVAQV-UHFFFAOYSA-N 0.000 description 1
- FHVGHVVFXOXCEN-UHFFFAOYSA-N CN(C)C(C(N)=NOC)=O Chemical compound CN(C)C(C(N)=NOC)=O FHVGHVVFXOXCEN-UHFFFAOYSA-N 0.000 description 1
- 241001212014 Cacoecia Species 0.000 description 1
- 235000017399 Caesalpinia tinctoria Nutrition 0.000 description 1
- 229910021532 Calcite Inorganic materials 0.000 description 1
- 239000006009 Calcium phosphide Substances 0.000 description 1
- 241000257160 Calliphora Species 0.000 description 1
- 241000333978 Caloglyphus Species 0.000 description 1
- 241001184747 Caloptilia theivora Species 0.000 description 1
- 241000282832 Camelidae Species 0.000 description 1
- 235000018970 Campomanesia grandiflora Nutrition 0.000 description 1
- 241000722666 Camponotus Species 0.000 description 1
- 241000589876 Campylobacter Species 0.000 description 1
- 241000613201 Campylomma livida Species 0.000 description 1
- 241000282465 Canis Species 0.000 description 1
- 241000282472 Canis lupus familiaris Species 0.000 description 1
- 241000253350 Capillaria Species 0.000 description 1
- 241000283707 Capra Species 0.000 description 1
- 240000004160 Capsicum annuum Species 0.000 description 1
- 235000008534 Capsicum annuum var annuum Nutrition 0.000 description 1
- KXDHJXZQYSOELW-UHFFFAOYSA-M Carbamate Chemical compound NC([O-])=O KXDHJXZQYSOELW-UHFFFAOYSA-M 0.000 description 1
- 229920002134 Carboxymethyl cellulose Polymers 0.000 description 1
- 241001466804 Carnivora Species 0.000 description 1
- 239000005973 Carvone Substances 0.000 description 1
- 241000162408 Cassida Species 0.000 description 1
- 241000614965 Catatropis Species 0.000 description 1
- 241000700198 Cavia Species 0.000 description 1
- 241000296609 Celastrus angulatus Species 0.000 description 1
- 235000017186 Celastrus paniculatus Nutrition 0.000 description 1
- 240000006739 Celastrus paniculatus Species 0.000 description 1
- 229940123982 Cell wall synthesis inhibitor Drugs 0.000 description 1
- 241000209441 Ceratophyllum Species 0.000 description 1
- 241000134979 Ceratovacuna lanigera Species 0.000 description 1
- 241000754688 Cercaria Species 0.000 description 1
- 241001660259 Cereus <cactus> Species 0.000 description 1
- 241000146399 Ceriporiopsis Species 0.000 description 1
- 241000293772 Cerrena Species 0.000 description 1
- 241000974009 Cervus canadensis Species 0.000 description 1
- 240000006122 Chenopodium album Species 0.000 description 1
- 235000009344 Chenopodium album Nutrition 0.000 description 1
- 240000006162 Chenopodium quinoa Species 0.000 description 1
- 241000700114 Chinchillidae Species 0.000 description 1
- 241000668556 Chionaspis Species 0.000 description 1
- 241000256135 Chironomus thummi Species 0.000 description 1
- 241000606161 Chlamydia Species 0.000 description 1
- 241000498849 Chlamydiales Species 0.000 description 1
- STUSTWKEFDQFFZ-UHFFFAOYSA-N Chlordimeform Chemical compound CN(C)C=NC1=CC=C(Cl)C=C1C STUSTWKEFDQFFZ-UHFFFAOYSA-N 0.000 description 1
- RAPBNVDSDCTNRC-UHFFFAOYSA-N Chlorobenzilate Chemical compound C=1C=C(Cl)C=CC=1C(O)(C(=O)OCC)C1=CC=C(Cl)C=C1 RAPBNVDSDCTNRC-UHFFFAOYSA-N 0.000 description 1
- 239000005747 Chlorothalonil Substances 0.000 description 1
- 239000004099 Chlortetracycline Substances 0.000 description 1
- 206010008631 Cholera Diseases 0.000 description 1
- 241000255945 Choristoneura Species 0.000 description 1
- 235000007516 Chrysanthemum Nutrition 0.000 description 1
- 244000035851 Chrysanthemum leucanthemum Species 0.000 description 1
- 235000008495 Chrysanthemum leucanthemum Nutrition 0.000 description 1
- 244000189548 Chrysanthemum x morifolium Species 0.000 description 1
- 241001273872 Chrysodeixis chalcites Species 0.000 description 1
- 241001124134 Chrysomelidae Species 0.000 description 1
- 241001292007 Chrysopa Species 0.000 description 1
- 241001635686 Cimex adjunctus Species 0.000 description 1
- 241001327638 Cimex lectularius Species 0.000 description 1
- 241000157855 Cinchona Species 0.000 description 1
- 235000001258 Cinchona calisaya Nutrition 0.000 description 1
- 244000037364 Cinnamomum aromaticum Species 0.000 description 1
- 235000014489 Cinnamomum aromaticum Nutrition 0.000 description 1
- 244000241235 Citrullus lanatus Species 0.000 description 1
- 235000012828 Citrullus lanatus var citroides Nutrition 0.000 description 1
- 241000207199 Citrus Species 0.000 description 1
- 235000007716 Citrus aurantium Nutrition 0.000 description 1
- 235000000228 Citrus myrtifolia Nutrition 0.000 description 1
- 240000003791 Citrus myrtifolia Species 0.000 description 1
- 241001672694 Citrus reticulata Species 0.000 description 1
- 235000016646 Citrus taiwanica Nutrition 0.000 description 1
- 240000000560 Citrus x paradisi Species 0.000 description 1
- 241000186650 Clavibacter Species 0.000 description 1
- 241001152840 Cleonus Species 0.000 description 1
- PITWUHDDNUVBPT-UHFFFAOYSA-N Cloethocarb Chemical compound CNC(=O)OC1=CC=CC=C1OC(CCl)OC PITWUHDDNUVBPT-UHFFFAOYSA-N 0.000 description 1
- 239000005654 Clofentezine Substances 0.000 description 1
- DBPRUZCKPFOVDV-UHFFFAOYSA-N Clorprenaline hydrochloride Chemical compound O.Cl.CC(C)NCC(O)C1=CC=CC=C1Cl DBPRUZCKPFOVDV-UHFFFAOYSA-N 0.000 description 1
- 241000008892 Cnaphalocrocis patnalis Species 0.000 description 1
- 241000131066 Coccinella Species 0.000 description 1
- 241000396583 Cochlearia Species 0.000 description 1
- 241001620713 Coeloides Species 0.000 description 1
- 241001427559 Collembola Species 0.000 description 1
- 208000035473 Communicable disease Diseases 0.000 description 1
- 239000005748 Coniothyrium minitans Strain CON/M/91-08 (DSM 9660) Substances 0.000 description 1
- 241001522723 Conoidea Species 0.000 description 1
- 241001126268 Cooperia Species 0.000 description 1
- RYGMFSIKBFXOCR-UHFFFAOYSA-N Copper Chemical compound [Cu] RYGMFSIKBFXOCR-UHFFFAOYSA-N 0.000 description 1
- 239000005752 Copper oxychloride Substances 0.000 description 1
- 241001509962 Coptotermes formosanus Species 0.000 description 1
- 241001640112 Cordobia Species 0.000 description 1
- 241000422839 Cornitermes cumulans Species 0.000 description 1
- 241000512048 Cotylophoron Species 0.000 description 1
- 241000606678 Coxiella burnetii Species 0.000 description 1
- 235000014493 Crataegus Nutrition 0.000 description 1
- 241001092040 Crataegus Species 0.000 description 1
- 235000013175 Crataegus laevigata Nutrition 0.000 description 1
- 241001516694 Cratoxylum Species 0.000 description 1
- 241000699800 Cricetinae Species 0.000 description 1
- 201000003075 Crimean-Congo hemorrhagic fever Diseases 0.000 description 1
- BOFHKBLZOYVHSI-UHFFFAOYSA-N Crufomate Chemical compound CNP(=O)(OC)OC1=CC=C(C(C)(C)C)C=C1Cl BOFHKBLZOYVHSI-UHFFFAOYSA-N 0.000 description 1
- 241000238424 Crustacea Species 0.000 description 1
- ORIGEOXWTMPZQD-DUFGSWQCSA-N Cryptocaryon Natural products O[C@H]1C=C[C@H]2OC(=O)C[C@H]2[C@@H]1C(=O)C=Cc3ccccc3 ORIGEOXWTMPZQD-DUFGSWQCSA-N 0.000 description 1
- 241001663425 Cryptocaryon Species 0.000 description 1
- 241001337994 Cryptococcus <scale insect> Species 0.000 description 1
- 241000195493 Cryptophyta Species 0.000 description 1
- 241000223935 Cryptosporidium Species 0.000 description 1
- 241001503016 Ctenomyces Species 0.000 description 1
- QPLDLSVMHZLSFG-UHFFFAOYSA-N CuO Inorganic materials [Cu]=O QPLDLSVMHZLSFG-UHFFFAOYSA-N 0.000 description 1
- 241001137883 Cucumaria Species 0.000 description 1
- 241000219112 Cucumis Species 0.000 description 1
- 235000015510 Cucumis melo subsp melo Nutrition 0.000 description 1
- 241000134316 Culicoides <genus> Species 0.000 description 1
- 241000371644 Curvularia ravenelii Species 0.000 description 1
- 239000005754 Cyazofamid Substances 0.000 description 1
- 239000005655 Cyflumetofen Substances 0.000 description 1
- 239000005891 Cyromazine Substances 0.000 description 1
- 241000987822 Cystoisospora Species 0.000 description 1
- 241001262815 Dactylogyrus Species 0.000 description 1
- 241000268912 Damalinia Species 0.000 description 1
- 235000002767 Daucus carota Nutrition 0.000 description 1
- 244000000626 Daucus carota Species 0.000 description 1
- 241001414890 Delia Species 0.000 description 1
- 241000627010 Delia brassica Species 0.000 description 1
- 241000975729 Delia florilega Species 0.000 description 1
- 241001609607 Delia platura Species 0.000 description 1
- 208000001490 Dengue Diseases 0.000 description 1
- 206010012310 Dengue fever Diseases 0.000 description 1
- 208000006558 Dental Calculus Diseases 0.000 description 1
- 241001480824 Dermacentor Species 0.000 description 1
- 244000147058 Derris elliptica Species 0.000 description 1
- 239000005696 Diammonium phosphate Substances 0.000 description 1
- 241000122105 Diatraea Species 0.000 description 1
- WGOWCPGHOCIHBW-UHFFFAOYSA-N Dichlofenthion Chemical compound CCOP(=S)(OCC)OC1=CC=C(Cl)C=C1Cl WGOWCPGHOCIHBW-UHFFFAOYSA-N 0.000 description 1
- 241001147667 Dictyocaulus Species 0.000 description 1
- 239000005893 Diflubenzuron Substances 0.000 description 1
- 241001389925 Digenea <Rhodophyta> Species 0.000 description 1
- 239000005947 Dimethoate Substances 0.000 description 1
- 239000005761 Dimethomorph Substances 0.000 description 1
- 239000005762 Dimoxystrobin Substances 0.000 description 1
- HDWLUGYOLUHEMN-UHFFFAOYSA-N Dinobuton Chemical compound CCC(C)C1=CC([N+]([O-])=O)=CC([N+]([O-])=O)=C1OC(=O)OC(C)C HDWLUGYOLUHEMN-UHFFFAOYSA-N 0.000 description 1
- 235000005903 Dioscorea Nutrition 0.000 description 1
- 244000281702 Dioscorea villosa Species 0.000 description 1
- 235000000504 Dioscorea villosa Nutrition 0.000 description 1
- 235000008597 Diospyros kaki Nutrition 0.000 description 1
- 244000236655 Diospyros kaki Species 0.000 description 1
- 241000511318 Diprion Species 0.000 description 1
- 241000123589 Dipsacus Species 0.000 description 1
- 239000005764 Dithianon Substances 0.000 description 1
- 241000399934 Ditylenchus Species 0.000 description 1
- 241001672142 Dolichovespula sylvestris Species 0.000 description 1
- 241000193907 Dreissena Species 0.000 description 1
- 241001595884 Drosicha Species 0.000 description 1
- 241001116742 Drynaria Species 0.000 description 1
- 241000196131 Dryopteris filix-mas Species 0.000 description 1
- 206010013883 Dwarfism Diseases 0.000 description 1
- 241000893563 Dysosma Species 0.000 description 1
- 241000770834 Dysphaea Species 0.000 description 1
- 241000504965 Echinoderma Species 0.000 description 1
- 241000257465 Echinoidea Species 0.000 description 1
- 241001074093 Echinopsis Species 0.000 description 1
- 241000578473 Echinorhynchida Species 0.000 description 1
- 241000578380 Echinorhynchus Species 0.000 description 1
- 241000258147 Echinus Species 0.000 description 1
- 241000400699 Elasmopalpus Species 0.000 description 1
- 241000661279 Eldana Species 0.000 description 1
- 206010014596 Encephalitis Japanese B Diseases 0.000 description 1
- 208000031912 Endemic Flea-Borne Typhus Diseases 0.000 description 1
- 241000224431 Entamoeba Species 0.000 description 1
- 241000284096 Epilachna borealis Species 0.000 description 1
- 241001147395 Epinotia Species 0.000 description 1
- 239000005767 Epoxiconazole Substances 0.000 description 1
- 241000283086 Equidae Species 0.000 description 1
- 241000283074 Equus asinus Species 0.000 description 1
- VGGSQFUCUMXWEO-UHFFFAOYSA-N Ethene Chemical compound C=C VGGSQFUCUMXWEO-UHFFFAOYSA-N 0.000 description 1
- 239000005977 Ethylene Substances 0.000 description 1
- 239000005896 Etofenprox Substances 0.000 description 1
- 241000266331 Eugenia Species 0.000 description 1
- 241001136540 Euleia Species 0.000 description 1
- 241000060469 Eupoecilia ambiguella Species 0.000 description 1
- 235000014066 European mistletoe Nutrition 0.000 description 1
- 241000502168 Eustigma Species 0.000 description 1
- 241000220485 Fabaceae Species 0.000 description 1
- 241000948950 Fallax Species 0.000 description 1
- 239000005772 Famoxadone Substances 0.000 description 1
- 241000371383 Fannia Species 0.000 description 1
- 241000322646 Felicola Species 0.000 description 1
- 241000282326 Felis catus Species 0.000 description 1
- 239000005774 Fenamidone Substances 0.000 description 1
- 239000005898 Fenoxycarb Substances 0.000 description 1
- 239000005779 Fenpyrazamine Substances 0.000 description 1
- 241000883990 Flabellum Species 0.000 description 1
- 239000005900 Flonicamid Substances 0.000 description 1
- 239000005780 Fluazinam Substances 0.000 description 1
- 239000005902 Flupyradifurone Substances 0.000 description 1
- 239000005785 Fluquinconazole Substances 0.000 description 1
- 239000005787 Flutriafol Substances 0.000 description 1
- 239000005788 Fluxapyroxad Substances 0.000 description 1
- UKSLKNUCVPZQCQ-UHFFFAOYSA-N Fluxofenim Chemical compound C=1C=C(Cl)C=CC=1C(C(F)(F)F)=NOCC1OCCO1 UKSLKNUCVPZQCQ-UHFFFAOYSA-N 0.000 description 1
- 239000005789 Folpet Substances 0.000 description 1
- AIKKULXCBHRFOS-UHFFFAOYSA-N Formothion Chemical compound COP(=S)(OC)SCC(=O)N(C)C=O AIKKULXCBHRFOS-UHFFFAOYSA-N 0.000 description 1
- 239000005790 Fosetyl Substances 0.000 description 1
- 241000654868 Frankliniella fusca Species 0.000 description 1
- 241000927584 Frankliniella occidentalis Species 0.000 description 1
- 241000585112 Galba Species 0.000 description 1
- 241000287828 Gallus gallus Species 0.000 description 1
- 239000005903 Gamma-cyhalothrin Substances 0.000 description 1
- 241001660203 Gasterophilus Species 0.000 description 1
- 239000005980 Gibberellic acid Substances 0.000 description 1
- 241001043186 Gibbium Species 0.000 description 1
- 241001315191 Gladiata Species 0.000 description 1
- 241000981782 Globularia Species 0.000 description 1
- 239000005562 Glyphosate Substances 0.000 description 1
- 241000695276 Glyphus Species 0.000 description 1
- 241000864400 Gomphus <basidiomycota> Species 0.000 description 1
- 239000007818 Grignard reagent Substances 0.000 description 1
- 241000241125 Gryllotalpa gryllotalpa Species 0.000 description 1
- 229920000084 Gum arabic Polymers 0.000 description 1
- 241001523601 Gyrodactylus Species 0.000 description 1
- 241000790933 Haematopinus Species 0.000 description 1
- 241000775881 Haematopota pluvialis Species 0.000 description 1
- 241000406101 Hammondia Species 0.000 description 1
- 241000208818 Helianthus Species 0.000 description 1
- 241000255990 Helicoverpa Species 0.000 description 1
- 241001147381 Helicoverpa armigera Species 0.000 description 1
- 241001351414 Hellula Species 0.000 description 1
- 108010034145 Helminth Proteins Proteins 0.000 description 1
- 241000130660 Hepialidae Species 0.000 description 1
- 239000005661 Hexythiazox Substances 0.000 description 1
- 241000218228 Humulus Species 0.000 description 1
- 241001251958 Hyalopterus Species 0.000 description 1
- 241001251909 Hyalopterus pruni Species 0.000 description 1
- 241001508558 Hypera Species 0.000 description 1
- 241000546188 Hypericum Species 0.000 description 1
- 235000017309 Hypericum perforatum Nutrition 0.000 description 1
- 241000257176 Hypoderma <fly> Species 0.000 description 1
- 241001595209 Idiocerus Species 0.000 description 1
- 206010061217 Infestation Diseases 0.000 description 1
- 241000500891 Insecta Species 0.000 description 1
- 239000005796 Ipconazole Substances 0.000 description 1
- 244000017020 Ipomoea batatas Species 0.000 description 1
- 235000002678 Ipomoea batatas Nutrition 0.000 description 1
- 239000005797 Iprovalicarb Substances 0.000 description 1
- 239000005908 Isaria fumosorosea Apopka strain 97 (formely Paecilomyces fumosoroseus) Substances 0.000 description 1
- 241001495069 Ischnocera Species 0.000 description 1
- 201000005807 Japanese encephalitis Diseases 0.000 description 1
- 241000710842 Japanese encephalitis virus Species 0.000 description 1
- 235000013757 Juglans Nutrition 0.000 description 1
- 241000758789 Juglans Species 0.000 description 1
- 241000721662 Juniperus Species 0.000 description 1
- 241001506109 Kalotermes Species 0.000 description 1
- 239000005909 Kieselgur Substances 0.000 description 1
- 241001467800 Knemidokoptes Species 0.000 description 1
- 241000186809 Kurthia Species 0.000 description 1
- NWUWYYSKZYIQAE-ZBFHGGJFSA-N L-(R)-iprovalicarb Chemical compound CC(C)OC(=O)N[C@@H](C(C)C)C(=O)N[C@H](C)C1=CC=C(C)C=C1 NWUWYYSKZYIQAE-ZBFHGGJFSA-N 0.000 description 1
- 241000490517 Labidura riparia Species 0.000 description 1
- 241001534110 Lactarius <percoid fish> Species 0.000 description 1
- 241000186660 Lactobacillus Species 0.000 description 1
- 241000131892 Lampyris Species 0.000 description 1
- 241001470017 Laodelphax striatella Species 0.000 description 1
- 241000222697 Leishmania infantum Species 0.000 description 1
- 208000004554 Leishmaniasis Diseases 0.000 description 1
- 241000270322 Lepidosauria Species 0.000 description 1
- 241000500881 Lepisma Species 0.000 description 1
- 241001358029 Leucotrichum Species 0.000 description 1
- 229920001732 Lignosulfonate Polymers 0.000 description 1
- 241000360065 Ligula Species 0.000 description 1
- 241000208204 Linum Species 0.000 description 1
- 241001074285 Liparis <scorpaeniform fish> Species 0.000 description 1
- 241000322707 Liposcelis Species 0.000 description 1
- 241001604074 Lippia Species 0.000 description 1
- 241000966204 Lissorhoptrus oryzophilus Species 0.000 description 1
- 206010024641 Listeriosis Diseases 0.000 description 1
- 241001535742 Listrophorus Species 0.000 description 1
- 241001261104 Lobesia botrana Species 0.000 description 1
- 241000408521 Lucida Species 0.000 description 1
- 241000254056 Luciola Species 0.000 description 1
- 244000241872 Lycium chinense Species 0.000 description 1
- 208000016604 Lyme disease Diseases 0.000 description 1
- 241000193386 Lysinibacillus sphaericus Species 0.000 description 1
- 241000779599 Malpighia Species 0.000 description 1
- 239000005802 Mancozeb Substances 0.000 description 1
- 239000005804 Mandipropamid Substances 0.000 description 1
- 241000255908 Manduca sexta Species 0.000 description 1
- 235000014826 Mangifera indica Nutrition 0.000 description 1
- 240000007228 Mangifera indica Species 0.000 description 1
- 241001354481 Mansonia <mosquito genus> Species 0.000 description 1
- 241000133232 Marshallia Species 0.000 description 1
- 241001232130 Maruca testulalis Species 0.000 description 1
- 241001375804 Mastigophora Species 0.000 description 1
- 241000590505 Melanitis leda Species 0.000 description 1
- 241000014130 Melanogaster sp. Species 0.000 description 1
- 235000013500 Melia azadirachta Nutrition 0.000 description 1
- 241000213996 Melilotus Species 0.000 description 1
- 241000243787 Meloidogyne hapla Species 0.000 description 1
- 241000243786 Meloidogyne incognita Species 0.000 description 1
- XADCESSVHJOZHK-UHFFFAOYSA-N Meperidine Chemical compound C=1C=CC=CC=1C1(C(=O)OCC)CCN(C)CC1 XADCESSVHJOZHK-UHFFFAOYSA-N 0.000 description 1
- 239000005806 Meptyldinocap Substances 0.000 description 1
- 241000016529 Meristotheca Species 0.000 description 1
- 241001483602 Mesocriconema onoense Species 0.000 description 1
- 241001268433 Mesocriconema ornatum Species 0.000 description 1
- 239000005808 Metalaxyl-M Substances 0.000 description 1
- 239000005868 Metconazole Substances 0.000 description 1
- 239000005809 Metiram Substances 0.000 description 1
- 241000775788 Metschnikowia fructicola Species 0.000 description 1
- 241000192701 Microcystis Species 0.000 description 1
- 241000398889 Micronema Species 0.000 description 1
- 241001154938 Microtermes Species 0.000 description 1
- PYCSFZRHAYWHQB-UHFFFAOYSA-N Mirasan Chemical compound CCN(CC)CCNC1=CC=C(C)C(Cl)=C1 PYCSFZRHAYWHQB-UHFFFAOYSA-N 0.000 description 1
- 241001653186 Mocis Species 0.000 description 1
- ZOKXTWBITQBERF-UHFFFAOYSA-N Molybdenum Chemical compound [Mo] ZOKXTWBITQBERF-UHFFFAOYSA-N 0.000 description 1
- 241001094463 Monellia Species 0.000 description 1
- 241001094800 Monelliopsis Species 0.000 description 1
- 241000700601 Moniliformis Species 0.000 description 1
- 241001524040 Monogenea Species 0.000 description 1
- 241001351098 Morellia Species 0.000 description 1
- 241000235395 Mucor Species 0.000 description 1
- 206010028282 Murine typhus Diseases 0.000 description 1
- 241000699670 Mus sp. Species 0.000 description 1
- 241000282339 Mustela Species 0.000 description 1
- 241001373727 Myobia Species 0.000 description 1
- 241001477928 Mythimna Species 0.000 description 1
- 241001494184 Myxozoa Species 0.000 description 1
- 241000165113 Myzus ligustri Species 0.000 description 1
- 241000180178 Myzus ornatus Species 0.000 description 1
- 241001140180 Myzus persicae nicotianae Species 0.000 description 1
- YRWLZFXJFBZBEY-UHFFFAOYSA-N N-(6-butyl-1H-benzimidazol-2-yl)carbamic acid methyl ester Chemical compound CCCCC1=CC=C2N=C(NC(=O)OC)NC2=C1 YRWLZFXJFBZBEY-UHFFFAOYSA-N 0.000 description 1
- MVTQIFVKRXBCHS-SMMNFGSLSA-N N-[(3S,6S,12R,15S,16R,19S,22S)-3-benzyl-12-ethyl-4,16-dimethyl-2,5,11,14,18,21,24-heptaoxo-19-phenyl-17-oxa-1,4,10,13,20-pentazatricyclo[20.4.0.06,10]hexacosan-15-yl]-3-hydroxypyridine-2-carboxamide (10R,11R,12E,17E,19E,21S)-21-hydroxy-11,19-dimethyl-10-propan-2-yl-9,26-dioxa-3,15,28-triazatricyclo[23.2.1.03,7]octacosa-1(27),6,12,17,19,25(28)-hexaene-2,8,14,23-tetrone Chemical compound CC(C)[C@H]1OC(=O)C2=CCCN2C(=O)c2coc(CC(=O)C[C@H](O)\C=C(/C)\C=C\CNC(=O)\C=C\[C@H]1C)n2.CC[C@H]1NC(=O)[C@@H](NC(=O)c2ncccc2O)[C@@H](C)OC(=O)[C@@H](NC(=O)[C@@H]2CC(=O)CCN2C(=O)[C@H](Cc2ccccc2)N(C)C(=O)[C@@H]2CCCN2C1=O)c1ccccc1 MVTQIFVKRXBCHS-SMMNFGSLSA-N 0.000 description 1
- XQJQCBDIXRIYRP-UHFFFAOYSA-N N-{2-[1,1'-bi(cyclopropyl)-2-yl]phenyl}-3-(difluoromethyl)-1-methyl-1pyrazole-4-carboxamide Chemical compound FC(F)C1=NN(C)C=C1C(=O)NC1=CC=CC=C1C1C(C2CC2)C1 XQJQCBDIXRIYRP-UHFFFAOYSA-N 0.000 description 1
- GRSMWKLPSNHDHA-UHFFFAOYSA-N Naphthalic anhydride Chemical compound C1=CC(C(=O)OC2=O)=C3C2=CC=CC3=C1 GRSMWKLPSNHDHA-UHFFFAOYSA-N 0.000 description 1
- 241000498271 Necator Species 0.000 description 1
- 206010062701 Nematodiasis Diseases 0.000 description 1
- 241001137882 Nematodirus Species 0.000 description 1
- 206010028980 Neoplasm Diseases 0.000 description 1
- 241001084186 Neotrombicula Species 0.000 description 1
- 241000238903 Nephila Species 0.000 description 1
- 241000359016 Nephotettix Species 0.000 description 1
- 241000358422 Nephotettix cincticeps Species 0.000 description 1
- 241000055277 Neritina Species 0.000 description 1
- RDXLYGJSWZYTFJ-UHFFFAOYSA-N Niridazole Chemical compound S1C([N+](=O)[O-])=CN=C1N1C(=O)NCC1 RDXLYGJSWZYTFJ-UHFFFAOYSA-N 0.000 description 1
- 241000216953 Notocotylus Species 0.000 description 1
- 241001338708 Nymphula Species 0.000 description 1
- SGMLAOIBDURVKL-UHFFFAOYSA-N O1N=C(C=C1)[P] Chemical compound O1N=C(C=C1)[P] SGMLAOIBDURVKL-UHFFFAOYSA-N 0.000 description 1
- 241001157094 Oiketicus Species 0.000 description 1
- 241000243981 Onchocerca Species 0.000 description 1
- 241000243985 Onchocerca volvulus Species 0.000 description 1
- 241000565675 Oncomelania Species 0.000 description 1
- 241000963703 Onychiurus armatus Species 0.000 description 1
- 241001491877 Operophtera brumata Species 0.000 description 1
- 241001184198 Orthosiphon Species 0.000 description 1
- 241000283973 Oryctolagus cuniculus Species 0.000 description 1
- 241000131102 Oryzaephilus Species 0.000 description 1
- 241001157806 Oscinella Species 0.000 description 1
- 241000243795 Ostertagia Species 0.000 description 1
- 241000131062 Oulema Species 0.000 description 1
- 241001160353 Oulema melanopus Species 0.000 description 1
- 241001570894 Oulema oryzae Species 0.000 description 1
- ZCQWOFVYLHDMMC-UHFFFAOYSA-N Oxazole Chemical compound C1=COC=N1 ZCQWOFVYLHDMMC-UHFFFAOYSA-N 0.000 description 1
- YXLXNENXOJSQEI-UHFFFAOYSA-L Oxine-copper Chemical compound [Cu+2].C1=CN=C2C([O-])=CC=CC2=C1.C1=CN=C2C([O-])=CC=CC2=C1 YXLXNENXOJSQEI-UHFFFAOYSA-L 0.000 description 1
- 108010004210 PF 1022A Proteins 0.000 description 1
- YJNUXGPXJFAUQJ-LYWANRAQSA-N PF1022A Chemical compound C([C@@H]1C(=O)N(C)[C@H](C(O[C@H](C)C(=O)N(C)[C@@H](CC(C)C)C(=O)O[C@H](CC=2C=CC=CC=2)C(=O)N(C)[C@@H](CC(C)C)C(=O)O[C@H](C)C(=O)N(C)[C@@H](CC(C)C)C(=O)O1)=O)CC(C)C)C1=CC=CC=C1 YJNUXGPXJFAUQJ-LYWANRAQSA-N 0.000 description 1
- 239000005960 Paecilomyces lilacinus strain 251 Substances 0.000 description 1
- 208000002193 Pain Diseases 0.000 description 1
- 241000488581 Panonychus citri Species 0.000 description 1
- 241000919536 Panstrongylus Species 0.000 description 1
- 239000005662 Paraffin oil Substances 0.000 description 1
- 241000887182 Paraphaeosphaeria minitans Species 0.000 description 1
- 206010033892 Paraplegia Diseases 0.000 description 1
- 241000899422 Parastrongyloides Species 0.000 description 1
- 241000216620 Pariana Species 0.000 description 1
- UOZODPSAJZTQNH-UHFFFAOYSA-N Paromomycin II Natural products NC1C(O)C(O)C(CN)OC1OC1C(O)C(OC2C(C(N)CC(N)C2O)OC2C(C(O)C(O)C(CO)O2)N)OC1CO UOZODPSAJZTQNH-UHFFFAOYSA-N 0.000 description 1
- NFHFRUOZVGFOOS-UHFFFAOYSA-N Pd(PPh3)4 Substances [Pd].C1=CC=CC=C1P(C=1C=CC=CC=1)C1=CC=CC=C1.C1=CC=CC=C1P(C=1C=CC=CC=1)C1=CC=CC=C1.C1=CC=CC=C1P(C=1C=CC=CC=1)C1=CC=CC=C1.C1=CC=CC=C1P(C=1C=CC=CC=1)C1=CC=CC=C1 NFHFRUOZVGFOOS-UHFFFAOYSA-N 0.000 description 1
- 241001494479 Pecora Species 0.000 description 1
- 241000606012 Pectinatus Species 0.000 description 1
- 241000228143 Penicillium Species 0.000 description 1
- 241000286209 Phasianidae Species 0.000 description 1
- 241001557903 Phlebia sp. Species 0.000 description 1
- 241001628505 Phlebopus Species 0.000 description 1
- 241000255129 Phlebotominae Species 0.000 description 1
- 241000722350 Phlebotomus <genus> Species 0.000 description 1
- 241001480007 Phomopsis Species 0.000 description 1
- IAJOBQBIJHVGMQ-UHFFFAOYSA-N Phosphinothricin Natural products CP(O)(=O)CCC(N)C(O)=O IAJOBQBIJHVGMQ-UHFFFAOYSA-N 0.000 description 1
- 241001439019 Phthorimaea operculella Species 0.000 description 1
- 241000921313 Phyllopodium Species 0.000 description 1
- 241001495084 Phylo Species 0.000 description 1
- IHPVFYLOGNNZLA-UHFFFAOYSA-N Phytoalexin Natural products COC1=CC=CC=C1C1OC(C=C2C(OCO2)=C2OC)=C2C(=O)C1 IHPVFYLOGNNZLA-UHFFFAOYSA-N 0.000 description 1
- 241000490567 Pinctada Species 0.000 description 1
- 235000008582 Pinus sylvestris Nutrition 0.000 description 1
- 241000722363 Piper Species 0.000 description 1
- 240000005428 Pistacia lentiscus Species 0.000 description 1
- 240000004713 Pisum sativum Species 0.000 description 1
- 206010035148 Plague Diseases 0.000 description 1
- 241000193804 Planococcus <bacterium> Species 0.000 description 1
- 108010064851 Plant Proteins Proteins 0.000 description 1
- 235000006753 Platycodon grandiflorum Nutrition 0.000 description 1
- 240000003582 Platycodon grandiflorus Species 0.000 description 1
- 241000092659 Pleuropterus Species 0.000 description 1
- 241000595629 Plodia interpunctella Species 0.000 description 1
- 241000189528 Polymorphida Species 0.000 description 1
- 239000004721 Polyphenylene oxide Substances 0.000 description 1
- 241000222640 Polyporus Species 0.000 description 1
- 241000908127 Porcellio scaber Species 0.000 description 1
- 241000258974 Porocephalida Species 0.000 description 1
- 241001506000 Porotermes Species 0.000 description 1
- 241001201614 Prays Species 0.000 description 1
- ZTHYODDOHIVTJV-UHFFFAOYSA-N Propyl gallate Chemical compound CCCOC(=O)C1=CC(O)=C(O)C(O)=C1 ZTHYODDOHIVTJV-UHFFFAOYSA-N 0.000 description 1
- GOOHAUXETOMSMM-UHFFFAOYSA-N Propylene oxide Chemical compound CC1CO1 GOOHAUXETOMSMM-UHFFFAOYSA-N 0.000 description 1
- 241000238705 Prostigmata Species 0.000 description 1
- 108010009736 Protein Hydrolysates Proteins 0.000 description 1
- 241000077191 Proteopsis Species 0.000 description 1
- QTXHFDHVLBDJIO-UHFFFAOYSA-N Prothoate Chemical compound CCOP(=S)(OCC)SCC(=O)NC(C)C QTXHFDHVLBDJIO-UHFFFAOYSA-N 0.000 description 1
- 241000196250 Prototheca Species 0.000 description 1
- 241001137874 Pseudophyllidea Species 0.000 description 1
- 241001415024 Psocoptera Species 0.000 description 1
- 241000517309 Pthirus Species 0.000 description 1
- 241001675082 Pulex Species 0.000 description 1
- 241000718000 Pulex irritans Species 0.000 description 1
- 241000083513 Punctum Species 0.000 description 1
- 239000005925 Pymetrozine Substances 0.000 description 1
- VQXSOUPNOZTNAI-UHFFFAOYSA-N Pyrethrin I Natural products CC(=CC1CC1C(=O)OC2CC(=O)C(=C2C)CC=C/C=C)C VQXSOUPNOZTNAI-UHFFFAOYSA-N 0.000 description 1
- 241000231139 Pyricularia Species 0.000 description 1
- 239000005828 Pyrimethanil Substances 0.000 description 1
- 239000005829 Pyriofenone Substances 0.000 description 1
- MWMQNVGAHVXSPE-UHFFFAOYSA-N Pyriprole Chemical compound ClC=1C=C(C(F)(F)F)C=C(Cl)C=1N1N=C(C#N)C(SC(F)F)=C1NCC1=CC=CC=N1 MWMQNVGAHVXSPE-UHFFFAOYSA-N 0.000 description 1
- 206010037688 Q fever Diseases 0.000 description 1
- 241000944747 Quesada gigas Species 0.000 description 1
- 241001408411 Raillietia Species 0.000 description 1
- 241000269435 Rana <genus> Species 0.000 description 1
- 241000283011 Rangifer Species 0.000 description 1
- 241000549289 Rastrococcus Species 0.000 description 1
- 241000700159 Rattus Species 0.000 description 1
- 108020004511 Recombinant DNA Proteins 0.000 description 1
- 241000244173 Rhabditis Species 0.000 description 1
- 241000156898 Rhagoletis cingulata Species 0.000 description 1
- 241000219093 Rhamnus Species 0.000 description 1
- 241001194723 Rhinoestrus Species 0.000 description 1
- 244000152640 Rhipsalis cassutha Species 0.000 description 1
- 235000012300 Rhipsalis cassutha Nutrition 0.000 description 1
- 241000316848 Rhodococcus <scale insect> Species 0.000 description 1
- 241000344244 Rhynchophorus Species 0.000 description 1
- 241001405974 Rhynchostylis Species 0.000 description 1
- 241000318997 Rhyzopertha dominica Species 0.000 description 1
- 241000606701 Rickettsia Species 0.000 description 1
- 241000220221 Rosales Species 0.000 description 1
- 241000702971 Rotylenchulus reniformis Species 0.000 description 1
- 241001092459 Rubus Species 0.000 description 1
- 229930001406 Ryanodine Natural products 0.000 description 1
- 125000000066 S-methyl group Chemical group [H]C([H])([H])S* 0.000 description 1
- AUVVAXYIELKVAI-UHFFFAOYSA-N SJ000285215 Natural products N1CCC2=CC(OC)=C(OC)C=C2C1CC1CC2C3=CC(OC)=C(OC)C=C3CCN2CC1CC AUVVAXYIELKVAI-UHFFFAOYSA-N 0.000 description 1
- 241000914334 Sahlbergella singularis Species 0.000 description 1
- OUNSASXJZHBGAI-UHFFFAOYSA-N Salithion Chemical compound C1=CC=C2OP(OC)(=S)OCC2=C1 OUNSASXJZHBGAI-UHFFFAOYSA-N 0.000 description 1
- 241000605112 Scapanulus oweni Species 0.000 description 1
- 241000726725 Scaptocoris castanea Species 0.000 description 1
- 241000253973 Schistocerca gregaria Species 0.000 description 1
- 241000242678 Schistosoma Species 0.000 description 1
- 241000630329 Scomberesox saurus saurus Species 0.000 description 1
- 241000207929 Scutellaria Species 0.000 description 1
- 241001313237 Scutigerella immaculata Species 0.000 description 1
- 239000005834 Sedaxane Substances 0.000 description 1
- 239000004113 Sepiolite Substances 0.000 description 1
- 241000347488 Silurus Species 0.000 description 1
- 241001503607 Simulium meridionale Species 0.000 description 1
- 241001177138 Sinoxylon Species 0.000 description 1
- PMZURENOXWZQFD-UHFFFAOYSA-L Sodium Sulfate Chemical compound [Na+].[Na+].[O-]S([O-])(=O)=O PMZURENOXWZQFD-UHFFFAOYSA-L 0.000 description 1
- 229920002125 Sokalan® Polymers 0.000 description 1
- 241001291279 Solanum galapagense Species 0.000 description 1
- 235000002597 Solanum melongena Nutrition 0.000 description 1
- 244000061458 Solanum melongena Species 0.000 description 1
- 241000219784 Sophora Species 0.000 description 1
- 235000011684 Sorghum saccharatum Nutrition 0.000 description 1
- 241000532885 Sphenophorus Species 0.000 description 1
- 235000009337 Spinacia oleracea Nutrition 0.000 description 1
- 244000300264 Spinacia oleracea Species 0.000 description 1
- 241001533587 Spironucleus Species 0.000 description 1
- 241000586493 Spirosoma Species 0.000 description 1
- 241000244042 Spirurida Species 0.000 description 1
- 241001406921 Squamosa Species 0.000 description 1
- 206010041896 St. Louis Encephalitis Diseases 0.000 description 1
- 241001161749 Stenchaetothrips biformis Species 0.000 description 1
- 241000448016 Stenoma Species 0.000 description 1
- 241000283614 Stephanitis nashi Species 0.000 description 1
- 241001636537 Stephanus Species 0.000 description 1
- 235000021282 Sterculia Nutrition 0.000 description 1
- 240000001058 Sterculia urens Species 0.000 description 1
- 241001369218 Sternula Species 0.000 description 1
- 241000975373 Sticta Species 0.000 description 1
- 241000063073 Stomopteryx Species 0.000 description 1
- 241000187747 Streptomyces Species 0.000 description 1
- 241001467541 Streptomyces galbus Species 0.000 description 1
- 241000187395 Streptomyces microflavus Species 0.000 description 1
- 241001194494 Strongylostoma Species 0.000 description 1
- 241000989659 Stropharia sp. Species 0.000 description 1
- 241000282887 Suidae Species 0.000 description 1
- 229940100389 Sulfonylurea Drugs 0.000 description 1
- 239000005935 Sulfuryl fluoride Substances 0.000 description 1
- 235000019486 Sunflower oil Nutrition 0.000 description 1
- 238000006069 Suzuki reaction reaction Methods 0.000 description 1
- 241001220316 Syngamus Species 0.000 description 1
- 241000255628 Tabanidae Species 0.000 description 1
- 241000244155 Taenia Species 0.000 description 1
- 241000228343 Talaromyces flavus Species 0.000 description 1
- 241000596504 Tamarindus Species 0.000 description 1
- 240000004460 Tanacetum coccineum Species 0.000 description 1
- 241000388430 Tara Species 0.000 description 1
- FEWJPZIEWOKRBE-UHFFFAOYSA-N Tartaric acid Natural products [H+].[H+].[O-]C(=O)C(O)C(O)C([O-])=O FEWJPZIEWOKRBE-UHFFFAOYSA-N 0.000 description 1
- 241000913329 Tecia Species 0.000 description 1
- 241000347415 Teladorsagia Species 0.000 description 1
- 241000270708 Testudinidae Species 0.000 description 1
- 241000787015 Tetanops Species 0.000 description 1
- 241001454295 Tetranychidae Species 0.000 description 1
- QUWSDLYBOVGOCW-UHFFFAOYSA-N Tetrasul Chemical compound C1=CC(Cl)=CC=C1SC1=CC(Cl)=C(Cl)C=C1Cl QUWSDLYBOVGOCW-UHFFFAOYSA-N 0.000 description 1
- 241000566961 Thelephora Species 0.000 description 1
- 244000299461 Theobroma cacao Species 0.000 description 1
- 235000009470 Theobroma cacao Nutrition 0.000 description 1
- 241000028626 Thermobia domestica Species 0.000 description 1
- 239000005940 Thiacloprid Substances 0.000 description 1
- 239000005843 Thiram Substances 0.000 description 1
- 241000910588 Thrips simplex Species 0.000 description 1
- 241000511627 Tipula paludosa Species 0.000 description 1
- GWEVSGVZZGPLCZ-UHFFFAOYSA-N Titan oxide Chemical compound O=[Ti]=O GWEVSGVZZGPLCZ-UHFFFAOYSA-N 0.000 description 1
- 239000005845 Tolclofos-methyl Substances 0.000 description 1
- CRPUJAZIXJMDBK-UHFFFAOYSA-N Toxaphene Natural products C1CC2C(=C)C(C)(C)C1C2 CRPUJAZIXJMDBK-UHFFFAOYSA-N 0.000 description 1
- 241000271862 Toxoptera Species 0.000 description 1
- 241001136888 Toxotrypana curvicauda Species 0.000 description 1
- 241000869417 Trematodes Species 0.000 description 1
- 241000589886 Treponema Species 0.000 description 1
- 239000005846 Triadimenol Substances 0.000 description 1
- 241001439624 Trichina Species 0.000 description 1
- 241000223261 Trichoderma viride Species 0.000 description 1
- 241000046051 Trichopsis Species 0.000 description 1
- 241001149076 Trichosanthes sp. Species 0.000 description 1
- 239000005627 Triclopyr Substances 0.000 description 1
- 239000005857 Trifloxystrobin Substances 0.000 description 1
- 241000736917 Trionyx Species 0.000 description 1
- 241000606278 Triplostegia Species 0.000 description 1
- 208000034784 Tularaemia Diseases 0.000 description 1
- 241001168740 Tychius Species 0.000 description 1
- 241000243782 Tylenchida Species 0.000 description 1
- 241000233948 Typha Species 0.000 description 1
- 241000841223 Typhlocyba Species 0.000 description 1
- 241000196252 Ulva Species 0.000 description 1
- 241001261505 Undaria Species 0.000 description 1
- 241001466100 Vaejovis Species 0.000 description 1
- XPHOBMULWMGEBA-UHFFFAOYSA-N Valienamine Natural products NC1C=C(CO)C(O)C(O)C1O XPHOBMULWMGEBA-UHFFFAOYSA-N 0.000 description 1
- 241000496694 Vasates Species 0.000 description 1
- 241001661641 Verrucosa Species 0.000 description 1
- 241000082085 Verticillium <Phyllachorales> Species 0.000 description 1
- 241000256856 Vespidae Species 0.000 description 1
- 241000607598 Vibrio Species 0.000 description 1
- 235000010749 Vicia faba Nutrition 0.000 description 1
- 240000006677 Vicia faba Species 0.000 description 1
- 235000002098 Vicia faba var. major Nutrition 0.000 description 1
- 239000004188 Virginiamycin Substances 0.000 description 1
- 108010080702 Virginiamycin Proteins 0.000 description 1
- 241001464837 Viridiplantae Species 0.000 description 1
- 241000726445 Viroids Species 0.000 description 1
- 241000221013 Viscum album Species 0.000 description 1
- 241001274788 Viteus vitifoliae Species 0.000 description 1
- 206010047642 Vitiligo Diseases 0.000 description 1
- 235000009754 Vitis X bourquina Nutrition 0.000 description 1
- 235000012333 Vitis X labruscana Nutrition 0.000 description 1
- 206010047697 Volvulus Diseases 0.000 description 1
- 241000216750 Wilhelmia Species 0.000 description 1
- 241000949975 Xeris Species 0.000 description 1
- 208000003152 Yellow Fever Diseases 0.000 description 1
- 235000010688 Yerba dulce Nutrition 0.000 description 1
- 241001035865 Zabrus Species 0.000 description 1
- HCHKCACWOHOZIP-UHFFFAOYSA-N Zinc Chemical compound [Zn] HCHKCACWOHOZIP-UHFFFAOYSA-N 0.000 description 1
- 239000006011 Zinc phosphide Substances 0.000 description 1
- 239000005870 Ziram Substances 0.000 description 1
- 241001123263 Zostera Species 0.000 description 1
- 241001414985 Zygentoma Species 0.000 description 1
- 241000839659 Zygina Species 0.000 description 1
- VXSIXFKKSNGRRO-MXOVTSAMSA-N [(1s)-2-methyl-4-oxo-3-[(2z)-penta-2,4-dienyl]cyclopent-2-en-1-yl] (1r,3r)-2,2-dimethyl-3-(2-methylprop-1-enyl)cyclopropane-1-carboxylate;[(1s)-2-methyl-4-oxo-3-[(2z)-penta-2,4-dienyl]cyclopent-2-en-1-yl] (1r,3r)-3-[(e)-3-methoxy-2-methyl-3-oxoprop-1-enyl Chemical class CC1(C)[C@H](C=C(C)C)[C@H]1C(=O)O[C@@H]1C(C)=C(C\C=C/C=C)C(=O)C1.CC1(C)[C@H](/C=C(\C)C(=O)OC)[C@H]1C(=O)O[C@@H]1C(C)=C(C\C=C/C=C)C(=O)C1 VXSIXFKKSNGRRO-MXOVTSAMSA-N 0.000 description 1
- BZMIHNKNQJJVRO-LVZFUZTISA-N [(e)-c-(3-chloro-2,6-dimethoxyphenyl)-n-ethoxycarbonimidoyl] benzoate Chemical compound COC=1C=CC(Cl)=C(OC)C=1C(=N/OCC)\OC(=O)C1=CC=CC=C1 BZMIHNKNQJJVRO-LVZFUZTISA-N 0.000 description 1
- KAATUXNTWXVJKI-QPIRBTGLSA-N [(s)-cyano-(3-phenoxyphenyl)methyl] 3-(2,2-dichloroethenyl)-2,2-dimethylcyclopropane-1-carboxylate Chemical compound CC1(C)C(C=C(Cl)Cl)C1C(=O)O[C@H](C#N)C1=CC=CC(OC=2C=CC=CC=2)=C1 KAATUXNTWXVJKI-QPIRBTGLSA-N 0.000 description 1
- FSAVDKDHPDSCTO-WQLSENKSSA-N [(z)-2-chloro-1-(2,4-dichlorophenyl)ethenyl] diethyl phosphate Chemical compound CCOP(=O)(OCC)O\C(=C/Cl)C1=CC=C(Cl)C=C1Cl FSAVDKDHPDSCTO-WQLSENKSSA-N 0.000 description 1
- UJLKLUQGBGSJOO-OWOJBTEDSA-N [1'-[(e)-3-(4-chlorophenyl)prop-2-enyl]-5-fluorospiro[2h-indole-3,4'-piperidine]-1-yl]-(2-chloropyridin-4-yl)methanone Chemical compound C12=CC(F)=CC=C2N(C(=O)C=2C=C(Cl)N=CC=2)CC1(CC1)CCN1C\C=C\C1=CC=C(Cl)C=C1 UJLKLUQGBGSJOO-OWOJBTEDSA-N 0.000 description 1
- KVIZNNVXXNFLMU-AIIUZBJTSA-N [2,3,5,6-tetrafluoro-4-(methoxymethyl)phenyl]methyl (1r,3r)-2,2-dimethyl-3-[(e)-prop-1-enyl]cyclopropane-1-carboxylate Chemical compound FC1=C(F)C(COC)=C(F)C(F)=C1COC(=O)[C@H]1C(C)(C)[C@@H]1\C=C\C KVIZNNVXXNFLMU-AIIUZBJTSA-N 0.000 description 1
- MWFQAAWRPDRKDG-KOLCDFICSA-N [2,3,5,6-tetrafluoro-4-(methoxymethyl)phenyl]methyl (1r,3s)-3-(2,2-dichloroethenyl)-2,2-dimethylcyclopropane-1-carboxylate Chemical compound FC1=C(F)C(COC)=C(F)C(F)=C1COC(=O)[C@H]1C(C)(C)[C@@H]1C=C(Cl)Cl MWFQAAWRPDRKDG-KOLCDFICSA-N 0.000 description 1
- JSPSGKJNCVNQBJ-FBWZZCNVSA-N [2-[[(3s,6s,7r,8r)-8-benzyl-6-methyl-7-(2-methylpropanoyloxy)-1,4,5,9-tetraoxononan-3-yl]carbamoyl]-4-methoxypyridin-3-yl]oxymethyl 2-methylpropanoate Chemical compound COC1=CC=NC(C(=O)N[C@@H](CC=O)C(=O)C(=O)[C@@H](C)[C@H](OC(=O)C(C)C)[C@@H](CC=2C=CC=CC=2)C=O)=C1OCOC(=O)C(C)C JSPSGKJNCVNQBJ-FBWZZCNVSA-N 0.000 description 1
- CFGPESLNPCIKIX-UHFFFAOYSA-N [2-[ethoxy(propylsulfanyl)phosphoryl]oxyphenyl] n-methylcarbamate Chemical compound CCCSP(=O)(OCC)OC1=CC=CC=C1OC(=O)NC CFGPESLNPCIKIX-UHFFFAOYSA-N 0.000 description 1
- ROVGZAWFACYCSP-MQBLHHJJSA-N [2-methyl-4-oxo-3-[(2z)-penta-2,4-dienyl]cyclopent-2-en-1-yl] (1r,3r)-2,2-dimethyl-3-(2-methylprop-1-enyl)cyclopropane-1-carboxylate Chemical compound CC1(C)[C@H](C=C(C)C)[C@H]1C(=O)OC1C(C)=C(C\C=C/C=C)C(=O)C1 ROVGZAWFACYCSP-MQBLHHJJSA-N 0.000 description 1
- YDHZUCLRCLIJRL-UHFFFAOYSA-N [3-(4-chloro-2-fluorophenyl)-5-(2,4-difluorophenyl)-1,2-oxazol-4-yl]-pyridin-3-ylmethanol Chemical compound C=1C=CN=CC=1C(O)C=1C(C=2C(=CC(Cl)=CC=2)F)=NOC=1C1=CC=C(F)C=C1F YDHZUCLRCLIJRL-UHFFFAOYSA-N 0.000 description 1
- CWVZGJORVTZXFW-UHFFFAOYSA-N [benzyl(dimethyl)silyl]methyl carbamate Chemical compound NC(=O)OC[Si](C)(C)CC1=CC=CC=C1 CWVZGJORVTZXFW-UHFFFAOYSA-N 0.000 description 1
- INISTDXBRIBGOC-CGAIIQECSA-N [cyano-(3-phenoxyphenyl)methyl] (2s)-2-[2-chloro-4-(trifluoromethyl)anilino]-3-methylbutanoate Chemical compound N([C@@H](C(C)C)C(=O)OC(C#N)C=1C=C(OC=2C=CC=CC=2)C=CC=1)C1=CC=C(C(F)(F)F)C=C1Cl INISTDXBRIBGOC-CGAIIQECSA-N 0.000 description 1
- IHVPAVRHNZFQKC-UHFFFAOYSA-N [cyano-(6-phenoxypyridin-2-yl)methyl] 3-(2,2-dichloroethenyl)-2,2-dimethylcyclopropane-1-carboxylate Chemical compound CC1(C)C(C=C(Cl)Cl)C1C(=O)OC(C#N)C1=CC=CC(OC=2C=CC=CC=2)=N1 IHVPAVRHNZFQKC-UHFFFAOYSA-N 0.000 description 1
- 230000036579 abiotic stress Effects 0.000 description 1
- 238000005299 abrasion Methods 0.000 description 1
- 239000000205 acacia gum Substances 0.000 description 1
- 235000010489 acacia gum Nutrition 0.000 description 1
- QDRXWCAVUNHOGA-UHFFFAOYSA-N acequinocyl Chemical group C1=CC=C2C(=O)C(CCCCCCCCCCCC)=C(OC(C)=O)C(=O)C2=C1 QDRXWCAVUNHOGA-UHFFFAOYSA-N 0.000 description 1
- ODFJOVXVLFUVNQ-UHFFFAOYSA-N acetarsol Chemical group CC(=O)NC1=CC([As](O)(O)=O)=CC=C1O ODFJOVXVLFUVNQ-UHFFFAOYSA-N 0.000 description 1
- 229940121373 acetyl-coa carboxylase inhibitor Drugs 0.000 description 1
- UELITFHSCLAHKR-UHFFFAOYSA-N acibenzolar-S-methyl Chemical group CSC(=O)C1=CC=CC2=C1SN=N2 UELITFHSCLAHKR-UHFFFAOYSA-N 0.000 description 1
- YLFSVIMMRPNPFK-WEQBUNFVSA-N acrinathrin Chemical compound CC1(C)[C@@H](\C=C/C(=O)OC(C(F)(F)F)C(F)(F)F)[C@H]1C(=O)O[C@H](C#N)C1=CC=CC(OC=2C=CC=CC=2)=C1 YLFSVIMMRPNPFK-WEQBUNFVSA-N 0.000 description 1
- 150000001252 acrylic acid derivatives Chemical class 0.000 description 1
- 239000012190 activator Substances 0.000 description 1
- 239000013543 active substance Substances 0.000 description 1
- 230000000996 additive effect Effects 0.000 description 1
- 230000002411 adverse Effects 0.000 description 1
- 239000000443 aerosol Substances 0.000 description 1
- LRZWFURXIMFONG-HRSIRGMGSA-N afidopyropen Chemical compound C([C@@]1(C)[C@H]2[C@]([C@H]3[C@@H](O)C=4C(=O)OC(=CC=4O[C@]3(C)[C@@H](O)C2)C=2C=NC=CC=2)(C)CC[C@@H]1OC(=O)C1CC1)OC(=O)C1CC1 LRZWFURXIMFONG-HRSIRGMGSA-N 0.000 description 1
- 229960000982 afoxolaner Drugs 0.000 description 1
- GMAUQNJOSOMMHI-JXAWBTAJSA-N alanycarb Chemical compound CSC(\C)=N/OC(=O)N(C)SN(CCC(=O)OCC)CC1=CC=CC=C1 GMAUQNJOSOMMHI-JXAWBTAJSA-N 0.000 description 1
- 229950010075 albendazole sulfoxide Drugs 0.000 description 1
- HFVAFDPGUJEFBQ-UHFFFAOYSA-M alizarin red S Chemical compound [Na+].O=C1C2=CC=CC=C2C(=O)C2=C1C=C(S([O-])(=O)=O)C(O)=C2O HFVAFDPGUJEFBQ-UHFFFAOYSA-M 0.000 description 1
- 150000008044 alkali metal hydroxides Chemical class 0.000 description 1
- 125000003342 alkenyl group Chemical group 0.000 description 1
- 125000004471 alkyl aminosulfonyl group Chemical group 0.000 description 1
- 150000004996 alkyl benzenes Chemical class 0.000 description 1
- 125000005907 alkyl ester group Chemical group 0.000 description 1
- 125000005376 alkyl siloxane group Chemical group 0.000 description 1
- 150000008051 alkyl sulfates Chemical class 0.000 description 1
- 125000004644 alkyl sulfinyl group Chemical group 0.000 description 1
- 229940045714 alkyl sulfonate alkylating agent Drugs 0.000 description 1
- 150000008052 alkyl sulfonates Chemical class 0.000 description 1
- HSFWRNGVRCDJHI-UHFFFAOYSA-N alpha-acetylene Natural products C#C HSFWRNGVRCDJHI-UHFFFAOYSA-N 0.000 description 1
- 229910000147 aluminium phosphate Inorganic materials 0.000 description 1
- 235000012211 aluminium silicate Nutrition 0.000 description 1
- RQVYBGPQFYCBGX-UHFFFAOYSA-N ametryn Chemical compound CCNC1=NC(NC(C)C)=NC(SC)=N1 RQVYBGPQFYCBGX-UHFFFAOYSA-N 0.000 description 1
- 230000002862 amidating effect Effects 0.000 description 1
- 230000009435 amidation Effects 0.000 description 1
- 238000007112 amidation reaction Methods 0.000 description 1
- 150000001409 amidines Chemical class 0.000 description 1
- 150000001413 amino acids Chemical class 0.000 description 1
- 125000005219 aminonitrile group Chemical group 0.000 description 1
- 229960002587 amitraz Drugs 0.000 description 1
- QXAITBQSYVNQDR-ZIOPAAQOSA-N amitraz Chemical compound C=1C=C(C)C=C(C)C=1/N=C/N(C)\C=N\C1=CC=C(C)C=C1C QXAITBQSYVNQDR-ZIOPAAQOSA-N 0.000 description 1
- 235000012538 ammonium bicarbonate Nutrition 0.000 description 1
- 239000001099 ammonium carbonate Substances 0.000 description 1
- 150000003863 ammonium salts Chemical class 0.000 description 1
- 229910052921 ammonium sulfate Inorganic materials 0.000 description 1
- 238000010171 animal model Methods 0.000 description 1
- 244000000054 animal parasite Species 0.000 description 1
- 229940124339 anthelmintic agent Drugs 0.000 description 1
- 239000000921 anthelmintic agent Substances 0.000 description 1
- 230000002528 anti-freeze Effects 0.000 description 1
- 230000001857 anti-mycotic effect Effects 0.000 description 1
- 230000000884 anti-protozoa Effects 0.000 description 1
- 239000002519 antifouling agent Substances 0.000 description 1
- 239000000427 antigen Substances 0.000 description 1
- 108091007433 antigens Proteins 0.000 description 1
- 102000036639 antigens Human genes 0.000 description 1
- 239000002543 antimycotic Substances 0.000 description 1
- 239000003963 antioxidant agent Substances 0.000 description 1
- 235000006708 antioxidants Nutrition 0.000 description 1
- 229940111121 antirheumatic drug quinolines Drugs 0.000 description 1
- 229910052786 argon Inorganic materials 0.000 description 1
- 150000001491 aromatic compounds Chemical class 0.000 description 1
- 125000006615 aromatic heterocyclic group Chemical group 0.000 description 1
- 125000005228 aryl sulfonate group Chemical group 0.000 description 1
- 238000006254 arylation reaction Methods 0.000 description 1
- 238000000889 atomisation Methods 0.000 description 1
- 229960000892 attapulgite Drugs 0.000 description 1
- 239000005667 attractant Substances 0.000 description 1
- RQVGAIADHNPSME-UHFFFAOYSA-N azinphos-ethyl Chemical group C1=CC=C2C(=O)N(CSP(=S)(OCC)OCC)N=NC2=C1 RQVGAIADHNPSME-UHFFFAOYSA-N 0.000 description 1
- CJJOSEISRRTUQB-UHFFFAOYSA-N azinphos-methyl Chemical group C1=CC=C2C(=O)N(CSP(=S)(OC)OC)N=NC2=C1 CJJOSEISRRTUQB-UHFFFAOYSA-N 0.000 description 1
- 239000000987 azo dye Substances 0.000 description 1
- ONHBDDJJTDTLIR-UHFFFAOYSA-N azocyclotin Chemical compound C1CCCCC1[Sn](N1N=CN=C1)(C1CCCCC1)C1CCCCC1 ONHBDDJJTDTLIR-UHFFFAOYSA-N 0.000 description 1
- 238000003287 bathing Methods 0.000 description 1
- 230000009286 beneficial effect Effects 0.000 description 1
- 150000001556 benzimidazoles Chemical class 0.000 description 1
- 150000008047 benzoylureas Chemical class 0.000 description 1
- 235000019445 benzyl alcohol Nutrition 0.000 description 1
- 125000001797 benzyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])* 0.000 description 1
- 239000003139 biocide Substances 0.000 description 1
- 229960000074 biopharmaceutical Drugs 0.000 description 1
- 238000010352 biotechnological method Methods 0.000 description 1
- 230000004790 biotic stress Effects 0.000 description 1
- QKSKPIVNLNLAAV-UHFFFAOYSA-N bis(2-chloroethyl) sulfide Chemical compound ClCCSCCCl QKSKPIVNLNLAAV-UHFFFAOYSA-N 0.000 description 1
- OIPMQULDKWSNGX-UHFFFAOYSA-N bis[[ethoxy(oxo)phosphaniumyl]oxy]alumanyloxy-ethoxy-oxophosphanium Chemical compound [Al+3].CCO[P+]([O-])=O.CCO[P+]([O-])=O.CCO[P+]([O-])=O OIPMQULDKWSNGX-UHFFFAOYSA-N 0.000 description 1
- 229960002326 bithionol Drugs 0.000 description 1
- JFIOVJDNOJYLKP-UHFFFAOYSA-N bithionol Chemical compound OC1=C(Cl)C=C(Cl)C=C1SC1=CC(Cl)=CC(Cl)=C1O JFIOVJDNOJYLKP-UHFFFAOYSA-N 0.000 description 1
- 201000000053 blastoma Diseases 0.000 description 1
- 229910052796 boron Inorganic materials 0.000 description 1
- 229940118790 boscalid Drugs 0.000 description 1
- WYEMLYFITZORAB-UHFFFAOYSA-N boscalid Chemical compound C1=CC(Cl)=CC=C1C1=CC=CC=C1NC(=O)C1=CC=CN=C1Cl WYEMLYFITZORAB-UHFFFAOYSA-N 0.000 description 1
- QSLZKWPYTWEWHC-UHFFFAOYSA-N broflanilide Chemical compound C=1C=CC(C(=O)NC=2C(=CC(=CC=2Br)C(F)(C(F)(F)F)C(F)(F)F)C(F)(F)F)=C(F)C=1N(C)C(=O)C1=CC=CC=C1 QSLZKWPYTWEWHC-UHFFFAOYSA-N 0.000 description 1
- RDHPKYGYEGBMSE-UHFFFAOYSA-N bromoethane Chemical compound CCBr RDHPKYGYEGBMSE-UHFFFAOYSA-N 0.000 description 1
- FOANIXZHAMJWOI-UHFFFAOYSA-N bromopropylate Chemical compound C=1C=C(Br)C=CC=1C(O)(C(=O)OC(C)C)C1=CC=C(Br)C=C1 FOANIXZHAMJWOI-UHFFFAOYSA-N 0.000 description 1
- 229950000536 butamisole Drugs 0.000 description 1
- 239000001273 butane Substances 0.000 description 1
- BEWFIPLBFJGWSR-AONZOJHOSA-N butyl (z,12r)-12-acetyloxyoctadec-9-enoate Chemical group CCCCCC[C@@H](OC(C)=O)C\C=C/CCCCCCCC(=O)OCCCC BEWFIPLBFJGWSR-AONZOJHOSA-N 0.000 description 1
- 239000006227 byproduct Substances 0.000 description 1
- 239000002775 capsule Substances 0.000 description 1
- JHRWWRDRBPCWTF-OLQVQODUSA-N captafol Chemical compound C1C=CC[C@H]2C(=O)N(SC(Cl)(Cl)C(Cl)Cl)C(=O)[C@H]21 JHRWWRDRBPCWTF-OLQVQODUSA-N 0.000 description 1
- 150000004657 carbamic acid derivatives Chemical class 0.000 description 1
- 239000004202 carbamide Substances 0.000 description 1
- 229960005286 carbaryl Drugs 0.000 description 1
- CVXBEEMKQHEXEN-UHFFFAOYSA-N carbaryl Chemical compound C1=CC=C2C(OC(=O)NC)=CC=CC2=C1 CVXBEEMKQHEXEN-UHFFFAOYSA-N 0.000 description 1
- PFKFTWBEEFSNDU-UHFFFAOYSA-N carbonyldiimidazole Chemical compound C1=CN=CN1C(=O)N1C=CN=C1 PFKFTWBEEFSNDU-UHFFFAOYSA-N 0.000 description 1
- 125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 description 1
- 239000001768 carboxy methyl cellulose Substances 0.000 description 1
- 235000010948 carboxy methyl cellulose Nutrition 0.000 description 1
- 239000008112 carboxymethyl-cellulose Substances 0.000 description 1
- 230000015556 catabolic process Effects 0.000 description 1
- 125000002091 cationic group Chemical group 0.000 description 1
- 230000032823 cell division Effects 0.000 description 1
- 239000004568 cement Substances 0.000 description 1
- 239000000919 ceramic Substances 0.000 description 1
- 239000002738 chelating agent Substances 0.000 description 1
- KXZJHVJKXJLBKO-UHFFFAOYSA-N chembl1408157 Chemical compound N=1C2=CC=CC=C2C(C(=O)O)=CC=1C1=CC=C(O)C=C1 KXZJHVJKXJLBKO-UHFFFAOYSA-N 0.000 description 1
- ALLOLPOYFRLCCX-UHFFFAOYSA-N chembl1986529 Chemical compound COC1=CC=CC=C1N=NC1=C(O)C=CC2=CC=CC=C12 ALLOLPOYFRLCCX-UHFFFAOYSA-N 0.000 description 1
- NDHXMRFNYMNBKO-PWSUYJOCSA-N chembl2227757 Chemical compound [O-][N+](=O)C([C@H]1CC[C@H](O1)N1CC2)=C1N2CC1=CC=C(Cl)N=C1 NDHXMRFNYMNBKO-PWSUYJOCSA-N 0.000 description 1
- 239000007795 chemical reaction product Substances 0.000 description 1
- 235000013330 chicken meat Nutrition 0.000 description 1
- BIWJNBZANLAXMG-YQELWRJZSA-N chloordaan Chemical compound ClC1=C(Cl)[C@@]2(Cl)C3CC(Cl)C(Cl)C3[C@]1(Cl)C2(Cl)Cl BIWJNBZANLAXMG-YQELWRJZSA-N 0.000 description 1
- 150000001805 chlorine compounds Chemical class 0.000 description 1
- QGTYWWGEWOBMAK-UHFFFAOYSA-N chlormephos Chemical compound CCOP(=S)(OCC)SCCl QGTYWWGEWOBMAK-UHFFFAOYSA-N 0.000 description 1
- HKMOPYJWSFRURD-UHFFFAOYSA-N chloro hypochlorite;copper Chemical compound [Cu].ClOCl HKMOPYJWSFRURD-UHFFFAOYSA-N 0.000 description 1
- 150000008422 chlorobenzenes Chemical class 0.000 description 1
- CRQQGFGUEAVUIL-UHFFFAOYSA-N chlorothalonil Chemical compound ClC1=C(Cl)C(C#N)=C(Cl)C(C#N)=C1Cl CRQQGFGUEAVUIL-UHFFFAOYSA-N 0.000 description 1
- 229960004475 chlortetracycline Drugs 0.000 description 1
- 235000019365 chlortetracycline Nutrition 0.000 description 1
- NZNRRXXETLSZRO-UHFFFAOYSA-N chlorthion Chemical compound COP(=S)(OC)OC1=CC=C([N+]([O-])=O)C(Cl)=C1 NZNRRXXETLSZRO-UHFFFAOYSA-N 0.000 description 1
- 238000004140 cleaning Methods 0.000 description 1
- 210000003555 cloaca Anatomy 0.000 description 1
- UXADOQPNKNTIHB-UHFFFAOYSA-N clofentezine Chemical compound ClC1=CC=CC=C1C1=NN=C(C=2C(=CC=CC=2)Cl)N=N1 UXADOQPNKNTIHB-UHFFFAOYSA-N 0.000 description 1
- 239000010941 cobalt Substances 0.000 description 1
- 229910017052 cobalt Inorganic materials 0.000 description 1
- GUTLYIVDDKVIGB-UHFFFAOYSA-N cobalt atom Chemical compound [Co] GUTLYIVDDKVIGB-UHFFFAOYSA-N 0.000 description 1
- 239000000084 colloidal system Substances 0.000 description 1
- 239000008139 complexing agent Substances 0.000 description 1
- 235000009508 confectionery Nutrition 0.000 description 1
- 238000007796 conventional method Methods 0.000 description 1
- 229910052802 copper Inorganic materials 0.000 description 1
- 239000010949 copper Substances 0.000 description 1
- 229910000366 copper(II) sulfate Inorganic materials 0.000 description 1
- OHGJVAFVIMGJTE-UHFFFAOYSA-L copper;naphthalene-2-carboxylate Chemical compound [Cu+2].C1=CC=CC2=CC(C(=O)[O-])=CC=C21.C1=CC=CC2=CC(C(=O)[O-])=CC=C21 OHGJVAFVIMGJTE-UHFFFAOYSA-L 0.000 description 1
- 239000006184 cosolvent Substances 0.000 description 1
- 229950002363 crufomate Drugs 0.000 description 1
- 101150065438 cry1Ab gene Proteins 0.000 description 1
- 229960004643 cupric oxide Drugs 0.000 description 1
- 238000005520 cutting process Methods 0.000 description 1
- YXKMMRDKEKCERS-UHFFFAOYSA-N cyazofamid Chemical compound CN(C)S(=O)(=O)N1C(C#N)=NC(Cl)=C1C1=CC=C(C)C=C1 YXKMMRDKEKCERS-UHFFFAOYSA-N 0.000 description 1
- 125000001995 cyclobutyl group Chemical group [H]C1([H])C([H])([H])C([H])(*)C1([H])[H] 0.000 description 1
- 125000000582 cycloheptyl group Chemical group [H]C1([H])C([H])([H])C([H])([H])C([H])([H])C([H])(*)C([H])([H])C1([H])[H] 0.000 description 1
- 125000000113 cyclohexyl group Chemical group [H]C1([H])C([H])([H])C([H])([H])C([H])(*)C([H])([H])C1([H])[H] 0.000 description 1
- 125000000640 cyclooctyl group Chemical group [H]C1([H])C([H])([H])C([H])([H])C([H])([H])C([H])(*)C([H])([H])C([H])([H])C1([H])[H] 0.000 description 1
- XCIXKGXIYUWCLL-UHFFFAOYSA-N cyclopentanol Chemical compound OC1CCCC1 XCIXKGXIYUWCLL-UHFFFAOYSA-N 0.000 description 1
- 125000001511 cyclopentyl group Chemical group [H]C1([H])C([H])([H])C([H])([H])C([H])(*)C1([H])[H] 0.000 description 1
- WMSPXQIQBQAWLL-UHFFFAOYSA-N cyclopropanesulfonamide Chemical compound NS(=O)(=O)C1CC1 WMSPXQIQBQAWLL-UHFFFAOYSA-N 0.000 description 1
- APJLTUBHYCOZJI-VZCXRCSSSA-N cyenopyrafen Chemical compound CC1=NN(C)C(\C(OC(=O)C(C)(C)C)=C(/C#N)C=2C=CC(=CC=2)C(C)(C)C)=C1C APJLTUBHYCOZJI-VZCXRCSSSA-N 0.000 description 1
- NNRSYETYEADPBW-UHFFFAOYSA-N cyhalodiamide Chemical compound CC1=CC(C(F)(C(F)(F)F)C(F)(F)F)=CC=C1NC(=O)C1=CC=CC(Cl)=C1C(=O)NC(C)(C)C#N NNRSYETYEADPBW-UHFFFAOYSA-N 0.000 description 1
- WCMMILVIRZAPLE-UHFFFAOYSA-M cyhexatin Chemical compound C1CCCCC1[Sn](C1CCCCC1)(O)C1CCCCC1 WCMMILVIRZAPLE-UHFFFAOYSA-M 0.000 description 1
- YUAUPYJCVKNAEC-SEYXRHQNSA-N cymiazole Chemical compound CC1=CC(C)=CC=C1\N=C/1N(C)C=CS\1 YUAUPYJCVKNAEC-SEYXRHQNSA-N 0.000 description 1
- LVQDKIWDGQRHTE-UHFFFAOYSA-N cyromazine Chemical compound NC1=NC(N)=NC(NC2CC2)=N1 LVQDKIWDGQRHTE-UHFFFAOYSA-N 0.000 description 1
- 229950000775 cyromazine Drugs 0.000 description 1
- 230000034994 death Effects 0.000 description 1
- 230000007123 defense Effects 0.000 description 1
- 238000006731 degradation reaction Methods 0.000 description 1
- PGRHXDWITVMQBC-UHFFFAOYSA-N dehydroacetic acid Natural products CC(=O)C1C(=O)OC(C)=CC1=O PGRHXDWITVMQBC-UHFFFAOYSA-N 0.000 description 1
- 208000025729 dengue disease Diseases 0.000 description 1
- DYVLXWPZFQQUIU-WGNDVSEMSA-N derquantel Chemical compound O1C(C)(C)C=COC2=C1C=CC1=C2NC[C@]11C(C)(C)[C@@H]2C[C@]3(N(C4)CC[C@@]3(C)O)C(=O)N(C)[C@]42C1 DYVLXWPZFQQUIU-WGNDVSEMSA-N 0.000 description 1
- 229950004278 derquantel Drugs 0.000 description 1
- 230000000249 desinfective effect Effects 0.000 description 1
- WOWBFOBYOAGEEA-UHFFFAOYSA-N diafenthiuron Chemical compound CC(C)C1=C(NC(=S)NC(C)(C)C)C(C(C)C)=CC(OC=2C=CC=CC=2)=C1 WOWBFOBYOAGEEA-UHFFFAOYSA-N 0.000 description 1
- GUJOJGAPFQRJSV-UHFFFAOYSA-N dialuminum;dioxosilane;oxygen(2-);hydrate Chemical compound O.[O-2].[O-2].[O-2].[Al+3].[Al+3].O=[Si]=O.O=[Si]=O.O=[Si]=O.O=[Si]=O GUJOJGAPFQRJSV-UHFFFAOYSA-N 0.000 description 1
- 150000001470 diamides Chemical class 0.000 description 1
- MNNHAPBLZZVQHP-UHFFFAOYSA-N diammonium hydrogen phosphate Chemical compound [NH4+].[NH4+].OP([O-])([O-])=O MNNHAPBLZZVQHP-UHFFFAOYSA-N 0.000 description 1
- 235000019838 diammonium phosphate Nutrition 0.000 description 1
- 229910000388 diammonium phosphate Inorganic materials 0.000 description 1
- RCJVRSBWZCNNQT-UHFFFAOYSA-N dichloridooxygen Chemical compound ClOCl RCJVRSBWZCNNQT-UHFFFAOYSA-N 0.000 description 1
- JZUKGAJJLZRHGL-UHFFFAOYSA-N diethoxy-[2-phenyl-5-(trifluoromethyl)pyrazol-3-yl]oxy-sulfanylidene-lambda5-phosphane Chemical compound CCOP(=S)(OCC)OC1=CC(C(F)(F)F)=NN1C1=CC=CC=C1 JZUKGAJJLZRHGL-UHFFFAOYSA-N 0.000 description 1
- RCKMWOKWVGPNJF-UHFFFAOYSA-N diethylcarbamazine Chemical compound CCN(CC)C(=O)N1CCN(C)CC1 RCKMWOKWVGPNJF-UHFFFAOYSA-N 0.000 description 1
- 229960003974 diethylcarbamazine Drugs 0.000 description 1
- 229940019503 diflubenzuron Drugs 0.000 description 1
- MCWXGJITAZMZEV-UHFFFAOYSA-N dimethoate Chemical compound CNC(=O)CSP(=S)(OC)OC MCWXGJITAZMZEV-UHFFFAOYSA-N 0.000 description 1
- VAYGXNSJCAHWJZ-UHFFFAOYSA-N dimethyl sulfate Chemical compound COS(=O)(=O)OC VAYGXNSJCAHWJZ-UHFFFAOYSA-N 0.000 description 1
- RDBIYWSVMRVKSG-UHFFFAOYSA-N dimetilan Chemical compound CN(C)C(=O)OC=1C=C(C)N(C(=O)N(C)C)N=1 RDBIYWSVMRVKSG-UHFFFAOYSA-N 0.000 description 1
- WXUZAHCNPWONDH-DYTRJAOYSA-N dimoxystrobin Chemical compound CNC(=O)C(=N\OC)\C1=CC=CC=C1COC1=CC(C)=CC=C1C WXUZAHCNPWONDH-DYTRJAOYSA-N 0.000 description 1
- 235000004879 dioscorea Nutrition 0.000 description 1
- FPKXBFWMIYHCID-UHFFFAOYSA-N dipymetitrone Chemical compound S1C=2C(=O)N(C)C(=O)C=2SC2=C1C(=O)N(C)C2=O FPKXBFWMIYHCID-UHFFFAOYSA-N 0.000 description 1
- 230000006806 disease prevention Effects 0.000 description 1
- PYZSVQVRHDXQSL-UHFFFAOYSA-N dithianon Chemical compound S1C(C#N)=C(C#N)SC2=C1C(=O)C1=CC=CC=C1C2=O PYZSVQVRHDXQSL-UHFFFAOYSA-N 0.000 description 1
- 239000010459 dolomite Substances 0.000 description 1
- 229910000514 dolomite Inorganic materials 0.000 description 1
- 238000010981 drying operation Methods 0.000 description 1
- 239000000428 dust Substances 0.000 description 1
- 238000010410 dusting Methods 0.000 description 1
- 230000001984 ectoparasiticidal effect Effects 0.000 description 1
- 230000002500 effect on skin Effects 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 235000013601 eggs Nutrition 0.000 description 1
- 239000005712 elicitor Substances 0.000 description 1
- 201000008184 embryoma Diseases 0.000 description 1
- AUVVAXYIELKVAI-CKBKHPSWSA-N emetine Chemical compound N1CCC2=CC(OC)=C(OC)C=C2[C@H]1C[C@H]1C[C@H]2C3=CC(OC)=C(OC)C=C3CCN2C[C@@H]1CC AUVVAXYIELKVAI-CKBKHPSWSA-N 0.000 description 1
- 229960002694 emetine Drugs 0.000 description 1
- QLHFZUMWECUDIA-UHFFFAOYSA-N emidine Natural products CC(O)C1CCC2(O)C3CC=C4CC(CCC4(C)C3CCC12C)OC5CC(O)C(OC6CC(O)C(OC7CC(O)C(O)C(C)O7)C(C)O6)C(C)O5 QLHFZUMWECUDIA-UHFFFAOYSA-N 0.000 description 1
- ZMQMTKVVAMWKNY-YSXLEBCMSA-N emodepside Chemical compound C([C@@H]1C(=O)N(C)[C@@H](CC(C)C)C(=O)O[C@H](C)C(=O)N(C)[C@H](C(O[C@H](CC=2C=CC(=CC=2)N2CCOCC2)C(=O)N(C)[C@@H](CC(C)C)C(=O)O[C@H](C)C(=O)N(C)[C@@H](CC(C)C)C(=O)O1)=O)CC(C)C)C(C=C1)=CC=C1N1CCOCC1 ZMQMTKVVAMWKNY-YSXLEBCMSA-N 0.000 description 1
- 108010056417 emodepside Proteins 0.000 description 1
- 229960001575 emodepside Drugs 0.000 description 1
- 201000005901 endemic typhus Diseases 0.000 description 1
- 238000005516 engineering process Methods 0.000 description 1
- 230000002708 enhancing effect Effects 0.000 description 1
- 206010014881 enterobiasis Diseases 0.000 description 1
- LGUDKOQUWIHXOV-UHFFFAOYSA-N epsiprantel Chemical compound C1C(C2=CC=CC=C2CCC2)N2C(=O)CN1C(=O)C1CCCCC1 LGUDKOQUWIHXOV-UHFFFAOYSA-N 0.000 description 1
- 229960005362 epsiprantel Drugs 0.000 description 1
- 230000008029 eradication Effects 0.000 description 1
- 230000008686 ergosterol biosynthesis Effects 0.000 description 1
- 230000032050 esterification Effects 0.000 description 1
- 238000005886 esterification reaction Methods 0.000 description 1
- RIZMRRKBZQXFOY-UHFFFAOYSA-N ethion Chemical compound CCOP(=S)(OCC)SCSP(=S)(OCC)OCC RIZMRRKBZQXFOY-UHFFFAOYSA-N 0.000 description 1
- 125000000219 ethylidene group Chemical group [H]C(=[*])C([H])([H])[H] 0.000 description 1
- 125000004705 ethylthio group Chemical group C(C)S* 0.000 description 1
- 125000002534 ethynyl group Chemical group [H]C#C* 0.000 description 1
- 229950005085 etofenprox Drugs 0.000 description 1
- 230000008020 evaporation Effects 0.000 description 1
- 239000003925 fat Substances 0.000 description 1
- 150000002191 fatty alcohols Chemical class 0.000 description 1
- 230000002349 favourable effect Effects 0.000 description 1
- 210000003746 feather Anatomy 0.000 description 1
- LMVPQMGRYSRMIW-KRWDZBQOSA-N fenamidone Chemical compound O=C([C@@](C)(N=C1SC)C=2C=CC=CC=2)N1NC1=CC=CC=C1 LMVPQMGRYSRMIW-KRWDZBQOSA-N 0.000 description 1
- 229950006668 fenfluthrin Drugs 0.000 description 1
- DIRFUJHNVNOBMY-UHFFFAOYSA-N fenobucarb Chemical compound CCC(C)C1=CC=CC=C1OC(=O)NC DIRFUJHNVNOBMY-UHFFFAOYSA-N 0.000 description 1
- 229960001419 fenoprofen Drugs 0.000 description 1
- HJUFTIJOISQSKQ-UHFFFAOYSA-N fenoxycarb Chemical compound C1=CC(OCCNC(=O)OCC)=CC=C1OC1=CC=CC=C1 HJUFTIJOISQSKQ-UHFFFAOYSA-N 0.000 description 1
- UTOHZQYBSYOOGC-UHFFFAOYSA-N fenpyrazamine Chemical compound O=C1N(C(C)C)N(C(=O)SCC=C)C(N)=C1C1=CC=CC=C1C UTOHZQYBSYOOGC-UHFFFAOYSA-N 0.000 description 1
- RWTNPBWLLIMQHL-UHFFFAOYSA-N fexofenadine Chemical compound C1=CC(C(C)(C(O)=O)C)=CC=C1C(O)CCCN1CCC(C(O)(C=2C=CC=CC=2)C=2C=CC=CC=2)CC1 RWTNPBWLLIMQHL-UHFFFAOYSA-N 0.000 description 1
- 239000007888 film coating Substances 0.000 description 1
- 238000009501 film coating Methods 0.000 description 1
- RLQJEEJISHYWON-UHFFFAOYSA-N flonicamid Chemical compound FC(F)(F)C1=CC=NC=C1C(=O)NCC#N RLQJEEJISHYWON-UHFFFAOYSA-N 0.000 description 1
- MXWAGQASUDSFBG-RVDMUPIBSA-N fluacrypyrim Chemical compound CO\C=C(\C(=O)OC)C1=CC=CC=C1COC1=CC(C(F)(F)F)=NC(OC(C)C)=N1 MXWAGQASUDSFBG-RVDMUPIBSA-N 0.000 description 1
- UZCGKGPEKUCDTF-UHFFFAOYSA-N fluazinam Chemical compound [O-][N+](=O)C1=CC(C(F)(F)F)=C(Cl)C([N+]([O-])=O)=C1NC1=NC=C(C(F)(F)F)C=C1Cl UZCGKGPEKUCDTF-UHFFFAOYSA-N 0.000 description 1
- YOWNVPAUWYHLQX-UHFFFAOYSA-N fluazuron Chemical compound FC1=CC=CC(F)=C1C(=O)NC(=O)NC1=CC=C(Cl)C(OC=2C(=CC(=CN=2)C(F)(F)F)Cl)=C1 YOWNVPAUWYHLQX-UHFFFAOYSA-N 0.000 description 1
- 229950006719 fluazuron Drugs 0.000 description 1
- QOIYTRGFOFZNKF-UHFFFAOYSA-N flupyradifurone Chemical compound C=1C(=O)OCC=1N(CC(F)F)CC1=CC=C(Cl)N=C1 QOIYTRGFOFZNKF-UHFFFAOYSA-N 0.000 description 1
- IJJVMEJXYNJXOJ-UHFFFAOYSA-N fluquinconazole Chemical compound C=1C=C(Cl)C=C(Cl)C=1N1C(=O)C2=CC(F)=CC=C2N=C1N1C=NC=N1 IJJVMEJXYNJXOJ-UHFFFAOYSA-N 0.000 description 1
- MLBZKOGAMRTSKP-UHFFFAOYSA-N fluralaner Chemical compound C1=C(C(=O)NCC(=O)NCC(F)(F)F)C(C)=CC(C=2CC(ON=2)(C=2C=C(Cl)C=C(Cl)C=2)C(F)(F)F)=C1 MLBZKOGAMRTSKP-UHFFFAOYSA-N 0.000 description 1
- 229960004498 fluralaner Drugs 0.000 description 1
- SXSGXWCSHSVPGB-UHFFFAOYSA-N fluxapyroxad Chemical compound FC(F)C1=NN(C)C=C1C(=O)NC1=CC=CC=C1C1=CC(F)=C(F)C(F)=C1 SXSGXWCSHSVPGB-UHFFFAOYSA-N 0.000 description 1
- HKIOYBQGHSTUDB-UHFFFAOYSA-N folpet Chemical compound C1=CC=C2C(=O)N(SC(Cl)(Cl)Cl)C(=O)C2=C1 HKIOYBQGHSTUDB-UHFFFAOYSA-N 0.000 description 1
- KVGLBTYUCJYMND-UHFFFAOYSA-N fonofos Chemical compound CCOP(=S)(CC)SC1=CC=CC=C1 KVGLBTYUCJYMND-UHFFFAOYSA-N 0.000 description 1
- WSFSSNUMVMOOMR-UHFFFAOYSA-N formaldehyde Substances O=C WSFSSNUMVMOOMR-UHFFFAOYSA-N 0.000 description 1
- 229960005102 foscarnet Drugs 0.000 description 1
- VUERQRKTYBIULR-UHFFFAOYSA-N fosetyl Chemical compound CCOP(O)=O VUERQRKTYBIULR-UHFFFAOYSA-N 0.000 description 1
- 239000003205 fragrance Substances 0.000 description 1
- HAWJXYBZNNRMNO-UHFFFAOYSA-N furathiocarb Chemical compound CCCCOC(=O)N(C)SN(C)C(=O)OC1=CC=CC2=C1OC(C)(C)C2 HAWJXYBZNNRMNO-UHFFFAOYSA-N 0.000 description 1
- 230000004927 fusion Effects 0.000 description 1
- ZXQYGBMAQZUVMI-GCMPRSNUSA-N gamma-cyhalothrin Chemical compound CC1(C)[C@@H](\C=C(/Cl)C(F)(F)F)[C@H]1C(=O)O[C@H](C#N)C1=CC=CC(OC=2C=CC=CC=2)=C1 ZXQYGBMAQZUVMI-GCMPRSNUSA-N 0.000 description 1
- 238000010413 gardening Methods 0.000 description 1
- 238000012239 gene modification Methods 0.000 description 1
- 230000005017 genetic modification Effects 0.000 description 1
- 235000013617 genetically modified food Nutrition 0.000 description 1
- 235000003869 genetically modified organism Nutrition 0.000 description 1
- IXORZMNAPKEEDV-UHFFFAOYSA-N gibberellic acid GA3 Natural products OC(=O)C1C2(C3)CC(=C)C3(O)CCC2C2(C=CC3O)C1C3(C)C(=O)O2 IXORZMNAPKEEDV-UHFFFAOYSA-N 0.000 description 1
- 239000011521 glass Substances 0.000 description 1
- IAJOBQBIJHVGMQ-BYPYZUCNSA-N glufosinate-P Chemical compound CP(O)(=O)CC[C@H](N)C(O)=O IAJOBQBIJHVGMQ-BYPYZUCNSA-N 0.000 description 1
- 229940097068 glyphosate Drugs 0.000 description 1
- XDDAORKBJWWYJS-UHFFFAOYSA-N glyphosate Chemical compound OC(=O)CNCP(O)(O)=O XDDAORKBJWWYJS-UHFFFAOYSA-N 0.000 description 1
- 235000002532 grape seed extract Nutrition 0.000 description 1
- 150000004795 grignard reagents Chemical class 0.000 description 1
- 239000003630 growth substance Substances 0.000 description 1
- 210000004209 hair Anatomy 0.000 description 1
- WIFXJBMOTMKRMM-UHFFFAOYSA-N halfenprox Chemical compound C=1C=C(OC(F)(F)Br)C=CC=1C(C)(C)COCC(C=1)=CC=CC=1OC1=CC=CC=C1 WIFXJBMOTMKRMM-UHFFFAOYSA-N 0.000 description 1
- 125000004438 haloalkoxy group Chemical group 0.000 description 1
- 125000005843 halogen group Chemical group 0.000 description 1
- 230000002140 halogenating effect Effects 0.000 description 1
- 210000003128 head Anatomy 0.000 description 1
- 230000002363 herbicidal effect Effects 0.000 description 1
- 125000004051 hexyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 description 1
- 235000012907 honey Nutrition 0.000 description 1
- 239000005556 hormone Substances 0.000 description 1
- 229940088597 hormone Drugs 0.000 description 1
- 239000003906 humectant Substances 0.000 description 1
- 239000010903 husk Substances 0.000 description 1
- MFZWMTSUNYWVBU-UHFFFAOYSA-N hycanthone Chemical compound S1C2=CC=CC=C2C(=O)C2=C1C(CO)=CC=C2NCCN(CC)CC MFZWMTSUNYWVBU-UHFFFAOYSA-N 0.000 description 1
- 229950000216 hycanthone Drugs 0.000 description 1
- WJRBRSLFGCUECM-UHFFFAOYSA-N hydantoin Chemical compound O=C1CNC(=O)N1 WJRBRSLFGCUECM-UHFFFAOYSA-N 0.000 description 1
- 229940091173 hydantoin Drugs 0.000 description 1
- 229930195733 hydrocarbon Natural products 0.000 description 1
- 150000002430 hydrocarbons Chemical class 0.000 description 1
- USZLCYNVCCDPLQ-UHFFFAOYSA-N hydron;n-methoxymethanamine;chloride Chemical compound Cl.CNOC USZLCYNVCCDPLQ-UHFFFAOYSA-N 0.000 description 1
- FYQGBXGJFWXIPP-UHFFFAOYSA-N hydroprene Chemical compound CCOC(=O)C=C(C)C=CCC(C)CCCC(C)C FYQGBXGJFWXIPP-UHFFFAOYSA-N 0.000 description 1
- 229930000073 hydroprene Natural products 0.000 description 1
- SCEVFJUWLLRELN-UHFFFAOYSA-N imidocarb Chemical compound C=1C=CC(C=2NCCN=2)=CC=1NC(=O)NC(C=1)=CC=CC=1C1=NCCN1 SCEVFJUWLLRELN-UHFFFAOYSA-N 0.000 description 1
- 229960004683 imidocarb Drugs 0.000 description 1
- VPRAQYXPZIFIOH-UHFFFAOYSA-N imiprothrin Chemical compound CC1(C)C(C=C(C)C)C1C(=O)OCN1C(=O)N(CC#C)CC1=O VPRAQYXPZIFIOH-UHFFFAOYSA-N 0.000 description 1
- 230000006872 improvement Effects 0.000 description 1
- 238000010348 incorporation Methods 0.000 description 1
- 230000002401 inhibitory effect Effects 0.000 description 1
- 238000002347 injection Methods 0.000 description 1
- 239000007924 injection Substances 0.000 description 1
- 239000002054 inoculum Substances 0.000 description 1
- 229910052500 inorganic mineral Inorganic materials 0.000 description 1
- 239000001023 inorganic pigment Substances 0.000 description 1
- 239000012194 insect media Substances 0.000 description 1
- 230000010354 integration Effects 0.000 description 1
- 201000007647 intestinal volvulus Diseases 0.000 description 1
- 239000011630 iodine Substances 0.000 description 1
- 229910052740 iodine Inorganic materials 0.000 description 1
- 239000002555 ionophore Substances 0.000 description 1
- 230000000236 ionophoric effect Effects 0.000 description 1
- QTYCMDBMOLSEAM-UHFFFAOYSA-N ipconazole Chemical compound C1=NC=NN1CC1(O)C(C(C)C)CCC1CC1=CC=C(Cl)C=C1 QTYCMDBMOLSEAM-UHFFFAOYSA-N 0.000 description 1
- 229910052741 iridium Inorganic materials 0.000 description 1
- GKOZUEZYRPOHIO-UHFFFAOYSA-N iridium atom Chemical compound [Ir] GKOZUEZYRPOHIO-UHFFFAOYSA-N 0.000 description 1
- DCYOBGZUOMKFPA-UHFFFAOYSA-N iron(2+);iron(3+);octadecacyanide Chemical compound [Fe+2].[Fe+2].[Fe+2].[Fe+3].[Fe+3].[Fe+3].[Fe+3].N#[C-].N#[C-].N#[C-].N#[C-].N#[C-].N#[C-].N#[C-].N#[C-].N#[C-].N#[C-].N#[C-].N#[C-].N#[C-].N#[C-].N#[C-].N#[C-].N#[C-].N#[C-] DCYOBGZUOMKFPA-UHFFFAOYSA-N 0.000 description 1
- 230000002262 irrigation Effects 0.000 description 1
- 238000003973 irrigation Methods 0.000 description 1
- 125000000959 isobutyl group Chemical group [H]C([H])([H])C([H])(C([H])([H])[H])C([H])([H])* 0.000 description 1
- WFKAJVHLWXSISD-UHFFFAOYSA-N isobutyramide Chemical compound CC(C)C(N)=O WFKAJVHLWXSISD-UHFFFAOYSA-N 0.000 description 1
- VFQXVTODMYMSMJ-UHFFFAOYSA-N isonicotinamide Chemical compound NC(=O)C1=CC=NC=C1 VFQXVTODMYMSMJ-UHFFFAOYSA-N 0.000 description 1
- 125000001972 isopentyl group Chemical group [H]C([H])([H])C([H])(C([H])([H])[H])C([H])([H])C([H])([H])* 0.000 description 1
- 125000000555 isopropenyl group Chemical group [H]\C([H])=C(\*)C([H])([H])[H] 0.000 description 1
- ITGSCCPVERXFGN-UHFFFAOYSA-N isoxadifen Chemical compound C1C(C(=O)O)=NOC1(C=1C=CC=CC=1)C1=CC=CC=C1 ITGSCCPVERXFGN-UHFFFAOYSA-N 0.000 description 1
- SDMSCIWHRZJSRN-UHFFFAOYSA-N isoxathion Chemical compound O1N=C(OP(=S)(OCC)OCC)C=C1C1=CC=CC=C1 SDMSCIWHRZJSRN-UHFFFAOYSA-N 0.000 description 1
- 150000002547 isoxazolines Chemical class 0.000 description 1
- NLYAJNPCOHFWQQ-UHFFFAOYSA-N kaolin Chemical compound O.O.O=[Al]O[Si](=O)O[Si](=O)O[Al]=O NLYAJNPCOHFWQQ-UHFFFAOYSA-N 0.000 description 1
- 229930001540 kinoprene Natural products 0.000 description 1
- 150000003951 lactams Chemical class 0.000 description 1
- 150000002596 lactones Chemical class 0.000 description 1
- 239000010985 leather Substances 0.000 description 1
- 239000000787 lecithin Substances 0.000 description 1
- 235000010445 lecithin Nutrition 0.000 description 1
- 239000004611 light stabiliser Substances 0.000 description 1
- 150000002632 lipids Chemical class 0.000 description 1
- YNESATAKKCNGOF-UHFFFAOYSA-N lithium bis(trimethylsilyl)amide Chemical compound [Li+].C[Si](C)(C)[N-][Si](C)(C)C YNESATAKKCNGOF-UHFFFAOYSA-N 0.000 description 1
- 244000144972 livestock Species 0.000 description 1
- 229950002303 lotilaner Drugs 0.000 description 1
- FBQPGGIHOFZRGH-UHFFFAOYSA-N lucanthone Chemical compound S1C2=CC=CC=C2C(=O)C2=C1C(C)=CC=C2NCCN(CC)CC FBQPGGIHOFZRGH-UHFFFAOYSA-N 0.000 description 1
- 235000019359 magnesium stearate Nutrition 0.000 description 1
- NXPHGHWWQRMDIA-UHFFFAOYSA-M magnesium;carbanide;bromide Chemical compound [CH3-].[Mg+2].[Br-] NXPHGHWWQRMDIA-UHFFFAOYSA-M 0.000 description 1
- 201000004792 malaria Diseases 0.000 description 1
- 230000036244 malformation Effects 0.000 description 1
- YKSNLCVSTHTHJA-UHFFFAOYSA-L maneb Chemical compound [Mn+2].[S-]C(=S)NCCNC([S-])=S YKSNLCVSTHTHJA-UHFFFAOYSA-L 0.000 description 1
- 229920000940 maneb Polymers 0.000 description 1
- WPBNNNQJVZRUHP-UHFFFAOYSA-L manganese(2+);methyl n-[[2-(methoxycarbonylcarbamothioylamino)phenyl]carbamothioyl]carbamate;n-[2-(sulfidocarbothioylamino)ethyl]carbamodithioate Chemical class [Mn+2].[S-]C(=S)NCCNC([S-])=S.COC(=O)NC(=S)NC1=CC=CC=C1NC(=S)NC(=O)OC WPBNNNQJVZRUHP-UHFFFAOYSA-L 0.000 description 1
- 239000004579 marble Substances 0.000 description 1
- 230000035800 maturation Effects 0.000 description 1
- 238000005259 measurement Methods 0.000 description 1
- 235000013372 meat Nutrition 0.000 description 1
- KLGMSAOQDHLCOS-UHFFFAOYSA-N mecarbam Chemical compound CCOC(=O)N(C)C(=O)CSP(=S)(OCC)OCC KLGMSAOQDHLCOS-UHFFFAOYSA-N 0.000 description 1
- 230000010534 mechanism of action Effects 0.000 description 1
- 239000002609 medium Substances 0.000 description 1
- 230000008099 melanin synthesis Effects 0.000 description 1
- 239000012528 membrane Substances 0.000 description 1
- XWPZUHJBOLQNMN-UHFFFAOYSA-N metconazole Chemical compound C1=NC=NN1CC1(O)C(C)(C)CCC1CC1=CC=C(Cl)C=C1 XWPZUHJBOLQNMN-UHFFFAOYSA-N 0.000 description 1
- 125000000956 methoxy group Chemical group [H]C([H])([H])O* 0.000 description 1
- 125000001160 methoxycarbonyl group Chemical group [H]C([H])([H])OC(*)=O 0.000 description 1
- 125000004184 methoxymethyl group Chemical group [H]C([H])([H])OC([H])([H])* 0.000 description 1
- GEPDYQSQVLXLEU-AATRIKPKSA-N methyl (e)-3-dimethoxyphosphoryloxybut-2-enoate Chemical compound COC(=O)\C=C(/C)OP(=O)(OC)OC GEPDYQSQVLXLEU-AATRIKPKSA-N 0.000 description 1
- 229940102396 methyl bromide Drugs 0.000 description 1
- HAMGRBXTJNITHG-UHFFFAOYSA-N methyl isocyanate Chemical compound CN=C=O HAMGRBXTJNITHG-UHFFFAOYSA-N 0.000 description 1
- 125000000250 methylamino group Chemical group [H]N(*)C([H])([H])[H] 0.000 description 1
- 229920000257 metiram Polymers 0.000 description 1
- 230000003641 microbiacidal effect Effects 0.000 description 1
- 229940124561 microbicide Drugs 0.000 description 1
- 239000011785 micronutrient Substances 0.000 description 1
- 235000013369 micronutrients Nutrition 0.000 description 1
- 230000001617 migratory effect Effects 0.000 description 1
- 235000013336 milk Nutrition 0.000 description 1
- 239000008267 milk Substances 0.000 description 1
- 210000004080 milk Anatomy 0.000 description 1
- 235000019713 millet Nutrition 0.000 description 1
- 230000003278 mimic effect Effects 0.000 description 1
- 235000010755 mineral Nutrition 0.000 description 1
- 201000002266 mite infestation Diseases 0.000 description 1
- 230000000394 mitotic effect Effects 0.000 description 1
- 230000004048 modification Effects 0.000 description 1
- 238000012986 modification Methods 0.000 description 1
- 239000003750 molluscacide Substances 0.000 description 1
- 230000002013 molluscicidal effect Effects 0.000 description 1
- 229910052750 molybdenum Inorganic materials 0.000 description 1
- 239000011733 molybdenum Substances 0.000 description 1
- WTERNLDOAPYGJD-SFHVURJKSA-N monepantel Chemical compound C([C@@](C)(NC(=O)C=1C=CC(SC(F)(F)F)=CC=1)C#N)OC1=CC(C#N)=CC=C1C(F)(F)F WTERNLDOAPYGJD-SFHVURJKSA-N 0.000 description 1
- 229950003439 monepantel Drugs 0.000 description 1
- 229910052901 montmorillonite Inorganic materials 0.000 description 1
- 235000010460 mustard Nutrition 0.000 description 1
- 238000002703 mutagenesis Methods 0.000 description 1
- 231100000350 mutagenesis Toxicity 0.000 description 1
- FTWUXYZHDFCGSV-UHFFFAOYSA-N n,n'-diphenyloxamide Chemical compound C=1C=CC=CC=1NC(=O)C(=O)NC1=CC=CC=C1 FTWUXYZHDFCGSV-UHFFFAOYSA-N 0.000 description 1
- BLCHMFQMHCCQCK-UHFFFAOYSA-N n-(2-bromo-6-fluorophenyl)-4-(2-chloro-4-fluorophenyl)-2,5-dimethylpyrazol-3-amine Chemical compound C=1C=C(F)C=C(Cl)C=1C=1C(C)=NN(C)C=1NC1=C(F)C=CC=C1Br BLCHMFQMHCCQCK-UHFFFAOYSA-N 0.000 description 1
- FXZGOEUQWCBASE-UHFFFAOYSA-N n-(2-bromophenyl)-4-(2-chloro-4-fluorophenyl)-2,5-dimethylpyrazol-3-amine Chemical compound C=1C=C(F)C=C(Cl)C=1C=1C(C)=NN(C)C=1NC1=CC=CC=C1Br FXZGOEUQWCBASE-UHFFFAOYSA-N 0.000 description 1
- IHYNKGRWCDKNEG-UHFFFAOYSA-N n-(4-bromophenyl)-2,6-dihydroxybenzamide Chemical compound OC1=CC=CC(O)=C1C(=O)NC1=CC=C(Br)C=C1 IHYNKGRWCDKNEG-UHFFFAOYSA-N 0.000 description 1
- QKEKUMRXLOHZQJ-UHFFFAOYSA-N n-(4-chloro-2,6-difluorophenyl)-4-(2-chloro-4-fluorophenyl)-2,5-dimethylpyrazol-3-amine Chemical compound C=1C=C(F)C=C(Cl)C=1C=1C(C)=NN(C)C=1NC1=C(F)C=C(Cl)C=C1F QKEKUMRXLOHZQJ-UHFFFAOYSA-N 0.000 description 1
- JEFUQUGZXLEHLD-UHFFFAOYSA-N n-[(5-chloro-2-propan-2-ylphenyl)methyl]-n-cyclopropyl-3-(difluoromethyl)-5-fluoro-1-methylpyrazole-4-carboxamide Chemical compound CC(C)C1=CC=C(Cl)C=C1CN(C(=O)C=1C(=NN(C)C=1F)C(F)F)C1CC1 JEFUQUGZXLEHLD-UHFFFAOYSA-N 0.000 description 1
- FMDLTPBLTVHTIM-UHFFFAOYSA-N n-[2-(5-amino-1,3,4-thiadiazol-2-yl)-4-chloro-6-methylphenyl]-5-bromo-2-(3-chloropyridin-2-yl)pyrazole-3-carboxamide Chemical compound C=1C(Br)=NN(C=2C(=CC=CN=2)Cl)C=1C(=O)NC=1C(C)=CC(Cl)=CC=1C1=NN=C(N)S1 FMDLTPBLTVHTIM-UHFFFAOYSA-N 0.000 description 1
- UWKQSUQMFIRFMM-UHFFFAOYSA-N n-[2-(tert-butylcarbamoyl)-4-chloro-6-methylphenyl]-2-(3-chloropyridin-2-yl)-5-(fluoromethoxy)pyrazole-3-carboxamide Chemical compound CC1=CC(Cl)=CC(C(=O)NC(C)(C)C)=C1NC(=O)C1=CC(OCF)=NN1C1=NC=CC=C1Cl UWKQSUQMFIRFMM-UHFFFAOYSA-N 0.000 description 1
- FVJQBZVCJVMBIP-UHFFFAOYSA-N n-[2-chloro-5-(trifluoromethyl)phenyl]-2,4-dinitro-6-(trifluoromethyl)aniline Chemical compound FC(F)(F)C1=CC([N+](=O)[O-])=CC([N+]([O-])=O)=C1NC1=CC(C(F)(F)F)=CC=C1Cl FVJQBZVCJVMBIP-UHFFFAOYSA-N 0.000 description 1
- HYMAFHMYSJZJIR-UHFFFAOYSA-L n-aminocarbamodithioate;nickel(2+) Chemical compound [Ni+2].NNC([S-])=S.NNC([S-])=S HYMAFHMYSJZJIR-UHFFFAOYSA-L 0.000 description 1
- IJDNQMDRQITEOD-UHFFFAOYSA-N n-butane Chemical compound CCCC IJDNQMDRQITEOD-UHFFFAOYSA-N 0.000 description 1
- 125000004108 n-butyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 description 1
- PEQJBOMPGWYIRO-UHFFFAOYSA-N n-ethyl-3,4-dimethoxyaniline Chemical compound CCNC1=CC=C(OC)C(OC)=C1 PEQJBOMPGWYIRO-UHFFFAOYSA-N 0.000 description 1
- CJYQZTZSYREQBD-UHFFFAOYSA-N n-fluorobenzenesulfonamide Chemical compound FNS(=O)(=O)C1=CC=CC=C1 CJYQZTZSYREQBD-UHFFFAOYSA-N 0.000 description 1
- 125000003136 n-heptyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 description 1
- OFBQJSOFQDEBGM-UHFFFAOYSA-N n-pentane Natural products CCCCC OFBQJSOFQDEBGM-UHFFFAOYSA-N 0.000 description 1
- 125000000740 n-pentyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 description 1
- LOWVXZYADKTOKN-QFWIXSRNSA-N n1c(OC\C=C(\C)/C(=N\OC)/C(=O)NC)ccn1-c1ccc(Cl)cc1F Chemical compound n1c(OC\C=C(\C)/C(=N\OC)/C(=O)NC)ccn1-c1ccc(Cl)cc1F LOWVXZYADKTOKN-QFWIXSRNSA-N 0.000 description 1
- PSZYNBSKGUBXEH-UHFFFAOYSA-N naphthalene-1-sulfonic acid Chemical class C1=CC=C2C(S(=O)(=O)O)=CC=CC2=C1 PSZYNBSKGUBXEH-UHFFFAOYSA-N 0.000 description 1
- 125000005609 naphthenate group Chemical group 0.000 description 1
- 201000003631 narcolepsy Diseases 0.000 description 1
- 229940042880 natural phospholipid Drugs 0.000 description 1
- 229920005615 natural polymer Polymers 0.000 description 1
- 229930014626 natural product Natural products 0.000 description 1
- 239000006199 nebulizer Substances 0.000 description 1
- 125000001971 neopentyl group Chemical group [H]C([*])([H])C(C([H])([H])[H])(C([H])([H])[H])C([H])([H])[H] 0.000 description 1
- XULACPAEUUWKFX-UHFFFAOYSA-N niclofolan Chemical compound C1=C(Cl)C=C([N+]([O-])=O)C(O)=C1C1=CC(Cl)=CC([N+]([O-])=O)=C1O XULACPAEUUWKFX-UHFFFAOYSA-N 0.000 description 1
- 229950006977 niclofolan Drugs 0.000 description 1
- 229960001920 niclosamide Drugs 0.000 description 1
- RJMUSRYZPJIFPJ-UHFFFAOYSA-N niclosamide Chemical compound OC1=CC=C(Cl)C=C1C(=O)NC1=CC=C([N+]([O-])=O)C=C1Cl RJMUSRYZPJIFPJ-UHFFFAOYSA-N 0.000 description 1
- 229960005130 niridazole Drugs 0.000 description 1
- NWBNORAVIXIZTL-UHFFFAOYSA-N nitro thiocyanate Chemical compound [O-][N+](=O)SC#N NWBNORAVIXIZTL-UHFFFAOYSA-N 0.000 description 1
- SVMGVZLUIWGYPH-UHFFFAOYSA-N nitroscanate Chemical compound C1=CC([N+](=O)[O-])=CC=C1OC1=CC=C(N=C=S)C=C1 SVMGVZLUIWGYPH-UHFFFAOYSA-N 0.000 description 1
- 229950009909 nitroscanate Drugs 0.000 description 1
- 239000003865 nucleic acid synthesis inhibitor Substances 0.000 description 1
- 238000010534 nucleophilic substitution reaction Methods 0.000 description 1
- 239000003921 oil Substances 0.000 description 1
- 235000019198 oils Nutrition 0.000 description 1
- 238000005457 optimization Methods 0.000 description 1
- 150000007524 organic acids Chemical class 0.000 description 1
- 235000005985 organic acids Nutrition 0.000 description 1
- 239000011368 organic material Substances 0.000 description 1
- 239000012074 organic phase Substances 0.000 description 1
- 239000003960 organic solvent Substances 0.000 description 1
- 150000002905 orthoesters Chemical class 0.000 description 1
- 235000010292 orthophenyl phenol Nutrition 0.000 description 1
- 239000002357 osmotic agent Substances 0.000 description 1
- 235000006408 oxalic acid Nutrition 0.000 description 1
- VRYKTHBAWRESFI-VOTSOKGWSA-N oxantel Chemical compound CN1CCCN=C1\C=C\C1=CC=CC(O)=C1 VRYKTHBAWRESFI-VOTSOKGWSA-N 0.000 description 1
- 229960000535 oxantel Drugs 0.000 description 1
- BEZZFPOZAYTVHN-UHFFFAOYSA-N oxfendazole Chemical compound C=1C=C2NC(NC(=O)OC)=NC2=CC=1S(=O)C1=CC=CC=C1 BEZZFPOZAYTVHN-UHFFFAOYSA-N 0.000 description 1
- 229960004454 oxfendazole Drugs 0.000 description 1
- 230000001590 oxidative effect Effects 0.000 description 1
- FMSOWMGJJIHFTQ-UHFFFAOYSA-N oxidobromine(.) Chemical compound Br[O] FMSOWMGJJIHFTQ-UHFFFAOYSA-N 0.000 description 1
- 125000003854 p-chlorophenyl group Chemical group [H]C1=C([H])C(*)=C([H])C([H])=C1Cl 0.000 description 1
- LXNAVEXFUKBNMK-UHFFFAOYSA-N palladium(II) acetate Substances [Pd].CC(O)=O.CC(O)=O LXNAVEXFUKBNMK-UHFFFAOYSA-N 0.000 description 1
- YJVFFLUZDVXJQI-UHFFFAOYSA-L palladium(ii) acetate Chemical compound [Pd+2].CC([O-])=O.CC([O-])=O YJVFFLUZDVXJQI-UHFFFAOYSA-L 0.000 description 1
- 229910052625 palygorskite Inorganic materials 0.000 description 1
- 239000012188 paraffin wax Substances 0.000 description 1
- UVZZDDLIOJPDKX-ITKQZBBDSA-N paraherquamide Chemical compound O1C(C)(C)C=COC2=C1C=CC1=C2NC(=O)[C@]11C(C)(C)[C@@H]2C[C@]3(N(C4)CC[C@@]3(C)O)C(=O)N(C)[C@]42C1 UVZZDDLIOJPDKX-ITKQZBBDSA-N 0.000 description 1
- UVZZDDLIOJPDKX-UHFFFAOYSA-N paraherquamide A Natural products O1C(C)(C)C=COC2=C1C=CC1=C2NC(=O)C11C(C)(C)C2CC3(N(C4)CCC3(C)O)C(=O)N(C)C42C1 UVZZDDLIOJPDKX-UHFFFAOYSA-N 0.000 description 1
- 229950007337 parbendazole Drugs 0.000 description 1
- UOZODPSAJZTQNH-LSWIJEOBSA-N paromomycin Chemical compound N[C@@H]1[C@@H](O)[C@H](O)[C@H](CN)O[C@@H]1O[C@H]1[C@@H](O)[C@H](O[C@H]2[C@@H]([C@@H](N)C[C@@H](N)[C@@H]2O)O[C@@H]2[C@@H]([C@@H](O)[C@H](O)[C@@H](CO)O2)N)O[C@@H]1CO UOZODPSAJZTQNH-LSWIJEOBSA-N 0.000 description 1
- 229960001914 paromomycin Drugs 0.000 description 1
- 235000020232 peanut Nutrition 0.000 description 1
- RGSFGYAAUTVSQA-UHFFFAOYSA-N pentamethylene Natural products C1CCCC1 RGSFGYAAUTVSQA-UHFFFAOYSA-N 0.000 description 1
- 229960000482 pethidine Drugs 0.000 description 1
- 239000003016 pheromone Substances 0.000 description 1
- BULVZWIRKLYCBC-UHFFFAOYSA-N phorate Chemical compound CCOP(=S)(OCC)SCSCC BULVZWIRKLYCBC-UHFFFAOYSA-N 0.000 description 1
- HOKBIQDJCNTWST-UHFFFAOYSA-N phosphanylidenezinc;zinc Chemical compound [Zn].[Zn]=P.[Zn]=P HOKBIQDJCNTWST-UHFFFAOYSA-N 0.000 description 1
- 150000003003 phosphines Chemical class 0.000 description 1
- 150000003904 phospholipids Chemical class 0.000 description 1
- 150000003014 phosphoric acid esters Chemical class 0.000 description 1
- UXCDUFKZSUBXGM-UHFFFAOYSA-N phosphoric tribromide Chemical compound BrP(Br)(Br)=O UXCDUFKZSUBXGM-UHFFFAOYSA-N 0.000 description 1
- 229910000073 phosphorus hydride Inorganic materials 0.000 description 1
- 239000001007 phthalocyanine dye Substances 0.000 description 1
- 239000000280 phytoalexin Substances 0.000 description 1
- 150000001857 phytoalexin derivatives Chemical class 0.000 description 1
- 230000003032 phytopathogenic effect Effects 0.000 description 1
- 230000000885 phytotoxic effect Effects 0.000 description 1
- 239000001839 pinus sylvestris Substances 0.000 description 1
- IWELDVXSEVIIGI-UHFFFAOYSA-N piperazin-2-one Chemical compound O=C1CNCCN1 IWELDVXSEVIIGI-UHFFFAOYSA-N 0.000 description 1
- 150000004885 piperazines Chemical class 0.000 description 1
- 125000004482 piperidin-4-yl group Chemical group N1CCC(CC1)* 0.000 description 1
- 239000005962 plant activator Substances 0.000 description 1
- 235000021118 plant-derived protein Nutrition 0.000 description 1
- 229920000058 polyacrylate Polymers 0.000 description 1
- 229920000570 polyether Polymers 0.000 description 1
- 229920005862 polyol Polymers 0.000 description 1
- 150000003077 polyols Chemical class 0.000 description 1
- 229920006324 polyoxymethylene Polymers 0.000 description 1
- 229920001184 polypeptide Polymers 0.000 description 1
- 229920001296 polysiloxane Polymers 0.000 description 1
- 229920001021 polysulfide Polymers 0.000 description 1
- 239000005077 polysulfide Substances 0.000 description 1
- 150000008117 polysulfides Polymers 0.000 description 1
- 239000001267 polyvinylpyrrolidone Substances 0.000 description 1
- 229920000036 polyvinylpyrrolidone Polymers 0.000 description 1
- 235000013855 polyvinylpyrrolidone Nutrition 0.000 description 1
- 229910052573 porcelain Inorganic materials 0.000 description 1
- NNFCIKHAZHQZJG-UHFFFAOYSA-N potassium cyanide Chemical compound [K+].N#[C-] NNFCIKHAZHQZJG-UHFFFAOYSA-N 0.000 description 1
- 239000004323 potassium nitrate Substances 0.000 description 1
- 235000010333 potassium nitrate Nutrition 0.000 description 1
- 235000012015 potatoes Nutrition 0.000 description 1
- LZLXHGFNOWILIY-APPDUMDISA-N pradofloxacin Chemical compound C12=C(C#N)C(N3C[C@H]4NCCC[C@H]4C3)=C(F)C=C2C(=O)C(C(=O)O)=CN1C1CC1 LZLXHGFNOWILIY-APPDUMDISA-N 0.000 description 1
- 229960001248 pradofloxacin Drugs 0.000 description 1
- 239000002243 precursor Substances 0.000 description 1
- 230000002265 prevention Effects 0.000 description 1
- 230000003449 preventive effect Effects 0.000 description 1
- 230000037452 priming Effects 0.000 description 1
- 108090000765 processed proteins & peptides Proteins 0.000 description 1
- 102000004196 processed proteins & peptides Human genes 0.000 description 1
- 230000035755 proliferation Effects 0.000 description 1
- 239000001294 propane Substances 0.000 description 1
- 235000010388 propyl gallate Nutrition 0.000 description 1
- 230000001681 protective effect Effects 0.000 description 1
- 239000003531 protein hydrolysate Substances 0.000 description 1
- 210000001938 protoplast Anatomy 0.000 description 1
- 229960003351 prussian blue Drugs 0.000 description 1
- 239000013225 prussian blue Substances 0.000 description 1
- 239000008262 pumice Substances 0.000 description 1
- QHMTXANCGGJZRX-WUXMJOGZSA-N pymetrozine Chemical compound C1C(C)=NNC(=O)N1\N=C\C1=CC=CN=C1 QHMTXANCGGJZRX-WUXMJOGZSA-N 0.000 description 1
- DDIQWGKUSJOETH-UHFFFAOYSA-N pyrafluprole Chemical compound ClC=1C=C(C(F)(F)F)C=C(Cl)C=1N1N=C(C#N)C(SCF)=C1NCC1=CN=CC=N1 DDIQWGKUSJOETH-UHFFFAOYSA-N 0.000 description 1
- VJFUPGQZSXIULQ-XIGJTORUSA-N pyrethrin II Chemical compound CC1(C)[C@H](/C=C(\C)C(=O)OC)[C@H]1C(=O)O[C@@H]1C(C)=C(C\C=C/C=C)C(=O)C1 VJFUPGQZSXIULQ-XIGJTORUSA-N 0.000 description 1
- 229940070846 pyrethrins Drugs 0.000 description 1
- 239000002728 pyrethroid Substances 0.000 description 1
- 229940015367 pyrethrum Drugs 0.000 description 1
- MIOBBYRMXGNORL-UHFFFAOYSA-N pyrifluquinazon Chemical compound C1C2=CC(C(F)(C(F)(F)F)C(F)(F)F)=CC=C2N(C(=O)C)C(=O)N1NCC1=CC=CN=C1 MIOBBYRMXGNORL-UHFFFAOYSA-N 0.000 description 1
- ZLIBICFPKPWGIZ-UHFFFAOYSA-N pyrimethanil Chemical compound CC1=CC(C)=NC(NC=2C=CC=CC=2)=N1 ZLIBICFPKPWGIZ-UHFFFAOYSA-N 0.000 description 1
- ITKAIUGKVKDENI-UHFFFAOYSA-N pyrimidifen Chemical compound CC1=C(C)C(CCOCC)=CC=C1OCCNC1=NC=NC(CC)=C1Cl ITKAIUGKVKDENI-UHFFFAOYSA-N 0.000 description 1
- 150000003230 pyrimidines Chemical class 0.000 description 1
- NMVCBWZLCXANER-UHFFFAOYSA-N pyriofenone Chemical compound COC1=C(OC)C(OC)=CC(C)=C1C(=O)C1=C(C)C(Cl)=CN=C1OC NMVCBWZLCXANER-UHFFFAOYSA-N 0.000 description 1
- DHTJFQWHCVTNRY-OEMAIJDKSA-N pyrisoxazole Chemical compound C1([C@@]2(C)CC(ON2C)C=2C=CC(Cl)=CC=2)=CC=CN=C1 DHTJFQWHCVTNRY-OEMAIJDKSA-N 0.000 description 1
- 239000010453 quartz Substances 0.000 description 1
- 239000001397 quillaja saponaria molina bark Substances 0.000 description 1
- 125000003410 quininyl group Chemical group 0.000 description 1
- 125000004548 quinolin-3-yl group Chemical group N1=CC(=CC2=CC=CC=C12)* 0.000 description 1
- MCJGNVYPOGVAJF-UHFFFAOYSA-N quinolin-8-ol Chemical compound C1=CN=C2C(O)=CC=CC2=C1 MCJGNVYPOGVAJF-UHFFFAOYSA-N 0.000 description 1
- MRUMAIRJPMUAPZ-UHFFFAOYSA-N quinolin-8-ol;sulfuric acid Chemical compound OS(O)(=O)=O.C1=CN=C2C(O)=CC=CC2=C1 MRUMAIRJPMUAPZ-UHFFFAOYSA-N 0.000 description 1
- 150000003248 quinolines Chemical class 0.000 description 1
- 150000007660 quinolones Chemical class 0.000 description 1
- VMXUWOKSQNHOCA-LCYFTJDESA-N ranitidine Chemical compound [O-][N+](=O)/C=C(/NC)NCCSCC1=CC=C(CN(C)C)O1 VMXUWOKSQNHOCA-LCYFTJDESA-N 0.000 description 1
- 229960000620 ranitidine Drugs 0.000 description 1
- 229940075993 receptor modulator Drugs 0.000 description 1
- 230000033458 reproduction Effects 0.000 description 1
- 238000011160 research Methods 0.000 description 1
- 239000011347 resin Substances 0.000 description 1
- 229920005989 resin Polymers 0.000 description 1
- 229950010867 resorantel Drugs 0.000 description 1
- 230000002441 reversible effect Effects 0.000 description 1
- 230000005070 ripening Effects 0.000 description 1
- 230000021749 root development Effects 0.000 description 1
- JUVIOZPCNVVQFO-HBGVWJBISA-N rotenone Chemical compound O([C@H](CC1=C2O3)C(C)=C)C1=CC=C2C(=O)[C@@H]1[C@H]3COC2=C1C=C(OC)C(OC)=C2 JUVIOZPCNVVQFO-HBGVWJBISA-N 0.000 description 1
- JJSYXNQGLHBRRK-SFEDZAPPSA-N ryanodine Chemical compound O([C@@H]1[C@]([C@@]2([C@]3(O)[C@]45O[C@@]2(O)C[C@]([C@]4(CC[C@H](C)[C@H]5O)O)(C)[C@@]31O)C)(O)C(C)C)C(=O)C1=CC=CN1 JJSYXNQGLHBRRK-SFEDZAPPSA-N 0.000 description 1
- MSHXTAQSSIEBQS-UHFFFAOYSA-N s-[3-carbamoylsulfanyl-2-(dimethylamino)propyl] carbamothioate;hydron;chloride Chemical compound [Cl-].NC(=O)SCC([NH+](C)C)CSC(N)=O MSHXTAQSSIEBQS-UHFFFAOYSA-N 0.000 description 1
- YGBMMMOLNODPBP-GWGZPXPZSA-N s-ethyl (2e,4e)-11-methoxy-3,7,11-trimethyldodeca-2,4-dienethioate Chemical compound CCSC(=O)\C=C(/C)\C=C\CC(C)CCCC(C)(C)OC YGBMMMOLNODPBP-GWGZPXPZSA-N 0.000 description 1
- 229960000581 salicylamide Drugs 0.000 description 1
- 229960001860 salicylate Drugs 0.000 description 1
- 229930182490 saponin Natural products 0.000 description 1
- 150000007949 saponins Chemical class 0.000 description 1
- 229960005393 sarolaner Drugs 0.000 description 1
- 125000002914 sec-butyl group Chemical group [H]C([H])([H])C([H])([H])C([H])(*)C([H])([H])[H] 0.000 description 1
- 125000003548 sec-pentyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])(*)C([H])([H])[H] 0.000 description 1
- 230000028327 secretion Effects 0.000 description 1
- 238000000926 separation method Methods 0.000 description 1
- 229910052624 sepiolite Inorganic materials 0.000 description 1
- 235000019355 sepiolite Nutrition 0.000 description 1
- 230000019491 signal transduction Effects 0.000 description 1
- 150000004760 silicates Chemical class 0.000 description 1
- 238000004088 simulation Methods 0.000 description 1
- 229950005194 sisapronil Drugs 0.000 description 1
- 210000003491 skin Anatomy 0.000 description 1
- 206010040872 skin infection Diseases 0.000 description 1
- 229940125794 sodium channel blocker Drugs 0.000 description 1
- QDRKDTQENPPHOJ-UHFFFAOYSA-N sodium ethoxide Chemical compound [Na+].CC[O-] QDRKDTQENPPHOJ-UHFFFAOYSA-N 0.000 description 1
- 229910052938 sodium sulfate Inorganic materials 0.000 description 1
- 235000011152 sodium sulphate Nutrition 0.000 description 1
- PYODKQIVQIVELM-UHFFFAOYSA-M sodium;2,3-bis(2-methylpropyl)naphthalene-1-sulfonate Chemical compound [Na+].C1=CC=C2C(S([O-])(=O)=O)=C(CC(C)C)C(CC(C)C)=CC2=C1 PYODKQIVQIVELM-UHFFFAOYSA-M 0.000 description 1
- 229930185156 spinosyn Natural products 0.000 description 1
- 230000002269 spontaneous effect Effects 0.000 description 1
- 239000007858 starting material Substances 0.000 description 1
- 229940059107 sterculia Drugs 0.000 description 1
- 230000001954 sterilising effect Effects 0.000 description 1
- 230000000638 stimulation Effects 0.000 description 1
- 150000005846 sugar alcohols Polymers 0.000 description 1
- 229950008545 sulfaclozine Drugs 0.000 description 1
- 125000000446 sulfanediyl group Chemical group *S* 0.000 description 1
- XZTNTFPEHWOKNK-UHFFFAOYSA-N sulfanylidenecyanamide Chemical compound S=NC#N XZTNTFPEHWOKNK-UHFFFAOYSA-N 0.000 description 1
- 229960003097 sulfaquinoxaline Drugs 0.000 description 1
- 229940124530 sulfonamide Drugs 0.000 description 1
- 150000003456 sulfonamides Chemical class 0.000 description 1
- BDHFUVZGWQCTTF-UHFFFAOYSA-M sulfonate Chemical compound [O-]S(=O)=O BDHFUVZGWQCTTF-UHFFFAOYSA-M 0.000 description 1
- 150000003457 sulfones Chemical class 0.000 description 1
- 150000003462 sulfoxides Chemical class 0.000 description 1
- 150000003467 sulfuric acid derivatives Chemical class 0.000 description 1
- OBTWBSRJZRCYQV-UHFFFAOYSA-N sulfuryl difluoride Chemical compound FS(F)(=O)=O OBTWBSRJZRCYQV-UHFFFAOYSA-N 0.000 description 1
- 239000002600 sunflower oil Substances 0.000 description 1
- 239000000725 suspension Substances 0.000 description 1
- 239000004546 suspension concentrate Substances 0.000 description 1
- 230000009182 swimming Effects 0.000 description 1
- 229920001059 synthetic polymer Polymers 0.000 description 1
- HOWHQWFXSLOJEF-MGZLOUMQSA-N systemin Chemical compound NCCCC[C@H](N)C(=O)N[C@@H](CCSC)C(=O)N[C@@H](CCC(N)=O)C(=O)N[C@@H]([C@@H](C)O)C(=O)N[C@@H](CC(O)=O)C(=O)OC(=O)[C@@H]1CCCN1C(=O)[C@H]1N(C(=O)[C@H](CC(O)=O)NC(=O)[C@H](CCCN=C(N)N)NC(=O)[C@H](CCCCN)NC(=O)[C@H](CO)NC(=O)[C@H]2N(CCC2)C(=O)[C@H]2N(CCC2)C(=O)[C@H](CCCCN)NC(=O)[C@H](CO)NC(=O)[C@H](CCC(N)=O)NC(=O)[C@@H](NC(=O)[C@H](C)N)C(C)C)CCC1 HOWHQWFXSLOJEF-MGZLOUMQSA-N 0.000 description 1
- 108010050014 systemin Proteins 0.000 description 1
- 239000000454 talc Substances 0.000 description 1
- 229910052623 talc Inorganic materials 0.000 description 1
- 239000003760 tallow Substances 0.000 description 1
- 235000002906 tartaric acid Nutrition 0.000 description 1
- 239000011975 tartaric acid Substances 0.000 description 1
- XOAAWQZATWQOTB-UHFFFAOYSA-N taurine Chemical class NCCS(O)(=O)=O XOAAWQZATWQOTB-UHFFFAOYSA-N 0.000 description 1
- LWLJEQHTPVPKSJ-UHFFFAOYSA-N tebufloquin Chemical compound C1=C(C(C)(C)C)C=C2C(OC(=O)C)=C(C)C(C)=NC2=C1F LWLJEQHTPVPKSJ-UHFFFAOYSA-N 0.000 description 1
- ROZUQUDEWZIBHV-UHFFFAOYSA-N tecloftalam Chemical compound OC(=O)C1=C(Cl)C(Cl)=C(Cl)C(Cl)=C1C(=O)NC1=CC=CC(Cl)=C1Cl ROZUQUDEWZIBHV-UHFFFAOYSA-N 0.000 description 1
- URHWNXDZOULUHC-UHFFFAOYSA-N tert-butyl n-[6-[[[(1-methyltetrazol-5-yl)-phenylmethylidene]amino]oxymethyl]pyridin-2-yl]carbamate Chemical compound CN1N=NN=C1C(C=1C=CC=CC=1)=NOCC1=CC=CC(NC(=O)OC(C)(C)C)=N1 URHWNXDZOULUHC-UHFFFAOYSA-N 0.000 description 1
- 125000001973 tert-pentyl group Chemical group [H]C([H])([H])C([H])([H])C(*)(C([H])([H])[H])C([H])([H])[H] 0.000 description 1
- JRMUNVKIHCOMHV-UHFFFAOYSA-M tetrabutylammonium bromide Chemical compound [Br-].CCCC[N+](CCCC)(CCCC)CCCC JRMUNVKIHCOMHV-UHFFFAOYSA-M 0.000 description 1
- 229940040944 tetracyclines Drugs 0.000 description 1
- MLGCXEBRWGEOQX-UHFFFAOYSA-N tetradifon Chemical compound C1=CC(Cl)=CC=C1S(=O)(=O)C1=CC(Cl)=C(Cl)C=C1Cl MLGCXEBRWGEOQX-UHFFFAOYSA-N 0.000 description 1
- 150000005326 tetrahydropyrimidines Chemical class 0.000 description 1
- 239000004753 textile Substances 0.000 description 1
- 235000019157 thiamine Nutrition 0.000 description 1
- 150000003544 thiamines Chemical class 0.000 description 1
- DNVLJEWNNDHELH-UHFFFAOYSA-N thiocyclam Chemical compound CN(C)C1CSSSC1 DNVLJEWNNDHELH-UHFFFAOYSA-N 0.000 description 1
- QSOHVSNIQHGFJU-UHFFFAOYSA-L thiosultap disodium Chemical compound [Na+].[Na+].[O-]S(=O)(=O)SCC(N(C)C)CSS([O-])(=O)=O QSOHVSNIQHGFJU-UHFFFAOYSA-L 0.000 description 1
- 229960002447 thiram Drugs 0.000 description 1
- KUAZQDVKQLNFPE-UHFFFAOYSA-N thiram Chemical compound CN(C)C(=S)SSC(=S)N(C)C KUAZQDVKQLNFPE-UHFFFAOYSA-N 0.000 description 1
- 239000013008 thixotropic agent Substances 0.000 description 1
- OGIDPMRJRNCKJF-UHFFFAOYSA-N titanium oxide Inorganic materials [Ti]=O OGIDPMRJRNCKJF-UHFFFAOYSA-N 0.000 description 1
- OBZIQQJJIKNWNO-UHFFFAOYSA-N tolclofos-methyl Chemical compound COP(=S)(OC)OC1=C(Cl)C=C(C)C=C1Cl OBZIQQJJIKNWNO-UHFFFAOYSA-N 0.000 description 1
- OEJNXTAZZBRGDN-UHFFFAOYSA-N toxaphene Chemical compound ClC1C(Cl)C2(Cl)C(CCl)(CCl)C(=C)C1(Cl)C2(Cl)Cl OEJNXTAZZBRGDN-UHFFFAOYSA-N 0.000 description 1
- YWSCPYYRJXKUDB-KAKFPZCNSA-N tralomethrin Chemical compound CC1(C)[C@@H](C(Br)C(Br)(Br)Br)[C@H]1C(=O)O[C@H](C#N)C1=CC=CC(OC=2C=CC=CC=2)=C1 YWSCPYYRJXKUDB-KAKFPZCNSA-N 0.000 description 1
- 230000014616 translation Effects 0.000 description 1
- 230000002258 trematocidal effect Effects 0.000 description 1
- BAZVSMNPJJMILC-UHFFFAOYSA-N triadimenol Chemical compound C1=NC=NN1C(C(O)C(C)(C)C)OC1=CC=C(Cl)C=C1 BAZVSMNPJJMILC-UHFFFAOYSA-N 0.000 description 1
- 150000003918 triazines Chemical class 0.000 description 1
- REEQLXCGVXDJSQ-UHFFFAOYSA-N trichlopyr Chemical compound OC(=O)COC1=NC(Cl)=C(Cl)C=C1Cl REEQLXCGVXDJSQ-UHFFFAOYSA-N 0.000 description 1
- NLOUTGCXBXLQIA-UHFFFAOYSA-N trichloro phosphate Chemical compound ClOP(=O)(OCl)OCl NLOUTGCXBXLQIA-UHFFFAOYSA-N 0.000 description 1
- 229960000323 triclabendazole Drugs 0.000 description 1
- DQJCHOQLCLEDLL-UHFFFAOYSA-N tricyclazole Chemical compound CC1=CC=CC2=C1N1C=NN=C1S2 DQJCHOQLCLEDLL-UHFFFAOYSA-N 0.000 description 1
- ONCZDRURRATYFI-TVJDWZFNSA-N trifloxystrobin Chemical compound CO\N=C(\C(=O)OC)C1=CC=CC=C1CO\N=C(/C)C1=CC=CC(C(F)(F)F)=C1 ONCZDRURRATYFI-TVJDWZFNSA-N 0.000 description 1
- 125000005034 trifluormethylthio group Chemical group FC(S*)(F)F 0.000 description 1
- 125000001889 triflyl group Chemical group FC(F)(F)S(*)(=O)=O 0.000 description 1
- 229960001082 trimethoprim Drugs 0.000 description 1
- IEDVJHCEMCRBQM-UHFFFAOYSA-N trimethoprim Chemical compound COC1=C(OC)C(OC)=CC(CC=2C(=NC(N)=NC=2)N)=C1 IEDVJHCEMCRBQM-UHFFFAOYSA-N 0.000 description 1
- 201000002311 trypanosomiasis Diseases 0.000 description 1
- 210000001944 turbinate Anatomy 0.000 description 1
- 229960005486 vaccine Drugs 0.000 description 1
- XPHOBMULWMGEBA-VZFHVOOUSA-N valienamine Chemical compound N[C@H]1C=C(CO)[C@@H](O)[C@H](O)[C@H]1O XPHOBMULWMGEBA-VZFHVOOUSA-N 0.000 description 1
- LESVOLZBIFDZGS-UHFFFAOYSA-N vamidothion Chemical compound CNC(=O)C(C)SCCSP(=O)(OC)OC LESVOLZBIFDZGS-UHFFFAOYSA-N 0.000 description 1
- 239000003981 vehicle Substances 0.000 description 1
- VRNFXUOQGOAQBZ-DYXAMGHASA-N veratrin Chemical compound C1[C@@H](C)CC[C@H]2[C@](O)(C)[C@@]3(O)[C@@H](O)C[C@@]4(O)[C@@H]5CC[C@H]6[C@]7(C)CC[C@H](OC(=O)C(\C)=C/C)[C@@]6(O)O[C@@]75C[C@@]4(O)[C@@H]3CN21.C1=C(OC)C(OC)=CC=C1C(=O)O[C@@H]1[C@@]2(O)O[C@@]34C[C@@]5(O)[C@H](CN6[C@@H](CC[C@H](C)C6)[C@@]6(C)O)[C@]6(O)[C@@H](O)C[C@@]5(O)[C@@H]4CC[C@H]2[C@]3(C)CC1 VRNFXUOQGOAQBZ-DYXAMGHASA-N 0.000 description 1
- 125000000391 vinyl group Chemical group [H]C([*])=C([H])[H] 0.000 description 1
- 229920002554 vinyl polymer Polymers 0.000 description 1
- 235000019373 virginiamycin Nutrition 0.000 description 1
- 229960003842 virginiamycin Drugs 0.000 description 1
- 239000012873 virucide Substances 0.000 description 1
- 239000002699 waste material Substances 0.000 description 1
- 239000001993 wax Substances 0.000 description 1
- 238000009736 wetting Methods 0.000 description 1
- 210000002268 wool Anatomy 0.000 description 1
- 239000000230 xanthan gum Substances 0.000 description 1
- 229920001285 xanthan gum Polymers 0.000 description 1
- 235000010493 xanthan gum Nutrition 0.000 description 1
- 229940082509 xanthan gum Drugs 0.000 description 1
- CXNIUSPIQKWYAI-UHFFFAOYSA-N xantphos Chemical compound C=12OC3=C(P(C=4C=CC=CC=4)C=4C=CC=CC=4)C=CC=C3C(C)(C)C2=CC=CC=1P(C=1C=CC=CC=1)C1=CC=CC=C1 CXNIUSPIQKWYAI-UHFFFAOYSA-N 0.000 description 1
- 239000005943 zeta-Cypermethrin Substances 0.000 description 1
- 229910052725 zinc Inorganic materials 0.000 description 1
- 239000011701 zinc Substances 0.000 description 1
- 229940048462 zinc phosphide Drugs 0.000 description 1
- DUBNHZYBDBBJHD-UHFFFAOYSA-L ziram Chemical compound [Zn+2].CN(C)C([S-])=S.CN(C)C([S-])=S DUBNHZYBDBBJHD-UHFFFAOYSA-L 0.000 description 1
Classifications
-
- A—HUMAN NECESSITIES
- A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
- A01N—PRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTS THEREOF; BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES OR AS HERBICIDES; PEST REPELLANTS OR ATTRACTANTS; PLANT GROWTH REGULATORS
- A01N43/00—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds
- A01N43/90—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having two or more relevant hetero rings, condensed among themselves or with a common carbocyclic ring system
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D519/00—Heterocyclic compounds containing more than one system of two or more relevant hetero rings condensed among themselves or condensed with a common carbocyclic ring system not provided for in groups C07D453/00 or C07D455/00
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P33/00—Antiparasitic agents
- A61P33/14—Ectoparasiticides, e.g. scabicides
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P43/00—Drugs for specific purposes, not provided for in groups A61P1/00-A61P41/00
Landscapes
- Life Sciences & Earth Sciences (AREA)
- Organic Chemistry (AREA)
- Chemical & Material Sciences (AREA)
- Health & Medical Sciences (AREA)
- General Health & Medical Sciences (AREA)
- Engineering & Computer Science (AREA)
- Dentistry (AREA)
- Plant Pathology (AREA)
- Wood Science & Technology (AREA)
- Zoology (AREA)
- Environmental Sciences (AREA)
- Pest Control & Pesticides (AREA)
- Agronomy & Crop Science (AREA)
- Veterinary Medicine (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Medicinal Chemistry (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Pharmacology & Pharmacy (AREA)
- Animal Behavior & Ethology (AREA)
- Public Health (AREA)
- Tropical Medicine & Parasitology (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Nitrogen Condensed Heterocyclic Rings (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Agricultural Chemicals And Associated Chemicals (AREA)
- Nitrogen And Oxygen Or Sulfur-Condensed Heterocyclic Ring Systems (AREA)
- Plural Heterocyclic Compounds (AREA)
- Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Abstract
本发明涉及新的式(I)的化合物,其中Aa、Ab、Ac、Ad、R1、Q和n具有说明书中所述的含义;其作为杀螨剂和/或杀虫剂用于防治动物害虫的用途;以及其制备方法和用于其制备的中间体产物。
Description
本发明涉及新的式(I)的稠合双环杂环衍生物;其作为杀螨剂和/或杀虫剂用于防治动物害虫、特别是节肢动物且尤其是昆虫和蛛形纲动物的用途;以及其制备方法和用于其制备的中间体。
具有杀虫特性的稠合双环杂环衍生物已记载于以下文献中:例如,WO 2010/125985、WO 2012/074135、WO 2012/086848、WO 2013/018928、WO 2013/191113、WO 2014/142292、WO 2014/148451、WO 2015/000715、WO 2016/124563、WO 2016/124557、WO 2016/162318、PCT/EP 2016/075365、PCT/EP 2016/078989、PCT/EP 2017/050773、EP16163912.5、EP 16168252.1、WO 2015/121136、WO 2015/002211、WO 2015/071180、WO2016/020286、WO 2015/059039、WO 2015/190316、WO 2016/091731、WO 2016/107742、EP16180168.3、EP 16180170.9、EP 16184163.0、EP 16189445.6、EP 16200177.0、EP17153317.7、WO 2017/026384。
然而,由上述文献已知的某些活性化合物在使用时具有缺点,不论是它们仅具有窄的施用范围,还是它们不具有令人满意的杀虫活性或杀螨活性。
现已发现新的稠合双环杂环衍生物,它们具有优于已知化合物的优点,例如更好的生物学特性或环境特性、更多的施用方法、更好的杀虫作用或杀螨作用,以及与作物植物良好的相容性。稠合双环杂环衍生物可以与用于改进功效的其他试剂结合使用,特别是对抗难以防治的昆虫。
因此,本发明提供了新的式(I)的化合物
其中(构型1-1)
Aa表示氮或=C(R7)-,
Ab表示=N-、-S(O)m-、-O-、-N(R15)-、=C(R2)-、–C(=O)-或–C(R9)(R10)-,
Ac表示=N-、-S(O)m-、-O-、=C(R3)-、–C(=O)-或–C(R11)(R12)-,
Ad表示=N-、-S(O)m-、-O-、-N(R15)-、=C(R8)-、–C(=O)-或–C(R13)(R14)-,
其中取代基Ab、Ac和Ad中只有一个可表示氧、–S(O)m-或–C(=O)-,
R1表示(C1-C6)-烷基、(C1-C6)-卤代烷基、(C1-C6)-氰基烷基、(C1-C6)-羟基烷基、(C1-C6)-烷氧基-(C1-C6)-烷基、(C1-C6)-卤代烷氧基-(C1-C6)-烷基、(C2-C6)-烯基、(C2-C6)-烯氧基-(C1-C6)-烷基、(C2-C6)-卤代烯氧基-(C1-C6)-烷基、(C2-C6)-卤代烯基、(C2-C6)-氰基烯基、(C2-C6)-炔基、(C2-C6)-炔氧基-(C1-C6)-烷基、(C2-C6)-卤代炔氧基-(C1-C6)-烷基、(C2-C6)-卤代炔基、(C2-C6)-氰基炔基、(C3-C8)-环烷基、(C3-C8)-环烷基-(C3-C8)-环烷基、(C1-C6)-烷基-(C3-C8)-环烷基、卤代-(C3-C8)-环烷基、氨基、(C1-C6)-烷基氨基、二-(C1-C6)-烷基-氨基、(C3-C8)-环烷基氨基、(C1-C6)-烷基羰基氨基、(C1-C6)-烷硫基-(C1-C6)-烷基、(C1-C6)-卤代烷硫基-(C1-C6)-烷基、(C1-C6)-烷基亚磺酰基-(C1-C6)-烷基、(C1-C6)-卤代烷基亚磺酰基-(C1-C6)-烷基、(C1-C6)-烷基磺酰基-(C1-C6)-烷基、(C1-C6)-卤代烷基磺酰基-(C1-C6)-烷基、(C1-C6)-烷氧基-(C1-C6)-烷硫基-(C1-C6)-烷基、(C1-C6)-烷氧基-(C1-C6)-烷基亚磺酰基-(C1-C6)-烷基、(C1-C6)-烷氧基-(C1-C6)-烷基磺酰基-(C1-C6)-烷基、(C1-C6)-烷基羰基-(C1-C6)-烷基、(C1-C6)-卤代烷基羰基-(C1-C6)-烷基、(C1-C6)-烷氧基羰基-(C1-C6)-烷基、(C1-C6)-卤代烷氧基羰基-(C1-C6)-烷基、(C1-C6)-烷基磺酰基氨基、氨基磺酰基-(C1-C6)-烷基、(C1-C6)-烷基氨基磺酰基-(C1-C6)-烷基、二-(C1-C6)-烷基-氨基磺酰基-(C1-C6)-烷基,
或表示(C1-C6)-烷基、(C1-C6)-烷氧基、(C2-C6)-烯基、(C2-C6)-炔基、(C3-C8)-环烷基,其各自任选地被相同或不同的芳基、杂芳基或杂环基取代基单取代或多取代,其中芳基、杂芳基或杂环基可各自任选地被相同或不同的以下取代基单取代或多取代:卤素、氰基、硝基、羟基、氨基、羧基、氨基甲酰基、氨基磺酰基、(C1-C6)-烷基、(C3-C6)-环烷基、(C1-C6)-烷氧基、(C1-C6)-卤代烷基、(C1-C6)-卤代烷氧基、(C1-C6)-烷硫基、(C1-C6)-烷基亚磺酰基、(C1-C6)-烷基磺酰基、(C1-C6)-烷基磺酰亚氨基((C1-C6)alkylsulfimino)、(C1-C6)-烷基磺酰亚氨基-(C1-C6)-烷基、(C1-C6)-烷基磺酰亚氨基-(C2-C6)-烷基羰基、(C1-C6)-烷基亚磺酰亚氨基((C1-C6)alkylsulfoximino)、(C1-C6)-烷基亚磺酰亚氨基-(C1-C6)-烷基、(C1-C6)-烷基亚磺酰亚氨基-(C2-C6)-烷基羰基、(C1-C6)-烷氧基羰基、(C1-C6)-烷基羰基、(C3-C6)-三烷基甲硅烷基或苄基,或
R1表示芳基、杂芳基或杂环基,其各自任选地被相同或不同的以下取代基单取代或多取代:卤素、氰基、硝基、羟基、氨基、羧基、氨基甲酰基、(C1-C6)-烷基、(C3-C8)-环烷基、(C1-C6)-烷氧基、(C1-C6)-卤代烷基、(C1-C6)-卤代烷氧基、(C1-C6)-烷硫基、(C1-C6)-烷基亚磺酰基、(C1-C6)-烷基磺酰基、(C1-C6)-烷基磺酰亚氨基、(C1-C6)-烷基磺酰亚氨基-(C1-C6)-烷基、(C1-C6)-烷基磺酰亚氨基-(C2-C6)-烷基羰基、(C1-C6)-烷基亚磺酰亚氨基、(C1-C6)-烷基亚磺酰亚氨基-(C1-C6)-烷基、(C1-C6)-烷基亚磺酰亚氨基-(C2-C6)-烷基羰基、(C1-C6)-烷氧基羰基、(C1-C6)-烷基羰基、(C3-C6)-三烷基甲硅烷基、(=O)(仅在杂环基的情况下)或(=O)2(仅在杂环基的情况下),
R2、R3、R8彼此独立地表示氢、氰基、卤素、硝基、乙酰基、羟基、氨基、SCN、三-(C1-C6)-烷基甲硅烷基、(C3-C8)-环烷基、(C3-C8)-环烷基-(C3-C8)-环烷基、(C1-C6)-烷基-(C3-C8)-环烷基、卤代-(C3-C8)-环烷基、(C1-C6)-烷基、(C1-C6)-卤代烷基、(C1-C6)-氰基烷基、(C1-C6)-羟基烷基、羟基羰基-(C1-C6)-烷氧基、(C1-C6)-烷氧基羰基-(C1-C6)-烷基、(C1-C6)-烷氧基-(C1-C6)-烷基、(C2-C6)-烯基、(C2-C6)-卤代烯基、(C2-C6)-氰基烯基、(C2-C6)-炔基、(C2-C6)-卤代炔基、(C2-C6)-氰基炔基、(C1-C6)-烷氧基、(C1-C6)-卤代烷氧基、(C1-C6)-氰基烷氧基、(C1-C6)-烷氧基羰基-(C1-C6)-烷氧基、(C1-C6)-烷氧基-(C1-C6)-烷氧基、(C1-C6)-烷基羟基亚氨基、(C1-C6)-烷氧基亚氨基、(C1-C6)-烷基-(C1-C6)-烷氧基亚氨基、(C1-C6)-卤代烷基-(C1-C6)-烷氧基亚氨基、(C1-C6)-烷硫基、(C1-C6)-卤代烷硫基、(C1-C6)-烷氧基-(C1-C6)-烷硫基、(C1-C6)-烷硫基-(C1-C6)-烷基、(C1-C6)-烷基亚磺酰基、(C1-C6)-卤代烷基亚磺酰基、(C1-C6)-烷氧基-(C1-C6)-烷基亚磺酰基、(C1-C6)-烷基亚磺酰基-(C1-C6)-烷基、(C1-C6)-烷基磺酰基、(C1-C6)-卤代烷基磺酰基、(C1-C6)-烷氧基-(C1-C6)-烷基磺酰基、(C1-C6)-烷基磺酰基-(C1-C6)-烷基、(C1-C6)-烷基磺酰基氧基、(C1-C6)-烷基羰基、(C1-C6)-烷基硫代羰基、(C1-C6)-卤代烷基羰基、(C1-C6)-烷基羰基氧基、(C1-C6)-烷氧基羰基、(C1-C6)-卤代烷氧基羰基、氨基羰基、(C1-C6)-烷基氨基羰基、(C1-C6)-烷基氨基硫代羰基、二-(C1-C6)-烷基氨基羰基、二-(C1-C6)-烷基氨基硫代羰基、(C2-C6)-烯基氨基羰基、二-(C2-C6)-烯基氨基羰基、(C3-C8)-环烷基氨基羰基、(C1-C6)-烷基磺酰基氨基、(C1-C6)-烷基氨基、二-(C1-C6)-烷基氨基、氨基磺酰基、(C1-C6)-烷基氨基磺酰基、二-(C1-C6)-烷基氨基磺酰基、(C1-C6)-烷基亚磺酰亚氨基、氨基硫代羰基、(C1-C6)-烷基氨基硫代羰基、二-(C1-C6)-烷基氨基硫代羰基、(C3-C8)-环烷基氨基或NHCO-(C1-C6)-烷基((C1-C6)-烷基羰基氨基),
R7表示氢、氰基、卤素、乙酰基、羟基、氨基、(C3-C8)-环烷基、卤代-(C3-C8)-环烷基、(C1-C6)-烷基、(C1-C6)-卤代烷基、(C1-C6)-氰基烷基、(C2-C6)-烯基、(C2-C6)-卤代烯基、(C2-C6)-炔基、(C2-C6)-卤代炔基、(C1-C6)-烷氧基、(C1-C6)-卤代烷氧基、(C1-C6)-烷硫基、(C1-C6)-卤代烷硫基、(C1-C6)-烷基亚磺酰基、(C1-C6)-卤代烷基亚磺酰基、(C1-C6)-烷基磺酰基或(C1-C6)-卤代烷基磺酰基,
R9、R10、R11、R12、R13、R14彼此独立地表示氢、卤素、(C1-C6)-烷基或(C1-C6)-卤代烷基,
R15表示氢、乙酰基、(C1-C4)-烷基、(C1-C4)-羟基烷基、(C1-C4)-卤代烷基、(C1-C4)-氰基烷基、(C1-C4)-烷氧基-(C1-C4)-烷基、(C1-C4)-卤代烷氧基-(C1-C4)-烷基、(C2-C4)-烯基、(C2-C4)-烯氧基-(C1-C4)-烷基、(C2-C4)-卤代烯氧基-(C1-C4)-烷基、(C2-C4)-卤代烯基、(C2-C4)-氰基烯基、(C2-C4)-炔基、(C2-C4)-炔氧基-(C1-C4)-烷基、(C2-C4)-卤代炔氧基-(C1-C4)-烷基、(C2-C4)-卤代炔基、(C2-C4)-氰基炔基、(C3-C6)-环烷基、(C1-C4)-烷基-(C3-C6)-环烷基、卤代-(C3-C6)-环烷基、(C1-C4)-烷硫基-(C1-C4)-烷基、(C1-C4)-卤代烷硫基-(C1-C4)-烷基、(C1-C4)-烷基亚磺酰基-(C1-C4)-烷基、(C1-C4)-卤代烷基亚磺酰基-(C1-C4)-烷基、(C1-C4)-烷基磺酰基-(C1-C4)-烷基、(C1-C4)-烷基羰基-(C1-C4)-烷基、(C1-C4)-卤代烷基羰基-(C1-C4)-烷基,
或表示(C1-C4)-烷基、(C2-C4)-烯基、(C2-C4)-炔基,其各自任选地被相同或不同的芳基或杂环基取代基单取代或二取代,其中芳基或杂环基在每种情况下可任选地被相同或不同的以下取代基单取代或二取代:卤素、氰基、(C1-C4)-烷基、(C3-C4)-环烷基、(C1-C4)-烷氧基、(C1-C4)-卤代烷基、(C1-C4)-卤代烷氧基、(C1-C4)-烷硫基、(C1-C4)-烷基亚磺酰基或(C1-C4)-烷基磺酰基,或
R15表示芳基或杂环基,其各自任选地被相同或不同的以下取代基单取代或二取代:卤素、氰基、(C1-C4)-烷基、(C3-C6)-环烷基、(C1-C4)-烷氧基、(C1-C4)-卤代烷基、(C1-C4)-卤代烷氧基、(C1-C4)-烷硫基、(C1-C4)-烷基亚磺酰基、(C1-C4)-烷基磺酰基、(C1-C4)-烷基亚磺酰亚氨基、(C1-C4)-烷基羰基、(=O)(仅在杂环基的情况下)或(=O)2(仅在杂环基的情况下),
Q表示部分饱和的或饱和的杂环或杂芳族8元、9元、10元、11元或12元稠合的双环或三环体系,其可任选地含有至少一个羰基基团和/或其中所述环体系任选地被相同或不同的取代基单取代或多取代且其中所述取代基可彼此独立地选自氰基、卤素、硝基、乙酰基、羟基、氨基、SCN、三-(C1-C6)-烷基甲硅烷基、(C3-C8)-环烷基、(C3-C8)-环烷基-(C3-C8)-环烷基、(C1-C6)-烷基-(C3-C8)-环烷基、卤代-(C3-C8)-环烷基、(C1-C6)-烷基、(C1-C6)-卤代烷基、(C1-C6)-氰基烷基、(C1-C6)-羟基烷基、羟基羰基-(C1-C6)-烷氧基、(C1-C6)-烷氧基羰基-(C1-C6)-烷基、(C1-C6)-烷氧基-(C1-C6)-烷基、(C2-C6)-烯基、(C2-C6)-卤代烯基、(C2-C6)-氰基烯基、(C2-C6)-炔基、(C2-C6)-炔氧基-(C1-C4)-烷基、(C2-C6)-卤代炔基、(C2-C6)-氰基炔基、(C1-C6)-烷氧基、(C1-C6)-卤代烷氧基、(C1-C6)-卤代烷氧基-(C1-C6)-烷基、(C2-C6)-烯氧基-(C1-C6)-烷基、(C2-C6)-卤代烯氧基-(C1-C6)-烷基、(C1-C6)-氰基烷氧基、(C1-C6)-烷氧基羰基-(C1-C6)-烷氧基、(C1-C6)-烷氧基-(C1-C6)-烷氧基、(C1-C6)-烷基羟基亚氨基、(C1-C6)-烷氧基亚氨基、(C1-C6)-烷基-(C1-C6)-烷氧基亚氨基、(C1-C6)-卤代烷基-(C1-C6)-烷氧基亚氨基、(C1-C6)-烷硫基、(C1-C6)-卤代烷硫基、(C1-C6)-烷氧基-(C1-C6)-烷硫基、(C1-C6)-烷硫基-(C1-C6)-烷基、(C1-C6)-烷基亚磺酰基、(C1-C6)-卤代烷基亚磺酰基、(C1-C6)-烷氧基-(C1-C6)-烷基亚磺酰基、(C1-C6)-烷基亚磺酰基-(C1-C6)-烷基、(C1-C6)-烷基磺酰基、(C1-C6)-卤代烷基磺酰基、(C1-C6)-烷氧基-(C1-C6)-烷基磺酰基、(C1-C6)-烷基磺酰基-(C1-C6)-烷基、(C1-C6)-烷基磺酰基氧基、(C1-C6)-烷基羰基、(C1-C6)-烷基羰基-(C1-C6)-烷基、(C1-C6)-烷基硫代羰基、(C1-C6)-卤代烷基羰基、(C1-C6)-烷基羰基氧基、(C1-C6)-烷氧基羰基、(C1-C6)-卤代烷氧基羰基、氨基羰基、(C1-C6)-烷基氨基羰基、(C1-C6)-烷基氨基硫代羰基、二-(C1-C6)-烷基-氨基羰基、二-(C1-C6)-烷基-氨基硫代羰基、(C2-C6)-烯基氨基羰基、二-(C2-C6)-烯基氨基羰基、(C3-C8)-环烷基氨基羰基、(C1-C6)-烷基磺酰基氨基、(C1-C6)-烷基氨基、二-(C1-C6)-烷基氨基、氨基磺酰基、(C1-C6)-烷基氨基磺酰基、二-(C1-C6)-烷基-氨基磺酰基、(C1-C6)-烷基亚磺酰亚氨基、氨基硫代羰基、(C1-C6)-烷基氨基硫代羰基、二-(C1-C6)-烷基-氨基硫代羰基、(C3-C8)-环烷基氨基、NHCO-(C1-C6)-烷基((C1-C6)-烷基羰基氨基),或其中所述取代基可彼此独立地选自苯基或5元或6元杂芳族环,其中苯基或所述环可任选地被相同或不同的以下取代基单取代或多取代:C1-C6-烷基、C2-C6-烯基、C2-C6-炔基、C3-C6-环烷基、C1-C6-卤代烷基、C2-C6-卤代烯基、C2-C6-卤代炔基、C3-C6-卤代环烷基、卤素、CN、NO2、C1-C4-烷氧基、C1-C4-卤代烷氧基,
m表示0、1或2,
n表示0、1或2,
还发现,式(I)的化合物作为农药、优选作为杀虫剂和/或杀螨剂具有非常好的功效,并且还通常具有非常好的植物相容性,特别是对作物植物而言。
一般而言,本发明的化合物由式(I)定义。在上文和下文提及的式中给出的优选的取代基或基团的范围在下文中举例说明:
构型2
Aa优选表示=C(R7)-,
Ab优选表示=N-、-S(O)m-、-O-、-N(R15)-、=C(R2)-、–C(=O)-或–C(R9)(R10)-,
Ac优选表示=C(R3)-、–C(=O)-或–C(R11)(R12)-,
Ad优选表示=N-、-S(O)m-、-O-、-N(R15)-、=C(R8)-、–C(=O)-或–C(R13)(R14)-,
其中取代基Ab、Ac和Ad中只有一个可表示氧、–S(O)m-或–C(=O)-,
优选得到以下结构单元A1至A14:
其中与取代基Q键合的键由波浪线标识,与硫原子键合的键由星号*标识,
R1优选表示(C1-C4)-烷基、(C1-C4)-羟基烷基、(C1-C4)-卤代烷基、(C2-C4)-烯基、(C2-C4)-卤代烯基、(C2-C4)-炔基、(C2-C4)-卤代炔基、(C3-C6)-环烷基、(C1-C4)-烷硫基-(C1-C4)-烷基、(C1-C4)-卤代烷硫基-(C1-C4)-烷基、(C1-C4)-烷基亚磺酰基-(C1-C4)-烷基、(C1-C4)-烷基磺酰基-(C1-C4)-烷基,
或表示(C1-C4)-烷基、(C2-C4)-烯基、(C2-C4)-炔基、(C3-C6)-环烷基,其各自任选地被相同或不同的芳基或杂环基取代基单取代或二取代,其中芳基或杂环基在每种情况下可任选地被相同或不同的以下取代基单取代或二取代:卤素、(C1-C4)-烷基、(C1-C4)-卤代烷基、(C3-C4)-环烷基、(C1-C4)-烷氧基或(C1-C4)-烷硫基,或
R1优选表示芳基、杂芳基或杂环基,其各自任选地被相同或不同的以下取代基单取代或二取代:卤素、氰基、(C1-C4)-烷基、(C3-C6)-环烷基、(C1-C4)-烷氧基、(C1-C4)-卤代烷基、(C1-C4)-卤代烷氧基、(C1-C4)-烷硫基、(=O)(仅在杂环基的情况下)或(=O)2(仅在杂环基的情况下),
R2、R3、R8优选彼此独立地表示氢、氰基、卤素、硝基、羟基、(C3-C6)-环烷基、(C1-C4)-烷基-(C3-C6)-环烷基、卤代-(C3-C6)-环烷基、(C1-C4)-烷基、(C1-C4)-卤代烷基、(C1-C4)-氰基烷基、(C1-C4)-烷氧基-(C1-C4)-烷基、(C2-C4)-烯基、(C2-C4)-卤代烯基、(C2-C4)-炔基、(C2-C4)-卤代炔基、(C1-C4)-烷氧基、(C1-C4)-卤代烷氧基、(C1-C4)-烷硫基、(C1-C4)-卤代烷硫基、(C1-C4)-烷基亚磺酰基、(C1-C4)-卤代烷基亚磺酰基、(C1-C4)-烷基磺酰基、(C1-C4)-卤代烷基磺酰基、(C1-C4)-烷基羰基、(C1-C4)-卤代烷基羰基、氨基羰基、(C1-C4)-烷基氨基羰基、二-(C1-C4)-烷基氨基羰基、(C1-C4)-烷基磺酰基氨基、(C1-C4)-烷基氨基、二-(C1-C4)-烷基氨基、氨基磺酰基、(C1-C4)-烷基氨基磺酰基、二-(C1-C4)-烷基氨基磺酰基或NHCO-(C1-C4)-烷基((C1-C4)-烷基羰基氨基),
R7优选表示氢、氰基、卤素、乙酰基、羟基、氨基、(C3-C6)-环烷基、卤代-(C3-C6)-环烷基、(C1-C4)-烷基、(C1-C4)-卤代烷基、(C1-C4)-氰基烷基、(C2-C4)-烯基、(C2-C4)-卤代烯基、(C2-C4)-炔基、(C2-C4)-卤代炔基、(C1-C4)-烷氧基、(C1-C4)-卤代烷氧基、(C1-C4)-烷硫基、(C1-C4)-卤代烷硫基、(C1-C4)-烷基亚磺酰基、(C1-C4)-卤代烷基亚磺酰基、(C1-C4)-烷基磺酰基或(C1-C4)-卤代烷基磺酰基,
R9、R10、R11、R12、R13、R14优选彼此独立地表示氢、卤素、(C1-C4)-烷基或(C1-C4)-卤代烷基,
R15优选表示氢、乙酰基、(C1-C4)-烷基、(C1-C4)-卤代烷基、(C1-C4)-氰基烷基、(C1-C4)-烷氧基-(C1-C4)-烷基、(C1-C4)-卤代烷氧基-(C1-C4)-烷基、(C3-C6)-环烷基、(C1-C4)-烷基-(C3-C6)-环烷基、卤代-(C3-C6)-环烷基、(C1-C4)-烷硫基-(C1-C4)-烷基,
或表示(C1-C4)-烷基,其在每种情况下任选地被相同或不同的芳基或杂环基取代基单取代或二取代,其中芳基或杂环基可在每种情况下任选地被相同或不同的以下取代基单取代或二取代:卤素、(C1-C4)-烷基、氰基、(C1-C4)-烷氧基、(C1-C4)-卤代烷基或(C1-C4)-卤代烷氧基,
Q优选表示杂芳族8元、9元、10元、11元或12元稠合的双环或三环体系,其中所述环体系任选地被相同或不同的取代基单取代或多取代,且其中所述取代基可彼此独立地选自氰基、卤素、硝基、乙酰基、羟基、氨基、SCN、三-(C1-C6)-烷基甲硅烷基、(C3-C8)-环烷基、(C3-C8)-环烷基-(C3-C8)-环烷基、(C1-C6)-烷基-(C3-C8)-环烷基、卤代-(C3-C8)-环烷基、(C1-C6)-烷基、(C1-C6)-卤代烷基、(C1-C6)-氰基烷基、(C1-C6)-羟基烷基、(C1-C6)-烷氧基-(C1-C6)-烷基、(C2-C6)-烯基、(C2-C6)-卤代烯基、(C2-C6)-氰基烯基、(C2-C6)-炔基、(C2-C6)-炔氧基-(C1-C4)-烷基、(C2-C6)-卤代炔基、(C1-C6)-烷氧基、(C1-C6)-卤代烷氧基、(C1-C6)-卤代烷氧基-(C1-C6)-烷基、(C2-C6)-烯氧基-(C1-C6)-烷基、(C2-C6)-卤代烯氧基-(C1-C6)-烷基、(C1-C6)-氰基烷氧基、(C1-C6)-烷氧基-(C1-C6)-烷氧基、(C1-C6)-烷基羟基亚氨基、(C1-C6)-烷氧基亚氨基、(C1-C6)-烷基-(C1-C6)-烷氧基亚氨基、(C1-C6)-烷硫基、(C1-C6)-卤代烷硫基、(C1-C6)-烷氧基-(C1-C6)-烷硫基、(C1-C6)-烷硫基-(C1-C6)-烷基、(C1-C6)-烷基亚磺酰基、(C1-C6)-卤代烷基亚磺酰基、(C1-C6)-烷氧基-(C1-C6)-烷基亚磺酰基、(C1-C6)-烷基亚磺酰基-(C1-C6)-烷基、(C1-C6)-烷基磺酰基、(C1-C6)-卤代烷基磺酰基、(C1-C6)-烷氧基-(C1-C6)-烷基磺酰基、(C1-C6)-烷基磺酰基-(C1-C6)-烷基、(C1-C6)-烷基磺酰基氧基、(C1-C6)-烷基羰基、(C1-C6)-烷基羰基-(C1-C6)-烷基、(C1-C6)-烷基硫代羰基、(C1-C6)-卤代烷基羰基、(C1-C6)-烷基羰基氧基、(C1-C6)-烷氧基羰基、(C1-C6)-卤代烷氧基羰基、氨基羰基、(C1-C6)-烷基氨基羰基、(C1-C6)-烷基氨基硫代羰基、二-(C1-C6)-烷基氨基羰基、二-(C1-C6)-烷基氨基硫代羰基、(C3-C8)-环烷基氨基羰基、(C1-C6)-烷基磺酰基氨基、(C1-C6)-烷基氨基、二-(C1-C6)-烷基氨基、氨基磺酰基、(C1-C6)-烷基氨基磺酰基、二-(C1-C6)-烷基氨基磺酰基、(C1-C6)-烷基亚磺酰亚氨基、氨基硫代羰基、(C1-C6)-烷基氨基硫代羰基、二-(C1-C6)-烷基氨基硫代羰基、(C3-C8)-环烷基氨基、NHCO-(C1-C6)-烷基((C1-C6)-烷基羰基氨基),或其中所述取代基可彼此独立地选自苯基或5元或6元杂芳族环,其中苯基或所述环可任选地被相同或不同的以下取代基单取代或多取代:C1-C6-烷基、C2-C6-烯基、C2-C6-炔基、C3-C6-环烷基、C1-C6-卤代烷基、C2-C6-卤代烯基、C2-C6-卤代炔基、C3-C6-卤代环烷基、卤素、CN、C1-C4-烷氧基、C1-C4-卤代烷氧基。
m优选表示0、1或2,
n优选表示0、1或2。
构型3
Aa特别优选表示=C(R7)-,
Ab特别优选表示=N-、-S(O)m-、-N(R15)-、=C(R2)-、–C(=O)-或–C(R9)(R10)-,
Ac特别优选表示=C(R3)-或–C(R11)(R12)-,
Ad特别优选表示=N-、-S(O)m-、-N(R15)-、=C(R8)-或–C(R13)(R14)-,
其中取代基Ab和Ad中只有一个可表示氧、–S(O)m-或–C(=O)-,
更优选得到以下结构单元:A1、A2、A5、A6、A9、A10、A11、A12、A13、A14,
R1特别优选表示(C1-C4)-烷基、(C1-C4)-羟基烷基、(C1-C4)-卤代烷基、(C2-C4)-烯基、(C2-C4)-卤代烯基、(C2-C4)-炔基、(C2-C4)-卤代炔基、(C3-C6)-环烷基、(C1-C4)-烷硫基-(C1-C4)-烷基、(C1-C4)-烷基亚磺酰基-(C1-C4)-烷基或(C1-C4)-烷基磺酰基-(C1-C4)-烷基,
R2、R3、R8特别优选彼此独立地表示氢、氰基、卤素、硝基、羟基、(C3-C6)-环烷基、(C1-C4)-烷基-(C3-C6)-环烷基、卤代-(C3-C6)-环烷基、(C1-C4)-烷基、(C1-C4)-卤代烷基、(C1-C4)-烷氧基-(C1-C4)-烷基、(C1-C4)-烷氧基、(C1-C4)-卤代烷氧基、(C1-C4)-烷硫基、(C1-C4)-卤代烷硫基、(C1-C4)-烷基亚磺酰基、(C1-C4)-卤代烷基亚磺酰基、(C1-C4)-烷基磺酰基、(C1-C4)-卤代烷基磺酰基、氨基磺酰基、(C1-C4)-烷基氨基磺酰基、二-(C1-C4)-烷基氨基磺酰基或NHCO-(C1-C4)-烷基((C1-C4)-烷基羰基氨基),
R7特别优选表示氢、卤素、氰基、(C1-C4)-烷基或(C1-C4)-卤代烷基,
R9、R10、R11、R12、R13、R14特别优选彼此独立地表示氢、卤素、(C1-C4)-烷基或(C1-C4)-卤代烷基,
R15特别优选表示氢、(C1-C4)-烷基、(C1-C4)-卤代烷基、(C1-C4)-氰基烷基或(C1-C4)-烷氧基-(C1-C4)-烷基,
Q特别优选表示选自Q1至Q20的杂芳族9元或12元稠合的双环或三环体系,
R4特别优选表示(C1-C4)-烷基、(C1-C4)-卤代烷基、(C1-C4)-氰基烷基、(C1-C4)-羟基烷基、(C1-C4)-烷氧基-(C1-C4)-烷基、(C1-C4)-卤代烷氧基-(C1-C4)-烷基、(C2-C4)-烯基、(C2-C4)-烯氧基-(C1-C4)-烷基、(C2-C4)-卤代烯氧基-(C1-C4)-烷基、(C2-C4)-卤代烯基、(C2-C4)氰基烯基、(C2-C4)-炔基、(C2-C4)-炔氧基-(C1-C4)-烷基、(C2-C4)-卤代炔基、(C3-C6)-环烷基、(C3-C6)-环烷基-(C3-C6)-环烷基、(C1-C4)-烷基-(C3-C6)-环烷基、卤代-(C3-C6)-环烷基、(C1-C4)-烷硫基-(C1-C4)-烷基、(C1-C4)-烷基亚磺酰基-(C1-C4)-烷基、(C1-C4)-烷基磺酰基-(C1-C4)-烷基或(C1-C4)-烷基羰基-(C1-C4)-烷基,
R5、R6特别优选彼此独立地表示氢、氰基、卤素、(C1-C4)-烷基、(C1-C4)-卤代烷基、(C2-C4)-烯基、(C2-C4)-卤代烯基、(C2-C4)-炔基、(C2-C4)-卤代炔基、(C3-C6)-环烷基、(C3-C6)-环烷基-(C3-C6)-环烷基、(C1-C4)-烷基-(C3-C6)-环烷基、(C1-C4)-烷氧基、(C1-C4)-卤代烷氧基、(C1-C4)-烷氧基亚氨基、(C1-C4)-烷硫基、(C1-C4)-卤代烷硫基、(C1-C4)-烷基亚磺酰基、(C1-C4)-卤代烷基亚磺酰基、(C1-C4)-烷基磺酰基、(C1-C4)-卤代烷基磺酰基、(C1-C4)-烷基磺酰基氧基、(C1-C4)-烷基羰基、(C1-C4)-卤代烷基羰基、氨基羰基、(C1-C4)-烷基氨基羰基、二-(C1-C4)-烷基氨基羰基、(C1-C4)-烷基磺酰基氨基、(C1-C4)-烷基氨基、二-(C1-C4)-烷基氨基、氨基磺酰基、(C1-C4)-烷基氨基磺酰基或二-(C1-C4)-烷基氨基磺酰基,
m特别优选表示0、1或2,
n特别优选表示0、1或2。
构型4
Aa非常特别优选表示=C(R7)-,
Ab非常特别优选表示=N-、-S(O)m-、-N(R15)-、=C(R2)-、–C(=O)-或–C(R9)(R10)-,
Ac非常特别优选表示=C(R3)-或–C(R11)(R12)-,
Ad非常特别优选表示=N-、-S(O)m-、-N(R15)-、=C(R8)-或–C(R13)(R14)-,
其中取代基Ab和Ad中只有一个可表示氧、–S(O)m-或–C(=O)-,
甚至更优选得到以下结构单元:A1、A2、A5、A6、A9、A10、A11、A12、A13、A14,
R1非常特别优选表示甲基、乙基、正丙基、异丙基或环丙基,
R2、R3、R8非常特别优选彼此独立地表示氢、氟、氯、溴、碘、氰基、甲基、乙基、甲氧基、三氟甲基、三氟甲氧基或三氟甲硫基,
R7非常特别优选表示氢、氟、氯、溴、氰基、甲基、乙基或三氟甲基,
R9、R10、R11、R12、R13、R14非常特别优选彼此独立地表示氢、氟、氯、溴、甲基、乙基或三氟甲基,
R15非常特别优选表示氢、甲基、乙基、正丙基、异丙基、仲丙基或叔丁基,
Q非常特别优选表示选自Q2、Q3、Q10、Q14和Q16的杂芳族9元稠合的双环体系,
R4非常特别优选表示甲基、乙基、异丙基、甲氧基甲基或甲氧基乙基,
R5非常特别优选表示氟、氯、溴、氟甲基、二氟甲基、三氟甲基、氟乙基(CH2CFH2、CHFCH3)、二氟乙基(CF2CH3、CH2CHF2、CHFCFH2)、三氟乙基(CH2CF3、CHFCHF2、CF2CFH2)、四氟乙基(CHFCF3、CF2CHF2)、五氟乙基、三氟甲氧基、二氟氯甲氧基、二氯氟甲氧基、三氟甲硫基、三氟甲基亚磺酰基或三氟甲基磺酰基,
R6非常特别优选表示氢,
m非常特别优选表示0,
n非常特别优选表示0、1或2。
构型5
Aa最优选表示=C(R7)-,
Ab最优选表示-S(O)m-或=C(R2)-,
Ac最优选表示=C(R3)-,
Ad最优选表示=N-、-S(O)m-或=C(R8)-,
最优选得到以下结构单元:A9、A10、A14
R1最优选表示乙基,
R2最优选表示氢,
R3最优选表示氢,
R7最优选表示氢,
R8最优选表示氢,
Q最优选表示选自Q2和Q3的杂芳族9元稠合的双环体系,
R4最优选表示甲基,
R5最优选表示三氟甲基,
R6最优选表示氢,
m最优选表示0,
n最优选表示0、1或2。
在另一优选的实施方案中,本发明涉及式(I)的化合物,其中Q表示Q2或Q3,且Aa、Ab、Ac、Ad、R1、R4、R5、R6和n具有实施方案(3)或实施方案(4)或实施方案(5)中给出的含义。
在另一优选的实施方案中,本发明涉及式(I)的化合物,其中Q表示Q2,且Aa、Ab、Ac、Ad、R1、R4、R5、R6和n具有实施方案(3)或实施方案(4)或实施方案(5)中给出的含义。
在另一优选的实施方案中,本发明涉及式(I)的化合物,其中Q表示Q3,且Aa、Ab、Ac、Ad、R1、R4、R5、R6和n具有实施方案(3)或实施方案(4)或实施方案(5)中给出的含义。
在另一优选的实施方案中,本发明涉及式(I)的化合物,其中Q表示
且Aa、Ab、Ac、Ad、R1和n具有实施方案(3)或实施方案(4)或实施方案(5)中给出的含义。
在另一优选的实施方案中,本发明涉及式(I)的化合物,其中Q表示
且Aa、Ab、Ac、Ad、R1和n具有实施方案(3)或实施方案(4)或实施方案(5)中给出的含义。
在另一优选的实施方案中,本发明涉及式(I)的化合物,其中
Aa表示=C(R7)-,
Ab表示-S(O)m-或=C(R2)-,
Ac表示=C(R3)-,
Ad表示=N-、-S(O)m-或=C(R8)-,
得到以下结构单元:A9、A10、A14
并且其中Q、R1、R2、R3、R7、R8、m和n具有实施方案(1)或实施方案(2)或实施方案(3)或实施方案(4)或实施方案(5)中给出的含义。
在另一优选的实施方案中,本发明涉及式(I)的化合物,其中
Aa表示=C(R7)-,
Ab表示-S(O)m-或=C(R2)-,
Ac表示=C(R3)-,
Ad表示=N-、-S(O)m-或=C(R8)-,
得到以下结构单元:A9、A10、A14
并且Q表示Q2或Q3
并且其中R1、R2、R3、R4、R5、R6、R7、R8、m和n具有实施方案(3)或实施方案(4)或实施方案(5)中给出的含义。
在另一优选的实施方案中,本发明涉及式(I)的化合物,其中
Aa表示=C(R7)-,
Ab表示=C(R2)-,
Ac表示=C(R3)-,
Ad表示-S(O)m-,
得到以下结构单元:A9
并且Q、R1、R2、R3、R7、m和n具有实施方案(1)或实施方案(2)或实施方案(3)或实施方案(4)或实施方案(5)中给出的含义。
在另一优选的实施方案中,本发明涉及式(I)的化合物,其中
Aa表示=C(H)-,
Ab表示=C(H)-,
Ac表示=C(H)-,
Ad表示-S-,
并且Q表示Q2或Q3
并且其中R1、R4、R5、R6和n具有实施方案(3)或实施方案(4)或实施方案(5)中给出的含义。
在另一优选的实施方案中,本发明涉及式(I)的化合物,其中
Aa表示=C(R7)-,
Ab表示-S(O)m-,
Ac表示=C(R3)-,
Ad表示=C(R8)-,
得到以下结构单元:A10
并且Q、R1、R3、R7、R8、m和n具有实施方案(1)或实施方案(2)或实施方案(3)或实施方案(4)或实施方案(5)中给出的含义。
在另一优选的实施方案中,本发明涉及式(I)的化合物,其中
Aa表示=C(H)-,
Ab表示-S-,
Ac表示=C(H)-,
Ad表示=C(H)-,
并且Q表示Q2或Q3
并且其中R1、R4、R5、R6和n具有实施方案(3)或实施方案(4)或实施方案(5)中给出的含义。
在另一优选的实施方案中,本发明涉及式(I)的化合物,其中
Aa表示=C(R7)-,
Ab表示-S(O)m-,
Ac表示=C(R3)-,
Ad表示=N-,
得到以下结构单元:A14
并且Q、R1、R3、R7、m和n具有实施方案(1)或实施方案(2)或实施方案(3)或实施方案(4)或实施方案(5)中给出的含义。
在另一优选的实施方案中,本发明涉及式(I)的化合物,其中
Aa表示=C(H)-,
Ab表示-S-,
Ac表示=C(H)-,
Ad表示=N-,
并且Q表示Q2或Q3
并且其中R1、R4、R5、R6和n具有实施方案(3)或实施方案(4)或实施方案(5)中给出的含义。
包含结构单元A1至A14,由此产生式(I)的以下主要结构:
其中R1、R2、R3、R7、R8、R9、R10、R11、R12、R13、R14、R15、Q、m和n具有上文给出的含义。
除非另有说明,在优选的定义中,
卤素选自氟、氯、溴和碘,依次优选选自氟、氯和溴。
除非另有说明,在特别优选的定义中,
卤素选自氟、氯、溴和碘,依次优选选自氟、氯和溴,
在本发明的上下文中,除非另有不同定义,术语“烷基”本身或与其他术语组合(例如卤代烷基)应理解为是指饱和脂族烃基的基团,其具有1至12个碳原子并且可以是支链或直链的。C1-C12-烷基的实例为甲基、乙基、正丙基、异丙基、正丁基、异丁基、仲丁基、叔丁基、正戊基、异戊基、新戊基、叔戊基、1-甲基丁基、2-甲基丁基、1-乙基丙基、1,2-二甲基丙基、己基、正庚基、正辛基、正壬基、正癸基、正十一烷基和正十二烷基。在这些烷基中,特别优选C1-C6-烷基。尤其优选C1-C4-烷基。
根据本发明,除非另有不同定义,术语“烯基”本身或与其他术语组合应理解为是指具有至少一个双键的直链或支链C2-C12-烯基,例如乙烯基、烯丙基、1-丙烯基、异丙烯基、1-丁烯基、2-丁烯基、3-丁烯基、1,3-丁二烯基、1-戊烯基、2-戊烯基、3-戊烯基、4-戊烯基、1,3-戊二烯基、1-己烯基、2-己烯基、3-己烯基、4-己烯基、5-己烯基和1,4-己二烯基。其中优选C2-C6-烯基,特别优选C2-C4-烯基。
根据本发明,除非另有不同定义,术语“炔基”本身或与其他术语组合应理解为是指具有至少一个三键的直链或支链C2-C12-炔基,例如乙炔基、1-丙炔基和炔丙基。其中,优选C3-C6-炔基,特别优选C3-C4-炔基。炔基还可以含有至少一个双键。
根据本发明,除非另有不同定义,术语“环烷基”本身或与其他术语组合应理解为是指C3-C8-环烷基,例如环丙基、环丁基、环戊基、环己基、环庚基和环辛基。其中,优选C3-C6-环烷基。
在本案中,术语“烷氧基”本身或与其他术语组合(例如卤代烷氧基)应理解为是指O-烷基,其中术语“烷基”如上文所定义。
卤素取代的基团(例如卤代烷基)为单卤代或多卤代的,至多为可能的取代基的最大数目。在多卤代的情况下,卤素原子可以相同或不同。在这种情况下,卤素表示氟、氯、溴或碘,特别是氟、氯或溴。
除非另有说明,任选取代的基团可以是单取代或多取代的,其中在多取代的情况下,取代基可以是相同的或不同的。
以一般性术语给出的或在优选范围内列出的基团定义或说明,相应地适用于终产物,以及原料和中间体。这些基团定义可以根据需要彼此组合,即包括各自优选范围之间的组合。
本发明优选使用式(I)的化合物,其含有上文作为优选列出的含义的组合。
本发明特别优选使用式(I)的化合物,其含有上文作为特别优选列出的含义的组合。
本发明非常特别优选使用式(I)的化合物,其含有上文作为非常特别优选列出的定义的组合。
本发明最优选使用式(I)的化合物,其含有上文作为最优选列出的含义的组合。
根据取代基的性质,式(I)的化合物可为几何异构体和/或光学活性异构体或相应的具有不同组成的异构体混合物的形式。这些立体异构体为例如对映异构体、非对映异构体、阻转异构体或几何异构体。因此,本发明包括纯的立体异构体和这些异构体的任何需要的混合物。
本发明的式(I)的化合物可以通过以下方案中所示的方法获得:
方法A
式(I)的化合物(其中Q表示Q1至Q9或Q16或Q19)可以通过已知方法制备,例如类似于WO 2009/131237、WO 2010/125985、WO 2011/043404、WO 2011/040629、WO 2012/086848、WO 2013/018928、WO 2015/000715和WO 2015/121136中所记载的方法。
基团R1、R4、R5、R6、Aa、Ab、Ac、Ad和n具有上文所述的含义,A2和A3表示CH或N,A4表示O、S或N-R4,X1表示卤素或三氟甲基磺酸根,且M表示碱金属(优选钠或钾)。
步骤a)
式(IV)的化合物可以类似于US 5576335中所记载的方法,通过使式(II)的化合物与式(III)的羧酸在缩合剂或碱的存在下反应来制备。
式(II)的化合物可商购获得或可通过已知方法制备,例如类似于US 2003/69257、WO 2006/65703、WO 2009/131237、WO 2010/125985、WO 2011/043404、WO 2011/040629、WO2012/086848、WO 2013/018928或WO 2015/000715中所记载的方法。
式(III)的羧酸可商购获得或可通过已知方法制备。可能的制备路线记载于方法E至G中。
式(II)的化合物与式(III)的羧酸的反应可以在无溶剂下或在溶剂中进行,优选在选自常规溶剂的溶剂中进行反应,所述常规溶剂在反应条件下呈惰性。优选醚类,例如二异丙基醚、二氧六环、四氢呋喃、1,2-二甲氧基乙烷;卤代烃类,例如二氯甲烷、氯仿、四氯化碳、1,2-二氯乙烷或氯苯;腈类,例如乙腈或丙腈;芳族烃类,例如甲苯或二甲苯;非质子极性溶剂,例如N,N-二甲基甲酰胺或N-甲基吡咯烷酮,或含氮化合物,例如吡啶。
合适的缩合剂为例如碳二亚胺,例如1-(3-二甲基氨基丙基)-3-乙基碳二亚胺盐酸盐(EDCI)或1,3-二环己基碳二亚胺。
合适的碱为通常用于这类反应的无机碱。优选使用的碱选自例如碱金属或碱土金属的乙酸盐、磷酸盐、碳酸盐和碳酸氢盐。在本文中,特别优选乙酸钠、磷酸钠、磷酸钾、碳酸铯、碳酸钠、碳酸钾、碳酸氢钠、碳酸氢钾。
该反应可以在减压下、在大气压下或在高压下并且在0℃至180℃的温度下进行;优选地,该反应在大气压下并且在20至140℃的温度下进行。
步骤b)
式(V)的化合物可以通过将式(IV)的化合物进行缩合来制备,例如类似于WO2009/131237、WO 2010/125985、WO 2011/043404、WO 2011/040629、WO 2012/086848、WO2013/018928、WO 2015/000715和WO 2015/121136中所记载的方法。
转化为式(V)的化合物可以在无溶剂下或在溶剂中进行,优选在选自常规溶剂的溶剂中进行反应,所述常规溶剂在反应条件下呈惰性。优选醚类,例如二异丙基醚、二氧六环、四氢呋喃、1,2-二甲氧基乙烷、叔丁基甲基醚;卤代烃类,例如二氯甲烷、氯仿、四氯化碳、1,2-二氯乙烷或氯苯;腈类,例如乙腈或丙腈;芳族烃类,例如甲苯或二甲苯;非质子极性溶剂,例如N,N-二甲基甲酰胺或N-甲基吡咯烷酮,或含氮化合物,例如吡啶。
该反应可以在缩合剂、酸、碱或氯化剂的存在下进行。
合适的缩合剂的实例为碳二亚胺,例如1-(3-二甲基氨基丙基)-3-乙基碳二亚胺盐酸盐(EDCI)或1,3-二环己基碳二亚胺;酸酐,例如乙酸酐、三氟乙酸酐;三苯基膦、碱和四氯化碳的混合物,或三苯基膦和偶氮二酯(例如偶氮二羧酸二乙酯)的混合物。
可用于所述反应的合适的酸的实例为磺酸,例如对甲苯磺酸;羧酸如乙酸,或多磷酸。
合适的碱的实例为含氮杂环类,例如吡啶、甲基吡啶、2,6-二甲基吡啶、1,8-二氮杂双环[5.4.0]-7-十一碳烯(DBU);叔胺,例如三乙胺和N,N-二异丙基乙胺;无机碱,例如磷酸钾、碳酸钾和氢化钠。
合适的氯化剂的实例为三氯氧化磷。
该反应可以在减压下、在大气压下或在高压下并且在0℃至200℃的温度下进行。
步骤c)
式(I)的化合物(其中n表示0)可以通过在碱的存在下,使式(V)的化合物与式(VIa)的化合物反应来制备。
式(VIa)的硫醇衍生物,例如甲硫醇、乙硫醇或异丙硫醇可商购获得或者可以通过已知方法制备,例如类似于US 2006/25633、US 2006/111591、US 2820062、ChemicalCommunications 2000,13,第1163-1164页或Journal of the American ChemicalSociety,1922,44,第1329页中所记载的方法。
转化为式(I)的化合物(其中n表示0)可以在无溶剂下或在溶剂中进行,优选在选自常规溶剂的溶剂中进行反应,所述常规溶剂在反应条件下呈惰性。优选醚类,例如二异丙基醚、二氧六环、四氢呋喃、1,2-二甲氧基乙烷、叔丁基甲基醚;腈类,例如乙腈或丙腈;芳族烃类,例如甲苯或二甲苯;非质子极性溶剂,例如N,N-二甲基甲酰胺、N-甲基吡咯烷酮或二甲基亚砜。
合适的碱的实例为选自碱金属或碱土金属的乙酸盐、磷酸盐和碳酸盐的无机碱。在本文中优选碳酸铯、碳酸钠和碳酸钾。其他合适的碱为碱金属氢化物,例如氢化钠。
该反应可以在减压下、在大气压下或在高压下并且在0℃至200℃的温度下进行。
在所述反应中,X1优选为氟或氯原子。
步骤d)
式(I)的化合物(其中n表示1)可以通过氧化其中n表示0的式(I)的化合物来制备。通常在选自常规溶剂的溶剂中进行氧化,所述常规溶剂在反应条件下呈惰性。优选卤代烃类,例如二氯甲烷、氯仿、四氯化碳、1,2-二氯乙烷或氯苯;醇类,例如甲醇或乙醇;甲酸、乙酸、丙酸或水。
合适的氧化剂的实例为过氧化氢、间氯过氧苯甲酸或高碘酸钠。
该反应可以在减压下、在大气压下或在高压下并且在-20℃至120℃的温度下进行。
步骤e)
式(I)的化合物(其中n表示2)可以通过氧化其中n表示1的式(I)的化合物来制备。通常在溶剂中进行氧化。优选卤代烃类,例如二氯甲烷、氯仿、四氯化碳、1,2-二氯乙烷或氯苯;醇类,例如甲醇或乙醇;甲酸、乙酸、丙酸或水。
合适的氧化剂的实例为过氧化氢和间氯过氧苯甲酸。
该反应可以在减压下、在大气压下或在高压下并且在-20℃至120℃的温度下进行。
步骤f)
式(I)的化合物(其中n表示2)还可以以一步法,通过氧化其中n表示0的式(I)的化合物来制备。通常在溶剂中进行氧化。优选卤代烃类,例如二氯甲烷、氯仿、四氯化碳、1,2-二氯乙烷或氯苯;醇类,例如甲醇或乙醇;甲酸、乙酸、丙酸或水。
合适的氧化剂的实例为过氧化氢和间氯过氧苯甲酸。
该反应可以在减压下、在大气压下或在高压下并且在-20℃至120℃的温度下进行。
步骤g)
或者,式(II)的化合物(其中n表示2)还可以以一步法制备,例如以类似于Journalof Organic Chemistry 2005,70,第2696-2700页中所记载的方法,由式(V)的化合物开始通过使用式(VIb)的化合物进行卤素-砜交换来制备。所述交换通常在溶剂中进行。优选使用极性非质子溶剂,例如二甲基亚砜和N,N-二甲基甲酰胺。
式(VIb)的化合物可商购获得或可通过已知的方法制备,例如类似于OrganicSynthesis 1977,57,第88-92页;Tetrahedron Letters 1979,9,第821-824页和Bulletinde la SociétéChimique de France 1958,4,第447-450页中所记载的方法。
合适的硫试剂的实例为亚磺酸的盐。
该反应可以在减压下、在大气压下或在高压下并且在-20℃至120℃的温度下进行。
方法B
式(I)的化合物(其中Q表示Q10、Q11、Q14或Q15)可通过已知的方法制备,例如类似于US 2009/203705、US 2012/258951、WO 2013/3298或J.Med.Chem.1988,31,第1590-1595页中所记载的方法。
基团R1、R5、R6、Aa、Ab、Ac、Ad和n具有上文所述的含义。A2、A3、A4和A5表示CH或N(其中A2、A3、A4和A5不同时表示N),X1表示卤素或三氟甲基磺酸根,且M表示碱金属(优选钠或钾)。
步骤a)
以类似于WO 2011/75643或EP 2671582中所记载的方法,在O,N-二甲基羟胺盐酸盐的存在下,使式(III)的羧酸转化为式(VI)的Weinreb酰胺。
式(III)的羧酸可商购获得或可通过已知方法制备。可能的制备路线记载于方法E至G中。
步骤b)和c)
然后可以通过已知方法,例如以类似于WO 2011/75643中所记载的方法,使用格氏试剂(例如甲基溴化镁),将式(VI)的化合物转化为式(VII)的酮。式(VIII)的化合物可以类似于例如US 2012/302573中所记载的已知方法通过随后的卤化来获得。
步骤d)
式(X)的化合物可通过利用式(IX)的胺使式(VIII)的化合物环化来制备。通过已知的方法例如在乙醇、乙腈或N,N-二甲基甲酰胺中进行环化,所述已知的方法类似于例如WO 2005/66177、WO 2012/88411、WO 2013/3298、US 2009/203705、US 2012/258951、WO2012/168733、WO 2014/187762或J.Med.Chem.1988,31,第1590-1595页中所记载的方法。
式(IX)的化合物可商购获得。
步骤e)
式(I)的化合物(其中n表示0)可通过在碱的存在下,使式(X)的化合物与式(VIa)的化合物反应来制备。式(VIa)的硫醇衍生物,例如甲硫醇、乙硫醇或异丙硫醇可商购获得或者可以通过已知方法制备,例如类似于US 2006/25633、US 2006/111591、US 2820062、Chemical Communications 2000,13,第1163-1164页或Journal of the AmericanChemical Society,1922,44,第1329页中所记载的方法。
步骤f)和g)
式(I)的化合物(其中n表示1)可以通过氧化其中n表示0的式(I)的化合物来制备。通过已知的方法使用合适的氧化剂进行氧化,所述氧化剂为例如过氧化氢、间氯过氧苯甲酸或高碘酸钠。
式(I)的化合物(其中n表示2)可以通过氧化其中n表示1的式(I)的化合物来制备。
通常在溶剂中进行氧化。优选卤代烃类,例如二氯甲烷、氯仿、四氯化碳、1,2-二氯乙烷或氯苯;醇类,例如甲醇或乙醇;甲酸、乙酸、丙酸或水。合适的氧化剂的实例为过氧化氢和间氯过氧苯甲酸。
步骤h)
式(I)的化合物(其中n表示2)还可以以一步法,通过氧化其中n表示0的式(I)的化合物来制备。通常在溶剂中进行氧化。优选卤代烃类,例如二氯甲烷、氯仿、四氯化碳、1,2-二氯乙烷或氯苯;醇类,例如甲醇或乙醇;甲酸、乙酸、丙酸或水。合适的氧化剂的实例为过氧化氢和间氯过氧苯甲酸。
步骤i)
或者,式(II)的化合物(其中n表示2)还可以以一步法制备,例如以类似于Journalof Organic Chemistry 2005,70,第2696-2700页中所记载的方法,由式(X)的化合物开始通过利用式(VIb)的化合物进行卤素-砜交换来制备。所述交换通常在溶剂中进行。优选使用极性非质子溶剂,例如二甲基亚砜和N,N-二甲基甲酰胺。
式(VIb)的化合物可商购获得或可通过已知的方法制备,例如类似于OrganicSynthesis 1977,57,第88-92页;Tetrahedron Letters 1979,9,第821-824页和Bulletinde la SociétéChimique de France 1958,4,第447-450页中所记载的方法。
合适的硫试剂的实例为亚磺酸的盐。
该反应可以在减压下、在大气压下或在高压下并且在-20℃至120℃的温度下进行。
方法C
式(I)的化合物(其中Q表示Q16)可通过已知的方法制备,例如类似于WO 2014/142292中所记载的方法。
基团R4、R5、R6、Aa、Ab、Ac和Ad具有上文所述的含义。X1表示卤素。
步骤a)
式(XI)的化合物可以类似于US 5374646或Bioorganic and MedicinalChemistry Letters 2003,13,第1093-1096页中所记载的方法,通过使式(III)的化合物与氨源在缩合剂的存在下反应来制备。
式(III)的羧酸可商购获得或可通过已知方法制备。可能的制备路线记载于方法E至G中。
式(III)的化合物与氨源的反应优选在选自常规溶剂的溶剂中进行,所述常规溶剂在反应条件下呈惰性。优选醚类,例如二氧六环或四氢呋喃。
合适的缩合剂为例如羰基二咪唑。
该反应可以在减压下、在大气压下或在高压下进行。优选地,该反应在大气压和20℃至70℃的温度下进行。
步骤b)
式(XIII)的化合物可以类似于WO 2014/142292中所记载的方法,通过使式(XI)的化合物与式(XII)的化合物在钯催化剂的存在下在碱性介质中进行反应来制备。
式(XII)的化合物可以例如类似于WO 2014/142292中所记载的方法进行制备。所用的钯催化剂可为例如[1,1'-双(二苯基膦)二茂铁]二氯化钯(II)。通常,使用的碱为无机碱,例如叔丁醇钾。
该反应在溶剂中进行。通常使用甲苯。
该反应可以在减压下、在大气压下或在高压下进行。优选地,该反应在大气压和20℃至110℃的温度下进行。
式(XIII)的化合物进一步转化为式(I)的化合物类似于方法A进行。
方法D
式(I)的化合物(其中Q表示Q12、Q13、Q17、Q18或Q20)可通过已知的方法进行制备,例如类似于WO 2010/091310、WO 2012/66061或WO 2013/099041中记载的方法。
基团R5、R6、Aa、Ab、Ac和Ad具有上文所述的含义。A2、A3和A6表示CH或N(其中A2、A3和A6不能同时表示N)。X1和X2表示卤素。
步骤a)
式(XVI)的化合物可通过使式(XIV)的化合物与式(XV)的化合物在碱性条件下反应来制备,例如类似于WO 2010/091310、WO 2012/66061、WO 2013/099041或Tetrahedron1993,49,第10997-11008页中所记载的方法。
式(XIV)的化合物可商购获得或可通过已知方法制备,例如类似于WO 2005/100353、WO 2012/66061或European Journal of Medicinal Chemistry 2010,45,第2214-2222页中所记载的方法。
式(XV)的化合物可商购获得或可通过已知方法(例如类似于方法E和G)制备。
所使用的碱通常为无机碱,例如氢化钠、碳酸钾或碳酸铯。
转化为式(XVI)的化合物通常在溶剂中进行,优选在腈类(例如乙腈或丙腈)或在非质子极性溶剂(例如N,N-二甲基甲酰胺或N-甲基吡咯烷酮)中进行。
该反应可以在减压下、在大气压下或在高压下并且在0℃至200℃的温度下进行。
或者,式(XIV)的化合物与式(XV)的化合物反应得到式(XVI)的化合物还可以通过钯催化的N-芳基化来进行,例如类似于Angewandte Chemie Int.Ed.2011,50,第8944-8947页中所记载的方法。
式(XVI)的化合物进一步转化为式(I)的化合物类似于方法A进行。
方法E
具有结构单元A1或A2的式(IIIa)的羧酸(Ab表示–C(=O)-或–C(R9)(R10)-)可通过以下方法来制备:
基团R7、R9、R10、R11、R12、R13和R14具有上文所述的含义。Ab表示–C(=O)-或–C(R9)(R10)-。X1、X2和X3表示卤素。R16表示(C1-C4)-烷基或芳基-(C1-C2)-烷基。
步骤a)
式(XVIII)的化合物可商购获得或可通过已知的方法,以类似于US 2008/003949中所记载的方法,由式(XVII)的化合物来制备,例如在作为溶剂的四氢呋喃中,使用二异丙基氨基锂作为碱和对甲苯磺酰氰作为亲电试剂。
式(XVII)的化合物可商购获得。
初始锂化步骤的反应温度任选地为-100℃至-75℃。
步骤b)
式(XIX)的化合物可商购获得或可通过已知的方法,以类似于Tetrahedron 2009,65,第748-751页中所记载的方法,由式(XVIII)的化合物经卤化来合成,例如在作为溶剂的四氢呋喃中,使用二异丙基氨基锂作为碱和碘作为卤化试剂。
初始锂化步骤的反应温度任选地为-100℃至-75℃。
步骤c)
式(XX)的化合物可商购获得或可通过已知的方法,以类似于Tetrahedron 2009,65,第748-751页中所记载的方法,由式(XIX)的化合物经Heck偶联来合成,例如在作为溶剂的乙腈中,使用丙烯酸甲酯、四丁基溴化铵、乙酸钯(II)作为催化剂,碳酸钾作为碱。
该反应可以在减压下、在大气压下或在高压下并且在0℃至200℃的温度下进行。
步骤d)
式(XXI)的化合物可商购获得或可通过已知的方法,例如以类似于Tetrahedron2009,65,第748-751页和Journal of the American Chemical Society 2002,124,第13097-13105页中所记载的方法,由式(XX)的化合物经氢化或亲核取代来制备。
该反应可以在减压下、在大气压下或在高压下并且在0℃至200℃的温度下进行。
步骤e)
式(XVaa)的化合物可商购获得或可通过已知的方法,以类似于Tetrahedron2009,65,第748-751页中所记载的方法,由式(XXI)的化合物来制备,例如在作为溶剂的四氢呋喃中使用叔丁醇钾作为碱,然后使用酸性条件,例如甲醇中的盐酸。
该反应可以在减压下、在大气压下或在高压下并且在0℃至200℃的温度下进行。
步骤f)
式(XXII)的化合物可通过已知的方法,以类似于European Journal of OrganicChemistry 2013,第4174-4180页和Organic Process Research and Development 2001,5,第572-574页中所记载的方法,由式(XVaa)的化合物经羰基化来合成。可以在过渡金属催化或非催化条件下,使用二氧化碳或金属烷基碳酸盐作为亲电试剂来进行官能化。
该反应可以在减压下、在大气压下或在高压下并且在0℃至200℃的温度下进行。
步骤g)
式(XXIII)的化合物可商购获得或可通过已知的方法,以类似于EP 1491531中所记载的方法,由式(XXII)的化合物来制备,例如在作为溶剂的四氢呋喃中使用六甲基二硅基胺基锂作为碱和N-氟苯磺酰胺作为亲电试剂。
该反应可以在减压下、在大气压下或在高压下并且在0℃至200℃的温度下进行。
步骤h)
式(XXIV)的化合物可通过已知的方法,例如以类似于WO 2015/024878,Synthesis1986,第770-772页和WO 2015/176267中所记载的方法,由式(XXIII)的化合物经还原或卤化来制备。
该反应可以在减压下、在大气压下或在高压下并且在-20℃至200℃的温度下进行。
步骤i)和j)
式(IIIaa)或(IIIa)的化合物可通过已知的方法由式(XXIII)或(XXIV)的化合物在酸性、碱性、热或氢解条件下经酯水解来制备。
方法F
具有结构单元A5、A6、A9、A10、A13或A14的式(IIIb)的羧酸(Ab表示=N-、-S(O)m-、-N(R15)-或=C(R2)-,且Ad表示=N-、-S(O)m-、-N(R15)-或=C(R8)-)可通过以下方法制备:
基团R2、R3、R7、R8和R15具有上文所述的含义。Ab表示=N-、-S(O)m、-N(R15)-或=C(R2)-。Ad表示=N-、-S(O)m-、-N(R15)-或=C(R8)-。X1表示卤素或三氟甲磺酸根。X2表示卤素。R16表示(C1-C4)-烷基。
步骤a)
式(XXVI)的化合物可商购获得或可通过已知的方法,以类似于US 2006/0199836中所记载的方法,由式(XXV)的化合物经氧化来合成,例如在作为溶剂的水中使用碳酸钾作为氧化剂。
式(XXV)的化合物可商购获得。
该反应可以在减压下、在大气压下或在高压下并且在0℃至200℃的温度下进行。
步骤b)
式(XXVII)的化合物可商购获得或可通过已知的方法,以类似于US 2006/0199836中所记载的方法,由式(XXVI)的化合物经酯化来合成,例如在作为溶剂的R16-OH中使用氯化亚砜。
该反应可以在减压下、在大气压下或在高压下并且在0℃至200℃的温度下进行。
步骤c)
式(XXVIII)的化合物可商购获得或可通过已知的方法,以类似于US 2006/0199836和US 2008/0004309中所记载的方法,由式(XXVII)的化合物来制备,例如在甲醇中使用氢氧化钠。
该反应可以在减压下、在大气压下或在高压下并且在0℃至200℃的温度下进行。
步骤d)
式(XXX)的化合物可商购获得或可通过已知的方法,以类似于US 2006/0199836和US 2008/0004309中所记载的方法,利用式(XXIX)的化合物使式(XXVIII)的化合物酰胺化来合成,例如使用乙二酰氯作为用于羧酸的活化剂和三乙胺作为碱。
式(XXIX)的化合物可商购获得。
该反应可以在减压下、在大气压下或在高压下并且在0℃至200℃的温度下进行。
步骤e)
式(XXXI)的化合物可商购获得或可通过已知的方法,以类似于US 2006/0199836和US 2008/0004309中所记载的方法,由式(XXX)的化合物经酰胺化来合成,例如在乙醇中使用乙醇钠。
该反应可以在减压下、在大气压下或在高压下并且在0℃至200℃的温度下进行。
步骤f)
式(XXXII)的化合物可商购获得或可通过已知的方法,以类似于US 2006/0199836和US 2008/0004309中所记载的方法,由式(XXXI)的化合物经卤化来合成,例如使用三氯氧化磷或三溴氧化磷。
该反应可以在减压下、在大气压下或在高压下并且在0℃至200℃的温度下进行。
步骤g)
式(XXXIII)的化合物可商购获得或可通过已知的方法,以类似于US 2006/0199836和US 2008/0004309中所记载的方法,由式(XXII)的化合物经氢化、Suzuki偶联或Stille偶联来合成,例如在作为溶剂的乙酸乙酯中使用负载在活性炭上的钯以及氢气,或者在作为溶剂的1,4-二氧六环或N,N-二甲基甲酰胺中使用R7-B(OH)2或Sn(R7)4、四(三苯基膦)钯(0)或双(三苯基膦)二氯化钯(II)作为催化剂和碳酸铯作为碱。
该反应可以在减压下、在大气压下或在高压下并且在0℃至200℃的温度下进行。
步骤h)
式(XXXIV)的化合物可商购获得或可通过已知的方法,以类似于WO 2005/103003中所记载的方法,由式(XXXIII)的化合物来制备,例如在作为溶剂的二氯甲烷中使用三氟甲磺酸酐和三乙胺。
该反应可以在减压下、在大气压下或在高压下并且在0℃至200℃的温度下进行。
步骤i)
式(IIIb)的化合物可商购获得或可通过已知的方法由式(XXXIV)的化合物在酸性、碱性、热或氢解条件下经酯水解来制备。
方法G
具有结构单元A11或A12的式(IIIc)的羧酸(Ab表示=N-或-N(R15)-且Ad表示=N-或-N(R15)-)可商购获得或可通过以下方法制备:
基团R3、R7和R15具有上文所述的含义。Ab表示=N-或-N(R15)-。Ad表示=N-或-N(R15)-。X1和X2表示卤素。R16表示(C1-C4)-烷基或芳基-(C1-C2)-烷基。
步骤a)
式(XXXVI)的化合物可商购获得或可通过已知的方法,以类似于WO 2013/007765中所记载的方法,由式(XXXV)的化合物来制备,例如在硫酸中使用硝酸钾。
式(XXXV)的化合物可商购获得。
该反应可以在减压下、在大气压下或在高压下并且在0℃至200℃的温度下进行。
步骤b)
式(XXXVII)的化合物可商购获得或可通过已知的方法,以类似于TetrahedronLetters 2013,54,第4054-4057页和Medicinal Chemical Communications 2013,第709-719页中所记载的方法,由式(XXVI)的化合物经还原来合成,例如在作为溶剂的甲醇、乙醇或乙酸乙酯中使用铁和乙酸。
该反应可以在减压下、在大气压下或在高压下并且在0℃至200℃的温度下进行。
步骤c)
式(XVc)的化合物(其中R15表示氢)可商购获得或可通过已知的方法以类似于Bioorganic Medicinal Chemistry 2012,第1644-1658页中所记载的方法,由式(XXXVII)的化合物经环化来合成。可使用酸R3-COOH或这类酸的类似物(如酸酐、酰氯、原酸酯)在酸性条件下来进行官能化。
该反应可以在减压下、在大气压下或在高压下并且在0℃至200℃的温度下进行。
步骤d)
式(XVc)的化合物可商购获得或可通过已知的方法,以类似于WO 2005/111047、WO2008/59238或WO 2009/16119中所记载的方法,由式(XVc)的化合物(其中R15表示氢)来制备,例如在作为溶剂的二甲基甲酰胺或二甲基亚砜中使用碱金属氢氧化物如氢氧化钠或无机碱如碳酸钾,以及式R15-X3的烷基化试剂如碘甲烷、溴乙烷或硫酸二甲酯。
步骤e)
式(XXXVIII)的化合物可商购获得或可通过已知的方法,以类似于EuropeanJournal of Organic Chemistry 2013,第4174-4180页和Organic Process Research andDevelopment 2001,5,第572-574页中所记载的方法,由式(XVc)的化合物经羰基化来合成。可在过渡金属催化或非催化条件下,使用二氧化碳或金属烷基碳酸盐作为亲电试剂来进行官能化。
该反应可以在减压下、在大气压下或在高压下并且在0℃至200℃的温度下进行。
步骤f)
式(IIIc)的化合物可商购获得或可通过已知的方法由式(XXXVIII)的化合物在酸性、碱性、热或氢解条件下经酯水解来制备。
方法H
式(I)的化合物(其中Q表示Q1至Q9或Q16或Q19)可通过已知的方法来制备,例如类似于WO 2009/131237、WO 2010/125985、WO 2011/043404、WO 2011/040629、WO 2012/086848、WO 2013/018928、WO 2015/000715和WO 2015/121136中所记载的方法。
基团R1、R4、R5、R6、Aa、Ab、Ac、Ad和n具有上文所述的含义,A2和A3表示CH或N,A4表示O、S或N-R4,X1表示卤素或三氟甲磺酸根,且R16表示(C1-C4)-烷基或芳基-(C1-C2)-烷基。
步骤a)
式(XL)的化合物可通过在碱的存在下,使式(XXXIX)的化合物与式(VIa)的化合物反应来制备。
式(XXXIX)的酯可商购获得或可通过已知的方法制备。可能的制备路线记载于方法E至G中。
式(VIa)的硫醇衍生物,例如甲硫醇、乙硫醇或异丙硫醇可商购获得或者可以通过已知方法制备,例如类似于US 2006/25633、US 2006/111591、US 2820062、ChemicalCommunications 2000,13,第1163-1164页或Journal of the American ChemicalSociety,1922,44,第1329页中所记载的方法。
转化为式(XL)的化合物可以在无溶剂下或在溶剂中进行,优选在选自常规溶剂的溶剂中进行反应,所述常规溶剂在反应条件下呈惰性。优选醚类,例如二异丙基醚、二氧六环、四氢呋喃、1,2-二甲氧基乙烷、叔丁基甲基醚;腈类,例如乙腈或丙腈;芳族烃类,例如甲苯或二甲苯;非质子极性溶剂,例如N,N-二甲基甲酰胺、N-甲基吡咯烷酮或二甲基亚砜。
合适的碱的实例为选自碱金属或碱土金属的乙酸盐、磷酸盐和碳酸盐的无机碱。在本文中优选碳酸铯、碳酸钠和碳酸钾。其他合适的碱是碱金属氢化物,例如氢化钠。
该反应可以在减压下、在大气压下或在高压下并且在0℃至200℃的温度下进行。
在所述反应中,X1优选表示氟或氯原子。
或者,式(XL)的化合物还可以以一步法制备,例如以类似于US2008/0171732中所记载的方法,由(XXXIX)式的化合物开始,通过利用式(VIa)的化合物进行卤素-硫交换来制备。所述交换通常在溶剂中进行。优选使用极性非质子溶剂,例如二甲基亚砜和N,N-二甲基甲酰胺。
该反应可以在减压下、在大气压下或在高压下并且在-20℃至120℃的温度下进行。
在所述反应中,X1优选表示溴原子或三氟甲磺酸根。
步骤b)
式(XLI)的化合物可商购获得或可通过已知的方法由式(XL)的化合物在酸性、碱性、热或氢解条件下经酯水解来制备。
步骤c)
式(XLII)的化合物可以类似于US 5576335中所记载的方法,通过使式(II)的化合物与式(XLI)的羧酸在缩合剂或碱的存在下反应来制备。
式(II)的化合物可商购获得或可通过已知方法制备,例如类似于US 2003/69257、WO 2006/65703、WO 2009/131237、WO 2010/125985、WO 2011/043404、WO 2011/040629、WO2012/086848、WO 2013/018928或WO 2015/000715中所记载的方法。
式(II)的化合物与式(XLI)的羧酸的反应可以在无溶剂下或在溶剂中进行,优选在选自常规溶剂的溶剂中进行反应,所述常规溶剂在反应条件下呈惰性。优选醚类,例如二异丙基醚、二氧六环、四氢呋喃、1,2-二甲氧基乙烷;卤代烃类,例如二氯甲烷、氯仿、四氯化碳、1,2-二氯乙烷或氯苯;腈类,例如乙腈或丙腈;芳族烃类,例如甲苯或二甲苯;非质子极性溶剂,例如N,N-二甲基甲酰胺或N-甲基吡咯烷酮,或含氮化合物,例如吡啶。
合适的缩合剂为例如碳二亚胺,例如1-(3-二甲基氨基丙基)-3-乙基碳二亚胺盐酸盐(EDCI)或1,3-二环己基碳二亚胺。
合适的碱为通常用于这类反应的无机碱。优选使用选自以下的碱:例如,碱金属或碱土金属的乙酸盐、磷酸盐、碳酸盐和碳酸氢盐。在本文中,特别优选乙酸钠、磷酸钠、磷酸钾、碳酸铯、碳酸钠、碳酸钾、碳酸氢钠、碳酸氢钾。
该反应可以在减压下、在大气压下或在高压下并且在0℃至180℃的温度下进行;其中优选地,该反应在大气压力下和在20至140℃的温度下进行。
步骤d)
式(I)的化合物(其中n表示0)可以通过将式(XLII)的化合物进行缩合来制备,例如类似于WO 2009/131237、WO 2010/125985、WO 2011/043404、WO 2011/040629、WO 2012/086848、WO 2013/018928、WO 2015/000715和WO 2015/121136中所记载的方法。
转化为式(I)的化合物(其中n表示0)可以在无溶剂下或在溶剂中进行,优选在选自常规溶剂的溶剂中进行反应,所述常规溶剂在反应条件下呈惰性。优选醚类,例如二异丙基醚、二氧六环、四氢呋喃、1,2-二甲氧基乙烷、叔丁基甲基醚;卤代烃类,例如二氯甲烷、氯仿、四氯化碳、1,2-二氯乙烷或氯苯;腈类,例如乙腈或丙腈;芳族烃类,例如甲苯或二甲苯;非质子极性溶剂,例如N,N-二甲基甲酰胺或N-甲基吡咯烷酮,或含氮化合物,例如吡啶。
该反应可以在缩合剂、酸、碱或氯化剂的存在下进行。
合适的缩合剂的实例为碳二亚胺,例如1-(3-二甲基氨基丙基)-3-乙基碳二亚胺盐酸盐(EDCI)或1,3-二环己基碳二亚胺;酸酐,例如乙酸酐、三氟乙酸酐;三苯基膦、碱和四氯化碳的混合物,或三苯基膦和偶氮二酯(例如偶氮二羧酸二乙酯)的混合物。
可用于所述反应的合适的酸的实例为磺酸,例如对甲苯磺酸;羧酸如乙酸,或多磷酸。
合适的碱的实例为含氮杂环类,例如吡啶、甲基吡啶、2,6-二甲基吡啶、1,8-二氮杂双环[5.4.0]-7-十一碳烯(DBU);叔胺,例如三乙胺和N,N-二异丙基乙胺;无机碱,例如磷酸钾、碳酸钾和氢化钠。
合适的氯化剂的实例为三氯氧化磷。
该反应可以在减压下、在大气压下或在高压下并且在0℃至200℃的温度下进行。
步骤e)
式(I)的化合物(其中n表示1)可通过氧化其中n表示0的式(I)的化合物来制备。通常在选自常规溶剂的溶剂中进行氧化,所述常规溶剂在反应条件下呈惰性。优选卤代烃类,例如二氯甲烷、氯仿、四氯化碳、1,2-二氯乙烷或氯苯;醇类,例如甲醇或乙醇;甲酸、乙酸、丙酸或水。
合适的氧化剂的实例为过氧化氢、间氯过氧苯甲酸或高碘酸钠。
该反应可以在减压下、在大气压下或在高压下并且在-20℃至120℃的温度下进行。
步骤f)
式(I)的化合物(其中n表示2)可通过氧化其中n表示1的式(I)的化合物来制备。通常在溶剂中进行氧化。优选卤代烃类,例如二氯甲烷、氯仿、四氯化碳、1,2-二氯乙烷或氯苯;醇类,例如甲醇或乙醇;甲酸、乙酸、丙酸或水。
合适的氧化剂的实例为过氧化氢和间氯过氧苯甲酸。
该反应可以在减压下、在大气压下或在高压下并且在-20℃至120℃的温度下进行。
步骤g)
式(I)的化合物(其中n表示2)还可以以一步法通过氧化其中n表示0的式(I)的化合物来制备。通常在溶剂中进行氧化。优选卤代烃类,例如二氯甲烷、氯仿、四氯化碳、1,2-二氯乙烷或氯苯;醇类,例如甲醇或乙醇;甲酸、乙酸、丙酸或水。
合适的氧化剂的实例为过氧化氢和间氯过氧苯甲酸。
该反应可以在减压下、在大气压下或在高压下并且在-20℃至120℃的温度下进行。
方法和用途
本发明还涉及防治动物害虫的方法,其中将式(I)的化合物作用于动物害虫和/或它们的生境。动物害虫的防治优选在农业和林业中、以及在材料保护中进行。这优选排除用于人体或动物体的外科或治疗处理的方法以及在人体或动物体上进行的诊断方法。
本发明还涉及式(I)的化合物作为农药的用途,尤其是作为作物保护剂的用途。
在本申请的上下文中,术语“农药”在每种情况下还总是涵盖术语“作物保护组合物”。
鉴于良好的植物耐受性、有利的恒温动物毒性和良好的环境相容性,式(I)的化合物适用于:保护植物和植物器官抵抗生物和非生物胁迫因素、提高采收产率、改善采收材料的品质,以及防治在农业、园艺、畜牧业、水产养殖业、林业、园林和休闲设施中、储存产品和材料的保护中以及卫生领域中遇到的动物害虫,尤其是昆虫、蛛形纲动物、蠕虫、尤其是线虫和软体动物。
在本专利申请的上下文中,术语“卫生”应理解为意指旨在预防疾病——特别是感染性疾病——并且用于保护人类和动物的健康和/或保护环境和/或保持清洁的任何和全部的措施、预防措施和方法。根据本发明,这特别地包括用于清洁、消毒和灭菌例如纺织品或硬表面(特别是由玻璃、木材、水泥、瓷器、陶瓷、塑料或金属制成的表面)以确保它们免受卫生害虫和/或它们的分泌物的措施。在这方面,本发明的保护范围优选排除应用于人体或动物体的外科处理或治疗处理的方法以及在人体或动物体上进行的诊断方法。
术语“卫生领域”涵盖其中这些卫生措施、预防措施和方法是重要的所有区域、技术领域和工业应用,例如在厨房、面包房、机场、浴场、游泳池、百货商店、酒店、医院、畜栏、动物饲养等中的卫生。
因此,术语“卫生害虫”应理解为意指一种或多种这样的动物害虫:其在卫生领域中的存在是有问题的,特别是出于健康原因。因此,主要目的是避免卫生害虫的存在和/或在卫生领域中对这些害虫的暴露,或将它们限制在最小的程度。这尤其可以通过使用既可以用于预防感染也可以用于预防已存在的感染的农药来实现。还可以使用预防或减少对害虫的暴露的制剂。例如,卫生害虫包括下文提及的生物体。
因此,术语“卫生保护”涵盖维持和/或改善这些卫生措施、预防措施和方法的所有行为。
式(I)的化合物可优选用作农药。它们对于通常敏感性和抗性的物种以及对于发育的全部或某些阶段均具有活性。上述害虫包括:
节肢动物门(Arthropoda)、尤其是蛛形纲(Arachnida)的害虫,例如粉螨属(例如粗脚粉螨(Acarus siro)、枸杞瘤瘿螨(Aceria kuko)、柑橘瘤瘿螨(Aceria sheldoni))、刺皮瘿螨属(Aculops spp.)、针刺瘿螨属(Aculus spp.)(例如佛氏刺瘿螨(Aculusfockeui)、苹果刺瘿螨(Aculus schlechtendali))、花蜱属(Amblyomma spp.)、山楂叶螨(Amphitetranychus viennensis)、锐缘蜱属(Argas spp.)、牛蜱属(Boophilus spp.)、短须螨属(Brevipalpus spp.)(例如紫红短须螨(Brevipalpus phoenicis))、蚜苔螨(Bryobia graminum)、苜蓿苔螨(Bryobia praetiosa)、刺尾蝎属(Centruroides spp.)、皮螨属(Chorioptes spp.)、鸡皮刺螨(Dermanyssus gallinae)、欧洲屋尘螨(Dermatophagoides pteronyssinus)、美洲屋尘螨(Dermatophagoides farinae)、革蜱属(Dermacentor spp.)、始叶螨属(Eotetranychus spp.)(例如核桃始叶螨(Eotetranychushicoriae))、梨上瘿螨(Epitrimerus pyri)、真叶螨属(Eutetranychus spp.)(例如班氏真叶螨(Eutetranychus banksi))、瘿螨属(Eriophyes spp.)(例如梨瘿螨(Eriophyespyri))、家甜食螨(Glycyphagus domesticus)、红足海镰螯螨(Halotydeus destructor)、半跗线螨属(Hemitarsonemus spp.)(例如茶半跗线螨(Hemitarsonemus latus)(=侧多食跗线螨(Polyphagotarsonemus latus)))、璃眼蜱属(Hyalomma spp.)、硬蜱属(Ixodesspp.)、毒蛛属(Latrodectus spp.)、斜蛛属(Loxosceles spp.)、秋收恙螨(Neutrombiculaautumnalis)、Nuphersa属、小爪螨属(Oligonychus spp.)(例如跗线螨(Oligonychuscoffeae)、Oligonychus coniferarum、冬青小爪螨(Oligonychus ilicis)、甘蔗小爪螨(Oligonychus indicus)、芒果小爪螨(Oligonychus mangiferus)、草地小爪螨(Oligonychus pratensis)、石榴小爪螨(Oligonychus punicae)、樟小爪螨(Oligonychusyothersi))、钝缘蜱属(Ornithodorus spp)、禽刺螨属(Ornithonyssus spp.)、全爪螨属(Panonychus spp.)(例如柑桔全爪螨(Panonychus citri(=Metatetranychus citri))、苹果全爪螨(Panonychus ulmi(=Metatetranychus ulmi)))、柑桔锈螨(Phyllocoptrutaoleivora)、多趾宽叶螨(Platytetranychus multidigituli)、侧多食跗线螨(Polyphagotarsonemus latus)、痒螨属(Psoroptes spp.)、扇头蜱属(Rhipicephalusspp.)、根螨属(Rhizoglyphus spp.)、疥螨属(Sarcoptes spp.)、中东金蝎(Scorpiomaurus)、狭跗线螨种(Stenotarsonemus spp.)、稻细螨(Steneotarsonemus spinki)、跗线螨属(Tarsonemus spp.)(例如乱跗线螨(Tarsonemus confusus)、樱草狭跗线螨(Tarsonemus pallidus))、叶螨属(Tetranychus spp.)(例如加拿大叶螨(Tetranychuscanadensis)、朱砂叶螨(Tetranychus cinnabarinus)、土耳其斯坦叶螨(Tetranychusturkestani)、二斑叶螨(Tetranychus urticae))、阿氏真恙螨(Trombiculaalfreddugesi)、Vaejovis属、番茄斜背瘤瘿螨(Vasates lycopersici);
唇足纲(Chilopoda)的害虫,例如,地蜈蚣属(Geophilus spp.)、蚰蜓属(Scutigera spp.);
弹尾目或弹尾纲(Collembola)的害虫,例如,武装棘跳虫(Onychiurus armatus);绿圆跳虫(Sminthurus viridis);
倍足纲(Diplopoda)的害虫,例如,千足虫(Blaniulus guttulatus);
昆虫纲的害虫,例如蜚蠊目(Blattodea),如东方蜚蠊(Blatta orientalis)、亚洲蜚蠊(Blattella asahinai)、德国小蠊(Blattella germanica)、马德拉蜚蠊(Leucophaeamaderae)、Loboptera decipiens、家屋斑蠊(Neostylopyga rhombifolia)、古巴蠊属(Panchlora spp.)、木蠊属(Parcoblatta spp.)、大蠊属(Periplaneta spp.)(例如美洲大蠊(Periplaneta americana)、澳洲大蠊(Periplaneta australasiae))、蔗蠊(Pycnoscelus surinamensis)、棕带蜚蠊(Supella longipalpa);
鞘翅目(Coleoptera)的害虫,例如,条纹南瓜甲(Acalymma vittatum)、菜豆象(Acanthoscelides obtectus)、喙丽金龟属(Adoretus spp.)、小蜂窝甲虫(Aethinatumida)、杨树萤叶甲(Agelastica alni)、叩甲属(Agriotes spp.)(例如直条叩头虫(Agriotes linneatus)、小麦叩头虫(Agriotes mancus))、黑菌虫(Alphitobiusdiaperinus)、马铃薯鳃角金龟(Amphimallon solstitialis)、家具窃蠹(Anobiumpunctatum)、星天牛属(Anoplophora spp.)、花象属(Anthonomus spp.)(例如棉铃象甲(Anthonomus grandis))、圆皮蠹属(Anthrenus spp.)、梨象属(Apion spp.)、阿鳃金龟属(Apogonia spp.)、隐食甲属(Atomaria spp.)(例如甜菜隐食甲(Atomaria linearis))、毛皮蠹属(Attagenus spp.)、Baris caerulescens、恶条豆象(Bruchidius obtectus)、豆象属(Bruchus spp.)(例如豌豆象(Bruchus pisorum)、蚕豆象(Bruchus rufimanus))、龟叶甲属(Cassida spp.)、菜豆莹叶甲(Cerotoma trifurcata)、龟象属(Ceuthorhynchusspp.)(例如白菜籽龟象(Ceutorrhynchus assimilis)、甘蓝茎龟象(Ceutorrhynchusquadridens)、白菜龟象(Ceutorrhynchus rapae))、跳甲属(Chaetocnema spp.)(例如甘薯跳甲(Chaetocnema confinis)、美国齿跳甲(Chaetocnema denticulata)、荒地玉米跳甲(Chaetocnema ectypa))、Cleonus mendicus、宽胸叩头虫属(Conoderus spp.)、根颈象属(Cosmopolites spp.)(例如香蕉根颈象甲(Cosmopolites sordidus))、褐新西兰肋翅鳃角金龟(Costelytra zealandica)、叩甲属(Ctenicera spp.)、象虫属(Curculio spp.)(例如美核桃象(Curculio caryae)、大栗象(Curculio caryatrypes)、美洲榛子象(Curculioobtusus)、小栗象(Curculio sayi))、锈赤扁谷盗(Cryptolestes ferrugineus)、长角扁谷盗(Cryptolestes pusillus)、杨干隐喙(Cryptorhynchus lapathi)、芒果果核象甲(Cryptorhynchus mangiferae)、细枝象属(Cylindrocopturus spp.)、密点细枝象(Cylindrocopturus adspersus)、洋松细枝象(Cylindrocopturus furnissi)、皮蠹属(Dermestes spp.)、叶甲属(Diabrotica spp.)(例如带斑黄瓜条叶甲(Diabroticabalteata)、北方玉米根叶甲(Diabrotica barberi)、南方十一星瓜叶甲(Diabroticaundecimpunctata howardi)、南方十一星瓜叶甲亚种(Diabrotica undecimpunctataundecimpunctata)、西方玉米根叶甲(Diabrotica virgifera virgifera)、墨西哥玉米根叶甲(Diabrotica virgifera zeae))、蛀野螟属(Dichocrocis spp.)、水稻铁甲(Dicladispa armigera)、Diloboderus属、Epicaerus属、食植瓢虫属(Epilachna spp.)(例如瓜食植瓢虫(Epilachna borealis)、墨西哥豆瓢虫(Epilachna varivestis))、毛跳甲属(Epitrix spp.)(例如黄瓜跳甲(Epitrix cucumeris)、茄子跳甲(Epitrix fuscula)、烟草跳甲(Epitrix hirtipennis)、美国马铃薯跳甲(Epitrix subcrinita)、块茎跳甲(Epitrixtuberis))、钻孔虫属(Faustinus spp.)、裸蛛甲(Gibbium psylloides)、阔角谷盗(Gnathocerus cornutus)、菜心野螟(Hellula undalis)、黑异爪蔗金龟(Heteronychusarator)、寡节鳃金龟属(Heteronyx spp.)、Hylamorpha elegans、北美家天牛(Hylotrupesbajulus)、紫苜蓿叶象(Hypera postica)、蓝绿象(Hypomeces squamosus)、咪小蠹属(Hypothenemus spp.)(例如咖啡果小蠹(Hypothenemus hampei)、苹枝小囊(Hypothenemusobscurus)、毛竹小蠹(Hypothenemus pubescens))、甘蔗大褐齿爪鳃金龟(Lachnosternaconsanguinea)、烟草甲(Lasioderma serricorne)、长头谷盗(Latheticus oryzae)、波缘薪甲属(Lathridius spp.)、负泥虫属(Lema spp.)、马铃薯甲虫(Leptinotarsadecemlineata)、潜叶蛾属(Leucoptera spp.)(例如咖啡潜叶蛾(Leucopteracoffeella))、稻根象(Lissorhoptrus oryzophilus)、Listronotus(=Hyperodes)属、筒喙象属(Lixus spp.)、Luperodes属、黄胸寡毛跳甲(Luperomorpha xanthodera)、粉蠹属(Lyctus spp.)、美洲叶甲属(Megascelis spp.)、梳爪叩头虫属(Melanotus spp.)(例如Melanotus longulus oregonensis)、油菜花露尾甲(Meligethes aeneus)、鳃金龟属(Melolontha spp.)(例如欧洲鳃金龟(Melolontha melolontha))、Migdolus属、墨天牛属(Monochamus spp.)、象甲(Naupactus xanthographus)、隐跗郭公虫属(Necrobia spp.)、Neogalerucella属、黄蛛甲(Niptus hololeucus)、椰蛀犀金龟(Oryctes rhinoceros)、锯谷盗(Oryzaephilus surinamensis)、Oryzaphagus oryzae、耳喙象属(Otiorrhynchusspp.)(例如苹果耳喙象(Otiorhynchus cribricollis)、苜蓿耳喙象(Otiorhynchusligustici)、草莓耳喙象(Otiorhynchus ovatus)、粗糙草莓耳喙象(Otiorhynchusrugosostriarus)、黑葡萄耳喙象(Otiorhynchus sulcatus))、负泥虫属(Oulema spp.)(例如橙足负泥虫(Oulema melanopus)、稻负泥虫(Oulema oryzae))、小青花金龟(Oxycetoniajucunda)、辣根猿叶虫(Phaedon cochleariae)、食叶鳃金龟属(Phyllophaga spp.)、鳃金龟(Phyllophaga helleri)、黄条跳甲属(Phyllotreta spp.)(例如辣根条跳甲(Phyllotreta armoraciae)、西方黑跳甲(Phyllotreta pusilla)、美条纹跳甲(Phyllotreta ramosa)、黄曲条跳甲(Phyllotreta striolata))、日本弧丽金龟(Popilliajaponica)、象甲属(Premnotrypes spp.)、大谷蠹(Prostephanus truncatus)、跳甲属(Psylliodes spp.)(例如马铃薯跳甲(Psylliodes affinis)、油菜兰跳甲(Psylliodeschrysocephala)、忽布跳甲(Psylliodes punctulata))、蛛甲属(Ptinus spp.)、暗色瓢虫(Rhizobius ventralis)、谷蠹(Rhizopertha dominica)、隐喙象属(Rhynchophorusspp.)、红棕象甲(Rhynchophorus ferrugineus)、棕榈象甲(Rhynchophorus palmarum)、Sinoxylon perforans、谷象属(Sitophilus spp.)(例如谷象(Sitophilus granarius)、罗望子象(Sitophilus linearis)、米象(Sitophilus oryzae)、玉米象(Sitophiluszeamais))、尖隐喙象属(Sphenophorus spp.)、药材甲(Stegobium paniceum)、茎干象属(Sternechus spp.)(例如豆茎象(Sternechus paludatus))、宽幅天牛属(Symphyletesspp.)、纤毛象属(Tanymecus spp.)(例如双宽隆突纤毛象(Tanymecus dilaticollis)、印度纤毛象(Tanymecus indicus)、红豆草灰象甲(Tanymecus palliatus))、黄粉虫(Tenebrio molitor)、大谷盗(Tenebrioides mauretanicus)、拟谷盗属(Tribolium spp.)(例如美洲黑拟谷盗(Tribolium audax)、赤拟谷盗(Tribolium castaneum)、杂拟谷盗(Tribolium confusum))、斑皮蠹属(Trogoderma spp.)、籽象属(Tychius spp.)、脊虎天牛属(Xylotrechus spp.)、距步甲属(Zabrus spp.)(例如玉米距步甲(Zabrustenebrioides));
革翅目(Dermaptera)的害虫,例如,肥螋(Anisolabis maritime)、欧洲球螋(Forficula auricularia)、溪岸蠼螋(Labidura riparia);
双翅目(Diptera)的害虫,例如,伊蚊属(Aedes spp.)(例如埃及伊蚊(Aedesaegypti)、白纹伊蚊(Aedes albopictus)、叮刺伊蚊(Aedes sticticus)、骚扰伊蚊(Aedesvexans))、潜蝇属(Agromyza spp.)(例如苜蓿斑潜蝇(Agromyza frontella)、美洲黍潜蝇(Agromyza parvicornis))、按实蝇属(Anastrepha spp.)、按蚊属(Anopheles spp.)(例如四斑按蚊(Anopheles quadrimaculatus)、冈比亚按蚊(Anopheles gambiae))、瘿蚊属(Asphondylia spp.)、果实蝇属(Bactrocera spp.)(例如瓜实蝇(Bactroceracucurbitae)、东方果实蝇(Bactrocera dorsalis)、油橄榄果实蝇(Bactrocera oleae))、花园毛蚊(Bibio hortulanus)、天青丽蝇(Calliphora erythrocephala)、红头丽蝇(Calliphora vicina)、地中海实蝇(Ceratitis capitata)、摇蚊属(Chironomus spp.)、金蝇属(Chrysomya spp.)、斑虻属(Chrysops spp.)、高额麻虻(Chrysozona pluvialis)、锥蝇属(Cochliomya spp.)、康瘿蚊属(Contarinia spp.)(例如葡萄瘿蚊(Contariniajohnsoni)、甘蓝瘿蚊(Contarinia nasturtii)、梨实康瘿蚊(Contarinia pyrivora)、向日葵瘿蚊(Contarinia schulzi)、高粱康瘿蚊(Contarinia sorghicola)、麦黄康癭蚊(Contarinia tritici))、人皮蝇(Cordylobia anthropophaga)、环足摇蚊(Cricotopussylvestris)、库蚊属(Culex spp.)(例如尖音库蚊(Culex pipiens)、致乏库蚊(Culexquinquefasciatus))、库蠓属(Culicoides spp.)、脉毛蚊属(Culiseta spp.)、黄蝇属(Cuterebra spp.)、橄榄大实蝇(Dacus oleae)、叶瘿蚊属(Dasyneura spp.)(例如油菜叶瘿蚊(Dasineura brassicae))、地种蝇属(Delia spp.)(例如葱蝇(Delia antiqua)、麦种蝇(Delia coarctata)、毛跗地种蝇(Delia florilega)、灰地种蝇(Delia platura)、甘蓝地种蝇(Delia radicum))、人肤蝇(Dermatobia hominis)、果蝇属(Drosophila spp.)(例如黑腹果蝇(Drosphila melanogaster)、樱桃果蝇(Drosophila suzukii))、稻象属(Echinocnemus spp.)、Euleia heraclei、厕蝇属(Fannia spp.)、胃蝇属(Gastrophilusspp.)、舌蝇属(Glossina spp.)、麻虻属(Haematopota spp.)、毛眼水蝇属(Hydrelliaspp.)、大麦毛眼水蝇(Hydrellia griseola)、黑蝇属(Hylemya spp.)、虱蝇属(Hippoboscaspp.)、皮蝇属(Hypoderma spp.)、斑潜蝇属(Liriomyza spp.)(例如菜斑潜蝇(Liriomyzabrassicae)、南美斑潜蝇(Liriomyza huidobrensis)、美洲斑潜蝇(Liriomyza sativae))、绿蝇属(Lucilia spp.)(例如铜绿蝇(Lucilia cuprina))、罗蛉属(Lutzomyia spp.)、曼蚊属(Mansonia spp.)、家蝇属(Musca spp.)(例如家蝇(Musca domestica)、舍蝇(Muscadomestica vicina))、狂蝇属(Oestrus spp.)、瑞典麦秆蝇(Oscinella frit)、拟长跑摇蚊属(Paratanytarsus spp.)、Paralauterborniella subcincta、泉蝇属(Pegomya或Pegomyia spp.)(例如甜菜泉蝇(Pegomya betae)、天仙子泉蝇(Pegomya hyoscyami)、悬钩子泉蝇(Pegomya rubivora))、白蛉属(Phlebotomus spp.)、草种蝇属(Phorbia spp.)、伏蝇属(Phormia spp.)、酪蝇(Piophila casei)、Platyparea poeciloptera、Prodiplosis属、胡萝卜茎蝇(Psila rosae)、绕实蝇属(Rhagoletis spp.)(例如东部樱桃实蝇(Rhagoletis cingulata)、核桃绕实蝇(Rhagoletis completa)、黑樱桃实蝇(Rhagoletisfausta)、西部樱桃实蝇(Rhagoletis indifferens)、越桔实蝇(Rhagoletis mendax)、苹果实蝇(Rhagoletis pomonella))、麻蝇属(Sarcophaga spp.)、蚋属(Simulium spp.)(例如南方蚋(Simulium meridionale))、螫蝇属(Stomoxys spp.)、虻属(Tabanus spp.)、根斑蝇属(Tetanops spp.)、大蚊属(Tipula spp.)(例如欧洲大蚊(Tipula paludosa)、牧场大蚊(Tipula simplex))、Toxotrypana curvicauda;
半翅目(Hemiptera)的害虫,例如Acizzia acaciaebaileyanae、Acizziadodonaeae、木虱(Acizzia uncatoides)、长头蝗(Acrida turrita)、无网长管蚜属(Acyrthosipon spp.)(例如豌豆长管蚜(Acyrthosiphon pisum))、Acrogonia属、Aeneolamia属、隆脉木虱属(Agonoscena spp.)、刺粉虱属(Aleurocanthus spp.)、欧洲甘蓝粉虱(Aleyrodes proletella)、蔗粉穴粉虱(Aleurolobus barodensis)、棉粉虱(Aleurothrixus floccosus)、植莲木风(Allocaridara malayensis)、芒果叶蝉属(Amrasca spp.)(例如小绿叶蝉(Amrasca bigutulla)、小叶蝉(Amrasca devastans))、圆尾蚜(Anuraphis cardui)、肾圆盾蚧属(Aonidiella spp.)(例如红肾圆盾蚧(Aonidiellaaurantii)、黄肾圆盾蚧(Aonidiella citrina)、苏铁肾盾蚧(Aonidiella inornata))、梨瘤蚜(Aphanostigma piri)、蚜属(Aphis spp)(例如绣线菊蚜(Aphis citricola)、黑豆蚜(Aphis craccivora)、甜菜蚜(Aphis fabae)、草莓根蚜(Aphis forbesi)、大豆蚜(Aphisglycines)、棉蚜(Aphis gossypii)、常春藤蚜(Aphis hederae)、葡萄藤蚜(Aphisillinoisensis)、Aphis middletoni、鼠李马铃薯蚜(Aphis nasturtii)、夹竹桃蚜(Aphisnerii)、苹果蚜(Aphis pomi)、卷叶蚜(Aphis spiraecola)、Aphis viburniphila)、葡萄叶蜂(Arboridia apicalis)、Arytainilla属、小圆盾蚧属(Aspidiella spp.)、圆盾蚧属(Aspidiotus spp.)(例如常春藤圆盾蚧(Aspidiotus nerii))、Atanus属、茄沟无网蚜(Aulacorthum solani)、烟粉虱(Bemisia tabaci)、澳大利亚木虱(Blastopsyllaoccidentalis)、Boreioglycaspis melaleucae、李短尾蚜(Brachycaudus helichrysii)、微管姆属(Brachycolus spp.)、甘蓝蚜(Brevicoryne brassicae)、喀木虱属(Cacopsyllaspp.)(例如梨木虱(Cacopsylla pyricola))、小褐稻虱(Calligypona marginata)、Capulinia属、丽黄头大叶蝉(Carneocephala fulgida)、甘蔗绵蚜(Ceratovacunalanigera)、沫蝉科(Cercopidae)、蜡蚧属(Ceroplastes spp.)、草莓钉蚜(Chaetosiphonfragaefolii)、蔗黄雪盾蚧(Chionaspis tegalensis)、茶绿叶蜂(Chlorita onukii)、台湾大蝗(Chondracris rosea)、核桃黑斑蚜(Chromaphis juglandicola)、黑褐圆盾蚧(Chrysomphalus aonidum)、黑褐圆盾蚧(Chrysomphalus ficus)、玉米叶蝉(Cicadulinambila)、Coccomytilus halli、软蚧属(Coccus spp.)(例如褐软蚧(Coccus hesperidum)、长椭圆软蚧(Coccus longulus)、桔软蜡蚧(Coccus pseudomagnoliarum)、咖啡绿蚧(Coccus viridis))、隐瘤蚜(Cryptomyzus ribis)、Cryptoneossa属、梳木风属(Ctenarytaina spp.)、黄翅叶蝶属(Dalbulus spp.)、Dialeurodes chittendeni、柑橘粉虱(Dialeurodes citri)、柑橘木虱(Diaphorina citri)、白背盾蚧属(Diaspis spp.)、Diuraphis属、Doralis属、履绵蚧属(Drosicha spp.)、西圆尾蚜属(Dysaphis spp.)(例如锈条蚜(Dysaphis apiifolia)、车前草蚜(Dysaphis plantaginea)、百合西圆尾蚜(Dysaphis tulipae))、灰粉蚧属(Dysmicoccus spp.)、小绿叶蝉属(Empoasca spp.)(例如西部马铃薯叶蝉(Empoasca abrupta)、蚕豆小叶蝉(Empoasca fabae)、苹果小绿叶蝉(Empoasca maligna)、茄微叶蝉(Empoasca solana)、Empoasca stevensi)、绵蚜属(Eriosoma spp.)(例如美洲绵蚜(Eriosoma americanum)、苹果绵蚜(Eriosomalanigerum)、梨根绵蚜(Eriosoma pyricola))、斑叶蝉属(Erythroneura spp.)、Eucalyptolyma属、褐木虱属(Euphyllura spp.)、殃叶蝉(Euscelis bilobatus)、拂粉阶属(Ferrisia spp.)、Fiorinia属、Furcaspis oceanica、咖啡地粉蚧(Geococcus coffeae)、Glycaspis属、银合欢木虱(Heteropsylla cubana)、颊木虱(Heteropsylla spinulosa)、假桃病毒叶蝉(Homalodisca coagulata)、梅大尾蚜(Hyalopterus arundinis)、桃大尾蚜(Hyalopterus pruni)、吹绵蚧属(Icerya spp.)(例如吹绵蚧壳虫(Icerya purchasi))、Idiocerus属、扁喙叶蝉属(Idioscopus spp.)、灰飞虱(Laodelphax striatellus)、蜡蚧属(Lecanium spp.)(例如水土坚蚧(Lecanium corni)(=Parthenolecanium corni))、盾蚧属(Lepidosaphes spp.)(例如榆蛎盾蚧(Lepidosaphes ulmi))、萝卜蚜(Lipaphiserysimi)、日本长白蚧(Lopholeucaspis japonica)、斑衣蜡蝉(Lycorma delicatula)、长管蚜属(Macrosiphum spp.)(例如马铃薯长管蚜(Macrosiphum euphorbiae)、百合长管蚜(Macrosiphum lilii)、蔷薇长管蚜(Macrosiphum rosae))、二点叶蜂(Macrostelesfacifrons)、沫蝶属(Mahanarva spp.)、高粱蚜(Melanaphis sacchari)、Metcalfiella属、Metcalfa pruinosa、麦无网蚜(Metopolophium dirhodum)、黑缘平翅斑蚜(Monelliacostalis)、Monelliopsis pecanis、瘤蚜属(Myzus spp.)(例如冬葱瘤蚜(Myzusascalonicus)、梅瘤蚜(Myzus cerasi)、女贞瘤蚜(Myzus ligustri)、堇菜瘤蚜(Myzusornatus)、桃蚜(Myzus persicae)、烟蚜(Myzus nicotianae))、莴苣衲长管蚜(Nasonoviaribisnigri)、Neomaskellia属、黑尾叶蝉属(Nephotettix spp.)(例如黑尾叶蝉(Nephotettix cincticeps)、二条黑尾叶蝉(Nephotettix nigropictus))、Nettigonicllaspectra、褐飞虱(Nilaparvata lugens)、Oncometopia属、Orthezia praelonga、中华稻蝗(Oxya chinensis)、Pachypsylla属、杨梅粉虱(Parabemisia myricae)、虱啮属(Paratrioza spp.)(例如马铃薯木虱(Paratrioza cockerelli))、片盾蚧属(Parlatoriaspp.)、瘿绵蚜属(Pemphigus spp.)(例如囊柄瘿绵蚜(Pemphigus bursarius)、Pemphiguspopulivenae)、玉米蜡蝉(Peregrinus maidis)、Perkinsiella属、绵粉蚧属(Phenacoccusspp.)(例如美地绵粉蚧(Phenacoccus madeirensis))、杨平翅绵蚜(Phloeomyzuspasserinii)、忽布疣蚜(Phorodon humuli)、葡萄根瘤蚜属(Phylloxera spp.)(例如Phylloxera devastatrix、警根瘤蚜(Phylloxera notabilis))、苏铁褐点并盾蚧(Pinnaspis aspidistrae)、臀纹粉蚧属(Planococcus spp.)(例如橘臀纹粉蚧(Planococcus citri))、Prosopidopsylla flava、梨形原绵腊蚧(Protopulvinariapyriformis)、桑白盾蚧(Pseudaulacaspis pentagona)、粉蚧属(Pseudococcus spp.)(例如柑栖粉蚧(Pseudococcus calceolariae)、康氏粉蚧(Pseudococcus comstocki)、拟长尾粉蚧(Pseudococcus longispinus)、葡萄粉蚧(Pseudococcus maritimus)、暗色粉蚧(Pseudococcus viburni))、Psyllopsis属、木虱属(Psylla spp.)(例如黄杨木虱(Psyllabuxi)、苹木虱(Psylla mali)、梨木虱(Psylla pyri))、金小蜂属(Pteromalus spp.)、桃绵蜡蚧(Pulvinaria spp.)、Pyrilla属、笠圆盾蚧属(Quadraspidiotus spp.)(例如胡桃园盾蚧(Quadraspidiotus juglansregiae)、杨笠圆盾蚧(Quadraspidiotus ostreaeformis)、梨笠盾蚧(Quadraspidiotus perniciosus))、Quesada gigas、平刺粉蚧属(Rastrococcusspp.)、缢管蚜属(Rhopalosiphum spp.)(例如玉米蚜(Rhopalosiphum maidis)、苹草缢管蚜(Rhopalosiphum oxyacanthae)、稻麦蚜(Rhopalosiphum padi)、红腹缢管蚜(Rhopalosiphum rufiabdominale))、黑盔蚧属(Saissetia spp.)(例如咖啡黑盔蚧(Saissetia coffeae)、Saissetia miranda、Saissetia neglecta、黑蜡蚧(Saissetiaoleae))、葡萄带叶蝉(Scaphoideus titanus)、麦二叉蚜(Schizaphis graminum)、苏铁刺圆盾蚧(Selenaspidus articulatus)、Sipha flava、麦长管蚜(Sitobion avenae)、长唇基飞虱属(Sogata spp.)、白背飞虱(Sogatella furcifera)、稻飞风属(Sogatodes spp.)、Stictocephala festina、树粉虱(Siphoninus phillyreae)、Tenalaphara malayensis、Tetragonocephela属、长斑蚜属(Tinocallis caryaefoliae)、广胸沫蝉属(Tomaspisspp.)、声蚜属(Toxoptera spp.)(例如小桔蚜(Toxoptera aurantii)、大桔蚜(Toxopteracitricidus))、温室粉虱(Trialeurodes vaporariorum)、尖翅木虱属(Trioza spp.)(例如柿木虱(Trioza diospyri))、小叶蝉属(Typhlocyba spp.)、尖盾蚧属(Unaspis spp.)、葡萄根瘤蚜(Viteus vitifolii)、么叶蝉属(Zygina spp.);
异翅亚目(Heteroptera)的害虫,例如,Aelia属、南瓜缘蝽(Anasa tristis)、拟丽蝽属(Antestiopsis spp.)、Boisea属、土长蝽属(Blissus spp.)、俊盲蝽属(Calocorisspp.)、斑腿微剌盲蝽(Campylomma livida)、异背长蝽属(Cavelerius spp.)、臭虫属(Cimex spp.)(例如Cimex adjunctus、热带臭虫(Cimex hemipterus)、温带臭虫(Cimexlectularius)、蝠臭虫(Cimex pilosellus))、白辧麦寄蝇属(Collaria spp.)、绿盲蝽(Creontiades dilutus)、胡椒缘蝽(Dasynus piperis)、Dichelops furcatus、厚氏长棒网蝽(Diconocoris hewetti)、棉红蝽属(Dysdercus spp.)、美洲蝽属(Euschistus spp.)(例如英雄美洲蝽(Euschistus heros)、褐美洲蝽(Euschistus servus)、三色美洲蝽(Euschistus tristigmus)、三点美洲蝽(Euschistus variolarius))、菜蝽属(Eurydemaspp.)、扁盾蝽属(Eurygaster spp.)、茶翅蝽(Halyomorpha halys)、盲蝽属(Heliopeltisspp.)、Horcias nobilellus、稻缘蝽属(Leptocorisa spp.)、异稻缘蝽(Leptocorisavaricornis)、西部喙缘蝽(Leptoglossus occidentalis)、叶缘缘蝽(Leptoglossusphyllopus)、丽盲蝽属(Lygocoris spp.)(例如原丽盲蝽(Lygocoris pabulinus))、草盲蝽属(Lygus spp.)(例如灰豆草盲蝽(Lygus elisus)、豆荚草盲蝽(Lygus hesperus)、美国牧草盲蝽(Lygus lineolaris))、蔗黑长蝽(Macropes excavatus)、Megacopta cribraria、Miridae、金光绿盲蝽(Monalonion atratum)、绿蝽属(Nezara spp.)(例如稻绿蝽(Nezaraviridula))、Nysius属、稻蝽属(Oebalus spp.)、Pentomidae、方背皮蝽(Piesmaquadrata)、璧蝽属(Piezodorus spp.)(例如盖德拟壁蝽(Piezodorus guildinii))、盲蝽属(Psallus spp.)、Pseudacysta persea、红猎蝽属(Rhodnius spp.)、可可褐盲蝽(Sahlbergella singularis)、Scaptocoris castanea、黑蝽属(Scotinophora spp.)、梨冠网蝽(Stephanitis nashi)、Tibraca属、锥猎蝽属(Triatoma spp.);
膜翅目(Hymenoptera)的害虫,例如,顶切叶蚁属(Acromyrmex spp.)、菜叶蜂属(Athalia spp.)(例如黄翅菜叶蜂(Athalia rosae))、美切叶蚁属(Atta spp.)、弓背蚁属(Camponotus spp.)、Dolichovespula属、松叶蜂属(Diprion spp.)(例如类欧松叶蜂(Diprion similis))、实叶蜂属(Hoplocampa spp.)(例如樱实叶蜂(Hoplocampa cookei)、苹叶蜂(Hoplocampa testudinea))、毛蚁属(Lasius spp.)、阿根廷蚁(Linepithema(Iridiomyrmex)humile)、小家蚁(Monomorium pharaonis)、立毛蚁属(Paratrechinaspp.)、Paravespula属、Plagiolepis属、树蜂属(Sirex spp.)、红火蚁(Solenopsisinvicta)、臭蚁属(Tapinoma spp.)、白足狡臭蚁(Technomyrmex albipes)、大树蜂属(Urocerus spp.)、胡蜂属(Vespa spp.)(例如黄边胡蜂(Vespa crabro))、小火蚁(Wasmannia auropunctata)、黑树蜂属(Xeris spp.);
等足目(Isopoda)的害虫,例如,鼠妇(Armadillidium vulgare)、栉水虱(Oniscusasellus)、球鼠妇(Porcellio scaber);
等翅目(Isoptera)的害虫,例如,家白蚁属(Coptotermes spp.)(例如台湾乳白蚁(Coptotermes formosanus))、堆角白蚁(Cornitermes cumulans)、堆砂白蚁属(Cryptotermes spp.)、楹白蚁属(Incisitermes spp.)、木白蚁属(Kalotermes spp.)、稻麦小白蚁(Microtermes obesi)、鼻白蚁属(Nasutitermes spp.)、土白蚁属(Odontotermesspp.)、Porotermes属、散白蚁属(Reticulitermes spp.)(例如黄肢散白蚁(Reticulitermes flavipes)、美国散白蚁(Reticulitermes hesperus));
鳞翅目(Lepidoptera)的害虫,例如,小蜡螟(Achroia grisella)、桑剑纹夜蛾(Acronicta major)、褐带卷蛾属(Adoxophyes spp.)(例如棉褐带卷蛾(Adoxophyesorana))、烦夜蛾(Aedia leucomelas)、地老虎属(Agrotis spp.)(例如黄地老虎(Agrotissegetum)、小地老虎(Agrotis ipsilon))、波纹夜蛾属(Alabama spp.)(例如棉叶波纹夜蛾(Alabama argillacea))、脐橙螟(Amyelois transitella)、条麦蛾属(Anarsia spp.)、干煞夜蛾属(Anticarsia spp.)(例如大豆夜蛾(Anticarsia gemmatalis))、条小卷蛾属(Argyroploce spp.)、苜蓿银纹夜蛾属(Autographa spp.)、甘蓝夜蛾(Barathrabrassicae)、苹髓尖蛾(Blastodacna atra)、籼弄蝶(Borbo cinnara)、棉潜蛾(Bucculatrix thurberiella)、松尺蠖(Bupalus piniarius)、蛀褐夜蛾属(Busseolaspp.)、卷叶蛾属(Cacoecia spp.)、茶细蛾(Caloptilia theivora)、烟卷蛾(Capuareticulana)、苹果小卷蛾(Carpocapsa pomonella)、桃蛀果蛾(Carposina niponensis)、冬尺蛾(Cheimatobia brumata)、禾草螟属(Chilo spp.)(例如Chilo plejadellus、二化螟(Chilo suppressalis))、Choreutis pariana、色卷蛾属(Choristoneura spp.)、Chrysodeixis chalcites、葡萄果蠹蛾(Clysia ambiguella)、纵卷叶野螟属(Cnaphalocerus spp.)、稻纵卷叶野螟(Cnaphalocrocis medinalis)、云卷蛾属(Cnephasia spp.)、茶枝尖细蛾属(Conopomorpha spp.)、球颈象属(Conotrachelusspp.)、Copitarsia属、小卷蛾属(Cydia spp.)(例如豆荚小卷蛾(Cydia nigricana)、苹果蠹蛾(Cydia pomonella))、Dalaca noctuides、绢野螟属(Diaphania spp.)、Diparopsis属、小蔗杆草螟(Diatraea saccharalis)、钻夜蛾属(Earias spp.)、Ecdytolophaaurantium、南美玉米苗斑螟(Elasmopalpus lignosellus)、甘薯杆螟(Eldanasaccharina)、粉斑螟属(Ephestia spp.)(例如烟草粉斑螟(Ephestia elutella)、地中海斑螟(Ephestia kuehniella))、叶小卷蛾属(Epinotia spp.)、苹淡褐卷蛾(Epiphyaspostvittana)、Erannis属、亚洲胡桃蛾(Erschoviella musculana)、荚斑螟属(Etiellaspp.)、Eudocima属、棕卷蛾属(Eulia spp.)、女贞细卷蛾(Eupoecilia ambiguella)、毒蛾属(Euproctis spp.)(例如黄毒蛾(Euproctis chrysorrhoea))、切夜蛾属(Euxoa spp.)、脏切夜蛾属(Feltia spp.)、大蜡螟(Galleria mellonella)、细蛾属(Gracillaria spp.)、小食心虫属(Grapholitha spp.)(例如梨小食心虫(Grapholita molesta)、杏小食心虫(Grapholita prunivora))、甘蔗螟属(Hedylepta spp.)、铃夜蛾属(Helicoverpa spp.)(例如棉铃虫(Helicoverpa armigera)、玉米夜蛾(Helicoverpa zea))、实夜蛾属(Heliothis spp.)(例如烟芽夜蛾(Heliothis virescens))、褐织蛾(Hofmannophilapseudospretella)、同斑螟属(Homoeosoma spp.)、长卷蛾属(Homona spp.)、苹果巢蛾(Hyponomeuta padella)、柿举枝蛾(Kakivoria flavofasciata)、亮灰蝶属(Lampidesspp.)、贪夜蛾属(Laphygma spp.)、蠹食心虫(Laspeyresia molesta)、茄白翅野螟(Leucinodes orbonalis)、纹潜蛾属(Leucoptera spp.)(例如咖啡潜叶蛾(Leucopteracoffeella))、潜叶细蛾属(Lithocolletis spp.)(例如苹果斑幕潜叶蛾(Lithocolletisblancardella))、绿果冬夜蛾(Lithophane antennata)、花翅小蛾属(Lobesia spp.)(例如葡萄花翅小卷蛾(Lobesia botrana))、豆白隆切根虫(Loxagrotis albicosta)、毒蛾属(Lymantria spp.)(例如舞毒蛾(Lymantria dispar))、潜蛾属(Lyonetia spp.)(例如桃潜叶蛾(Lyonetia clerkella))、黄褐天幕毛虫(Malacosoma neustria)、豆荚野螟(Marucatestulalis)、甘蓝夜蛾(Mamstra brassicae)、稻暮眼蝶(Melanitis leda)、毛胫夜蛾属(Mocis spp.)、Monopis obviella、粘虫(Mythimna separata)、橡长角蛾(Nemapogoncloacellus)、水螟属(Nymphula spp.)、Oiketicus属、楸属(Omphisa spp.)、Operophtera属、麦秆夜蛾属(Oria spp.)、瘤丛螟属(Orthaga spp.)、秆野螟属(Ostrinia spp.)(例如欧洲玉米螟(Ostrinia nubilalis))、小眼夜蛾(Panolis flammea)、稻弄蝶属(Parnaraspp.)、红铃虫属(Pectinophora spp.)(例如棉红铃虫(Pectinophora gossypiella))、潜跳甲属(Perileucoptera spp.)、茄麦蛾属(Phthorimaea spp.)(例如马铃薯麦蛾(Phthorimaea operculella))、桔潜蛾(Phyllocnistis citrella)、小潜细蛾属(Phyllonorycter spp.)(例如金纹小潜细蛾(Phyllonorycter blancardella)、山楂潜叶蛾(Phyllonorycter crataegella))、粉蝶属(Pieris spp.)(例如菜粉蝶(Pierisrapae))、荷兰石竹小卷蛾(Platynota stultana)、印度谷斑螟(Plodia interpunctella)、金翅夜蛾属(Plusia spp.)、菜蛾(Plutella xylostella)(=钻石背蛾(Plutellamaculipennis))、小白巢蛾属(Prays spp.)、斜纹夜蛾属(Prodenia spp.)、烟草天蛾属(Protoparce spp.)、粘虫属(Pseudaletia spp.)(例如一星粘虫(Pseudaletiaunipuncta))、大豆尺夜蛾(Pseudoplusia includens)、玉米螟(Pyrausta nubilalis)、薄荷灰夜蛾(Rachiplusia nu)、禾螟属(Schoenobius spp.)(例如三化螟(Schoenobiusbipunctifer))、白禾螟属(Scirpophaga spp.)(例如稻白螟(Scirpophaga innotata))、黄地老虎(Scotia segetum)、茎夜蛾属(Sesamia spp.)(例如大螟(Sesamia inferens))、长须卷蛾属(Sparganothis spp.)、灰翅夜蛾属(Spodoptera spp.)(例如Spodopteraeradiana、甜菜夜蛾(Spodoptera exigua)、草地贪夜蛾(Spodoptera frugiperda)、Spodoptera praefica)、展足蛾属(Stathmopoda spp.)、Stenoma属、花生麦蛾(Stomopteryx subsecivella)、透翅蛾属(Synanthedon spp.)、安第斯马铃薯块茎蛾(Tecia solanivora)、异舟蛾属(Thaumetopoea spp.)、大豆夜蛾(Thermesiagemmatalis)、木塞谷蛾(Tinea cloacella)、袋谷蛾(Tinea pellionella)、幕谷蛾(Tineola bisselliella)、卷蛾属(Tortrix spp.)、毛毡衣蛾(Trichophaga tapetzella)、粉夜蛾属(Trichoplusia spp.)(例如粉纹夜蛾(Trichoplusia ni))、三化螟(Tryporyzaincertulas)、番茄斑潜蝇(Tuta absoluta)、灰蝶属(Virachola spp.);
直翅目(Orthoptera)或跳跃目(Saltatoria)的害虫,例如,家蟋蟀(Achetadomesticus)、Dichroplus属、蝼蛄属(Gryllotalpa spp.)(例如欧洲蝼蛄(Gryllotalpagryllotalpa))、蔗蝗属(Hieroglyphus spp.)、飞蝗属(Locusta spp.)(例如飞蝗(Locustamigratoria))、黑蝗属(Melanoplus spp.)(例如迁飞黑蝗(Melanoplus devastator)、Paratlanticus ussuriensis)、沙漠蝗(Schistocerca gregaria);
虱目(Phthiraptera)的害虫,例如,例如畜虱属(Damalinia spp.)、血虱属(Haematopinus spp.)、毛虱属(Linognathus spp.)、虱属(Pediculus spp.)、根瘤蚜(Phylloxera vastatrix)、阴虱(Ptirus pubis)、啮毛虱属(Trichodectes spp.);
啮虫目(Psocoptera)的害虫,例如,粉啮虫属(Lepinatus spp.)、书虱属(Liposcelis spp.);
蚤目(Siphonaptera)的害虫,例如,角叶蚤属(Ceratophyllus spp.)、栉首蚤属(Ctenocephalides spp.)(例如犬栉头蚤(Ctenocephalides canis),猫栉首蚤(Ctenocephalides felis))、跳蚤(Pulex irritans)、穿皮潜蚤(Tunga penetrans)、印鼠客蚤(Xenopsylla cheopis);
缨翅目(Thysanoptera)的害虫,例如,玉米黄呆蓟马(Anaphothrips obscurus)、稻蓟马(Baliothrips biformis)、Chaetanaphothrips leeuweni、葡萄镰蓟马(Drepanothris reuteri)、Enneothrips flavens、花蓟马属(Frankliniella spp.)(例如烟褐蓟马(Frankliniella fusca)、西花蓟马(Frankliniella occidentalis)、苏花蓟马(Frankliniella schultzei)、麦花蓟马(Frankliniella tritici)、越桔花蓟马(Frankliniella vaccinii)、威廉期花蓟马(Frankliniella williamsi))、蓟马属(Haplothrips spp.)、阳蓟马属(Heliothrips spp.)、温室条篱蓟马(Hercinothripsfemoralis)、卡蓟马属(Kakothrips spp.)、葡萄蓟马(Rhipiphorothrips cruentatus)、硬蓟马属(Scirtothrips spp.)、小豆蘧带蓟马(Taeniothrips cardamomi)、蓟马属(Thripsspp.)(例如棕榈蓟马(Thrips palmi)、烟蓟马(Thrips tabaci));
衣鱼目(Zygentoma)(=缨尾亚目(Thysanura))的害虫,例如,栉衣鱼属(Ctenolepisma spp.)、衣鱼(Lepisma saccharina)、盗火虫(Lepismodes inquilinus)、家衣鱼(Thermobia domestica);
综合纲(Symphyla)的害虫,例如,幺蚰属(Scutigerella spp.)(例如无斑点幺蚰(Scutigerella immaculata));
软体动物门(Mollusca)的害虫,例如双壳纲(Bivalvia)的害虫,如饰贝属(Dreissena spp.),
以及腹足纲(Gastropoda)的害虫,如阿勇蛞蝓属(Arion spp.)(例如黑红阿勇蛞蝓(Arion ater rufus))、双脐螺属(Biomphalaria spp.)、小泡螺属(Bulinus spp.)、野蛞蝓属(Deroceras spp.)(例如田灰蛞蝓(Deroceras laeve))、土蜗属(Galba spp.)、椎实螺属(Lymnaea spp.)、钉螺属(Oncomelania spp.)、福寿螺属(Pomacea spp.)、琥珀螺属(Succinea spp.);
线虫纲(Nematoda)的植物害虫,即植物寄生性线虫,尤其是野外垫刃线虫属(Aglenchus spp.)(例如居农野外垫刃线虫(Aglenchus agricola))、粒线虫属(Anguinaspp.)(例如小麦粒线虫(Anguina tritici))、滑刃线虫属(Aphelenchoides spp.)(例如花生滑刃线虫(Aphelenchoides arachidis)、草莓滑刃线虫(Aphelenchoides fragariae))、刺线虫属(Belonolaimus spp.)(例如细小刺线虫(Belonolaimus gracilis)、长尾刺线虫(Belonolaimus longicaudatus)、诺顿刺线虫(Belonolaimus nortoni))、伞滑刃线虫属(Bursaphelenchus spp.)(例如椰子红环腐线虫(Bursaphelenchus cocophilus)、荒漠伞滑刃线虫(Bursaphelenchus eremus)、松材线虫(Bursaphelenchus xylophilus))、坏死线虫属(Cacopaurus spp.)(例如瘟疫坏死线虫(Cacopaurus pestis))、小环线虫属(Criconemella spp.)(例如弯曲小环线虫(Criconemella curvata)、刻线小环线虫(Criconemella onoensis)、装饰小环线虫(Criconemella ornata)、畸形小环线虫(Criconemella rusium)、薄叶小环线虫(Criconemella xenoplax(=环腐线虫(Mesocriconema xenoplax))))、轮线虫属(Criconemoides spp.)(例如Criconemoidesferniae、Criconemoides onoense、Criconemoides ornatum)、双垫刃属(Ditylenchusapp.)(例如续断双垫刃线虫(Ditylenchus dipsaci))、锥线虫属(Dolichodorus spp.)、球异皮线虫属(Globodera spp.)(例如马铃薯白线虫(Globodera pallida)、马铃薯金线虫(Globodera rostochiensis))、螺旋线虫属(Helicotylenchus spp.)(例如双宫螺旋线虫(Helicotylenchus dihystera))、半轮线虫属(Hemicriconemoides spp.)、鞘线虫属(Hemicycliophora spp.)、异皮线虫属(Heterodera spp.)(例如燕麦胞囊线虫(Heterodera avenae)、大豆胞囊线虫(Heterodera glycines)、甜菜胞囊线虫(Heteroderaschachtii))、Hirschmaniella属、纽带线虫属(Hoplolaimus spp.)、长针线虫属(Longidorus spp.)(例如非洲长针线虫(Longidorus africanus))、根结线虫属(Meloidogyne spp.)(例如哥伦比亚根结线虫(Meloidogyne chitwoodi)、伪根结线虫(Meloidogyne fallax)、北方根结线虫(Meloidogyne hapla)、南方根结线虫(Meloidogyneincognita))、瓢线虫属(Meloinema spp.)、珍珠线虫属(Nacobbus spp.)、拟茎线虫属(Neotylenchus spp.)、拟长针线虫属(Paralongidorus spp.)、拟滑刃线虫属(Paraphelenchus spp.)、拟毛刺线虫属(Paratrichodorus spp.)(例如次拟毛刺线虫(Paratrichodorus minor))、针线虫属(Paratylenchus spp.)、短体线虫属(Pratylenchusspp.)(例如穿刺短体线虫(Pratylenchus penetrans))、Pseudohalenchus属、平滑垫刃属(Psilenchus spp.)、斑皮胞囊线虫属(Punctodera spp.)、五沟线虫属(Quinisulciusspp.)、穿孔线虫属(Radopholus spp.)(例如柑桔穿孔线虫(Radopholus citrophilus)、香蕉穿孔线虫(Radopholus similis))、肾状线虫属(Rotylenchulus spp.)、盘旋线虫属(Rotylenchus spp.)、盾线虫属(Scutellonema spp.)、亚蛇形线虫属(Subanguina spp.)、毛刺线虫属(Trichodorus spp.)(例如短粗根毛刺线虫(Trichodorus obtusus)、原始毛刺线虫(Trichodorus primitivus))、矮化线虫属(Tylenchorhynchus spp.)(例如饰环矮化线虫(Tylenchorhynchus annulatus))、麦线虫属(Tylenchulus spp.)(例如柑桔根线虫(Tylenchulus semipenetrans))、剑线虫属(Xiphinema spp.)(例如标准剑线虫(Xiphinema index))。
在一定的浓度或施用率下,还可视情况将式(I)的化合物用作除草剂、安全剂、生长调节剂或改善植物特性的试剂,用作杀微生物剂或杀配子剂,例如用作杀真菌剂、抗霉菌剂、杀细菌剂、杀病毒剂(包括对抗类病毒的试剂)或用作对抗MLO(类支原体生物)和RLO(类立克次氏体生物)的试剂。视情况,还可将它们用作用于合成其他活性化合物的中间体或前体。
制剂
本发明还涉及作为农药的包含至少一种式(I)化合物的制剂和由其制备的使用形式,例如浇灌、滴注和喷洒液体。任选地,使用形式包含其他农药和/或改善作用的佐剂,例如渗透剂,例如植物油(如油菜籽油、向日葵油)、矿物油(如石蜡油)、植物脂肪酸的烷基酯(如油菜籽油甲酯或大豆油甲酯)、或烷醇烷氧基化物;和/或展着剂(spreader),例如烷基硅氧烷和/或盐(如有机或无机铵盐或鏻盐,例如硫酸铵或磷酸氢二铵);和/或保留促进剂,例如磺基丁二酸二辛酯或羟丙基瓜尔胶聚合物;和/或湿润剂,例如甘油;和/或肥料,例如含铵、含钾或含磷的肥料。
常规的制剂为,例如水溶性液体剂(SL)、乳液浓缩剂(EC)、水包乳剂(EW)、悬浮浓缩剂(SC、SE、FS、OD)、水分散性颗粒剂(WG)、颗粒剂(GR)和胶囊浓缩剂(CS);这些制剂和其他可能的制剂类型例如被国际作物生命组织(Crop Life International)记载并在以下文献中描述:《农药标准》、《联合国粮农组织(FAO)和世界卫生组织(WHO)农药标准制订和使用手册》、《联合国粮农组织(FAO)植物生产与保护文件-173》(由联合国粮农组织(FAO)/世界卫生组织(WHO)农药标准联席会议编写,2004,ISBN:9251048576)。除了一种或多种式(I)的化合物外,所述制剂还任选地包含其他农用化学活性化合物。
优选的是包含下述物质的制剂或使用形式:助剂,如增量剂、溶剂、自发性促进剂、载体、乳化剂、分散剂、防冻剂、杀生物剂(biocide)、增稠剂;和/或其他助剂,如佐剂。在本发明的上下文中,佐剂是增强制剂的生物功效的组分,而该组分本身不具有任何生物功效。佐剂的实例为促进保留、铺展、附着到叶面或渗透的试剂。
这些制剂以已知方式制备,例如通过将式(I)的化合物与助剂如增量剂、溶剂和/或固体载体和/或其他助剂如表面活性剂相混合。所述制剂在合适的设备中制备或在施用前或施用过程中制备。
所使用的助剂可为适合用于向式(I)的化合物的制剂或由这些制剂制备的使用形式(如即用型农药,如喷雾液体或拌种剂产品)赋予特定特性(例如某些物理、技术和/或生物特性)的物质。
合适的增量剂为例如水、极性和非极性有机化学液体,例如选自:芳族烃和非芳族烃(如石蜡、烷基苯、烷基萘、氯苯)、醇和多元醇(如果合适的话,其还可被取代、醚化和/或酯化)、酮(如丙酮、环己酮)、酯(包括脂肪和油)和(聚)醚,简单和取代的胺、酰胺、内酰胺(如N-烷基吡咯烷酮)和内酯、砜和亚砜(如二甲基亚砜)。
如果所用的增量剂是水,则还可使用例如有机溶剂作为助溶剂。有用的液体溶剂主要为:芳族化合物,如二甲苯、甲苯或烷基萘;氯代芳族烃或氯代脂族烃,如氯苯、氯乙烯或二氯甲烷;脂族烃,如环己烷或石蜡,如石油馏分、矿物油和植物油;醇,如丁醇或乙二醇及其醚和酯;酮,如丙酮、甲基乙基酮、甲基异丁基酮或环己酮;强极性溶剂,如二甲基甲酰胺和二甲基亚砜;以及水。
原则上,可使用所有合适的溶剂。合适的溶剂的实例为:芳族烃,如二甲苯、甲苯或烷基萘;氯代芳族烃或氯代脂族烃,如氯苯、氯乙烯或二氯甲烷;脂族烃,如环己烷、石蜡、石油馏分、矿物油和植物油;醇,如甲醇、乙醇、异丙醇、丁醇或乙二醇及其醚和酯;酮,如丙酮、甲基乙基酮、甲基异丁基酮或环己酮;强极性溶剂,如二甲基亚砜;以及水。
原则上,可使用所有合适的载体。更具体而言,有用的载体包括以下物质:例如,铵盐和精细研磨的天然岩石,如高岭土、氧化铝、滑石、白垩、石英、绿坡缕石、蒙脱石或硅藻土;和精细研磨的合成岩石,如高度分散的二氧化硅、氧化铝和天然或合成的硅酸盐;树脂;蜡;和/或固体肥料。同样可使用这些载体的混合物。用于颗粒剂的有用载体包括:例如,压碎并分级的天然岩石,如方解石、大理石、浮石、海泡石、白云石;以及无机粉和有机粉的合成颗粒;以及有机材料的颗粒,如锯屑、纸、椰壳、玉米穗轴和烟草茎。
还可使用液化的气体增量剂或溶剂。特别合适的是在标准温度和大气压下为气态的那些增量剂或载体,例如,气溶胶推进剂(aerosol propellant),如卤代烃,以及丁烷、丙烷、氮气和二氧化碳。
具有离子或非离子性质的乳化剂和/或发泡剂、分散剂或润湿剂、或这些表面活性物质的混合物的实例为:聚丙烯酸的盐;木素磺酸的盐;苯酚磺酸或萘磺酸的盐;环氧乙烷与脂肪醇或与脂肪酸或与脂肪胺的缩聚物、环氧乙烷与取代的酚(优选烷基酚或芳基酚)的缩聚物;磺基丁二酸酯的盐;牛磺酸衍生物(优选牛磺酸烷基酯);聚乙氧基化醇或酚的磷酸酯;多元醇的脂肪酸酯;以及含硫酸根、磺酸根和磷酸根的化合物的衍生物,例如烷基芳基聚乙二醇醚、烷基磺酸盐、烷基硫酸盐、芳基磺酸盐、蛋白质水解产物、木质素亚硫酸盐废液和甲基纤维素。如果式(I)的化合物之一和/或惰性载体之一不溶于水并且如果施用在水中进行时,则表面活性剂的存在是有利的。
可存在于制剂和由其获得的使用形式中的其他助剂包括:染料,例如无机颜料,如氧化铁、氧化钛和普鲁士蓝;和有机染料,如茜素染料、偶氮染料和金属酞菁染料;以及营养物和微量营养物,如铁盐、锰盐、硼盐、铜盐、钴盐、钼盐和锌盐。
可以存在的另外的组分为稳定剂,如低温稳定剂、防腐剂、抗氧化剂、光稳定剂或其他提高化学和/或物理稳定性的试剂。还可存在发泡剂和消泡剂。
此外,制剂和由其获得的使用形式还可包含下述物质作为另外的助剂:粘着剂,如羧甲基纤维素;以及呈粉末、颗粒或乳胶形式的天然和合成的聚合物,如阿拉伯树胶、聚乙烯醇和聚乙酸乙烯酯;或者天然磷脂,如脑磷脂和卵磷脂;和合成磷脂。其他助剂可以为矿物油和植物油。
如果合适的话,在制剂和由其获得的使用形式中还可以存在其他助剂。这些添加剂的实例为香料、保护胶体、粘合剂、胶粘剂、增稠剂、触变剂、渗透剂、保留促进剂、稳定剂、螯合剂、络合剂、润湿剂和展着剂。一般而言,式(I)的化合物可与通常用于制剂目的的任何固体或液体添加剂相结合。
有用的保留促进剂包括所有那些降低动态表面张力的物质(如磺基丁二酸二辛酯)或增加粘弹性的物质(如羟丙基瓜尔胶聚合物)。
在本发明的上下文中,有用的渗透剂为所有那些通常用于增强农用化学活性化合物向植物内渗透的物质。在本发明的上下文中,渗透剂通过这样的方式定义:它们从(通常水性)施用液体和/或从喷洒涂层渗透到植物的表皮,从而增加活性化合物在表皮中的移动性的能力。文献(Baur等人,1997,Pesticide Science 51,131-152)中记载的方法可用于测定这种特性。实例包括:醇烷氧基化物,如椰子脂肪乙氧基化物(10)或异十三烷基乙氧基化物(12);脂肪酸酯,如油菜籽油甲酯或大豆油甲酯;脂肪胺烷氧基化物,如牛油胺乙氧基化物(15);或铵盐和/或鏻盐,如硫酸铵或磷酸氢二铵。
所述制剂优选包含0.00000001重量%至98重量%的式(I)的化合物,更优选0.01重量%至95重量%的式(I)的化合物,最优选0.5重量%至90重量%的式(I)的化合物,基于所述制剂的重量计。
在由制剂制备的使用形式(尤其是农药)中,式(I)的化合物的含量可在宽的范围内变化。在使用形式中,式(I)的化合物的浓度通常可为0.00000001重量%至95重量%的式(I)的化合物,优选为0.00001重量%至1重量%,基于使用形式的重量计。施用以适合于使用形式的常规方式进行。
混合物
式(I)的化合物还可与一种或多种合适的如下物质混合使用:杀真菌剂、杀细菌剂、杀螨剂、杀软体动物剂、杀线虫剂、杀昆虫剂、微生物剂、有益生物体、除草剂、肥料、驱鸟剂、phytotonic、止繁殖剂、安全剂、化学信息素和/或植物生长调节剂,从而例如拓宽作用谱、延长作用时间、提高作用速率、防止排斥或防止抗性发展。另外,这类活性化合物结合物可以改善植物生长和/或对非生物因素的耐受性,如对高温或低温、对干旱或对高水含量或土壤盐度的耐受性。还可改善开花和结果性能、优化发芽能力和根系发育、促进采收和提高产量、影响熟化、改善采收产品的品质和/或营养价值、延长储存期和/或改善采收产品的可加工性。
此外,式(I)的化合物可与其他活性化合物或化学信息素如引诱剂和/或驱鸟剂和/或植物活化剂和/或生长调节剂和/或肥料混合存在。同样地,式(I)的化合物可用于改善植物性能如采收材料的生长、产量和品质。
在本发明的一个特别的实施方案中,式(I)的化合物与其他化合物(优选下文所述的那些化合物)混合存在于制剂或由这些制剂制备的使用形式中。
如果下文提到的化合物之一可以不同的互变异构形式存在,则这些形式即使在各种情况下没有被明确提及,也包括在内。所提及的所有混合组分视情况还可与合适的碱或酸形成盐,如果它们基于其官能团能形成盐的话。
杀昆虫剂/杀螨剂/杀线虫剂
本文中以其“通用名称”提及的活性化合物是已知的,并且记载于例如“农药手册(The Pesticide Manual)”,第16版,British Crop Protection Council 2012中,或者可以在互联网(例如http://www.alanwood.net/pesticides)上检索到。该分类以提交该专利申请时适用的IRAC作用方式分类方案为基础。
(1)乙酰胆碱酯酶(AChE)抑制剂,例如氨基甲酸酯类,例如棉铃威(alanycarb)、涕灭威(aldicarb)、噁虫威(bendiocarb)、丙硫克百威(benfuracarb)、丁酮威(butocarboxim)、丁酮砜威(butoxycarboxim)、胺甲萘(carbaryl)、虫螨威(carbofuran)、丁硫克百威(carbosulfan)、乙硫苯威(ethiofencarb)、仲丁威(fenobucarb)、伐虫脒(formetanate)、呋线威(furathiocarb)、异丙威(isoprocarb)、灭虫威(methiocarb)、灭多虫(methomyl)、速灭威(metolcarb)、杀线威(oxamyl)、抗蚜威(pirimicarb)、残杀威(propoxur)、硫双威(thiodicarb)、久效威(thiofanox)、唑蚜威(triazamate)、混杀威(trimethacarb)、灭除威(XMC)和灭杀威(xylylcarb);或有机磷酸酯类,例如乙酰甲胺磷(acephate)、甲基吡噁磷(azamethiphos)、乙基谷硫磷(azinphos-ethyl)、甲基谷硫磷(azinphos-methyl)、硫线磷(cadusafos)、氯氧磷(chlorethoxyfos)、毒虫畏(chlorfenvinphos)、氯甲硫磷(chlormephos)、甲基毒死蜱(chloropyrifos-methyl)、蝇毒磷(coumaphos)、杀螟腈(cyanophos)、甲基内吸磷(demeton-S-methyl)、二嗪农(diazinon)、敌敌畏(dichlorvos/DDVP)、百治磷(dicrotophos)、乐果(dimethoate)、甲基毒虫畏(dimethylvinphos)、乙拌磷(disulfoton)、苯硫磷(EPN)、乙硫磷(ethion)、灭线磷(ethoprophos)、伐灭磷(famphur)、苯线磷(fenamiphos)、杀螟松(fenitrothion)、倍硫磷(fenthion)、噻唑磷(fosthiazate)、庚烯磷(heptenophos)、氰咪唑硫磷(imicyafos)、异柳磷(isofenphos)、邻-(甲氧基氨基硫代磷酰基)水杨酸异丙酯、异噁唑磷(isoxathion)、马拉硫磷(malathion)、灭蚜磷(mecarbam)、甲胺磷(methamidophos)、杀扑磷(methidathion)、速灭磷(mevinphos)、久效磷(monocrotophos)、二溴磷(naled)、氧乐果(omethoate)、亚砜磷(oxydemeton-methyl)、对硫磷甲酯(parathion-methyl)、稻丰散(phenthoate)、甲拌磷(phorate)、伏杀磷(phosalone)、亚胺硫磷(phosmet)、磷胺(phosphamidon)、肟硫磷(phoxim)、甲基吡啶磷(pirimiphos-methyl)、丙溴磷(profenofos)、胺丙畏(propetamphos)、丙硫磷(prothiofos)、吡唑硫磷(pyraclofos)、哒嗪硫磷(pyridaphenthion)、喹硫磷(quinalphos)、治螟磷(sulfotep)、丁基吡啶磷(tebupirimfos)、双硫磷(temephos)、特丁硫磷(terbufos)、杀虫畏(tetrachlorvinphos)、甲基乙拌磷(thiometon)、三唑磷(triazophos)、敌百虫(triclorfon)和蚜灭磷(vamidothion)。
(2)GABA-门控氯化物通道阻断剂,例如环戊二烯有机氯类,例如氯丹(chlordane)和硫丹(endosulfan);或苯基吡唑类(fiproles),例如乙虫腈(ethiprole)和氟虫腈(fipronil)。
(3)钠通道调节剂,例如拟除虫菊酯(pyrethroid)类,例如氟丙菊酯(acrinathrin)、丙烯除虫菊酯(allethrin)、d-顺-反丙烯除虫菊酯(d-cis-transallethrin)、d-反丙烯除虫菊酯(d-trans allethrin)、联苯菊酯(bifenthrin)、生物烯丙菊酯(bioallethrin)、生物烯丙菊酯S-环戊烯基异构体(bioallethrin S-cyclopentenylisomer)、生物苄呋菊酯(bioresmethrin)、乙氰菊酯(cycloprothrin)、氟氯氰菊酯(cyfluthrin)、β-氟氯氰菊酯(beta-cyfluthrin)、氯氟氰菊酯(cyhalothrin)、λ-氯氟氰菊酯(lambda-cyhalothrin)、γ-氯氟氰菊酯(gamma-cyhalothrin)、氯氰菊酯(cypermethrin)、α-氯氰菊酯(alpha-cypermethrin)、β-氯氰菊酯(beta-cypermethrin)、θ-氯氰菊酯(theta-cypermethrin)、δ-氯氰菊酯(zeta-cypermethrin)、苯醚氰菊酯[(1R)-反式异构体](cyphenothrin[(1R)-trans isomers])、溴氰菊酯(deltamethrin)、右旋烯炔菊酯[(EZ)-(1R)异构体](empenthrin[(EZ)-(1R)isomers])、高氰戊菊酯(esfenvalerate)、醚菊酯(etofenprox)、甲氰菊酯(fenpropathrin)、氰戊菊酯(fenvalerate)、氟氰戊菊酯(flucythrinate)、氟氯苯菊酯(flumethrin)、τ-氟胺氰菊酯(tau-fluvalinate)、苄螨醚(halfenprox)、炔咪菊酯(imiprothrin)、噻嗯菊酯(kadethrin)、甲氧苄氟菊酯(momfluorothrin)、苄氯菊酯(permethrin)、苯醚菊酯[(1R)-反式异构体](phenothrin[(1R)-trans isomer])、炔丙菊酯(prallethrin)、除虫菊酯(pyrethrine、pyrethrum)、苄呋菊酯(resmethrin)、氟硅菊酯(silafluofen)、七氟菊酯(tefluthrin)、胺菊酯(tetramethrin)、胺菊酯[(1R)异构体)](tetramethrin[(1R)isomers])、四溴菊酯(tralomethrin)和四氟苯菊酯(transfluthrin);或DDT;或甲氧氯。
(4)烟碱乙酰胆碱受体(nAChR)竞争调节剂,例如新烟碱类(neonicotinoids),例如啶虫脒(acetamiprid)、噻虫胺(clothianidin)、呋虫胺(dinotefuran)、吡虫啉(imidacloprid)、烯啶虫胺(nitenpyram)、噻虫啉(thiacloprid)和噻虫嗪(thiamethoxam)或尼古丁(nicotine)或氟啶虫胺腈(sulfoxaflor)或氟吡呋喃酮(flupyradifurone)。
(5)烟碱乙酰胆碱受体(nAChR)变构调节剂,例如多杀菌素类(spinosyns),如乙基多杀菌素(spinetoram)和多杀菌素(spinosad)。
(6)谷氨酸门控氯化物通道(GluCl)变构调节剂,例如,阿凡曼维菌素类/米尔倍霉素类(avermectins/milbemycins),例如阿巴克丁(abamectin)、甲氨基阿维菌素苯甲酸盐(emamectin benzoate)、雷皮菌素(lepimectin)和灭螨菌素(milbemectin)。
(7)保幼激素模仿物,例如,保幼激素类似物如烯虫乙酯(hydroprene)、烯虫炔酯(kinoprene)和烯虫酯(methoprene)或苯氧威(fenoxycarb)或蚊蝇醚(pyriproxyfen)。
(8)其他非特异性(多位点)抑制剂,例如烷基卤化物,例如甲基溴化物和其他烷基卤化物;或氯化苦(chloropicrin)或硫酰氟或硼砂或吐酒石(tartar emetic)或异氰酸甲酯生成剂,如棉隆(diazomet)或威百亩(metam)。
(9)弦音器官调节剂,例如吡蚜酮(pymetrozine)或氟啶虫酰胺(flonicamide)。
(10)螨生长抑制剂,例如四螨嗪、噻螨酮和氟螨嗪(diflovidazin)或乙螨唑(etoxazole)。
(11)昆虫中肠膜的微生物干扰剂,例如苏云金芽孢杆菌以色列亚种(Bacillusthuringiensis subspecies israelensis)、球形芽孢杆菌(Bacillus sphaericus)、苏云金芽胞杆菌鲇泽亚种(Bacillus thuringiensis subspecies aizawai)、苏云金芽孢杆菌库尔斯塔克亚种(Bacillus thuringiensis subspecies kurstaki)、苏云金芽孢杆菌拟步行甲亚种(Bacillus thuringiensis subspecies tenebrionis)和B.t.植物蛋白:Cry1Ab、Cry1Ac、Cry1Fa、Cry1A.105、Cry2Ab、VIP3A、mCry3A、Cry3Ab、Cry3Bb、Cry34Ab1/35Ab1。
(12)线粒体ATP合成酶的抑制剂,例如ATP干扰剂,例如丁醚脲或有机锡化合物,例如三唑锡、三环锡和苯丁锡(fenbutatin oxide)或快螨特(propargite)或四氯杀螨砜(tetradifon)。
(13)通过阻断质子梯度的氧化磷酸化的解偶联剂,例如虫螨腈(chlorfenapyr)、二硝甲酚(DNOC)和氟虫胺(sulphluramid)。
(14)烟碱乙酰胆碱受体通道阻断剂,例如杀虫磺(bensultap)、杀螟丹盐酸盐(cartap hydrochloride)、杀虫环(thiocyclam)和杀虫双(thiosultap-sodium)。
(15)几丁质生物合成抑制剂,0型,例如双三氟虫脲(bistrifluron)、定虫隆(chlofluazuron)、二氟苯隆(diflubenzuron)、氟环脲(flucycloxuron)、氟虫脲(flufenoxuron)、氟铃脲(hexaflumuron)、氯芬奴隆(lufenuron)、双苯氟脲(novaluron)、多氟脲(noviflumuron)、氟苯脲(teflubenzuron)和杀铃脲(triflumuron)。
(16)几丁质生物合成抑制剂,1型,例如噻嗪酮(buprofezin)。
(17)蜕皮干扰剂(特别是对于双翅目(Diptera)),例如灭蝇胺(cyromazine)。
(18)蜕皮激素受体激动剂,例如环虫酰胺(chromafenozide)、氯虫酰肼(halofenozide)、甲氧虫酰肼(methoxyfenozide)和虫酰肼(tebufenozide)。
(19)章鱼胺受体激动剂,例如双甲脒(amitraz)。
(20)线粒体复合物III电子传递抑制剂,例如氟蚁腙(hydramethylnone),或灭螨醌(acequinocyl),或嘧螨酯(fluacrypyrim)。
(21)线粒体复合物I电子传递抑制剂,例如METI杀螨剂,例如喹螨醚(fenazaquin)、唑螨酯(fenpyroximate)、嘧螨醚(pyrimidifen)、哒螨灵(pyridaben)、吡螨胺(tebufenpyrad)和唑虫酰胺(tolfenpyrad);或鱼藤酮(rotenone)(鱼藤)。
(22)电压依赖型的钠通道阻断剂,例如茚虫威(indoxacarb)或氰氟虫腙(metaflumizone)。
(23)乙酰基-CoA羧化酶的抑制剂,例如特窗酸(tetronic acid)和特特拉姆酸(tetramic acid)衍生物,例如螺螨酯(spirodiclofen)、螺甲螨酯(spiromesifen)和螺虫乙酯(spirotetramat)。
(24)线粒体复合物IV电子传递抑制剂,例如膦类,如磷化铝、磷化钙、膦和磷化锌;或氰化物,如氰化钙、氰化钾和氰化钠。
(25)线粒体复合物II电子传递抑制剂,如β-酮腈衍生物,例如腈吡螨酯(cyenopyrafen)和丁氟螨酯(cyflumetofen)和甲酰苯胺,如pyflubumide。
(28)鱼尼丁受体调节剂,例如二酰胺类,如氯虫苯甲酰胺(chlorantraniliprole)、溴氰虫酰胺(cyantraniliprole)和氟虫双酰胺(flubendiamide);
其它活性化合物,例如afidopyropen、阿福拉纳(afoxolaner)、印楝素(azadirachtin)、benclothiaz、苯螨特(benzoximate)、联苯肼酯(bifenazate)、broflanilide、溴螨酯(bromopropylate)、灭螨锰(chinomethionat)、chloroprallethrin、冰晶石(cryolite)、环溴虫酰胺(cyclaniliprole)、环氧虫啶(cycloxaprid)、氯氟氰虫酰胺(cyhalodiamide)、dicloromezotiaz、三氯杀螨醇(dicofol)、ε-甲氧苄氟菊酯(epsilonmetofluthrin)、epsilon momfluthrin、flometoquin、三氟咪啶酰胺(fluazaindolizine)、氟噻虫砜(fluensulfone)、嘧虫胺(flufenerim)、氟菌螨酯(flufenoxystrobin)、丁虫腈(flufiprole)、fluhexafon、氟吡菌酰胺(fluopyram)、氟雷拉纳(fluralaner)、fluxametamide、呋喃虫酰肼(fufenozide)、guadipyr、右旋七氟甲醚菊酯(heptafluthrin)、氯噻啉(imidaclothiz)、异菌脲(iprodione)、κ-联苯菊酯(kappabifenthrin)、κ-七氟菊酯(kappa tefluthrin)、lotilaner、氯氟醚菊酯(meperfluthrin)、哌虫啶(paichongding)、三氟甲吡醚(pyridalyl)、pyrifluquinazon、嘧螨胺(pyriminostrobin)、spirobudiclofen、四氟醚菊酯(tetramethylfluthrin)、氟氰虫酰胺(tetraniliprole)、氟氰虫酰胺(tetrachlorantraniliprole)、tioxazafen、硫氟肟醚(thiofluoximate)、triflumezopyrim和碘甲烷(iodomethane);以及基于坚强芽孢杆菌(Bacillus firmus,I-1582,BioNeem,Votivo)的制品,以及下列化合物:1-{2-氟-4-甲基-5-[(2,2,2-三氟乙基)亚磺酰基]苯基}-3-(三氟甲基)-1H-1,2,4-三唑-5-胺(由WO2006/043635已知)(CAS 885026-50-6)、{1'-[(2E)-3-(4-氯苯基)丙-2-烯-1-基]-5-氟螺[吲哚-3,4'-哌啶]-1(2H)-基}(2-氯吡啶-4-基)甲酮(由WO 2003/106457已知)(CAS 637360-23-7)、2-氯-N-[2-{1-[(2E)-3-(4-氯苯基)丙-2-烯-1-基]哌啶-4-基}-4-(三氟甲基)苯基]异烟酰胺(由WO2006/003494已知)(CAS 872999-66-1)、3-(4-氯-2,6-二甲基苯基)-4-羟基-8-甲氧基-1,8-二氮杂螺[4.5]癸-3-烯-2-酮(由WO 2010052161已知)(CAS 1225292-17-0)、3-(4-氯-2,6-二甲基苯基)-8-甲氧基-2-氧代-1,8-二氮杂螺[4.5]癸-3-烯-4-基乙基碳酸酯(由EP 2647626已知)(CAS-1440516-42-6)、4-(丁-2-炔-1-基氧基)-6-(3,5-二甲基哌啶-1-基)-5-氟嘧啶(由WO2004/099160已知)(CAS 792914-58-0)、PF1364(由JP2010/018586已知)(CAS登记号1204776-60-2)、N-[(2E)-1-[(6-氯吡啶-3-基)甲基]吡啶-2(1H)-亚基]-2,2,2-三氟乙酰胺(由WO2012/029672已知)(CAS 1363400-41-2)、(3E)-3-[1-[(6-氯-3-吡啶基)甲基]-2-吡啶基亚基]-1,1,1-三氟丙-2-酮(由WO2013/144213已知)(CAS1461743-15-6)、N-[3-(苄基氨基甲酰基)-4-氯苯基]-1-甲基-3-(五氟乙基)-4-(三氟甲基)-1H-吡唑-5-甲酰胺(由WO2010/051926已知)(CAS 1226889-14-0)、5-溴-4-氯-N-[4-氯-2-甲基-6-(甲基氨基甲酰基)苯基]-2-(3-氯-2-吡啶基)吡唑-3-甲酰胺(由CN103232431已知)(CAS 1449220-44-3)、4-[5-(3,5-二氯苯基)-4,5-二氢-5-(三氟甲基)-3-异噁唑基]-2-甲基-N-(顺式-1-氧化-3-硫杂环丁烷基)苯甲酰胺、4-[5-(3,5-二氯苯基)-4,5-二氢-5-(三氟甲基)-3-异噁唑基]-2-甲基-N-(反式-1-氧化-3-硫杂环丁烷基)苯甲酰胺和4-[(5S)-5-(3,5-二氯苯基)-4,5-二氢-5-(三氟甲基)-3-异噁唑基]-2-甲基-N-(顺式-1-氧化-3-硫杂环丁烷基)苯甲酰胺(由WO 2013/050317 A1已知)(CAS 1332628-83-7)、N-[3-氯-1-(3-吡啶基)-1H-吡唑-4-基]-N-乙基-3-[(3,3,3-三氟丙基)亚磺酰基]丙酰胺、(+)-N-[3-氯-1-(3-吡啶基)-1H-吡唑-4-基]-N-乙基-3-[(3,3,3-三氟丙基)亚磺酰基]丙酰胺和(-)-N-[3-氯-1-(3-吡啶基)-1H-吡唑-4-基]-N-乙基-3-[(3,3,3-三氟丙基)亚磺酰基]丙酰胺(由WO 2013/162715 A2、WO 2013/162716 A2、US 2014/0213448 A1已知)(CAS1477923-37-7)、5-[[(2E)-3-氯-2-丙烯-1-基]氨基]-1-[2,6-二氯-4-(三氟甲基)苯基]-4-[(三氟甲基)亚磺酰基]-1H-吡唑-3-甲腈(由CN 101337937 A已知)(CAS 1105672-77-2)、3-溴-N-[4-氯-2-甲基-6-[(甲基氨基)硫代甲基]苯基]-1-(3-氯-2-吡啶基)-1H-吡唑-5-甲酰胺、(Liudaibenjiaxuanan,由CN 103109816 A已知)(CAS 1232543-85-9);N-[4-氯-2-[[(1,1-二甲基乙基)氨基]羰基]-6-甲基苯基]-1-(3-氯-2-吡啶基)-3-(氟甲氧基)-1H-吡唑-5-甲酰胺(由WO 2012/034403 A1已知)(CAS 1268277-22-0)、N-[2-(5-氨基-1,3,4-噻二唑-2-基)-4-氯-6-甲基苯基]-3-溴-1-(3-氯-2-吡啶基)-1H-吡唑-5-甲酰胺(由WO2011/085575 A1已知)(CAS 1233882-22-8)、4-[3-[2,6-二氯-4-[(3,3-二氯-2-丙烯-1-基)氧基]苯氧基]丙氧基]-2-甲氧基-6-(三氟甲基)嘧啶(由CN 101337940 A已知)(CAS1108184-52-6);(2E)-和2(Z)-2-[2-(4-氰基苯基)-1-[3-(三氟甲基)苯基]亚乙基]-N-[4-(二氟甲氧基)苯基]肼甲酰胺(由CN 101715774 A已知)(CAS 1232543-85-9);3-(2,2-二氯乙烯基)-2,2-二甲基-4-(1H-苯并咪唑-2-基)苯基环丙烷羧酸酯(由CN 103524422 A已知)(CAS 1542271-46-4);(4aS)-7-氯-2,5-二氢-2-[[(甲氧基羰基)[4-[(三氟甲基)硫代]苯基]氨基]羰基]茚并[1,2-e][1,3,4]噁二嗪-4a(3H)-羧酸甲酯(由CN 102391261 A已知)(CAS 1370358-69-2);6-脱氧-3-O-乙基-2,4-二-O-甲基-1-[N-[4-[1-[4-(1,1,2,2,2-五氟乙氧基)苯基]-1H-1,2,4-三唑-3-基]苯基]氨基甲酸酯]-α-L-吡喃甘露糖(由US 2014/0275503 A1已知)(CAS 1181213-14-8);8-(2-环丙基甲氧基-4-三氟甲基苯氧基)-3-(6-三氟甲基哒嗪-3-基)-3-氮杂二环[3.2.1]辛烷(CAS 1253850-56-4)、(8-反)-8-(2-环丙基甲氧基-4-三氟甲基苯氧基)-3-(6-三氟甲基哒嗪-3-基)-3-氮杂二环[3.2.1]辛烷(CAS933798-27-7)、(8-顺)-8-(2-环丙基甲氧基-4-三氟甲基苯氧基)-3-(6-三氟甲基哒嗪-3-基)-3-氮杂二环[3.2.1]辛烷(由WO 2007040280 A1、WO 2007040282 A1已知)(CAS934001-66-8)和N-[3-氯-1-(3-吡啶基)-1H-吡唑-4-基]-N-乙基-3-[(3,3,3-三氟丙基)硫代]丙酰胺(由WO 2015/058021 A1、WO 2015/058028A1已知)(CAS 1477919-27-9)。
杀真菌剂
本文通过其“通用名称”提及的活性化合物是已知的,并且例如记载于“农药手册”(第16版,British Crop Protection Council)中或可在互联网(例如:http://www.alanwood.net/pesticides)上检索。
在类别(1)至(15)中提及的所有混合组分,可视情况与合适的碱或酸形成盐,如果它们基于其官能团能形成盐的话。所提及的类别(1)至(15)中的所有杀真菌混合组分可视情况包括互变异构形式。
1)麦角甾醇生物合成抑制剂,例如(1.001)环丙唑醇(cyproconazole)、(1.002)苯醚甲环唑(difenoconazole)、(1.003)氟环唑(epoxiconazole)、(1.004)环酰菌胺(fenhexamide)、(1.005)苯锈啶(fenpropidin)、(1.006)丁苯吗啉(fenpropimorph)、(1.007)胺苯吡菌酮(fenpyrazamine)、(1.008)氟喹唑(fluquinconazole)、(1.009)粉唑醇(flutriafol)、(1.010)烯菌灵(imazalil)、(1.011)烯菌灵硫酸盐(imazalil sulfate)、(1.012)种菌唑(ipconazole)、(1.013)叶菌唑(metconazole)、(1.014)腈菌唑(myclobutanil)、(1.015)多效唑(paclobutrazol)、(1.016)咪鲜胺(prochloraz)、(1.017)丙环唑(propiconazole)、(1.018)丙硫菌唑(prothioconazole)、(1.019)啶菌唑(pyrisoxazole)、(1.020)螺环菌胺(spiroxamine)、(1.021)戊唑醇(tebuconazole)、(1.022)氟醚唑(tetraconazole)、(1.023)三唑醇(triadimenol)、(1.024)克啉菌(tridemorph)、(1.025)灭菌唑(triticonazole)、(1.026)(1R,2S,5S)-5-(4-氯苄基)-2-(氯甲基)-2-甲基-1-(1H-1,2,4-三唑-1-基甲基)环戊醇、(1.027)(1S,2R,5R)-5-(4-氯苄基)-2-(氯甲基)-2-甲基-1-(1H-1,2,4-三唑-1-基甲基)环戊醇、(1.028)(2R)-2-(1-氯环丙基)-4-[(1R)-2,2-二氯环丙基]-1-(1H-1,2,4-三唑-1-基)丁-2-醇(1.029)(2R)-2-(1-氯环丙基)-4-[(1S)-2,2-二氯环丙基]-1-(1H-1,2,4-三唑-1-基)丁-2-醇、(1.030)(2R)-2-[4-(4-氯苯氧基)-2-(三氟甲基)苯基]-1-(1H-1,2,4-三唑-1-基)丙-2-醇、(1.031)(2S)-2-(1-氯环丙基)-4-[(1R)-2,2-二氯环丙基]-1-(1H-1,2,4-三唑-1-基)丁-2-醇、(1.032)(2S)-2-(1-氯环丙基)-4-[(1S)-2,2-二氯环丙基]-1-(1H-1,2,4-三唑-1-基)丁-2-醇、(1.033)(2S)-2-[4-(4-氯苯氧基)-2-(三氟甲基)苯基]-1-(1H-1,2,4-三唑-1-基)丙-2-醇、(1.034)(R)-[3-(4-氯-2-氟苯基)-5-(2,4-二氟苯基)-1,2-噁唑-4-基](吡啶-3-基)甲醇、(1.035)(S)-[3-(4-氯-2-氟苯基)-5-(2,4-二氟苯基)-1,2-噁唑-4-基](吡啶-3-基)甲醇、(1.036)[3-(4-氯-2-氟苯基)-5-(2,4-二氟苯基)-1,2-噁唑-4-基](吡啶-3-基)甲醇、(1.037)1-({(2R,4S)-2-[2-氯-4-(4-氯苯氧基)苯基]-4-甲基-1,3-二氧戊环-2-基}甲基)-1H-1,2,4-三唑、(1.038)1-({(2S,4S)-2-[2-氯-4-(4-氯苯氧基)苯基]-4-甲基-1,3-二氧戊环-2-基}甲基)-1H-1,2,4-三唑、(1.039)1-{[3-(2-氯苯基)-2-(2,4-二氟苯基)环氧乙烷-2-基]甲基}-1H-1,2,4-三唑-5-基硫氰酸酯、(1.040)1-{[rel(2R,3R)-3-(2-氯苯基)-2-(2,4-二氟苯基)环氧乙烷-2-基]甲基}-1H-1,2,4-三唑-5-基硫氰酸酯、(1.041)1-{[rel(2R,3S)-3-(2-氯苯基)-2-(2,4-二氟苯基)环氧乙烷-2-基]甲基}-1H-1,2,4-三唑-5-基硫氰酸酯、(1.042)2-[(2R,4R,5R)-1-(2,4-二氯苯基)-5-羟基-2,6,6-三甲基庚-4-基]-2,4-二氢-3H-1,2,4-三唑-3-硫酮、(1.043)2-[(2R,4R,5S)-1-(2,4-二氯苯基)-5-羟基-2,6,6-三甲基庚-4-基]-2,4-二氢-3H-1,2,4-三唑-3-硫酮、(1.044)2-[(2R,4S,5R)-1-(2,4-二氯苯基)-5-羟基-2,6,6-三甲基庚-4-基]-2,4-二氢-3H-1,2,4-三唑-3-硫酮、(1.045)2-[(2R,4S,5S)-1-(2,4-二氯苯基)-5-羟基-2,6,6-三甲基庚-4-基]-2,4-二氢-3H-1,2,4-三唑-3-硫酮、(1.046)2-[(2S,4R,5R)-1-(2,4-二氯苯基)-5-羟基-2,6,6-三甲基庚-4-基]-2,4-二氢-3H-1,2,4-三唑-3-硫酮、(1.047)2-[(2S,4R,5S)-1-(2,4-二氯苯基)-5-羟基-2,6,6-三甲基庚-4-基]-2,4-二氢-3H-1,2,4-三唑-3-硫酮、(1.048)2-[(2S,4S,5R)-1-(2,4-二氯苯基)-5-羟基-2,6,6-三甲基庚-4-基]-2,4-二氢-3H-1,2,4-三唑-3-硫酮、(1.049)2-[(2S,4S,5S)-1-(2,4-二氯苯基)-5-羟基-2,6,6-三甲基庚-4-基]-2,4-二氢-3H-1,2,4-三唑-3-硫酮、(1.050)2-[1-(2,4-二氯苯基)-5-羟基-2,6,6-三甲基庚-4-基]-2,4-二氢-3H-1,2,4-三唑-3-硫酮、(1.051)2-[2-氯-4-(2,4-二氯苯氧基)苯基]-1-(1H-1,2,4-三唑-1-基)丙-2-醇、(1.052)2-[2-氯-4-(4-氯苯氧基)苯基]-1-(1H-1,2,4-三唑-1-基)丁-2-醇、(1.053)2-[4-(4-氯苯氧基)-2-(三氟甲基)苯基]-1-(1H-1,2,4-三唑-1-基)丁-2-醇、(1.054)2-[4-(4-氯苯氧基)-2-(三氟甲基)苯基]-1-(1H-1,2,4-三唑-1-基)戊-2-醇、(1.055)2-[4-(4-氯苯氧基)-2-(三氟甲基)苯基]-1-(1H-1,2,4-三唑-1-基)丙-2-醇、(1.056)2-{[3-(2-氯苯基)-2-(2,4-二氟苯基)环氧乙烷-2-基]甲基}-2,4-二氢-3H-1,2,4-三唑-3-硫酮、(1.057)2-{[rel(2R,3R)-3-(2-氯苯基)-2-(2,4-二氟苯基)环氧乙烷-2-基]甲基}-2,4-二氢-3H-1,2,4-三唑-3-硫酮、(1.058)2-{[rel(2R,3S)-3-(2-氯苯基)-2-(2,4-二氟苯基)环氧乙烷-2-基]甲基}-2,4-二氢-3H-1,2,4-三唑-3-硫酮、(1.059)5-(4-氯苄基)-2-(氯甲基)-2-甲基-1-(1H-1,2,4-三唑-1-基甲基)环戊醇、(1.060)5-(烯丙基硫基)-1-{[3-(2-氯苯基)-2-(2,4-二氟苯基)环氧乙烷-2-基]甲基}-1H-1,2,4-三唑、(1.061)5-(烯丙基硫基)-1-{[rel(2R,3R)-3-(2-氯苯基)-2-(2,4-二氟苯基)环氧乙烷-2-基]甲基}-1H-1,2,4-三唑、(1.062)5-(烯丙基硫基)-1-{[rel(2R,3S)-3-(2-氯苯基)-2-(2,4-二氟苯基)环氧乙烷-2-基]甲基}-1H-1,2,4-三唑、(1.063)N'-(2,5-二甲基-4-{[3-(1,1,2,2-四氟乙氧基)苯基]硫基}苯基)-N-乙基-N-甲基亚氨基甲酰胺、(1.064)N'-(2,5-二甲基-4-{[3-(2,2,2-三氟乙氧基)苯基]硫基}苯基)-N-乙基-N-甲基亚氨基甲酰胺、(1.065)N'-(2,5-二甲基-4-{[3-(2,2,3,3-四氟丙氧基)苯基]硫基}苯基)-N-乙基-N-甲基甲亚氨基甲酰胺、(1.066)N'-(2,5-二甲基-4-{[3-(五氟乙氧基)苯基]硫基}苯基)-N-乙基-N-甲基亚氨基甲酰胺、(1.067)N'-(2,5-二甲基-4-{3-[(1,1,2,2-四氟乙基)硫基]苯氧基}苯基)-N-乙基-N-甲基亚氨基甲酰胺、(1.068)N'-(2,5-二甲基-4-{3-[(2,2,2-三氟乙基)硫基]苯氧基}苯基)-N-乙基-N-甲基亚氨基甲酰胺、(1.069)N'-(2,5-二甲基-4-{3-[(2,2,3,3-四氟丙基)硫基]苯氧基}苯基)-N-乙基-N-甲基亚氨基甲酰胺、(1.070)N'-(2,5-二甲基-4-{3-[(五氟乙基)硫基]苯氧基}苯基)-N-乙基-N-甲基亚氨基甲酰胺、(1.071)N'-(2,5-二甲基-4-苯氧基苯基)-N-乙基-N-甲基亚氨基甲酰胺、(1.072)N'-(4-{[3-(二氟甲氧基)苯基]硫基}-2,5-二甲基苯基)-N-乙基-N-甲基亚氨基甲酰胺、(1.073)N'-(4-{3-[(二氟甲基)硫基]苯氧基}-2,5-二甲基苯基)-N-乙基-N-甲基亚氨基甲酰胺、(1.074)N'-[5-溴-6-(2,3-二氢-1H-茚-2-基氧基)-2-甲基吡啶-3-基]-N-乙基-N-甲基亚氨基甲酰胺、(1.075)N'-{4-[(4,5-二氯-1,3-噻唑-2-基)氧基]-2,5-二甲基苯基}-N-乙基-N-甲基亚氨基甲酰胺、(1.076)N'-{5-溴-6-[(1R)-1-(3,5-二氟苯基)乙氧基]-2-甲基吡啶-3-基}-N-乙基-N-甲基亚氨基甲酰胺、(1.077)N'-{5-溴-6-[(1S)-1-(3,5-二氟苯基)乙氧基]-2-甲基吡啶-3-基}-N-乙基-N-甲基亚氨基甲酰胺、(1.078)N'-{5-溴-6-[(顺式-4-异丙基环己基)氧基]-2-甲基吡啶-3-基}-N-乙基-N-甲基亚氨基甲酰胺、(1.079)N'-{5-溴-6-[(反式-4-异丙基环己基)氧基]-2-甲基吡啶-3-基}-N-乙基-N-甲基亚氨基甲酰胺、(1.080)N'-{5-溴-6-[1-(3,5-二氟苯基)乙氧基]-2-甲基吡啶-3-基}-N-乙基-N-甲基亚氨基甲酰胺。
2)呼吸链复合物I或II的抑制剂,例如(2.001)苯并烯氟菌唑(benzovindiflupyr)、(2.002)联苯吡菌胺(bixafen)、(2.003)啶酰菌胺(boscalid)、(2.004)萎锈灵(carboxin)、(2.005)氟吡菌酰胺(fluopyram)、(2.006)氟酰胺(flutolanil)、(2.007)氟唑菌酰胺(fluxapyroxad)、(2.008)呋吡菌胺(furametpyr)、(2.009)噻吩酰菌酮(isofetamid)、(2.010)吡唑萘菌胺(isopyrazam)(反式差向异构对映异构体1R,4S,9S)、(2.011)吡唑萘菌胺(反式差向异构对映异构体1S,4R,9R)、(2.012)吡唑萘菌胺(反式差向异构外消旋体1RS,4SR,9SR)、(2.013)吡唑萘菌胺(顺式差向异构外消旋体1RS,4SR,9RS和反式差向异构外消旋体1RS,4SR,9SR的混合物)、(2.014)吡唑萘菌胺(顺式差向异构对映异构体1R,4S,9R)、(2.015)吡唑萘菌胺(顺式差向异构对映异构体1S,4R,9S)、(2.016)吡唑萘菌胺(顺式差向异构外消旋体1RS,4SR,9RS)、(2.017)氟唑菌苯胺(penflufen)、(2.018)吡噻菌胺(penthiopyrad)、(2.019)pydiflumetofen、(2.020)pyraziflumid、(2.021)氟唑环菌胺(sedaxane)、(2.022)1,3-二甲基-N-(1,1,3-三甲基-2,3-二氢-1H-茚-4-基)-1H-吡唑-4-甲酰胺、(2.023)1,3-二甲基-N-[(3R)-1,1,3-三甲基-2,3-二氢-1H-茚-4-基]-1H-吡唑-4-甲酰胺、(2.024)1,3-二甲基-N-[(3S)-1,1,3-三甲基-2,3-二氢-1H-茚-4-基]-1H-吡唑-4-甲酰胺、(2.025)1-甲基-3-(三氟甲基)-N-[2'-(三氟甲基)联苯基-2-基]-1H-吡唑-4-甲酰胺、(2.026)2-氟-6-(三氟甲基)-N-(1,1,3-三甲基-2,3-二氢-1H-茚-4-基)苯甲酰胺、(2.027)3-(二氟甲基)-1-甲基-N-(1,1,3-三甲基-2,3-二氢-1H-茚-4-基)-1H-吡唑-4-甲酰胺、(2.028)3-(二氟甲基)-1-甲基-N-[(3R)-1,1,3-三甲基-2,3-二氢-1H-茚-4-基]-1H-吡唑-4-甲酰胺、(2.029)3-(二氟甲基)-1-甲基-N-[(3S)-1,1,3-三甲基-2,3-二氢-1H-茚-4-基]-1H-吡唑-4-甲酰胺、(2.030)3-(二氟甲基)-N-(7-氟-1,1,3-三甲基-2,3-二氢-1H-茚-4-基)-1-甲基-1H-吡唑-4-甲酰胺、(2.031)3-(二氟甲基)-N-[(3R)-7-氟-1,1,3-三甲基-2,3-二氢-1H-茚-4-基]-1-甲基-1H-吡唑-4-甲酰胺、(2.032)3-(二氟甲基)-N-[(3S)-7-氟-1,1,3-三甲基-2,3-二氢-1H-茚-4-基]-1-甲基-1H-吡唑-4-甲酰胺、(2.033)5,8-二氟-N-[2-(2-氟-4-{[4-(三氟甲基)吡啶-2-基]氧基}苯基)乙基]喹唑啉-4-胺、(2.034)N-(2-环戊基-5-氟苄基-)-N-环丙基-3-(二氟甲基)-5-氟-1-甲基-1H-吡唑-4-甲酰胺、(2.035)N-(2-叔丁基-5-甲基苄基-)-N-环丙基-3-(二氟甲基)-5-氟-1-甲基-1H-吡唑-4-甲酰胺、(2.036)N-(2-叔丁基苄基-)-N-环丙基-3-(二氟甲基)-5-氟-1-甲基-1H-吡唑-4-甲酰胺、(2.037)N-(5-氯-2-乙基苄基-)-N-环丙基-3-(二氟甲基)-5-氟-1-甲基-1H-吡唑-4-甲酰胺、(2.038)N-(5-氯-2-异丙基苄基-)-N-环丙基-3-(二氟甲基)-5-氟-1-甲基-1H-吡唑-4-甲酰胺、(2.039)N-[(1R,4S)-9-(二氯亚甲基)-1,2,3,4-四氢-1,4-亚甲基萘-5-基]-3-(二氟甲基)-1-甲基-1H-吡唑-4-甲酰胺、(2.040)N-[(1S,4R)-9-(二氯亚甲基)-1,2,3,4-四氢-1,4-亚甲基萘-5-基]-3-(二氟甲基)-1-甲基-1H-吡唑-4-甲酰胺、(2.041)N-[1-(2,4-二氯苯基)-1-甲氧基丙-2-基]-3-(二氟甲基)-1-甲基-1H-吡唑-4-甲酰胺、(2.042)N-[2-氯-6-(三氟甲基)苄基-]-N-环丙基-3-(二氟甲基)-5-氟-1-甲基-1H-吡唑-4-甲酰胺、(2.043)N-[3-氯-2-氟-6-(三氟甲基)苄基-]-N-环丙基-3-(二氟甲基)-5-氟-1-甲基-1H-吡唑-4-甲酰胺、(2.044)N-[5-氯-2-(三氟甲基)苄基-]-N-环丙基-3-(二氟甲基)-5-氟-1-甲基-1H-吡唑-4-甲酰胺、(2.045)N-环丙基-3-(二氟甲基)-5-氟-1-甲基-N-[5-甲基-2-(三氟甲基)苄基-]-1H-吡唑-4-羧酰胺、(2.046)N-环丙基-3-(二氟甲基)-5-氟-N-(2-氟-6-异丙基苄基-)-1-甲基-1H-吡唑-4-甲酰胺、(2.047)N-环丙基-3-(二氟甲基)-5-氟-N-(2-异丙基-5-甲基苄基-)-1-甲基-1H-吡唑-4-甲酰胺、(2.048)N-环丙基-3-(二氟甲基)-5-氟-N-(2-异丙基苄基-)-1-甲基-1H-吡唑-4-硫代酰胺、(2.049)N-环丙基-3-(二氟甲基)-5-氟-N-(2-异丙基苄基-)-1-甲基-1H-吡唑-4-甲酰胺、(2.050)N-环丙基-3-(二氟甲基)-5-氟-N-(5-氟-2-异丙基苄基-)-1-甲基-1H-吡唑-4-甲酰胺、(2.051)N-环丙基-3-(二氟甲基)-N-(2-乙基-4,5-二甲基苄基-)-5-氟-1-甲基-1H-吡唑-4-甲酰胺、(2.052)N-环丙基-3-(二氟甲基)-N-(2-乙基-5-氟苄基-)-5-氟-1-甲基-1H-吡唑-4-甲酰胺、(2.053)N-环丙基-3-(二氟甲基)-N-(2-乙基-5-甲基苄基-)-5-氟-1-甲基-1H-吡唑-4-甲酰胺、(2.054)N-环丙基-N-(2-环丙基-5-氟苄基-)-3-(二氟甲基)-5-氟-1-甲基-1H-吡唑-4-甲酰胺、(2.055)N-环丙基-N-(2-环丙基-5-甲基苄基-)-3-(二氟甲基)-5-氟-1-甲基-1H-吡唑-4-甲酰胺、(2.056)N-环丙基-N-(2-环丙基苄基-)-3-(二氟甲基)-5-氟-1-甲基-1H-吡唑-4-甲酰胺。
3)呼吸链复合物III的抑制剂,例如(3.001)唑嘧菌胺(ametoctradin)、(3.002)安美速(amisulbrom)、(3.003)腈嘧菌酯(azoxystrobin)、(3.004)甲香菌酯(coumethoxystrobin)、(3.005)丁香菌酯(coumoxystrobin)、(3.006)氰霜唑(cyazofamid)、(3.007)醚菌胺(dimoxystrobin)、(3.008)烯肟菌酯(enoxastrobin)、(3.009)噁唑菌酮(famoxadon)、(3.010)咪唑菌酮(fenamidon)、(3.011)氟菌螨酯(flufenoxystrobin)、(3.012)氟嘧菌酯(fluoxastrobin)、(3.013)醚菌酯(kresoxim-methyl)、(3.014)苯氧菌胺(metominostrobin)、(3.015)肟醚菌胺(orysastrobin)、(3.016)啶氧菌酯(picoxystrobin)、(3.017)唑菌胺酯(pyraclostrobin)、(3.018)唑胺菌酯(pyrametostrobin)、(3.019)唑胺菌酯(pyraoxystrobin)、(3.020)肟菌酯(trifloxystrobin)、(3.021)(2E)-2-{2-[({[(1E)-1-(3-{[(E)-1-氟-2-苯基乙烯基]氧基}苯基)亚乙基]氨基}氧基)甲基]苯基}-2-(甲氧基亚氨基)-N-甲基乙酰胺、(3.022)(2E,3Z)-5-{[1-(4-氯苯基)-1H-吡唑-3-基]氧基}-2-(甲氧基亚氨基)-N,3-二甲基戊-3-烯酰胺、(3.023)(2R)-2-{2-[(2,5-二甲基苯氧基)甲基]苯基}-2-甲氧基-N-甲基乙酰胺、(3.024)(2S)-2-{2-[(2,5-二甲基苯氧基)甲基]苯基}-2-甲氧基-N-甲基乙酰胺、(3.025)(3S,6S,7R,8R)-8-苄基--3-[({3-[(异丁酰基氧基)甲氧基]-4-甲氧基吡啶-2-基}羰基)氨基]-6-甲基-4,9-二氧代-1,5-二氧杂环壬烷-7-基2-甲基丙酸酯、(3.026)2-{2-[(2,5-二甲基苯氧基)甲基]苯基}-2-甲氧基-N-甲基乙酰胺、(3.027)N-(3-乙基-3,5,5-三甲基环己基)-3-甲酰胺基-2-羟基苯甲酰胺、(3.028)(2E,3Z)-5-{[1-(4-氯-2-氟苯基)-1H-吡唑-3-基]氧基}-2-(甲氧基亚氨基)-N,3-二甲基戊-3-烯酰胺。
4)有丝分裂和细胞分裂抑制剂,例如(4.001)多菌灵(carbendazim)、(4.002)乙霉威(diethofencarb)、(4.003)噻唑菌胺(ethaboxam)、(4.004)氟吡菌胺(fluopicolide)、(4.005)戊菌隆(pencycuron)、(4.006)噻苯咪唑(thiabendazole)、(4.007)甲基硫菌灵(thiophanate-methyl)、(4.008)苯酰菌胺(zoxamide)、(4.009)3-氯-4-(2,6-二氟苯基)-6-甲基-5-苯基哒嗪、(4.010)3-氯-5-(4-氯苯基)-4-(2,6-二氟苯基)-6-甲基哒嗪、(4.011)3-氯-5-(6-氯吡啶-3-基)-6-甲基-4-(2,4,6-三氟苯基)哒嗪、(4.012)4-(2-溴-4-氟苯基)-N-(2,6-二氟苯基)-1,3-二甲基-1H-吡唑-5-胺、(4.013)4-(2-溴-4-氟苯基)-N-(2-溴-6-氟苯基)-1,3-二甲基-1H-吡唑-5-胺、(4.014)4-(2-溴-4-氟苯基)-N-(2-溴苯基)-1,3-二甲基-1H-吡唑-5-胺、(4.015)4-(2-溴-4-氟苯基)-N-(2-氯-6-氟苯基)-1,3-二甲基-1H-吡唑-5-胺、(4.016)4-(2-溴-4-氟苯基)-N-(2-氯苯基)-1,3-二甲基-1H-吡唑-5-胺、(4.017)4-(2-溴-4-氟苯基)-N-(2-氟苯基)-1,3-二甲基-1H-吡唑-5-胺、(4.018)4-(2-氯-4-氟苯基)-N-(2,6-二氟苯基)-1,3-二甲基-1H-吡唑-5-胺、(4.019)4-(2-氯-4-氟苯基)-N-(2-氯-6-氟苯基)-1,3-二甲基-1H-吡唑-5-胺、(4.020)4-(2-氯-4-氟苯基)-N-(2-氯苯基)-1,3-二甲基-1H-吡唑-5-胺、(4.021)4-(2-氯-4-氟苯基)-N-(2-氟苯基)-1,3-二甲基-1H-吡唑-5-胺、(4.022)4-(4-氯苯基)-5-(2,6-二氟苯基)-3,6-二甲基哒嗪、(4.023)N-(2-溴-6-氟苯基)-4-(2-氯-4-氟苯基)-1,3-二甲基-1H-吡唑-5-胺、(4.024)N-(2-溴苯基)-4-(2-氯-4-氟苯基)-1,3-二甲基-1H-吡唑-5-胺、(4.025)N-(4-氯-2,6-二氟苯基)-4-(2-氯-4-氟苯基)-1,3-二甲基-1H-吡唑-5-胺。
5)能够具有多位点活性的化合物,例如(5.001)波尔多液(Bordeaux mixture)、(5.002)敌菌丹(captafol)、(5.003)克菌丹(captan)、(5.004)百菌清(chlorothalonil)、(5.005)氢氧化铜、(5.006)环烷酸铜(copper naphthenate)、(5.007)氧化铜、(5.008)氧氯化铜(copper oxychloride)、(5.009)硫酸铜(2+)(copper(2+)sulfate)、(5.010)二噻农(dithianon)、(5.011)多果定(dodine)、(5.012)灭菌丹(folpet)、(5.013)代森锰锌(mancozeb)、(5.014)代森锰(maneb)、(5.015)代森联(metiram)、(5.016)代森联锌(zincmetiram)、(5.017)喹啉铜(copper oxine)、(5.018)丙森锌(propineb)、(5.019)硫和硫制剂包括多硫化钙、(5.020)福美双(thiram)、(5.021)代森锌(zineb)、(5.022)福美锌(ziram)。
6)能够触发宿主防御的化合物,例如(6.001)苯并噻二唑(acibenzolar-S-methyl)、(6.002)异噻菌胺(isotianil)、(6.003)烯丙苯噻唑(probenazole)、(6.004)噻酰菌胺(tiadinil)。
7)氨基酸和/或蛋白质生物合成抑制剂,例如(7.001)嘧菌环胺(cyprodinil)、(7.002)春雷霉素(kasugamycin)、(7.003)春雷霉素盐酸盐水合物(kasugamycinhydrochloride hydrate)、(7.004)土霉素(oxytetracycline)、(7.005)嘧霉胺(pyrimethanil)、(7.006)3-(5-氟-3,3,4,4-四甲基-3,4-二氢异喹啉-1-基)喹啉。
8)ATP生成抑制剂,例如(8.001)硅噻菌胺(silthiofam)。
9)细胞壁合成抑制剂,例如(9.001)苯噻菌胺(benthiavalicarb)、(9.002)烯酰吗啉(dimethomorph)、(9.003)氟吗啉(flumorph)、(9.004)缬霉威(iprovalicarb)、(9.005)双炔酰菌胺(mandipropamid)、(9.006)丁吡吗啉(pyrimorph)、(9.007)缬菌胺(valifenalate)、(9.008)(2E)-3-(4-叔丁基苯基)-3-(2-氯吡啶-4-基)-1-(吗啉-4-基)丙-2-烯-1-酮、(9.009)(2Z)-3-(4-叔丁基苯基)-3-(2-氯吡啶-4-基)-1-(吗啉-4-基)丙-2-烯-1-酮。
10)脂和膜合成抑制剂,例如(10.001)霜霉威(propamocarb)、(10.002)霜霉威盐酸盐(propamocarb hydrochloride)、(10.003)甲基立枯磷(tolclofos-methyl)。
11)黑色素生物合成抑制剂,例如(11.001)三环唑(tricyclazole)、(11.002)2,2,2-三氟乙基{3-甲基-1-[(4-甲基苯甲酰基)氨基]丁-2-基}氨基甲酸酯。
12)核酸合成抑制剂,例如(12.001)苯霜灵(benalaxyl)、(12.002)高效苯霜灵(benalaxyl-M)(kiralaxyl)、(12.003)甲霜灵(metalaxyl)、(12.004)高效甲霜灵(metalaxyl-M)(mefenoxam)。
13)信号转导抑制剂,例如(13.001)咯菌腈(fludioxonil)、(13.002)异菌脲(iprodione)、(13.003)腐霉利(procymidone)、(13.004)丙氧喹啉(proquinazid)、(13.005)喹氧灵(quinoxyfen)、(13.006)乙烯菌核利(vinclozolin)。
14)能作为解偶联剂的化合物,例如(14.001)氟啶胺(fluazinam)、(14.002)消螨多(meptyldinocap)。
15)其他化合物,例如(15.001)脱落酸(abscisic acid)、(15.002)苯噻硫氰(benthiazole)、(15.003)bethoxazin、(15.004)卡巴西霉素(capsimycin)、(15.005)香芹酮(carvone)、(15.006)灭螨锰(chinomethionat)、(15.007)硫杂灵(cufraneb)、(15.008)环氟菌胺(cyflufenamid)、(15.009)霜脲氰(cymoxanil)、(15.010)环丙磺酰胺(cyprosulfamide)、(15.011)flutianil、(15.012)三乙膦酸铝(fosetyl-aluminium)、(15.013)乙膦酸钙(fosetyl-calcium)、(15.014)乙膦酸钠(fosetyl-sodium)、(15.015)异硫氰酸甲酯(methyl isothiocyanate)、(15.016)苯菌酮(metrafenone)、(15.017)灭粉霉素(mildiomycin)、(15.018)游霉素(natamycin)、(15.019)二甲基二硫代氨基甲酸镍(nickel dimethyldithiocarbamate)、(15.020)酞菌酯(nitrothal-isopropyl)、(15.021)oxamocarb、(15.022)oxathiapiprolin、(15.023)oxyfenthiin、(15.024)五氯苯酚(pentachlorophenol)及盐、(15.025)磷酸及其盐、(15.026)霜霉威-乙膦酸盐(propamocarb-fosetylate)、(15.027)pyriofenone(chlazafenone)(15.028)tebufloquin、(15.029)叶枯酞(tecloftalam)、(15.030)tolnifanide、(15.031)1-(4-{4-[(5R)-5-(2,6-二氟苯基)-4,5-二氢-1,2-噁唑-3-基]-1,3-噻唑-2-基}哌啶-1-基)-2-[5-甲基-3-(三氟甲基)-1H-吡唑-1-基]乙酮、(15.032)1-(4-{4-[(5S)-5-(2,6-二氟苯基)-4,5-二氢-1,2-噁唑-3-基]-1,3-噻唑-2-基}哌啶-1-基)-2-[5-甲基-3-(三氟甲基)-1H-吡唑-1-基]乙酮、(15.033)2-(6-苄基-吡啶-2-基)喹唑啉、(15.034)2,6-二甲基-1H,5H-[1,4]二噻英并[2,3-c:5,6-c']二吡咯-1,3,5,7(2H,6H)-四酮、(15.035)2-[3,5-二(二氟甲基)-1H-吡唑-1-基]-1-[4-(4-{5-[2-(丙-2-炔-1-基氧基)苯基]-4,5-二氢-1,2-噁唑-3-基}-1,3-噻唑-2-基)哌啶-1-基]乙酮、(15.036)2-[3,5-二(二氟甲基)-1H-吡唑-1-基]-1-[4-(4-{5-[2-氯-6-(丙-2-炔-1-基氧基)苯基]-4,5-二氢-1,2-噁唑-3-基}-1,3-噻唑-2-基)哌啶-1-基]乙酮、(15.037)2-[3,5-二(二氟甲基)-1H-吡唑-1-基]-1-[4-(4-{5-[2-氟-6-(丙-2-炔-1-基氧基)苯基]-4,5-二氢-1,2-噁唑-3-基}-1,3-噻唑-2-基)哌啶-1-基]乙酮、(15.038)2-[6-(3-氟-4-甲氧基苯基)-5-甲基吡啶-2-基]喹唑啉、(15.039)2-{(5R)-3-[2-(1-{[3,5-二(二氟甲基)-1H-吡唑-1-基]乙酰基}哌啶-4-基)-1,3-噻唑-4-基]-4,5-二氢-1,2-噁唑-5-基}-3-氯苯基甲磺酸酯、(15.040)2-{(5S)-3-[2-(1-{[3,5-二(二氟甲基)-1H-吡唑-1-基]乙酰基}哌啶-4-基)-1,3-噻唑-4-基]-4,5-二氢-1,2-噁唑-5-基}-3-氯苯基甲磺酸酯、(15.041)2-{2-[(7,8-二氟-2-甲基喹啉-3-基)氧基]-6-氟苯基}丙-2-醇、(15.042)2-{2-氟-6-[(8-氟-2-甲基喹啉-3-基)氧基]苯基}丙-2-醇、(15.043)2-{3-[2-(1-{[3,5-二(二氟甲基)-1H-吡唑-1-基]乙酰基}哌啶-4-基)-1,3-噻唑-4-基]-4,5-二氢-1,2-噁唑-5-基}-3-氯苯基甲磺酸酯、(15.044)2-{3-[2-(1-{[3,5-二(二氟甲基)-1H-吡唑-1-基]乙酰基}哌啶-4-基)-1,3-噻唑-4-基]-4,5-二氢-1,2-噁唑-5-基}苯基甲磺酸酯、(15.045)2-苯基苯酚及其盐、(15.046)3-(4,4,5-三氟-3,3-二甲基-3,4-二氢异喹啉-1-基)喹啉、(15.047)3-(4,4-二氟-3,3-二甲基-3,4-二氢异喹啉-1-基)喹啉、(15.048)4-氨基-5-氟嘧啶-2-醇(互变异构形式:4-氨基-5-氟嘧啶-2(1H)-酮)、(15.049)4-氧代-4-[(2-苯基乙基)氨基]丁酸、(15.050)5-氨基-1,3,4-噻二唑-2-硫醇、(15.051)5-氯-N'-苯基-N'-(丙-2-炔-1-基)噻吩2-磺酰肼、(15.052)5-氟-2-[(4-氟苄基-)氧基]嘧啶-4-胺、(15.053)5-氟-2-[(4-甲基苄基-)氧基]嘧啶-4-胺、(15.054)9-氟-2,2-二甲基-5-(喹啉-3-基)-2,3-二氢-1,4-苯并氧杂吖庚因、(15.055)丁-3-炔-1-基{6-[({[(Z)-(1-甲基-1H-四唑-5-基)(苯基)亚甲基]氨基}氧基)甲基]吡啶-2-基}氨基甲酸酯、(15.056)(2Z)-3-氨基-2-氰基-3-苯基丙烯酸乙酯、(15.057)吩嗪-1-羧酸、(15.058)3,4,5-三羟基苯甲酸丙酯、(15.059)喹啉-8-醇、(15.060)喹啉-8-醇硫酸酯(2:1)、(15.061){6-[({[(1-甲基-1H-四唑-5-基)(苯基)亚甲基]氨基}氧基)甲基]吡啶-2-基}氨基甲酸叔丁酯。
作为混合组分的生物农药
式(I)的化合物可与生物农药结合。
生物农药尤其包括细菌、真菌、酵母菌、植物提取物和由微生物形成的产物,包括蛋白质和次级代谢物。
生物农药包括细菌如产芽孢细菌(spore-forming bacteria)、根定殖细菌(root-colonizing bacteria)和作为生物杀昆虫剂、杀真菌剂或杀线虫剂起作用的细菌。
用作或可用作生物农药的这类细菌的实例为:
解淀粉芽孢杆菌(Bacillus amyloliquefaciens),菌株FZB42(DSM 231179);或蜡样芽胞杆菌(Bacillus cereus),尤其是蜡样芽孢杆菌菌株CNCM I-1562;或者坚强芽孢杆菌(Bacillus firmus),菌株I-1582(登录号CNCMI-1582);或短小芽胞杆菌(Bacilluspumilus),尤其是菌株GB34(登录号ATCC 700814)和菌株QST2808(登录号NRRL B-30087);或枯草芽孢杆菌(Bacillus subtilis),尤其是菌株GB03(登录号ATCC SD-1397),或枯草芽孢杆菌菌株QST713(登录号NRRL B-21661)或枯草芽孢杆菌菌株OST 30002(登录号NRRL B-50421);苏云金芽孢杆菌(Bacillus thuringiensis),尤其是苏云金杆菌以色列亚种(B.thuringiensis subspecies israelensis)(血清型H-14)、菌株AM65-52(登录号ATCC1276),或苏云金杆菌鲇泽亚种(B.thuringiensis subsp.aizawai),尤其是菌株ABTS-1857(SD-1372),或苏云金杆菌库尔斯塔克亚种(B.thuringiensis subsp.kurstaki)菌株HD-1,或苏云金杆菌粉虫变种(thuringiensis subsp.tenebrionis)菌株NB 176(SD-5428);侵入巴斯德氏芽菌(Pasteuria penetrans)、巴斯德氏芽菌属(Pasteuria spp.)(肾形肾状线虫(Rotylenchulus reniformis nematode))-PR3(登录号ATCC SD-5834);细黄链霉菌(Streptomyces microflavus)菌株AQ6121(=QRD 31.013,NRRL B-50550);鲜黄链霉菌(Streptomyces galbus)菌株AQ 6047(登录号NRRL 30232)。
用作或可用作生物农药的真菌和酵母菌的实例为:
巴西安白僵菌(Beauveria bassiana),尤其是菌株ATCC 74040;盾壳霉(Coniothyrium minitans),尤其是菌株CON/M/91-8(登录号DSM-9660);轮枝孢属(Lecanicillium spp.),尤其是菌株HRO LEC 12;蜡蚧轮枝菌(Lecanicillium lecanii),(以前称为Verticillium lecanii),尤其是菌株KV01;金龟子绿僵菌(Metarhiziumanisopliae),尤其是菌株F52(DSM3884/ATCC 90448);梅奇酵母菌(Metschnikowiafructicola),尤其是菌株NRRL Y-30752;玫烟色拟青霉(Paecilomyces fumosoroseus)(现名:玫烟色棒束孢(Isaria fumosorosea)),尤其是菌株IFPC 200613,或菌株Apopka 97(登录号ATCC 20874);淡紫拟青霉(Paecilomyces lilacinus),尤其是淡紫拟青霉菌株251(AGAL 89/030550);黄色蠕形霉(Talaromyces flavus),尤其是菌株V117b;深绿木霉(Trichoderma atroviride),尤其是菌株SC1(登录号CBS 122089);哈茨木霉(Trichodermaharzianum),尤其是哈茨木霉T39(登录号CNCM I-952)。
用作或可用作生物农药的病毒的实例为:
棉褐带卷蛾(Adoxophyes orana)(夏季水果卷叶蛾(summer fruit tortrix))颗粒型病毒(GV)、苹果蠹蛾(Cydia pomonella(codling moth))颗粒型病毒(GV)、棉铃虫(Helicoverpa armigera(cotton bollworm))核型多角体病毒(NPV)、甜菜夜蛾(Spodoptera exigua(beet armyworm))mNPV、草地贪夜蛾(Spodoptera frugiperda(秋夜蛾(fall armyworm)))mNPV、海灰翅夜蛾(Spodoptera littoralis(非洲棉树叶虫(Africancotton leafworm)))NPV。
还包括作为“接种剂”添加到植物或植物部位或植物器官中的细菌和真菌,这些细菌和真菌通过其特定性质促进植物生长和植物健康。可提及以下实例:
土壤杆菌属(Agrobacterium spp.)、茎瘤固氮根瘤菌(Azorhizobiumcaulinodans)、固氮螺菌属(Azospirillum spp.)、固氮菌属(Azotobacter spp.)、短根瘤菌属(Bradyrhizobium spp.)、伯霍尔德杆菌属(Burkholderia spp.),尤其是洋葱伯霍尔德杆菌(Burkholderia cepacia)(以前称为洋葱假单胞菌(Pseudomonas cepacia))、巨孢囊霉属(Gigaspora spp.)、或Gigaspora monosporum、球囊霉属(Glomus spp.)、蜡蘑属(Laccaria spp.)、布赫纳乳杆菌(Lactobacillus buchneri)、类球囊霉属(Paraglomusspp.)、豆包菌(Pisolithus tinctorus)、假单胞菌属(Pseudomonas spp.)、根瘤菌属(Rhizobium spp.)尤其是三叶草根瘤菌(Rhizobium trifolii)、须腹菌属(Rhizopogonspp.)、硬皮锈菌属(Scleroderma spp.)、乳牛肝菌属(Suillus spp.)、链霉菌属(Streptomyces spp.)。
用作或可用作生物农药的植物提取物和由微生物形成的产物(包括蛋白和次级代谢物)的实例为:
大蒜(Allium sativum)、苦艾(Artemisia absinthium)、印楝素(azadirachtin)、Biokeeper WP、Cassia nigricans、苦皮藤(Celastrus angulatus)、Chenopodiumanthelminticum、壳多糖(chitin)、Armour-Zen、鳞毛蕨(Dryopteris filix-mas)、问荆(Equisetum arvense)、Fortune Aza、Fungastop、Heads Up(奎奴亚藜(Chenopodiumquinoa)皂苷提取物)、除虫菊/除虫菊酯类、苏里南苦木(Quassia amara)、栎树属(Quercus)、皂树属(Quillaja)、Regalia、“RequiemTM杀昆虫剂”、鱼藤酮(rotenone)、鱼尼丁/兰尼碱、聚合草(Symphytum officinale)、艾菊(Tanacetum vulgare)、麝香草酚(thymol)、Triact 70、TriCon、旱金莲(Tropaeulum majus)、大荨麻(Urtica dioica)、Veratrin、槲寄生(Viscum album)、十字花科(Brassicaceae)提取物,尤其是油菜籽粉末或芥末粉末。
作为混合组分的安全剂
式(I)的化合物可与安全剂结合,例如解草酮(benoxacor)、喹氧乙酸(解草酯)(cloquintocet(-mexyl))、解草胺腈(cyometrinil)、环丙磺酰胺(cyprosulfamide)、二氯丙烯胺(dichlormid)、解草唑(fenchlorazole(-ethyl))、解草啶(fenclorim)、解草胺(flurazole)、氟草肟(fluxofenim)、解草噁唑(furilazole)、双苯噁唑酸(乙酯)(isoxadifen(-ethyl))、吡唑解草酯(mefenpyr(-diethyl))、萘二甲酸酐(naphthalicanhydride)、解草腈(oxabetrinil)、2-甲氧基-N-{4-[(甲基氨基甲酰基)氨基]苯基}磺酰基)苯甲酰胺(CAS129531-12-0)、4-(二氯乙酰基)-1-氧杂-4-氮杂螺[4.5]癸烷(CAS71526-07-3)、2,2,5-三甲基-3-(二氯乙酰基)-1,3-噁唑烷(CAS52836-31-4)。
植物和植物部位
所有的植物和植物部位均可根据本发明进行处理。在本文中植物应理解为意指所有植物和植物种群,例如期望和不期望的野生植物或作物植物(包括天然存在的作物植物),例如谷物(小麦、稻、黑小麦、大麦、黑麦、燕麦)、玉米、大豆、马铃薯、糖用甜菜、甘蔗、番茄、甜椒、黄瓜、甜瓜、胡萝卜、西瓜、洋葱、莴苣、菠菜、韭、豆类、甘蓝(如卷心菜)和其他蔬菜品种,棉花、烟草、油菜,以及水果植物(水果为苹果、梨、柑橘类水果和葡萄)。作物植物可以为可通过常规的育种和优化方法或者通过生物技术方法和基因工程方法或这些方法的组合而获得的植物,包括转基因植物以及包括可受或不受植物育种者的权利(plantbreeders’right)保护的植物栽培种。植物应理解为意指所有发育阶段,例如种子、幼苗和早期(未成熟)植物直至并包括成熟植物。植物部位应理解为意指植物的地上和地下的所有部位和器官,如芽、叶、花和根,给出的实例为叶、针叶、茎、枝干、花、子实体、果实和种子,以及根、块茎和根茎。植物部位还包括采收植物或采收植物部位以及无性和有性繁殖的材料,例如插条、块茎、根茎、分檗(slip)和种子。
本发明的使用式(I)的化合物对植物和植物部位进行处理通过常规处理方法直接进行或使所述化合物作用于其环境、生境或储存空间来进行,例如通过浸渍、喷雾、蒸发、雾化、撒播、涂抹、注射进行,以及在繁殖材料、尤其是种子的情况下,还通过施用一层或多层包衣来进行。
如上所述,可根据本发明处理所有植物及其部位。在一个优选的实施方案中,处理野生植物物种和植物栽培种,或通过常规生物育种方法如杂交或原生质体融合而获得的那些,及其部位。在另一优选的实施方案中,处理通过基因工程方法—如果合适,与常规方法结合—而获得的转基因植物和植物栽培种(遗传修饰生物体)及其部位。术语“部位”或“植物的部位”或“植物部位”已在上文中作出解释。特别优选的是,根据本发明处理各自市售的常规植物栽培种或正在使用的那些植物。植物栽培种应理解为意指具有新特性(“性状”)并且已通过常规育种、通过诱变或通过重组DNA技术获得的植物。它们可以是栽培种、变种、生物型或基因型。
转基因植物、种子处理和整合株系(integration event)
根据本发明进行处理的优选的转基因植物或植物栽培种(通过基因工程获得的那些植物)包括通过基因修饰接受了赋予这些植物特别有利的有用特性(“性状”)的基因材料的所有植物。这些特性的实例为:更好的植物生长、对高温或低温的增强的耐受性、对干旱或对水或土壤盐度水平的增强的耐受性、提高的开花性能、更容易采收、加速成熟、更高的采收产量、采收产品的更高的品质和/或更高的营养价值、采收产品的更好的储存性和/或可加工性。这些特性的其他和特别强调的实例为:增强植物对动物害虫和微生物害虫的抗性,例如昆虫、蛛形纲动物、线虫、螨、蛞蝓以及蜗牛,例如这归因于在植物中形成的毒素、特别是通过苏云金芽孢杆菌的基因材料(例如通过基因CryIA(a)、CryIA(b)、CryIA(c)、CryIIA、CryIIIA、CryIIIB2、Cry9c、Cry2Ab、Cry3Bb和CryIF及其组合)在植物中形成的那些毒素,以及增强的植物对植物病原性真菌、细菌和/或病毒的抗性,其例如由内吸性获得的抗性(SAR)、系统素(systemin)、植物抗毒素、激发子和抗性基因及相应表达的蛋白质和毒素引起,以及增强的植物对某些活性除草化合物的耐受性,例如咪唑啉酮类、磺酰脲类、草甘膦或膦丝菌素(phosphinothricin)(例如“PAT”基因)。赋予了所述所需特性(“性状”)的基因还可互相结合地存在于转基因植物中。所提及的转基因植物的实例包括重要的作物植物,例如谷物(小麦、稻、黑小麦、大麦、黑麦、燕麦)、玉米、大豆、马铃薯、糖用甜菜、甘蔗、番茄、豌豆和其他蔬菜类型,棉花、烟草、油菜,以及水果植物(水果为苹果、梨、柑橘类水果和葡萄),尤其强调的是玉米、大豆、小麦、稻、马铃薯、棉花、甘蔗、烟草和油菜。特别强调的特性(“性状”)是增强的植物对昆虫、蛛形纲动物、线虫和蛞蝓以及蜗牛的抗性。
作物保护——处理的类型
使用常规处理方法利用式(I)的化合物对植物和植物部位进行直接处理或通过作用于其环境、生境或储存空间来进行处理,所述常规处理方法为例如浸渍、喷雾、雾化、灌溉、蒸发、撒粉、成雾、撒播、发泡、涂抹、撒布、注射、浇水(浇灌)、滴灌,以及在繁殖材料、尤其是种子的情况下,还通过干种子处理、液体种子处理、浆体处理、通过结壳、通过用一层或多层包衣包覆等进行处理。还可以通过超低容量方法施用式(I)的化合物或者将式(I)的化合物的施用形式或其本身注射到土壤中。
优选的对植物的直接处理为叶面施用,即将式(I)的化合物施用到叶面上,在该情况下处理频率和施用率应根据所述害虫的侵染水平来调节。
在内吸性活性化合物的情况下,式(I)的化合物还经由根系统进入植物。然后通过将式(I)的化合物作用于植物的生境来处理该植物。这可以通过下述方式完成:例如,浇灌;或者通过混入土壤或营养液中,这意味着植物的生长场所(例如土壤或水培体系)被液体形式的式(I)的化合物浸渍;或通过土壤施用,这意味着将本发明的式(I)的化合物以固体形式(例如以颗粒剂的形式)引入到植物的生长场所。在水稻作物的情况下,这还可以通过将式(I)的化合物以固体施用形式(例如作为颗粒剂)计量加入水稻田来完成。
种子处理
人们早已知道通过处理植物种子来防治动物害虫并且这是不断改进的主题。然而,种子处理涉及一系列不能总是以令人满意的方式得以解决的问题。因此,需要开发保护种子和发芽植物的方法,该方法不需要或至少显著地减少了在储存过程中、在播种后或在植物出苗后农药的额外施用。此外还需要优化所使用的活性化合物的量,以便为种子和发芽植物提供最佳的保护以免受动物害虫的侵害,而所使用的活性化合物则不会损害植物本身。特别地,处理种子的方法还应考虑到害虫抗性或害虫耐受性转基因植物的固有的杀昆虫或杀线虫特性,以便用最少量的农药来实现对种子以及发芽植物的最佳保护。
因此,特别地,本发明还涉及一种通过用式(I)的化合物之一处理种子来保护种子和发芽植物免受害虫侵害的方法。本发明的保护种子和发芽植物免受害虫侵害的方法还包括在一个操作中同时或依序用式(I)的化合物和混合组分处理种子的方法。其还包括在不同的时间用式(I)的化合物和混合组分处理种子的方法。
本发明还涉及式(I)的化合物用于处理种子以保护种子和所得植物免受动物害虫侵害的用途。
本发明还涉及用本发明的式(I)的化合物处理过以保护其免受动物害虫侵害的种子。本发明还涉及用式(I)的化合物和混合组分同时处理过的种子。本发明还涉及用式(I)的化合物和混合组分在不同时间处理过的种子。在用式(I)的化合物和混合组分在不同时间处理过的种子的情况下,各物质可以不同的层存在于种子上。在这种情况下,包含式(I)的化合物和混合组分的层可以任选地被中间层分隔。本发明还涉及其中已经施用了式(I)的化合物和混合组分作为包衣的一部分或作为除了包衣外的另一层或另几层的种子。
本发明还涉及在用式(I)的化合物处理后,进行薄膜包衣过程以防止种子遭受灰尘磨损的种子。
当式(I)的化合物内吸性地起作用时,产生的优点之一在于:通过处理种子,不仅保护种子本身还保护由其得到的植物在出苗后免受动物害虫的侵害。以这种方式,可无需在播种时或在其之后不久对作物进行即时处理。
另一个优势在于,用式(I)的化合物处理种子可促进已处理过的种子的发芽和出苗。
同样认为有利的是,式(I)的化合物还可特别地用于转基因种子。
此外,式(I)的化合物还可与信号技术组分结合使用,从而导致共生体(例如根瘤菌、菌根和/或内生细菌或真菌)更好的定殖(colonization),和/或优化的固氮作用。
式(I)的化合物适于保护在农业、温室、林业或园艺中使用的任何植物品种的种子。更具体而言,其为以下植物的种子:谷物(例如小麦、大麦、黑麦、粟和燕麦)、玉米、棉花、大豆、稻、马铃薯、向日葵、咖啡、烟草、加拿大油菜、油菜、甜菜(例如糖用甜菜和饲用甜菜)、花生、蔬菜(例如番茄、黄瓜、菜豆、十字花科蔬菜、洋葱和莴苣)、水果植物、草坪植物和观赏性植物。特别重要的是处理谷物(小麦、大麦、黑麦、燕麦)、玉米、大豆、棉花、加拿大油菜、油菜、蔬菜和稻的种子。
如上所述,用式(I)的化合物处理转基因种子也是特别重要的。其包括通常包含至少一种异源基因的植物的种子,所述异源基因控制特别是具有杀昆虫和/或杀线虫特性的多肽的表达。转基因种子中的异源基因可源自微生物如芽孢杆菌属(Bacillus)、根瘤菌属(Rhizobium)、假单孢菌属(Pseudomonas)、沙雷氏菌属(Serratia)、木霉属(Trichoderma)、棍状杆菌属(Clavibacter)、球囊霉属(Glomus)或胶霉属(Gliocladium)。本发明特别适合用于处理包含至少一种源自芽孢杆菌属的异源基因的转基因种子。所述异源基因更优选衍生自苏云金芽孢杆菌(Bacillus thuringiensis)。
在本发明的上下文中,将式(I)的化合物施用于种子。优选在这样的状态下处理种子:其足够稳定以使得在处理过程中不发生损害。一般而言,可在采收和播种之间的任意时间处理种子。通常使用已与植物分离并且已除去穗轴、壳、茎、荚(coat)、毛或果肉的种子。例如,可使用已采收、清洁并干燥至允许贮存的水分含量的种子。或者,还可使用在干燥之后例如用水处理然后再干燥(例如引发(priming))的种子。在稻种子的情况下,还可以使用例如已浸泡在水中直至其达到稻胚芽的某一阶段(“胚乳(pigeon breast)阶段”)的种子,这导致刺激了发芽和更均匀的出芽。
在处理种子时,通常必须确保选择施用于种子的式(I)的化合物的量和/或其他添加剂的量,使得不对种子的发芽产生不利的影响,或不损害所得的植物。特别是对于在某些施用率下可能会表现出植物毒性效应的活性化合物,必须保证这点。
通常,将式(I)的化合物以合适的制剂形式施用于种子。用于种子处理的合适的制剂和方法是本领域技术人员已知的。
可将式(I)的化合物转化为常规的拌种制剂,例如溶液剂、乳剂、悬浮剂、粉剂、泡沫剂、浆剂(slurry)或其他种子包衣组合物,以及ULV制剂。
这些制剂用已知方式通过使式(I)的化合物与常规添加剂(例如常规的增量剂以及溶剂或稀释剂、染料、润湿剂、分散剂、乳化剂、消泡剂、防腐剂、二次增稠剂、胶粘剂、赤霉素以及水)进行混合而制备。
可存在于可根据本发明使用的拌种制剂中的染料为常用于此目的的所有染料。可使用微溶于水的颜料或溶于水的染料。实例包括已知的名称为罗丹明B(Rhodamine B)、C.I.颜料红112和C.I.溶剂红1的染料。
可存在于可根据本发明使用的拌种制剂中的有用的润湿剂为促进润湿并通常用于配制农用化学活性化合物的所有物质。优选使用萘磺酸烷基酯,如萘磺酸二异丙酯或萘磺酸二异丁酯。
可存在于可根据本发明使用的拌种制剂中的合适的分散剂和/或乳化剂为常用于配制农用化学活性化合物的所有非离子、阴离子和阳离子分散剂。可优选使用非离子或阴离子分散剂,或者非离子或阴离子分散剂的混合物。合适的非离子分散剂特别地包括环氧乙烷/环氧丙烷嵌段聚合物、烷基酚聚乙二醇醚和三苯乙烯基苯酚聚乙二醇醚,以及其磷酸化或硫酸化衍生物。合适的阴离子分散剂特别为木素磺酸盐、聚丙烯酸盐和芳基磺酸盐-甲醛缩合物。
可存在于可根据本发明使用的拌种制剂中的消泡剂为常用于配制农业化学活性化合物的所有抑制泡沫的物质。可优选使用硅酮消泡剂和硬脂酸镁。
可存在于可根据本发明使用的拌种制剂中的防腐剂为可在农用化学组合物中用于此目的的所有物质。实例包括二氯酚和苄醇半缩甲醛。
可存在于可根据本发明使用的拌种制剂中的二次增稠剂为可在农用化学组合物中用于此目的的所有物质。优选的实例包括纤维素衍生物、丙烯酸衍生物、黄原胶、改性粘土以及细分散二氧化硅。
可存在于可根据本发明使用的拌种制剂中的有用的粘着剂为可用于拌种产品的所有常规的粘合剂。优选的实例包括聚乙烯基吡咯烷酮、聚乙酸乙烯酯、聚乙烯醇和甲基纤维素。
可存在于可根据本发明使用的拌种制剂中的赤霉素优选为赤霉素A1、A3(=赤霉酸)、A4和A7;特别优选使用赤霉酸。所述赤霉素是已知的(参见R.Wegler“Chemie derPflanzenschutz-und”,第2卷,Springer Verlag,1970,第401-412页)。
可根据本发明使用的拌种制剂可以直接地或预先用水稀释后,用于处理各种不同类型的种子。例如,浓缩剂或可通过用水稀释而由其获得的制剂可用于拌种以下植物的种子:谷物(例如小麦、大麦、黑麦、燕麦和黑小麦),以及玉米、稻、油菜、豌豆、豆类、棉花、向日葵、大豆和甜菜,或各种不同的蔬菜。可根据本发明使用的拌种制剂或其稀释使用形式还可用于拌种转基因植物的种子。
对于用可根据本发明使用的拌种制剂或通过加入水而由其制得的使用形式来处理种子,所有常用于拌种的混合装置都是有用的。具体而言,拌种过程为将种子置于间歇操作或连续操作的混合器中;加入特定所需量的拌种制剂(以其本身或预先用水稀释后);以及进行混合直到制剂均匀地分布在种子上。如果合适,之后进行干燥操作。
可根据本发明使用的拌种制剂的施用率可在较宽的范围内变化。这由制剂中式(I)的化合物的具体含量以及种子决定。式(I)的化合物的施用率通常为0.001至50g/Kg种子,优选0.01至15g/Kg种子。
动物健康
在动物健康领域,即兽医学领域,式(I)的化合物对于动物寄生虫、特别是外寄生虫或内寄生虫是有活性的。术语“内寄生虫”特别包括蠕虫和原生动物,如球虫目(coccidia)。外寄生虫通常且优选为节肢动物,尤其是昆虫或螨类。
在兽医学领域中,具有有利的温血动物毒性的式(I)的化合物适用于防治在家畜、繁育动物、动物园动物、实验室动物、实验动物和家养动物中在动物繁育和动物畜牧中出现的寄生虫。它们在对抗寄生虫的所有或特定发育阶段具有活性。
农业家畜包括,例如,哺乳动物,如绵羊、山羊、马、驴、骆驼、水牛、兔、驯鹿、扁角鹿,尤其是牛和猪;或家禽,如火鸡、鸭、鹅,尤其是鸡;或鱼或甲壳动物,如在水产养殖中;或可视情况,昆虫如蜜蜂。
家养动物包括,例如,哺乳动物,如仓鼠、豚鼠、大鼠、小鼠、毛丝鼠、雪貂,特别是狗、猫、笼鸟;爬行动物、两栖动物或观赏鱼。
在一个具体的实施方案中,将式(I)的化合物施用于哺乳动物。
在另一个具体的实施方案中,将式(I)的化合物施用于禽类,即笼鸟或特别是家禽。
使用式(I)的化合物来防治动物寄生虫,旨在减少或预防疾病、死亡病例和性能下降(在肉、奶、毛、皮、蛋、蜜等情况下),从而使得动物饲养更经济且更简单,并可实现更好的动物健康。
在本文的上下文中,关于动物健康领域,术语“防治”(control或controlling)意指式(I)的化合物有效地将被寄生虫感染的动物中的特定寄生虫的发生率降低至无害水平。更具体而言,在本文的上下文中,“防治”意指式(I)的化合物杀死各种寄生虫、抑制其生长或抑制其增殖。
节肢动物包括,例如,但不限于:
虱目(Anoplurida),例如血虱属(Haematopinus spp.)、毛虱属(Linognathusspp.)、虱属(Pediculus spp.)、Phtirus属和管虱属(Solenopotes spp.);
食毛目(Mallophagida)和钝角亚目(Amblycerina)和丝角亚目(Ischnocerina),例如牛羽虱属(Bovicola spp.)、畜虱属(Damalina spp.)、猫虱属(Felicola spp.)、Lepikentron属、禽虱属(Menopon spp.)、嚼虱属(Trichodectes spp.)、毛羽虱属(Trimenopon spp.)、巨羽虱属(Trinoton spp.)、Werneckiella属;
双翅目(Diptera)和长角亚目(Nematocerina)和短角亚目(Brachycerina),例如伊蚊属(Aedes spp.)、按蚊属(Anopheles spp.)、黄虻属(Atylotus spp.)、蜂虱蝇属(Braula spp.)、丽蝇属(Calliphora spp.)、金蝇属(Chrysomyia spp.)、斑虻属(Chrysopsspp.)、库蚊属(Culex spp.)、库蠓属(Culicoides spp.)、真蚋属(Eusimulium spp.)、厕蝇属(Fannia spp.)、胃蝇属(Gasterophilus spp.)、舌蝇属(Glossina spp.)、角蝇属(Haematobia spp.)、麻虻属(Haematopota spp.)、虱蝇属(Hippobosca spp.)、瘤虻属(Hybomitra spp.)、齿股蝇属(Hydrotaea spp.)、皮蝇属(Hypoderma spp.)、羊虱蝇属(Lipoptena spp.)、绿蝇属(Lucilia spp.)、罗蛉属(Lutzomyia spp.)、蜱蝇属(Melophagus spp.)、莫蝇属(Morellia spp.)、家蝇属(Musca spp.)、短蚋属(Odagmiaspp.)、狂蝇属(Oestrus spp.)、Philipomyia属、白蛉属(Phlebotomus spp.)、鼻狂蝇属(Rhinoestrus spp.)、麻蝇属(Sarcophaga spp.)、蚋属(Simulium spp.)、螫蝇属(Stomoxys spp.)、虻属(Tabanus spp.)、大蚊属(Tipula spp.)、维蚋属(Wilhelmiaspp.)、污蝇属(Wohlfahrtia spp.);
蚤目(Siphonapterida),例如角叶蚤属(Ceratophyllus spp.)、栉头蚤属(Ctenocephalides spp.)、蚤属(Pulex spp.)、潜蚤属(Tunga spp.)、客蚤属(Xenopsyllaspp.);
异翅目(Heteropterida),例如臭虫属(Cimex spp.)、锥蝽属(Panstrongylusspp.)、红猎蝽属(Rhodnius spp.)、锥猎蝽属(Triatoma spp.);以及来自蜚蠊目(Blattarida)的公害和卫生害虫。
此外,在节肢动物的情况下,应提及例如但不限于以下蜱螨亚纲(Acari):
蜱螨亚纲(Acari)(蜱螨目(Acarina))和后气门目(Metastigmata),例如软蜱科(Argasidae)如锐缘蜱属(Argas spp.)、钝缘蜱属(Ornithodorus spp.)、耳蜱属(Otobiusspp.),硬蜱科(Ixodidae)如花蜱属(Amblyomma spp.)、革蜱属(Dermacentor spp.)、血蜱属(Haemophysalis spp.)、璃眼蜱属(Hyalomma spp.)、硬蜱属(Ixodes spp.)、扇头蜱属(Rhipicephalus(牛蜱属(Boophilus))spp.)、扇头蜱属(Rhipicephalus spp.)(多宿主蜱的原始属);中气门目(Mesostigmata)如皮刺螨属(Dermanyssus spp.)、禽刺螨属(Ornithonyssus spp.)、肺刺螨属(Pneumonyssus spp.)、刺利螨属(Raillietia spp.)、胸孔螨属(Sternostoma spp.)、厉螨属(Tropilaelaps spp.)、瓦螨属(Varroa spp.);辐螨目(Actinedida)(前气门目(Prostigmata)),例如蜂盾螨属(Acarapis spp.)、姬螯螨属(Cheyletiella spp.)、蠕形螨属(Demodex spp.)、Listrophorus属、肉螨属(Myobiaspp.)、新恙螨属(Neotrombicula spp.)、禽螯螨属(Ornithocheyletia spp.)、疮螨属(Psorergates spp.)、恙螨属(Trombicula spp.);和粉螨目(Acaridida)(无气门目(Astigmata)),例如粉螨属(Acarus spp.)、嗜木螨属(Caloglyphus spp.)、皮螨属(Chorioptes spp.)、气囊螨属(Cytodites spp.)、颈下螨属(Hypodectes spp.)、鸟疥螨属(Knemidocoptes spp.)、鸡雏螨属(Laminosioptes spp.)、耳螨属(Notoedres spp.)、耳疥螨属(Otodectes spp.)、痒螨属(Psoroptes spp.)、翅螨属(Pterolichus spp.)、疥螨属(Sarcoptes spp.)、Trixacarus属、食酪螨属(Tyrophagus spp.)。
寄生性原生动物的实例包括但不限于:
鞭毛纲(Mastigophora)(鞭毛虫纲(Flagellata)),例如:
后滴门(Metamonada):双滴虫目(Diplomonadida),例如贾第虫属(Giardiaspp.)、螺旋核虫属(Spironucleus spp.)。
Parabasala:毛滴虫目(Trichomonadida),例如组织滴虫属(Histomonas spp.)、五鞭毛滴虫属(Pentatrichomonas spp.)、四毛滴虫属(Tetratrichomonas spp.)、毛滴虫属(Trichomonas spp.)、三毛滴虫属(Tritrichomonas spp.)。
眼虫门(Euglenozoa):锥体虫目(Trypanosomatida),例如利什曼原虫属(Leishmania spp.)、锥体虫属(Trypanosoma spp.)。
肉鞭虫亚门(Sarcomastigophora)(肉足亚门(Rhizopoda)),例如内阿米巴科(Entamoebidae),例如内阿米巴属(Entamoeba spp.)、Centramoebidae,例如棘变形虫属(Acanthamoeba sp.)、Euamoebidae,例如哈氏虫属(Harmanella sp.)。
囊泡虫类(Alveolata),如顶复亚门(Apicomplexa)(孢子重亚门(Sporozoa)):如隐孢子虫属(Cryptosporidium spp.);艾美耳球虫目(Eimeriida),例如贝诺孢子虫属(Besnoitia spp.)、囊等孢虫属(Cystoisospora spp.)、艾美球虫属(Eimeria spp.)、哈蒙德虫属(Hammondia spp.)、等孢子球虫属(Isospora spp.)、新孢子虫属(Neospora spp.)、肉孢子虫属(Sarcocystis spp.)、弓形虫属(Toxoplasma spp.);Adeleida目,例如肝簇虫属(Hepatozoon spp.)、克洛虫属(Klossiella spp.);血孢子虫目(Haemosporida),例如住白虫属(Leucocytozoon spp.)、疟原虫属(Plasmodium spp.);梨形虫目(Piroplasmida),例如巴贝虫属(Babesia spp.)、纤毛虫属(Ciliophora spp.)、Echinozoon属、泰勒虫属(Theileria spp.);Vesibuliferida目,例如肠袋虫属(Balantidium spp.)、布克斯顿纤毛虫属(Buxtonella spp.)。
微孢子门(Microspora),例如脑胞内原虫属(Encephalitozoon spp.)、肠孢虫属(Enterocytozoon spp.)、球形虫属(Globidium spp.)、微粒子虫属(Nosema spp.)、以及例如粘原虫属(Myxozoa spp.)。
对人或动物致病的蠕虫包括例如棘头虫纲(Acanthocephala)、Nematoden、舌形动物门(Pentastoma)和扁形动物门(Platyhelminthes)(如,单殖亚纲(Monogenea)、绦虫(Cestode)和吸虫类(trematodes))。
示例性的蠕虫包括但不限于:
单殖亚纲:例如:指环虫属(Dactylogyrus spp.)、三代虫属(Gyrodactylusspp.)、Microbothrium属、多盘吸虫属(Polystoma spp.)、Troglecephalus属;
绦虫:假叶目(Pseudophyllidea),例如:吸叶绦虫属(Bothridium spp.)、裂头绦虫属(Diphyllobothrium spp.)、复殖孔绦虫属(Diplogonoporus spp.)、Ichthyobothrium属、舌状绦虫属(Ligula spp.)、Schistocephalus属、迭宫绦虫属(Spirometra spp.);
圆叶目(Cyclophyllidea),例如:Andyra属、裸头绦虫属(Anoplocephala spp.)、无卵黄腺绦虫属(Avitellina spp.)、伯特绦虫属(Bertiella spp.)、鸣绦虫属(Cittotaenia spp.)、代凡绦虫属(Davainea spp.)、双睾绦虫属(Diorchis spp.)、复孔绦虫属(Diplopylidium spp.)、犬复孔绦虫属(Dipylidium spp.)、棘球绦虫属(Echinococcus spp.)、棘叶绦虫属(Echinocotyle spp.)、棘鳞绦虫属(Echinolepisspp.)、泡尾绦虫属(Hydatigera spp.)、膜壳绦虫属(Hymenolepis spp.)、约优克斯绦虫属(Joyeuxiella spp.)、中殖孔绦虫属(Mesocestoides spp.)、蒙尼茨绦虫属(Monieziaspp.)、副裸头绦虫属(Paranoplocehala spp.)、瑞利绦虫属(Raillietina spp.)、西里西亚绦虫属(Stilesia spp.)、带绦虫属(Taenia spp.)、曲子宫绦虫属(Thysaniezia spp.)、Thysanosomsa属;
吸虫:选自复殖纲(Digenea),例如:澳毕吸虫属(Austrobilharzia spp.)、短咽吸虫属(Brachylaima spp.)、杯殖吸虫属(Calicophoron spp.)、下弯吸虫属(Catatropisspp.)、支睾吸虫属(Clonorchis spp.)、肛瘤吸虫属(Collyriclum spp.)、殖盘吸虫属(Cotylophoron spp.)、环腔吸虫属(Cyclocoelum spp.)、双腔吸虫属(Dicrocoeliumspp.)、双穴吸虫属(Diplostomum spp.)、棘隙吸虫属(Echinochasmus spp.)、棘缘吸虫属(Echinoparyphium spp.)、棘口吸虫属(Echinostoma spp.)、阔盘吸虫属(Eurytemaspp.)、片形吸虫属(Fasciola spp.)、片形吸虫属(Fascioloides spp.)、姜片吸虫属(Fasciolopsis spp.)、菲策吸虫(Fischoederius spp.)、腹袋吸虫属(Gastrothylacusspp.)、巨毕吸虫属(Gigantobilharzia spp.)、巨盘吸虫属(Gigantoctyle spp.)、异形吸虫属(Heterophyes spp.)、低颈吸虫属(Hypoderaeum spp.)、彩蚴吸虫属(Leucochloridium spp.)、后殖吸虫属(Metagonimus spp.)、次睾吸虫属(Metorchisspp.)、侏形吸虫属(Nanophyetus spp.)、背孔吸虫属(Notocotylus spp.)、后睾吸虫属(Opisthorchis spp.)、鸟毕吸虫属(Ornithobilharzia spp.)、并殖吸虫属(Paragonimusspp.)、同端盘吸虫属(Paramphistomum spp.)、斜睾吸虫属(Plagiorchis spp.)、茎双穴吸虫属(Posthodiplostomum spp.)、前殖吸虫属(Prosthogonimus spp.)、血吸虫属(Schistosoma spp.)、毛毕吸虫属(Trichobilharzia spp.)、鲑吸虫属(Troglotremaspp.)、盲腔吸虫属(Typhlocoelum spp.);
线虫:毛线目(Trichinellida),例如:毛细线虫属(Capillaria spp.)、旋毛虫属(Trichinella spp.)、Trichomosoides属、鞭虫属(Trichuris spp.);
垫刃目(Tylenchida),例如:细丝鲶属(Micronema spp.)、Parastrangyloides属、类圆线虫属(Strongyloides spp.);
杆形目(Rhabditina),例如:猫圆线虫属(Aelurostrongylus spp.)、裂口线虫属(Amidostomum spp.)、钩虫线虫属(Ancylostoma spp.)、血管圆线虫属(Angiostrongylusspp.)、Bronchonema属、仰口线虫属(Bunostomum spp.)、夏伯特线虫属(Chabertia spp.)、古柏线虫属(Cooperia spp.)、Cooperioides属、环体线虫属(Crenosoma spp.)、杯口属(Cyathostomum spp.)、Cyclococercus属、Cyclodontostomum属、杯杯属(Cylicocyclusspp.)、杯冠属(Cylicostephanus spp.)、柱咽属(Cylindropharynx spp.)、囊尾线虫属(Cystocaulus spp.)、网尾线虫属(Dictyocaulus spp.)、鹿圆线虫属(Elaphostrongylusspp.)、类丝虫属(Filaroides spp.)、球首属(Globocephalus spp.)、细纹线虫属(Graphidium spp.)、辐首线虫属(Gyalocephalus spp.)、血矛线虫属(Haemonchus spp.)、螺旋线虫属(Heligmosomoides spp.)、猪圆线虫属(Hyostrongylus spp.)、马歇尔线虫属(Marshallagia spp.)、后圆线虫属(Metastrongylus spp.)、缪勒线虫属(Muelleriusspp.)、板口线虫属(Necator spp.)、细颈线虫属(Nematodirus spp.)、新圆线虫属(Neostrongylus spp.)、日本圆线虫属(Nippostrongylus spp.)、尖柱线虫属(Obeliscoides spp.)、食道齿属(Oesophagodontus spp.)、食道口线虫属(Oesophagostomum spp.)、沃鲁线虫属(Ollulanus spp.)、鸟圆线虫属(Ornithostrongylus spp.)、奥斯勒线虫属(Oslerus spp.)、奥斯特线虫属(Ostertagiaspp.)、副库柏属(Paracooperia spp.)、Paracrenosoma属、副类丝虫属(Parafilaroidesspp.)、拟马鹿圆线虫属(Parelaphostrongylus spp.)、肺尾属(Pneumocaulus spp.)、肺圆线虫属(Pneumostrongylus spp.)、杯口线虫属(Poteriostomum spp.)、原圆线虫属(Protostrongylus spp.)、Spicocaulus属、冠尾线属(Stephanurus spp.)、圆线虫属(Strongylus spp.)、比翼属(Syngamus spp.)、背带线虫属(Teladorsagia spp.)、毛线属(Trichonema spp.)、毛圆线虫属(Trichostrongylus spp.)、三齿属(Triodontophorusspp.)、隐圆线虫属(Troglostrongylus spp.)、弯口属(Uncinaria spp.);
旋尾目(Spirurida),例如:棘唇线虫属(Acanthocheilonema spp.)、异尖线虫属(Anisakis spp.)、禽蛔虫属(Ascaridia spp.)、蛔虫属(Ascaris spp.)、斜环咽线虫属(Ascarops spp.)、无刺线虫属(Aspiculuris spp.)、贝利蛔线虫属(Baylisascarisspp.)、布鲁线虫属(Brugia spp.)、Cercopithifilaria属、Crassicauda属、棘唇线虫属(Dipetalonema spp.)、恶丝虫属(Dirofilaria spp.)、龙线虫属(Dracunculus spp.)、德拉西线虫属(Draschia spp.)、蛲虫属(Enterobius spp.)、丝虫属(Filaria spp.)、颚口线虫属(Gnathostoma spp.)、筒线虫属(Gongylonema spp.)、丽线虫属(Habronema spp.)、异刺线虫属(Heterakis spp.);光丝虫属(Litomosoides spp.)、罗阿丝虫属(Loa spp.)、盘尾丝虫属(Onchocerca spp.)、尖尾线虫属(Oxyuris spp.)、副柔线属(Parabronemaspp.)、副丝虫属(Parafilaria spp.)、副蛔虫属(Parascaris spp.)、栓尾线虫属(Passalurus spp.)、泡翼线虫属(Physaloptera spp.)、普氏线虫属(Probstmayriaspp.)、Pseudofilaria属、腹腔丝虫属(Setaria spp.)、Skjrabinema属、旋毛线虫属(Spirocerca spp.)、冠丝虫属(Stephanofilaria spp.)、Strongyluris属、管状线虫属(Syphacia spp.)、吸吮线虫属(Thelazia spp.)、弓蛔线虫属(Toxascaris spp.)、弓蛔虫属(Toxocara spp.)、吴策线虫属(Wuchereria spp.);
棘头虫纲(Acanthocephala):寡棘吻目(Oligacanthorhynchida),例如:巨吻棘头虫属(Macracanthorhynchus spp.)、前睾棘头虫属(Prosthenorchis spp.);Moniliformida目,例如:念珠棘虫属(Moniliformis spp.);
多形目(Polymorphida),例如细颈棘头虫属(Filicollis spp.);棘吻目(Echinorhynchida),例如棘头花属(Acanthocephalus spp.)、棘吻虫属(Echinorhynchusspp.)、似细吻棘头虫属(Leptorhynchoides spp.);
舌形动物门(Pentastoma):蛇舌状虫目(Porocephalida),例如舌形虫属(Linguatula spp.)。
在兽医领域和动物饲养中,通过本领域通常已知的方法(例如经肠内、胃肠外、真皮或经鼻途径)以合适的制剂形式施用式(I)的化合物。施用可以是预防性的、补救性(metaphylactic)的或治疗性的。
因此,本发明的一个实施方案涉及用作药物的式(I)的化合物。
另一个方面涉及用作抗内寄生虫剂的式(I)的化合物。
本发明的另一具体的方面涉及用作抗蠕虫剂(antithelminthic)、尤其是用作杀线虫剂、杀扁形动物剂、杀棘头虫剂或杀舌形动物剂的式(I)的化合物。
本发明的另一具体的方面涉及用作抗原生动物剂的式(I)的化合物。
另一方面涉及用作抗外寄生虫剂、尤其是杀节肢动物剂、非常特别是杀昆虫剂或杀螨剂的式(I)的化合物。
本发明的其他方面为兽药制剂,其包含有效量的至少一种式(I)的化合物和至少一种以下物质:药学上可接受的赋形剂(例如固体或液体稀释剂)、药学上可接受的助剂(例如表面活性剂),尤其是常规用于兽药制剂中的药学上可接受的赋形剂和/或常规用于兽药制剂中的药学上可接受的助剂。
本发明的一个相关方面是一种制备如本文所述的兽药制剂的方法,其包括以下步骤:将至少一种式(I)的化合物与药学上可接受的赋形剂和/或助剂、尤其是与常规用于兽药制剂中的药学上可接受的赋形剂和/或常规用于兽药制剂中的助剂进行混合。
本发明的另一具体方面是选自杀外寄生虫和杀内寄生虫制剂的兽药制剂以及其制备方法,所述兽药制剂尤其选自上述方面的驱虫、抗原生动物和杀节肢动物制剂,非常特别选自杀线虫、杀扁形动物、杀棘头虫、杀舌形动物、杀昆虫和杀螨制剂。
另一方面涉及一种通过在具有需求的动物、尤其是非人动物中,使用有效量的式(I)的化合物治疗寄生虫感染的方法,尤其是治疗由选自本文中所提及的外寄生虫和内寄生虫的寄生虫所引起的感染的方法。
另一方面涉及一种通过在具有需求的动物、尤其是非人动物中使用本文所定义的兽药制剂治疗寄生虫感染的方法,尤其是治疗由选自本文中所提及的外寄生虫和内寄生虫的寄生虫所引起的感染的方法。
另一方面涉及式(I)的化合物在治疗动物、尤其是非人动物的寄生虫感染、尤其是由选自本文中所提及的外寄生虫和内寄生虫的寄生虫所引起的感染的用途。
在本发明的动物健康或兽医学的上下文中,术语“治疗”包括预防性的、补救性的或治疗性的治疗。
在一个特别的实施方案中,以此方式,提供用于兽医学领域的至少一种式(I)的化合物与其他活性化合物、尤其是与杀内寄生虫剂和杀外寄生虫剂的混合物。
在动物健康领域,“混合物”不仅是指将两种(或更多种)不同的活性化合物以常规制剂进行配制并相应地一起使用,而且还涉及包含针对每种活性化合物分开的制剂的产品。因此,当使用两种以上的活性化合物时,可将所有活性化合物以常规制剂进行配制或者可将所有活性化合物以单独制剂进行配制;还可为混合的形式,其中一些活性化合物一起配制而一些活性化合物单独配制。单独的制剂可以单独或依次施用所述活性化合物。
本文中以其“通用名称”提及的活性化合物是已知的,并且记载于例如农药手册(the“Pesticide Manual”)中(参见上文),或者可以在互联网(例如http://www.alanwood.net/pesticides)上检索。
作为混合组分的杀外寄生虫剂的示例性活性化合物,包括但无任何意图限于,上文详细列出的杀昆虫剂和杀螨剂。其他可使用的活性化合物根据上述基于现行的IRAC作用方式分类方案的分类列于下文中:(1)乙酰胆碱酯酶(AChE)抑制剂;(2)GABA-门控氯化物通道阻断剂;(3)钠通道调节剂;(4)烟碱乙酰胆碱受体(nAChR)竞争性调节剂;(5)烟碱乙酰胆碱受体(nAChR)变构调节剂;(6)谷氨酸门控氯化物通道(GluCl)变构调节剂;(7)保幼激素模仿物;(8)其他非特异性(多位点)抑制剂;(9)弦音器官调节剂;(10)螨生长抑制剂;(12)线粒体ATP合成酶抑制剂,如ATP干扰剂;(13)通过阻断质子梯度的氧化磷酸化的解偶联剂;(14)烟碱乙酰胆碱受体通道阻断剂;(15)几丁质生物合成抑制剂,0型;(16)几丁质生物合成抑制剂,1型;(17)蜕皮干扰剂(尤其是对于双翅目(Diptera));(18)蜕皮激素受体激动剂;(19)章鱼胺受体激动剂;(21)线粒体复合物I电子传递抑制剂;(25)线粒体复合物II电子传递抑制剂;(20)线粒体复合物III电子传递抑制剂;(22)电压依赖型钠通道阻断剂;(23)乙酰基-CoA羧化酶抑制剂;(28)鱼尼丁受体调节剂;
具有未知或非特异性的作用机理的活性化合物,如fentrifanil、氧嘧酰胺(fenoxacrim)、cycloprene、乙酯杀螨醇(chlorobenzilate)、杀虫脒(chlordimeform)、氟苯灭(flubenzimin)、地昔尼尔(dicyclanil)、磺胺螨酯(amidoflumet)、灭螨猛(quinomethionat)、三苯噻螨吩(triarathene)、clothiazoben、杀螨氯硫(tetrasul)、油酸钾(potassium oleate)、石油(petroleum)、恶虫酮(metoxadiazone)、gossyplur、氟螨嗪(flutenzine)、溴满酯(brompropylate)、氟铝酸钠(cryolite);
其他种类的化合物,例如畜虫威(butacarb)、敌蝇威(dimetilan)、除线威(cloethocarb)、磷虫威(phosphocarb)、嘧啶磷(乙基嘧啶磷)(pirimiphos(-ethyl))、对硫磷(乙基对硫磷)(parathion(-ethyl))、虫螨畏(methacrifos)、水杨酸异丙酯(isopropylo-salicylate)、三氯膦酸酯(trichlorfon)、硫丙磷(sulprofos)、丙虫磷(propaphos)、克线丹(sebufos)、哒硫磷(pyridathion)、发硫磷(prothoate)、除线磷(dichlofenthion)、甲基砜内吸磷(demeton-S-methyl sulfone)、氯唑磷(isazofos)、苯腈膦(cyanofenphos)、氯亚胺硫磷(dialifos)、三硫磷(carbophenothion)、特嘧硫磷(autathiofos)、aromfenvinfos(-methyl)、谷硫磷(乙基谷硫磷)(azinphos(-ethyl))、毒死蜱(乙基毒死蜱)(chlorpyrifos(-ethyl))、丁苯硫磷(fosmethilan)、碘硫磷(iodofenphos)、蔬果磷(dioxabenzofos)、安果(formothion)、地虫磷(fonofos)、吡氟硫磷(flupyrazofos)、丰索磷(fensulfothion)、乙嘧硫磷(etrimfos);
有机氯化物,例如毒杀芬(camphechlor)、林丹(lindane)、七氯(heptachlor);或苯基吡唑类,如acetoprole、pyrafluprole、pyriprole、vaniliprole、维吉霉素(sisapronil);或异噁唑啉类,如sarolaner、afoxolaner、lotilaner、fluralaner;
除虫菊酯(pyrethroids),如(顺式-、反式-)甲氧苄氟菊酯((cis-,trans-)metofluthrin)、丙氟菊酯(profluthrin)、三氟醚菊酯(flufenprox)、溴氟菊酯(flubrocythrinate)、气丙笨酸(fubfenprox)、芬氟司林(fenfluthrin)、protrifenbut、pyresmethrin、RU15525、环戊烯丙菊酯(terallethrin)、苄呋菊酯(cis-resmethrin)、heptafluthrin、bioethanomethrin、生物氯菊酯(biopermethrin)、吡氯氰菊酯(fenpyrithrin)、氯氰菊酯(cis-cypermethrin)、苄氯菊酯(cis-permethrin)、氰菊酯(clocythrin)、氯氟氰菊酯(cyhalothrin(lambda-))、二氯炔戊菊酯(chlovaporthrin),或卤代烃化合物(HCH),
新烟碱类,如硝乙脲噻唑(nithiazine);
Dicloromezotiaz,三氟苯嘧啶(triflumezopyrim);
大环内酯类,如奈马克丁(nemadectin)、伊维菌素(ivermectin)、拉替待克丁(latidectin)、莫昔克丁(moxidectin)、司拉克丁(selamectin)、依立诺克丁(eprinomectin)、多拉克丁(doramectin)、埃玛菌素(emamectin benzoate);米尔贝肟(milbemycin oxime)
烯虫硫酯(triprene)、保幼醚(epofenonane)、苯虫醚(diofenolan);
生物制剂、激素或信息素,例如天然产物,如苏云金素(thuringiensin)、十二碳二烯醇(codlemone)或印楝(neem)成分
二硝基酚类,例如敌螨普(dinocap)、消螨通(dinobuton)、乐杀螨(binapacryl);
苯甲酰基脲类,例如氟佐隆(fluazuron)、氟幼脲(penfluron),
脒衍生物,例如chlormebuform、螨蜱胺(cymiazole)、得米地曲(demiditraz)
beehive蜂螨属杀螨剂(beehive varroa acaricides),例如有机酸,如甲酸、乙二酸。
作为混合组分的杀内寄生虫剂的示例性活性化合物包括但不限于活性驱虫化合物和活性抗原生动物(antiprotozoic)化合物。
活性驱虫化合物包括但不限于以下活性杀线虫、杀吸虫(trematicidal)和/或杀绦虫(cestocidal)化合物:
大环内酯类,例如:依立诺克丁(eprinomectin)、阿巴克丁(abamectin)、奈马克丁(nemadectin)、莫昔克丁(moxidectin)、多拉克丁(doramectin)、司拉克丁(selamectin)、雷皮菌素(lepimectin)、拉替待克丁(latidectin)、弥拜菌素(milbemectin)、伊维菌素(ivermectin)、依马菌素(emamectin)、米尔倍霉素(milbemycin);
苯并咪唑类和probenzimidazole,例如:奥苯达唑(oxibendazole)、甲苯咪唑(mebendazole)、三氯苯咪唑(triclabendazole)、托布津(thiophanate)、丁苯咪唑(parbendazole)、奥吩达唑(oxfendazole)、奈托比胺(netobimin)、芬苯达唑(fenbendazole)、非班太(febantel)、噻苯哒唑(thiabendazole)、环苯达唑(cyclobendazole)、坎苯达唑(cambendazole)、阿苯达唑亚砜(albendazole sulfoxide)、阿苯达唑(albendazole)、氟苯达唑(flubendazole);
缩肽类,优选环状缩肽,尤其是24元环状缩肽,例如:依吗德塞(emodepside)、PF1022A;
四氢嘧啶类,例如:莫仑太尔(morantel)、噻嘧啶(pyrantel)、奥克太尔(oxantel);
咪唑并噻唑类,例如:布他咪唑(butamisole)、左旋咪唑(levamisole)、四咪唑(tetramisole);
氨基苯基脒类,例如:阿米太尔(amidantel)、脱酰化阿米太尔(dAMD)、三苯双脒(tribendimidine);
氨基乙腈类,例如:莫奈太尔(monepantel);
Paraherquamides类,例如:paraherquamide、德奎太尔(derquantel);
水杨酰苯胺类,例如:三溴沙仑(tribromsalan)、溴沙尼特(bromoxanide)、溴替尼特(brotianide)、氯碘沙尼(clioxanide)、氯生太尔(closantel)、氯硝柳胺(niclosamide)、羟氯扎胺(oxyclozanide)、雷复尼特(rafoxanide);
取代的酚类,例如:硝碘酚腈(nitroxynil)、硫氯酚(bithionol)、二碘硝酚(disophenol)、六氯芬(hexachlorophene)、联硝氯酚(niclofolan)、meniclopholan;
有机磷酸酯类,例如:三氯磷酸酯(trichlorfon)、naphthalofos、敌敌畏(dichlorvos/DDVP)、克芦磷酯(crufomate)、蝇毒磷(coumaphos)、哈洛克酮(haloxon);
哌嗪酮/喹啉,例如:吡喹酮(praziquantel)、依西太尔(epsiprantel);
哌嗪类,例如:哌嗪(piperazine)、羟嗪(hydroxyzine);
四环素类,例如:四环素(tetracycline)、金霉素(chlorotetracycline)、多西环素(doxycycline)、土霉素(oxytetracycline)、罗利环素(rolitetracycline);
各种其他种类,例如:丁萘脒(bunamidine)、尼立达唑(niridazole)、雷琐太尔(resorantel)、omphalotin、奥替普拉(oltipraz)、硝硫氰酯(nitroscanate)、硝碘酚腈(nitroxynil)、奥沙尼喹(oxamniquin)、mirasan、米拉西尔(miracil)、硫坎酮(lucanthon)、羟胺硫蒽酮(hycanthon)、海涛林(hetolin)、依米丁(emetin)、乙胺嗪(diethylcarbamazine)、双氯酚(dichlorophen)、地芬尼太(diamfenetide)、氯硝西泮(clonazepam)、苄酚宁(bephenium)、硝硫氰胺(amoscanate)、氯舒隆(clorsulon)。
活性抗原生动物化合物包括但不限于以下活性化合物:
三嗪类,例如:地克珠利(diclazuril)、帕那珠利(ponazuril)、来曲珠利(letrazuril)、托曲珠利(toltrazuril);
聚醚离子载体类,例如:莫能菌素(monensin)、盐霉素(salinomycin)、马度米星(maduramicin)、甲基盐霉素(narasin);
大环内酯类,例如:米尔倍霉素(milbemycin)、红霉素(erythromycin);
喹诺酮类,例如:恩氟沙星(enrofloxacin)、普拉沙星(pradofloxacin);
奎宁类,例如:氯喹(chloroquine);
嘧啶类,例如:乙胺嘧啶(pyrimethamine);
磺酰胺类,例如:磺胺喹噁啉(sulfaquinoxaline)、甲氧苄氨嘧啶(trimethoprim)、磺胺氯吡嗪(sulfaclozin);
硫胺素类,例如:安普罗铵(amprolium);
林可胺类,例如:克林霉素(clindamycin);
碳酰苯胺类,例如:咪多卡(imidocarb);
硝基呋喃类,例如:硝呋莫司(nifurtimox);
喹唑啉酮生物碱类,例如:卤夫酮(halofuginone);
各种其他种类,例如:奥沙尼喹(Oxamniquin)、巴龙霉素(Paromomycin);
来自微生物的疫苗或抗原,所述微生物为例如:罗氏巴贝斯虫亚种(Babesiacanis rossi)、柔嫩艾美耳球虫(Eimeria tenella)、早熟艾美尔球虫(Eimeria praecox)、毒害艾美球虫(Eimeria necatrix)、和缓艾美球虫(Eimeria mitis)、巨型艾美耳球虫(Eimeria maxima)、布氏艾美耳球虫(Eimeria brunetti)、堆型艾美耳球虫(Eimeriaacervulina)、韦氏巴贝斯虫亚种(Babesia canis vogeli)、婴儿利什曼虫(Leishmaniainfantum)、犬巴贝斯虫亚种(Babesia canis canis)、胎生网尾线虫(Dictyocaulusviviparus)。
视情况,所提及的所有混合组分还可与合适的碱或酸形成盐,如果它们基于其官能团能形成盐的话。
病媒防治
式(I)的化合物还可用于病媒防治。在本发明的上下文中,病媒为节肢动物,尤其是昆虫或蛛形纲动物,其能够将病原体例如病毒、蠕虫、单细胞生物和细菌从贮主(植物、动物、人等)传播给宿主。病原体可以机械地传播给宿主(例如通过无刺蝇(non-stinging)传播沙眼),或者可以在注射后传播给宿主(例如通过蚊传播疟原虫)。
病媒以及它们传播的疾病或病原体的实例为:
1)蚊
-按蚊属:疟疾、丝虫病;
-库蚊属:日本脑炎、丝虫病、其他病毒性疾病、其他蠕虫传播;
-伊蚊属:黄热病、登革热、其他病毒性疾病、丝虫病;
-蚋科:蠕虫传播,尤其是盘尾丝虫(Onchocerca volvulus);
-毛蠓科:利什曼病传播;
2)虱:皮肤感染、流行性斑疹伤寒(epidemic typhus);
3)跳蚤:鼠疫、地方性斑疹伤寒、绦虫;
4)蝇:昏睡病(锥虫病(trypanosomiasis));霍乱、其他细菌性疾病;
5)螨:壁虱病、流行性斑疹伤寒、立克次氏体痘、土拉菌病、圣路易斯脑炎(SaintLouis encephalitis)、蜱媒脑炎(tick-borne encephalitis)(TBE)、克里米亚-刚果出血热(Crimean–Congo haemorrhagic fever)、疏螺旋体病(borreliosis);
6)蜱:borellioses,如Borrelia bungdorferi sensu lato.、达氏疏螺旋体(Borrelia duttoni)、蜱媒脑炎、Q热(贝氏柯克斯体(Coxiella burnetii))、焦虫病(babesioses)(犬巴贝斯虫(Babesia canis canis))、埃立克体病。
在本发明的上下文中,病媒的实例为昆虫,例如蚜虫、蝇、叶蝉或蓟马(thrip),其可向植物传播植物病毒。能够传播植物病毒的其他病媒是蜘蛛螨、虱、甲虫和线虫。
在本发明的上下文中,病媒的其他实例为昆虫和蛛形纲动物,例如蚊,尤其是伊蚊属、按蚊属,例如冈比亚按蚊(A.gambiae)、阿拉伯按蚊(A.arabiensis)、不吉按蚊(A.funestus)、大劣按蚊(A.dirus)(疟疾)和库蚊属、毛蠓科,如白蛉属、罗岭属、虱、跳蚤、蝇、螨和蜱,其可向动物和/或人类传播病原体。
如果式(I)的化合物为抗性突破(resistance-breaking)的,则病媒防治也是可能的。
式(I)的化合物适合用于预防由病媒传播的疾病和/或病原体。因此,本发明的另一方面为式(I)的化合物在例如农业、园艺、林业、园林以及休闲设备中、以及在材料和贮存产品的保护中用于病媒防治的用途。
工业材料的保护
式(I)的化合物适合用于保护工业材料免受昆虫的侵害或破坏,所述昆虫例如来自鞘翅目、膜翅目、等翅目、鳞翅目、啮虫目和衣鱼目(Zygentoma)。
在本发明的上下文中,工业材料应理解为意指无生命材料,例如,优选塑料、粘合剂、胶料(size)、纸和卡片、皮革、木材、加工的木制品和涂料组合物。特别优选本发明的用于保护木材的用途。
在另一实施方案中,式(I)的化合物与至少一种其他杀昆虫剂和/或至少一种杀真菌剂一起使用。
在另一实施方案中,式(I)的化合物采取即用型(ready-to-use)农药的形式,意味着它不需要进一步修饰即可施用于所述材料。有用的其他杀昆虫剂或杀真菌剂特别地包括上述提及的那些。
出乎意料地,还发现式(I)的化合物可用于保护与盐水或微咸水接触的物体免受沾污,所述物体特别是船体、隔板、网、建筑物、系泊设备及信号体系。同样可以将式(I)的化合物单独或与其他活性化合物结合用作防污剂。
卫生领域中动物害虫的防治
式(I)的化合物适合用于防治卫生领域的动物害虫。更具体而言,本发明可以用于室内保护领域、卫生保护领域以及储存产品的保护,尤其是用于防治密闭空间中遇到的昆虫、蛛形纲动物、壁虱和螨,所述密闭空间为例如住所、工厂大厅、办公室、车辆舱室、动物育种设施。为了防治动物害虫,将式(I)的化合物单独使用或与其他活性化合物和/或助剂结合使用。它们优选用于室内杀昆虫剂产品中。式(I)的化合物有效地对抗敏感性物种及抗性物种,以及其全部的发育阶段。
这些害虫包括,例如,下述害虫:蛛形纲,蝎目(Scorpiones)、蜘蛛目(Araneae)和盲蛛目(Opiliones);唇足纲和倍足纲;昆虫纲蜚蠊目、鞘翅目、革翅目、双翅目、异翅亚目、膜翅目、等翅目、鳞翅目、虱目、啮虫目、跳跃亚目(Saltatoria)或直翅目、蚤目和衣鱼目;软甲纲等足目。
施用如下进行:例如,气溶胶、无压喷雾器产品如泵式喷雾器和雾化喷雾器、自动雾化系统、雾化器、泡沫、凝胶、具有由纤维素或塑料制成的蒸发器片的蒸发器产品、液体蒸发器、凝胶和薄膜蒸发器、螺旋桨驱动的蒸发器、无动力(energy-free)或无源(passive)的蒸发系统、蛾纸、蛾袋和蛾胶中,作为颗粒剂或粉剂,用于撒播的诱饵或诱饵站。
制备实施例:
7-(乙基磺酰基)-6-[3-甲基-6-(三氟甲基)-3H-咪唑并[4,5-b]吡啶-2-基][1,3]噻唑并[4,5-c]吡啶(I-1)
在室温下,将64mg(0.16mmol)7-(乙基硫基)-6-[3-甲基-6-(三氟甲基)咪唑并[4,5-b]吡啶-2-基][1,3]噻唑并-[4,5-c]吡啶溶于7.5mL二氯甲烷,加入37mg(0.81mmol)甲酸和110mg(1.13mmol)过氧化氢,然后将混合物在室温下搅拌4小时。将混合物在减压下除去溶剂。残余物通过HPLC,使用乙腈/水+0.1%甲酸为流动相,在RP18上进行纯化。
logP[a]:2.60;logP[n]:2.53;MH+:428;1H-NMR(400MHz,CD3CN)δppm:1.29(t,3H),3.80(s,3H),3.87(q,2H),8.44(s,1H),8.84(s,1H),9.51(s,1H),9.66(s,1H)。
7-(乙基亚磺酰基)-6-[3-甲基-6-(三氟甲基)-3H-咪唑并[4,5-b]吡啶-2-基][1,3]噻唑并[4,5-c]吡啶(I-2)
在室温下,将64mg(0.16mmol)7-(乙基硫基)-6-[3-甲基-6-(三氟甲基)咪唑并[4,5-b]吡啶-2-基][1,3]噻唑并-[4,5-c]吡啶溶于7.5mL二氯甲烷,加入37mg(0.81mmol)甲酸和110mg(1.13mmol)过氧化氢,然后将混合物在室温下搅拌4小时。将混合物在减压下除去溶剂。残余物通过HPLC,使用乙腈/水+0.1%甲酸为流动相,在RP18上进行纯化。
logP[a]:3.09;logP[n]:2.98;MH+:412;1H-NMR(400MHz,d6-DMSO)δppm:1.43(t,3H),3.70(m,2H),4.24(s,3H),8.73(s,1H),8.91(s,1H),9.68(s,1H),9.77(s,1H)。
7-(乙基硫基)-6-[3-甲基-6-(三氟甲基)-3H-咪唑并[4,5-b]吡啶-2-基][1,3]噻唑并[4,5-c]吡啶(I-3)
在120℃下,将68mg(0.36mmol)N2-甲基-5-(三氟甲基)吡啶-2,3-二胺、121mg(0.43mmol)7-(乙基硫基)[1,3]噻唑并[4,5-c]吡啶-6-甲酸和136mg(0.71mmol)1-(3-二甲基氨基丙基)-3-乙基碳二亚胺盐酸盐(EDCI)在15mL吡啶中搅拌18小时。将混合物用乙腈稀释、过滤并在减压下除去溶剂。残余物通过柱色谱法,使用梯度的乙酸乙酯/甲醇作为流动相,进行纯化。所需馏分通过HPLC,使用乙腈/水+0.1%甲酸为流动相,在RP18上进行纯化。
logP[a]:2.96;logP[n]:2.94;MH+:396;1H-NMR(400MHz,CD3CN)δppm:1.08(t,3H),2.96(q,2H),3.83(s,3H),8.43(s,1H),8.81(s,1H),9.39(s,1H),9.42(s,1H)。
7-(乙基硫基)[1,3]噻唑并[4,5-c]吡啶-6-甲酸(XLI-1)
在室温下,将113mg(0.421mmol)7-(乙基硫基)[1,3]噻唑并[4,5-c]吡啶-6-甲酸乙酯和20mg(0.84mmol)氢氧化锂在2.1mL四氢呋喃和0.7mL水中搅拌18小时。加入1N盐酸水溶液,并将混合物在减压下除去溶剂。将甲苯加入残余物中并将混合物在减压下除去溶剂,该过程进行两次。
logP[a]:0.88;MH+:241;1H-NMR(400MHz,d6-DMSO)δppm:1.11(t,3H),3.03(q,2H),9.32(s,1H),9.66(s,1H)。
7-(乙基硫基)[1,3]噻唑并[4,5-c]吡啶-6-甲酸乙酯(XL-1)
将166mg(0.47mmol)7-{[(三氟甲基)磺酰基]氧基}[1,3]噻唑并[4,5-c]吡啶-6-甲酸乙酯、59mg 4,5-双二苯基膦-9,9-二甲基氧杂蒽(xantphos)(0.10mmol)、0.25mL乙硫醇(3.36mmol)和0.25mL(1.49mmol)N,N-二异丙基乙胺于6.6mL二氧六环的溶液,用氩气脱气。加入68mg(0.065mmol)三(二亚苄基丙酮)二钯/氯仿加合物,并将溶液在微波中在160℃下搅拌5分钟。将混合物在减压下除去溶剂。残余物通过柱色谱法,使用梯度的环己烷/乙酸乙酯作为流动相,进行纯化。
logP[a]:2.23;logP[n]:2.17;MH+:269;1H-NMR(400MHz,CD3CN)δppm:1.17(t,3H),1.39(t,3H),3.03(q,2H),4.45(q,2H),9.25(s,1H),9.315(s,1H)。
7-{[(三氟甲基)磺酰基]氧基}[1,3]噻唑并[4,5-c]吡啶-6-甲酸乙酯(XXXIV-1)
[7-羟基[1,3]噻唑并[4,5-c]吡啶-6-甲酸乙酯根据US 2008/0004309的方法制备]将200mg(0.89mmol)7-羟基[1,3]噻唑并[4,5-c]吡啶-6-甲酸乙酯和0.62mL(4.46mmol)三乙胺溶于2mL二氯甲烷中并冷却至0℃。在0℃下,滴加0.45mL(2.68mmol)三氟甲磺酸酐。将混合物在0℃下搅拌10分钟,并用水/乙酸乙酯萃取。将有机相使用硫酸钠干燥、过滤并在减压下除去溶剂。残余物通过柱色谱法,使用梯度的环己烷/乙酸乙酯作为流动相,进行纯化。
logP[a]:2.58;logP[n]:2.57;MH+:357;1H-NMR(400MHz,CD3CN)δppm:1.41(t,3H),4.47(q,2H),9.42(s,1H),9.445(s,1H)。
类似于实施例并根据上述制备方法,可以获得以下式(I)的化合物:
根据EEC Directive 79/831附录V.A8通过HPLC(高效液相色谱)在反相柱(C18)上测量logP值。温度:55℃。
酸性范围内的LC-MS测定使用0.1%甲酸水溶液和乙腈(含有0.1%甲酸)作为流动相在pH 2.7下进行;线性梯度为从10%乙腈至95%乙腈。在表中称为logP(HCOOH)或logP[a]。
中性范围内的LC-MS测定使用0.001摩尔碳酸氢铵水溶液和乙腈作为流动相在pH7.8下进行;线性梯度为从10%乙腈至95%乙腈。在表中称为logP(中性)或logP[n]。
使用具有已知logP值的非支链烷-2-酮(具有3至16个碳原子)进行校准(logP值基于保留时间通过两个连续烷酮之间的线性插值测定)。
所选实例的NMR数据以常规形式(δ值,多重峰分裂,氢原子数)或作为NMR峰列表列出。
在每种情况下,说明了被记录的NMR谱的溶剂。
NMR峰列表方法
所选实例的1H NMR数据以1H NMR峰列表的形式表示。对于每个信号峰,首先列出以ppm计的δ值,然后在圆括号内列出信号强度。对于不同信号峰的一对δ值-信号强度数,通过分号彼此间隔列出。
因此,一个实例的峰列表具有以下形式:
δ1(强度1);δ2(强度2);...;δi(强度i);...;δn(强度n)
尖峰信号的强度与NMR谱的打印例中的信号高度(以厘米计)相关,并且显示出信号强度的真实比例。对于宽峰信号,可以显示数个峰或信号的中间部分及它们与谱图中最强信号相比的相对强度。
为了标定1H NMR谱的化学位移,我们使用四甲基硅烷和/或溶剂的化学位移,特别是在DMSO中测量的谱图的情况下。因此,四甲基硅烷峰可以但不一定在NMR峰列表中出现。
1H NMR峰的列表类似于常规1H NMR打印件,因此,其通常含有在常规NMR说明中列出的所有峰。
另外,如同常规1H NMR打印件,它们可显示出溶剂信号、目标化合物的立体异构体(其同样由本发明提供)的信号,和/或杂质的峰。
在记录化合物在溶剂和/或水的δ范围内的信号时,我们的1H NMR峰列表显示出标准溶剂峰,例如在d6-DMSO中的DMSO的峰和水的峰,这通常具有高的平均强度。
目标化合物的立体异构体的峰和/或杂质的峰通常具有比目标化合物(例如具有>90%的纯度)的峰更低的平均强度。
此类立体异构体和/或杂质对于特定的制备方法可以是特有的。因此,通过参考“副产品指纹”,它们的峰可有助于确定制备方法的再现性。
视需要,通过已知方法(MestreC,ACD模拟,以及凭经验评估的预期值)计算目标化合物的峰的专业人员可以任选地使用另外的强度滤波器分离出目标化合物的峰。这种分离类似于在常规1H NMR说明中所选的相关的峰。
1H NMR峰列表的其他详情可参见Research Disclosure Database Number564025。
用途实施例
桃蚜(Myzus persicae)–经口测试(oral test)
溶剂:100重量份的丙酮
为了制备合适的活性化合物制剂,将1重量份的活性化合物使用指定重量份的溶剂来溶解,并用水补充直至获得所需的浓度。
将50μL的活性化合物制剂转移至微量滴定板,并用150μL的IPL41昆虫培养基(33%+15%糖)补充至200μL的最终体积。随后,使用石蜡膜密封该板,在第二个微量滴定板内桃蚜(Myzus persicae)的混合种群能够刺破并穿过石蜡膜而吸收溶液。
5天后,测定以%计的功效。100%表示所有蚜虫都已被杀死;0%表示没有蚜虫被杀死。
在本测试中,例如,来自制备实施例的下列化合物在施用率为4ppm下显示出100%的功效:I-1、I-4、I-7、I-8。
桃蚜–喷洒测试
溶剂:78重量份的丙酮
1.5重量份的二甲基甲酰胺
乳化剂:烷基芳基聚乙二醇醚
为了制备合适的活性化合物制剂,使用指定重量份的溶剂来溶解1重量份的活性化合物,并用含有浓度为1000ppm的乳化剂的水补充直至获得所需浓度。为了制备其他测试浓度,用含有乳化剂的水稀释制剂。
在被所有阶段的桃蚜(Myzus persicae)侵染的大白菜(白菜(Brassicapekinensis))叶的叶面上,喷洒具有所需浓度的活性化合物制剂。
5天后,测定以%计的功效。100%表示所有蚜虫都已被杀死;0%表示没有蚜虫被杀死。
在本测试中,例如,来自制备实施例的下列化合物在施用率为20g/ha下显示出100%的功效:I-7、I-8。
在本测试中,例如,来自制备实施例的下列化合物在施用率为20g/ha下显示出90%的功效:I-1、I-4、I-5。
辣根猿叶虫(Phaedon cochleariae)–喷洒测试
溶剂:78.0重量份的丙酮
1.5重量份的二甲基甲酰胺
乳化剂:烷基芳基聚乙二醇醚
为了制备合适的活性化合物制剂,使用指定重量份的溶剂来溶解1重量份的活性化合物,并用含有浓度为1000ppm的乳化剂的水补充直至获得所需浓度。为了制备其他测试浓度,用含有乳化剂的水稀释制剂。
在大白菜(白菜(Brassica pekinensis))叶的叶面上喷洒具有所需浓度的活性化合物制剂,并在干燥后使芥菜甲虫(辣根猿叶甲虫)的幼虫栖居于叶面。
7天后,测定以%计的功效。100%表示所有甲虫幼虫都已被杀死;0%表示没有甲虫幼虫被杀死。
在本测试中,例如,来自制备实施例的下列化合物在施用率为100g/ha下显示出100%的功效:I-4。
在本测试中,例如,来自制备实施例的下列化合物在施用率为100g/ha下显示出83%的功效:I-1。
Claims (11)
1.式(I)的化合物
其中
Aa表示=C(R7)-,
Ab表示-S(O)m-或=C(R2)-,
Ac表示=C(R3),
Ad表示=N-、-S(O)m-或=C(R8)-,
其中取代基Ab和Ad中只有一个可表示–S(O)m-,
得到以下结构单元:A9、A10、A14,
其中与取代基Q键合的键由波浪线标识,并且与硫原子键合的键由星号*标识,
R1表示(C1-C4)-烷基,
R2、R3、R8彼此独立地表示氢,
R7表示氢,
Q表示杂芳族9元稠合的双环体系,其选自Q2或Q3
R4表示(C1-C4)-烷基,
R5、R6彼此独立地表示氢、氰基、卤素、(C1-C4)-烷基或(C1-C4)-卤代烷基,
m表示0,
n表示0、1或2。
2.根据权利要求1所述的式(I)的化合物,其中
Aa表示=C(R7)-,
Ab表示-S(O)m-或=C(R2)-,
Ac表示=C(R3)-,
Ad表示=N-、-S(O)m-或=C(R8)-,
其中取代基Ab和Ad中只有一个可表示–S(O)m-,
得到以下结构单元:A9、A10、A14,
R1表示甲基、乙基、正丙基、异丙基或环丙基,
R2、R3、R8彼此独立地表示氢,
R7表示氢,
Q表示杂芳族9元稠合的双环体系,其选自Q2和Q3,
R4表示甲基、乙基或异丙基,
R5表示氟、氯、溴、氟甲基、二氟甲基、三氟甲基、氟乙基、二氟乙基、三氟乙基、四氟乙基或五氟乙基,
R6表示氢,
m表示0,
n表示0、1或2。
3.根据权利要求2所述的式(I)的化合物,其中氟乙基是CH2CFH2或CHFCH3。
4.根据权利要求2所述的式(I)的化合物,其中二氟乙基是CF2CH3、CH2CHF2或CHFCFH2。
5.根据权利要求2所述的式(I)的化合物,其中三氟乙基是CH2CF3、CHFCHF2或CF2CFH2。
6.根据权利要求2所述的式(I)的化合物,其中四氟乙基是CHFCF3或CF2CHF2。
7.根据权利要求1所述的式(I)的化合物,其中
Aa表示=C(R7)-,
Ab表示-S(O)m-或=C(R2)-,
Ac表示=C(R3)-,
Ad表示=N-、-S(O)m-或=C(R8)-,
得到以下结构单元:A9、A10、A14,
R1表示乙基,
R2表示氢,
R3表示氢,
R7表示氢,
R8表示氢,
Q表示选自Q2和Q3的杂芳族9元稠合的双环体系,
R4表示甲基,
R5表示三氟甲基,
R6表示氢,
m表示0,
n表示0、1或2。
8.农用化学制剂,其包含权利要求1的式(I)的化合物以及增量剂和/或表面活性剂。
9.根据权利要求8所述的农用化学制剂,其还包含另外的农用化学活性化合物。
10.防治动物害虫的方法,其特征在于,使权利要求1的式(I)的化合物或权利要求8或9的农用化学制剂作用于动物害虫和/或其生境;
其中所述方法排除用于人体或动物体的诊断和治疗方法。
11.权利要求1的式(I)的化合物或权利要求8或9的农用化学制剂作为作物保护剂用于防治动物害虫的用途。
Applications Claiming Priority (3)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
EP16180168.3 | 2016-07-19 | ||
EP16180168 | 2016-07-19 | ||
PCT/EP2017/067838 WO2018015289A1 (de) | 2016-07-19 | 2017-07-14 | Kondensierte bicyclische heterocyclen-derivate als schädlingsbekämpfungsmittel |
Publications (2)
Publication Number | Publication Date |
---|---|
CN109689662A CN109689662A (zh) | 2019-04-26 |
CN109689662B true CN109689662B (zh) | 2022-03-15 |
Family
ID=56464118
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
CN201780054877.0A Expired - Fee Related CN109689662B (zh) | 2016-07-19 | 2017-07-14 | 作为害虫防治剂的稠合双环杂环衍生物 |
Country Status (21)
Country | Link |
---|---|
US (1) | US10561145B2 (zh) |
EP (1) | EP3487860B1 (zh) |
JP (1) | JP6967064B2 (zh) |
KR (1) | KR102435080B1 (zh) |
CN (1) | CN109689662B (zh) |
AR (1) | AR109076A1 (zh) |
AU (1) | AU2017298972B2 (zh) |
BR (1) | BR112019001135B1 (zh) |
CA (1) | CA3031139A1 (zh) |
CL (1) | CL2019000125A1 (zh) |
CO (1) | CO2019000503A2 (zh) |
ES (1) | ES2877571T3 (zh) |
IL (1) | IL264204B (zh) |
MX (1) | MX2019000793A (zh) |
PE (1) | PE20190206A1 (zh) |
PH (1) | PH12019500139A1 (zh) |
RU (1) | RU2019104378A (zh) |
TW (1) | TWI747924B (zh) |
UY (1) | UY37327A (zh) |
WO (1) | WO2018015289A1 (zh) |
ZA (1) | ZA201901024B (zh) |
Families Citing this family (7)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
KR102309351B1 (ko) | 2016-03-10 | 2021-10-05 | 닛산 가가쿠 가부시키가이샤 | 축합 복소 고리 화합물 및 유해 생물 방제제 |
JP7165126B2 (ja) | 2016-09-19 | 2022-11-02 | バイエル・クロップサイエンス・アクチェンゲゼルシャフト | ピラゾロ[1,5-a]ピリジン誘導体及びそれの殺有害生物剤としての使用 |
EP3305786A3 (de) * | 2018-01-22 | 2018-07-25 | Bayer CropScience Aktiengesellschaft | Kondensierte bicyclische heterocyclen-derivate als schädlingsbekämpfungsmittel |
JP2021514949A (ja) * | 2018-02-21 | 2021-06-17 | バイエル・アクチエンゲゼルシヤフト | 有害生物防除剤としての縮合二環式ヘテロ環誘導体 |
AR119140A1 (es) * | 2019-06-13 | 2021-11-24 | Pi Industries Ltd | Compuestos heterocíclicos fusionados y su uso como agentes de control de plagas |
CN115181116B (zh) | 2022-07-29 | 2024-11-26 | 江苏中旗科技股份有限公司 | 具有含硫取代基的稠环化合物、制备方法、杀虫剂组合物及用途 |
WO2024189139A1 (en) | 2023-03-14 | 2024-09-19 | Syngenta Crop Protection Ag | Control of pests resistant to insecticides |
Citations (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO2005066177A1 (en) * | 2003-12-31 | 2005-07-21 | Schering-Plough Ltd. | Control of parasites in animals by the use of imidazo[1,2-b]pyridazine derivatives |
WO2016020286A1 (en) * | 2014-08-07 | 2016-02-11 | Syngenta Participations Ag | Pesticidally active heterocyclic derivatives with sulphur containing substituents |
CN105473558A (zh) * | 2013-06-20 | 2016-04-06 | 拜耳作物科学股份公司 | 作为杀螨剂和杀昆虫剂的芳基硫化物衍生物和芳基硫氧化物衍生物 |
WO2016091731A1 (en) * | 2014-12-11 | 2016-06-16 | Syngenta Participations Ag | Pesticidally active tetracyclic derivatives with sulfur containing substituents |
WO2016107742A1 (en) * | 2014-12-29 | 2016-07-07 | Syngenta Participations Ag | Pesticidally active tetracyclic derivatives with sulfur containing substituents |
Family Cites Families (89)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US2820062A (en) | 1954-08-11 | 1958-01-14 | Pure Oil Co | Preparation of organic thiols |
US5374646A (en) | 1989-12-01 | 1994-12-20 | Glaxo Group Limited | Benzofuran derivatives |
US5576335A (en) | 1994-02-01 | 1996-11-19 | Nisshin Flour Milling Co., Ltd. | Urea derivatives and their use as ACAT inhibitors |
PA8535601A1 (es) | 2000-12-21 | 2002-11-28 | Pfizer | Derivados benzimidazol y piridilimidazol como ligandos para gabaa |
ES2297141T3 (es) | 2002-03-29 | 2008-05-01 | EISAI R&D MANAGEMENT CO., LTD. | Derivados de (1-indanona)-(1,2,3,6-tetrahidropiridina). |
GB0213715D0 (en) | 2002-06-14 | 2002-07-24 | Syngenta Ltd | Chemical compounds |
FR2844794B1 (fr) | 2002-09-25 | 2004-12-03 | Atofina | Procede catalytique de fabrication d'alkylmercaptans par addition d'hydrogene |
FR2844726B1 (fr) | 2002-09-25 | 2004-12-03 | Atofina | Procede catalytique de fabricaton de mercaptans a partir de thioethers |
TWI312272B (en) | 2003-05-12 | 2009-07-21 | Sumitomo Chemical Co | Pyrimidine compound and pests controlling composition containing the same |
ES2241496B1 (es) | 2004-04-15 | 2006-12-01 | Almirall Prodesfarma, S.A. | Nuevos derivados de piridina. |
EP1756103A2 (en) | 2004-04-26 | 2007-02-28 | Pfizer, Inc. | Pyrrolopyridine derivatives and their use as hiv-integrase inhibitors |
AU2005243439B2 (en) | 2004-05-17 | 2011-09-29 | Tibotec Pharmaceuticals Ltd. | 1-heterocyclyl-1,5-dihydro-pyrido(3,2-b)indol-2-ones |
GB0414438D0 (en) | 2004-06-28 | 2004-07-28 | Syngenta Participations Ag | Chemical compounds |
UA86251C2 (uk) | 2004-10-20 | 2009-04-10 | Кумиай Кемикал Индастри Ко., Лтд. | Похідне 3-тріазолілсульфіду і інсектицид, акарицид або нематоцид, що містять його як активний інгредієнт |
EP1828186A1 (en) | 2004-12-13 | 2007-09-05 | Sunesis Pharmaceuticals, Inc. | Pyrido pyrimidinones, dihydro pyrimido pyrimidinones and pteridinones useful as raf kinase inhibitors |
EP1866318B1 (en) | 2005-03-02 | 2011-06-22 | Fibrogen, Inc. | Thienopyridine compounds, and methods of use thereof |
WO2007040282A1 (ja) | 2005-10-06 | 2007-04-12 | Nippon Soda Co., Ltd. | 架橋環状アミン化合物および有害生物防除剤 |
US7696223B2 (en) | 2006-04-04 | 2010-04-13 | Fibrogen, Inc. | Pyrrolo- and Thiazolo-pyridine compounds, and methods of use thereof |
US8606259B2 (en) | 2006-06-28 | 2013-12-10 | Samsung Electronics Co., Ltd. | Method and system for testing a software-defined radio device |
WO2008059238A1 (en) | 2006-11-17 | 2008-05-22 | Astrazeneca Ab | Benzenesulfonamide compounds as edg-1 antagonists useful in the treatment of cancer |
TW200833335A (en) | 2007-01-12 | 2008-08-16 | Astrazeneca Ab | New pyridine analogues |
DE102007035334A1 (de) | 2007-07-27 | 2009-01-29 | Boehringer Ingelheim Pharma Gmbh & Co. Kg | Neue substituierte Arylsulfonylglycine, deren Herstellung und deren Verwendung als Arzneimittel |
TW200944520A (en) | 2008-01-29 | 2009-11-01 | Glaxo Group Ltd | Spiro compounds as NPY Y5 receptor antagonists |
JP5369854B2 (ja) | 2008-04-21 | 2013-12-18 | 住友化学株式会社 | 有害節足動物防除組成物および縮合複素環化合物 |
JP5268461B2 (ja) | 2008-07-14 | 2013-08-21 | Meiji Seikaファルマ株式会社 | Pf1364物質、その製造方法、生産菌株、及び、それを有効成分とする農園芸用殺虫剤 |
CN101337937B (zh) | 2008-08-12 | 2010-12-22 | 国家农药创制工程技术研究中心 | 具有杀虫活性的n-苯基-5-取代氨基吡唑类化合物 |
CN101337940B (zh) | 2008-08-12 | 2012-05-02 | 国家农药创制工程技术研究中心 | 具杀虫活性的含氮杂环二氯烯丙醚类化合物 |
CN101715774A (zh) | 2008-10-09 | 2010-06-02 | 浙江化工科技集团有限公司 | 一个具有杀虫活性化合物制备及用途 |
EP2184273A1 (de) | 2008-11-05 | 2010-05-12 | Bayer CropScience AG | Halogen-substituierte Verbindungen als Pestizide |
GB0820344D0 (en) | 2008-11-06 | 2008-12-17 | Syngenta Ltd | Herbicidal compositions |
WO2010091310A1 (en) | 2009-02-06 | 2010-08-12 | Elan Pharmaceuticals, Inc. | Inhibitors of jun n-terminal kinase |
WO2010125985A1 (en) | 2009-04-28 | 2010-11-04 | Sumitomo Chemical Company, Limited | Fused heterocyclic compound and use thereof |
WO2011040629A1 (en) | 2009-09-30 | 2011-04-07 | Sumitomo Chemical Company, Limited | Composition and method for controlling arthropod pests |
JP5540640B2 (ja) | 2009-10-07 | 2014-07-02 | 住友化学株式会社 | 複素環化合物及びその有害節足動物防除用途 |
US8759359B2 (en) | 2009-12-18 | 2014-06-24 | Incyte Corporation | Substituted heteroaryl fused derivatives as PI3K inhibitors |
CA2782601C (en) | 2009-12-18 | 2015-07-21 | Mitsubishi Tanabe Pharma Corporation | Novel antiplatelet agent |
WO2011085575A1 (zh) | 2010-01-15 | 2011-07-21 | 江苏省农药研究所股份有限公司 | 邻杂环甲酰苯胺类化合物及其合成方法和应用 |
PH12013500237A1 (en) | 2010-08-31 | 2013-03-11 | Mitsui Chemicals Crop & Life Solutions Inc | Pest control agent |
CN101967139B (zh) | 2010-09-14 | 2013-06-05 | 中化蓝天集团有限公司 | 一种含一氟甲氧基吡唑的邻甲酰氨基苯甲酰胺类化合物、其合成方法及应用 |
BR112013011520A2 (pt) | 2010-11-19 | 2019-09-24 | Hoffmann La Roche | pirazolo piridinas e pirazolo piridinas e seu uso como inibidores de tyk2 |
TW201242962A (en) | 2010-12-01 | 2012-11-01 | Sumitomo Chemical Co | Pyrimidine compound and use for pest control thereof |
TWI617559B (zh) | 2010-12-22 | 2018-03-11 | 江蘇恆瑞醫藥股份有限公司 | 2-芳基咪唑并[1,2-b]嗒.2-苯基咪唑并[1,2-a]吡啶,和2-苯基咪唑并[1,2-a]吡衍生物 |
MX2013006847A (es) | 2010-12-24 | 2013-07-29 | Sumitomo Chemical Co | Compuesto heterociclico fusionado y su uso para el control de plagas. |
CN103298468A (zh) | 2011-02-01 | 2013-09-11 | 协和发酵麒麟株式会社 | 稠环杂环衍生物 |
US20120302573A1 (en) | 2011-05-25 | 2012-11-29 | Paul Francis Jackson | Methods of inhibiting pro matrix metalloproteinase activation |
GB201109763D0 (en) | 2011-06-10 | 2011-07-27 | Ucl Business Plc | Compounds |
US8975276B2 (en) | 2011-06-29 | 2015-03-10 | Bristol-Myers Squibb Company | Inhibitors of PDE10 |
WO2013007765A1 (en) | 2011-07-13 | 2013-01-17 | F. Hoffmann-La Roche Ag | Fused tricyclic compounds for use as inhibitors of janus kinases |
TWI589570B (zh) | 2011-08-04 | 2017-07-01 | 住友化學股份有限公司 | 稠合雜環化合物及其在病蟲害防制上之用途 |
WO2013050317A1 (en) | 2011-10-03 | 2013-04-11 | Syngenta Limited | Polymorphs of an isoxazoline derivative |
CN102391261A (zh) | 2011-10-14 | 2012-03-28 | 上海交通大学 | 一种n-取代噁二嗪类化合物及其制备方法和应用 |
MY188000A (en) | 2011-12-28 | 2021-11-08 | Fujifilm Corp | Novel nicotinamide derivative or salt thereof |
JP2015512907A (ja) | 2012-03-30 | 2015-04-30 | ビーエーエスエフ ソシエタス・ヨーロピアBasf Se | 有害動物を駆除するためのn−置換ピリジニリデン化合物および誘導体 |
EP2647626A1 (en) | 2012-04-03 | 2013-10-09 | Syngenta Participations AG. | 1-Aza-spiro[4.5]dec-3-ene and 1,8-diaza-spiro[4.5]dec-3-ene derivatives as pesticides |
MX2014013071A (es) | 2012-04-27 | 2015-01-12 | Dow Agrosciences Llc | Composiciones pesticidas y procesos relacionados con ellas. |
US9282739B2 (en) | 2012-04-27 | 2016-03-15 | Dow Agrosciences Llc | Pesticidal compositions and processes related thereto |
US9271500B2 (en) | 2012-06-18 | 2016-03-01 | Sumitomo Chemical Company, Limited | Fused heterocyclic compound |
CN103109816B (zh) | 2013-01-25 | 2014-09-10 | 青岛科技大学 | 硫代苯甲酰胺类化合物及其应用 |
CN103232431B (zh) | 2013-01-25 | 2014-11-05 | 青岛科技大学 | 一种二卤代吡唑酰胺类化合物及其应用 |
WO2014158644A1 (en) | 2013-03-13 | 2014-10-02 | Dow Agrosciences Llc | Process for the preparation of triaryl rhamnose carbamates |
UY35421A (es) | 2013-03-15 | 2014-10-31 | Nihon Nohyaku Co Ltd | Compuesto heterocíclico condensado o su sal, insecticida agrícola u hortícola que comprende el comp uesto y método de uso del insecticida |
WO2014148451A1 (ja) | 2013-03-19 | 2014-09-25 | 日本農薬株式会社 | 縮合複素環化合物又はその塩類及び該化合物を含有する農園芸用殺虫剤並びにその使用方法 |
BR112015025140A2 (pt) | 2013-05-23 | 2017-07-18 | Hoffmann La Roche | 2-fenilimidazo[1,2-a]pirimidinas como agentes de imagem |
CN105358555B (zh) | 2013-07-01 | 2018-01-30 | 住友化学株式会社 | 稠合杂环化合物及其有害生物防除用途 |
WO2015000715A1 (en) | 2013-07-02 | 2015-01-08 | Syngenta Participations Ag | Pesticidally active bi- or tricyclic heterocycles with sulfur containing substituents |
WO2015024203A1 (en) | 2013-08-20 | 2015-02-26 | Leo Pharma A/S | Novel neurokinin 1 receptor antagonist compounds ii |
CN103524422B (zh) | 2013-10-11 | 2015-05-27 | 中国农业科学院植物保护研究所 | 苯并咪唑衍生物及其制备方法和用途 |
EP3057430A4 (en) | 2013-10-17 | 2017-09-13 | Dow AgroSciences LLC | Processes for the preparation of pesticidal compounds |
KR20160072155A (ko) | 2013-10-17 | 2016-06-22 | 다우 아그로사이언시즈 엘엘씨 | 살충성 화합물의 제조 방법 |
WO2015059039A1 (en) | 2013-10-24 | 2015-04-30 | Syngenta Participations Ag | Method of protecting a plant propagation material |
EP2873668A1 (en) | 2013-11-13 | 2015-05-20 | Syngenta Participations AG. | Pesticidally active bicyclic heterocycles with sulphur containing substituents |
KR102362756B1 (ko) | 2014-02-17 | 2022-02-11 | 바이엘 크롭사이언스 악티엔게젤샤프트 | 해충 방제제로서의 2-(헤트)아릴-치환된 융합 비사이클릭 헤테로사이클 유도체 |
WO2015176267A1 (en) | 2014-05-22 | 2015-11-26 | Merck Sharp & Dohme Corp. | Antidiabetic tricyclic compounds |
US9708341B2 (en) | 2014-06-09 | 2017-07-18 | Sumitomo Chemical Company, Limited | Method for producing pyridine compound |
JP6675404B2 (ja) * | 2014-12-17 | 2020-04-01 | シンジェンタ パーティシペーションズ アーゲー | 硫黄含有置換基を有する殺有害生物的に活性な複素環式誘導体 |
UY36548A (es) | 2015-02-05 | 2016-06-01 | Bayer Cropscience Ag | Derivados heterocíclicos condensados bicíclicos sustituidos por 2-(het)arilo como pesticidas |
UY36547A (es) | 2015-02-05 | 2016-06-01 | Bayer Cropscience Ag | Derivados heterocíclicos condensados bicíclicos sustituidos por 2-(het)arilo como pesticidas |
EP3280716B1 (de) | 2015-04-08 | 2020-02-12 | Bayer CropScience AG | Imidazo[1,2-a]pyridin-2-yl-derivate als schädlingsbekämpfungsmittel und deren zwischenprodukte |
WO2017026384A1 (ja) | 2015-08-07 | 2017-02-16 | 日本農薬株式会社 | インダゾール化合物又はその塩類及び該化合物を含有する農園芸用殺虫剤並びにその使用方法 |
JP6916175B2 (ja) * | 2015-10-26 | 2021-08-11 | バイエル・クロップサイエンス・アクチェンゲゼルシャフト | 有害生物防除剤としての縮合二環式ヘテロ環誘導体 |
WO2017093180A1 (de) | 2015-12-01 | 2017-06-08 | Bayer Cropscience Aktiengesellschaft | Kondensierte bicyclische heterocyclen-derivate als schädlingsbekämpfungsmittel |
WO2017125340A1 (de) | 2016-01-22 | 2017-07-27 | Bayer Cropscience Aktiengesellschaft | Kondensierte bicyclische heterocyclen-derivate als schädlingsbekämpfungsmittel |
WO2017174414A1 (de) | 2016-04-05 | 2017-10-12 | Bayer Cropscience Aktiengesellschaft | Naphthalin-derivate als schädlingsbekämpfungsmittel |
EP3241830A1 (de) | 2016-05-04 | 2017-11-08 | Bayer CropScience Aktiengesellschaft | Kondensierte bicyclische heterocyclen-derivate als schädlingsbekämpfungsmittel |
WO2018033455A1 (de) | 2016-08-15 | 2018-02-22 | Bayer Cropscience Aktiengesellschaft | Kondensierte bicyclische heterocyclen-derivate als schädlingsbekämpfungsmittel |
JP7165126B2 (ja) | 2016-09-19 | 2022-11-02 | バイエル・クロップサイエンス・アクチェンゲゼルシャフト | ピラゾロ[1,5-a]ピリジン誘導体及びそれの殺有害生物剤としての使用 |
US10765116B2 (en) | 2016-11-23 | 2020-09-08 | Bayer Cropscience Aktiengesellschaft | 2-[3-(alkylsulfonyl)-2H-indazol-2-yl]-3H-imidazo[4,5-B]pyridine derivatives and similar compounds as pesticides |
WO2018138050A1 (de) | 2017-01-26 | 2018-08-02 | Bayer Aktiengesellschaft | Kondensierte bicyclische heterocyclen-derivate als schädlingsbekämpfungsmittel |
EP3305786A3 (de) | 2018-01-22 | 2018-07-25 | Bayer CropScience Aktiengesellschaft | Kondensierte bicyclische heterocyclen-derivate als schädlingsbekämpfungsmittel |
-
2017
- 2017-07-14 KR KR1020197004746A patent/KR102435080B1/ko active Active
- 2017-07-14 CN CN201780054877.0A patent/CN109689662B/zh not_active Expired - Fee Related
- 2017-07-14 PE PE2019000225A patent/PE20190206A1/es unknown
- 2017-07-14 CA CA3031139A patent/CA3031139A1/en not_active Abandoned
- 2017-07-14 JP JP2019502171A patent/JP6967064B2/ja active Active
- 2017-07-14 WO PCT/EP2017/067838 patent/WO2018015289A1/de active Application Filing
- 2017-07-14 MX MX2019000793A patent/MX2019000793A/es unknown
- 2017-07-14 AU AU2017298972A patent/AU2017298972B2/en not_active Ceased
- 2017-07-14 EP EP17739984.7A patent/EP3487860B1/de active Active
- 2017-07-14 US US16/318,592 patent/US10561145B2/en not_active Expired - Fee Related
- 2017-07-14 BR BR112019001135-8A patent/BR112019001135B1/pt not_active IP Right Cessation
- 2017-07-14 ES ES17739984T patent/ES2877571T3/es active Active
- 2017-07-14 RU RU2019104378A patent/RU2019104378A/ru not_active Application Discontinuation
- 2017-07-17 AR ARP170101988A patent/AR109076A1/es not_active Application Discontinuation
- 2017-07-17 TW TW106123759A patent/TWI747924B/zh not_active IP Right Cessation
- 2017-07-19 UY UY0001037327A patent/UY37327A/es not_active Application Discontinuation
-
2019
- 2019-01-10 IL IL264204A patent/IL264204B/en unknown
- 2019-01-16 CL CL2019000125A patent/CL2019000125A1/es unknown
- 2019-01-18 PH PH12019500139A patent/PH12019500139A1/en unknown
- 2019-01-18 CO CONC2019/0000503A patent/CO2019000503A2/es unknown
- 2019-02-18 ZA ZA2019/01024A patent/ZA201901024B/en unknown
Patent Citations (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO2005066177A1 (en) * | 2003-12-31 | 2005-07-21 | Schering-Plough Ltd. | Control of parasites in animals by the use of imidazo[1,2-b]pyridazine derivatives |
CN105473558A (zh) * | 2013-06-20 | 2016-04-06 | 拜耳作物科学股份公司 | 作为杀螨剂和杀昆虫剂的芳基硫化物衍生物和芳基硫氧化物衍生物 |
WO2016020286A1 (en) * | 2014-08-07 | 2016-02-11 | Syngenta Participations Ag | Pesticidally active heterocyclic derivatives with sulphur containing substituents |
WO2016091731A1 (en) * | 2014-12-11 | 2016-06-16 | Syngenta Participations Ag | Pesticidally active tetracyclic derivatives with sulfur containing substituents |
WO2016107742A1 (en) * | 2014-12-29 | 2016-07-07 | Syngenta Participations Ag | Pesticidally active tetracyclic derivatives with sulfur containing substituents |
Also Published As
Publication number | Publication date |
---|---|
CN109689662A (zh) | 2019-04-26 |
KR102435080B1 (ko) | 2022-08-22 |
KR20190027919A (ko) | 2019-03-15 |
CL2019000125A1 (es) | 2019-06-14 |
UY37327A (es) | 2018-02-28 |
US20190239510A1 (en) | 2019-08-08 |
ZA201901024B (en) | 2022-07-27 |
MX2019000793A (es) | 2019-06-20 |
IL264204A (en) | 2019-02-28 |
ES2877571T3 (es) | 2021-11-17 |
EP3487860A1 (de) | 2019-05-29 |
CA3031139A1 (en) | 2018-01-25 |
AU2017298972B2 (en) | 2021-03-04 |
JP2019527221A (ja) | 2019-09-26 |
TW201811804A (zh) | 2018-04-01 |
AR109076A1 (es) | 2018-10-24 |
JP6967064B2 (ja) | 2021-11-17 |
AU2017298972A1 (en) | 2019-01-31 |
PE20190206A1 (es) | 2019-02-07 |
IL264204B (en) | 2022-03-01 |
WO2018015289A1 (de) | 2018-01-25 |
PH12019500139A1 (en) | 2019-10-28 |
BR112019001135A2 (pt) | 2019-04-30 |
RU2019104378A (ru) | 2020-08-19 |
US10561145B2 (en) | 2020-02-18 |
EP3487860B1 (de) | 2021-04-14 |
TWI747924B (zh) | 2021-12-01 |
CO2019000503A2 (es) | 2019-04-30 |
BR112019001135B1 (pt) | 2022-11-01 |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
CN108430986B (zh) | 作为有害生物控制剂的稠合双环杂环衍生物 | |
CN107810188B (zh) | 作为害虫防治剂和中间体产物的稠合双环杂环衍生物 | |
JP6913076B2 (ja) | 有害生物防除剤としての2−(ヘタ)アリール−置換縮合ヘテロ環誘導体 | |
JP6871917B2 (ja) | 有害生物防除剤としての2−(ヘタ)アリール−置換縮合二環式ヘテロ環誘導体 | |
CN110382485B (zh) | 作为害虫防治剂的杂环烯衍生物 | |
CN109996799B (zh) | 作为害虫防治剂的稠合双环杂环衍生物 | |
CN112189011A (zh) | 作为农药的杂芳基三唑和杂芳基四唑化合物 | |
CN112204021A (zh) | 作为农药的新的杂芳基三唑和杂芳基四唑化合物 | |
CN112135819A (zh) | 作为杀虫剂的杂芳基-三唑与杂芳基-四唑化合物 | |
CN109689662B (zh) | 作为害虫防治剂的稠合双环杂环衍生物 | |
CN110312718B (zh) | 作为害虫防治剂的杂环烯衍生物 | |
CN111108106B (zh) | 作为害虫防治剂的杂环衍生物 | |
CN110248938A (zh) | 用作农药的2-[3-(烷基磺酰基)-2h-吲唑-2-基]-3h-咪唑并[4,5-b]吡啶衍生物和类似化合物 | |
CN111433215A (zh) | 用作害虫防治剂的杂环化合物的衍生物 | |
CN111741958A (zh) | 作为害虫防治剂的稠合双环杂环衍生物 | |
CN110637019B (zh) | 作为有害物防治剂的2-(杂)芳基-取代的稠合双环杂环衍生物 | |
CN110573513B (zh) | 作为害虫防治剂的2-(杂)芳基取代的稠合双环杂环衍生物 | |
JP6892452B2 (ja) | 有害生物防除剤としての置換イミダゾリル−カルボキサミド類 | |
CN113710669A (zh) | 作为农药的稠合双环杂环衍生物 | |
CN112912377A (zh) | 作为害虫防治剂的杂环衍生物 | |
CN113727983A (zh) | 作为害虫防治剂的稠合双环杂环衍生物 | |
CN112368280A (zh) | 作为害虫防治剂的杂环衍生物 | |
CN111886238A (zh) | 作为害虫防治剂的稠合双环杂环衍生物 | |
CN110691781A (zh) | 用作杀虫剂的介离子咪唑并吡啶 | |
CN111989328B (zh) | 作为害虫防治剂的杂环衍生物 |
Legal Events
Date | Code | Title | Description |
---|---|---|---|
PB01 | Publication | ||
PB01 | Publication | ||
SE01 | Entry into force of request for substantive examination | ||
SE01 | Entry into force of request for substantive examination | ||
GR01 | Patent grant | ||
GR01 | Patent grant | ||
CF01 | Termination of patent right due to non-payment of annual fee | ||
CF01 | Termination of patent right due to non-payment of annual fee |
Granted publication date: 20220315 |