ZA200102715B - Oral combination of lufenuron and nitenpyram against fleas. - Google Patents
Oral combination of lufenuron and nitenpyram against fleas. Download PDFInfo
- Publication number
- ZA200102715B ZA200102715B ZA200102715A ZA200102715A ZA200102715B ZA 200102715 B ZA200102715 B ZA 200102715B ZA 200102715 A ZA200102715 A ZA 200102715A ZA 200102715 A ZA200102715 A ZA 200102715A ZA 200102715 B ZA200102715 B ZA 200102715B
- Authority
- ZA
- South Africa
- Prior art keywords
- hydrogen
- halogen
- formula
- fleas
- partially
- Prior art date
Links
- 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 title description 10
- 229940079888 nitenpyram Drugs 0.000 title description 10
- 239000005912 Lufenuron Substances 0.000 title description 4
- 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 title description 4
- 229960000521 lufenuron Drugs 0.000 title description 4
- 229910052739 hydrogen Inorganic materials 0.000 claims abstract description 42
- 239000001257 hydrogen Substances 0.000 claims abstract description 40
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims abstract description 28
- 229910052736 halogen Inorganic materials 0.000 claims abstract description 26
- 150000002367 halogens Chemical group 0.000 claims abstract description 23
- 150000001875 compounds Chemical class 0.000 claims abstract description 15
- 125000005843 halogen group Chemical group 0.000 claims abstract description 11
- 238000002360 preparation method Methods 0.000 claims abstract description 9
- 150000002431 hydrogen Chemical class 0.000 claims abstract description 8
- 239000000203 mixture Substances 0.000 claims abstract description 8
- 125000004430 oxygen atom Chemical group O* 0.000 claims abstract description 6
- 238000009472 formulation Methods 0.000 claims abstract description 4
- 239000000546 pharmaceutical excipient Substances 0.000 claims abstract description 3
- 241001465754 Metazoa Species 0.000 claims description 46
- 238000000034 method Methods 0.000 claims description 11
- 125000000623 heterocyclic group Chemical group 0.000 claims description 5
- 229910052799 carbon Inorganic materials 0.000 claims description 4
- 238000004519 manufacturing process Methods 0.000 claims description 2
- 239000004480 active ingredient Substances 0.000 claims 1
- 239000002552 dosage form Substances 0.000 claims 1
- 125000004435 hydrogen atom Chemical group [H]* 0.000 abstract 4
- 125000004169 (C1-C6) alkyl group Chemical group 0.000 abstract 3
- 125000006273 (C1-C3) alkyl group Chemical group 0.000 abstract 2
- 125000004191 (C1-C6) alkoxy group Chemical group 0.000 abstract 2
- 125000000882 C2-C6 alkenyl group Chemical group 0.000 abstract 1
- 241000258242 Siphonaptera Species 0.000 description 24
- 230000000694 effects Effects 0.000 description 14
- 241000282326 Felis catus Species 0.000 description 10
- 241000282472 Canis lupus familiaris Species 0.000 description 7
- HRYILSDLIGTCOP-UHFFFAOYSA-N N-benzoylurea Chemical class NC(=O)NC(=O)C1=CC=CC=C1 HRYILSDLIGTCOP-UHFFFAOYSA-N 0.000 description 7
- -1 cyciobutyl Chemical group 0.000 description 7
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 7
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 7
- 239000000460 chlorine Substances 0.000 description 6
- 235000013601 eggs Nutrition 0.000 description 6
- 239000000126 substance Substances 0.000 description 6
- ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 description 5
- 239000008280 blood Substances 0.000 description 5
- 210000004369 blood Anatomy 0.000 description 5
- 229910052801 chlorine Inorganic materials 0.000 description 5
- 229910052731 fluorine Inorganic materials 0.000 description 4
- 239000002917 insecticide Substances 0.000 description 4
- 241000490513 Ctenocephalides canis Species 0.000 description 3
- 241000258924 Ctenocephalides felis Species 0.000 description 3
- PXGOKWXKJXAPGV-UHFFFAOYSA-N Fluorine Chemical compound FF PXGOKWXKJXAPGV-UHFFFAOYSA-N 0.000 description 3
- 241000282412 Homo Species 0.000 description 3
- 206010061217 Infestation Diseases 0.000 description 3
- 239000011737 fluorine Substances 0.000 description 3
- 230000000366 juvenile effect Effects 0.000 description 3
- 150000002903 organophosphorus compounds Chemical class 0.000 description 3
- 231100000614 poison Toxicity 0.000 description 3
- 239000000843 powder Substances 0.000 description 3
- 125000001424 substituent group Chemical group 0.000 description 3
- WKBOTKDWSSQWDR-UHFFFAOYSA-N Bromine atom Chemical compound [Br] WKBOTKDWSSQWDR-UHFFFAOYSA-N 0.000 description 2
- 241000196324 Embryophyta Species 0.000 description 2
- 208000006004 Flea Infestations Diseases 0.000 description 2
- 241000238631 Hexapoda Species 0.000 description 2
- 208000003251 Pruritus Diseases 0.000 description 2
- 241000382353 Pupa Species 0.000 description 2
- 125000000217 alkyl group Chemical group 0.000 description 2
- 150000008047 benzoylureas Chemical class 0.000 description 2
- GDTBXPJZTBHREO-UHFFFAOYSA-N bromine Substances BrBr GDTBXPJZTBHREO-UHFFFAOYSA-N 0.000 description 2
- 229910052794 bromium Inorganic materials 0.000 description 2
- 125000004432 carbon atom Chemical group C* 0.000 description 2
- 230000029142 excretion Effects 0.000 description 2
- 230000002147 killing effect Effects 0.000 description 2
- 125000004076 pyridyl group Chemical group 0.000 description 2
- 239000007921 spray Substances 0.000 description 2
- 230000009885 systemic effect Effects 0.000 description 2
- 125000003718 tetrahydrofuranyl group Chemical group 0.000 description 2
- 125000000335 thiazolyl group Chemical group 0.000 description 2
- 229920002554 vinyl polymer Polymers 0.000 description 2
- 125000004973 1-butenyl group Chemical group C(=CCC)* 0.000 description 1
- 125000006040 2-hexenyl group Chemical group 0.000 description 1
- 125000003903 2-propenyl group Chemical group [H]C([*])([H])C([H])=C([H])[H] 0.000 description 1
- 125000004070 6 membered heterocyclic group Chemical group 0.000 description 1
- 201000004384 Alopecia Diseases 0.000 description 1
- 206010003399 Arthropod bite Diseases 0.000 description 1
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical group [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 1
- 241000242722 Cestoda Species 0.000 description 1
- 241000935794 Dipylidium Species 0.000 description 1
- 206010020751 Hypersensitivity Diseases 0.000 description 1
- 241000118205 Ovicides Species 0.000 description 1
- 206010040880 Skin irritation Diseases 0.000 description 1
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical compound [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 description 1
- 239000005864 Sulphur Substances 0.000 description 1
- 208000027418 Wounds and injury Diseases 0.000 description 1
- 241000607479 Yersinia pestis Species 0.000 description 1
- 230000000895 acaricidal effect Effects 0.000 description 1
- 239000000642 acaricide Substances 0.000 description 1
- 230000002506 adulticidal effect Effects 0.000 description 1
- 125000001931 aliphatic group Chemical group 0.000 description 1
- 125000003342 alkenyl group Chemical group 0.000 description 1
- 208000026935 allergic disease Diseases 0.000 description 1
- 230000000172 allergic effect Effects 0.000 description 1
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 description 1
- 208000010668 atopic eczema Diseases 0.000 description 1
- 238000003287 bathing Methods 0.000 description 1
- 238000004820 blood count Methods 0.000 description 1
- 230000036765 blood level Effects 0.000 description 1
- 125000000484 butyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- 210000001520 comb Anatomy 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
- 125000001511 cyclopentyl group Chemical group [H]C1([H])C([H])([H])C([H])([H])C([H])(*)C1([H])[H] 0.000 description 1
- 125000001559 cyclopropyl group Chemical group [H]C1([H])C([H])([H])C1([H])* 0.000 description 1
- 230000006378 damage Effects 0.000 description 1
- 125000004852 dihydrofuranyl group Chemical group O1C(CC=C1)* 0.000 description 1
- 125000005043 dihydropyranyl group Chemical group O1C(CCC=C1)* 0.000 description 1
- 125000000532 dioxanyl group Chemical group 0.000 description 1
- 125000005879 dioxolanyl group Chemical group 0.000 description 1
- 239000000428 dust Substances 0.000 description 1
- 238000010410 dusting Methods 0.000 description 1
- 230000007613 environmental effect Effects 0.000 description 1
- 230000002349 favourable effect Effects 0.000 description 1
- 235000013305 food Nutrition 0.000 description 1
- 125000002541 furyl group Chemical group 0.000 description 1
- 230000002650 habitual effect Effects 0.000 description 1
- 208000024963 hair loss Diseases 0.000 description 1
- 230000003676 hair loss 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
- 125000002632 imidazolidinyl group Chemical group 0.000 description 1
- 125000002636 imidazolinyl group Chemical group 0.000 description 1
- 125000002883 imidazolyl group Chemical group 0.000 description 1
- 238000000338 in vitro Methods 0.000 description 1
- 208000015181 infectious disease Diseases 0.000 description 1
- 238000002347 injection Methods 0.000 description 1
- 239000007924 injection Substances 0.000 description 1
- 208000014674 injury Diseases 0.000 description 1
- PNDPGZBMCMUPRI-UHFFFAOYSA-N iodine Chemical compound II PNDPGZBMCMUPRI-UHFFFAOYSA-N 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
- 125000004491 isohexyl group Chemical group C(CCC(C)C)* 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
- 125000001449 isopropyl group Chemical group [H]C([H])([H])C([H])(*)C([H])([H])[H] 0.000 description 1
- 125000000842 isoxazolyl group Chemical group 0.000 description 1
- 230000007803 itching Effects 0.000 description 1
- 125000002757 morpholinyl group Chemical group 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
- 229910052757 nitrogen Inorganic materials 0.000 description 1
- 125000004433 nitrogen atom Chemical group N* 0.000 description 1
- 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 1
- 235000015097 nutrients Nutrition 0.000 description 1
- 230000017448 oviposition Effects 0.000 description 1
- 125000000160 oxazolidinyl group Chemical group 0.000 description 1
- 125000005968 oxazolinyl group Chemical group 0.000 description 1
- 125000002971 oxazolyl group Chemical group 0.000 description 1
- 239000001301 oxygen Substances 0.000 description 1
- 229910052760 oxygen Inorganic materials 0.000 description 1
- 244000045947 parasite Species 0.000 description 1
- 125000001147 pentyl group Chemical group C(CCCC)* 0.000 description 1
- 230000000361 pesticidal effect Effects 0.000 description 1
- 239000000575 pesticide Substances 0.000 description 1
- 125000003386 piperidinyl group Chemical group 0.000 description 1
- 125000001436 propyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- 125000000719 pyrrolidinyl group Chemical group 0.000 description 1
- 125000000168 pyrrolyl group Chemical group 0.000 description 1
- 238000006748 scratching Methods 0.000 description 1
- 230000002393 scratching effect Effects 0.000 description 1
- 230000001568 sexual effect Effects 0.000 description 1
- 239000002453 shampoo Substances 0.000 description 1
- 230000036556 skin irritation Effects 0.000 description 1
- 231100000475 skin irritation Toxicity 0.000 description 1
- 230000005808 skin problem Effects 0.000 description 1
- 241000894007 species Species 0.000 description 1
- 239000004544 spot-on Substances 0.000 description 1
- 238000005507 spraying Methods 0.000 description 1
- 238000004381 surface treatment Methods 0.000 description 1
- 239000011885 synergistic combination Substances 0.000 description 1
- 238000012360 testing method Methods 0.000 description 1
- 125000001412 tetrahydropyranyl group Chemical group 0.000 description 1
- 125000001544 thienyl group Chemical group 0.000 description 1
- 230000001988 toxicity Effects 0.000 description 1
- 231100000419 toxicity Toxicity 0.000 description 1
- 230000009466 transformation Effects 0.000 description 1
- 230000001052 transient effect Effects 0.000 description 1
- 230000007704 transition Effects 0.000 description 1
- 125000000876 trifluoromethoxy group Chemical group FC(F)(F)O* 0.000 description 1
- 125000000391 vinyl group Chemical group [H]C([*])=C([H])[H] 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
- A01N47/00—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom not being member of a ring and having no bond to a carbon or hydrogen atom, e.g. derivatives of carbonic acid
- A01N47/08—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom not being member of a ring and having no bond to a carbon or hydrogen atom, e.g. derivatives of carbonic acid the carbon atom having one or more single bonds to nitrogen atoms
- A01N47/28—Ureas or thioureas containing the groups >N—CO—N< or >N—CS—N<
- A01N47/34—Ureas or thioureas containing the groups >N—CO—N< or >N—CS—N< containing the groups, e.g. biuret; Thio analogues thereof; Urea-aldehyde condensation products
-
- 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
- A01N43/34—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with one nitrogen atom as the only ring hetero atom
- A01N43/40—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with one nitrogen atom as the only ring hetero atom six-membered rings
-
- 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
Landscapes
- Life Sciences & Earth Sciences (AREA)
- Health & Medical Sciences (AREA)
- General Health & Medical Sciences (AREA)
- Dentistry (AREA)
- Wood Science & Technology (AREA)
- Environmental Sciences (AREA)
- Zoology (AREA)
- Engineering & Computer Science (AREA)
- Plant Pathology (AREA)
- Pest Control & Pesticides (AREA)
- Agronomy & Crop Science (AREA)
- Veterinary Medicine (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Public Health (AREA)
- Chemical & Material Sciences (AREA)
- Pharmacology & Pharmacy (AREA)
- Organic Chemistry (AREA)
- Animal Behavior & Ethology (AREA)
- Tropical Medicine & Parasitology (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Medicinal Chemistry (AREA)
- General Chemical & Material Sciences (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
- Agricultural Chemicals And Associated Chemicals (AREA)
- Cosmetics (AREA)
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| CH204198 | 1998-10-09 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| ZA200102715B true ZA200102715B (en) | 2005-01-17 |
Family
ID=4224562
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| ZA200102715A ZA200102715B (en) | 1998-10-09 | 2001-04-03 | Oral combination of lufenuron and nitenpyram against fleas. |
Country Status (17)
| Country | Link |
|---|---|
| US (2) | US20020058683A1 (de) |
| EP (1) | EP1119256B1 (de) |
| JP (1) | JP2002527362A (de) |
| KR (1) | KR20010075604A (de) |
| CN (1) | CN1323161A (de) |
| AT (1) | ATE241908T1 (de) |
| AU (1) | AU757825B2 (de) |
| BR (1) | BR9914365A (de) |
| CA (1) | CA2345132A1 (de) |
| DE (1) | DE69908626T2 (de) |
| DK (1) | DK1119256T3 (de) |
| ES (1) | ES2201775T3 (de) |
| NZ (1) | NZ510846A (de) |
| PT (1) | PT1119256E (de) |
| RU (1) | RU2233590C2 (de) |
| WO (1) | WO2000021371A1 (de) |
| ZA (1) | ZA200102715B (de) |
Families Citing this family (25)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| ATE411799T1 (de) * | 2003-11-04 | 2008-11-15 | Intervet Int Bv | Ectoparasitische formulierungen von spinosyns und azol-pestiziden |
| CA2545543A1 (en) * | 2003-12-02 | 2005-06-16 | Schwarz Pharma Ag | Novel use of peptide compounds for treating central neuropathic pain |
| US20050158367A1 (en) * | 2004-01-16 | 2005-07-21 | The Procter & Gamble Company | Liquid compositions comprising one or more medicaments |
| CA2558848C (en) | 2004-03-05 | 2013-11-19 | Nissan Chemical Industries, Ltd. | Isoxazoline-substituted benzamide compound and pesticide |
| ES2353312T3 (es) | 2004-07-28 | 2011-03-01 | Intervet International Bv | Composición veterinaria que comprende un arilpirazol y una nitroenamina con actividad antiparasitaria potenciada. |
| IL165021A0 (en) * | 2004-11-04 | 2005-12-18 | Makhteshim Chem Works Ltd | Pesticidal composition |
| CN100353840C (zh) * | 2005-08-12 | 2007-12-12 | 南京第一农药有限公司 | 一种杀虫组合物及其应用 |
| CN100353839C (zh) * | 2005-08-12 | 2007-12-12 | 南京第一农药有限公司 | 一种含虱螨脲和啶虫脒的杀虫组合物及其应用 |
| CN100353841C (zh) * | 2005-08-12 | 2007-12-12 | 南京第一农药有限公司 | 一种含虱螨脲和吡虫啉的杀虫组合物及其应用 |
| CN100353843C (zh) * | 2005-08-12 | 2007-12-12 | 南京第一农药有限公司 | 一种含高效氯氟氰菊酯和虱螨脲的增效杀虫组合物及应用 |
| CN100353845C (zh) * | 2005-08-12 | 2007-12-12 | 南京第一农药有限公司 | 一种含虱螨脲和毒死蜱的增效杀虫组合物及其应用 |
| CN100353842C (zh) * | 2005-08-12 | 2007-12-12 | 南京第一农药有限公司 | 一种含高效氯氰菊酯和虱螨脲的增效杀虫组合物及其应用 |
| DE102005038585A1 (de) * | 2005-08-16 | 2007-02-22 | Bayer Cropscience Ag | Synergistische insektizide Mischungen |
| BRPI0601078B1 (pt) * | 2006-03-24 | 2015-10-06 | Champion Farmoquímico Ltda | Uso de Diflubenzuron |
| CN101795568A (zh) * | 2007-06-07 | 2010-08-04 | 达沃股份有限公司 | 外寄生物的防控 |
| AU2008268321C1 (en) | 2007-06-27 | 2018-09-27 | E. I. Du Pont De Nemours And Company | Animal pest control method |
| CN102613235B (zh) * | 2008-12-31 | 2014-08-20 | 浙江世佳科技有限公司 | 虱螨脲和苯醚甲环唑的悬浮剂 |
| CN101755788B (zh) * | 2008-12-31 | 2012-06-27 | 浙江世佳科技有限公司 | 含虱螨脲和烯啶虫胺以及有机硅增效剂的杀虫组合物 |
| CN102613225A (zh) * | 2008-12-31 | 2012-08-01 | 浙江世佳科技有限公司 | 虱螨脲和烯啶虫胺的水剂 |
| CN102613234A (zh) * | 2008-12-31 | 2012-08-01 | 浙江世佳科技有限公司 | 虱螨脲和烯啶虫胺的微乳剂 |
| WO2013056730A1 (en) | 2011-10-18 | 2013-04-25 | In2Care B.V. | Systemic use of compounds in humans that kill free-living blood-feeding ectoparasites |
| CN105992517B (zh) * | 2013-12-10 | 2020-03-06 | 英特维特国际股份有限公司 | 异噁唑啉化合物的抗寄生虫用途 |
| BR112017023059B1 (pt) | 2015-04-28 | 2022-07-05 | Mars, Incorporated | Processo para preparar um produto de ração úmida esterilizada, produto de ração úmida esterilizada, e seu uso |
| US10736318B2 (en) | 2017-03-28 | 2020-08-11 | Piedmont Animal Health Inc. | Combinations of acaricides and insect growth regulators for control of fleas without emesis in animals |
| CA3224225A1 (en) * | 2021-06-25 | 2022-12-29 | In The Bowl Animal Health, Inc. | Oral feline feed and methods for controlling flea infestations in a feline |
Family Cites Families (7)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US5153224A (en) * | 1984-10-18 | 1992-10-06 | Ciba-Geigy Corporation | Benzoylphenylureas |
| EP0179022B1 (de) * | 1984-10-18 | 1990-11-07 | Ciba-Geigy Ag | Benzoylphenylharnstoffe |
| WO1993024002A1 (de) * | 1992-05-23 | 1993-12-09 | Ciba-Geigy Ag | 1-[n-(halo-3-pyridylmethyl)]-n-methylamino-1-alkylamino-2-nitroethylen-derivate zur bekämpfung von flöhen bei haustieren |
| US5750548A (en) * | 1994-01-24 | 1998-05-12 | Novartis Corp. | 1- N-(halo-3-pyridylmethyl)!-N-methylamino-1-alklamino-2-nitroethylene derivatives for controlling fleas in domestic animals |
| EP2260707A3 (de) * | 1994-06-08 | 2013-07-24 | Syngenta Participations AG. | Lufenuron enthaltende synergistische Zusammensetzungen |
| IT1290845B1 (it) * | 1996-12-12 | 1998-12-14 | Isagro Spa | Composizioni per il controllo sistemico di parassiti di animali a sangue caldo |
| WO1999018796A2 (en) * | 1997-10-09 | 1999-04-22 | Rhone-Poulenc Agro | Pesticidal combination |
-
1999
- 1999-10-07 ES ES99947481T patent/ES2201775T3/es not_active Expired - Lifetime
- 1999-10-07 CN CN99811951A patent/CN1323161A/zh active Pending
- 1999-10-07 KR KR1020017004459A patent/KR20010075604A/ko not_active Application Discontinuation
- 1999-10-07 BR BR9914365-8A patent/BR9914365A/pt not_active IP Right Cessation
- 1999-10-07 DE DE69908626T patent/DE69908626T2/de not_active Expired - Fee Related
- 1999-10-07 RU RU2001111880/15A patent/RU2233590C2/ru not_active IP Right Cessation
- 1999-10-07 DK DK99947481T patent/DK1119256T3/da active
- 1999-10-07 CA CA002345132A patent/CA2345132A1/en not_active Abandoned
- 1999-10-07 AU AU60905/99A patent/AU757825B2/en not_active Ceased
- 1999-10-07 PT PT99947481T patent/PT1119256E/pt unknown
- 1999-10-07 NZ NZ510846A patent/NZ510846A/en unknown
- 1999-10-07 WO PCT/EP1999/007538 patent/WO2000021371A1/en not_active Application Discontinuation
- 1999-10-07 JP JP2000575367A patent/JP2002527362A/ja not_active Withdrawn
- 1999-10-07 AT AT99947481T patent/ATE241908T1/de not_active IP Right Cessation
- 1999-10-07 EP EP99947481A patent/EP1119256B1/de not_active Expired - Lifetime
-
2001
- 2001-04-03 US US09/825,114 patent/US20020058683A1/en not_active Abandoned
- 2001-04-03 ZA ZA200102715A patent/ZA200102715B/en unknown
-
2002
- 2002-12-12 US US10/317,551 patent/US20030139459A1/en not_active Abandoned
Also Published As
| Publication number | Publication date |
|---|---|
| DE69908626T2 (de) | 2004-05-13 |
| CA2345132A1 (en) | 2000-04-20 |
| JP2002527362A (ja) | 2002-08-27 |
| KR20010075604A (ko) | 2001-08-09 |
| BR9914365A (pt) | 2001-06-26 |
| EP1119256B1 (de) | 2003-06-04 |
| EP1119256A1 (de) | 2001-08-01 |
| CN1323161A (zh) | 2001-11-21 |
| AU757825B2 (en) | 2003-03-06 |
| US20030139459A1 (en) | 2003-07-24 |
| ATE241908T1 (de) | 2003-06-15 |
| DE69908626D1 (de) | 2003-07-10 |
| ES2201775T3 (es) | 2004-03-16 |
| DK1119256T3 (da) | 2003-09-29 |
| RU2233590C2 (ru) | 2004-08-10 |
| US20020058683A1 (en) | 2002-05-16 |
| AU6090599A (en) | 2000-05-01 |
| NZ510846A (en) | 2003-07-25 |
| WO2000021371A1 (en) | 2000-04-20 |
| PT1119256E (pt) | 2003-10-31 |
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