IL100698A - Polyamine Theolytes and anti-radiation drugs containing them - Google Patents

Polyamine Theolytes and anti-radiation drugs containing them

Info

Publication number: IL100698A
Authority: IL; Israel
Prior art keywords: bis; compound; phenyl; appropriate; give
Prior art date: 1991-01-23

Application number

IL10069892A

Other languages

English (en)

Hebrew (he)

Other versions

IL100698A0 (en

Original Assignee

Merrell Dow Pharma

Priority date (The priority date 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 date listed.)

1991-01-23

Filing date

1992-01-19

Publication date

1998-08-16

1992-01-19 Application filed by Merrell Dow Pharma filed Critical Merrell Dow Pharma

1992-09-06 Publication of IL100698A0 publication Critical patent/IL100698A0/xx

1998-08-16 Publication of IL100698A publication Critical patent/IL100698A/en

Links

239000000203 mixture Substances 0.000 title description 31
150000003573 thiols Chemical class 0.000 title description 22
229920000768 polyamine Polymers 0.000 title description 5
230000004223 radioprotective effect Effects 0.000 title description 2
150000001875 compounds Chemical class 0.000 claims abstract description 189
125000002947 alkylene group Chemical group 0.000 claims abstract description 10
239000003795 chemical substances by application Substances 0.000 claims description 46
210000004027 cell Anatomy 0.000 claims description 43
206010028980 Neoplasm Diseases 0.000 claims description 31
230000002939 deleterious effect Effects 0.000 claims description 28
230000001413 cellular effect Effects 0.000 claims description 27
230000001681 protective effect Effects 0.000 claims description 27
201000011510 cancer Diseases 0.000 claims description 24
238000001959 radiotherapy Methods 0.000 claims description 22
230000005865 ionizing radiation Effects 0.000 claims description 20
239000008194 pharmaceutical composition Substances 0.000 claims description 16
238000002512 chemotherapy Methods 0.000 claims description 15
239000002246 antineoplastic agent Substances 0.000 claims description 13
229940127089 cytotoxic agent Drugs 0.000 claims description 13
239000000546 pharmaceutical excipient Substances 0.000 claims description 8
239000003937 drug carrier Substances 0.000 claims description 4
210000004962 mammalian cell Anatomy 0.000 claims description 3
239000000718 radiation-protective agent Substances 0.000 abstract description 19
125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 description 123
-1 saturated hydrocarbylene radical Chemical class 0.000 description 122
239000002904 solvent Substances 0.000 description 95
XEKOWRVHYACXOJ-UHFFFAOYSA-N Ethyl acetate Chemical compound CCOC(C)=O XEKOWRVHYACXOJ-UHFFFAOYSA-N 0.000 description 90
125000002088 tosyl group Chemical group [H]C1=C([H])C(=C([H])C([H])=C1C([H])([H])[H])S(*)(=O)=O 0.000 description 72
238000010898 silica gel chromatography Methods 0.000 description 66
ZMXDDKWLCZADIW-UHFFFAOYSA-N N,N-Dimethylformamide Chemical compound CN(C)C=O ZMXDDKWLCZADIW-UHFFFAOYSA-N 0.000 description 63
RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 56
239000001257 hydrogen Substances 0.000 description 55
229910052739 hydrogen Inorganic materials 0.000 description 55
VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 48
HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 48
238000003756 stirring Methods 0.000 description 48
239000000376 reactant Substances 0.000 description 46
UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 description 45
125000000217 alkyl group Chemical group 0.000 description 44
UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 description 42
239000000243 solution Substances 0.000 description 36
238000010992 reflux Methods 0.000 description 35
DNJIEGIFACGWOD-UHFFFAOYSA-N ethanethiol Chemical compound CCS DNJIEGIFACGWOD-UHFFFAOYSA-N 0.000 description 34
XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 34
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 31
238000000034 method Methods 0.000 description 31
HEDRZPFGACZZDS-UHFFFAOYSA-N Chloroform Chemical compound ClC(Cl)Cl HEDRZPFGACZZDS-UHFFFAOYSA-N 0.000 description 28
238000006243 chemical reaction Methods 0.000 description 28
125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 28
LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 27
125000003236 benzoyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C(*)=O 0.000 description 27
239000000872 buffer Substances 0.000 description 22
OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 21
125000002768 hydroxyalkyl group Chemical group 0.000 description 19
239000012074 organic phase Substances 0.000 description 19
JUJWROOIHBZHMG-UHFFFAOYSA-N Pyridine Chemical compound C1=CC=NC=C1 JUJWROOIHBZHMG-UHFFFAOYSA-N 0.000 description 18
WYURNTSHIVDZCO-UHFFFAOYSA-N Tetrahydrofuran Chemical compound C1CCOC1 WYURNTSHIVDZCO-UHFFFAOYSA-N 0.000 description 18
QGZKDVFQNNGYKY-UHFFFAOYSA-N Ammonia Chemical compound N QGZKDVFQNNGYKY-UHFFFAOYSA-N 0.000 description 17
150000001356 alkyl thiols Chemical class 0.000 description 17
NLXLAEXVIDQMFP-UHFFFAOYSA-N Ammonia chloride Chemical class [NH4+].[Cl-] NLXLAEXVIDQMFP-UHFFFAOYSA-N 0.000 description 16
PAYRUJLWNCNPSJ-UHFFFAOYSA-N Aniline Chemical compound NC1=CC=CC=C1 PAYRUJLWNCNPSJ-UHFFFAOYSA-N 0.000 description 16
239000003960 organic solvent Substances 0.000 description 16
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 15
238000005192 partition Methods 0.000 description 15
239000011734 sodium Substances 0.000 description 15
229910052708 sodium Inorganic materials 0.000 description 15
VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 14
KRKNYBCHXYNGOX-UHFFFAOYSA-N citric acid Natural products OC(=O)CC(O)(C(O)=O)CC(O)=O KRKNYBCHXYNGOX-UHFFFAOYSA-N 0.000 description 14
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 14
150000001412 amines Chemical group 0.000 description 13
150000002431 hydrogen Chemical class 0.000 description 13
125000000472 sulfonyl group Chemical group *S(*)(=O)=O 0.000 description 13
238000003786 synthesis reaction Methods 0.000 description 13
241000124008 Mammalia Species 0.000 description 12
230000015572 biosynthetic process Effects 0.000 description 12
239000012299 nitrogen atmosphere Substances 0.000 description 12
239000007858 starting material Substances 0.000 description 12
125000001424 substituent group Chemical group 0.000 description 12
UIIMBOGNXHQVGW-UHFFFAOYSA-M Sodium bicarbonate Chemical class [Na+].OC([O-])=O UIIMBOGNXHQVGW-UHFFFAOYSA-M 0.000 description 11
229910052943 magnesium sulfate Inorganic materials 0.000 description 11
229920006395 saturated elastomer Polymers 0.000 description 11
238000011282 treatment Methods 0.000 description 11
RYYWUUFWQRZTIU-UHFFFAOYSA-N Thiophosphoric acid Chemical class OP(O)(S)=O RYYWUUFWQRZTIU-UHFFFAOYSA-N 0.000 description 10
238000001704 evaporation Methods 0.000 description 10
230000008020 evaporation Effects 0.000 description 10
RYHBNJHYFVUHQT-UHFFFAOYSA-N 1,4-Dioxane Chemical compound C1COCCO1 RYHBNJHYFVUHQT-UHFFFAOYSA-N 0.000 description 9
KWYUFKZDYYNOTN-UHFFFAOYSA-M Potassium hydroxide Chemical compound [OH-].[K+] KWYUFKZDYYNOTN-UHFFFAOYSA-M 0.000 description 9
KEAYESYHFKHZAL-UHFFFAOYSA-N Sodium Chemical compound [Na] KEAYESYHFKHZAL-UHFFFAOYSA-N 0.000 description 9
201000010099 disease Diseases 0.000 description 9
208000037265 diseases, disorders, signs and symptoms Diseases 0.000 description 9
230000006698 induction Effects 0.000 description 9
UMJSCPRVCHMLSP-UHFFFAOYSA-N pyridine Natural products COC1=CC=CN=C1 UMJSCPRVCHMLSP-UHFFFAOYSA-N 0.000 description 9
239000012312 sodium hydride Substances 0.000 description 9
229910000104 sodium hydride Inorganic materials 0.000 description 9
YLQBMQCUIZJEEH-UHFFFAOYSA-N tetrahydrofuran Natural products C=1C=COC=1 YLQBMQCUIZJEEH-UHFFFAOYSA-N 0.000 description 9
YYROPELSRYBVMQ-UHFFFAOYSA-N 4-toluenesulfonyl chloride Chemical compound CC1=CC=C(S(Cl)(=O)=O)C=C1 YYROPELSRYBVMQ-UHFFFAOYSA-N 0.000 description 8
238000002560 therapeutic procedure Methods 0.000 description 8
QAEDZJGFFMLHHQ-UHFFFAOYSA-N trifluoroacetic anhydride Chemical compound FC(F)(F)C(=O)OC(=O)C(F)(F)F QAEDZJGFFMLHHQ-UHFFFAOYSA-N 0.000 description 8
PXRKCOCTEMYUEG-UHFFFAOYSA-N 5-aminoisoindole-1,3-dione Chemical compound NC1=CC=C2C(=O)NC(=O)C2=C1 PXRKCOCTEMYUEG-UHFFFAOYSA-N 0.000 description 7
FAMRKDQNMBBFBR-BQYQJAHWSA-N diethyl azodicarboxylate Substances CCOC(=O)\N=N\C(=O)OCC FAMRKDQNMBBFBR-BQYQJAHWSA-N 0.000 description 7
FAMRKDQNMBBFBR-UHFFFAOYSA-N ethyl n-ethoxycarbonyliminocarbamate Chemical compound CCOC(=O)N=NC(=O)OCC FAMRKDQNMBBFBR-UHFFFAOYSA-N 0.000 description 7
QJGQUHMNIGDVPM-UHFFFAOYSA-N nitrogen group Chemical group [N] QJGQUHMNIGDVPM-UHFFFAOYSA-N 0.000 description 7
125000001037 p-tolyl group Chemical group [H]C1=C([H])C(=C([H])C([H])=C1*)C([H])([H])[H] 0.000 description 7
125000002924 primary amino group Chemical group [H]N([H])* 0.000 description 7
230000005855 radiation Effects 0.000 description 7
208000011581 secondary neoplasm Diseases 0.000 description 7
239000001509 sodium citrate Substances 0.000 description 7
NLJMYIDDQXHKNR-UHFFFAOYSA-K sodium citrate Chemical compound O.O.[Na+].[Na+].[Na+].[O-]C(=O)CC(O)(CC([O-])=O)C([O-])=O NLJMYIDDQXHKNR-UHFFFAOYSA-K 0.000 description 7
150000003456 sulfonamides Chemical class 0.000 description 7
DYHSDKLCOJIUFX-UHFFFAOYSA-N tert-butoxycarbonyl anhydride Chemical compound CC(C)(C)OC(=O)OC(=O)OC(C)(C)C DYHSDKLCOJIUFX-UHFFFAOYSA-N 0.000 description 7
VOVUARRWDCVURC-UHFFFAOYSA-N thiirane Chemical compound C1CS1 VOVUARRWDCVURC-UHFFFAOYSA-N 0.000 description 7
QOXOZONBQWIKDA-UHFFFAOYSA-N 3-hydroxypropyl Chemical group [CH2]CCO QOXOZONBQWIKDA-UHFFFAOYSA-N 0.000 description 6
AOJJSUZBOXZQNB-TZSSRYMLSA-N Doxorubicin Chemical compound O([C@H]1C[C@@](O)(CC=2C(O)=C3C(=O)C=4C=CC=C(C=4C(=O)C3=C(O)C=21)OC)C(=O)CO)[C@H]1C[C@H](N)[C@H](O)[C@H](C)O1 AOJJSUZBOXZQNB-TZSSRYMLSA-N 0.000 description 6
241001465754 Metazoa Species 0.000 description 6
NWIBSHFKIJFRCO-WUDYKRTCSA-N Mytomycin Chemical compound C1N2C(C(C(C)=C(N)C3=O)=O)=C3[C@@H](COC(N)=O)[C@@]2(OC)[C@@H]2[C@H]1N2 NWIBSHFKIJFRCO-WUDYKRTCSA-N 0.000 description 6
239000002253 acid Substances 0.000 description 6
VSCWAEJMTAWNJL-UHFFFAOYSA-K aluminium trichloride Chemical compound Cl[Al](Cl)Cl VSCWAEJMTAWNJL-UHFFFAOYSA-K 0.000 description 6
229910021529 ammonia Inorganic materials 0.000 description 6
239000000706 filtrate Substances 0.000 description 6
238000002360 preparation method Methods 0.000 description 6
238000010791 quenching Methods 0.000 description 6
239000000741 silica gel Substances 0.000 description 6
229910002027 silica gel Inorganic materials 0.000 description 6
229940124530 sulfonamide Drugs 0.000 description 6
125000000565 sulfonamide group Chemical group 0.000 description 6
RMVRSNDYEFQCLF-UHFFFAOYSA-N thiophenol Chemical compound SC1=CC=CC=C1 RMVRSNDYEFQCLF-UHFFFAOYSA-N 0.000 description 6
VLVCWODDMDGANW-UHFFFAOYSA-N 4-methyl-n-phenylbenzenesulfonamide Chemical compound C1=CC(C)=CC=C1S(=O)(=O)NC1=CC=CC=C1 VLVCWODDMDGANW-UHFFFAOYSA-N 0.000 description 5
QGZKDVFQNNGYKY-UHFFFAOYSA-O Ammonium Chemical compound [NH4+] QGZKDVFQNNGYKY-UHFFFAOYSA-O 0.000 description 5
FRPHFZCDPYBUAU-UHFFFAOYSA-N Bromocresolgreen Chemical compound CC1=C(Br)C(O)=C(Br)C=C1C1(C=2C(=C(Br)C(O)=C(Br)C=2)C)C2=CC=CC=C2S(=O)(=O)O1 FRPHFZCDPYBUAU-UHFFFAOYSA-N 0.000 description 5
239000002168 alkylating agent Substances 0.000 description 5
229940100198 alkylating agent Drugs 0.000 description 5
150000001408 amides Chemical class 0.000 description 5
239000002585 base Substances 0.000 description 5
229940079593 drug Drugs 0.000 description 5
239000003814 drug Substances 0.000 description 5
230000001613 neoplastic effect Effects 0.000 description 5
230000002829 reductive effect Effects 0.000 description 5
BEOOHQFXGBMRKU-UHFFFAOYSA-N sodium cyanoborohydride Chemical compound [Na+].[B-]C#N BEOOHQFXGBMRKU-UHFFFAOYSA-N 0.000 description 5
125000005931 tert-butyloxycarbonyl group Chemical group [H]C([H])([H])C(OC(*)=O)(C([H])([H])[H])C([H])([H])[H] 0.000 description 5
239000003039 volatile agent Substances 0.000 description 5
NHQDETIJWKXCTC-UHFFFAOYSA-N 3-chloroperbenzoic acid Chemical compound OOC(=O)C1=CC=CC(Cl)=C1 NHQDETIJWKXCTC-UHFFFAOYSA-N 0.000 description 4
FMMWHPNWAFZXNH-UHFFFAOYSA-N Benz[a]pyrene Chemical compound C1=C2C3=CC=CC=C3C=C(C=C3)C2=C2C3=CC=CC2=C1 FMMWHPNWAFZXNH-UHFFFAOYSA-N 0.000 description 4
108020004414 DNA Proteins 0.000 description 4
231100001074 DNA strand break Toxicity 0.000 description 4
208000017604 Hodgkin disease Diseases 0.000 description 4
208000010747 Hodgkins lymphoma Diseases 0.000 description 4
HMMUPZWQTYSHGC-UHFFFAOYSA-N N-[4-[7-(4-aminobutylamino)heptylamino]butyl]benzamide Chemical compound C(C1=CC=CC=C1)(=O)NCCCCNCCCCCCCNCCCCN HMMUPZWQTYSHGC-UHFFFAOYSA-N 0.000 description 4
AXCZMVOFGPJBDE-UHFFFAOYSA-L calcium dihydroxide Chemical compound [OH-].[OH-].[Ca+2] AXCZMVOFGPJBDE-UHFFFAOYSA-L 0.000 description 4
239000000920 calcium hydroxide Substances 0.000 description 4
229910001861 calcium hydroxide Inorganic materials 0.000 description 4
239000002775 capsule Substances 0.000 description 4
239000000969 carrier Substances 0.000 description 4
239000003638 chemical reducing agent Substances 0.000 description 4
238000004821 distillation Methods 0.000 description 4
125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 4
IKDUDTNKRLTJSI-UHFFFAOYSA-N hydrazine hydrate Chemical compound O.NN IKDUDTNKRLTJSI-UHFFFAOYSA-N 0.000 description 4
125000005191 hydroxyalkylamino group Chemical group 0.000 description 4
239000007788 liquid Substances 0.000 description 4
239000012280 lithium aluminium hydride Substances 0.000 description 4
239000011777 magnesium Substances 0.000 description 4
239000000463 material Substances 0.000 description 4
LULAYUGMBFYYEX-UHFFFAOYSA-N metachloroperbenzoic acid Natural products OC(=O)C1=CC=CC(Cl)=C1 LULAYUGMBFYYEX-UHFFFAOYSA-N 0.000 description 4
FKSLYSSVKFYJKE-UHFFFAOYSA-N n,n-diethylethanamine;methanol Chemical compound OC.CCN(CC)CC FKSLYSSVKFYJKE-UHFFFAOYSA-N 0.000 description 4
150000002825 nitriles Chemical group 0.000 description 4
XKJCHHZQLQNZHY-UHFFFAOYSA-N phthalimide Chemical compound C1=CC=C2C(=O)NC(=O)C2=C1 XKJCHHZQLQNZHY-UHFFFAOYSA-N 0.000 description 4
125000000612 phthaloyl group Chemical group C(C=1C(C(=O)*)=CC=CC1)(=O)* 0.000 description 4
239000012857 radioactive material Substances 0.000 description 4
239000011541 reaction mixture Substances 0.000 description 4
239000000126 substance Substances 0.000 description 4
239000000725 suspension Substances 0.000 description 4
125000000954 2-hydroxyethyl group Chemical group [H]C([*])([H])C([H])([H])O[H] 0.000 description 3
GNFTZDOKVXKIBK-UHFFFAOYSA-N 3-(2-methoxyethoxy)benzohydrazide Chemical compound COCCOC1=CC=CC(C(=O)NN)=C1 GNFTZDOKVXKIBK-UHFFFAOYSA-N 0.000 description 3
WEVYAHXRMPXWCK-UHFFFAOYSA-N Acetonitrile Chemical compound CC#N WEVYAHXRMPXWCK-UHFFFAOYSA-N 0.000 description 3
NLHHRLWOUZZQLW-UHFFFAOYSA-N Acrylonitrile Chemical compound C=CC#N NLHHRLWOUZZQLW-UHFFFAOYSA-N 0.000 description 3
WVDDGKGOMKODPV-UHFFFAOYSA-N Benzyl alcohol Chemical compound OCC1=CC=CC=C1 WVDDGKGOMKODPV-UHFFFAOYSA-N 0.000 description 3
CMSMOCZEIVJLDB-UHFFFAOYSA-N Cyclophosphamide Chemical compound ClCCN(CCCl)P1(=O)NCCCO1 CMSMOCZEIVJLDB-UHFFFAOYSA-N 0.000 description 3
YMWUJEATGCHHMB-UHFFFAOYSA-N Dichloromethane Chemical compound ClCCl YMWUJEATGCHHMB-UHFFFAOYSA-N 0.000 description 3
241000699670 Mus sp. Species 0.000 description 3
PKUWKAXTAVNIJR-UHFFFAOYSA-N O,O-diethyl hydrogen thiophosphate Chemical compound CCOP(O)(=S)OCC PKUWKAXTAVNIJR-UHFFFAOYSA-N 0.000 description 3
DNIAPMSPPWPWGF-UHFFFAOYSA-N Propylene glycol Chemical compound CC(O)CO DNIAPMSPPWPWGF-UHFFFAOYSA-N 0.000 description 3
FAPWRFPIFSIZLT-UHFFFAOYSA-M Sodium chloride Chemical compound [Na+].[Cl-] FAPWRFPIFSIZLT-UHFFFAOYSA-M 0.000 description 3
230000001154 acute effect Effects 0.000 description 3
JKOQGQFVAUAYPM-UHFFFAOYSA-N amifostine Chemical compound NCCCNCCSP(O)(O)=O JKOQGQFVAUAYPM-UHFFFAOYSA-N 0.000 description 3
239000012267 brine Substances 0.000 description 3
230000030833 cell death Effects 0.000 description 3
108091092356 cellular DNA Proteins 0.000 description 3
DQLATGHUWYMOKM-UHFFFAOYSA-L cisplatin Chemical compound N[Pt](N)(Cl)Cl DQLATGHUWYMOKM-UHFFFAOYSA-L 0.000 description 3
229960004316 cisplatin Drugs 0.000 description 3
229960004397 cyclophosphamide Drugs 0.000 description 3
229960004679 doxorubicin Drugs 0.000 description 3
230000007613 environmental effect Effects 0.000 description 3
238000002474 experimental method Methods 0.000 description 3
229960004857 mitomycin Drugs 0.000 description 3
VLKZOEOYAKHREP-UHFFFAOYSA-N n-Hexane Chemical compound CCCCCC VLKZOEOYAKHREP-UHFFFAOYSA-N 0.000 description 3
230000000269 nucleophilic effect Effects 0.000 description 3
238000011275 oncology therapy Methods 0.000 description 3
150000007530 organic bases Chemical class 0.000 description 3
125000001436 propyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])[H] 0.000 description 3
125000006239 protecting group Chemical group 0.000 description 3
HPALAKNZSZLMCH-UHFFFAOYSA-M sodium;chloride;hydrate Chemical compound O.[Na+].[Cl-] HPALAKNZSZLMCH-UHFFFAOYSA-M 0.000 description 3
238000012360 testing method Methods 0.000 description 3
IBODDUNKEPPBKW-UHFFFAOYSA-N 1,5-dibromopentane Chemical compound BrCCCCCBr IBODDUNKEPPBKW-UHFFFAOYSA-N 0.000 description 2
HZAXFHJVJLSVMW-UHFFFAOYSA-N 2-Aminoethan-1-ol Chemical compound NCCO HZAXFHJVJLSVMW-UHFFFAOYSA-N 0.000 description 2
CXMYWOCYTPKBPP-UHFFFAOYSA-N 3-(3-hydroxypropylamino)propan-1-ol Chemical compound OCCCNCCCO CXMYWOCYTPKBPP-UHFFFAOYSA-N 0.000 description 2
BMYNFMYTOJXKLE-UHFFFAOYSA-N 3-azaniumyl-2-hydroxypropanoate Chemical compound NCC(O)C(O)=O BMYNFMYTOJXKLE-UHFFFAOYSA-N 0.000 description 2
YKFROQCFVXOUPW-UHFFFAOYSA-N 4-(methylthio) aniline Chemical compound CSC1=CC=C(N)C=C1 YKFROQCFVXOUPW-UHFFFAOYSA-N 0.000 description 2
QRVYABWJVXXOTN-UHFFFAOYSA-N 4-methylsulfanylbenzaldehyde Chemical compound CSC1=CC=C(C=O)C=C1 QRVYABWJVXXOTN-UHFFFAOYSA-N 0.000 description 2
208000031261 Acute myeloid leukaemia Diseases 0.000 description 2
CIWBSHSKHKDKBQ-JLAZNSOCSA-N Ascorbic acid Chemical compound OC[C@H](O)[C@H]1OC(=O)C(O)=C1O CIWBSHSKHKDKBQ-JLAZNSOCSA-N 0.000 description 2
TXVHTIQJNYSSKO-UHFFFAOYSA-N BeP Natural products C1=CC=C2C3=CC=CC=C3C3=CC=CC4=CC=C1C2=C34 TXVHTIQJNYSSKO-UHFFFAOYSA-N 0.000 description 2
241000282472 Canis lupus familiaris Species 0.000 description 2
201000009030 Carcinoma Diseases 0.000 description 2
PEDCQBHIVMGVHV-UHFFFAOYSA-N Glycerine Chemical compound OCC(O)CO PEDCQBHIVMGVHV-UHFFFAOYSA-N 0.000 description 2
241000282412 Homo Species 0.000 description 2
OAKJQQAXSVQMHS-UHFFFAOYSA-N Hydrazine Chemical compound NN OAKJQQAXSVQMHS-UHFFFAOYSA-N 0.000 description 2
239000012359 Methanesulfonyl chloride Substances 0.000 description 2
208000033776 Myeloid Acute Leukemia Diseases 0.000 description 2
WBNQDOYYEUMPFS-UHFFFAOYSA-N N-nitrosodiethylamine Chemical compound CCN(CC)N=O WBNQDOYYEUMPFS-UHFFFAOYSA-N 0.000 description 2
HBTROEQVZQSAKI-UHFFFAOYSA-N NCCCNCCCN.C(C)S Chemical compound NCCCNCCCN.C(C)S HBTROEQVZQSAKI-UHFFFAOYSA-N 0.000 description 2
208000015914 Non-Hodgkin lymphomas Diseases 0.000 description 2
241000700159 Rattus Species 0.000 description 2
206010039491 Sarcoma Diseases 0.000 description 2
229930006000 Sucrose Natural products 0.000 description 2
CZMRCDWAGMRECN-UGDNZRGBSA-N Sucrose Chemical compound O[C@H]1[C@H](O)[C@@H](CO)O[C@@]1(CO)O[C@@H]1[C@H](O)[C@@H](O)[C@H](O)[C@@H](CO)O1 CZMRCDWAGMRECN-UGDNZRGBSA-N 0.000 description 2
YHPLKWQJMAYFCN-UHFFFAOYSA-N WR-1065 Chemical compound NCCCNCCS YHPLKWQJMAYFCN-UHFFFAOYSA-N 0.000 description 2
239000004480 active ingredient Substances 0.000 description 2
239000002671 adjuvant Substances 0.000 description 2
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201000008968 osteosarcoma Diseases 0.000 description 1
210000001672 ovary Anatomy 0.000 description 1
210000000496 pancreas Anatomy 0.000 description 1
208000008443 pancreatic carcinoma Diseases 0.000 description 1
210000000578 peripheral nerve Anatomy 0.000 description 1
235000021317 phosphate Nutrition 0.000 description 1
150000003013 phosphoric acid derivatives Chemical class 0.000 description 1
229910052698 phosphorus Inorganic materials 0.000 description 1
239000011574 phosphorus Substances 0.000 description 1
CYQAYERJWZKYML-UHFFFAOYSA-N phosphorus pentasulfide Chemical compound S1P(S2)(=S)SP3(=S)SP1(=S)SP2(=S)S3 CYQAYERJWZKYML-UHFFFAOYSA-N 0.000 description 1
239000004033 plastic Substances 0.000 description 1
229920003023 plastic Polymers 0.000 description 1
239000003755 preservative agent Substances 0.000 description 1
230000002062 proliferating effect Effects 0.000 description 1
FVSKHRXBFJPNKK-UHFFFAOYSA-N propionitrile Chemical compound CCC#N FVSKHRXBFJPNKK-UHFFFAOYSA-N 0.000 description 1
150000003254 radicals Chemical class 0.000 description 1
230000003537 radioprotector Effects 0.000 description 1
238000005932 reductive alkylation reaction Methods 0.000 description 1
230000004044 response Effects 0.000 description 1
210000003660 reticulum Anatomy 0.000 description 1
CVHZOJJKTDOEJC-UHFFFAOYSA-N saccharin Chemical compound C1=CC=C2C(=O)NS(=O)(=O)C2=C1 CVHZOJJKTDOEJC-UHFFFAOYSA-N 0.000 description 1
229940081974 saccharin Drugs 0.000 description 1
235000019204 saccharin Nutrition 0.000 description 1
239000000901 saccharin and its Na,K and Ca salt Substances 0.000 description 1
239000012056 semi-solid material Substances 0.000 description 1
239000004208 shellac Substances 0.000 description 1
229940113147 shellac Drugs 0.000 description 1
ZLGIYFNHBLSMPS-ATJNOEHPSA-N shellac Chemical compound OCCCCCC(O)C(O)CCCCCCCC(O)=O.C1C23[C@H](C(O)=O)CCC2[C@](C)(CO)[C@@H]1C(C(O)=O)=C[C@@H]3O ZLGIYFNHBLSMPS-ATJNOEHPSA-N 0.000 description 1
235000013874 shellac Nutrition 0.000 description 1
210000000813 small intestine Anatomy 0.000 description 1
239000011780 sodium chloride Substances 0.000 description 1
235000010267 sodium hydrogen sulphite Nutrition 0.000 description 1
239000011343 solid material Substances 0.000 description 1
239000011877 solvent mixture Substances 0.000 description 1
241000894007 species Species 0.000 description 1
238000012289 standard assay Methods 0.000 description 1
239000008107 starch Substances 0.000 description 1
235000019698 starch Nutrition 0.000 description 1
210000002784 stomach Anatomy 0.000 description 1
239000000829 suppository Substances 0.000 description 1
230000001629 suppression Effects 0.000 description 1
OKZDCLQORQPGLE-UHFFFAOYSA-N tert-butyl N-(3-aminopropyl)-N-[3-(2-sulfanylethylamino)propyl]carbamate Chemical compound SCCNCCCN(CCCN)C(=O)OC(C)(C)C OKZDCLQORQPGLE-UHFFFAOYSA-N 0.000 description 1
OROJZNZIQBPZLT-UHFFFAOYSA-N tert-butyl n,n-bis(3-anilinopropyl)carbamate Chemical compound C=1C=CC=CC=1NCCCN(C(=O)OC(C)(C)C)CCCNC1=CC=CC=C1 OROJZNZIQBPZLT-UHFFFAOYSA-N 0.000 description 1
SFOZKAHBJOBGPP-UHFFFAOYSA-N tert-butyl n,n-bis[3-[(2-methylpropan-2-yl)oxycarbonyl-[(4-sulfanylphenyl)methyl]amino]propyl]carbamate Chemical compound C=1C=C(S)C=CC=1CN(C(=O)OC(C)(C)C)CCCN(C(=O)OC(C)(C)C)CCCN(C(=O)OC(C)(C)C)CC1=CC=C(S)C=C1 SFOZKAHBJOBGPP-UHFFFAOYSA-N 0.000 description 1
HZHBOIOMRJRCNA-UHFFFAOYSA-N tert-butyl n-(4-chlorobutyl)-n-(4-methylphenyl)sulfonylcarbamate Chemical compound CC1=CC=C(S(=O)(=O)N(CCCCCl)C(=O)OC(C)(C)C)C=C1 HZHBOIOMRJRCNA-UHFFFAOYSA-N 0.000 description 1
ISHLCKAQWKBMAU-UHFFFAOYSA-N tert-butyl n-diazocarbamate Chemical compound CC(C)(C)OC(=O)N=[N+]=[N-] ISHLCKAQWKBMAU-UHFFFAOYSA-N 0.000 description 1
150000003512 tertiary amines Chemical class 0.000 description 1
125000005490 tosylate group Chemical group 0.000 description 1
BDZBKCUKTQZUTL-UHFFFAOYSA-N triethyl phosphite Chemical compound CCOP(OCC)OCC BDZBKCUKTQZUTL-UHFFFAOYSA-N 0.000 description 1
239000003981 vehicle Substances 0.000 description 1
230000035899 viability Effects 0.000 description 1
235000012431 wafers Nutrition 0.000 description 1
239000008215 water for injection Substances 0.000 description 1

Classifications

- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C323/00—Thiols, sulfides, hydropolysulfides or polysulfides substituted by halogen, oxygen or nitrogen atoms, or by sulfur atoms not being part of thio groups
- C07C323/23—Thiols, sulfides, hydropolysulfides or polysulfides substituted by halogen, oxygen or nitrogen atoms, or by sulfur atoms not being part of thio groups containing thio groups and nitrogen atoms, not being part of nitro or nitroso groups, bound to the same carbon skeleton
- C07C323/24—Thiols, sulfides, hydropolysulfides or polysulfides substituted by halogen, oxygen or nitrogen atoms, or by sulfur atoms not being part of thio groups containing thio groups and nitrogen atoms, not being part of nitro or nitroso groups, bound to the same carbon skeleton having the sulfur atoms of the thio groups bound to acyclic carbon atoms of the carbon skeleton
- C07C323/25—Thiols, sulfides, hydropolysulfides or polysulfides substituted by halogen, oxygen or nitrogen atoms, or by sulfur atoms not being part of thio groups containing thio groups and nitrogen atoms, not being part of nitro or nitroso groups, bound to the same carbon skeleton having the sulfur atoms of the thio groups bound to acyclic carbon atoms of the carbon skeleton the carbon skeleton being acyclic and saturated
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P39/00—General protective or antinoxious agents
- A61P39/02—Antidotes
- 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
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C323/00—Thiols, sulfides, hydropolysulfides or polysulfides substituted by halogen, oxygen or nitrogen atoms, or by sulfur atoms not being part of thio groups
- C07C323/23—Thiols, sulfides, hydropolysulfides or polysulfides substituted by halogen, oxygen or nitrogen atoms, or by sulfur atoms not being part of thio groups containing thio groups and nitrogen atoms, not being part of nitro or nitroso groups, bound to the same carbon skeleton
- C07C323/31—Thiols, sulfides, hydropolysulfides or polysulfides substituted by halogen, oxygen or nitrogen atoms, or by sulfur atoms not being part of thio groups containing thio groups and nitrogen atoms, not being part of nitro or nitroso groups, bound to the same carbon skeleton having the sulfur atom of at least one of the thio groups bound to a carbon atom of a six-membered aromatic ring of the carbon skeleton
- C07C323/32—Thiols, sulfides, hydropolysulfides or polysulfides substituted by halogen, oxygen or nitrogen atoms, or by sulfur atoms not being part of thio groups containing thio groups and nitrogen atoms, not being part of nitro or nitroso groups, bound to the same carbon skeleton having the sulfur atom of at least one of the thio groups bound to a carbon atom of a six-membered aromatic ring of the carbon skeleton having at least one of the nitrogen atoms bound to an acyclic carbon atom of the carbon skeleton
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C323/00—Thiols, sulfides, hydropolysulfides or polysulfides substituted by halogen, oxygen or nitrogen atoms, or by sulfur atoms not being part of thio groups
- C07C323/23—Thiols, sulfides, hydropolysulfides or polysulfides substituted by halogen, oxygen or nitrogen atoms, or by sulfur atoms not being part of thio groups containing thio groups and nitrogen atoms, not being part of nitro or nitroso groups, bound to the same carbon skeleton
- C07C323/31—Thiols, sulfides, hydropolysulfides or polysulfides substituted by halogen, oxygen or nitrogen atoms, or by sulfur atoms not being part of thio groups containing thio groups and nitrogen atoms, not being part of nitro or nitroso groups, bound to the same carbon skeleton having the sulfur atom of at least one of the thio groups bound to a carbon atom of a six-membered aromatic ring of the carbon skeleton
- C07C323/33—Thiols, sulfides, hydropolysulfides or polysulfides substituted by halogen, oxygen or nitrogen atoms, or by sulfur atoms not being part of thio groups containing thio groups and nitrogen atoms, not being part of nitro or nitroso groups, bound to the same carbon skeleton having the sulfur atom of at least one of the thio groups bound to a carbon atom of a six-membered aromatic ring of the carbon skeleton having at least one of the nitrogen atoms bound to a carbon atom of the same non-condensed six-membered aromatic ring
- C07C323/34—Thiols, sulfides, hydropolysulfides or polysulfides substituted by halogen, oxygen or nitrogen atoms, or by sulfur atoms not being part of thio groups containing thio groups and nitrogen atoms, not being part of nitro or nitroso groups, bound to the same carbon skeleton having the sulfur atom of at least one of the thio groups bound to a carbon atom of a six-membered aromatic ring of the carbon skeleton having at least one of the nitrogen atoms bound to a carbon atom of the same non-condensed six-membered aromatic ring the thio group being a mercapto group
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07F—ACYCLIC, CARBOCYCLIC OR HETEROCYCLIC COMPOUNDS CONTAINING ELEMENTS OTHER THAN CARBON, HYDROGEN, HALOGEN, OXYGEN, NITROGEN, SULFUR, SELENIUM OR TELLURIUM
- C07F9/00—Compounds containing elements of Groups 5 or 15 of the Periodic Table
- C07F9/02—Phosphorus compounds
- C07F9/06—Phosphorus compounds without P—C bonds
- C07F9/16—Esters of thiophosphoric acids or thiophosphorous acids
- C07F9/165—Esters of thiophosphoric acids
- C07F9/1651—Esters of thiophosphoric acids with hydroxyalkyl compounds with further substituents on alkyl

Landscapes

Chemical & Material Sciences (AREA)
Organic Chemistry (AREA)
Health & Medical Sciences (AREA)
Life Sciences & Earth Sciences (AREA)
General Health & Medical Sciences (AREA)
Molecular Biology (AREA)
Medicinal Chemistry (AREA)
Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
Pharmacology & Pharmacy (AREA)
General Chemical & Material Sciences (AREA)
Animal Behavior & Ethology (AREA)
Chemical Kinetics & Catalysis (AREA)
Public Health (AREA)
Veterinary Medicine (AREA)
Biochemistry (AREA)
Engineering & Computer Science (AREA)
Toxicology (AREA)
Bioinformatics & Cheminformatics (AREA)
Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
Polymers With Sulfur, Phosphorus Or Metals In The Main Chain (AREA)
Materials For Medical Uses (AREA)
Polyurethanes Or Polyureas (AREA)
Macromolecular Compounds Obtained By Forming Nitrogen-Containing Linkages In General (AREA)
Display Devices Of Pinball Game Machines (AREA)
Polyethers (AREA)
Coating Of Shaped Articles Made Of Macromolecular Substances (AREA)
Heterocyclic Compounds That Contain Two Or More Ring Oxygen Atoms (AREA)

IL10069892A 1991-01-23 1992-01-19 Polyamine Theolytes and anti-radiation drugs containing them IL100698A (en)

Applications Claiming Priority (1)

Application Number	Priority Date	Filing Date	Title
US07/644,810 US5217964A (en)	1991-01-23	1991-01-23	Polyamine thiols as radioprotective agents

Publications (2)

Publication Number	Publication Date
IL100698A0 IL100698A0 (en)	1992-09-06
IL100698A true IL100698A (en)	1998-08-16

Family

ID=24586432

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
IL10069892A IL100698A (en)	1991-01-23	1992-01-19	Polyamine Theolytes and anti-radiation drugs containing them

Country Status (16)

Country	Link
US (1)	US5217964A (de)
EP (1)	EP0497202B1 (de)
JP (1)	JP3203582B2 (de)
KR (1)	KR100195420B1 (de)
AT (1)	ATE127785T1 (de)
AU (1)	AU647570B2 (de)
CA (1)	CA2059817C (de)
DE (1)	DE69204698T2 (de)
ES (1)	ES2079695T3 (de)
FI (1)	FI111251B (de)
IE (1)	IE67961B1 (de)
IL (1)	IL100698A (de)
NO (1)	NO179003C (de)
NZ (1)	NZ241347A (de)
PT (1)	PT100045B (de)
ZA (1)	ZA92360B (de)

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US5677351A (en) *	1986-12-02	1997-10-14	University Of Florida Research Foundation, Inc.	Sterically hindered tetraamines and method for their production
US5393757A (en) *	1986-12-02	1995-02-28	University Of Florida	Polyamines and anti-diarrheal and gastrointestinal anti-spasmodic pharmaceutical compositions and methods of treatment
US5342945A (en) *	1986-12-02	1994-08-30	University Of Florida Research Foundation, Inc.	Anti-neoplastic, anti-viral or anti-retroviral spermine derivatives
US5354782A (en) *	1991-01-17	1994-10-11	Merrell Dow Pharmaceuticals Inc.	Polyamine phenols as radioprotective agents
US5488042A (en) *	1992-03-13	1996-01-30	Arch Development Corporation	Method for protection against genotoxic mutagenesis
JPH08509699A (ja) *	1993-02-23	1996-10-15	メレルダウファーマスーティカルズインコーポレイテッド	放射線防護剤としてのポリアミン誘導体類
CN1124483A (zh) *	1993-05-26	1996-06-12	默里尔多药物公司	作为放射保护剂的n-烷硫基多胺衍生物
US5994409A (en)	1997-12-09	1999-11-30	U.S. Bioscience, Inc.	Methods for treatment of neuro--and nephro--disorders and therapeutic toxicities using aminothiol compounds
US6482943B1 (en)	1999-04-30	2002-11-19	Slil Biomedical Corporation	Quinones as disease therapies
US6649587B1 (en)	1999-04-30	2003-11-18	Slil Biomedical Corporation	Polyamine analog conjugates and quinone conjugates as therapies for cancers and prostate diseases
WO2002038105A2 (en) *	2000-11-08	2002-05-16	Slil Biomedical Corporation	Novel polyamine analog-amino acid conjugates useful as anticancer agents
WO2000066175A2 (en) *	1999-04-30	2000-11-09	Slil Biomedical Corporation	Conjugates as therapies for cancer and prostate diseases
EP1698629A3 (de)	1999-04-30	2006-11-29	Cellgate, Inc.	Polyamine und ihre therapeutische Verwendung
US6489312B1 (en) *	1999-06-15	2002-12-03	Medimmune Oncology, Inc.	Pharmaceutical formulations comprising aminoalkyl phosphorothioates
WO2001085142A1 (en) *	2000-05-05	2001-11-15	Wisconsin Alumni Research Foundation	Compositions and methods for protecting cells during cancer chemotherapy and radiotherapy
US7053072B2 (en)	2001-05-11	2006-05-30	Medimmune Oncology, Inc.	Methods for the administration of amifostine and related compounds
US7045550B2 (en) *	2001-08-07	2006-05-16	Wisconsin Alumni Research Foundation	Polyamines and analogs for protecting cells during cancer chemotherapy and radiotherapy
AU2002364539A1 (en)	2001-12-07	2003-06-23	Cellgate, Inc.	Cycloalkyl substituted polyamines for cancer therapy and methods of synthesis therefor
EP1478618A1 (de) *	2002-02-07	2004-11-24	Wisconsin Alumni Research Foundation	Polyaminverbindungen und zusammensetzungen zur verwendung im zusammenhang mit einer krebstherapie
US7314959B2 (en) *	2003-08-07	2008-01-01	Wisconsin Alumni Research Foundation	Amino thiol compounds and compositions for use in conjunction with cancer therapy
US7754463B2 (en) *	2006-06-20	2010-07-13	Dana-Farber Cancer Institute	Inhibitors of USP1 Deubiquitinating Enzyme Complex
CA2797719C (en)	2010-04-30	2019-11-26	Dana-Farber Cancer Institute, Inc.	Small molecule inhibitors of usp1 deubiquitinating enzyme activity
US9725425B1 (en)	2014-02-25	2017-08-08	Dana-Farber Cancer Institute, Inc.	Compounds and methods for treating cancer
TWM528362U (zh) *	2016-04-15	2016-09-11	Calendar Entpr Co Ltd	無繩式電動節能捲簾結構改良

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Publication number	Priority date	Publication date	Assignee	Title
US2901503A (en) *	1956-08-28	1959-08-25	Campbell Pharmaceuticals Inc	Dialkylaminophenyl esters of thiophosphoric acids
US3368972A (en) *	1965-01-06	1968-02-13	Mobil Oil Corp	High molecular weight mannich bases as engine oil additives
AU602186B2 (en) *	1987-02-03	1990-10-04	Merrell Dow Pharmaceuticals Inc.	Novel polyamine derivatives
ZA887410B (en) *	1987-10-08	1989-06-28	Merrell Dow Pharma	Polyamine derivatives as antineoplastic agents

1991
- 1991-01-23 US US07/644,810 patent/US5217964A/en not_active Expired - Fee Related
1992
- 1992-01-17 ZA ZA92360A patent/ZA92360B/xx unknown
- 1992-01-17 AU AU10304/92A patent/AU647570B2/en not_active Ceased
- 1992-01-19 IL IL10069892A patent/IL100698A/en not_active IP Right Cessation
- 1992-01-21 NZ NZ241347A patent/NZ241347A/en unknown
- 1992-01-22 NO NO920283A patent/NO179003C/no unknown
- 1992-01-22 ES ES92101017T patent/ES2079695T3/es not_active Expired - Lifetime
- 1992-01-22 PT PT100045A patent/PT100045B/pt not_active IP Right Cessation
- 1992-01-22 IE IE920189A patent/IE67961B1/en not_active IP Right Cessation
- 1992-01-22 AT AT92101017T patent/ATE127785T1/de not_active IP Right Cessation
- 1992-01-22 KR KR1019920000836A patent/KR100195420B1/ko not_active IP Right Cessation
- 1992-01-22 EP EP92101017A patent/EP0497202B1/de not_active Expired - Lifetime
- 1992-01-22 FI FI920271A patent/FI111251B/fi active
- 1992-01-22 CA CA002059817A patent/CA2059817C/en not_active Expired - Fee Related
- 1992-01-22 DE DE69204698T patent/DE69204698T2/de not_active Expired - Fee Related
- 1992-01-23 JP JP03128092A patent/JP3203582B2/ja not_active Expired - Fee Related

Also Published As

Publication number	Publication date
JP3203582B2 (ja)	2001-08-27
CA2059817A1 (en)	1992-07-24
NO179003C (no)	1996-07-17
IL100698A0 (en)	1992-09-06
FI111251B (fi)	2003-06-30
FI920271A0 (fi)	1992-01-22
AU1030492A (en)	1992-07-30
IE67961B1 (en)	1996-05-15
EP0497202B1 (de)	1995-09-13
KR100195420B1 (ko)	1999-06-15
FI920271A (fi)	1992-07-24
ES2079695T3 (es)	1996-01-16
NO179003B (no)	1996-04-09
DE69204698D1 (de)	1995-10-19
NO920283D0 (no)	1992-01-22
NO920283L (no)	1992-07-24
DE69204698T2 (de)	1996-02-15
EP0497202A1 (de)	1992-08-05
PT100045B (pt)	1999-10-29
PT100045A (pt)	1993-03-31
AU647570B2 (en)	1994-03-24
JPH04334362A (ja)	1992-11-20
ATE127785T1 (de)	1995-09-15
KR920014772A (ko)	1992-08-25
IE920189A1 (en)	1992-07-29
ZA92360B (en)	1992-11-25
NZ241347A (en)	1994-04-27
CA2059817C (en)	2003-07-15
US5217964A (en)	1993-06-08

Publication	Publication Date	Title
EP0497202B1 (de)	1995-09-13	Polyaminthiole als Strahlenschutzmittel
US5434145A (en)	1995-07-18	N-alkythio polyamine derivatives as radioprotective agents
US5109024A (en)	1992-04-28	Polyamine derivatives as antineoplastic agents
KR100311851B1 (ko)	2002-04-24	방사선보호제로서의폴리아민유도체
US5354782A (en)	1994-10-11	Polyamine phenols as radioprotective agents
US5654484A (en)	1997-08-05	Polyamine derivatives as antineoplastic agents
EP0495450B1 (de)	1995-07-26	Polyamin-Phenole als Röntgenschutzwirkstoffe
EP0378146A2 (de)	1990-07-18	Polyamin-Derivate als antineoplastische Mittel
JPH09500105A (ja)	1997-01-07	放射線防護剤としてのｎ−アルキルチオポリアミン誘導体類

Legal Events

Date	Code	Title
1998-12-27	FF	Patent granted
1999-08-17	KB	Patent renewed
2002-09-12	MM9K	Patent not in force due to non-payment of renewal fees