SK172098A3 - New amidino derivatives and their use as thrombin inhibitors - Google Patents
New amidino derivatives and their use as thrombin inhibitors Download PDFInfo
- Publication number
- SK172098A3 SK172098A3 SK1720-98A SK172098A SK172098A3 SK 172098 A3 SK172098 A3 SK 172098A3 SK 172098 A SK172098 A SK 172098A SK 172098 A3 SK172098 A3 SK 172098A3
- Authority
- SK
- Slovakia
- Prior art keywords
- formula
- ethoxy
- aminoiminomethylphenyl
- phenyl
- compound
- Prior art date
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- 229940122388 Thrombin inhibitor Drugs 0.000 title description 9
- 239000003868 thrombin inhibitor Substances 0.000 title description 9
- 125000003739 carbamimidoyl group Chemical group C(N)(=N)* 0.000 title description 2
- 150000001875 compounds Chemical class 0.000 claims abstract description 309
- 108090000190 Thrombin Proteins 0.000 claims abstract description 34
- 229960004072 thrombin Drugs 0.000 claims abstract description 29
- 230000005764 inhibitory process Effects 0.000 claims abstract description 15
- 238000011282 treatment Methods 0.000 claims abstract description 12
- 208000007536 Thrombosis Diseases 0.000 claims abstract description 10
- 239000003146 anticoagulant agent Substances 0.000 claims abstract description 9
- 229940127219 anticoagulant drug Drugs 0.000 claims abstract description 8
- XEKOWRVHYACXOJ-UHFFFAOYSA-N Ethyl acetate Natural products CCOC(C)=O XEKOWRVHYACXOJ-UHFFFAOYSA-N 0.000 claims description 110
- -1 C 13 alkylnaphthyl Chemical group 0.000 claims description 103
- 238000000034 method Methods 0.000 claims description 84
- 125000001301 ethoxy group Chemical group [H]C([H])([H])C([H])([H])O* 0.000 claims description 59
- 125000000217 alkyl group Chemical group 0.000 claims description 51
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims description 47
- 239000000460 chlorine Substances 0.000 claims description 36
- 125000004182 2-chlorophenyl group Chemical group [H]C1=C([H])C(Cl)=C(*)C([H])=C1[H] 0.000 claims description 31
- 239000012634 fragment Substances 0.000 claims description 30
- XEEYBQQBJWHFJM-UHFFFAOYSA-N Iron Chemical compound [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 claims description 20
- 125000005037 alkyl phenyl group Chemical group 0.000 claims description 19
- 229910052760 oxygen Inorganic materials 0.000 claims description 18
- 229910052736 halogen Inorganic materials 0.000 claims description 17
- 150000002367 halogens Chemical class 0.000 claims description 17
- 229910052717 sulfur Inorganic materials 0.000 claims description 17
- 229910052757 nitrogen Inorganic materials 0.000 claims description 15
- 125000001424 substituent group Chemical group 0.000 claims description 15
- 238000006243 chemical reaction Methods 0.000 claims description 13
- 230000035602 clotting Effects 0.000 claims description 13
- 206010053567 Coagulopathies Diseases 0.000 claims description 12
- 150000003839 salts Chemical class 0.000 claims description 12
- 229910052739 hydrogen Inorganic materials 0.000 claims description 11
- 125000003545 alkoxy group Chemical group 0.000 claims description 10
- 125000002887 hydroxy group Chemical group [H]O* 0.000 claims description 10
- 229940092714 benzenesulfonic acid Drugs 0.000 claims description 9
- 210000004369 blood Anatomy 0.000 claims description 9
- 239000008280 blood Substances 0.000 claims description 9
- 229910052799 carbon Inorganic materials 0.000 claims description 9
- 125000004093 cyano group Chemical group *C#N 0.000 claims description 9
- QGZKDVFQNNGYKY-UHFFFAOYSA-N Ammonia Chemical compound N QGZKDVFQNNGYKY-UHFFFAOYSA-N 0.000 claims description 8
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 claims description 8
- 125000000449 nitro group Chemical group [O-][N+](*)=O 0.000 claims description 8
- 229910052801 chlorine Inorganic materials 0.000 claims description 7
- ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 claims description 6
- 125000002490 anilino group Chemical group [H]N(*)C1=C([H])C([H])=C([H])C([H])=C1[H] 0.000 claims description 6
- 239000008194 pharmaceutical composition Substances 0.000 claims description 6
- 125000000753 cycloalkyl group Chemical group 0.000 claims description 5
- 230000008569 process Effects 0.000 claims description 5
- XPSHLXRBQBOXPR-UHFFFAOYSA-N CCOC(=O)CN(C1=CC(=CC(=C1)C)OCCC2=CC=C(C=C2)C=NN)S(=O)(=O)C3=CC=CC=C3Cl Chemical compound CCOC(=O)CN(C1=CC(=CC(=C1)C)OCCC2=CC=C(C=C2)C=NN)S(=O)(=O)C3=CC=CC=C3Cl XPSHLXRBQBOXPR-UHFFFAOYSA-N 0.000 claims description 4
- 125000003118 aryl group Chemical group 0.000 claims description 4
- 238000002360 preparation method Methods 0.000 claims description 4
- VIYPBXWLXCOTCK-UHFFFAOYSA-N 2,4,5-trichloro-n-[2-[2-(4-methanehydrazonoylphenyl)ethylsulfanyl]phenyl]benzenesulfonamide Chemical compound C1=CC(C=NN)=CC=C1CCSC1=CC=CC=C1NS(=O)(=O)C1=CC(Cl)=C(Cl)C=C1Cl VIYPBXWLXCOTCK-UHFFFAOYSA-N 0.000 claims description 3
- JJAFAAWADDIEHZ-UHFFFAOYSA-N 2-chloro-n-[3-[2-(4-methanehydrazonoylphenyl)ethoxy]phenyl]benzenesulfonamide Chemical compound C1=CC(C=NN)=CC=C1CCOC1=CC=CC(NS(=O)(=O)C=2C(=CC=CC=2)Cl)=C1 JJAFAAWADDIEHZ-UHFFFAOYSA-N 0.000 claims description 3
- ZDTGQOSIABKQFX-UHFFFAOYSA-N 2-cyano-n-[3-[2-(4-methanehydrazonoylphenyl)ethoxy]phenyl]benzenesulfonamide Chemical compound C1=CC(C=NN)=CC=C1CCOC1=CC=CC(NS(=O)(=O)C=2C(=CC=CC=2)C#N)=C1 ZDTGQOSIABKQFX-UHFFFAOYSA-N 0.000 claims description 3
- 239000004480 active ingredient Substances 0.000 claims description 3
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims description 3
- JUQZCOUERXMZDM-UHFFFAOYSA-N n-[2-[2-(4-methanehydrazonoylphenyl)ethylsulfanyl]phenyl]benzenesulfonamide Chemical compound C1=CC(C=NN)=CC=C1CCSC1=CC=CC=C1NS(=O)(=O)C1=CC=CC=C1 JUQZCOUERXMZDM-UHFFFAOYSA-N 0.000 claims description 3
- TZYFIHILTWFVFO-UHFFFAOYSA-N n-[3-[2-(4-methanehydrazonoylphenyl)ethoxy]-2-methylphenyl]benzenesulfonamide Chemical compound C1=CC=C(OCCC=2C=CC(C=NN)=CC=2)C(C)=C1NS(=O)(=O)C1=CC=CC=C1 TZYFIHILTWFVFO-UHFFFAOYSA-N 0.000 claims description 3
- VLNVAOIFEQCTIB-UHFFFAOYSA-N n-[3-[2-(4-methanehydrazonoylphenyl)ethoxy]-5-methylphenyl]benzenesulfonamide Chemical compound C=1C(OCCC=2C=CC(C=NN)=CC=2)=CC(C)=CC=1NS(=O)(=O)C1=CC=CC=C1 VLNVAOIFEQCTIB-UHFFFAOYSA-N 0.000 claims description 3
- QMLSYOLBVAUPHO-UHFFFAOYSA-N n-[3-[2-(4-methanehydrazonoylphenyl)ethoxy]phenyl]benzenesulfonamide Chemical compound C1=CC(C=NN)=CC=C1CCOC1=CC=CC(NS(=O)(=O)C=2C=CC=CC=2)=C1 QMLSYOLBVAUPHO-UHFFFAOYSA-N 0.000 claims description 3
- HJNWVQKSKQPACN-UHFFFAOYSA-N n-[5-[2-(4-methanehydrazonoylphenyl)ethoxy]-2-methylphenyl]benzenesulfonamide Chemical compound C1=C(NS(=O)(=O)C=2C=CC=CC=2)C(C)=CC=C1OCCC1=CC=C(C=NN)C=C1 HJNWVQKSKQPACN-UHFFFAOYSA-N 0.000 claims description 3
- 125000004433 nitrogen atom Chemical group N* 0.000 claims description 3
- 230000009467 reduction Effects 0.000 claims description 3
- 125000004955 1,4-cyclohexylene group Chemical group [H]C1([H])C([H])([H])C([H])([*:1])C([H])([H])C([H])([H])C1([H])[*:2] 0.000 claims description 2
- 125000001140 1,4-phenylene group Chemical group [H]C1=C([H])C([*:2])=C([H])C([H])=C1[*:1] 0.000 claims description 2
- DCBXKBOKMOUHLK-UHFFFAOYSA-N 2,5-dichloro-n-[2-[2-(4-methanehydrazonoylphenyl)ethylsulfanyl]phenyl]benzenesulfonamide Chemical compound C1=CC(C=NN)=CC=C1CCSC1=CC=CC=C1NS(=O)(=O)C1=CC(Cl)=CC=C1Cl DCBXKBOKMOUHLK-UHFFFAOYSA-N 0.000 claims description 2
- IMUNGGYEMMRXSY-UHFFFAOYSA-N 2,5-dichloro-n-[3-[2-(4-methanehydrazonoylphenyl)ethoxy]phenyl]thiophene-3-sulfonamide Chemical compound C1=CC(C=NN)=CC=C1CCOC1=CC=CC(NS(=O)(=O)C2=C(SC(Cl)=C2)Cl)=C1 IMUNGGYEMMRXSY-UHFFFAOYSA-N 0.000 claims description 2
- SVWIDTIEKDMZOM-UHFFFAOYSA-N 2-(benzenesulfonamido)propan-2-yl-oxido-oxophosphanium Chemical compound CC(C)(NS(=O)(=O)c1ccccc1)P(=O)=O SVWIDTIEKDMZOM-UHFFFAOYSA-N 0.000 claims description 2
- SXYIRMGNMOHKTP-UHFFFAOYSA-N 2-[n-(2-chlorophenyl)sulfonyl-3-[2-(4-methanehydrazonoylphenyl)ethoxy]-5-methylanilino]acetic acid Chemical compound C=1C(N(CC(O)=O)S(=O)(=O)C=2C(=CC=CC=2)Cl)=CC(C)=CC=1OCCC1=CC=C(C=NN)C=C1 SXYIRMGNMOHKTP-UHFFFAOYSA-N 0.000 claims description 2
- ZOANUIGMJGECCT-UHFFFAOYSA-N 2-[n-(2-chlorophenyl)sulfonyl-3-[2-(4-methanehydrazonoylphenyl)ethoxy]-5-methylanilino]propanoic acid Chemical compound C=1C=CC=C(Cl)C=1S(=O)(=O)N(C(C)C(O)=O)C(C=1)=CC(C)=CC=1OCCC1=CC=C(C=NN)C=C1 ZOANUIGMJGECCT-UHFFFAOYSA-N 0.000 claims description 2
- JKWKDCLQRIYOKA-UHFFFAOYSA-N 2-[n-(benzenesulfonyl)-3-[2-(4-methanehydrazonoylphenyl)ethoxy]anilino]acetic acid Chemical compound C1=CC(C=NN)=CC=C1CCOC1=CC=CC(N(CC(O)=O)S(=O)(=O)C=2C=CC=CC=2)=C1 JKWKDCLQRIYOKA-UHFFFAOYSA-N 0.000 claims description 2
- KAEXKJWWYZBVQX-UHFFFAOYSA-N 2-chloro-4-fluoro-n-[2-[2-(4-methanehydrazonoylphenyl)ethylsulfanyl]phenyl]benzenesulfonamide Chemical compound C1=CC(C=NN)=CC=C1CCSC1=CC=CC=C1NS(=O)(=O)C1=CC=C(F)C=C1Cl KAEXKJWWYZBVQX-UHFFFAOYSA-N 0.000 claims description 2
- VKHVVVQVGFDCJW-UHFFFAOYSA-N 3,4-dibromo-n-[2-[2-(4-methanehydrazonoylphenyl)ethylsulfanyl]phenyl]benzenesulfonamide Chemical compound C1=CC(C=NN)=CC=C1CCSC1=CC=CC=C1NS(=O)(=O)C1=CC=C(Br)C(Br)=C1 VKHVVVQVGFDCJW-UHFFFAOYSA-N 0.000 claims description 2
- SODNDLJETLIHHH-UHFFFAOYSA-N 3-bromo-n-[2-[2-(4-methanehydrazonoylphenyl)ethylsulfanyl]phenyl]benzenesulfonamide Chemical compound C1=CC(C=NN)=CC=C1CCSC1=CC=CC=C1NS(=O)(=O)C1=CC=CC(Br)=C1 SODNDLJETLIHHH-UHFFFAOYSA-N 0.000 claims description 2
- ZZJKRCJENKBNOA-UHFFFAOYSA-N 4-fluoro-n-[3-[2-(4-methanehydrazonoylphenyl)ethoxy]phenyl]benzenesulfonamide Chemical compound C1=CC(C=NN)=CC=C1CCOC1=CC=CC(NS(=O)(=O)C=2C=CC(F)=CC=2)=C1 ZZJKRCJENKBNOA-UHFFFAOYSA-N 0.000 claims description 2
- FAJATWKXQOVACU-UHFFFAOYSA-N 5-chloro-n-[3-[2-(4-methanehydrazonoylphenyl)ethoxy]phenyl]thiophene-2-sulfonamide Chemical compound C1=CC(C=NN)=CC=C1CCOC1=CC=CC(NS(=O)(=O)C=2SC(Cl)=CC=2)=C1 FAJATWKXQOVACU-UHFFFAOYSA-N 0.000 claims description 2
- HOMNCAFHHMHLLA-UHFFFAOYSA-N CC1=CC(=CC(=C1)OCCC2=CC=C(C=C2)C=NN)N(C(C)C(=O)OC)S(=O)(=O)C3=CC=CC=C3Cl Chemical compound CC1=CC(=CC(=C1)OCCC2=CC=C(C=C2)C=NN)N(C(C)C(=O)OC)S(=O)(=O)C3=CC=CC=C3Cl HOMNCAFHHMHLLA-UHFFFAOYSA-N 0.000 claims description 2
- NMVZRPKPAXCEOG-UHFFFAOYSA-N CC1=CC(=CC(=C1)OS(=O)(=O)C2=CC=CC=C2Cl)OCCC3=CC=C(C=C3)C=NN Chemical compound CC1=CC(=CC(=C1)OS(=O)(=O)C2=CC=CC=C2Cl)OCCC3=CC=C(C=C3)C=NN NMVZRPKPAXCEOG-UHFFFAOYSA-N 0.000 claims description 2
- NUVLKGIFLPMJMP-UHFFFAOYSA-N CCC1=CC(=CC(=C1)OS(=O)(=O)C2=CC=CC=C2Cl)OCCC3=CC=C(C=C3)C=NN Chemical compound CCC1=CC(=CC(=C1)OS(=O)(=O)C2=CC=CC=C2Cl)OCCC3=CC=C(C=C3)C=NN NUVLKGIFLPMJMP-UHFFFAOYSA-N 0.000 claims description 2
- 239000003085 diluting agent Substances 0.000 claims description 2
- 239000003814 drug Substances 0.000 claims description 2
- MBXQDYSRZRFGCY-UHFFFAOYSA-N ethyl 4-[n-(2-chlorophenyl)sulfonyl-3-[2-(4-methanehydrazonoylphenyl)ethoxy]-5-methylanilino]pentanoate Chemical compound C=1C=CC=C(Cl)C=1S(=O)(=O)N(C(C)CCC(=O)OCC)C(C=1)=CC(C)=CC=1OCCC1=CC=C(C=NN)C=C1 MBXQDYSRZRFGCY-UHFFFAOYSA-N 0.000 claims description 2
- 125000005842 heteroatom Chemical group 0.000 claims description 2
- 230000003301 hydrolyzing effect Effects 0.000 claims description 2
- 125000002883 imidazolyl group Chemical group 0.000 claims description 2
- 125000000842 isoxazolyl group Chemical group 0.000 claims description 2
- 125000000956 methoxy group Chemical group [H]C([H])([H])O* 0.000 claims description 2
- FTSASJXRLLORTF-UHFFFAOYSA-N n-[2-[2-(4-methanehydrazonoylphenyl)ethylsulfanyl]phenyl]-2-methoxy-5-methylbenzenesulfonamide Chemical compound COC1=CC=C(C)C=C1S(=O)(=O)NC1=CC=CC=C1SCCC1=CC=C(C=NN)C=C1 FTSASJXRLLORTF-UHFFFAOYSA-N 0.000 claims description 2
- XRISKDXCJKJFJY-UHFFFAOYSA-N n-[2-[2-(4-methanehydrazonoylphenyl)ethylsulfanyl]phenyl]-3,4-dimethoxybenzenesulfonamide Chemical compound C1=C(OC)C(OC)=CC=C1S(=O)(=O)NC1=CC=CC=C1SCCC1=CC=C(C=NN)C=C1 XRISKDXCJKJFJY-UHFFFAOYSA-N 0.000 claims description 2
- LSTIKTUDDORGRM-UHFFFAOYSA-N n-[3-[2-(4-methanehydrazonoylphenyl)ethoxy]phenyl]-2,5-dimethylbenzenesulfonamide Chemical compound CC1=CC=C(C)C(S(=O)(=O)NC=2C=C(OCCC=3C=CC(C=NN)=CC=3)C=CC=2)=C1 LSTIKTUDDORGRM-UHFFFAOYSA-N 0.000 claims description 2
- AKQQLSUXNFQFOS-UHFFFAOYSA-N n-[3-[2-(4-methanehydrazonoylphenyl)ethoxy]phenyl]-3,5-dimethyl-1,2-oxazole-4-sulfonamide Chemical compound CC1=NOC(C)=C1S(=O)(=O)NC1=CC=CC(OCCC=2C=CC(C=NN)=CC=2)=C1 AKQQLSUXNFQFOS-UHFFFAOYSA-N 0.000 claims description 2
- BNYREDCQRBWCNQ-UHFFFAOYSA-N n-[3-[2-(4-methanehydrazonoylphenyl)ethoxy]phenyl]-3-methyl-2h-imidazole-1-sulfonamide Chemical compound C1=CN(C)CN1S(=O)(=O)NC1=CC=CC(OCCC=2C=CC(C=NN)=CC=2)=C1 BNYREDCQRBWCNQ-UHFFFAOYSA-N 0.000 claims description 2
- DJPQYCDMGLZKKF-UHFFFAOYSA-N n-[3-[2-(4-methanehydrazonoylphenyl)ethylsulfanyl]phenyl]benzenesulfonamide Chemical compound C1=CC(C=NN)=CC=C1CCSC1=CC=CC(NS(=O)(=O)C=2C=CC=CC=2)=C1 DJPQYCDMGLZKKF-UHFFFAOYSA-N 0.000 claims description 2
- 125000001624 naphthyl group Chemical group 0.000 claims description 2
- 125000006574 non-aromatic ring group Chemical group 0.000 claims description 2
- 230000001590 oxidative effect Effects 0.000 claims description 2
- IPWFJLQDVFKJDU-UHFFFAOYSA-N pentanamide Chemical compound CCCCC(N)=O IPWFJLQDVFKJDU-UHFFFAOYSA-N 0.000 claims description 2
- 239000000546 pharmaceutical excipient Substances 0.000 claims description 2
- 125000001544 thienyl group Chemical group 0.000 claims description 2
- 125000004705 ethylthio group Chemical group C(C)S* 0.000 claims 4
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims 2
- 239000001257 hydrogen Substances 0.000 claims 2
- 238000004519 manufacturing process Methods 0.000 claims 2
- ZNQQZJCWFWWUQY-UHFFFAOYSA-N 2-fluoro-n-[3-[2-(4-methanehydrazonoylphenyl)ethoxy]phenyl]benzenesulfonamide Chemical compound C1=CC(C=NN)=CC=C1CCOC1=CC=CC(NS(=O)(=O)C=2C(=CC=CC=2)F)=C1 ZNQQZJCWFWWUQY-UHFFFAOYSA-N 0.000 claims 1
- FFKVFRHTHWVIQK-UHFFFAOYSA-N 3-[n-(2-chlorophenyl)sulfonyl-3-[2-(4-methanehydrazonoylphenyl)ethoxy]-5-methylanilino]butanamide Chemical compound C=1C=CC=C(Cl)C=1S(=O)(=O)N(C(CC(N)=O)C)C(C=1)=CC(C)=CC=1OCCC1=CC=C(C=NN)C=C1 FFKVFRHTHWVIQK-UHFFFAOYSA-N 0.000 claims 1
- KZXXBGHWTCMNRO-UHFFFAOYSA-N 3-[n-(2-chlorophenyl)sulfonyl-3-[2-(4-methanehydrazonoylphenyl)ethoxy]-5-methylanilino]butanoic acid Chemical compound C=1C=CC=C(Cl)C=1S(=O)(=O)N(C(CC(O)=O)C)C(C=1)=CC(C)=CC=1OCCC1=CC=C(C=NN)C=C1 KZXXBGHWTCMNRO-UHFFFAOYSA-N 0.000 claims 1
- PXFLZLNBSUZGEO-UHFFFAOYSA-N 5-[n-(2-chlorophenyl)sulfonyl-3-[2-(4-methanehydrazonoylphenyl)ethoxy]-5-methylanilino]hexanoic acid Chemical compound C=1C=CC=C(Cl)C=1S(=O)(=O)N(C(CCCC(O)=O)C)C(C=1)=CC(C)=CC=1OCCC1=CC=C(C=NN)C=C1 PXFLZLNBSUZGEO-UHFFFAOYSA-N 0.000 claims 1
- IBJLVYOMOBJPAF-UHFFFAOYSA-N 5-[n-(2-chlorophenyl)sulfonyl-3-[2-(4-methanehydrazonoylphenyl)ethoxy]-5-methylanilino]pentanamide Chemical compound C=1C(N(CCCCC(N)=O)S(=O)(=O)C=2C(=CC=CC=2)Cl)=CC(C)=CC=1OCCC1=CC=C(C=NN)C=C1 IBJLVYOMOBJPAF-UHFFFAOYSA-N 0.000 claims 1
- AWJHTUNJHDQDBW-UHFFFAOYSA-N C(C)OC(CCCC(C)N(S(=O)(=O)C1=C(C=CC=C1)Cl)C1=CC(=CC(=C1)C)OCCC1=CC=C(C=C1)C=NN)=O Chemical compound C(C)OC(CCCC(C)N(S(=O)(=O)C1=C(C=CC=C1)Cl)C1=CC(=CC(=C1)C)OCCC1=CC=C(C=C1)C=NN)=O AWJHTUNJHDQDBW-UHFFFAOYSA-N 0.000 claims 1
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- 238000004895 liquid chromatography mass spectrometry Methods 0.000 description 69
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- 238000001704 evaporation Methods 0.000 description 29
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- 238000003818 flash chromatography Methods 0.000 description 29
- 229920006395 saturated elastomer Polymers 0.000 description 28
- ZMANZCXQSJIPKH-UHFFFAOYSA-N Triethylamine Chemical compound CCN(CC)CC ZMANZCXQSJIPKH-UHFFFAOYSA-N 0.000 description 24
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- 125000004801 4-cyanophenyl group Chemical group [H]C1=C([H])C(C#N)=C([H])C([H])=C1* 0.000 description 13
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Classifications
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D333/00—Heterocyclic compounds containing five-membered rings having one sulfur atom as the only ring hetero atom
- C07D333/02—Heterocyclic compounds containing five-membered rings having one sulfur atom as the only ring hetero atom not condensed with other rings
- C07D333/04—Heterocyclic compounds containing five-membered rings having one sulfur atom as the only ring hetero atom not condensed with other rings not substituted on the ring sulphur atom
- C07D333/26—Heterocyclic compounds containing five-membered rings having one sulfur atom as the only ring hetero atom not condensed with other rings not substituted on the ring sulphur atom with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
- C07D333/30—Hetero atoms other than halogen
- C07D333/34—Sulfur atoms
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/16—Amides, e.g. hydroxamic acids
- A61K31/18—Sulfonamides
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P7/00—Drugs for disorders of the blood or the extracellular fluid
- A61P7/02—Antithrombotic agents; Anticoagulants; Platelet aggregation inhibitors
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C309/00—Sulfonic acids; Halides, esters, or anhydrides thereof
- C07C309/63—Esters of sulfonic acids
- C07C309/71—Esters of sulfonic acids having sulfur atoms of esterified sulfo groups bound to carbon atoms of rings other than six-membered aromatic rings
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C309/00—Sulfonic acids; Halides, esters, or anhydrides thereof
- C07C309/63—Esters of sulfonic acids
- C07C309/72—Esters of sulfonic acids having sulfur atoms of esterified sulfo groups bound to carbon atoms of six-membered aromatic rings of a carbon skeleton
- C07C309/73—Esters of sulfonic acids having sulfur atoms of esterified sulfo groups bound to carbon atoms of six-membered aromatic rings of a carbon skeleton to carbon atoms of non-condensed six-membered aromatic rings
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C311/00—Amides of sulfonic acids, i.e. compounds having singly-bound oxygen atoms of sulfo groups replaced by nitrogen atoms, not being part of nitro or nitroso groups
- C07C311/15—Sulfonamides having sulfur atoms of sulfonamide groups bound to carbon atoms of six-membered aromatic rings
- C07C311/21—Sulfonamides having sulfur atoms of sulfonamide groups bound to carbon atoms of six-membered aromatic rings having the nitrogen atom of at least one of the sulfonamide groups bound to a carbon atom of a six-membered aromatic ring
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C311/00—Amides of sulfonic acids, i.e. compounds having singly-bound oxygen atoms of sulfo groups replaced by nitrogen atoms, not being part of nitro or nitroso groups
- C07C311/22—Sulfonamides, the carbon skeleton of the acid part being further substituted by singly-bound oxygen atoms
- C07C311/29—Sulfonamides, the carbon skeleton of the acid part being further substituted by singly-bound oxygen atoms having the sulfur atom of at least one of the sulfonamide groups bound to a carbon atom of a six-membered aromatic ring
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- 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
- C07C323/50—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 carboxyl groups bound to the same carbon skeleton
- C07C323/51—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 carboxyl groups bound to the same carbon skeleton having the sulfur atoms of the thio groups bound to acyclic carbon atoms of the carbon skeleton
- C07C323/60—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 carboxyl groups bound to the same carbon skeleton having the sulfur atoms of the thio groups bound to acyclic carbon atoms of the carbon skeleton with the carbon atom of at least one of the carboxyl groups bound to nitrogen atoms
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D233/00—Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings
- C07D233/54—Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings having two double bonds between ring members or between ring members and non-ring members
- C07D233/66—Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings having two double bonds between ring members or between ring members and non-ring members with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
- C07D233/84—Sulfur atoms
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D261/00—Heterocyclic compounds containing 1,2-oxazole or hydrogenated 1,2-oxazole rings
- C07D261/02—Heterocyclic compounds containing 1,2-oxazole or hydrogenated 1,2-oxazole rings not condensed with other rings
- C07D261/06—Heterocyclic compounds containing 1,2-oxazole or hydrogenated 1,2-oxazole rings not condensed with other rings having two or more double bonds between ring members or between ring members and non-ring members
- C07D261/10—Heterocyclic compounds containing 1,2-oxazole or hydrogenated 1,2-oxazole rings not condensed with other rings having two or more double bonds between ring members or between ring members and non-ring members with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
- C07D261/14—Nitrogen atoms
- C07D261/16—Benzene-sulfonamido isoxazoles
-
- 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
- C07F9/28—Phosphorus compounds with one or more P—C bonds
- C07F9/50—Organo-phosphines
- C07F9/53—Organo-phosphine oxides; Organo-phosphine thioxides
- C07F9/5304—Acyclic saturated phosphine oxides or thioxides
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- Chemical & Material Sciences (AREA)
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- Veterinary Medicine (AREA)
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- Medicinal Chemistry (AREA)
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- Diabetes (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Hematology (AREA)
- Epidemiology (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Peptides Or Proteins (AREA)
- Plural Heterocyclic Compounds (AREA)
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Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
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SE9602646A SE9602646D0 (sv) | 1996-07-04 | 1996-07-04 | Pharmaceutically-useful compounds |
PCT/SE1997/001150 WO1998001422A1 (en) | 1996-07-04 | 1997-06-26 | New amidino derivatives and their use as thrombin inhibitors |
Publications (1)
Publication Number | Publication Date |
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SK172098A3 true SK172098A3 (en) | 1999-06-11 |
Family
ID=20403276
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
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SK1720-98A SK172098A3 (en) | 1996-07-04 | 1997-06-26 | New amidino derivatives and their use as thrombin inhibitors |
Country Status (24)
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US (2) | US6221898B1 (et) |
EP (1) | EP0917528B1 (et) |
JP (1) | JP2000515505A (et) |
KR (1) | KR20000022437A (et) |
CN (1) | CN1228765A (et) |
AR (1) | AR007614A1 (et) |
AT (1) | ATE224365T1 (et) |
BR (1) | BR9710142A (et) |
CA (1) | CA2260190A1 (et) |
CZ (1) | CZ1299A3 (et) |
DE (1) | DE69715635T2 (et) |
EE (1) | EE9900006A (et) |
HU (1) | HUP9902410A3 (et) |
ID (1) | ID19479A (et) |
IL (1) | IL127885A0 (et) |
IS (1) | IS4930A (et) |
NO (1) | NO986180L (et) |
NZ (1) | NZ333394A (et) |
PL (1) | PL331047A1 (et) |
SE (1) | SE9602646D0 (et) |
SK (1) | SK172098A3 (et) |
TR (1) | TR199802767T2 (et) |
WO (1) | WO1998001422A1 (et) |
ZA (1) | ZA975591B (et) |
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SE9602646D0 (sv) | 1996-07-04 | 1996-07-04 | Astra Ab | Pharmaceutically-useful compounds |
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AR013084A1 (es) | 1997-06-19 | 2000-12-13 | Astrazeneca Ab | Derivados de amidino utiles como inhibidores de la trombina, composicion farmaceutica, utilizacion de dichos compuestos para la preparacion demedicamentos y proceso para la preparacion de los compuestos mencionados |
SE9704543D0 (sv) | 1997-12-05 | 1997-12-05 | Astra Ab | New compounds |
AR023510A1 (es) | 1999-04-21 | 2002-09-04 | Astrazeneca Ab | Un equipo de partes, formulacion farmaceutica y uso de un inhibidor de trombina. |
EP2314564A3 (en) * | 1999-12-23 | 2012-04-04 | Ampac Fine Chemicals LLC | Improved preparation of 2S,3S-N-isobutyl-N-(2-hydroxy-3-amino-4-phenylbutyl)-p-nitrobenzenesulfonylamide hydrochloride and other derivatives of 2-hydroxy-1,3-diamines |
US6548706B2 (en) | 1999-12-23 | 2003-04-15 | Aerojet Fine Chemicals Llc | Preparation of 2S,3S-N-isobutyl-N-(2-hydroxy-3-amino-4-phenylbutyl) -p-nitrobenzenesulfonylamide hydrochloride and other derivatives of 2-hydroxy-1,3-diamines |
AU9233101A (en) * | 2000-10-04 | 2002-04-15 | Kissei Pharmaceutical | 5-amidino-2-hydroxybenzenesulfonamide derivatives, pharmaceutical compositions containing the same and intermediates for their preparation |
AR035216A1 (es) * | 2000-12-01 | 2004-05-05 | Astrazeneca Ab | Derivados de acido mandelico ,derivados farmaceuticamente aceptables, uso de estos derivados para la fabricacion de medicamentos, metodos de tratamiento ,procesos para la preparacion de estos derivados, y compuestos intermediarios |
US7129233B2 (en) | 2000-12-01 | 2006-10-31 | Astrazeneca Ab | Mandelic acid derivatives and their use as thrombin inhibitors |
US7067539B2 (en) | 2001-02-08 | 2006-06-27 | Schering Corporation | Cannabinoid receptor ligands |
US7507767B2 (en) | 2001-02-08 | 2009-03-24 | Schering Corporation | Cannabinoid receptor ligands |
AR034517A1 (es) * | 2001-06-21 | 2004-02-25 | Astrazeneca Ab | Formulacion farmaceutica |
EP1312602A1 (en) * | 2001-11-15 | 2003-05-21 | Eisai Co., Ltd. | Amidino derivatives, and anticoagulants and thrombosis therapeutic agents containing them |
JP4209659B2 (ja) | 2001-11-15 | 2009-01-14 | エーザイ・アール・アンド・ディー・マネジメント株式会社 | アミジノ誘導体並びにそれを用いた抗血液凝固剤および血栓症治療剤 |
SI1465861T1 (sl) * | 2001-12-20 | 2009-12-31 | Bristol Myers Squibb Co | Alfa-(n-sulfonamido)acetamidni derivati kot beta-amiloid inhibitorji |
SE0201659D0 (sv) * | 2002-05-31 | 2002-05-31 | Astrazeneca Ab | Modified release pharmaceutical formulation |
SE0201661D0 (sv) | 2002-05-31 | 2002-05-31 | Astrazeneca Ab | New salts |
US20050026168A1 (en) * | 2002-12-13 | 2005-02-03 | Genesis Group Inc. | Method for the detection of risk factors associated with myocardial infarction |
US7781424B2 (en) * | 2003-05-27 | 2010-08-24 | Astrazeneca Ab | Modified release pharmaceutical formulation |
US7524354B2 (en) * | 2005-07-07 | 2009-04-28 | Research Foundation Of State University Of New York | Controlled synthesis of highly monodispersed gold nanoparticles |
TW200827336A (en) * | 2006-12-06 | 2008-07-01 | Astrazeneca Ab | New crystalline forms |
US20090061000A1 (en) * | 2007-08-31 | 2009-03-05 | Astrazeneca Ab | Pharmaceutical formulation use 030 |
CA2728511A1 (en) * | 2008-06-23 | 2009-12-30 | Astellas Pharma Inc. | Sulfonamide compounds or salts thereof |
GB0815782D0 (en) | 2008-08-29 | 2008-10-08 | Xention Ltd | Novel potassium channel blockers |
GB0815781D0 (en) | 2008-08-29 | 2008-10-08 | Xention Ltd | Novel potassium channel blockers |
GB0815784D0 (en) | 2008-08-29 | 2008-10-08 | Xention Ltd | Novel potassium channel blockers |
AU2011344148B2 (en) * | 2010-12-16 | 2017-04-27 | Allergan, Inc. | Phosphorous derivatives as chemokine receptor modulators |
CN102358753B (zh) * | 2011-10-14 | 2013-06-05 | 山西大学 | 一种胰蛋白酶抑制剂活性片段衍生物及其制备方法和应用 |
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SE9602646D0 (sv) | 1996-07-04 | 1996-07-04 | Astra Ab | Pharmaceutically-useful compounds |
DE19632773A1 (de) | 1996-08-14 | 1998-02-19 | Basf Ag | Neue Thrombininhibitoren |
DE19632772A1 (de) | 1996-08-14 | 1998-02-19 | Basf Ag | Neue Benzamidine |
US6285302B1 (en) | 1998-12-28 | 2001-09-04 | Texas Instruments Incorporated | Runlength-limited code and method |
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1996
- 1996-07-04 SE SE9602646A patent/SE9602646D0/xx unknown
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1997
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- 1997-06-24 ZA ZA975591A patent/ZA975591B/xx unknown
- 1997-06-26 NZ NZ333394A patent/NZ333394A/xx not_active IP Right Cessation
- 1997-06-26 EP EP97932085A patent/EP0917528B1/en not_active Expired - Lifetime
- 1997-06-26 JP JP10505123A patent/JP2000515505A/ja not_active Ceased
- 1997-06-26 DE DE69715635T patent/DE69715635T2/de not_active Expired - Fee Related
- 1997-06-26 KR KR1019980710870A patent/KR20000022437A/ko not_active Application Discontinuation
- 1997-06-26 EE EEP199900006A patent/EE9900006A/et unknown
- 1997-06-26 IL IL12788597A patent/IL127885A0/xx unknown
- 1997-06-26 PL PL97331047A patent/PL331047A1/xx unknown
- 1997-06-26 AT AT97932085T patent/ATE224365T1/de not_active IP Right Cessation
- 1997-06-26 CN CN97197578A patent/CN1228765A/zh active Pending
- 1997-06-26 HU HU9902410A patent/HUP9902410A3/hu unknown
- 1997-06-26 CZ CZ9912A patent/CZ1299A3/cs unknown
- 1997-06-26 WO PCT/SE1997/001150 patent/WO1998001422A1/en not_active Application Discontinuation
- 1997-06-26 CA CA002260190A patent/CA2260190A1/en not_active Abandoned
- 1997-06-26 BR BR9710142A patent/BR9710142A/pt unknown
- 1997-06-26 US US08/894,833 patent/US6221898B1/en not_active Expired - Fee Related
- 1997-06-26 SK SK1720-98A patent/SK172098A3/sk unknown
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1998
- 1998-12-21 IS IS4930A patent/IS4930A/is unknown
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2001
- 2001-04-23 US US09/839,609 patent/US7074820B2/en not_active Expired - Fee Related
Also Published As
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HUP9902410A3 (en) | 2001-10-29 |
ZA975591B (en) | 1998-12-24 |
CN1228765A (zh) | 1999-09-15 |
KR20000022437A (ko) | 2000-04-25 |
ID19479A (id) | 1998-07-16 |
HUP9902410A2 (hu) | 1999-11-29 |
US7074820B2 (en) | 2006-07-11 |
NZ333394A (en) | 2000-08-25 |
EE9900006A (et) | 1999-06-15 |
AU3562897A (en) | 1998-02-02 |
US20020040043A1 (en) | 2002-04-04 |
WO1998001422A1 (en) | 1998-01-15 |
BR9710142A (pt) | 1999-08-10 |
US6221898B1 (en) | 2001-04-24 |
AR007614A1 (es) | 1999-11-10 |
IL127885A0 (en) | 1999-10-28 |
ATE224365T1 (de) | 2002-10-15 |
NO986180D0 (no) | 1998-12-29 |
AU726236B2 (en) | 2000-11-02 |
EP0917528A1 (en) | 1999-05-26 |
NO986180L (no) | 1999-03-04 |
DE69715635D1 (de) | 2002-10-24 |
DE69715635T2 (de) | 2003-08-07 |
PL331047A1 (en) | 1999-06-21 |
TR199802767T2 (xx) | 1999-04-21 |
JP2000515505A (ja) | 2000-11-21 |
IS4930A (is) | 1998-12-21 |
CA2260190A1 (en) | 1998-01-15 |
CZ1299A3 (cs) | 1999-06-16 |
EP0917528B1 (en) | 2002-09-18 |
SE9602646D0 (sv) | 1996-07-04 |
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