JP5318094B2 - 凝固因子阻害剤としてのジペプチド類似体 - Google Patents
凝固因子阻害剤としてのジペプチド類似体 Download PDFInfo
- Publication number
- JP5318094B2 JP5318094B2 JP2010512311A JP2010512311A JP5318094B2 JP 5318094 B2 JP5318094 B2 JP 5318094B2 JP 2010512311 A JP2010512311 A JP 2010512311A JP 2010512311 A JP2010512311 A JP 2010512311A JP 5318094 B2 JP5318094 B2 JP 5318094B2
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- Prior art keywords
- methyl
- substituted
- ylmethyl
- alkyl
- nhco
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
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- 0 C*C(C)(C)C(NN)=O Chemical compound C*C(C)(C)C(NN)=O 0.000 description 57
- BOABMNOKLJDCMR-UHFFFAOYSA-N CC(C)C(C)C1C2C(C3CCCC3)=C2C2C1C2 Chemical compound CC(C)C(C)C1C2C(C3CCCC3)=C2C2C1C2 BOABMNOKLJDCMR-UHFFFAOYSA-N 0.000 description 1
- UCQGMLJPPPLFGP-YYSDWVBWSA-N CC(Nc(cc1)ccc1NC([C@H](Cc1ccccc1)NC(/C=C/c(cc(cc1)Cl)c1-[n]1nnnc1)=O)=O)=O Chemical compound CC(Nc(cc1)ccc1NC([C@H](Cc1ccccc1)NC(/C=C/c(cc(cc1)Cl)c1-[n]1nnnc1)=O)=O)=O UCQGMLJPPPLFGP-YYSDWVBWSA-N 0.000 description 1
- UAOZOBSOELDIKI-NRFANRHFSA-N CC[n]1nc(C[C@@H](C(Nc(cc2)ccc2C(O)=O)=O)NC(CCc2cc(Cl)ccc2-[n]2nnnc2)=O)cc1 Chemical compound CC[n]1nc(C[C@@H](C(Nc(cc2)ccc2C(O)=O)=O)NC(CCc2cc(Cl)ccc2-[n]2nnnc2)=O)cc1 UAOZOBSOELDIKI-NRFANRHFSA-N 0.000 description 1
- ASCZNPSXZUYWFO-UHFFFAOYSA-N CCc1n[n](CCCO2)c2c1 Chemical compound CCc1n[n](CCCO2)c2c1 ASCZNPSXZUYWFO-UHFFFAOYSA-N 0.000 description 1
- RATDEFSYEXUKHF-LNYGYFNRSA-N CN(C)CCCC[C@@H](C(Nc(cc1)ccc1C(O)=O)=O)NC(/C=C/c1cc(Cl)ccc1-[n]1nnnc1)=O Chemical compound CN(C)CCCC[C@@H](C(Nc(cc1)ccc1C(O)=O)=O)NC(/C=C/c1cc(Cl)ccc1-[n]1nnnc1)=O RATDEFSYEXUKHF-LNYGYFNRSA-N 0.000 description 1
- MGXNWVKSTKFQNB-ZSIUJALASA-N COC(c(cc1)ccc1NC([C@H](CC(N(CC1)CCS1(=O)=O)=O)NC(/C=C/c1cc(Cl)ccc1-[n]1nnnc1)=O)=O)=O Chemical compound COC(c(cc1)ccc1NC([C@H](CC(N(CC1)CCS1(=O)=O)=O)NC(/C=C/c1cc(Cl)ccc1-[n]1nnnc1)=O)=O)=O MGXNWVKSTKFQNB-ZSIUJALASA-N 0.000 description 1
- BDKOKJWERFRBRM-MEJUDOHFSA-N COC(c1ccc(NC([C@H](Cc2ccccc2)NC(/C=C/c(c(-[n]2nnnc2)ccc2Cl)c2F)=O)=O)nc1)=O Chemical compound COC(c1ccc(NC([C@H](Cc2ccccc2)NC(/C=C/c(c(-[n]2nnnc2)ccc2Cl)c2F)=O)=O)nc1)=O BDKOKJWERFRBRM-MEJUDOHFSA-N 0.000 description 1
- BECKLZLYKXCODA-URPWPPKMSA-N COCC[C@@H](C(Nc(cc1)ccc1C(O)=O)=O)NC(/C=C/c1cc(Cl)ccc1-[n]1nnnc1)=O Chemical compound COCC[C@@H](C(Nc(cc1)ccc1C(O)=O)=O)NC(/C=C/c1cc(Cl)ccc1-[n]1nnnc1)=O BECKLZLYKXCODA-URPWPPKMSA-N 0.000 description 1
- YHUHYOWYUCZSAL-PYPKYNKJSA-N CS(CC[C@@H](C(Nc(cc1)ccc1C(O)=O)=O)NC(/C=C/c1cc(Cl)ccc1-[n]1nnnc1)=O)=O Chemical compound CS(CC[C@@H](C(Nc(cc1)ccc1C(O)=O)=O)NC(/C=C/c1cc(Cl)ccc1-[n]1nnnc1)=O)=O YHUHYOWYUCZSAL-PYPKYNKJSA-N 0.000 description 1
- HPNHDBZGRHZCQY-DQPCJIFYSA-N C[C@@H](C(Nc(cc1)ccc1NC(OC)=O)=O)NC(/C=C/c1cc(Cl)ccc1-[n]1nnnc1)=O Chemical compound C[C@@H](C(Nc(cc1)ccc1NC(OC)=O)=O)NC(/C=C/c1cc(Cl)ccc1-[n]1nnnc1)=O HPNHDBZGRHZCQY-DQPCJIFYSA-N 0.000 description 1
- JDBWCTCREIJODM-UHFFFAOYSA-N C[n]1c2ncccc2c(CO)c1 Chemical compound C[n]1c2ncccc2c(CO)c1 JDBWCTCREIJODM-UHFFFAOYSA-N 0.000 description 1
- KMEYZHACDFMRCW-UHFFFAOYSA-N C[n]1nc(CO)c2c1cccc2 Chemical compound C[n]1nc(CO)c2c1cccc2 KMEYZHACDFMRCW-UHFFFAOYSA-N 0.000 description 1
- AVBPTIYKXNVKNJ-UHFFFAOYSA-N Cc(cc1C=CN2)ccc1C2=O Chemical compound Cc(cc1C=CN2)ccc1C2=O AVBPTIYKXNVKNJ-UHFFFAOYSA-N 0.000 description 1
- UYZJTSNVWCNCIR-UHFFFAOYSA-N Cc(cc1CCN2)ccc1C2=O Chemical compound Cc(cc1CCN2)ccc1C2=O UYZJTSNVWCNCIR-UHFFFAOYSA-N 0.000 description 1
- GAUKCDPSYQUYQL-UHFFFAOYSA-N Cc1n[o]c2ccccc12 Chemical compound Cc1n[o]c2ccccc12 GAUKCDPSYQUYQL-UHFFFAOYSA-N 0.000 description 1
- PHORCHZMUAPHRU-YDSNZTKKSA-N NC(c(c1c2)c[nH]c1ccc2NC([C@H](Cc1ccccc1)NC(/C=C/c1cc(Cl)ccc1-[n]1nnnc1)=O)=O)=O Chemical compound NC(c(c1c2)c[nH]c1ccc2NC([C@H](Cc1ccccc1)NC(/C=C/c1cc(Cl)ccc1-[n]1nnnc1)=O)=O)=O PHORCHZMUAPHRU-YDSNZTKKSA-N 0.000 description 1
- YZNMGAIGBKRLJI-SEYIPAOBSA-N NC(c1cccc([C@H](C2)C2(C(Nc(cc2)ccc2C(O)=O)=O)NC(/C=C/c2cc(Cl)ccc2-[n]2nnnc2)=O)c1)=O Chemical compound NC(c1cccc([C@H](C2)C2(C(Nc(cc2)ccc2C(O)=O)=O)NC(/C=C/c2cc(Cl)ccc2-[n]2nnnc2)=O)c1)=O YZNMGAIGBKRLJI-SEYIPAOBSA-N 0.000 description 1
- FEGPFKUMKHFVRG-OGCVIRRGSA-N O=C(/C=C/c1cc(Cl)ccc1-[n]1nnnc1)N/C(/C(Nc1cccc(-c2nnn[nH]2)c1)=O)=C/c1ccccc1 Chemical compound O=C(/C=C/c1cc(Cl)ccc1-[n]1nnnc1)N/C(/C(Nc1cccc(-c2nnn[nH]2)c1)=O)=C/c1ccccc1 FEGPFKUMKHFVRG-OGCVIRRGSA-N 0.000 description 1
- YOCYPSUBCRUCJY-YRNVUSSQSA-N O=C(C(Cc1ccccc1)NC(/C=C/c1cc(Cl)ccc1-[n]1nnnc1)=O)Nc1ccc(C=CNC2=O)c2c1 Chemical compound O=C(C(Cc1ccccc1)NC(/C=C/c1cc(Cl)ccc1-[n]1nnnc1)=O)Nc1ccc(C=CNC2=O)c2c1 YOCYPSUBCRUCJY-YRNVUSSQSA-N 0.000 description 1
- GXQWFGQPENKDGB-MCEVJEMCSA-N O=C([C@@](C1)([C@@H]1c1ccccc1)NC(/C=C/c(cc(cc1)Cl)c1-[n]1nnnc1)=O)Nc(cc1)ccc1C(NO1)=NC1=O Chemical compound O=C([C@@](C1)([C@@H]1c1ccccc1)NC(/C=C/c(cc(cc1)Cl)c1-[n]1nnnc1)=O)Nc(cc1)ccc1C(NO1)=NC1=O GXQWFGQPENKDGB-MCEVJEMCSA-N 0.000 description 1
- YMSQQUSRXPEQSF-KVTOOOBYSA-N O=C([C@H](CCc1ccccc1)NC(/C=C/c(cc(cc1)Cl)c1-[n]1nnnc1)=O)Nc(cc1)ccc1-[n]1ncnc1 Chemical compound O=C([C@H](CCc1ccccc1)NC(/C=C/c(cc(cc1)Cl)c1-[n]1nnnc1)=O)Nc(cc1)ccc1-[n]1ncnc1 YMSQQUSRXPEQSF-KVTOOOBYSA-N 0.000 description 1
- NYKUIVGARDHMCO-BGVYSJOJSA-N O=C([C@H](Cc1ccccc1)NC(/C=C/c1cc(Cl)ccc1-[n]1nnnc1)=O)Nc1n[o]c2c1cccc2 Chemical compound O=C([C@H](Cc1ccccc1)NC(/C=C/c1cc(Cl)ccc1-[n]1nnnc1)=O)Nc1n[o]c2c1cccc2 NYKUIVGARDHMCO-BGVYSJOJSA-N 0.000 description 1
- YSAIHMUQKYDLSZ-DAFODLJHSA-N OC(/C=C/c(c(-[n]1nnnc1)ccc1Cl)c1F)=O Chemical compound OC(/C=C/c(c(-[n]1nnnc1)ccc1Cl)c1F)=O YSAIHMUQKYDLSZ-DAFODLJHSA-N 0.000 description 1
- RODHDNAJXSCYJK-ICFOYXHFSA-N OC(C[C@@H](C(Nc(cc1)ccc1C(O)=O)=O)NC(/C=C/c1cc(Cl)ccc1-[n]1nnnc1)=O)=O Chemical compound OC(C[C@@H](C(Nc(cc1)ccc1C(O)=O)=O)NC(/C=C/c1cc(Cl)ccc1-[n]1nnnc1)=O)=O RODHDNAJXSCYJK-ICFOYXHFSA-N 0.000 description 1
- DRNNIJVASSWYII-NWMLYGLHSA-N OC(Cc(cc1)ccc1NC([C@H](Cc1ccccc1)NC(/C=C/c1cc(Cl)ccc1-[n]1nnnc1)=O)=O)=O Chemical compound OC(Cc(cc1)ccc1NC([C@H](Cc1ccccc1)NC(/C=C/c1cc(Cl)ccc1-[n]1nnnc1)=O)=O)=O DRNNIJVASSWYII-NWMLYGLHSA-N 0.000 description 1
- NKMPQTZHXMQROY-KPKJPENVSA-N OC(c(cc1)ccc1NC(C(Cc1nc(cccc2)c2nc1)NC(/C=C/c1cc(Cl)ccc1-[n]1nnnc1)=O)=O)=O Chemical compound OC(c(cc1)ccc1NC(C(Cc1nc(cccc2)c2nc1)NC(/C=C/c1cc(Cl)ccc1-[n]1nnnc1)=O)=O)=O NKMPQTZHXMQROY-KPKJPENVSA-N 0.000 description 1
- XDIWADWJPBZWHA-RAHHNWTCSA-N OC(c(cc1)ccc1NC([C@@](C1)([C@@H]1c1cc(C(O)=O)ccc1)NC(/C=C/c1cc(Cl)ccc1-[n]1nnnc1)=O)=O)=O Chemical compound OC(c(cc1)ccc1NC([C@@](C1)([C@@H]1c1cc(C(O)=O)ccc1)NC(/C=C/c1cc(Cl)ccc1-[n]1nnnc1)=O)=O)=O XDIWADWJPBZWHA-RAHHNWTCSA-N 0.000 description 1
- XMICRACKVBKENR-OYCQWZNWSA-N OC(c(cc1)ccc1NC([C@H](CC1CCOCC1)NC(/C=C/c1cc(Cl)ccc1-[n]1nnnc1)=O)=O)=O Chemical compound OC(c(cc1)ccc1NC([C@H](CC1CCOCC1)NC(/C=C/c1cc(Cl)ccc1-[n]1nnnc1)=O)=O)=O XMICRACKVBKENR-OYCQWZNWSA-N 0.000 description 1
- OPBKVSOYGHXWAL-FQEVSTJZSA-N OC(c(cc1)ccc1NC([C@H](Cc1ccccc1)NC(CS(c1cc(Cl)ccc1-[n]1nnnc1)(=O)=O)=O)=O)=O Chemical compound OC(c(cc1)ccc1NC([C@H](Cc1ccccc1)NC(CS(c1cc(Cl)ccc1-[n]1nnnc1)(=O)=O)=O)=O)=O OPBKVSOYGHXWAL-FQEVSTJZSA-N 0.000 description 1
- BHXIVJNUCBWSFO-UHFFFAOYSA-N OCc1n[n](CCOC2)c2c1 Chemical compound OCc1n[n](CCOC2)c2c1 BHXIVJNUCBWSFO-UHFFFAOYSA-N 0.000 description 1
- KSFQACWNSBYUPR-NWMLYGLHSA-N OP(Cc(cc1)ccc1NC([C@H](Cc1ccccc1)NC(/C=C/c1cc(Cl)ccc1-[n]1nnnc1)=O)=O)(O)=O Chemical compound OP(Cc(cc1)ccc1NC([C@H](Cc1ccccc1)NC(/C=C/c1cc(Cl)ccc1-[n]1nnnc1)=O)=O)(O)=O KSFQACWNSBYUPR-NWMLYGLHSA-N 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D257/00—Heterocyclic compounds containing rings having four nitrogen atoms as the only ring hetero atoms
- C07D257/02—Heterocyclic compounds containing rings having four nitrogen atoms as the only ring hetero atoms not condensed with other rings
- C07D257/04—Five-membered rings
-
- 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
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P9/00—Drugs for disorders of the cardiovascular system
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P9/00—Drugs for disorders of the cardiovascular system
- A61P9/04—Inotropic agents, i.e. stimulants of cardiac contraction; Drugs for heart failure
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P9/00—Drugs for disorders of the cardiovascular system
- A61P9/10—Drugs for disorders of the cardiovascular system for treating ischaemic or atherosclerotic diseases, e.g. antianginal drugs, coronary vasodilators, drugs for myocardial infarction, retinopathy, cerebrovascula insufficiency, renal arteriosclerosis
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C237/00—Carboxylic acid amides, the carbon skeleton of the acid part being further substituted by amino groups
- C07C237/02—Carboxylic acid amides, the carbon skeleton of the acid part being further substituted by amino groups having the carbon atoms of the carboxamide groups bound to acyclic carbon atoms of the carbon skeleton
- C07C237/22—Carboxylic acid amides, the carbon skeleton of the acid part being further substituted by amino groups having the carbon atoms of the carboxamide groups bound to acyclic carbon atoms of the carbon skeleton having nitrogen atoms of amino groups bound to the carbon skeleton of the acid part, further acylated
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D231/00—Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings
- C07D231/54—Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings condensed with carbocyclic rings or ring systems
- C07D231/56—Benzopyrazoles; Hydrogenated benzopyrazoles
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D249/00—Heterocyclic compounds containing five-membered rings having three nitrogen atoms as the only ring hetero atoms
- C07D249/02—Heterocyclic compounds containing five-membered rings having three nitrogen atoms as the only ring hetero atoms not condensed with other rings
- C07D249/04—1,2,3-Triazoles; Hydrogenated 1,2,3-triazoles
- C07D249/06—1,2,3-Triazoles; Hydrogenated 1,2,3-triazoles with aryl radicals directly attached to ring atoms
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D401/00—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom
- C07D401/02—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings
- C07D401/12—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings linked by a chain containing hetero atoms as chain links
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D403/00—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00
- C07D403/02—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00 containing two hetero rings
- C07D403/12—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00 containing two hetero rings linked by a chain containing hetero atoms as chain links
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D405/00—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom
- C07D405/02—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom containing two hetero rings
- C07D405/12—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom containing two hetero rings linked by a chain containing hetero atoms as chain links
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D409/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having sulfur atoms as the only ring hetero atoms
- C07D409/02—Heterocyclic compounds containing two or more hetero rings, at least one ring having sulfur atoms as the only ring hetero atoms containing two hetero rings
- C07D409/12—Heterocyclic compounds containing two or more hetero rings, at least one ring having sulfur atoms as the only ring hetero atoms containing two hetero rings linked by a chain containing hetero atoms as chain links
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D413/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms
- C07D413/02—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms containing two hetero rings
- C07D413/12—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms containing two hetero rings linked by a chain containing hetero atoms as chain links
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D417/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00
- C07D417/02—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00 containing two hetero rings
- C07D417/12—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00 containing two hetero rings linked by a chain containing hetero atoms as chain links
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D417/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00
- C07D417/14—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00 containing three or more hetero rings
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D471/00—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00
- C07D471/02—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00 in which the condensed system contains two hetero rings
- C07D471/04—Ortho-condensed systems
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D487/00—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, not provided for by groups C07D451/00 - C07D477/00
- C07D487/02—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, not provided for by groups C07D451/00 - C07D477/00 in which the condensed system contains two hetero rings
- C07D487/04—Ortho-condensed systems
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D498/00—Heterocyclic compounds containing in the condensed system at least one hetero ring having nitrogen and oxygen atoms as the only ring hetero atoms
- C07D498/02—Heterocyclic compounds containing in the condensed system at least one hetero ring having nitrogen and oxygen atoms as the only ring hetero atoms in which the condensed system contains two hetero rings
- C07D498/04—Ortho-condensed systems
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- Engineering & Computer Science (AREA)
- Bioinformatics & Cheminformatics (AREA)
- General Health & Medical Sciences (AREA)
- Veterinary Medicine (AREA)
- General Chemical & Material Sciences (AREA)
- Medicinal Chemistry (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Pharmacology & Pharmacy (AREA)
- Life Sciences & Earth Sciences (AREA)
- Animal Behavior & Ethology (AREA)
- Cardiology (AREA)
- Public Health (AREA)
- Heart & Thoracic Surgery (AREA)
- Diabetes (AREA)
- Hematology (AREA)
- Hospice & Palliative Care (AREA)
- Urology & Nephrology (AREA)
- Vascular Medicine (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Plural Heterocyclic Compounds (AREA)
- Nitrogen Condensed Heterocyclic Rings (AREA)
- Nitrogen And Oxygen Or Sulfur-Condensed Heterocyclic Ring Systems (AREA)
- Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
- Peptides Or Proteins (AREA)
- Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
- Pyridine Compounds (AREA)
Applications Claiming Priority (5)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US94379107P | 2007-06-13 | 2007-06-13 | |
| US60/943,791 | 2007-06-13 | ||
| US4951608P | 2008-05-01 | 2008-05-01 | |
| US61/049,516 | 2008-05-01 | ||
| PCT/US2008/066506 WO2008157162A1 (en) | 2007-06-13 | 2008-06-11 | Dipeptide analogs as coagulation factor inhibitors |
Publications (3)
| Publication Number | Publication Date |
|---|---|
| JP2010529991A JP2010529991A (ja) | 2010-09-02 |
| JP2010529991A5 JP2010529991A5 (cg-RX-API-DMAC7.html) | 2010-11-04 |
| JP5318094B2 true JP5318094B2 (ja) | 2013-10-16 |
Family
ID=39714076
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2010512311A Expired - Fee Related JP5318094B2 (ja) | 2007-06-13 | 2008-06-11 | 凝固因子阻害剤としてのジペプチド類似体 |
Country Status (12)
| Country | Link |
|---|---|
| US (1) | US8367709B2 (cg-RX-API-DMAC7.html) |
| EP (1) | EP2152664B1 (cg-RX-API-DMAC7.html) |
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| AU2010240527A1 (en) * | 2009-04-22 | 2011-12-01 | Actelion Pharmaceuticals Ltd | Thiazole derivatives and their use as P2Y12 receptor antagonists |
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| TW201319068A (zh) | 2011-08-05 | 2013-05-16 | 必治妥美雅史谷比公司 | 作為xia因子抑制劑之環狀p1接合劑 |
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| BR112015002081A2 (pt) | 2012-08-03 | 2017-07-04 | Bristol Myers Squibb Co | di-hidropiridona p1 como inibidores de fator xia |
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| CN112805001B (zh) | 2018-08-29 | 2024-07-23 | 莫菲克医疗股份有限公司 | 抑制αvβ6整联蛋白 |
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| CN113943259A (zh) * | 2020-07-17 | 2022-01-18 | 西安禾渼生物医药有限公司 | 一种氨基酸衍生物、其制备方法及应用 |
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| MX2009012847A (es) | 2009-12-08 |
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| CN101784516B (zh) | 2014-07-02 |
| EP2152664B1 (en) | 2014-09-03 |
| KR20100037600A (ko) | 2010-04-09 |
| US20100173899A1 (en) | 2010-07-08 |
| US8367709B2 (en) | 2013-02-05 |
| EP2152664A1 (en) | 2010-02-17 |
| AU2008266228A1 (en) | 2008-12-24 |
| JP2010529991A (ja) | 2010-09-02 |
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