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公开(公告)号:US5100917A
公开(公告)日:1992-03-31
申请号:US580759
申请日:1990-09-11
申请人: Gary A. Flynn , Philippe Bey , Thomas R. Blohm
发明人: Gary A. Flynn , Philippe Bey , Thomas R. Blohm
CPC分类号: C07J61/00
摘要: The present invention relates to novel A-nor-steroid-3-carboxylic acid derivatives and to their use as inhibitors of mammalian 5.alpha.-reductase.
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2.Mercaptoacetylamide derivatives useful as inhibitors of enkephalinase and ace 失效
标题翻译: 巯基乙酰胺衍生物,可用作脑啡肽酶和ace的抑制剂公开(公告)号:US5527795A
公开(公告)日:1996-06-18
申请号:US417179
申请日:1995-04-05
申请人: Gary A. Flynn , Philippe Bey , Alan M. Warshawsky , Douglas W. Beight , Shujaath Mehdi , Eugene L. Giroux , Timothy P. Burkholder , Edward D. Daugs , John F. French
发明人: Gary A. Flynn , Philippe Bey , Alan M. Warshawsky , Douglas W. Beight , Shujaath Mehdi , Eugene L. Giroux , Timothy P. Burkholder , Edward D. Daugs , John F. French
IPC分类号: A61K38/00 , C07D471/04 , C07D487/04 , C07K5/078 , A61K31/55 , C07D457/04
CPC分类号: C07D471/04 , C07D487/04 , C07K5/06139 , A61K38/00
摘要: The present invention relates to certain novel mercaptoacetylamide derivatives useful as inhibitors of enkephalinase and of ACE.
摘要翻译: 本发明涉及可用作脑啡肽酶和ACE抑制剂的某些新型巯基乙酰胺衍生物。
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3.Mercaptoacetylamide derivatives useful as inhibitors of enkephalinase and ACE 失效
标题翻译: 巯基乙酰胺衍生物可用作脑啡肽酶和ACE的抑制剂公开(公告)号:US5491143A
公开(公告)日:1996-02-13
申请号:US417424
申请日:1995-04-05
申请人: Gary A. Flynn , Philippe Bey , Alan M. Warshawsky , Douglas W. Beight , Shujaath Mehdi , Eugene L. Giroux , Timothy P. Burkholder , Edward D. Daugs , John F. French
发明人: Gary A. Flynn , Philippe Bey , Alan M. Warshawsky , Douglas W. Beight , Shujaath Mehdi , Eugene L. Giroux , Timothy P. Burkholder , Edward D. Daugs , John F. French
IPC分类号: A61K38/00 , C07D471/04 , C07D487/04 , C07K5/078 , A61K31/55
CPC分类号: C07D471/04 , C07D487/04 , C07K5/06139 , A61K38/00
摘要: The present invention relates to certain novel mercaptoacetylamide derivatives useful as inhibitors of enkephalinase and of ACE.
摘要翻译: 本发明涉及可用作脑啡肽酶和ACE抑制剂的某些新型巯基乙酰胺衍生物。
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4.Mercaptoacetylamide derivatives useful as inhibitors of enkephalinase and ace 失效
标题翻译: 新型巯基乙酰胺衍生物可用作脑啡肽酶抑制剂和ace公开(公告)号:US5430145A
公开(公告)日:1995-07-04
申请号:US149572
申请日:1993-11-09
申请人: Gary A. Flynn , Philippe Bey , Alan M. Warshawsky , Douglas W. Beight , Shujaath Mehdi , Eugene L. Giroux , Timothy P. Burkholder , Edward D. Daugs , John F. French
发明人: Gary A. Flynn , Philippe Bey , Alan M. Warshawsky , Douglas W. Beight , Shujaath Mehdi , Eugene L. Giroux , Timothy P. Burkholder , Edward D. Daugs , John F. French
IPC分类号: A61K38/00 , C07D471/04 , C07D487/04 , C07K5/078 , A61K31/55 , C07D223/16 , C07D498/04 , C07D513/04
CPC分类号: C07D471/04 , C07D487/04 , C07K5/06139 , A61K38/00
摘要: The present invention relates to certain novel mercaptoacetylamide derivatives useful as inhibitors of enkephalinase and of ACE.
摘要翻译: 本发明涉及可用作脑啡肽酶和ACE抑制剂的某些新型巯基乙酰胺衍生物。
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公开(公告)号:US07858666B2
公开(公告)日:2010-12-28
申请号:US12135571
申请日:2008-06-09
CPC分类号: C07C65/21 , A61K31/11 , A61K31/135 , A61K31/166 , A61K31/192 , A61K31/357 , A61K31/381 , A61K31/505 , A61K31/5375 , A61K31/5377 , C07C47/55 , C07C47/565 , C07C47/575 , C07C65/11 , C07C65/26 , C07C65/30 , C07C205/44 , C07C205/61 , C07C223/02 , C07C233/65 , C07C235/42 , C07C235/84 , C07C251/24 , C07C317/24 , C07C321/04 , C07C2601/02 , C07C2601/08 , C07C2601/14 , C07D213/48 , C07D213/64 , C07D213/69 , C07D213/74 , C07D215/14 , C07D217/16 , C07D231/12 , C07D235/08 , C07D239/26 , C07D239/54 , C07D241/18 , C07D249/18 , C07D261/08 , C07D277/34 , C07D295/125 , C07D295/15 , C07D295/192 , C07D307/80 , C07D317/54 , C07D319/08 , C07D319/18 , C07D321/10 , C07D333/22 , C07D333/58 , C07D401/12 , C07D403/12 , C07D417/10 , Y02A50/389 , Y02A50/393
摘要: Compounds which directly inhibit IRE-1α activity in vitro, prodrugs, and pharmaceutically acceptable salts thereof. Such compounds and prodrugs are useful for treating diseases associated with the unfolded protein response and can be used as single agents or in combination therapies.
摘要翻译: 在体外直接抑制IRE-1α活性的化合物,其前药和药学上可接受的盐。 这样的化合物和前药可用于治疗与未折叠的蛋白质应答相关的疾病,并可用作单一药剂或联合疗法。
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公开(公告)号:US06358978B1
公开(公告)日:2002-03-19
申请号:US09599390
申请日:2000-06-22
申请人: Olaf Ritzeler , Hans Ulrich Stilz , Bernhard Neises , William Jerome Bock, Jr. , Armin Walser , Gary A. Flynn , Jörg Habermann , Gerhard Jähne
发明人: Olaf Ritzeler , Hans Ulrich Stilz , Bernhard Neises , William Jerome Bock, Jr. , Armin Walser , Gary A. Flynn , Jörg Habermann , Gerhard Jähne
IPC分类号: A61K31445
CPC分类号: C07D401/04 , C07D401/14 , C07D409/14 , C07D471/04
摘要: Compounds of formula I are suitable for the production of pharmaceuticals for the prophylaxis and therapy of disorders in whose course an increased activity of NF&kgr;B is involved.
摘要翻译: 式I化合物适用于生产用于预防和治疗疾病的药物,其中涉及NFκB活性增加。
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7.Mercaptoacetylamino 1,3,4,5-tetrahydro-benzo(C)azepin-2-one disulfide derivatives useful as inhibitors of enkephalinase and ACE 失效
标题翻译: 巯基乙酰氨基1,3,4,5-四氢 - 苯并(C)氮杂-2-酮二硫化物衍生物,可用作脑啡肽酶和ACE的抑制剂公开(公告)号:US5880119A
公开(公告)日:1999-03-09
申请号:US910053
申请日:1997-08-12
申请人: Gary A. Flynn , Douglas W. Beight , Alan M. Warshawsky , Shujaath Mehdi , John F. French , John H. Kehne
发明人: Gary A. Flynn , Douglas W. Beight , Alan M. Warshawsky , Shujaath Mehdi , John F. French , John H. Kehne
IPC分类号: C12N9/99 , A61K38/00 , A61K38/55 , A61P1/04 , A61P7/10 , A61P9/00 , A61P9/12 , A61P25/00 , A61P25/04 , A61P43/00 , C07K1/06 , C07K5/06 , C07K5/078 , A61K31/55 , A01N43/46 , C07D498/04
CPC分类号: C07K5/06139 , A61K38/00
摘要: The present invention relates to certain novel mercaptoacetylamido 1,3,4,5-tetrahydro-benzo�c!azepin-3-one disulfide derivatives useful as inhibitors of enkephalinase and of ACE.
摘要翻译: 本发明涉及可用作脑啡肽酶和ACE抑制剂的某些新的巯基乙酰氨基1,3,4,5-四氢 - 苯并[c]氮杂-3-酮二硫化物衍生物。
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公开(公告)号:US5849908A
公开(公告)日:1998-12-15
申请号:US967075
申请日:1997-11-10
IPC分类号: A61K38/00 , C07D401/06 , C07D401/10 , C07D401/14 , C07D405/00 , C07D405/14 , C07D409/00 , C07D409/14 , C07D471/04 , C07D491/00 , C07D495/00 , C07K5/06 , C07K5/078 , C07D417/04
CPC分类号: C07D401/06 , C07D471/04 , C07K5/06139 , A61K38/00
摘要: The present invention relates to novel processes for preparing intermediates of the formula I ##STR1## and to novel intermediates thereof which are useful in the preparation of inhibitors of enkephalinase and angiotensin converting enzyme.
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9.2-substituted indane-2-mercaptoacetylamide tricyclic derivatives useful as inhibitors of enkephalinase 失效
标题翻译: 可用作脑啡肽酶抑制剂的2-取代的茚满-2-巯基乙酰胺三环衍生物公开(公告)号:US5491142A
公开(公告)日:1996-02-13
申请号:US396945
申请日:1995-03-01
申请人: Alan M. Warshawsky , Gary A. Flynn
发明人: Alan M. Warshawsky , Gary A. Flynn
IPC分类号: A61K31/55 , A61P7/10 , A61P9/00 , A61P9/04 , A61P9/12 , A61P13/12 , A61P25/04 , A61P25/24 , A61P25/30 , A61P27/06 , A61P43/00 , C07D471/04 , C07D487/04 , C07D498/04 , C07D513/04
CPC分类号: C07D471/04 , C07D487/04 , C07D513/04
摘要: The present invention relates to novel 2-substituted indane-2-mercaptoacetylamide tricyclic derivatives which are useful as inhibitors of Enkephalise.
摘要翻译: 本发明涉及可用作脑啡肽抑制剂的新型2-取代的茚满-2-巯基乙酰胺三环衍生物。
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10.
公开(公告)号:US5472959A
公开(公告)日:1995-12-05
申请号:US348778
申请日:1994-12-01
申请人: Alan M. Warshawsky , Gary A. Flynn
发明人: Alan M. Warshawsky , Gary A. Flynn
IPC分类号: A61K31/535 , A61K31/54 , A61K31/55 , A61K38/00 , A61P7/10 , A61P9/00 , A61P9/12 , A61P25/04 , A61P25/28 , A61P43/00 , C07D471/04 , C07D487/04 , C07D498/04 , C07D507/00 , C07D513/04 , C07K5/078
CPC分类号: C07K5/06139 , A61K38/00
摘要: The invention relates to compounds of the formula ##STR1## wherein B.sub.1 and B.sub.2 are each independently hydrogen; hydroxy; --OR.sub.2 wherein R.sub.2 is a C.sub.1 -C.sub.4 alkyl or an Ar--Y group wherein Ar is aryl and Y is a hydrogen or C.sub.1 -C.sub.4 alkyl; or, where B.sub.1 and B.sub.2 are attached to adjacent carbon atoms, B.sub.1 and B.sub.2 can be taken together with said adjacent carbons to form a benzene ring or methylenedioxy;A is a bond, methylene or oxygen, sulfur, NR.sub.4 or NCOR.sub.5 wherein R.sub.4 is hydrogen, a C.sub.1 -C.sub.4 alkyl or an Ar--Y-- group and R.sub.5 is --CF.sub.3, a C.sub.1 -C.sub.10 alkyl or an Ar--Y-- group; R.sub.3 is hydrogen or --CH.sub.2 OC(O)C(CH.sub.3).sub.3 ; R.sub.1 is hydrogen, C.sub.1 -C.sub.4 alkyl or --CH.sub.2 OC(O)--C(CH.sub.3).sub.3 ; and n is an integer 1 to 3,that are useful as inhibitors of enkephalinase and ACE.
摘要翻译: 本发明涉及下式化合物:其中B1和B2各自独立地为氢; 羟基; -OR 2,其中R 2是C 1 -C 4烷基或Ar-Y基团,其中Ar是芳基,Y是氢或C 1 -C 4烷基; 或者其中B1和B2连接到相邻的碳原子上,可以将B1和B2与所述相邻的碳原子一起形成苯环或亚甲二氧基; A是键,亚甲基或氧,硫,NR 4或NCOR 5,其中R 4是氢,C 1 -C 4烷基或Ar-Y-基,R 5是-CF 3,C 1 -C 10烷基或Ar-Y-基团; R3是氢或-CH2OC(O)C(CH3)3; R1是氢,C1-C4烷基或-CH2OC(O)-C(CH3)3; 且n为1〜3的整数,可用作脑啡肽酶和ACE的抑制剂。
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