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公开(公告)号:US6069160A
公开(公告)日:2000-05-30
申请号:US631516
申请日:1996-04-12
申请人: Andreas Stolle , Dieter Habich , Stephan Bartel , Bernd Riedl , Martin Ruppelt , Hanno Wild , Rainer Endermann , Klaus-Dieter Bremm , Hein-Peter Kroll , Harald Labischinski , Klaus Schaller , Hans-Otto Werling
发明人: Andreas Stolle , Dieter Habich , Stephan Bartel , Bernd Riedl , Martin Ruppelt , Hanno Wild , Rainer Endermann , Klaus-Dieter Bremm , Hein-Peter Kroll , Harald Labischinski , Klaus Schaller , Hans-Otto Werling
IPC分类号: A61K31/40 , A61K31/42 , A61K31/423 , A61K31/425 , A61K31/44 , A61K31/445 , A61K31/655 , A61K31/66 , A61P31/04 , C07D263/58 , C07D413/04 , C07D413/12 , C07D413/14 , C07D417/04 , C07D417/14 , C07D419/04 , C07F9/6558 , C07F9/6584 , A61K31/428 , C07D263/54 , C07D277/62
CPC分类号: C07D263/58 , C07D413/04 , C07D413/14 , C07D417/04 , C07D417/14 , C07D419/04 , C07F9/6558 , C07F9/65842
摘要: The invention relates to heteroatom-containing benzocyclopentaneoxazolidinones, to processes for their preparation and their use as medicaments, especially as antibacterial medicaments.
摘要翻译: 本发明涉及含杂原子的苯并环戊恶唑烷酮,其制备方法及其作为药物的用途,特别是作为抗菌药物。
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公开(公告)号:US5529998A
公开(公告)日:1996-06-25
申请号:US508245
申请日:1995-07-27
申请人: Dieter Habich , Bernd Riedl , Martin Ruppelt , Andreas Stolle , Hanno Wild , Rainer Endermann , Klaus D. Bremm , Hein-Peter Kroll , Harald Labischinski , Klaus Schaller , Hans-Otto Werling
发明人: Dieter Habich , Bernd Riedl , Martin Ruppelt , Andreas Stolle , Hanno Wild , Rainer Endermann , Klaus D. Bremm , Hein-Peter Kroll , Harald Labischinski , Klaus Schaller , Hans-Otto Werling
IPC分类号: C07D491/113 , A61K31/42 , A61K31/423 , A61K31/425 , A61K31/44 , A61K31/445 , A61K31/495 , A61K31/496 , A61K31/505 , A61K31/535 , A61K31/5377 , A61K31/55 , A61P31/04 , C07D247/02 , C07D263/38 , C07D263/56 , C07D263/58 , C07D413/04 , C07D417/04 , C07D417/12 , C07D417/14 , C07D419/12 , C07D491/10 , C07D413/02 , C07D417/02
CPC分类号: C07D263/58 , C07D417/04 , C07D417/14 , C07D491/10
摘要: The invention relates to benzoxazolyl- and benzothiazolyloxazolidinones, processes for their preparation and their use as medicaments, in particular as antibacterial medicaments.
摘要翻译: 本发明涉及苯并恶唑基和苯并噻唑基恶唑烷酮,其制备方法及其作为药物的用途,特别是抗菌药物。
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3.Use of substituted chromans, some of which are known, as medicaments, new active compounds and processes for their preparation 失效
标题翻译: 取代的苯并二氢吡喃酮(其中一些已知的)用作药物,新的活性化合物及其制备方法公开(公告)号:US5492918A
公开(公告)日:1996-02-20
申请号:US251986
申请日:1994-06-01
申请人: Hanno Wild , Wolfgang Bender , Dieter Habich , Hans-Georg Heine , Siegfried Raddatz , Wolfgang Roben , Jutta Hansen , Arnold Paessens
发明人: Hanno Wild , Wolfgang Bender , Dieter Habich , Hans-Georg Heine , Siegfried Raddatz , Wolfgang Roben , Jutta Hansen , Arnold Paessens
IPC分类号: A61K31/443 , A61K31/445 , A61P31/12 , C07D405/06 , C07D405/14
CPC分类号: C07D405/06 , C07D405/14
摘要: The present invention relates to the use of substituted chromans of the general formula (I) ##STR1## in which the substituents have the meaning indicated in the description, for the production of medicaments, in particular as HIV protease-inhibiting agents, new active compounds and processes for their preparation.
摘要翻译: 本发明涉及通式(I)的取代苯并二氢吡喃的用途,其中取代基具有说明书中指出的含义,用于生产药物,特别是作为HIV蛋白酶抑制剂,新的活性化合物 及其制备方法。
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4.Phosphonopyrrolidine- and piperidine-containing pseudopeptides of the statin type, a process for their preparation and their use as medicaments against retroviruses 失效
标题翻译: 苯妥英类和苯哌啶类药物的类型,其制备方法及其作为抗逆转录病毒药物使用的方法公开(公告)号:US5147865A
公开(公告)日:1992-09-15
申请号:US746272
申请日:1991-08-15
申请人: Dieter Habich , Jutta Hansen , Arnold Paessens
发明人: Dieter Habich , Jutta Hansen , Arnold Paessens
IPC分类号: A61K31/675 , A61K38/00 , A61P31/12 , A61P31/18 , C07F9/572 , C07F9/59 , C07K5/02 , C07K5/06 , C07K5/08
CPC分类号: C07K5/0205 , C07F9/5726 , A61K38/00
摘要: The invention relates to new phosphonopyrrolidine- and piperidine-containing pseudopeptides, to a process for their preparation and to their use as medicaments, in particular as antiviral agents in human and veterinary medicine.
摘要翻译: 本发明涉及新的膦酰基吡咯烷和哌啶的伪肽,涉及其制备方法和用作药物,特别是作为人和兽医学中的抗病毒剂。
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公开(公告)号:US5843967A
公开(公告)日:1998-12-01
申请号:US749581
申请日:1996-11-15
申请人: Bernd Riedl , Dieter Habich , Andreas Stolle , Hanno Wild , Rainer Endermann , Klaus Dieter Bremm , Hein-Peter Kroll , Harald Labischinski , Klaus Schaller , Hans-Otto Werling
发明人: Bernd Riedl , Dieter Habich , Andreas Stolle , Hanno Wild , Rainer Endermann , Klaus Dieter Bremm , Hein-Peter Kroll , Harald Labischinski , Klaus Schaller , Hans-Otto Werling
IPC分类号: C07D237/20 , A61K31/44 , A61K31/4418 , A61K31/47 , A61K31/495 , A61K31/50 , A61P31/04 , C07D213/72 , C07D215/38 , C07D215/48 , C07D239/42 , C07D241/44 , C07D413/04 , C07D413/14 , C07D417/14 , C07D471/04 , C07D401/04
CPC分类号: C07D413/04 , C07D413/14 , C07D417/14
摘要: The invention relates to 6-membered nitrogen-containing heteroaryloxazolidinones, processes for their preparation and their use as medicaments, in particular as antibacterial medicaments.
摘要翻译: 本发明涉及6元含氮杂芳基恶唑烷酮,其制备方法及其作为药物的用途,特别是抗菌药物。
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公开(公告)号:US5698574A
公开(公告)日:1997-12-16
申请号:US503183
申请日:1995-07-17
申请人: Bernd Riedl , Dieter Habich , Andreas Stolle , Hanno Wild , Rainer Endermann , Klaus Dieter Bremm , Hein-Peter Kroll , Harald Labischinski , Klaus Schaller , Hans-Otto Werling
发明人: Bernd Riedl , Dieter Habich , Andreas Stolle , Hanno Wild , Rainer Endermann , Klaus Dieter Bremm , Hein-Peter Kroll , Harald Labischinski , Klaus Schaller , Hans-Otto Werling
IPC分类号: C07D333/38 , A61K31/42 , A61K31/421 , A61K31/4245 , A61K31/425 , A61K31/426 , A61K31/44 , A61K31/655 , A61P31/04 , C07D263/32 , C07D263/48 , C07D277/20 , C07D277/44 , C07D333/66 , C07D413/04 , C07D413/08 , C07D413/14 , C07D417/04 , C07D417/14 , C07D413/00
CPC分类号: C07D413/04 , C07D263/48 , C07D413/08 , C07D413/14 , C07D417/04
摘要: The present invention relates to 5-membered heteroaryl-oxazolidinones, to processes for their preparation and to their use as medicaments, in particular as antibacterial medicaments.
摘要翻译: 本发明涉及5元杂芳基 - 恶唑烷酮,其制备方法和用作药物,特别是抗菌药物。
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7.
公开(公告)号:US5430151A
公开(公告)日:1995-07-04
申请号:US920216
申请日:1992-07-24
申请人: Dieter Habich , Wolfgang Roben , Jutta Hansen , Arnold Paessens
发明人: Dieter Habich , Wolfgang Roben , Jutta Hansen , Arnold Paessens
IPC分类号: A61K31/16 , A61K31/40 , A61K31/403 , A61K31/404 , A61K31/435 , A61K31/4427 , A61K31/445 , A61K31/47 , A61K31/535 , A61K31/5375 , A61K31/66 , A61K38/00 , A61P31/12 , A61P31/18 , C07C237/22 , C07C271/22 , C07C317/44 , C07D207/08 , C07D209/42 , C07D211/18 , C07D215/12 , C07D217/14 , C07D295/16 , C07D295/18 , C07D401/12 , C07F9/40 , C07F9/572 , C07F9/59 , C07F9/62 , C07K5/06 , C07K5/08 , C07K5/083 , C07D211/06 , C07D207/04
CPC分类号: C07D207/08 , C07C317/44 , C07D211/18 , C07D217/14 , C07K5/06191 , C07K5/081 , C07K5/0827 , A61K38/00
摘要: The present invention relates to new trifluoromethyl-containing pseudopeptides of the general formula (I) ##STR1## in which W, A, B, D, E, R.sub.1, R.sub.2 and R.sub.3 have the meaning as outlined of their making and use as pharmaceuticals.
摘要翻译: 本发明涉及通式(I)的新的含三氟甲基的伪肽,其中W,A,B,D,E,R 1,R 2和R 3具有其制备和使用概述的含义 作为药物。
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8.Dithiolanylglycine-containing HIV protease inhibitors of the hydroxyethylene isostere type 失效
标题翻译: 含二硫醇基甘氨酸的HIV蛋白酶抑制剂是羟基乙烯异构体型公开(公告)号:US5424426A
公开(公告)日:1995-06-13
申请号:US59488
申请日:1993-05-10
申请人: Dieter Habich , Wolfgang Bender , Jutta Hansen , Arnold Paessens
发明人: Dieter Habich , Wolfgang Bender , Jutta Hansen , Arnold Paessens
IPC分类号: A61K31/44 , A61K31/385 , A61K31/4433 , A61K31/445 , A61K31/47 , A61K38/00 , A61K38/55 , A61P31/12 , A61P31/18 , C07D215/48 , C07D339/06 , C07D409/12 , C07D409/14 , C07K5/02 , C07K5/03
CPC分类号: C07D409/12 , C07D409/14 , C07K5/0207 , A61K38/00
摘要: The invention relates to dithiolanylglycine-containing HIV protease inhibitors of the hydroxyethylene isostere type of the general formula (I) ##STR1## processes for their preparation and their use as retroviral agents.
摘要翻译: 本发明涉及通式(I)的羟基亚乙基异构体类型的二硫醇基甘氨酸的HIV蛋白酶抑制剂,其制备及其用作逆转录病毒剂。
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公开(公告)号:US4863916A
公开(公告)日:1989-09-05
申请号:US47371
申请日:1987-05-06
IPC分类号: C07D477/00 , A61K31/397 , A61K31/40 , A61P31/04 , C07D477/20
CPC分类号: C07D477/20
摘要: Substituted 6-hydroxymethyl-carbapenem antibiotics of the formula ##STR1## in which R.sup.1 is --OR.sup.4, ##STR2## A is a direct bond, or an alkylene and/or cycloalkylene radical, R.sup.2 is a group of the formula ##STR3## an aryl or heterocyclic radical, ##STR4## R.sup.3 is a COOH radical, or salt or ester thereof.
摘要翻译: 取代的式“IMAGE”的6-羟甲基 - 碳青霉烯类抗生素,其中R 1为-OR 4,A为直接键,或亚烷基和/或亚环烷基,R 2为下式基团: 或杂环基,R 3是COOH基团,或其盐或酯。
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公开(公告)号:US5922708A
公开(公告)日:1999-07-13
申请号:US790869
申请日:1997-02-03
申请人: Bernd Riedl , Dieter Habich , Andreas Stolle , Martin Ruppelt , Stephan Bartel , Walter Guarnieri , Rainer Endermann , Hein-Peter Kroll
发明人: Bernd Riedl , Dieter Habich , Andreas Stolle , Martin Ruppelt , Stephan Bartel , Walter Guarnieri , Rainer Endermann , Hein-Peter Kroll
IPC分类号: A01N43/76 , A61K31/42 , A61K31/44 , A61K31/47 , A61P31/04 , C07D413/04 , C07D413/14 , A61K31/535
CPC分类号: C07D413/04 , C07D413/14 , H04Q2213/13003 , H04Q2213/13196 , H04Q2213/13202 , H04Q2213/13203 , H04Q2213/13209 , H04Q2213/1329 , H04Q2213/13292 , H04Q2213/13299
摘要: The invention relates to novel heteroaryl-oxazolidinones of the general formula (I): ##STR1## in which the substituents are as defined in the description, to processes for their preparation and to their use as drugs, especially as antibacterial drugs.
摘要翻译: 本发明涉及通式(I)的新型杂芳基 - 恶唑烷酮:其中取代基如说明书中所定义,其制备方法及其作为药物,特别是抗菌药物的用途。
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