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公开(公告)号:US20090029981A1
公开(公告)日:2009-01-29
申请号:US12087904
申请日:2007-01-18
申请人: Peter Herold , Robert Mah , Vincenzo Tschinke , Dirk Behnke , Nathalie Jotterand , Aleksandar Stojanovic , Stefan Stutz , Stjepan Jelakovic , Michael Quirmbach
发明人: Peter Herold , Robert Mah , Vincenzo Tschinke , Dirk Behnke , Nathalie Jotterand , Aleksandar Stojanovic , Stefan Stutz , Stjepan Jelakovic , Michael Quirmbach
IPC分类号: A61K31/538 , A61P9/00 , C07D413/12 , C07D413/14
CPC分类号: C07D401/12 , C07D413/12 , C07D413/14
摘要: The application relates to substituted 4-phenylpiperidines of the general formula and their salts, preferably their pharmaceutically acceptable salts, in which R2, R3, W and X have the meanings explained in the description, a process for their preparation and the use of these compounds as medicines, especially as renin inhibitors.
摘要翻译: 本申请涉及通式的取代的4-苯基哌啶及其盐,优选其药学上可接受的盐,其中R 2,R 3,W和X具有说明书中所述的含义,其制备方法和这些化合物的用途 作为药物,特别是作为肾素抑制剂。
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公开(公告)号:US20070066604A1
公开(公告)日:2007-03-22
申请号:US11522313
申请日:2006-09-18
申请人: Peter Herold , Robert Mah , Stefan Stutz , Vincenzo Tschinke , Aleksandar Stojanovic , Christiane Marti , Dirk Behnke , Nathalie Jotterand , Michael Quirmbach , Christoph Schumacher
发明人: Peter Herold , Robert Mah , Stefan Stutz , Vincenzo Tschinke , Aleksandar Stojanovic , Christiane Marti , Dirk Behnke , Nathalie Jotterand , Michael Quirmbach , Christoph Schumacher
IPC分类号: A61K31/542 , A61K31/5415 , A61K31/538 , A61K31/519 , A61K31/517 , A61K31/455 , A61K31/47
CPC分类号: A61K31/404 , Y02A50/411
摘要: Use of compounds of the general formula (I) or a pharmaceutically usable salt thereof; wherein R1, R2, R3, R4, R5 and X have the definitions elucidated in more detail in the description, as beta-secretase, cathepsin D, plasmepsin II and/or HIV protease inhibitors.
摘要翻译: 使用通式(I)的化合物或其药学上可用的盐; 其中R 1,R 2,R 3,R 4,R 5, 和X具有在说明书中更详细阐述的定义,如β-分泌酶,组织蛋白酶D,浆细胞素II和/或HIV蛋白酶抑制剂。
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公开(公告)号:US20090270380A1
公开(公告)日:2009-10-29
申请号:US11887354
申请日:2006-03-30
申请人: Peter Herold , Robert Mah , Vincenzo Tschinke , Nathalie Jotterand , Dirk Behnke , Aleksandar Stojanovic , Stefan Stuz , Michael Quirmbach , Stjepan Jelakovic
发明人: Peter Herold , Robert Mah , Vincenzo Tschinke , Nathalie Jotterand , Dirk Behnke , Aleksandar Stojanovic , Stefan Stuz , Michael Quirmbach , Stjepan Jelakovic
IPC分类号: A61K31/538 , C07D265/36 , A61P9/00 , A61P9/12 , A61P13/12
CPC分类号: C07D413/14 , C07D413/12
摘要: The application relates to novel substituted piperidines of the general formula (II) in which R1, R2′, R2″, R4′, X, Z, m and n have the meanings defined in the description, to a process for the preparation thereof and to the use of these compounds as medicines, especially as renin inhibitors.
摘要翻译: 本申请涉及其中R1,R2',R2“,R4”,X,Z,m和n具有本说明书中定义的含义的通式(II)的新型取代哌啶与其制备方法 以及使用这些化合物作为药物,特别是作为肾素抑制剂。
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公开(公告)号:US07842688B2
公开(公告)日:2010-11-30
申请号:US12068443
申请日:2008-02-06
申请人: Peter Herold , Robert Mah , Stefan Stutz , Aleksandar Stojanovic , Vincenzo Tschinke , Nathalie Jotterand
发明人: Peter Herold , Robert Mah , Stefan Stutz , Aleksandar Stojanovic , Vincenzo Tschinke , Nathalie Jotterand
IPC分类号: C07D401/12 , A61K31/4427
CPC分类号: C07D211/42 , C07D401/12 , C07D413/12
摘要: Novel substituted piperidines of the general formulae (I) and (II) with the substituent definitions as explained in detail in the description are described. The compounds are suitable in particular as renin inhibitors and are highly potent.
摘要翻译: 描述通式(I)和(II)的新颖取代的哌啶与具有如在说明书中详细说明的取代基定义。 该化合物特别适合作为肾素抑制剂,并且是非常有效的。
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公开(公告)号:US20090012055A1
公开(公告)日:2009-01-08
申请号:US12068443
申请日:2008-02-06
申请人: Peter Herold , Robert Mah , Stefan Stutz , Aleksandar Stojanovic , Vincenzo Tschinke , Nathalie Jotterand
发明人: Peter Herold , Robert Mah , Stefan Stutz , Aleksandar Stojanovic , Vincenzo Tschinke , Nathalie Jotterand
IPC分类号: A61K31/397 , C07D211/40 , A61K31/445 , C07D265/36 , A61K31/538 , C07D413/02 , A61K31/454 , A61K31/4525 , A61K31/5415 , A61P13/12 , A61P9/00 , C07D279/16 , C07D401/02 , C07D215/00 , A61K31/4709 , A61K31/5377 , C07D239/24 , A61K31/506
CPC分类号: C07D211/42 , C07D401/12 , C07D413/12
摘要: Novel substituted piperidines of the general formulae (I) and (II) with the substituent definitions as explained in detail in the description are described. The compounds are suitable in particular as renin inhibitors and are highly potent.
摘要翻译: 描述通式(I)和(II)的新颖取代的哌啶与具有如在说明书中详细说明的取代基定义。 该化合物特别适合作为肾素抑制剂,并且是非常有效的。
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公开(公告)号:US20070010511A1
公开(公告)日:2007-01-11
申请号:US10574108
申请日:2004-09-30
申请人: Peter Herold , Robert Mah , Stefan Stutz , Aleksandar Stojanovic , Vincenzo Tschinke , Nathalie Jotterand
发明人: Peter Herold , Robert Mah , Stefan Stutz , Aleksandar Stojanovic , Vincenzo Tschinke , Nathalie Jotterand
IPC分类号: A61K31/541 , A61K31/5377 , A61K31/496 , A61K31/46 , C07D453/02
CPC分类号: C07D211/42 , C07D401/12 , C07D413/12
摘要: Novel substituted piperidines of the general formulae (I) and (II) with the substituent definitions as explained in detail in the description are described. The compounds are suitable in particular as renin inhibitors and are highly potent.
摘要翻译: 描述通式(I)和(II)的新颖取代的哌啶与具有如在说明书中详细说明的取代基定义。 该化合物特别适合作为肾素抑制剂,并且是非常有效的。
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公开(公告)号:US07790715B2
公开(公告)日:2010-09-07
申请号:US10574108
申请日:2004-09-30
申请人: Peter Herold , Robert Mah , Stefan Stutz , Aleksandar Stojanovic , Vincenzo Tschinke , Nathalie Jotterand
发明人: Peter Herold , Robert Mah , Stefan Stutz , Aleksandar Stojanovic , Vincenzo Tschinke , Nathalie Jotterand
IPC分类号: C07D401/12 , A61K31/4427
CPC分类号: C07D211/42 , C07D401/12 , C07D413/12
摘要: Novel substituted piperidines of the general formulae (I) and (II) with the substituent definitions as explained in detail in the description are described. The compounds are suitable in particular as renin inhibitors and are highly potent.
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公开(公告)号:US08324235B2
公开(公告)日:2012-12-04
申请号:US12450521
申请日:2008-03-27
申请人: Peter Herold , Robert Mah , Stefan Stutz , Vincenzo Tschinke , Aleksandar Stojanovic , Nathalie Jotterand , Bibia Bennacer
发明人: Peter Herold , Robert Mah , Stefan Stutz , Vincenzo Tschinke , Aleksandar Stojanovic , Nathalie Jotterand , Bibia Bennacer
IPC分类号: A61K31/4188 , C07D401/14 , C07D235/02
CPC分类号: C07D491/20
摘要: The patent application relates to new heterocyclic compounds of the general formula (I), in which R, R1, R2, Q, T, n and p have the definitions elucidated in more detail in the description, to a process for preparing them and to the use of these compounds as medicaments, particularly as aldosterone synthase inhibitors.
摘要翻译: 该专利申请涉及通式(I)的新的杂环化合物,其中R,R 1,R 2,Q,T,n和p具有在说明书中更详细阐述的定义,涉及其制备方法和 使用这些化合物作为药物,特别是作为醛固酮合成酶抑制剂。
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公开(公告)号:US20100144774A1
公开(公告)日:2010-06-10
申请号:US12450521
申请日:2008-03-27
申请人: Peter Herold , Robert Mah , Stefan Stutz , Vincenzo Tschinke , Aleksandar Stojanovic , Nathalie Jotterand , Bibia Bennacer
发明人: Peter Herold , Robert Mah , Stefan Stutz , Vincenzo Tschinke , Aleksandar Stojanovic , Nathalie Jotterand , Bibia Bennacer
IPC分类号: A61K31/438 , C07D491/20 , A61K31/4188 , A61P9/12 , A61P9/00 , A61P29/00 , A61P3/00
CPC分类号: C07D491/20
摘要: The patent application relates to new heterocyclic compounds of the general formula (I), in which R, R1, R2, Q, T, n and p have the definitions elucidated in more detail in the description, to a process for preparing them and to the use of these compounds as medicaments, particularly as aldosterone synthase inhibitors.
摘要翻译: 该专利申请涉及通式(I)的新的杂环化合物,其中R,R 1,R 2,Q,T,n和p具有在说明书中更详细阐述的定义,涉及其制备方法和 使用这些化合物作为药物,特别是作为醛固酮合酶抑制剂。
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公开(公告)号:US07687495B2
公开(公告)日:2010-03-30
申请号:US12076221
申请日:2008-03-14
申请人: Peter Herold , Robert Mah , Vincenzo Tschinke , Christiane Marti , Stefan Stutz , Stjepan Jelakovic , Zenon D. Konteatis , Jennifer L. Ludington , Michael Quirmbach , Aleksandar Stojanovic , Dirk Behnke , Frank Hollinger
发明人: Peter Herold , Robert Mah , Vincenzo Tschinke , Christiane Marti , Stefan Stutz , Stjepan Jelakovic , Zenon D. Konteatis , Jennifer L. Ludington , Michael Quirmbach , Aleksandar Stojanovic , Dirk Behnke , Frank Hollinger
IPC分类号: C07D401/02 , A61K31/50 , A61K31/4965
CPC分类号: C07D413/12 , C07D413/14
摘要: Substituted piperidines of formulae (I) and (II) with the substituent definitions as explained in the specification. The compounds are suitable in particular as renin inhibitors and are highly potent.
摘要翻译: 式(I)和(II)的取代的哌啶与说明书中所述的取代基定义相同。 该化合物特别适合作为肾素抑制剂,并且是非常有效的。
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