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公开(公告)号:US08957064B2
公开(公告)日:2015-02-17
申请号:US13201277
申请日:2010-02-02
申请人: Matthias Vennemann , Thomas Bär , Thomas Maier , Swen Hölder , Gerrit Beneke , Florian Dehmel , Armin Zülch , Andreas Strub , Stuart Ince , Hartmut Rehwinkel , Ningshu Liu , Ulf Bömer , Barbara Beckers
发明人: Matthias Vennemann , Thomas Bär , Thomas Maier , Swen Hölder , Gerrit Beneke , Florian Dehmel , Armin Zülch , Andreas Strub , Thomas Beckers , Stuart Ince , Hartmut Rehwinkel , Ningshu Liu , Ulf Bömer
IPC分类号: A61K31/495 , A61K31/519 , A61K31/505 , C07D401/12 , C07D487/04 , A61K45/06 , C07D471/04
CPC分类号: A61K31/519 , A61K31/495 , A61K31/505 , A61K45/06 , C07D401/12 , C07D471/04 , C07D487/04
摘要: Compounds of formula (I) or an N-oxide, a salt, a tautomer or a stereoisomer of said compound, or a salt of said N-oxide, tautomer or stereoisomer, wherein ring B and the pyrimidine to which it is fused, R4, R5, R6, R7, m and n have the meanings as given in the description and the claims, which are effective inhibitors of the Pi3K/Akt pathway, processes for their production and their use as pharmaceuticals.
摘要翻译: 式(I)化合物或所述化合物的N-氧化物,盐,互变异构体或立体异构体,或所述N-氧化物,互变异构体或立体异构体的盐,其中环B和与其稠合的嘧啶,R4 R5,R6,R7,m和n具有在描述和权利要求中给出的含义,它们是Pi3K / Akt途径的有效抑制剂,其生产方法及其作为药物的用途。
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公开(公告)号:US08614218B2
公开(公告)日:2013-12-24
申请号:US12731880
申请日:2010-03-25
申请人: Swen Hölder , Matthias Vennemann , Gerrit Beneke , Armin Zülch , Volker Gekeler , Thomas Beckers , Astrid Zimmermann , Hemant Joshi
发明人: Swen Hölder , Matthias Vennemann , Gerrit Beneke , Armin Zülch , Volker Gekeler , Thomas Beckers , Astrid Zimmermann , Hemant Joshi
IPC分类号: A01N43/90 , A61K31/519 , C07D487/00
CPC分类号: C07D487/04
摘要: Compounds of formula (I) a tautomer or stereoisomer thereof, or a salt thereof, wherein ring B and the pyrimidine to which it is fused, R4, R5, R6 and R7 have the meanings as given in the description and the claims, are effective inhibitors of the Pi3K/Akt pathway.
摘要翻译: 式(I)化合物其互变异构体或立体异构体或其盐,其中环B和其稠合的嘧啶,R4,R5,R6和R7具有在说明书和权利要求书中给出的含义,是有效的 Pi3K / Akt途径的抑制剂。
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公开(公告)号:US07776864B2
公开(公告)日:2010-08-17
申请号:US12191703
申请日:2008-08-14
申请人: Swen Hölder , Matthias Vennemann , Gerrit Beneke , Armin Zülch , Volker Gekeler , Thomas Beckers , Astrid Zimmermann , Hemant Joshi
发明人: Swen Hölder , Matthias Vennemann , Gerrit Beneke , Armin Zülch , Volker Gekeler , Thomas Beckers , Astrid Zimmermann , Hemant Joshi
IPC分类号: A61K31/4965 , A61K31/505 , A61K31/519 , A61K31/445 , C07D471/04 , C07D471/22 , C07D487/00 , C07D491/00 , C07D403/00 , C07D239/02 , A01N43/54 , A01N43/90 , A01N43/40
CPC分类号: C07D487/04
摘要: Compounds of formula (I) a tautomer or stereoisomer thereof, or a salt thereof, wherein ring B and the pyrimidine to which it is fused, R4, R5, R6 and R7 have the meanings as given in the description and the claims, are effective inhibitors of the Pi3K/Akt pathway.
摘要翻译: 式(I)化合物其互变异构体或立体异构体或其盐,其中环B和其稠合的嘧啶,R4,R5,R6和R7具有在说明书和权利要求书中给出的含义,是有效的 Pi3K / Akt途径的抑制剂。
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公开(公告)号:US20100184782A1
公开(公告)日:2010-07-22
申请号:US12731880
申请日:2010-03-25
申请人: Swen Hölder , Matthias Vennemann , Gerrit Beneke , Armin Zülch , Volker Gekeler , Thomas Beckers , Astrid Zimmermann , Hemant Joshi
发明人: Swen Hölder , Matthias Vennemann , Gerrit Beneke , Armin Zülch , Volker Gekeler , Thomas Beckers , Astrid Zimmermann , Hemant Joshi
IPC分类号: A61K31/519 , A61P35/00 , A61P35/02
CPC分类号: C07D487/04
摘要: Compounds of formula (I) a tautomer or stereoisomer thereof, or a salt thereof, wherein ring B and the pyrimidine to which it is fused, R4, R5, R6 and R7 have the meanings as given in the description and the claims, are effective inhibitors of the Pi3K/Akt pathway.
摘要翻译: 式(I)化合物其互变异构体或立体异构体或其盐,其中环B和其稠合的嘧啶,R4,R5,R6和R7具有在说明书和权利要求书中给出的含义,是有效的 Pi3K / Akt途径的抑制剂。
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公开(公告)号:US20090137607A1
公开(公告)日:2009-05-28
申请号:US12191703
申请日:2008-08-14
申请人: Swen Holder , Matthias Vennemann , Gerrit Beneke , Armin Zulch , Volker Gekeler , Thomas Beckers , Astrid Zimmermann , Hemant Joshi
发明人: Swen Holder , Matthias Vennemann , Gerrit Beneke , Armin Zulch , Volker Gekeler , Thomas Beckers , Astrid Zimmermann , Hemant Joshi
IPC分类号: A61K31/497 , C07D487/02 , A61K31/519 , A61P35/00
CPC分类号: C07D487/04
摘要: Compounds of formula (I) a tautomer or stereoisomer thereof, or a salt thereof, wherein ring B and the pyrimidine to which it is fused, R4, R5, R6 and R7 have the meanings as given in the description and the claims, are effective inhibitors of the Pi3K/Akt pathway.
摘要翻译: 式(I)化合物其互变异构体或立体异构体或其盐,其中环B和其稠合的嘧啶,R4,R5,R6和R7具有在说明书和权利要求书中给出的含义,是有效的 Pi3K / Akt途径的抑制剂。
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公开(公告)号:US20130317002A1
公开(公告)日:2013-11-28
申请号:US13201277
申请日:2010-02-02
申请人: Barbara Beckers
发明人: Matthias Vennemann , Thomas Bär , Thomas Maier , Swen Hölder , Gerrit Beneke , Florian Dehmel , Armin Zülch , Andreas Strub , Thomas Beckers , Stuart Ince , Hartmut Rehwinkel , Ningshu Liu , Ulf Bömer
IPC分类号: A61K31/519 , A61K45/06 , C07D471/04 , C07D487/04
CPC分类号: A61K31/519 , A61K31/495 , A61K31/505 , A61K45/06 , C07D401/12 , C07D471/04 , C07D487/04
摘要: Compounds of formula (I) or an N-oxide, a salt, a tautomer or a stereoisomer of said compound, or a salt of said N-oxide, tautomer or stereoisomer, wherein ring B and the pyrimidine to which it is fused, R4, R5, R6, R7, m and n have the meanings as given in the description and the claims, which are effective inhibitors of the Pi3K/Akt pathway, processes for their production and their use as pharmaceuticals.
摘要翻译: 式(I)化合物或所述化合物的N-氧化物,盐,互变异构体或立体异构体,或所述N-氧化物,互变异构体或立体异构体的盐,其中环B和与其稠合的嘧啶,R4 R5,R6,R7,m和n具有在描述和权利要求中给出的含义,它们是Pi3K / Akt途径的有效抑制剂,其生产方法及其作为药物的用途。
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公开(公告)号:US20130310362A1
公开(公告)日:2013-11-21
申请号:US13201227
申请日:2010-02-05
申请人: Barbara Beckers
发明人: Matthias Vennemann , Thomas Bär , Thomas Maier , Swen Hölder , Gerrit Beneke , Florian Dehmel , Armin Zülch , Andreas Strub , Thomas Beckers , Stuart Ince , Hartmut Rehwinkel , Ningshu Liu , Ulf Bömer
IPC分类号: A61K31/519 , A61K45/06 , C07D487/04
CPC分类号: A61K31/519 , A61K45/06 , C07D487/04
摘要: The present invention relates to compounds of formula (I), a N-oxide or tautomer or stereoisomer thereof, or a salt thereof, wherein ring B and the imidazole to which it is fused, R4, R6, R7, R10, m and n have the meanings as given in the description and the claims, which are effective inhibitors of the Pi3K/Akt pathway, processes for their production and their use as pharmaceuticals.
摘要翻译: 本发明涉及式(I)化合物,其N-氧化物或互变异构体或其立体异构体或其盐,其中环B和与其稠合的咪唑R4,R6,R7,R10,m和n 具有在描述和权利要求中给出的含义,其是Pi3K / Akt通路的有效抑制剂,其生产方法及其作为药物的用途。
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