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公开(公告)号:US20080161338A1
公开(公告)日:2008-07-03
申请号:US11794497
申请日:2006-01-11
申请人: Matthias Vennemann , Thomas Bar , Jurgen Braunger , Paola Ciapetti , Jean-Marie Contreras , Camille George Wermuth
发明人: Matthias Vennemann , Thomas Bar , Jurgen Braunger , Paola Ciapetti , Jean-Marie Contreras , Camille George Wermuth
IPC分类号: A61K31/44
CPC分类号: C07D471/04
摘要: The invention relates to novel pyrrolodihydroisoquinoline derivatives, which are efficacious inhibitors of PDE10.
摘要翻译: 本发明涉及新的吡咯二氢异喹啉衍生物,它们是PDE10的有效抑制剂。
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公开(公告)号:US20080064714A1
公开(公告)日:2008-03-13
申请号:US11794494
申请日:2006-01-11
申请人: Matthias Vennemann , Thomas Bar , Juergen Braunger , Volker Gekeler , Petra Gimmnich , Paola Ciapetti , Jean-Marie Contreras , Camille Wermuth
发明人: Matthias Vennemann , Thomas Bar , Juergen Braunger , Volker Gekeler , Petra Gimmnich , Paola Ciapetti , Jean-Marie Contreras , Camille Wermuth
IPC分类号: A61K31/47 , A61P35/00 , C07D217/00
CPC分类号: C07D471/04
摘要: The invention relates to novel pyrrolodihydroisoquinoline derivatives which are efficacious inhibitors of cellular (hyper)proliferation and/or inducers of apoptosis in cancer cells.
摘要翻译: 本发明涉及新的吡咯二氢异喹啉衍生物,其是癌细胞中细胞(超)增殖和/或凋亡诱导剂的有效抑制剂。
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3.
公开(公告)号:US20080125452A1
公开(公告)日:2008-05-29
申请号:US11795762
申请日:2006-01-26
申请人: Matthias Vennemann , Thomas Bar , Jurgen Braunger , Petra Gimmnich , Thomas Beckers , Mathias Schmidt , Thomas Ciossek , Sandra Nappe
发明人: Matthias Vennemann , Thomas Bar , Jurgen Braunger , Petra Gimmnich , Thomas Beckers , Mathias Schmidt , Thomas Ciossek , Sandra Nappe
IPC分类号: A61K31/4745 , C07D491/14 , C07D498/14 , C07D487/14
CPC分类号: C07D471/14 , C07D491/14 , C07D495/14
摘要: Compounds of a certain formula (I), in which R1, R2, R3, R4, R5 and X have the meanings indicated in the description, are novel effective compounds with anti-proliferative and/or apoptosis inducing activity.
摘要翻译: 其中R1,R2,R3,R4,R5和X具有说明书中所示含义的某种式(I)的化合物是具有抗增殖和/或凋亡诱导活性的新型有效化合物。
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4.Novel Indolopyridines, Benzofuranopyridines and Benzothienopyridines 审中-公开
标题翻译: 新型吲哚啉,苯并呋喃并吡啶和苯并噻吩并吡啶公开(公告)号:US20080114017A1
公开(公告)日:2008-05-15
申请号:US11795763
申请日:2006-01-26
IPC分类号: A61K31/435 , A61P35/00 , C07D471/22
CPC分类号: C07D471/14
摘要: Compounds of a certain formula (I), in which R1, R2, R3, R4, R5, R6 and X have the meanings indicated in the description, are novel effective compounds with anti-proliferative and/or apoptosis inducing activity.
摘要翻译: 其中R1,R2,R3,R4,R5,R6和X具有说明书中所示含义的某种式(I)的化合物是具有抗增殖和/或凋亡诱导活性的新型有效化合物。
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公开(公告)号:US20060148840A1
公开(公告)日:2006-07-06
申请号:US10562137
申请日:2004-06-30
申请人: Matthias Vennemann , Thomas Bar , Jurgen Braunger
发明人: Matthias Vennemann , Thomas Bar , Jurgen Braunger
IPC分类号: A61K31/4745 , C07D451/02
CPC分类号: C07D471/04 , A61K31/4745
摘要: The invention relates to novel pyrrolodihydroisoquinoline derivatives, which are efficacious inhibitors of PDE10.
摘要翻译: 本发明涉及新的吡咯二氢异喹啉衍生物,它们是PDE10的有效抑制剂。
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6.
公开(公告)号:US20060148838A1
公开(公告)日:2006-07-06
申请号:US10562149
申请日:2004-06-30
IPC分类号: A61K31/4745 , C07D491/02 , C07D451/02
CPC分类号: C07D471/04 , A61K31/4745
摘要: The invention relates to novel pyrrolodihydroisoquinoline derivatives, which are efficacious inhibitors of cellular (hyper)proliferation and/or inducers of apoptosis in cancer cells.
摘要翻译: 本发明涉及新型吡咯二氢异喹啉衍生物,其是癌细胞中细胞(超)增殖和/或凋亡诱导剂的有效抑制剂。
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公开(公告)号:US20070232596A1
公开(公告)日:2007-10-04
申请号:US11659738
申请日:2005-08-17
申请人: Matthias Vennemann , Thomas Baer , Gudrun Groegor , Jurgen Braunger , Petra Gimmnich , Thomas Maier , Heike Rothfels
发明人: Matthias Vennemann , Thomas Baer , Gudrun Groegor , Jurgen Braunger , Petra Gimmnich , Thomas Maier , Heike Rothfels
IPC分类号: A61K31/4523 , A61K31/5377 , A61K31/541 , C07D417/14 , C07D419/14
CPC分类号: C07D471/14 , C07D495/14
摘要: Compounds of the formula (1) in which R1, R2, R3, R4 and X have the meanings indicated in the description, are novel effective compounds with Eg5 inhibitory, anti-proliferative and/or apoptosis inducing activity.
摘要翻译: 其中R1,R2,R3,R4和X具有说明书中所示含义的式(1)化合物是具有Eg5抑制,抗增殖和/或凋亡诱导活性的新型有效化合物。
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8.
公开(公告)号:US20070105840A1
公开(公告)日:2007-05-10
申请号:US10562142
申请日:2004-06-30
申请人: Thomas Bar , Matthias Vennemann
发明人: Thomas Bar , Matthias Vennemann
IPC分类号: A61K31/55 , A61K31/541 , A61K31/5377 , A61K31/506 , A61K31/496 , A61K31/4745 , C07D471/04
CPC分类号: A61K31/4745
摘要: The invention relates to the use of a pyrrolo ‘2,1-a’ isoquinoline structure-element as an integral part of the overall structure of compounds which inhibit PDE10.
摘要翻译: 本发明涉及吡咯并[2,1-a'异喹啉结构元素作为抑制PDE10的化合物整体结构的组成部分的用途。
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公开(公告)号:US20090246169A1
公开(公告)日:2009-10-01
申请号:US12280264
申请日:2007-02-21
IPC分类号: A61K38/20 , C07D471/12 , A61K31/437 , C07D401/14 , A61K31/496 , C07D413/14 , A61K31/5377 , A61K31/55 , A61K31/397 , A61P35/00
CPC分类号: C07D471/14
摘要: Compounds of a certain formula I, in which R1, R2, R3, R4, R5 and R6 have the meanings indicated in the description, are effective compounds with anti-proliferative and/or apoptosis inducing activity.
摘要翻译: 其中R1,R2,R3,R4,R5和R6具有说明书中所示含义的某种式I化合物是具有抗增殖和/或凋亡诱导活性的有效化合物。
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公开(公告)号:US07842820B2
公开(公告)日:2010-11-30
申请号:US10591477
申请日:2005-03-10
申请人: Thomas Maier , Thomas Beckers , Thomas Baer , Petra Gimmnich , Frank Dullweber , Matthias Vennemann
发明人: Thomas Maier , Thomas Beckers , Thomas Baer , Petra Gimmnich , Frank Dullweber , Matthias Vennemann
IPC分类号: C07D207/46 , A61K31/40
CPC分类号: A61K31/40 , C07D207/48 , C07D401/12 , C07D403/12 , C07D409/12 , C07D409/14 , C07D413/12
摘要: Compounds of the formula I in which the substitutents have the definitions provided in the specification, are novel, effective HDAC inhibitors.
摘要翻译: 其中取代基具有说明书中提供的定义的式I化合物是新的有效的HDAC抑制剂。
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