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公开(公告)号:US20150018332A1
公开(公告)日:2015-01-15
申请号:US14235342
申请日:2012-07-26
申请人: Vincent P. Sandanayaka , Sharon Shacham , Michael Kauffman , Sharon Shechter , Dilara McCauley , Yosef Landesman , William Senapedis , Jean-Richard Saint-Martin
发明人: Vincent P. Sandanayaka , Sharon Shacham , Michael Kauffman , Sharon Shechter , Dilara McCauley , Yosef Landesman , William Senapedis , Jean-Richard Saint-Martin
IPC分类号: C07D403/06 , C07D401/14 , C07D487/10 , C07D413/12 , C07D403/12 , C07D401/06 , C07D401/12
CPC分类号: C07D487/10 , C07D213/50 , C07D401/06 , C07D401/08 , C07D401/12 , C07D401/14 , C07D403/06 , C07D403/12 , C07D403/14 , C07D405/14 , C07D413/12
摘要: The invention generally relates to nuclear transport modulators, e.g CRM1 inhibitors, and more particularly to a compound represented by formula (I): or a pharmaceutically acceptable salt thereof, wherein the variables are as defined and described herein. The invention also includes the synthesis and use of a compound of structural formula (I), or a pharmaceutically acceptable salt or composition thereof, e.g, in the treatment, modulation and/or prevention of physiological conditions associated with CRM1 activity.
摘要翻译: 本发明通常涉及核转运调节剂,例如CRM1抑制剂,更具体地涉及由式(I)表示的化合物或其药学上可接受的盐,其中变量如本文所定义和描述。 本发明还包括结构式(I)化合物或其药学上可接受的盐或组合物的合成和用途,例如用于治疗,调节和/或预防与CRM1活性相关的生理条件。
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公开(公告)号:US09428490B2
公开(公告)日:2016-08-30
申请号:US14235342
申请日:2012-07-26
申请人: Vincent P. Sandanayaka , Sharon Shacham , Michael Kauffman , Sharon Shechter , Dilara McCauley , Yosef Landesman , William Senapedis , Jean-Richard Saint-Martin
发明人: Vincent P. Sandanayaka , Sharon Shacham , Michael Kauffman , Sharon Shechter , Dilara McCauley , Yosef Landesman , William Senapedis , Jean-Richard Saint-Martin
IPC分类号: C07D403/06 , C07D403/12 , C07D401/14 , C07D405/14 , C07D401/08 , C07D401/12 , C07D403/14 , C07D413/12 , C07D487/10 , C07D401/06
CPC分类号: C07D487/10 , C07D213/50 , C07D401/06 , C07D401/08 , C07D401/12 , C07D401/14 , C07D403/06 , C07D403/12 , C07D403/14 , C07D405/14 , C07D413/12
摘要: The invention generally relates to nuclear transport modulators, e.g CRM1 inhibitors, and more particularly to a compound represented by formula (I): or a pharmaceutically acceptable salt thereof, wherein the variables are as defined and described herein. The invention also includes the synthesis and use of a compound of structural formula (I), or a pharmaceutically acceptable salt or composition thereof, e.g, in the treatment, modulation and/or prevention of physiological conditions associated with CRM1 activity.
摘要翻译: 本发明通常涉及核转运调节剂,例如CRM1抑制剂,更具体地涉及由式(I)表示的化合物或其药学上可接受的盐,其中变量如本文所定义和描述。 本发明还包括结构式(I)化合物或其药学上可接受的盐或组合物的合成和用途,例如用于治疗,调节和/或预防与CRM1活性相关的生理条件。
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