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公开(公告)号:US07741324B2
公开(公告)日:2010-06-22
申请号:US11185599
申请日:2005-07-20
IPC分类号: C07D487/04 , C07D487/12 , A61K31/53 , A61K35/00
CPC分类号: C07D487/04
摘要: Compounds of the formula and pharmaceuticaly acceptable salts thereof, wherein Q1 and R1 are defined herein, inhibit the IGF-1R enzyme and are useful for the treatment and/or prevention of various diseases and conditions that respond to treatment by inhibition of tyrosine kinases.
摘要翻译: 其中Q1和R1在本文中定义的式及其药学上可接受的盐的化合物抑制IGF-1R酶,并且可用于治疗和/或预防通过抑制酪氨酸激酶对治疗作出反应的各种疾病和病症。
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公开(公告)号:US20110281888A1
公开(公告)日:2011-11-17
申请号:US13108024
申请日:2011-05-16
申请人: Mark J. Mulvihill , Amo G. Steinig , Andrew Philip Crew , Meizhong Jin , Andrew Kleinberg , An-Hu Li , Jing Wang
发明人: Mark J. Mulvihill , Amo G. Steinig , Andrew Philip Crew , Meizhong Jin , Andrew Kleinberg , An-Hu Li , Jing Wang
IPC分类号: A61K31/497 , A61P35/00 , A61K31/437 , C07D471/04 , C07D401/14
CPC分类号: C07D471/04
摘要: Compounds of Formula I, as shown below and defined herein: pharmaceutically acceptable salts thereof, synthesis, intermediates, formulations, and methods of disease treatment therewith, including treatment of cancers, such as tumors driven at least in part by at least one of RON, MET or ALK. This Abstract is not limiting of the invention.
摘要翻译: 式I化合物,如下文所示和定义:其药学上可接受的盐,合成,中间体,制剂及其治疗方法,包括治疗癌症,例如至少部分地通过至少一种RON, MET或ALK。 本发明并不限于本发明。
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公开(公告)号:US07659274B2
公开(公告)日:2010-02-09
申请号:US11657156
申请日:2007-01-24
IPC分类号: A61K31/4985
CPC分类号: C07D487/04
摘要: Compounds represented by Formula (I) or a pharmaceutically acceptable salt thereof, are inhibitors of mTOR and useful in the treatment of cancer.
摘要翻译: 由式(I)表示的化合物或其药学上可接受的盐是mTOR的抑制剂,可用于治疗癌症。
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