发明申请
- 专利标题: SUBSTITUTED QUINAZOLINE COMPOUNDS AND METHODS OF USE THEREOF
- 专利标题(中): 取代的喹唑啉化合物及其使用方法
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申请号: PCT/US2016026573申请日: 2016-04-08
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公开(公告)号: WO2016164675A8公开(公告)日: 2017-05-11
- 发明人: LI LIANSHENG , FENG JUN , LONG YUN OLIVER , LIU YUAN , WU TAO , REN PINGDA , LIU YI
- 申请人: ARAXES PHARMA LLC
- 专利权人: ARAXES PHARMA LLC
- 当前专利权人: ARAXES PHARMA LLC
- 优先权: US201562145705 2015-04-10; US201562145818 2015-04-10; US201562255891 2015-11-16; US201562265320 2015-12-09; US201562265316 2015-12-09
- 主分类号: C07D403/12
- IPC分类号: C07D403/12 ; C07D239/74 ; C07D239/94 ; C07D239/95 ; C07D401/04 ; C07D401/12 ; C07D401/14 ; C07D403/04 ; C07D403/14 ; C07D405/12 ; C07D405/14 ; C07D409/12 ; C07D413/12 ; C07D417/04 ; C07D471/08
摘要:
Compounds having activity as inhibitors of G12C mutant KRAS protein are provided. The compounds have one of the following structures (I), (II) or (III): or a pharmaceutically acceptable salt, stereoisomer or prodrug thereof, wherein R1, R2a, R2b, R2c, R3a, R3b, R4a, R4b, R5a, R5b, R6, A, B, G1, G2, L1, L2, m1, m2, n, x, y, X and E are as defined herein. Methods associated with preparation and use of such compounds, pharmaceutical compositions comprising such compounds and methods to modulate the activity of G12C mutant KRAS protein for treatment of disorders, such as cancer, are also provided.