发明申请
US20080004270A1 3,4-Disubstituted Pyrazoles as Cyclin Dependent Kinases (Cdk) or Aurora Kinase or Glycogen Synthase 3 (Gsk-3) Inhibitors
审中-公开
作为细胞周期蛋白依赖性激酶(Cdk)或极光激酶或糖原合酶3(Gsk-3)抑制剂的3,4-二取代吡唑类
- 专利标题: 3,4-Disubstituted Pyrazoles as Cyclin Dependent Kinases (Cdk) or Aurora Kinase or Glycogen Synthase 3 (Gsk-3) Inhibitors
- 专利标题(中): 作为细胞周期蛋白依赖性激酶(Cdk)或极光激酶或糖原合酶3(Gsk-3)抑制剂的3,4-二取代吡唑类
-
申请号: US11571713申请日: 2005-07-05
-
公开(公告)号: US20080004270A1公开(公告)日: 2008-01-03
- 发明人: Adrian Gill , Maria Carr , Michael O'Brien , Paul Wyatt , Valerio Berdini
- 申请人: Adrian Gill , Maria Carr , Michael O'Brien , Paul Wyatt , Valerio Berdini
- 申请人地址: UK UK Cambridge CB4 0QA
- 专利权人: ASTEX THERAPEUTICS LIMITED
- 当前专利权人: ASTEX THERAPEUTICS LIMITED
- 当前专利权人地址: UK UK Cambridge CB4 0QA
- 优先权: GB0415082.7 20040705; GB0415084.3 20040705
- 国际申请: PCT/GB05/02629 WO 20050705
- 主分类号: A61K31/5377
- IPC分类号: A61K31/5377 ; A61K31/4188 ; A61P25/28 ; A61P35/00 ; C07D235/02 ; C07D471/02 ; C07D265/34 ; A61P37/00 ; A61P31/12 ; A61K31/47
摘要:
The invention provides compounds of the formula (I); or salts or solvates or N-oxides thereof; wherein: Rq is selected from groups (a), (b) and (c); the asterisk denoting the point of attachment to the pyrazole ring; X is N or CR5; X″ is NR4; O, S or S(O); A is a bond or —(CH2)m—(B)n—; B is C═O, NRg(C═O) or O(C═O) wherein Rg is hydrogen or C1-4 hydrocarbyl optionally substituted by hydroxy or C1-4 alkoxy; m is 0, 1 or 2; n is 0 or 1; R0 is hydrogen or, together with NRg when present, forms a group —(CH2)p— wherein p is 2 to 4; and R1 to R6b are as defined in the description. Compounds of the formula (I) have activity as inhibitors of CDK, aurora and GSK-3 kinases are useful in treating or preventing diseases such as cancers that are mediated by the said kinases.
信息查询
IPC分类: