发明申请
- 专利标题: Pyrazole Derivatives for the Inhibition of CDK'S and GSK'S
- 专利标题(中): 吡唑衍生物抑制CDK和GSK'S
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申请号: US11814443申请日: 2006-01-20
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公开(公告)号: US20080306069A1公开(公告)日: 2008-12-11
- 发明人: Paul Graham Wyatt , Valerio Berdini , Adrian Liam Gill , Gary Trewartha , Andrew James Woodhead , Eva Figueroa Navarro , Michael Alistair O'Brien , Theresa Rachael Phillips
- 申请人: Paul Graham Wyatt , Valerio Berdini , Adrian Liam Gill , Gary Trewartha , Andrew James Woodhead , Eva Figueroa Navarro , Michael Alistair O'Brien , Theresa Rachael Phillips
- 申请人地址: UK Cambridge
- 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 Cambridge
- 优先权: GB0501480.8 20050122; GB0501748.8 20050127
- 国际申请: PCT/GB2006/000191 WO 20060120
- 主分类号: A61K31/415
- IPC分类号: A61K31/415 ; A61P35/00 ; C07D401/12 ; C07D401/14 ; C07D413/14 ; A61K31/4439 ; C07D231/38 ; A61K31/454 ; A61K31/4545 ; A61K31/5377
摘要:
The invention provides compounds of the formula (I), or salts, tautomers, N-oxides or solvates thereof wherein: R1 is selected from: (a) 2,6-dichlorophenyl; (b) 2,6-difluorophenyl; (c) a 2,3,6-trisubstituted phenyl group wherein the substituents for the phenyl group are selected from fluorine, chlorine, methyl and methoxy; (d) a group RO; (e) a group R a; (f) a group RIb; (g) a group RIc; (h) a group RId; and 0) 2,6-difluorophenylamino; wherein R) 0υ, r R>llaa, T Rj HbD, T R) HcC, r R>Iidα, r R>>2zaa, r R>22bD and RJ are as defined in the claims. The compounds have activity as inhibitors of cdk kinase (such as cdk1 or cdk2) and glycogen synthase kinase-3 activity.
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