发明名称 PYRAZOLE DERIVATIVES FOR THE INHIBITION OF CDK'S AND GSK'S
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 R0; (e) a group R a; (f) a group Rlb; (g) a group Rlc; (h) a group Rld; and 0) 2,6-difluorophenylamino ; wherein R)0e, r R> llaa, T Rj I1bD, T R) I1cC, r R> IidE, 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 cdkl or cdk2) and glycogen synthase kinase-3 activity.
申请公布号 KR20070098928(A) 申请公布日期 2007.10.05
申请号 KR20077018917 申请日期 2007.08.17
申请人 ASTEX THERAPEUTICS LIMITED 发明人 WYATT PAUL GRAHAM;BERDINI VALERIO;GILL ADRIAN LIAM;TREWARTHA GARY;WOODHEAD ANDREW JAMES;NAVARRO EVA FIGUEROA;O'BRIEN MICHAEL ALISTAIR;PHILLIPS THERESA RACHEL
分类号 C07D231/40;A61K31/415;A61P35/00 主分类号 C07D231/40
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