PHARMACEUTICAL COMPOUNDS
    8.
    发明申请
    PHARMACEUTICAL COMPOUNDS 审中-公开
    药物化合物

    公开(公告)号:US20100004243A1

    公开(公告)日:2010-01-07

    申请号:US12373659

    申请日:2007-07-13

    摘要: The invention provides a cyclin dependent kinase (e.g. cdk-4 kinase) inhibitor of the formula (I) or a salt, tautomer, solvate or N-oxide thereof; wherein R1 is an optionally substituted monocyclic or bicyclic aryl or heteroaryl group containing 0-2 heteroatoms selected from O, N and S wherein the optional substituents are selected from halogen, C1-4 alkyl, C1-4 alkoxy, C3-4 cycloalkyl and cyano, and wherein the C1-4 alkyl and C1-4 alkoxy groups are each optionally further substituted by C1-2 alkoxy or one or more halogen atoms; and E is a group E1, E2, E3 or E4: formulae E1, E2, E3, E4 wherein n, q, A5 B, T, U, V, W, Z, R2, R5, R6 and R7 are as defined in the claims.

    摘要翻译: 本发明提供了式(I)的细胞周期蛋白依赖性激酶(例如cdk-4激酶)抑制剂或其盐,互变异构体,溶剂合物或N-氧化物; 其中R 1是含有0-2个选自O,N和S的杂原子的任选取代的单环或双环芳基或杂芳基,其中任选的取代基选自卤素,C 1-4烷基,C 1-4烷氧基,C 3-4环烷基和氰基 并且其中所述C 1-4烷基和C 1-4烷氧基各自任选进一步被C 1-2烷氧基或一个或多个卤素原子取代; 并且E是E1,E2,E3或E4基团:式E1,E2,E3,E4其中n,q,A5B,T,U,V,W,Z,R2,R5,R6和R7如 索赔。