The present invention discloses compounds of formula (I);(I);Wherein, R 2, R 7, R 13, R 14 and R 15 are independently hydrogen, (un) substituted lower alkyl, (un) alkenyl substituted lower alkenyl, (un) substituted lower alkynyl, or (un) substituted - (CH 2 ) n R 12 ; R 5 is halogen, cyano, nitro, -R 9 , -NR 9 R 10 or -OR 9 ; R 6 is halogen, cyano, nitro, -R 9, -NR 9 R 1O , -OR 9, -C0 2 R 9, -COR 9, -CONR 9 R 10, -NR 9 COR 10, ( de) substituted Lower alkenyl or (un) substituted lower alkynyl; R 8 is -CO 2 R 13, -COR 13, -CONR 13 R l4, -CSNR l3 R l4, -C (NR 13) NR l4 R l5, -S0 3 R 13, -SO 2 R 13, -S0 2 NR 13 R 14 , -PO 3 R 13 R 14 , -POR 13 R 14, or -PO (NR 13 R 14 ) 2 ; R 9 and R 10 are independently hydrogen or (un) substituted lower alkyl; R 11 is a heteroaryl group or a heterocyclic group; R 12 is a cycloalkyl group, a heterocyclic group, an aryl group or a heteroaryl group; n is 0, 1, 2 or 3;;These compounds and pharmaceutical compositions thereof are useful for the treatment of cell proliferative diseases such as cancer and restenosis. These compounds are potent inhibitors of cdk and growth factor-mediated kinase.
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机译:本发明公开了式(I);(I)的化合物,其中,R 2, Sup> R 7, Sup> R 13, Sup> R 14 Sup>和R 15 Sup>独立地为氢,(un)取代的低级烷基,(un)烯基取代的低级烯基,(un)取代的低级炔基或(un)取代的-(CH 2 Sub>) n Sub> R 12 Sup>; R 5 Sup>是卤素,氰基,硝基,-R 9 Sup>,-NR 9 Sup> R 10 Sup>或-OR < Sup> 9 Sup>; R 6 Sup>是卤素,氰基,硝基,-R 9--NR 9 R 1O Sup>,-OR 9--C0 2 R 9--COR 9--CONR 9 R 10,-NR 9 COR 10,(de)取代的低级烯基或(un)取代的低级炔基; R 8 Sup>是 -CO 2 R 13,-COR 13, Sup> Sub> -CONR 13 R l4,-CSNR l3 R l4,-C(NR 13)NR l4 R l5,-S0 3 R 13,-SO 2 R 13,-S0 2 Sub> NR 13 Sup> R 14 Sup>,-PO 3 Sub> R 13 Sup> R 14 Sup>,-POR 13 Sup> R 14, Sup>或-PO (NR 13 Sup> R 14 Sup>) 2 Sub>; R 9 Sup>和R 10 Sup>独立地是氢或(未)取代的低级烷基; R 11 Sup>为杂芳基或杂环基。 R 12 Sup>为环烷基,杂环基,芳基或杂芳基; n为0、1、2或3;这些化合物及其药物组合物可用于治疗细胞增生性疾病,例如癌症和再狭窄。这些化合物是cdk和生长因子介导的激酶的有效抑制剂。
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