This invention provides pyridopyrimidines and 4-aminopyrimidines that are useful for treating cell proliferatives disorders, such as cancer and restenosis. We have now discovered a group of 7,8-dihydro-2 (amino and thio)pyrido[2,3-d]pyrimidines and 2,4-diaminopyrimidines that are potent inhibitors of cyclin-dependent kinases (cdks) and growth factor-mediated kinases. The compounds are readily synthesized and can be administered by a variety of routes, including orally, and have sufficient bioavailability. This invention provides compounds of Formula (I) and Formula (II) where W is NH, S, SO, or SO
2
, R
1
includes phenyl and substituted phenyl, R
2
includes alkyl and cycloalkyl, R
3
includes alkyl and hydrogen, R
8
and R
9
include hydrogen and alkyl, and Z is carboxy. This invention also provide pharmaceutical formulations comprising a compound of Formula (I or II) together with a pharmaceutically acceptable carrier, diluent, or excipient therefor.
1
这项发明提供了对治疗细胞增殖性疾病(如癌症和再狭窄)有用的
吡啶吡嘧啶和4-
氨基
吡嘧啶。我们现在发现了一组7,8-二
氢-2(
氨基和
硫)
吡啶嘧啶和
2,4-二
氨基
吡嘧啶,它们是细胞周期依赖性激酶(cdk)和生长因子介导的激酶的有效
抑制剂。这些化合物易于合成,并且可以通过多种途径(包括口服)给药,具有足够的
生物利用度。该发明提供了式(I)和式(II)的化合物,其中W为NH、S、SO或SO2,R1包括
苯基和取代
苯基,R2包括烷基和
环烷基,R3包括烷基和
氢,R8和R9包括
氢和烷基,Z为羧基。该发明还提供了含有式(I或II)化合物的制剂,与其一起使用的药用可接受载体、稀释剂或赋形剂。