This invention relates to substituted thiazolylaminotetrahydropyridopyrimidines derivatives of the following general formula, the substituent groups of which are as defined in the specification herein: ##STR1## These compounds are useful as inhibitors of platelet aggregation and inhibitors of adhesion molecules and may be provided in pharmaceutical compositions and in methods of treating reperfusion thrombosis injury in patients.
本发明涉及以下一般公式的取代
噻唑基
氨基
四氢吡咯二
嘧啶衍
生物,其中取代基团如本说明书中所定义: ##STR1## 这些化合物可用作血小板聚集
抑制剂和粘附分子
抑制剂,并可在治疗患者的再灌注血栓形成损伤的方法和制药组合物中提供。