Novel 6-substituted-4(3H)-quinazolinones are described as well as methods for the preparation and pharmaceutical composition of same, which inhabit the enzyme thymidylate synthase (TS) and are thus useful as anticancer agents.
描述了一种新型的6-取代-4(3H)-
喹唑啉酮,以及其制备和药物组合物的方法,这些化合物抑制了酶
胸苷酸甲基化酶(
TS),因此可用作抗癌药物。