Provided are compounds of formula (I), wherein: ring A and ring B are each independently an optionally substituted 5-6 membered monocyclic aryl or heteroaryl; one of X, Y and W is CH and the two others are N; and Z is H or -C(R1)(R2)(R3). The compounds are inhibitors of isocitrate dehydronenase 2 (IDH2) mutants useful for treating cancer.
提供的是化合物的公式(I),其中:环A和环B分别是可选择地取代的5-6成员单环芳基或杂环芳基;X、Y和W中的一个是CH,另外两个是N;Z是H或-C(R1)(R2)(R3)。这些化合物是
异柠檬酸脱氢酶2(IDH2)突变体的
抑制剂,可用于治疗癌症。