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. The compounds are inhibitors of isocitrate dehydrogenase 2 (IDH2) mutants useful for treating cancer.
提供的是化合物的结构式(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。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。