Provided are aryl sulfonamide diarylurea derivative compounds that are inhibitors of mutant isocitrate dehydrogenase 1/2 (IDH 1/2), useful for treating cancer. Also provided are methods of treating cancer comprising administering to a subject in need thereof a compound described herein. Cancers that are treatable by the compounds of the invention are glioblastoma, myelodysplastic syndrome, myeloproliferative neoplasm, acute myelogenous leukemia, sarcoma, melanoma, non-small cell lung cancer, chondrosarcoma, and non-Hodgkin's lymphoma (NHL).
提供的是芳基磺
酰胺二芳基
脲衍
生物化合物,它们是突变
异柠檬酸脱氢酶1/2(IDH1/2)的
抑制剂,用于治疗癌症。还提供了一种治疗癌症的方法,包括向需要治疗的受试者投与本文所述的化合物。本发明的化合物可治疗的癌症包括胶质母细胞瘤、骨髓增生异常综合征、骨髓增生性肿瘤、急性髓系白血病、肉瘤、
黑色素瘤、非小细胞肺癌、软骨肉瘤和非霍奇
金淋巴瘤(NHL)。