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).
本发明提供的芳基磺酰胺二芳基
脲衍
生物化合物是突变型
异柠檬酸脱氢酶 1/2(IDH 1/2)的
抑制剂,可用于治疗癌症。还提供了治疗癌症的方法,包括向有需要的受试者施用本文所述的化合物。本发明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、急性骨髓性白血病、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)。