The present invention is directed to substituted 5-trifluoromethyl oxadiazole compounds of generic formula (I) (I) or a pharmaceutically acceptable salt thereof. In particular, the invention is directed to a class of aryl and heteroaryl substituted 5-trifluoromethyl oxadiazole compounds of formula I which may be useful as HDAC6 inhibitors for treating cellular proliferative diseases, including cancer, neurodegenerative diseases, such as schizophrenia and stroke, as well as other diseases.
本发明涉及通式(I)(I)的取代5-三
氟甲基
噁唑化合物或其药学上可接受的盐。特别地,本发明涉及一类芳基和杂环芳基取代的式I的5-三
氟甲基
噁唑化合物,可用作H
DAC6
抑制剂,用于治疗细胞增殖性疾病,包括癌症、神经退行性疾病,如精神分裂症和中风,以及其他疾病。