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SELECTIVE INHIBITORS OF HISTONE DEACETYLASE ISOFORM 6 AND METHODS THEREOF

机译:组氨酸去乙酰化异构体6的选择性抑制剂及其方法

摘要

The described invention provides histone deacetylase (HDAC) inhibitor compounds with substituted benzimidazole, benzimidazolone and benzotriazole heterocycles showing selective inhibition of histone deacetylase isoform HDAC6. The described invention further provides methods of making such compounds and methods of inhibiting HDAC, treating HDAC- associated diseases, including cell proliferative disorders, such as cancer, autoimmune or inflammatory diseases and neurodegenerative diseases.
机译:所描述的发明提供了具有取代的苯并咪唑,苯并咪唑酮和苯并三唑杂环的组蛋白脱乙酰基酶(HDAC)抑制剂化合物,其显示出对组蛋白脱乙酰基酶同工型HDAC6的选择性抑制。所描述的发明进一步提供了制备此类化合物的方法和抑制HDAC,治疗与HDAC相关的疾病的方法,所述疾病包括细胞增殖性疾病,例如癌症,自身免疫或炎性疾病和神经退行性疾病。

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