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开发选择性组蛋白去乙酰化酶 3 抑制剂的过程和策略。

The Process and Strategy for Developing Selective Histone Deacetylase 3 Inhibitors.

机构信息

Chemical and Pharmaceutical Biology, Groningen Research Institute of Pharmacy, University of Groningen, 9713AV Groningen, The Netherlands.

出版信息

Molecules. 2018 Mar 2;23(3):551. doi: 10.3390/molecules23030551.

Abstract

Histone deacetylases (HDACs) are epigenetic drug targets that have gained major scientific attention. Inhibition of these important regulatory enzymes is used to treat cancer, and has the potential to treat a host of other diseases. However, currently marketed HDAC inhibitors lack selectivity for the various HDAC isoenzymes. Several studies have shown that HDAC3, in particular, plays an important role in inflammation and degenerative neurological diseases, but the development of selective HDAC3 inhibitors has been challenging. This review provides an up-to-date overview of selective HDAC3 inhibitors, and aims to support the development of novel HDAC3 inhibitors in the future.

摘要

组蛋白去乙酰化酶(HDACs)是表观遗传药物靶点,受到了极大的科学关注。抑制这些重要的调节酶被用于治疗癌症,并有可能治疗许多其他疾病。然而,目前市场上的 HDAC 抑制剂对各种 HDAC 同工酶缺乏选择性。多项研究表明,HDAC3 尤其在炎症和退行性神经疾病中发挥着重要作用,但选择性 HDAC3 抑制剂的开发一直具有挑战性。本综述提供了选择性 HDAC3 抑制剂的最新概述,并旨在为未来新型 HDAC3 抑制剂的开发提供支持。

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