罗咪酯肽
组蛋白脱乙酰基酶
伏立诺他
药理学
医学
去肽
组蛋白
组蛋白脱乙酰酶抑制剂
化学
癌症研究
生物化学
基因
作者
Jagannath Behera,Venkatesan Jayaprakash,Barij Nayan Sinha
出处
期刊:Mini-reviews in Medicinal Chemistry
[Bentham Science]
日期:2015-05-25
卷期号:15 (9): 731-750
被引量:21
标识
DOI:10.2174/1389557515666150521162237
摘要
Histone Deacetylase (HDAC) is an established and validated target for the treatment of cancer. It has been attempted to present a comprehensive review on the inhibitors for Class-I Histone Deacetylase enzyme family, reported during the period from 2002 to 2012. This review has summarized the inhibitors, based on their specificity towards different isoforms within this class. Further various recent United State (US) patents and the HDAC inhibitors, used singly or in combination undergoing clinical trial as anticancer agents have been reviewed. Three such inhibitors SAHA, Romidepsin and Belinostat have already been approved by the US-FDA for the treatment of cancer.
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