化学
事后诸葛亮
组蛋白脱乙酰基酶
癌症化疗
组蛋白脱乙酰酶抑制剂
组蛋白
药理学
癌症研究
癌症
内科学
生物化学
心理学
医学
基因
认知心理学
作者
Terence C. S. Ho,Alex H. Y. Chan,A. Ganesan
标识
DOI:10.1021/acs.jmedchem.0c00830
摘要
It is now 30 years since the first report of a potent zinc-dependent histone deacetylase (HDAC) inhibitor appeared. Since then, five HDAC inhibitors have received regulatory approval for cancer chemotherapy while many others are in clinical development for oncology as well as other therapeutic indications. This Perspective reviews the biological and medicinal chemistry advances over the past 3 decades with an emphasis on the design of selective inhibitors that discriminate between the 11 human HDAC isoforms.
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