Computational Studies on the Histone Deacetylases and the Design of Selective Histone Deacetylase Inhibitors

被引:46
|
作者
Wang, Difei [1 ]
机构
[1] NCI, Cell Biol Lab, NIH, Bethesda, MD 20892 USA
关键词
SMALL-MOLECULE INHIBITOR; 2 CATALYTIC DOMAINS; CRYSTAL-STRUCTURE; ZINC-BINDING; STRUCTURAL BASIS; HDAC INHIBITORS; BIOLOGICAL EVALUATION; PROTEIN DEACETYLASE; SUBSTRATE-BINDING; HYDROXAMIC ACIDS;
D O I
10.2174/156802609788085287
中图分类号
R914 [药物化学];
学科分类号
100701 ;
摘要
The catalytic activity of the histone deacetylase ( HDAC) enzymes is directly relevant to the pathogenesis of cancer as well as several other diseases. HDAC inhibitors have been shown to have the potential to treat several types of cancers. The role of computational study of the HDAC enzymes is reviewed, with particular emphasis on the important role of molecular modeling to the development of HDAC inhibitors with improved efficacy and selectivity. The use of two computational approaches - one structure-based, and the second ligand-based - toward inhibitors against the different HDAC sub-classes, are summarized.
引用
收藏
页码:241 / 256
页数:16
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