Aminosuberoyl hydroxamic acids (ASHAs): A potent new class of HDAC inhibitors

被引:32
作者
Belvedere, Sandro
Witter, David J.
Yan, Jiaming
Secrist, J. Paul
Richon, Victoria
Miller, Thomas A.
机构
[1] Merck Res Labs, Dept Drug Design & Optimizat, Boston, MA 02115 USA
[2] Merck Res Labs, Dept Canc & Biol Therapeut, Boston, MA 02115 USA
[3] ARMGO Pharma Inc, New York, NY 10032 USA
关键词
HDAC; histone deacetylase inhibitor; HDAC inhibitor; anticancer drug; SAHA; hydroxamic acids;
D O I
10.1016/j.bmcl.2007.04.089
中图分类号
R914 [药物化学];
学科分类号
100701 ;
摘要
Histone deacetylase (HDAC) inhibitors that target Class I and Class II HDACs are currently in advanced clinical trials for the treatment of cancer. Vorinostat (Zolinza (TM), SAHA) is a hydroxamic acid approved for the treatment of patients with cutaneous T-cell lymphoma who have progressive, persistent or recurrent disease on or following two systemic therapies. As part of an on-going effort to better understand the nature of the HDAC enzyme/inhibitor interaction and design highly effective HDAC inhibitors, we herein report the design, synthesis and HDAC inhibitory activity of a vorinostat-derived series of substrate-based HDAC inhibitors. (C) 2007 Elsevier Ltd. All rights reserved.
引用
收藏
页码:3969 / 3971
页数:3
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