Synthesis and biological activity of diaryl ether inhibitors of malarial enoyl acyl carrier protein reductase.: Part 2:: 2′-substituted triclosan derivatives

被引:57
作者
Freundlich, JS
Yu, M
Lucumi, E
Kuo, M
Tsai, HC
Valderramos, JC
Karagyozov, L
Jacobs, WR
Schiehser, GA
Fidock, DA
Jacobus, DP
Sacchettini, JC
机构
[1] Jacobus Pharmaceut Co, Dept Med Chem, Princeton, NJ 08540 USA
[2] Yeshiva Univ Albert Einstein Coll Med, Dept Microbiol & Immunol, Bronx, NY 10461 USA
[3] Yeshiva Univ Albert Einstein Coll Med, Howard Hughes Med Inst, Bronx, NY 10461 USA
[4] Texas A&M Univ, Dept Biochem & Biophys, College Stn, TX 77843 USA
关键词
antimalarial; diaryl ether; phenol;
D O I
10.1016/j.bmcl.2006.01.051
中图分类号
R914 [药物化学];
学科分类号
100701 ;
摘要
2'-substituted analogs of triclosan have been synthesized to target inhibition of the key malarial enzyme Plasmodium falciparum enoyl acyl carrier protein reductase (PfENR). Many of these compounds exhibit good potency (EC50<500 nM) against in vitro cultures of drug-resistant and drug-sensitive strains of the P. falciparum parasite and modest (I-50=1-20 mu M) potency against purified PfENR enzyme. Compared to triclosan, this survey of 2'-substituted derivatives has afforded gains in excess of 20- and 30-fold versus the 3D7 and Dd2 strains of parasite, respectively. (C) 2006 Elsevier Ltd. All rights reserved.
引用
收藏
页码:2163 / 2169
页数:7
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