Synthesis and structure-activity relationships of antimalarial 4-oxo-3-carboxyl quinolones

被引:37
作者
Zhang, Yiqun [1 ]
Guiguemde, W. Armand [1 ]
Sigal, Martina [1 ]
Zhu, Fangyi [1 ]
Connelly, Michele C. [1 ]
Nwaka, Solomon [2 ]
Guy, R. Kiplin [1 ]
机构
[1] St Jude Childrens Res Hosp, Dept Chem Biol & Therapeut, Memphis, TN 38105 USA
[2] WHO, Special Programme Res & Training Trop Dis, CH-1211 Geneva, Switzerland
关键词
Malaria; Quinolones; Plasmodium; Synthesis; DRUGS; INHIBITORS; WR-243251;
D O I
10.1016/j.bmc.2010.02.013
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Malaria is endemic in tropical and subtropical regions of Africa, Asia, and the Americas. The increasing prevalence of multi-drug-resistant Plasmodium falciparum drives the ongoing need for the development of new antimalarial drugs. In this light, novel scaffolds to which the parasite has not been exposed are of particular interest. Recently, workers at the Swiss Tropical Institute discovered two novel 4-oxo-3-carboxyl quinolones active against the intra-erythrocytic stages of P. falciparum while carrying out rationally directed low-throughput screening of potential antimalarial agents as part of an effort directed by the World Health Organization. Here we report the design, synthesis, and preliminary pharmacologic characterization of a series of analogues of 4-oxo-3-carboxyl quinolones. These studies indicate that the series has good potential for preclinical development. (C) 2010 Elsevier Ltd. All rights reserved.
引用
收藏
页码:2756 / 2766
页数:11
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