Modifications of the chemical structure of terpenes in antiplasmodial and antifungal drug research

被引:37
|
作者
Olagnier, David
Costes, Philippe
Berry, Antoine
Linas, Marie-Denise
Urrutigoity, Martine
Dechy-Cabaret, Odile
Benoit-Vical, Francoise [1 ]
机构
[1] CHU Rangueil, Serv Parasitol Mycol, TSA 50032, F-31059 Toulouse, France
[2] CNRS, Lab Chim Coordinat, ENSIACET, F-31077 Toulouse, France
[3] CNRS, Lab Chim Coordinat, F-31077 Toulouse, France
关键词
monoterpenes; Plasmodium; Candida; bioactive products and chemistry;
D O I
10.1016/j.bmcl.2007.09.056
中图分类号
R914 [药物化学];
学科分类号
100701 ;
摘要
Pure natural monoterpenes were evaluated in vitro for their antiplasmodial activities against Plasmodium falciparum. Chemically modified terpenes were also tested to see whether the introduction of an alkyne, a cyclopropane, a diene, or a cyclopentenone moiety had an influence on the biological activity. The IC50 obtained on a chloroquine-resistant strain of Plasmodium (FcM29-Cameroon) showed moderate activity, but with the alkyne and the cyclopentenone derivatives showing a promising enhancement of activity compared with the parent molecules. On the contrary, no antifungal activity was found in vitro using Candida albicans. Given the observed antiplasmodial activity of some of these modified monoterpenes, new monoterpene derivatives could be the basis for new antimalarial drugs to be researched. (C) 2007 Elsevier Ltd. All rights reserved.
引用
收藏
页码:6075 / 6078
页数:4
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