Antileishmanial 2-substituted quinolines:: In vitro behaviour towards biological components

被引:25
作者
Desrivot, Julie
Herrenknecht, Christine
Ponchel, Gilles
Garbi, Najla
Prina, Eric
Fournet, Alain
Bories, Christian
Figadere, Bruno
Hocquemiller, Reynald
Loiseau, Philippe M.
机构
[1] Univ Paris 11, BioCIS UMR 8076, Ctr Etud Pharmaceut, Lab Pharmacognosie & Chimiotherapie Antiparasitai, F-92290 Chatenay Malabry, France
[2] Univ Paris 11, CNRS, UMR 8612,Ctr Etud Pharmaceut, Lab Pharmacotech & Biopharm, F-92290 Chatenay Malabry, France
[3] Inst Pasteur, Unite Immunophysiol & Parasitisme Intracellulaire, F-75724 Paris 15, France
[4] Univ Paris 11, IRD US 084, Ctr Etud Pharmaceut, Lab Pharmacognosie, F-92290 Chatenay Malabry, France
关键词
2-Substituted quinolines; in vitro interaction;
D O I
10.1016/j.biopha.2007.03.004
中图分类号
R-3 [医学研究方法]; R3 [基础医学];
学科分类号
1001 ;
摘要
Quinolines substituted on their carbon 2 have in vivo antileishmanial activity but some of them could not be detected in plasma when assayed for pharmacokinetic studies, suggesting a sequestration of the drugs by components of the blood compartment. The present study, performed on three quinolines (1, 2 and 3), showed strong affinity for two of them (2 and 3) with red blood cells (RBCs), whereas quinoline 1 did not react with them. This process was saturable, temperature dependant and positively correlated with the in vitro antileishmanial activity, of the quinolines. In addition, a rapid and spontaneous reaction with thiol groups was demonstrated for unsaturated quinolines 2 and 3. The reactivity with RBCs could be part of the compounds targeting to the parasite. These results illustrate that derivatives of the quinoline series with similar antileishmanial in vivo activity have different behaviour in. the blood compartment. (c) 2007 Elsevier Masson SAS. All rights reserved.
引用
收藏
页码:441 / 450
页数:10
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