Jagu Elodie, Pomel Sébastien, Diez-Martinez Alba, Rascol Estelle, Pethe Stéphanie, Loiseau Philippe M, Labruère Raphaël
Institut de Chimie Moléculaire et des Matériaux d'Orsay (ICMMO), CNRS, Univ Paris Sud, Université Paris-Saclay, 15 rue Georges Clemenceau, 91405 Orsay Cedex, France.
Chimiothérapie antiparasitaire, UMR 8076 BioCis, CNRS, Univ Paris Sud, Université Paris-Saclay, 5 rue Jean-Baptiste Clément, 92290 Châtenay-Malabry, France.
Eur J Med Chem. 2018 Apr 25;150:655-666. doi: 10.1016/j.ejmech.2018.02.087. Epub 2018 Mar 6.
This study describes the synthesis and the biological evaluation of twenty-four original bis(benzyl)spermidines. Structural modifications of the polyamine scaffold were performed in order to avoid easily metabolized bonds. Some bis(benzyl)polyamine derivatives have demonstrated promising activity in vitro against Trypanosoma brucei gambiense and Leishmania donovani. From the enzymatic experiments on trypanothione reductase, we observed that this enzyme was not targeted by our compounds. In vivo evaluation on Swiss mice model infected by T. b. gambiense or L. donovani was done with the most interesting compound of the series.
本研究描述了24种新型双(苄基)亚精胺的合成及生物学评价。对多胺骨架进行结构修饰以避免易代谢的键。一些双(苄基)多胺衍生物在体外对布氏冈比亚锥虫和杜氏利什曼原虫表现出有前景的活性。从对锥虫硫醇还原酶的酶学实验中,我们观察到该酶不是我们化合物的作用靶点。用该系列中最具活性的化合物对感染布氏冈比亚锥虫或杜氏利什曼原虫的瑞士小鼠模型进行了体内评价。