Antileishmanial Thioureas: Synthesis, Biological Activity and in Silico Evaluations of New Promising Derivatives
Abstract
Leishmaniasis is a neglected tropical disease caused by protozoan parasites belonging to the genus Leishmania.Currently, the drugs available for treatment of this disease present high toxicity, along with development of parasite resistance.In order to overcome these problems, efforts have been made to search for new and more effective leishmanicidal drugs.The aim of this study was to synthesize and investigate the leishmanicidal effect of N,N′-disubstituted thioureas against Leishmania amazonensis, with evaluation of their in silico pharmacokinetics and toxicity profiles.Our results showed that different thioureas could be obtained in high to moderate yields using simple reaction conditions.Nine thiourea derivatives (3e, 3i, 3k, 3l, 3p, 3q, 3v, 3x and 3z) were active against parasite promastigotes (IC 50 21.48-189.10µM), with low cytotoxicity on mice peritoneal macrophages (CC 50 >200 µM), except for thiourea 3e (CC 50 =49.22µM).After that, the most promising thioureas (3k, 3l, 3p, 3q and 3v) showed IC 50 ranging from 70 to 150 µM against L. amazonensis amastigotes in infected macrophages.Except for thiourea 3p, the leishmanicidal activity of the derivatives were independent of nitric oxide (NO) production.Thioureas 3q and 3v affected promastigotes cell cycle without disturbing the mitochondrial membrane potential.Furthermore, our derivatives showed satisfactory theoretical absorption, distribution, metabolism, excretion, toxicity (ADMET) properties.These data indicate that…
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