ChemMedChem · 2026
Synthesis, Antiparasitic Activity, and ADME Profile of Morpholinephenylbenzamides: A Pharmacological Study Against Chagas Disease and Visceral Leishmaniasis.
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Farago Danilo Nascimento, de Melo Resende Daniela, de Moura Lodi Cruz Mariza Gabriela Faleiro, Sousa Rafaela Marçal, Chelucci Rafael Consolin, Michelan-Duarte Simone, da Silva Mendonça de Melo Felipe, da Silva Oliveira Douglas Davison, Macruz Paula Derksen, Dos Santos Carvalho Alexandra Maria, Pilau Eduardo Jorge, Bastos Izabela Marques Dourado, Andricopulo Adriano D, Ferreira Leonardo L G, Murta Silvane Maria Fonseca, de Oliveira Rezende Júnior Celso
Аннотация
Chagas disease and leishmaniasis are neglected tropical diseases with limited treatment options. This study reports a hit-to-lead optimization of morpholinephenylbenzamides, starting from hit 1, which showed potent activity against Trypanosoma cruzi (IC50 0.29-0.76 μM) and Leishmania infantum (IC50 10.7 μM), despite a suboptimal ADME profile. A structure-activity relationship study of twenty-four novel derivatives provided key pharmacophoric insights. While Trypanosoma cruzi was less susceptible to chemical modifications, compound 20 exhibited potency comparable to benznidazole (IC50 3.58 μM) with significantly improved selectivity, lipophilicity, and solubility relative to compound 1. Against Leishmania infantum, six derivatives maintained activity, with compound 24 showing a 1.5-fold potency increase IC50 7.6 μM). Additionally, compound 16 stood out for its superior ADME profile, including enhanced permeability and metabolic stability. These findings validate the morpholinephenylbenzamide scaffold as a robust class with dual antiparasitic activity.