
ABSTRACT 2-(2″-Dichloroacetamidobenzyl)-3-(3′-indolylquinoline), designated indolylquinoline derivative A, reduced the splenic and the liver parasite burdens by >93.0% in Leishmania donovani -infected hamsters, whereas sodium antimony gluconate (SAG) reduced the burdens approximately 80.0%. Complete clearance of parasitemia from the livers and spleens was noticed when infected animals received indolylquinoline derivative A plus SAG, suggesting that indolylquinoline derivative A has potential as a new agent for sole or conjunctive therapy for leishmaniasis.
Disease Models, Animal, Indoles, Treatment Outcome, Antimony Sodium Gluconate, Cricetinae, Antiprotozoal Agents, Quinolines, Animals, Leishmaniasis, Visceral, Drug Therapy, Combination
Disease Models, Animal, Indoles, Treatment Outcome, Antimony Sodium Gluconate, Cricetinae, Antiprotozoal Agents, Quinolines, Animals, Leishmaniasis, Visceral, Drug Therapy, Combination
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