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Bioorg Med Chem Lett ; 22(4): 1712-5, 2012 Feb 15.
Article in English | MEDLINE | ID: mdl-22248858

ABSTRACT

A series of 25 N,N'-substituted diamines were prepared by controlled reductive amination of free aliphatic diamines with different substituted benzaldehydes. The library was screened in vitro for antiparasitic activity on the causative agents of human African trypanosomiasis, Chagas' disease and visceral leishmaniasis. The most potent compounds were derived from a subset of diamines that contained a 4-OBn substitution, having a 50% parasite growth inhibition in the submicromolar (against Trypanosoma cruzi) or nanomolar (against Trypanosoma brucei and Leishmania donovani) range. We conclude that members of this series of N,N'-substituted diamines provide new lead structures that have potential to treat trypanosomal and leishmanial infections.


Subject(s)
Antiprotozoal Agents/chemical synthesis , Antiprotozoal Agents/pharmacology , Diamines/chemical synthesis , Diamines/pharmacology , Kinetoplastida/drug effects , Animals , Chagas Disease/drug therapy , Diamines/chemistry , Humans , Inhibitory Concentration 50 , Leishmaniasis, Visceral/drug therapy , Molecular Structure , Small Molecule Libraries/chemical synthesis , Small Molecule Libraries/chemistry , Small Molecule Libraries/pharmacology , Trypanosomiasis, African/drug therapy
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