| Literature DB >> 22138896 |
Bruno Demoro1, Cynthia Sarniguet, Roberto Sánchez-Delgado, Miriam Rossi, Daniel Liebowitz, Francesco Caruso, Claudio Olea-Azar, Virtudes Moreno, Andrea Medeiros, Marcelo A Comini, Lucía Otero, Dinorah Gambino.
Abstract
In the search for new therapeutic tools against neglected diseases produced by trypanosomatid parasites, and particularly against African Trypanosomiasis, whose etiological agent is Trypanosoma brucei, organoruthenium compounds with bioactive nitrofuran containing thiosemicarbazones (L) as co-ligands were obtained. Four ruthenium(II) complexes with the formula [Ru(2)(p-cymene)(2)(L)(2)]X(2), where X = Cl or PF(6), were synthesized and the crystal structures of two of them were solved by X-ray diffraction methods. Two of the complexes show significant in vitro growth inhibition activity against Trypanosoma brucei brucei and are highly selective towards trypanosomal cells with respect to mammalian cells (J774 murine macrophages). These promising results make the title organoruthenium compounds good lead candidates for further developments towards potential antitrypanosomal organometallic drugs.Entities:
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Year: 2011 PMID: 22138896 PMCID: PMC3299570 DOI: 10.1039/c1dt11519g
Source DB: PubMed Journal: Dalton Trans ISSN: 1477-9226 Impact factor: 4.390