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J Pharm Pharmacol ; 61(2): 257-66, 2009 Feb.
Artículo en Inglés | MEDLINE | ID: mdl-19178775

RESUMEN

OBJECTIVES: The known anti-protozoal activity of flavonoids has stimulated the testing of other derivatives from natural and synthetic sources. METHODS: As part of our efforts to find potential lead compounds, a number of flavonoids isolated from Neoraputia paraensis, N. magnifica, Murraya paniculata, (Rutaceae), Lonchocarpus montanus, L. latifolius, L. subglaucescens, L. atropurpureus, L. campestris, Deguelia hatschbachii (Leguminosae), dibenzoylmethanes from L. subglaucescens and synthetic analogues were tested for in-vitro activity against chloroquine-sensitive Plasmodium falciparum and Trypanosoma brucei rhodesiense bloodstream form trypomastigotes. An assay with KB cells has been developed in order to compare in-vitro cytotoxicity of flavonoids with a selective action on the parasites. KEY FINDINGS: Thirteen of the compounds tested had IC50 values ranging from 4.6 to 9.9 microm against T. brucei rhodesiense. In contrast, a small number of compounds showed significant activity against P. falciparum; seven of those tested had IC50 values ranging from 2.7 to 9.5 microm. Among the flavones only one had IC50 < 10 microm (7.6 microm), whereas against T. brucei rhodesiense seven had IC50 < 10 microm. Synthetic dibenzoylmethanes were the most active in terms of number (five) of compounds and the IC50 values (2.7-9.5 microm) against P. falciparum. CONCLUSIONS: Dibenzoylmethanes represent a novel class of compounds tested for the first time as antimalarial and trypanocidal agents.


Asunto(s)
Antimaláricos/uso terapéutico , Descubrimiento de Drogas , Flavonoides/química , Tripanocidas/uso terapéutico , Animales , Antimaláricos/química , Antimaláricos/aislamiento & purificación , Antimaláricos/toxicidad , Chalconas/química , Chalconas/uso terapéutico , Chalconas/toxicidad , Chalonas/química , Chalonas/uso terapéutico , Chalonas/toxicidad , Química Farmacéutica/métodos , Química Farmacéutica/tendencias , Fabaceae/química , Flavonoides/aislamiento & purificación , Flavonoides/uso terapéutico , Humanos , Concentración 50 Inhibidora , Células KB , Estructura Molecular , Plasmodium falciparum/efectos de los fármacos , Rutaceae/química , Tripanocidas/química , Tripanocidas/aislamiento & purificación , Tripanocidas/toxicidad , Trypanosoma brucei rhodesiense/efectos de los fármacos
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