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Merck

Anti-leishmanial lindenane sesquiterpenes from Hedyosmum angustifolium.

Planta medica (2009-10-16)
Lucia Acebey, Valérie Jullian, Denis Sereno, Séverine Chevalley, Yannick Estevez, Claude Moulis, Stephan Beck, Alex Valentin, Alberto Gimenez, Michel Sauvain
摘要

The aim of this work is the isolation of anti-leishmanial compounds from the ethyl acetate extracts of the bark of HEDYOSMUM ANGUSTIFOLIUM. We have successfully isolated and characterized five sesquiterpenes: one new compound (oxyonoseriolide, 1), one compound isolated for the first time from a natural source (hedyosmone, 2), and three known sesquiterpenes (onoseriolide, 3; chloranthalactone A, 4; and spathulenol, 5) that had not been previously isolated from H. ANGUSTIFOLIUM. The biological activities of 1- 5 showed that onoseriolide ( 3) was the most active compound against axenic amastigotes from LEISHMANIA AMAZONENSIS and L. INFANTUM. Moreover, it was still active on the intramacrophagic amastigotes of L. INFANTUM. The isolated compounds have also been tested on PLASMODIUM FALCIPARUM and against various mammalian cell lines.

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Sigma-Aldrich
氯喹 二磷酸盐, powder or crystals, 98.5-101.0% (EP)
Sigma-Aldrich
喷他脒 羟乙基磺酸盐, powder