We have investigated the in vitro leishmanicidal activity of representative
members from series II-V of combretastatin analogues and heteroanalogues.
Most of them exhibited different degrees of activity against various strain
s of Leishmania spp. The diaryl(heteroaryl)ethane system or the more comple
x fused heterocyclic stilbenoids, constitute useful skeletal bases to suppo
rt some kind of antiparasitic activity. Particularly, the incorporation of
2-furyl substituents led to potent antileishmanial compounds, which have be
en selected for in vivo testing on murine models. (C) 1999 Elsevier Science
Ltd. All rights reserved.