Here we report details of the isolation and determination of the absol
ute configurations and comparative anti-HIV activities of novel, atrop
isomeric naphthylisoquinoline alkaloid dimers, michellamines A, B, and
C, from a newly described species of Ancistrocladus from the Korup ra
inforest of Cameroon. We further provide a more extensive analysis of
the range of anti-HIV activity of michellamine B, the most potent and
abundant member of the series. Michellamine B inhibited HIV-induced ce
ll killing and viral replication in a variety of human cell lines, as
well as in cultures of human peripheral blood leukocytes and monocytes
. Michellamine B was active against a panel of biologically diverse la
boratory and clinical strains of HIV-1, including the AZT-resistant st
rain G910-6 and the pyridinone-resistant strain A17; the compound also
inhibited several strains of HIV-2.