New type of febrifugine analogues, bearing a quinolizidine moiety, show potent antimalarial activity against Plasmodium malaria parasite

Febrifugine (1) and isofebrifugine (2), isolated from the roots of Dichroa febrifuga Lour. (Chinese name: Chang Shan), are active principles against m alaria. Adducts of 1 and 2 with acetone, Df-l (3) and Df-2 (4), respectivel y, were obtained using silica gel and acetone. They showed high activity ag ainst P. falciparum malaria in vitro. Compound 3 was found to be equally ef fective against P. berghei in vivo as the clinically used drug chloroquine, whereas 4 showed only 1/24 of the activity of 3. Metabolism studies of the se compounds revealed that compound 4 is readily metabolized in mouse liver . Accordingly, the dose of 4 must be higher than that of 3 to attain blood levels sufficient for a favorable therapeutic effect.