New Type of Febrifugine Analogues, Bearing a Quinolizidine Moiety, Show Potent Antimalarial Activity against <i>Plasmodium</i> Malaria Parasite

Yoshiaki Takaya, Hidehisa Tasaka, Tomoyuki Chiba, Koji Uwai, Masa-aki Tanitsu, Hye‐Sook Kim, Yusuke Wataya, Masatomo Miura, Mitsuhiro Takeshita, Yoshiteru Oshima

Journal of Medicinal Chemistry · 1999 · 139 citations · 4 references

Concepts

Abstract

Febrifugine (1) and isofebrifugine (2), isolated from the roots of Dichroa febrifuga Lour. (Chinese name: Cháng Shan), are active principles against malaria. Adducts of 1 and 2 with acetone, Df-1 (3) and Df-2 (4), respectively, were obtained using silica gel and acetone. They showed high activity against P. falciparum malaria in vitro. Compound 3 was found to be equally effective 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 these 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.

References

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