Publication | Closed Access
New Type of Febrifugine Analogues, Bearing a Quinolizidine Moiety, Show Potent Antimalarial Activity against <i>Plasmodium</i> Malaria Parasite
139
Citations
4
References
1999
Year
New TypeAntiparasitic AgentMalariaCháng ShanPharmaceutical ChemistryMedicinal ChemistryPhytopharmacologyPhytochemicalDrug ChloroquineBiochemistryFebrifugine AnaloguesMetabolomicsPharmacologyAntiviral CompoundNatural SciencesHerb-drug InteractionQuinolizidine MoietyFavorable Therapeutic EffectMedicineDrug Discovery
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.
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