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Bioorg Med Chem Lett ; 14(17): 4439-43, 2004 Sep 06.
Article in English | MEDLINE | ID: mdl-15357968

ABSTRACT

Synthesis of a new family of quinolylhydrazone derivatives and evaluation of their activity against a chloroquine-resistant strain of Plasmodium falciparum are described. The best compound displayed an activity 6-fold higher than chloroquine. None of the active compounds were found to inhibit beta-hematin formation in vitro in the same range as chloroquine and five among them displayed lower calculated vacuolar accumulation ratios, suggesting the implication of a different mechanism of action.


Subject(s)
Antimalarials/chemical synthesis , Glyoxylates/chemical synthesis , Hydrazones/chemical synthesis , Animals , Antimalarials/pharmacology , Glyoxylates/pharmacology , Hydrazones/pharmacology , Plasmodium falciparum/drug effects , Plasmodium falciparum/growth & development
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