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Antimicrob Agents Chemother ; 56(3): 1564-70, 2012 Mar.
Article in English | MEDLINE | ID: mdl-22155838

ABSTRACT

Novel conjugates of the antimalarial drug primaquine (compound 1) with ferrocene, named primacenes, have been synthesized and screened for their activities against blood stage and liver stage malaria in vitro and host-vector transmission in vivo. Both transmission-blocking and blood-schizontocidal activities of the parent drug were conserved only in primacenes bearing a basic aliphatic amine group. Liver stage activity did not require this structural feature, and all metallocenes tested were comparable to or better than primaquine in this regard. Remarkably, the replacement of primaquine's aliphatic chain by hexylferrocene, as in compound 7, led to a ~45-fold-higher level activity against liver stage parasitemia than that of primaquine.


Subject(s)
Antimalarials/chemical synthesis , Ferrous Compounds/chemistry , Liver/drug effects , Malaria/prevention & control , Plasmodium berghei/drug effects , Plasmodium falciparum/drug effects , Primaquine/analogs & derivatives , Primaquine/chemistry , Animals , Antimalarials/pharmacology , Erythrocytes/drug effects , Erythrocytes/parasitology , Ferrous Compounds/pharmacology , Genes, Reporter , Green Fluorescent Proteins/genetics , Humans , Inhibitory Concentration 50 , Liver/parasitology , Malaria/parasitology , Malaria/transmission , Metallocenes , Mice , Mice, Inbred BALB C , Oocysts/drug effects , Oocysts/physiology , Plasmodium berghei/physiology , Plasmodium falciparum/physiology , Primaquine/pharmacology , Sporozoites/drug effects , Sporozoites/physiology
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