Author:
Matos Joana,da Cruz Filipa P.,Cabrita Élia,Gut Jiri,Nogueira Fátima,do Rosário Virgílio E.,Moreira Rui,Rosenthal Philip J.,Prudêncio Miguel,Gomes Paula
Abstract
ABSTRACTNovel 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 malariain vitroand host-vector transmissionin 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.
Publisher
American Society for Microbiology
Subject
Infectious Diseases,Pharmacology (medical),Pharmacology
Cited by
35 articles.
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