| Literature DB >> 22155838 |
Joana Matos1, Filipa P da Cruz, Élia Cabrita, Jiri Gut, Fátima Nogueira, Virgílio E do Rosário, Rui Moreira, Philip J Rosenthal, Miguel Prudêncio, Paula Gomes.
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.Entities:
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Year: 2011 PMID: 22155838 PMCID: PMC3294896 DOI: 10.1128/AAC.05345-11
Source DB: PubMed Journal: Antimicrob Agents Chemother ISSN: 0066-4804 Impact factor: 5.191