Antimalarial potential of xestoquinone, a protein kinase inhibitor isolated from a Vanuatu marine sponge Xestospongia sp

As part of our search for new antimalarial drugs, we have screened for inhibitors of Pfnek-1, a protein kinase of Plasmodium falciparum, in south Pacific marine sponges. On the basis of a preliminary screening, the ethanolic crude extract of a new species of Xestospongia collected in Vanuatu was sel...

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Veröffentlicht in:Bioorganic & medicinal chemistry 2006-07, Vol.14 (13), p.4477-4482
Hauptverfasser: Laurent, Dominique, Jullian, Valérie, Parenty, Arnaud, Knibiehler, Martine, Dorin, Dominique, Schmitt, Sophie, Lozach, Olivier, Lebouvier, Nicolas, Frostin, Maryvonne, Alby, Frédéric, Maurel, Séverine, Doerig, Christian, Meijer, Laurent, Sauvain, Michel
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Sprache:eng
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Zusammenfassung:As part of our search for new antimalarial drugs, we have screened for inhibitors of Pfnek-1, a protein kinase of Plasmodium falciparum, in south Pacific marine sponges. On the basis of a preliminary screening, the ethanolic crude extract of a new species of Xestospongia collected in Vanuatu was selected for its promising activity. A bioassay-guided fractionation led us to isolate xestoquinone which inhibits Pfnek-1 with an IC(50) around 1 microM. Among a small panel of plasmodial protein kinases, xestoquinone showed modest protein kinase inhibitory activity toward PfPK5 and no activity toward PfPK7 and PfGSK-3. Xestoquinone showed in vitro antiplasmodial activity against a FCB1 P. falciparum strain with an IC(50) of 3 microM and a weak selectivity index (SI 7). Xestoquinone exhibited a weak in vivo activity at 5mg/kg in Plasmodium berghei NK65 infected mice and was toxic at higher doses.
ISSN:0968-0896
1464-3391
DOI:10.1016/j.bmc.2006.02.026