New bioactive halenaquinone derivatives from South Pacific marine sponges of the genus Xestospongia.
Bioorg Med Chem
; 18(16): 6006-11, 2010 Aug 15.
Article
en En
| MEDLINE
| ID: mdl-20634081
Bioassay-directed fractionation of South Pacific marine sponges of the genus Xestospongia has led to the isolation of a number of halenaquinone-type polyketides, including two new derivatives named xestosaprol C methylacetal 7 and orhalquinone 8. Chemical characterization of these two new compounds was achieved by extensive 1D and 2D NMR spectroscopic studies. Evaluation of anti-phospholipase A(2), anti-farnesyltransferase and antiplasmodial activities of this series is presented and structure/activity relationships are discussed. Orhalquinone 8 displayed a significant inhibition of both human and yeast farnesyltransferase enzymes, with IC(50) value of 0.40 microM and was a moderate growth inhibitor of Plasmodium falciparum.
Texto completo:
1
Banco de datos:
MEDLINE
Asunto principal:
Plasmodium falciparum
/
Quinonas
/
Xestospongia
/
Farnesiltransferasa
/
Inhibidores de Fosfolipasa A2
/
Antimaláricos
Límite:
Animals
/
Humans
Idioma:
En
Año:
2010
Tipo del documento:
Article