| Literature DB >> 17190441 |
Pierre Sauleau1, Marie-Thérèse Martin, Marie-Elise Tran Huu Dau, Diaa T A Youssef, Marie-Lise Bourguet-Kondracki.
Abstract
Biological and chemical investigations of the methanolic crude extract of the Red Sea marine sponge Hyrtios erectus led to the isolation of a novel azepino-indole-type alkaloid named hyrtiazepine (2) and 5-hydroxy-1H-indole-3-carboxylic acid methyl ester (3), together with the known metabolites hyrtiosulawesine (1), 5-hydroxyindole-3-carbaldehyde (4), hyrtiosin A (5), and hyrtiosin B (6). Their structures were elucidated on the basis of mass spectrometry and detailed 2D NMR spectroscopic data. Hyrtiosulawesine (1) displayed a significant antiphospholipase A2 activity with an IC50 value of 14 microM in a fluorometric assay using Crotalus adamanteus venom phospholipase A2.Entities:
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Year: 2006 PMID: 17190441 DOI: 10.1021/np060132r
Source DB: PubMed Journal: J Nat Prod ISSN: 0163-3864 Impact factor: 4.050