Article ID | Journal | Published Year | Pages | File Type |
---|---|---|---|---|
9895192 | Steroids | 2005 | 6 Pages |
Abstract
Chemical investigation of the dichloromethane extract of the Red Sea marine sponge Lamellodysidea herbacea led to the isolation of four novel polyhydroxysteroids: cholesta-8-en-3β,5α,6α,25-tetrol (1), cholesta-8(14)-en-3β,5α,6α,25-tetrol (2), cholesta-8,24-dien-3β,5α,6α-triol (3), and cholesta-8(14),24-dien-3β,5α,6α-triol (4). Their structures were identified through 1D and 2D NMR studies. Relative stereochemistries were established by analysis of chemical shifts, coupling constants, and NOESY correlations. Compounds 3-4 showed antifungal activity against Candida tropicalis, with an inhibition diameter of 13 and 11 mm at 10 μg/disc, respectively.
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Authors
Pierre Sauleau, Marie-Lise Bourguet-Kondracki,