Article ID | Journal | Published Year | Pages | File Type |
---|---|---|---|---|
10847785 | Steroids | 2005 | 6 Pages |
Abstract
The apolar fraction of the crude alcoholic extract of the sponge Euryspongia n. sp. was shown to display anti-inflammatory activity. Bioassay guided chromatographic purification led to the isolation of a known compound petrosterol (1) of 3β-hydroxy-24-norchol-5-en-23-oic acid (2), which has never yet been found as a natural substance, and of a new steroid, 3β-hydroxy-26-norcampest-5-en-25-oic acid (3). The absolute configurations of 2 and 3 were deduced from comparative 1H NMR data of the (S)- and (R)-phenylglycine methyl ester derivatives. These compounds were evaluated for their anti-inflammatory activity against 6-keto-prostaglandinF1α release in a human keratinocyte cell line HaCaT.
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Authors
Anne Mandeau, Cecile Debitus, Marie-Françoise Ariès, Bruno David,