Pachymoside A A novel glycolipid isolated from the marine sponge Pachymatisma johnstonia
Crude extracts of the North Sea marine sponge Pachymatisma johnstonia showed promising activity in a new assay for inhibitors of bacterial type III secretion. Bioassay-guided fractionation resulted in the isolation of the pachymosides, a new family of sponge glycolipids. A major part of the structur...
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Veröffentlicht in: | Canadian journal of chemistry 2004-02, Vol.82 (2), p.102-112 |
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Format: | Artikel |
Sprache: | eng |
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Zusammenfassung: | Crude extracts of the North Sea marine sponge Pachymatisma johnstonia showed promising activity in a new assay for inhibitors of bacterial type III secretion. Bioassay-guided fractionation resulted in the isolation of the pachymosides, a new family of sponge glycolipids. A major part of the structural diversity in this family of glycolipids involves increasing degrees of acetylation and differing positions of acetylation on a common pachymoside glycolipid template. All of the metabolites with these variations in acetylation pattern were converted into the same peracetylpachymoside methyl ester (
2
) for purification and spectroscopic analysis. Pachymoside A (
1
) is the component of the mixture that has natural acetylation at the eight galactose hydroxyls and at the C-6 hydroxyls of glucose-B and glucose-D. Chemical degradation and transformation in conjunction with extensive analysis of 800 MHz NMR data was used to elucidate the structure of pachymoside A (
1
).
Key words: Pachymatisma johnstonia, marine sponge, pachymoside, glycolipid. |
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ISSN: | 0008-4042 1480-3291 |
DOI: | 10.1139/v03-183 |