Thyonosides A and B, two new saponins isolated from the holothurian Thyone aurea |
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Authors: | Isabelle Bonnard Kenneth L. Rinehart |
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Affiliation: | Roger Adam Laboratory, University of Illinois at Urbana-Champaign, Urbana, IL, USA |
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Abstract: | The structures of two saponins, thyonosides A and B, isolated from the holothurian Thyone aurea collected in Namibia, were elucidated by 1D and 2D NMR (1H, 13C, 1H-1H COSY, 1H-1H J-resolved, TOCSY, HMQC, HMBC and NOESY). The two compounds have the same aglycon but different oligosaccharidic chains. Thyonoside A has a 3-O-methyl-β-d-xylopyranosyl-(1→3)-6-O-sodium sulphate-β-d-glucopyranosyl-(1→4)-β-d-quinovopyranosyl-(1→2)-4-O-sodium sulphate-β-d-xylopyranosyl chain, and thyonoside B a 3-O-methyl-β-d-xylopyranosyl-(1→4)-β-d-xylopyranosyl-(1→4)-β-d-quinovopyranosyl-(1→2)-4-O-sodium sulphate-β-d-xylopyranosyl chain. The holostane-type aglycon features an endocyclic double bond at position 7-8, a double bond at position 25-26 and a β-acetoxy group at C16. |
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Keywords: | Thyone aurea Holothurian Triterpene saponin Holostane aglycon |
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