Chemistry of Natural Compounds

, Volume 18, Issue 2, pp 177–182 | Cite as

Glycosides of marine invertegrates. XI. Two new triterpene glycosides from holothurians of the familyStichopadidae

  • V. A. Stonik
  • I. I. Mal'tsev
  • A. I. Kalinovskii
  • C. Conde
  • G. B. Elyakov


By repeated column chromatography on silica gel new glycosides have been isolated from the holothuriansAstichopus multifidus andStichopus chloronotus — astichoposide C and stichoposide C (I and II, respectively). Their structures have been studied with the aid of chemical and physicochemical methods. The complete structures of the glycosides have been established as 23(S)-acetoxy-3β-{4′-O-[O-(3-O-methyl-β-D-glucopyranosyl)-(1→3)-β-D-glucopyranosyl]-2′-O-[O-(3-O-methyl-β-D-glucopyranosyl)-(1→3)-O-β-D-xylopyranosyl-(1→4)-β-D-quinovopyranosyl]-β-D-xylopyranosyloxy}holosta-7,25-diene and -holost-7-ene.


Xylose Glycoside Triterpene Glycoside Xylose Residue Peracetates 


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Copyright information

© Plenum Publishing Corporation 1983

Authors and Affiliations

  • V. A. Stonik
  • I. I. Mal'tsev
  • A. I. Kalinovskii
  • C. Conde
  • G. B. Elyakov

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