Cytotoxic triterpene glycosides from the sea cucumber Pseudocolochirus violaceus

Fitoterapia. 2007 Jun;78(4):283-7. doi: 10.1016/j.fitote.2007.02.010. Epub 2007 Apr 11.

Abstract

A new triterpene glycoside (1) along with the known intercedenside B (2) was isolated from the sea cucumber Pseudocolochirus violaceus. Glycoside 1 was elucidated as 3-O-{6-O-sodiumsulfate-3-O-methyl-beta-D-glucopyranosyl-(1-->3)-beta-D-xylopyranosyl-(1-->4)-[beta-D-xylopyranosyl(1-->2)]-beta-D-quinovopyranosyl-(1-->2)-4-O-sodiumsulfate-beta-D-xylopyranosyl}-16beta-acetoxy-holosta-7, 24-diene-3beta-ol on the basis of extensive spectral studies and chemical evidence. Both the glycosides exhibited significant cytotoxicity against cancer cell lines MKN-45 and HCT-116.

MeSH terms

  • Animals
  • Antineoplastic Agents / administration & dosage
  • Antineoplastic Agents / chemistry
  • Antineoplastic Agents / pharmacology*
  • Antineoplastic Agents / therapeutic use
  • Cell Line, Tumor / drug effects
  • Glycosides / administration & dosage
  • Glycosides / chemistry
  • Glycosides / pharmacology
  • Glycosides / therapeutic use
  • Magnetic Resonance Spectroscopy
  • Phytotherapy*
  • Sea Cucumbers*
  • Structure-Activity Relationship
  • Triterpenes / administration & dosage
  • Triterpenes / chemistry
  • Triterpenes / pharmacology
  • Triterpenes / therapeutic use

Substances

  • Antineoplastic Agents
  • Glycosides
  • Triterpenes