Structure and cytotoxicity of a new lanostane-type triterpene glycoside from the sea cucumber Holothuria hilla

Chem Biodivers. 2006 Nov;3(11):1249-54. doi: 10.1002/cbdv.200690126.

Abstract

A new triterpene glycoside, hillaside C (1), was isolated from the sea cucumber Holothuria hilla Lesson, which is found in the South China Sea, and its structure has been elucidated by spectral analysis (ESI-MS and NMR) and chemical transformations. Four known compounds, holothuria A, thymine, uracil, and cholesterol, were also obtained. Compound 1 exhibited significant cytotoxicity against eight human tumor cell lines (A-549, MCF-7, IA9, CAKI-1, PC-3, KB, KB-VIN, and HCT-8) with IC50 values in the range of 0.15-3.20 microg/ml.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Antineoplastic Agents / pharmacology
  • Cell Line, Tumor
  • Cholesterol / chemistry
  • Drug Screening Assays, Antitumor
  • Glycosides / chemistry*
  • Glycosides / pharmacology
  • Humans
  • Inhibitory Concentration 50
  • Magnetic Resonance Spectroscopy
  • Models, Chemical
  • Sea Cucumbers
  • Spectrometry, Mass, Electrospray Ionization
  • Thymine / chemistry
  • Triterpenes / chemistry*
  • Triterpenes / pharmacology
  • Uracil / chemistry

Substances

  • Antineoplastic Agents
  • Glycosides
  • Triterpenes
  • hillaside C
  • Uracil
  • Cholesterol
  • Thymine