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Two new subergane-based sesquiterpenes from a Taiwanese Gorgonian coral Subergorgia suberosa.

Abstract
Chemical investigation of the ethyl acetate extract of the Taiwanese Gorgonian coral Subergorgia suberosa has resulted in the isolation of two new subergane-based sesquiterpenes, subergorgiol (1) and 2beta-acetoxysubergorgic acid (2), along with four known compounds, subergorgic acid methyl ester (3), 2beta-acetoxy methyl ester of subergorgic acid (4), 2beta-hydroxysubergorgic acid (5), and subergorgic acid (6). The structures of the new metabolites 1 and 2 were determined on the basis of extensive spectral analyses. Subergorgiol (1) may be the biosynthetic precursor of 2-6. Compound 3 was found to exhibit moderate cytotoxicity against the growth of HeLa cancer cells.
AuthorsGuey-Horng Wang, Atallah F Ahmed, Yao-Haur Kuo, Jyh-Horng Sheu
JournalJournal of natural products (J Nat Prod) Vol. 65 Issue 7 Pg. 1033-6 (Jul 2002) ISSN: 0163-3864 [Print] United States
PMID12141868 (Publication Type: Journal Article, Research Support, Non-U.S. Gov't)
Chemical References
  • 2beta-acetoxysubergorgic acid
  • Antineoplastic Agents
  • Sesquiterpenes
  • subergorgiol
Topics
  • Animals
  • Antineoplastic Agents (chemistry, isolation & purification, pharmacology)
  • Chromatography, High Pressure Liquid
  • Cnidaria
  • Drug Screening Assays, Antitumor
  • HeLa Cells
  • Humans
  • KB Cells
  • Molecular Conformation
  • Molecular Structure
  • Nuclear Magnetic Resonance, Biomolecular
  • Sesquiterpenes (chemistry, isolation & purification, pharmacology)
  • Stereoisomerism
  • Taiwan
  • Tumor Cells, Cultured (drug effects)

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