Junceol A, a new sesquiterpenoid from the sea pen Virgularia juncea

J Nat Prod. 2001 Sep;64(9):1241-2. doi: 10.1021/np010192r.

Abstract

A new sesquiterpenoid, junceol A(1), as well as two known diterpenoids, sclerophytin A (2) and cladiellisin (3), have been isolated from the sea pen octocoral Virgularia juncea. The structure of metabolite 1 was determined by extensive spectral analysis. Compounds 1-3 have been shown to exhibit cytotoxicity toward P-388 cancer cells.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Bridged-Ring Compounds / chemistry
  • Bridged-Ring Compounds / isolation & purification
  • Bridged-Ring Compounds / pharmacology
  • Chromatography, Thin Layer
  • Cnidaria / chemistry*
  • Drug Screening Assays, Antitumor
  • Furans / chemistry
  • Furans / isolation & purification
  • Furans / pharmacology
  • Inhibitory Concentration 50
  • Leukemia P388
  • Magnetic Resonance Spectroscopy
  • Molecular Conformation
  • Molecular Structure
  • Sesquiterpenes / chemistry
  • Sesquiterpenes / isolation & purification*
  • Sesquiterpenes / pharmacology
  • Spectrophotometry, Infrared
  • Taiwan
  • Tumor Cells, Cultured / drug effects

Substances

  • Bridged-Ring Compounds
  • Furans
  • Sesquiterpenes
  • junceol A
  • sclerophytin A