Dysideanones A-C, unusual sesquiterpene quinones from the South China Sea sponge Dysidea avara

J Nat Prod. 2014 Feb 28;77(2):346-50. doi: 10.1021/np4009392. Epub 2014 Feb 18.

Abstract

Dysideanones A-C (1-3), three unusual sesquiterpene quinones with unprecedented carbon skeletons, were isolated from the South China Sea sponge Dysidea avara. Their structures including absolute configurations were determined by a combination of spectroscopic analyses and calculated ECD spectra. Within the sesquiterpene quinone structures, dysideanones A (1) and B (2) share an unprecedented 6/6/6/6-fused tetracyclic carbon skeleton, while dysideanone C (3) possesses an unusual 6/6/5/6-fused tetracyclic core. Dysideanone B (2) showed cytotoxicity against two human cancer cell lines, HeLa and HepG2, with IC50 values of 7.1 and 9.4 μM, respectively.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Benzoquinones
  • China
  • Drug Screening Assays, Antitumor
  • Dysidea / chemistry*
  • HeLa Cells
  • Hep G2 Cells
  • Humans
  • Inhibitory Concentration 50
  • Molecular Structure
  • Oceans and Seas
  • Quinones / chemistry
  • Quinones / isolation & purification*
  • Quinones / pharmacology
  • Sesquiterpenes / chemistry
  • Sesquiterpenes / isolation & purification*
  • Sesquiterpenes / pharmacology

Substances

  • Benzoquinones
  • Quinones
  • Sesquiterpenes
  • dysideanone A
  • dysideanone B
  • dysideanone C
  • quinone