Anti-inflammatory sesquiterpene-quinones from the New Zealand sponge Dysidea cf. cristagalli

J Nat Prod. 2005 Sep;68(9):1431-3. doi: 10.1021/np050171n.

Abstract

The inhibition of superoxide production by human neutrophils has been used to screen New Zealand's unique biota for anti-inflammatory natural products. Bioactivity-directed isolation on an extract of the sponge Dysidea cf. cristagalli led to a new sesquiterpene-quinone (4) with anti-inflammatory activity, plus acetylated hydroquinone (3). These compounds inhibited superoxide production in vitro with IC50's of 3 microM (3) and 11 microM (4).

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Anti-Inflammatory Agents, Non-Steroidal / chemistry
  • Anti-Inflammatory Agents, Non-Steroidal / isolation & purification*
  • Anti-Inflammatory Agents, Non-Steroidal / pharmacology
  • Dysidea / chemistry*
  • Humans
  • Inhibitory Concentration 50
  • Molecular Structure
  • Neutrophils / drug effects
  • New Zealand
  • Quinones / chemistry
  • Quinones / isolation & purification*
  • Quinones / pharmacology
  • Sesquiterpenes / chemistry
  • Sesquiterpenes / isolation & purification*
  • Sesquiterpenes / pharmacology
  • Superoxides / metabolism

Substances

  • 20-O-acetyl-21-hydroxy-ent-isozonarol
  • 21-hydroxy-ent-isozonarone
  • Anti-Inflammatory Agents, Non-Steroidal
  • Quinones
  • Sesquiterpenes
  • Superoxides