Cymatherelactone and cymatherols A-C, polycyclic oxylipins from the marine brown alga Cymathere triplicata

Phytochemistry. 2012 Jan;73(1):134-41. doi: 10.1016/j.phytochem.2011.09.014. Epub 2011 Nov 7.

Abstract

An investigation of the oxylipin chemistry of the temperate brown alga Cymathere triplicata led to the isolation of several secondary metabolites, cymatherelactone (1) and cymatherols A-C (2-4), the latter as their methyl ester derivatives (5-7), which contained cyclopentyl, cyclopropyl, epoxide and lactone rings. Their structures were elucidated using a combination of spectroscopic techniques and synthetic chemistry. Cymatherelactone (1), as well as R- and S-Mosher's esters of its seco acid, exhibited moderate sodium channel blocking activity.

Publication types

  • Research Support, N.I.H., Extramural

MeSH terms

  • Marine Biology
  • Molecular Structure
  • Nuclear Magnetic Resonance, Biomolecular
  • Oxylipins / chemistry
  • Oxylipins / isolation & purification*
  • Oxylipins / pharmacology
  • Phaeophyceae / chemistry*
  • Sodium Channel Blockers / chemistry
  • Sodium Channel Blockers / isolation & purification*
  • Sodium Channel Blockers / pharmacology

Substances

  • Oxylipins
  • Sodium Channel Blockers
  • cymatherelactone
  • cymatherol A
  • cymatherol B
  • cymatherol C