Isolation and identification of a cis-C8-diol-ester of okadaic acid from Dinophysis acuta in New Zealand

Toxicon. 2006 Aug;48(2):195-203. doi: 10.1016/j.toxicon.2006.04.018. Epub 2006 May 22.

Abstract

A cis-isomer of a C(8)-diol ester of okadaic acid (1) was isolated during large-scale purification of pectenotoxins (PTXs) from extracts of Dinophysis acuta collected from the west coast of South Island, New Zealand. The compound was identified by NMR spectroscopic and liquid chromatography-mass spectrometry (LC-MS) studies, and is the first reported cis-isomer of an okadaic acid C(8)-diol-ester identified in Dinophysis. The more abundant trans-C(8)-diol ester of okadaic acid (2) isolated from the same Dinophysis extract was rapidly hydrolyzed to okadaic acid in vitro by the supernatant from green-lipped mussel hepatopancreas.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Chromatography, High Pressure Liquid
  • Dinoflagellida / chemistry*
  • Esterification
  • Furans / pharmacology
  • Hepatopancreas / metabolism
  • Hydrolysis / drug effects
  • Macrolides
  • Magnetic Resonance Spectroscopy
  • Marine Toxins / chemistry
  • Marine Toxins / isolation & purification*
  • Molecular Structure
  • Okadaic Acid / analogs & derivatives
  • Okadaic Acid / analysis
  • Okadaic Acid / isolation & purification*
  • Pyrans / chemistry*
  • Pyrans / pharmacology
  • Spectrometry, Mass, Electrospray Ionization

Substances

  • Furans
  • Macrolides
  • Marine Toxins
  • Pyrans
  • Okadaic Acid
  • dinophysistoxin 1
  • pectenotoxin 2