Stereostructure and biological activity of 42-hydroxy-palytoxin: a new palytoxin analogue from Hawaiian Palythoa subspecies

Chem Res Toxicol. 2009 Nov;22(11):1851-9. doi: 10.1021/tx900259v.

Abstract

This paper reports on the analysis of the toxin content from Palythoa tuberculosa and Palythoa toxica samples collected off of the Hawaiian coast. Our work, based on in-depth high-resolution liquid chromatography-mass spectrometry analysis along with extensive NMR study, led us to structurally characterize 42-hydroxy-palytoxin, a new palytoxin congener. This toxin and palytoxin itself appeared to be the major components of toxic extract from a P. tuberculosa sample, while 42-hydroxy-palytoxin was proven by far to be the main palytoxin derivative in P. toxica. Functional studies on this new palytoxin-like compound suggest that the new palytoxin analogue and palytoxin itself present similar biological activities.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Acrylamides / chemistry*
  • Animals
  • Anthozoa / chemistry*
  • Cells, Cultured
  • Chromatography, High Pressure Liquid
  • Cnidarian Venoms / chemistry
  • Cnidarian Venoms / therapeutic use*
  • Hawaii
  • Magnetic Resonance Spectroscopy
  • Mice
  • Pyrans / chemistry
  • Pyrans / therapeutic use*
  • Spectrometry, Mass, Electrospray Ionization
  • Stereoisomerism

Substances

  • Acrylamides
  • Cnidarian Venoms
  • Pyrans
  • 42-hydroxypalytoxin
  • palytoxin