The hoiamides, structurally intriguing neurotoxic lipopeptides from Papua New Guinea marine cyanobacteria

J Nat Prod. 2010 Aug 27;73(8):1411-21. doi: 10.1021/np100468n.

Abstract

Two related peptide metabolites, one a cyclic depsipeptide, hoiamide B (2), and the other a linear lipopeptide, hoiamide C (3), were isolated from two different collections of marine cyanobacteria obtained in Papua New Guinea. Their structures were elucidated by combining various techniques in spectroscopy, chromatography, and synthetic chemistry. Both metabolites belong to the unique hoiamide structural class, characterized by possessing an acetate extended and S-adenosyl methionine modified isoleucine unit, a central triheterocyclic system comprised of two alpha-methylated thiazolines and one thiazole, and a highly oxygenated and methylated C-15 polyketide unit. In neocortical neurons, the cyclic depsipeptide 2 stimulated sodium influx and suppressed spontaneous Ca(2+) oscillations with EC(50) values of 3.9 microM and 79.8 nM, respectively, while 3 had no significant effects in these assays.

Publication types

  • Research Support, N.I.H., Extramural
  • Research Support, Non-U.S. Gov't
  • Research Support, U.S. Gov't, Non-P.H.S.

MeSH terms

  • Animals
  • Cyanobacteria / chemistry*
  • Depsipeptides / chemistry
  • Depsipeptides / isolation & purification*
  • Depsipeptides / pharmacology
  • Female
  • Humans
  • Lipopeptides / chemistry
  • Lipopeptides / isolation & purification*
  • Lipopeptides / pharmacology
  • Marine Biology
  • Mice
  • Molecular Structure
  • Neurons / drug effects
  • Neurotoxins / chemistry
  • Neurotoxins / isolation & purification*
  • Neurotoxins / pharmacology
  • Nuclear Magnetic Resonance, Biomolecular
  • Papua New Guinea
  • Pregnancy

Substances

  • Depsipeptides
  • Lipopeptides
  • Neurotoxins
  • hoiamide A
  • hoiamide B
  • hoiamide C