Alcohol dehydrogenase-catalyzed in vitro oxidation of anandamide to N-arachidonoyl glycine, a lipid mediator: synthesis of N-acyl glycinals

Bioorg Med Chem Lett. 2009 Jan 1;19(1):237-41. doi: 10.1016/j.bmcl.2008.10.087. Epub 2008 Nov 1.

Abstract

N-Arachidonoyl ethanolamide or anandamide is an endocannabinoid found in most tissues where it acts as an important signaling mediator in a number of physiological and pathophysiological processes. Consequently, intense effort has been focused on understanding all its biosynthetic and metabolic pathways. Herein we report human alcohol dehydrogenase-catalyzed sequential oxidation of anandamide to N-arachidonoyl glycine, a prototypical member of the class of long chain fatty acyl glycines, a new group of lipid mediators with a wide array of physiological effects. We also present a straightforward synthesis for a series of N-acyl glycinals including N-arachidonoyl glycinal, an intermediate in the alcohol dehydrogenase-catalyzed oxidation of anandamide.

Publication types

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

MeSH terms

  • Alcohol Dehydrogenase / metabolism*
  • Arachidonic Acids / metabolism*
  • Catalysis
  • Endocannabinoids
  • Glycine / biosynthesis*
  • Humans
  • Metabolic Networks and Pathways
  • Oxidation-Reduction
  • Polyunsaturated Alkamides / metabolism*

Substances

  • Arachidonic Acids
  • Endocannabinoids
  • Polyunsaturated Alkamides
  • Alcohol Dehydrogenase
  • Glycine
  • anandamide