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

      Bioorganic & Medicinal Chemistry Letters
      Alcohol Dehydrogenase, metabolism, Arachidonic Acids, Catalysis, Endocannabinoids, Glycine, biosynthesis, Humans, Metabolic Networks and Pathways, Oxidation-Reduction, Polyunsaturated Alkamides

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          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.

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          Author and article information

          Journal
          19013794
          2798806
          10.1016/j.bmcl.2008.10.087

          Chemistry
          Alcohol Dehydrogenase,metabolism,Arachidonic Acids,Catalysis,Endocannabinoids,Glycine,biosynthesis,Humans,Metabolic Networks and Pathways,Oxidation-Reduction,Polyunsaturated Alkamides

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