(S)-<wbr/>(?)-<wbr/>Eicosapentaenyl-<wbr/>1'-<wbr/>Hydroxy-<wbr/>2'-<wbr/>Propylamide

(S)-(?)-Eicosapentaenyl-1′-Hydroxy-2′-Propylamide

CAT N°: 9001227
Price:

From 122.00 103.70

N-Acyl ethanolamines (NAEs) have diverse biological actions that are strongly affected by the associated acyl group. Eicosapentaenoyl ethanolamide (EPEA) has potential signaling roles in aging, cancer, inflammation, and neurological development.{21496,19917,19740,19623} At least some of EPEA’s effects are mediated through cannabinoid (CB) receptors, while some NAEs also act as vanilloid receptor agonists.{21496,19780} S-(?)-Eicosapentaenyl-1’-hydroxy-2’-propylamide is a homolog of EPEA, characterized by the addition of an (S)-?-methyl group at the methylene carbon adjacent to the amide nitrogen. A similar modification of arachidonoyl ethanolamide (Item No. 90050) to produce S-1 methanandamide (Item No. 90072) results in a diminished affinity for the CB receptor but greatly improved metabolic stability to aminopeptidase hydrolysis.{1092} The physiological actions of this compound have not been evaluated.

Territorial Availability: Available through Bertin Technologies only in France

  • Synonyms
    • N-((S)-1-hydroxypropan-2-yl)icosa-5Z,8Z,11Z,14Z,17Z-pentaenamide
  • Correlated keywords
    • 1638355-66-4 EPA EPEA ethanolamide acylethanolamine NAE homolog eicosapentaenoyl hydroxypropylamide AEA
  • Product Overview:
    N-Acyl ethanolamines (NAEs) have diverse biological actions that are strongly affected by the associated acyl group. Eicosapentaenoyl ethanolamide (EPEA) has potential signaling roles in aging, cancer, inflammation, and neurological development.{21496,19917,19740,19623} At least some of EPEA’s effects are mediated through cannabinoid (CB) receptors, while some NAEs also act as vanilloid receptor agonists.{21496,19780} S-(?)-Eicosapentaenyl-1’-hydroxy-2’-propylamide is a homolog of EPEA, characterized by the addition of an (S)-?-methyl group at the methylene carbon adjacent to the amide nitrogen. A similar modification of arachidonoyl ethanolamide (Item No. 90050) to produce S-1 methanandamide (Item No. 90072) results in a diminished affinity for the CB receptor but greatly improved metabolic stability to aminopeptidase hydrolysis.{1092} The physiological actions of this compound have not been evaluated.

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