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Stearoylethanolamide

From Wikipedia, the free encyclopedia
Chemical compound
Stearoylethanolamide
Names
IUPAC name
N-(2-Hydroxyethyl)octadecanamide
Identifiers
3D model (JSmol)
ChemSpider
ECHA InfoCard100.003.531Edit this at Wikidata
UNII
  • InChI=1S/C20H41NO2/c1-2-3-4-5-6-7-8-9-10-11-12-13-14-15-16-17-20(23)21-18-19-22/h22H,2-19H2,1H3,(H,21,23)
    Key: OTGQIQQTPXJQRG-UHFFFAOYSA-N
  • CCCCCCCCCCCCCCCCCC(=O)NCCO
Properties
C20H41NO2
Molar mass327.553 g·mol−1
Except where otherwise noted, data are given for materials in theirstandard state (at 25 °C [77 °F], 100 kPa).
Chemical compound

Stearoylethanolamide (SEA) is anendocannabinoidneurotransmitter.[1]

Stearoylethanolamide (C20H41NO2; 18:0), also called N-(octadecanoyl)ethanolamine, is anN-acylethanolamine and theethanolamide ofoctadecanoic acid (C18H36O2; 18:0) andethanolamine (MEA: C2H7NO), and functionally related to an octadecanoic acid.[2]

Levels of SEA correlate with changes in pain intensity, indicating this SEA change, reflect the pain reduction effects of IPRP.[3]

References

[edit]
  1. ^Mauro Maccarrone, Riccardo Pauselli, Marianna Di Rienzo, Alessandro Finazzi-Agrò (2002)."Binding, degradation and apoptotic activity of stearoylethanolamide in rat C6 glioma cells".Biochem J.366 (Pt 1):137–144.doi:10.1042/BJ20020438.PMC 1222758.PMID 12010121.{{cite journal}}: CS1 maint: multiple names: authors list (link)
  2. ^PubChem."N-(2-Hydroxyethyl)octadecanamide".pubchem.ncbi.nlm.nih.gov. Retrieved2022-09-27.
  3. ^Stensson, Niclas; Gerdle, Björn; Rönne-Petersén, Linn; Yang, Liu L.; Lavebratt, Catharina; Falkenberg, Torkel; Ghafouri, Bijar (2022-02-26)."Investigating the Long-Term Effect of an Interdisciplinary Multimodal Rehabilitation Program on Levels of Bioactive Lipids and Telomerase Activity in Blood from Patients with Chronic Pain".Journal of Clinical Medicine.11 (5): 1291.doi:10.3390/jcm11051291.ISSN 2077-0383.PMC 8911430.PMID 35268382.


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