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LGEQQWMQCRIYKG-DOFZRALJSA-N
SpectraBase Compound ID BCh61tpUUUC
InChI InChI=1S/C22H37NO2/c1-2-3-4-5-6-7-8-9-10-11-12-13-14-15-16-17-18-19-22(25)23-20-21-24/h6-7,9-10,12-13,15-16,24H,2-5,8,11,14,17-21H2,1H3,(H,23,25)/b7-6-,10-9-,13-12-,16-15-
InChIKey LGEQQWMQCRIYKG-DOFZRALJSA-N
Mol Weight 347.5 g/mol
Molecular Formula C22H37NO2
Exact Mass 347.282429 g/mol
Copyright Copyright © 2024 DigiLab GmbH and Wiley-VCH GmbH. All Rights Reserved.
Source of Spectrum DigiLab GmbH (C) 2024
Technique GC/MS
Copyright Copyright © 2020-2024 John Wiley & Sons, Inc. All Rights Reserved.
Source of Spectrum SWG-33-2669-0
Copyright Copyright © 2020-2024 John Wiley & Sons, Inc. All Rights Reserved.
Source of Spectrum CAY-2023-1242-0
Catalog Number <a href=https://www.caymanchem.com/product/90050>90050</a>
Copyright Copyright © 2020-2024 John Wiley & Sons, Inc. All Rights Reserved.
Source of Spectrum CAY-2023-2038-0
Catalog Number <a href=https://www.caymanchem.com/product/90050>90050</a>
Copyright Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved.
Solvent CDCl3
Copyright Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved.
Solvent CDCl3
  • (5Z,8Z,11Z,14Z)-N-(2-HYDROXYETHYL)-5,8,11,14-EICOSATETRAENAMIDE;ENANDAMIDE
  • Anandamide
  • Arachidonoyl ethanolamide (AEA)
  • Arachidonoyl Ethanolamide
  • Arachidonic acid-N-(hydroxyethyl)amide
  • Arachidonylethanolamide
  • AEA
Title Journal or Book Year
Synthesis and Evaluation of Fatty Acid Amides on the <i>N</i>-Oleoylethanolamide-Like Activation of Peroxisome Proliferator Activated Receptor α CHEMICAL & PHARMACEUTICAL BULLETIN 2015
1H,13C and15N NMR assignments forN- andO-acylethanolamines, important family of naturally occurring bioactive lipid mediators Magnetic Resonance in Chemistry 2012

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