An intermediate in the synthesis of linoleoylethanolamide
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Linoleoyl Ethanolamide Phosphate

Item No. 9001837

Technical Information
Formal Name
N-[2-(phosphonooxy)ethyl]-9Z,12Z-octadecadienamide, disodium salt
CAS Number
419566-71-5
Synonyms
  • phospho-LEA
  • phospho-Linoleoyl Ethanolamide
Molecular Formula
C20H38NO5P • 2Na
Formula Weight
Purity
≥95%
A crystalline solid
PBS (pH 7.2): 2 mg/ml
SMILES
O=C(CCCCCCC/C=C\C/C=C\CCCCC)NCCOP(O)(O)=O.[Na].[Na]
InChi Code
InChI=1S/C20H38NO5P.2Na/c1-2-3-4-5-6-7-8-9-10-11-12-13-14-15-16-17-20(22)21-18-19-26-27(23,24)25;;/h6-7,9-10H,2-5,8,11-19H2,1H3,(H,21,22)(H2,23,24,25);;/b7-6-,10-9-;;
InChi Key
HRQCOAVPHQCYQI-JFHYDWJLSA-N
Shipping & Storage Information
Storage
-20°C
Shipping
Wet ice in continental US; may vary elsewhere
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    Product Description

    Linoleoyl ethanolamide phosphate is an intermediate in the biosynthesis of linoleoyl ethanolamide (Item No. 90155) that can be generated through phospholipase C-mediated hydrolysis of N-acylphosphatidylethanolamine.1 Linoleoyl ethanolamide phosphate, along with other endogenous N-acylethanolamines, is thought to play a role in the regulation of food intake by selective prolongation of feeding latency and post-meal interval.2

    WARNING This product is not for human or veterinary use.

    References & Product Citations
    Product Description References

    1. Liu, J., Wang, L., Harvey-White, J., et alMultiple pathways involved in the biosynthesis of anandamide. Neuropharmacology 54(1), 1-7 (2008).

    2. Hansen, H.S., and Diep, T.A. N-acylethanolamines, anandamide and food intake. Biochem. Pharmacol. 78(6), 553-560 (2009).