Palmitoylethanolamide
Tocris Bioscience, part of Bio-Techne | Catalog # 0879
Selective GPR55 agonist. FAAH and PAA substrate
Key Product Details
Description
Selective GPR55 agonist. FAAH and PAA substrate
Alternative Names
PEA
Product Description
Palmitoylethanolamide is an endogenous lipid that acts as a selective GPR55 agonist (EC50 values are 4, 19 800 and > 30 000 nM at GPR55, CB2 and CB1 receptors respectively). Substrate for fatty acid amide hydrolase (FAAH) and PEA-preferring acid amidase (PAA) and exhibits antinociceptive and anticonvulsant in vivo. Directly activates PPARα (EC50 = 3 μM) producing robust anti-inflammatory actions.Product Specifications
Molecular Weight
299.50
Formula
C18H37NO2
Storage
Store at RT
Chemical Name
N-(2-Hydroxyethyl)hexadecanamide
CAS Number
544-31-0
PubChem ID
4671
InChI Key
HXYVTAGFYLMHSO-UHFFFAOYSA-N
SMILES
O=C(CCCCCCCCCCCCCCC)NCCO
The technical data provided above is for guidance only. For batch specific data refer to the Certificate of Analysis.
Solubility
| Solvent | Max Conc. mg/mL | Max Conc. mM | |
|---|---|---|---|
| Solubility | |||
| DMSO | 5.99 | 20 | |
| Ethanol | 7.49 | 25 |
Preparing Stock Solutions
for Palmitoylethanolamide
The following data is based on the product molecular weight 299.50
Batch specific molecular weights may vary from batch to batch due to the degree of hydration, which all affect the solvent volumes required to prepare stock solutions.
| Concentration / Solvent Volume / Mass | 1 mg | 5 mg | 10 mg |
|---|---|---|---|
| 0.25 mM | 13.36 mL | 66.78 mL | 133.56 mL |
| 1.25 mM | 2.67 mL | 13.36 mL | 26.71 mL |
| 2.5 mM | 1.34 mL | 6.68 mL | 13.36 mL |
| 12.5 mM | 0.27 mL | 1.34 mL | 2.67 mL |
Calculators
Molarity Calculator
Dilution Calculator
Reconstitution Calculator
Background References
References are publications that support the biological activity of the product.
- Ryberg The orphan receptor GPR55 is a novel cannabinoid receptor. Br.J.Pharmacol. 2007 PMID: 17876302
- Re Palmitoylethanolamide, endocannabinoids and related cannabimimetic compounds in protection against tissue inflammation and pain: potential use in companion animals. Vet.J. 2005 PMID: 16324856
- Lambert The palmitoylethanolamide family: a new class of anti-inflammatory agents? Curr.Med.Chem. 2002 PMID: 11945130
- Lo Verme The search for the palmitoylethanolamide receptor. Life Sci. 2005 PMID: 15963531
- Lambert Anticonvulsant activity of N-palmitoylethanolamide, a putative endocannabinoid, in mice. Epilepsia 2001 PMID: 11442148
Product Specific Notices for Palmitoylethanolamide
For research use only
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