γ-Linolenoyl monoethanolamide
γ-Linolenoyl monoethanolamide, a kind of fatty N-acyl ethanolamine, is an endocannabinoid.
For research use only. We do not sell to patients.
- CAS No.: 150314-37-7
- Formula: C20H35NO2
- Molecular Weight:321.50
-
Storage:
Please store the product under the recommended conditions in the Certificate of Analysis.
To place orders, for customer services and technical support, please contact: MedChemExpress USA
Tel: 609-228-6898 E-mail: [email protected] [email protected]
-
Biological Activity
-
Chemical Information
- Purity & Documentation
- References
-
Help & FAQs
-
HY-W130610
Stearamide
-
HY-120963
N-Oleoyl Taurine
-
HY-W009123
Erucamide
-
HY-W130610R
Stearamide (Standard)
-
HY-120968
Arachidoyl ethanolamide
-
HY-119723
Myristoyl ethanolamide
-
HY-120969
Docosanoyl ethanolamide
-
HY-120961
Oleoyl ethyl amide
-
HY-134055
Arachidonoyl-N,N-dimethyl amide
-
HY-130311
2-Linoleoyl glycerol
-
HY-121389
Hexadecanamide
-
HY-120965
N-Palmitoyl Taurine
Biological Activity
Chemical Information
-
CAS No. 150314-37-7
-
Molecular Weight 321.50
-
Formula C20H35NO2
-
SMILES
CCCCC/C=C\C/C=C\C/C=C\CCCCC(NCCO)=O
-
Shipping
Room temperature in continental US; may vary elsewhere.
-
Storage
Please store the product under the recommended conditions in the Certificate of Analysis.
Purity & Documentation
References
[1]. M Van Der Stelt, et al. Formation of a new class of oxylipins from N-acyl(ethanol)amines by the lipoxygenase pathway. Eur J Biochem. 2000 Apr;267(7):2000-7. [Content Brief]
[2]. Matthew W Buczynski, et al. Inflammatory hyperalgesia induces essential bioactive lipid production in the spinal cord. J Neurochem. 2010 Aug;114(4):981-93. [Content Brief]
Calculators
Concentration (start) × Volume (start) = Concentration (final) × Volume (final)
γ-Linolenoyl monoethanolamide Related Classifications
HY-162298 Related Classifications
Powered by Bioz