| Identification | Back Directory | [Name]
N-(2-hydroxyethyl)docosanamide | [CAS]
94109-05-4 | [Synonyms]
BEHENAMIDE MEA
Docosanoyl Ethanolamide
N-(2-hydroxyethyl)docosanamide
N-(2-hydroxyethyl)-docosanamid
Docosanamide, N-(2-hydroxyethyl)-
Docosanoyl Ethanolamide Exclusive | [EINECS(EC#)]
302-442-2 | [Molecular Formula]
C24H49NO2 | [MOL File]
94109-05-4.mol | [Molecular Weight]
383.65 |
| Chemical Properties | Back Directory | [Melting point ]
102-104 °C(Solv: water (7732-18-5)) | [Boiling point ]
533.4±33.0 °C(Predicted) | [density ]
0.896±0.06 g/cm3(Predicted) | [solubility ]
Chloroform: 0.3 mg/ml | [form ]
A crystalline solid | [pka]
14.49±0.10(Predicted) | [LogP]
8.853 (est) |
| Hazard Information | Back Directory | [Description]
The endocannabinoids present a rich system of central cannabinoid (CB1), peripheral cannabinoid (CB2), and non-CB receptor-mediated pharmacology that has stimulated research in many fields including memory, weight loss and appetite, neurodegeneration, tumor surveillance, analgesia, and inflammation. Docosanoyl ethanolamide is a saturated N-acylethanolamide. Non-cannabinoid receptor-mediated pharmacology of the saturated ethanolamides is still being elucidated. Other studies indicate they may have a role in the functioning of ion channels. | [Uses]
Docosanoyl Ethanolamide is saturated N-acylethanolamide. | [Definition]
ChEBI: N-(docosanoyl)ethanolamine is an N-(long-chain-acyl)ethanolamine that is the ethanolamide of docosanoic acid. It is a N-(saturated fatty acyl)ethanolamine and a N-(long-chain-acyl)ethanolamine. It is functionally related to a docosanoic acid. | [References]
[1] DARREN SMART. ‘Entourage’ effects of N-acyl ethanolamines at human vanilloid receptors. Comparison of effects upon anandamide-induced vanilloid receptor activation and upon anandamide metabolism[J]. British Journal of Pharmacology, 2009, 136 3: 452-458. DOI: 10.1038/sj.bjp.0704732
[2] MURAT OZ . Effects of saturated long-chain N-acylethanolamines on voltage-dependent Ca2+ fluxes in rabbit T-tubule membranes[J]. Archives of biochemistry and biophysics, 2005, 434 2: Pages 344-351. DOI: 10.1016/j.abb.2004.11.010 |
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Alfa Chemistry
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1-516-6625404 |
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https://www.alfa-chemistry.com |
| Company Name: |
Enzo Biochem Inc
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Enzo Biochem Inc. 13797054060 |
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www.enzo.com |
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