| Identification | Back Directory | [Name]
Lignoceroyl Ethanolamide Exclusive | [CAS]
10015-68-6 | [Synonyms]
Lignoceroyl Ethanolamide
Tetracosanamide, N-(2-hydroxyethyl)-
Lignoceroyl Ethanolamide Exclusive | [Molecular Formula]
C26H53NO2 | [MOL File]
10015-68-6.mol | [Molecular Weight]
411.7 |
| Hazard Information | Back Directory | [Description]
Lignoceroyl ethanolamide is a member of the family of fatty N-acyl ethanolamines collectively called endocannabinoids. Whereas lignoceric acid has been detected at relatively high levels in rat cerebrospinal fluid, the specific role and relative importance of its ethanolamine metabolite have not been determined. | [Uses]
N-(2-Hydroxyethyl)tetracosanamide acts as a crude oil emulsifier. | [Definition]
ChEBI:Lignoceroyl-EA is a N-(saturated fatty acyl)ethanolamine. | [References]
[1] N. BACHUR S U. Microsomal synthesis of fatty acid amides.[J]. The Journal of Biological Chemistry, 1966, 72 1: 1308-1313. DOI: 10.1016/s0021-9258(18)96775-x
[2] PAUL W. DOETSCH. Monomeric Base Damage Products from Guanine, Adenine, and Thymine Induced by Exposure of DNA to Ultraviolet Radiation[J]. Biochemistry Biochemistry, 1995, 34 3: 737-742. DOI: 10.1021/bi00003a005
[3] ALAN SAGHATELIAN. Assignment of Endogenous Substrates to Enzymes by Global Metabolite Profiling?[J]. Biochemistry Biochemistry, 2004, 43 45: 14332-14339. DOI: 10.1021/bi0480335
[4] MATTHEW W. BUCZYNSKI. Inflammatory hyperalgesia induces essential bioactive lipid production in the spinal cord[J]. Journal of Neurochemistry, 2010, 114 4: 981-993. DOI: 10.1111/j.1471-4159.2010.06815.x |
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