R-Palmitoyl-(1-methyl) Ethanolamide

A synthetic analog of palmitoyl ethanolamide

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货号: ajci10622
CAS: 142128-47-0
别名: R-1 PMA
分子式: C19H39NO2
分子量: 313.5
纯度: >98%
溶解度: ≤10mg/ml in ethanol;25mg/ml in DMSO;3.3mg/ml in dimethyl formamide
储存: Store at -20°C
库存: 现货

Background

R-Palmitoyl-(1-methyl) ethanolamide, a synthetic analog of Palmitoyl ethanolamide (PEA), incorporates the (R)-methyl group vicinal to the alcohol on the ethanolamine moiety. The analogous modification to arachidonoyl ethanolamide (AEA) protects the molecule from hydrolysis by fatty acid amide hydrolase, prolongs duration of action and enhances potency in vivo [1].

PEA is an endogenous cannabinoid existed in mammalian tissues, such as liver and brain. PEA has also been isolated from egg yolk [2, 3]. PEA is a compound with documented anti-nociceptive and anti-inflammatory effects. During inflammation, PEA is accumulated and exihibits anti-inflammatory effects, including beneficial effects in clinically relevant animal models of inflammatory pain [4].

参考文献:
[1] Abadji V, Lin S, Taha G, et al.? (R)-methanandamide: a chiral novel anandamide possessing higher potency and metabolic stability[J]. Journal of medicinal chemistry, 1994, 37(12): 1889-1893.
[2] Bachur N R, Masek K, Melmon K L, et al.? Fatty acid amides of ethanol-amine in mammalian tissues[J]. Journal of Biological Chemistry, 1965, 240: 1019-1024.
[3] Ganley O H, Graessle O E, Robinson H J, et al.? Anti-inflammatory activity of compounds obtained from egg yolk, peanut oil, and soybean lecithin[J]. Journal of Laboratory and Clinical Medicine, 1958, 51: 709-714.
[4] Lambert D M, Vandevoorde S, Jonsson K O, et al.? The palmitoylethanolamide family: a new class of anti-inflammatory agents [J]. Current medicinal chemistry, 2002, 9(6): 663-674.