产品名称
棕榈酰,
InChI key
HXYVTAGFYLMHSO-UHFFFAOYSA-N
InChI
1S/C18H37NO2/c1-2-3-4-5-6-7-8-9-10-11-12-13-14-15-18(21)19-16-17-20/h20H,2-17H2,1H3,(H,19,21)
SMILES string
CCCCCCCCCCCCCCCC(=O)NCCO
form
powder
storage temp.
−20°C
Gene Information
human ... CNR1(1268), CNR2(1269)
rat ... Faah(29347)
Application
棕榈酰乙醇胺已用作质谱分析(MS/MS)的标准品。
Biochem/physiol Actions
棕榈酰乙醇胺(PEA)是由乙醇胺和棕榈酸形成的天然脂肪酸酰胺,存在于大豆、蛋黄等多种食物中。棕榈酰乙醇胺是一种内源性大麻素受体激动剂。它是过氧化物酶体增殖物激活受体α(PPAR-α)的配体。棕榈酰乙醇胺具有抗炎、抗过敏、神经保护和镇痛活性。它属于脂质介质和N-酰基乙醇胺家族。棕榈酰乙醇胺可抑制活化的肥大细胞释放促炎介质,并阻止活化的肥大细胞在神经损伤位点募集。
Other Notes
大麻素的结构类似物。
signalword
Danger
hcodes
Hazard Classifications
Aquatic Chronic 2 - Eye Dam. 1 - Skin Irrit. 2
存储类别
13 - Non Combustible Solids
wgk
WGK 2
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
Eyeshields, Gloves, type N95 (US)
Lili He et al.
Journal of chromatographic science, 54(8), 1428-1434 (2016-05-04)
This article aims to build up a simple, rapid and accurate capillary zone electrophoresis (CZE) method for the separation of biogenic amines (BAs). Here, 10 key BAs (phenethylamine, histamine, tryptamine, tyramine, 5-hydroxytryptamine, octopamine, dopamine, norepinephrine, epinephrine and carnosine) owning significant
Xiao Shi et al.
PloS one, 11(3), e0152581-e0152581 (2016-04-01)
Methamphetamine (MA) and neurotransmitter precursors and metabolites such as tyramine, octopamine, and β-phenethylamine stimulate the G protein-coupled trace amine-associated receptor 1 (TAAR1). TAAR1 has been implicated in human conditions including obesity, schizophrenia, depression, fibromyalgia, migraine, and addiction. Additionally TAAR1 is
Melania Melis et al.
The Laryngoscope, 129(9), E307-E312 (2019-01-25)
Taste sensitivity varies greatly among individuals influencing eating behavior and health, consequently the disorders of this sense can affect the quality of life. The ability to perceive the bitter of thiourea compounds, such as phenylthiocarbamide (PTC), has been largely reported
Didier M Lambert et al.
Current medicinal chemistry, 9(6), 663-674 (2002-04-12)
The discovery of anandamide as an endogenous ligand for the cannabinoid receptors has led to a resurgence of interest in the fatty acid amides. However, N-palmitoylethanolamine (PEA), a shorter and fully saturated analogue of anandamide, has been known since the
Giulia Donvito et al.
The Journal of pharmacology and experimental therapeutics, 359(2), 310-318 (2016-10-21)
Chemotherapy-induced peripheral neuropathy (CIPN) represents a serious complication associated with antineoplastic drugs. Although there are no medications available that effectively prevent CIPN, many classes of drugs have been used to treat this condition, including anticonvulsants, serotonin and noradrenaline reuptake inhibitors
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