P0359
Palmitoylethanolamide
≥98% (HPLC), powder, cannabinoid receptor agonist
동의어(들):
N-(2-Hydroxyethyl)hexadecanamide, PEA, Palmidrol
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모든 사진(1)
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10 MG
₩203,711
50 MG
₩716,184
About This Item
실험식(Hill 표기법):
C18H37NO2
CAS Number:
Molecular Weight:
299.49
EC Number:
MDL number:
UNSPSC 코드:
12352200
PubChem Substance ID:
NACRES:
NA.77
추천 제품
제품명
Palmitoylethanolamide,
양식
powder
저장 온도
−20°C
SMILES string
CCCCCCCCCCCCCCCC(=O)NCCO
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)
InChI key
HXYVTAGFYLMHSO-UHFFFAOYSA-N
유전자 정보
human ... CNR1(1268) , CNR2(1269)
rat ... Faah(29347)
1 of 4
이 품목 | SML0906 | SML0384 | SML2594 |
|---|---|---|---|
| Quality Level 200 | Quality Level 100 | Quality Level 100 | Quality Level - |
| storage temp. −20°C | storage temp. 2-8°C | storage temp. −20°C | storage temp. −20°C |
| Gene Information human ... CNR1(1268), CNR2(1269) | Gene Information - | Gene Information - | Gene Information - |
애플리케이션
Palmitoylethanolamide has been used as a reference standard in mass spectrometry (MS/MS).[1]
생화학적/생리학적 작용
Palmitoylethanolamide (PEA) is a natural fatty acid[2] amide of ethanolamine and palmitic acid.[3] It is found in soybeans, egg yolk, and many other food sources.[4] PEA is an endogenous cannabinoid receptor agonist.[5] It is a peroxisome proliferator-activated receptor α (PPAR-α) ligand. PEA possesses anti-inflammatory, anti-allergic[4], neuroprotective, and analgesic activities.[6] It belongs to the class of lipid mediators and the N-acylethanolamine family. PEA blocks the release of pro-inflammatory mediators from activated mast cells and prevents the recruitment of activated mast cells at the site of nerve injury.[2]
결합
Structural analog of anandamide.
신호어
Danger
유해 및 위험 성명서
Hazard Classifications
Aquatic Chronic 2 - Eye Dam. 1 - Skin Irrit. 2
Storage Class Code
13 - Non Combustible Solids
WGK
WGK 2
Flash Point (°F)
Not applicable
Flash Point (°C)
Not applicable
개인 보호 장비
Eyeshields, Gloves, type N95 (US)
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시험 성적서(COA)
Lot/Batch Number
이미 열람한 고객
Jonathan C van Zijl et al.
Annals of clinical and translational neurology, 5(4), 386-396 (2018-04-25)
Posthypoxic myoclonus (PHM) in the first few days after resuscitation can be divided clinically into generalized and focal (uni- and multifocal) subtypes. The former is associated with a subcortical origin and poor prognosis in patients with postanoxic encephalopathy (PAE), and
Tessa L Crume et al.
American journal of obstetrics and gynecology, 215(5), 609-609 (2016-10-30)
Consistent evidence of an influence of maternal dietary intake during pregnancy on infant body size and composition in human populations is lacking, despite robust evidence in animal models. We sought to evaluate the influence of maternal macronutrient intake and balance
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
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
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
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