CAS:544-31-0|十六酰胺乙醇

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CAS:544-31-0|十六酰胺乙醇

产品别名：
Palmitoylethanolamide
CAS 号：
544-31-0
分子量：
299.492
分子式：
C18H37NO2
产品纯度：
≥95%
产品规格：
100mg，500mg（可根据需求定制）
运输条件：
顺丰速运包邮
产品说明：
此产品仅用于科研，不能用于人体治疗、药物开发、和其他商业用途。
更新时间：
2023-03-01 10:34:19

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产品名称：十六酰胺乙醇
英文名称：Palmitoylethanolamide
别名：N-(2-Hydroxyethyl)hexadecanamide; PEA; Palmidrol
英文别名：N-(2-Hydroxyethyl)hexadecanamide; PEA; Palmidrol
规格或纯度：10mM in DMSO
运输条件：超低温冰袋运输
生化机理
Endogenous CB2 cannabinoid receptor agonist.Endogenous lipid that acts as a potent, selective GPR55 agonist (EC 50 = 4 nM). Highly selective over CB 2 and CB 1 receptors (EC 50 values are 19.8 and >30 μM, respectively). Fatty acid amide hydrolase (FAAH) and PEA-preferring acid amidase (PAA) substra
Palmitoylethanolamide is an endogenous cannabinoid. It is a weak ligand of the cannabinoid 1 (CB1) and cannabinoid 2 (CB2) receptors. It has been found to inhibit FAAH (fatty acid amide hydrolase). Palmitoylethanolamide exhibits anti-nociceptive, anti-inflammatory, anti-convulsant and immunosuppresant activity. Palmitoylethanolamide acts by binding to an unidentified cannabinoid receptor that is similar to CB2. It also acts as a selective activator of the GPR55 receptor. In addition, this compound directly activates PPARα, producing an anti-inflammatory response.
Palmitoylethanolamide is an endogenous cannabinoid. It is a weak ligand of the cannabinoid 1 (CB1) and cannabinoid 2 (CB2) receptors. It has been found to inhibit FAAH (fatty acid amide hydrolase). Palmitoylethanolamide exhibits anti-nociceptive, anti-inflammatory, anti-convulsant and immunosuppresant activity. Palmitoylethanolamide acts by binding to an unidentified cannabinoid receptor that is similar to CB2. It also acts as a selective activator of the GPR55 receptor. In addition, this compound directly activates PPARα, producing an anti-inflammatory response.An endogenous cannabinoid agonist, FAAH inhibitor, and PPARα agonist
CAS编号：544-31-0
敏感性：对热敏感
熔点：99 °C

储存温度-80℃储存
分子量：299.492
分子式：C18H37NO2
PubChem CID：4671