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十六酰胺乙醇

    
10mM in DMSO

Palmitoylethanolamide

源叶(MedMol)
T91747 一键复制产品信息
544-31-0
C18H37NO2
299.492
N-(2-Hydroxyethyl)hexadecanamide; PEA; Palmidrol;N-(2-Hydroxyethyl)hexadecanamide; PEA; Palmidrol
货号 规格 价格 上海 北京 珠海 重庆 武汉 购买数量
T91747-1ml促销
10mM in DMSO

¥720.00 ¥648.00

货期:3-5天 - - - -
产品介绍 参考文献 质检证书(COA) 摩尔浓度计算器 相关产品
产品描述: 强大的选择性GPR55激动剂;Potent, selective GPR55 agonist;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
保存条件: -80℃(运输条件:冰袋低温运输)
配置溶液浓度参考:
1mg 5mg 10mg
1 mM 3.339 ml 16.695 ml 33.39 ml
5 mM 0.668 ml 3.339 ml 6.678 ml
10 mM 0.334 ml 1.669 ml 3.339 ml
50 mM 0.067 ml 0.334 ml 0.668 ml
注意: 部分产品我司仅能提供部分信息,我司不保证所提供信息的权威性,仅供客户参考交流研究之用。

参考文献

质检证书(COA)

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摩尔浓度计算器

质量 (mg) = 浓度 (mM) x 体积 (mL) x 分子摩尔量 (g/mol)

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