Mead ethanolamide

上海金畔生物科技有限公司为生命科学和医药研发人员提供生物活性分子抑制剂、激动剂、特异性抑制剂、化合物库、重组蛋白、同位素标记物,专注于信号通路和疾病研究领域。
Mead ethanolamide 

Mead ethanolamide 是一种内源性大麻素受体(cannabinoid receptor)激动剂,对 CB1CB2Kd 值分别为 753 nM 和 1810 nM。

Mead ethanolamide

Mead ethanolamide Chemical Structure

CAS No. : 169232-04-6

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生物活性

Mead ethanolamide is an endogenous cannabinoid receptor agonist with Kd values of 753 nM and 1810 nM against CB1 and CB2, respectively[1].

IC50 & Target

CB1

753 nM (Kd)

CB2

1810 nM (Kd)

体外研究
(In Vitro)

Mead ethanolamide inhibits cAMP accumulation in CHO-hCB1 and CHO-hCB2 cells with IC50s of 431 nM and 156 nM, respectively[1].
Mead ethanolamide (1-1000 nM) inhibits N-type calcium currents in a concentration-dependent manner. Inhibition was halfmaximal at a Mead ethanolamide concentration of 124 ± 19 nM[1].

Shanghai Jinpan Biotech Co Ltd has not independently confirmed the accuracy of these methods. They are for reference only.

Mead ethanolamide 相关抗体:

分子量

349.55

Formula

C22H39NO2

CAS 号

169232-04-6

结构分类
  • Alkaloids
  • Other Alkaloids
初始来源
  • 内源性代谢物
运输条件

Room temperature in continental US; may vary elsewhere.

储存方式

Please store the product under the recommended conditions in the Certificate of Analysis.

纯度 & 产品资料
Data Sheet (524 KB) 产品使用指南 (1538 KB)

参考文献
  • [1]. Priller J, et al. Mead ethanolamide, a novel eicosanoid, is an agonist for the central (CB1) and peripheral (CB2) cannabinoid receptors. Mol Pharmacol. 1995 Aug;48(2):288-92.  [Content Brief]

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