OMDM-2

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。
OMDM-2 

OMDM-2 是一种有效选择性的,代谢稳定的 anandamide 细胞摄取 (ACU) 抑制剂,Ki 值为 3.0 μM。

OMDM-2

OMDM-2 Chemical Structure

CAS No. : 616884-63-0

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OMDM-2 相关产品

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生物活性

OMDM-2 is a potent, selective and metabolically stable inhibitor of anandamide cellular uptake (ACU), with a Ki of 3.0 μM[1].

IC50 & Target

Ki: 3.0 μM (anandamide cellular uptake)[1]

体外研究
(In Vitro)

OMDM-2 shows poor affinity for either CB1 (Ki=5.1 μM) or CB2 (Ki>10 μM) receptors in rat brain and spleen membranes, respectively; OMDM-2 has almost no activity at vanilloid receptors in the intracellular calcium assay carried out with intact cells over-expressing the human VR1 (EC50=10 μM), and no activity as inhibitors of FAAH in N18TG2 cell membranes (Ki>50 μM)[1].

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

OMDM-2 相关抗体:

分子量

431.65

Formula

C27H45NO3

CAS 号

616884-63-0

结构分类
  • Alkaloids
  • Other Alkaloids
  • Phenols
  • Monophenols
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 (520 KB) 产品使用指南 (1538 KB)

参考文献
  • [1]. Ortar G, et al. Novel selective and metabolically stable inhibitors of anandamide cellular uptake. Biochem Pharmacol. 2003 May 1;65(9):1473-81.  [Content Brief]

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