1. GPCR/G Protein Neuronal Signaling
  2. Opioid Receptor
  3. MOR agonist-5

MOR agonist-5 是一种选择性、强效的 μ-阿片受体 (MOR) 激动剂,其 EC50 值为 0.25 nM。MOR agonist-5 对 δ-阿片受体 (DOR) 的 EC50 为 10 nM,对 κ- 阿片受体 (KOR) 和痛敏肽受体 (NOR) 的 EC50 均大于10000 nM。MOR agonist-5 具有显著的抗伤害感受活性,可用于疼痛相关研究。

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MOR agonist-5

MOR agonist-5 Chemical Structure

CAS No. : 3085132-31-3

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  • 生物活性

  • 纯度 & 产品资料

  • 参考文献

生物活性

MOR agonist-5 is a selective and potent mu-opioid receptor (MOR) agonist with an EC50 of 0.25 nM. MOR agonist-5 shows an EC50 of 10 nM for DOR and >10000 nM for KOR and NOR. MOR agonist-5 exerts significant antinociceptive activity. MOR agonist-5 can be used for the research of pain[1].

IC50 & Target[1]

μ Opioid Receptor/MOR

0.25 nM (EC50)

δ Opioid Receptor/DOR

10 nM (EC50)

κ Opioid Receptor/KOR

>10000 nM (EC50)

NOP Receptor/ORL1

>10000 nM (EC50)

体外研究
(In Vitro)

MOR agonist-5 (Compound 13) 表现出较弱的 β-阻断蛋白 2 募集作用,pEC50 值为 7.8[1]
MOR agonist-5 对 DOR 的 EC50 为 10 nM,对 KOR 和 NOR 的 EC50 均大于 10000 nM[1]

MCE has not independently confirmed the accuracy of these methods. They are for reference only.

体内研究
(In Vivo)

MOR agonist-5 (Compound 13) (腹腔注射) 具有显著的抗伤害感受活性,在 B6129/F1 杂交小鼠热板试验中,其 ED50 为 0.6581 mg/kg,且其抗伤害感受作用可被 Naloxone (HY-17417A) 完全拮抗[1]

MCE has not independently confirmed the accuracy of these methods. They are for reference only.

分子量

349.47

Formula

C22H27N3O

CAS 号
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
参考文献
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  • Do most proteins show cross-species activity?

    Species cross-reactivity must be investigated individually for each product. Many human cytokines will produce a nice response in mouse cell lines, and many mouse proteins will show activity on human cells. Other proteins may have a lower specific activity when used in the opposite species.

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产品名称:
MOR agonist-5
目录号:
HY-179705
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