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SR17018

更新时间:2025-08-25 13:28:56

SR17018结构式
SR17018结构式
品牌特惠专场
常用名 SR17018 英文名 SR17018
CAS号 2134602-45-0 分子量 410.72
密度 N/A 沸点 N/A
分子式 C19H18Cl3N3O 熔点 N/A
MSDS N/A 闪点 N/A

 SR17018用途


SR17018 是一种 mu 型阿片受体 (mu-opioid-receptor) 激动剂,能够与 GTPγS 结合,EC50 值为 97 nM。

 SR17018名称

中文名 SR17018
英文名 SR17018

 SR17018生物活性

描述 SR17018 是一种 mu 型阿片受体 (mu-opioid-receptor) 激动剂,能够与 GTPγS 结合,EC50 值为 97 nM。
相关类别
靶点实验

EC50: 97 nM (MOR)[1]

体外研究 SR17018是一种μ-阿片受体(MOR)激动剂,与GTPγS结合,EC50为97 nM。 SR17018对低于10μM的MOR诱导βarrestin2募集没有明显影响。 SR17018通过G蛋白或βarrestin2促进信号传导[1]。
参考文献

[1]. Schmid CL, et al. Bias Factor and Therapeutic Window Correlate to Predict Safer Opioid Analgesics. Cell. 2017 Nov 16;171(5):1165-1175.e13.

 SR17018物理化学性质

分子式 C19H18Cl3N3O
分子量 410.72
储存条件 2-8℃

 SR17018靶点实验

查看更多实验

实验名称:cAMP inhibition assays from US Patent US10751335: "Signaling-biased mu opioid recepto...
来源:BindingDB
靶标:N/A
External Id:BindingDB_9312_2
实验名称:G protein signaling assays from US Patent US10751335: "Signaling-biased mu opioid rec...
来源:BindingDB
靶标:N/A
External Id:BindingDB_9312_1
实验名称:Ratio of EC50 for human mu opioid receptor expressed in human U2OS cells co-transfect...
来源:ChEMBL
靶标:Mu-type opioid receptor
External Id:CHEMBL4371661
实验名称:Agonist activity at human MOR expressed in CHOK1 cells assessed as inhibition of fors...
来源:ChEMBL
靶标:Mu-type opioid receptor
External Id:CHEMBL4680511
实验名称:Agonist activity at human MOR expressed in CHOK1 cells assessed as inhibition of fors...
来源:ChEMBL
靶标:Mu-type opioid receptor
External Id:CHEMBL4680510
实验名称:Agonist activity at human KOR expressed in CHOK1 cells assessed as inhibition of fors...
来源:ChEMBL
靶标:Kappa-type opioid receptor
External Id:CHEMBL4680513
实验名称:Agonist activity at human KOR expressed in CHOK1 cells assessed as inhibition of fors...
来源:ChEMBL
靶标:Kappa-type opioid receptor
External Id:CHEMBL4680512
实验名称:Agonist activity at human mu opioid receptor expressed in CHO cell membranes after 1 ...
来源:ChEMBL
靶标:Mu-type opioid receptor
External Id:CHEMBL4371526
实验名称:Agonist activity at human mu opioid receptor expressed in human U2OS cells co-transfe...
来源:ChEMBL
靶标:Mu-type opioid receptor
External Id:CHEMBL4371528
实验名称:Inhibition of human mu-opioid receptor assessed as reduction in intracellular cAMP ac...
来源:ChEMBL
靶标:Mu-type opioid receptor
External Id:CHEMBL4409290
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