1. GPCR/G Protein Neuronal Signaling
  2. Opioid Receptor
  3. KOR agonist 4

KOR agonist 4 (compound 39) 是 κ 阿片受体 (Kappa Opioid Receptor) 的激动剂。KOR agonist 4是 G 蛋白信号传导的激活剂。KOR agonist 4 与 GTPγS 结合的 EC50 为 14 nM,Emax 为 83%。KOR agonist 4 在人肝细胞中表现出中等至高的内在清除率。KOR agonist 4 对相关的 μ (MOR)和 δ (DOR) 阿片受体的选择性是 κ (KOR) 阿片受体的 60 倍和 810 倍。KOR agonist 4 适用于中枢神经系统 (CNS) 疾病研究。

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KOR agonist 4 Chemical Structure

KOR agonist 4 Chemical Structure

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  • 生物活性

  • 纯度 & 产品资料

  • 参考文献

生物活性

KOR agonist 4 (compound 39) is an agonist of Kappa Opioid Receptor. KOR agonist 4 is an activator of G-protein signaling. KOR agonist 4 binds with GTPγS with an EC50 of 14 nM and with an Emax of 83 %. KOR agonist 4 demonstrates moderate to high intrinsic clearance in human hepatocytes. KOR agonist 4 exhibits 60- and 810-fold selectivities versus the related mu (MOR) and delta (DOR) opioid receptors. KOR agonist 4 is potential for central nervous system (CNS) disorders research[1].

IC50 & Target[1]

human κ-opioid receptor (hKOR)

14 nM (EC50)

human κ-opioid receptor (hKOR)

4.8 nM (Ki)

human μ-opioid receptor

280 nM (Ki)

δ Opioid Receptor/DOR

3900 nM (Ki)

分子量

319.44

Formula

C21H25N3

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
  • 摩尔计算器

  • 稀释计算器

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Concentration (start) × Volume (start) = Concentration (final) × Volume (final)

This equation is commonly abbreviated as: C1V1 = C2V2

浓度 (start) × 体积 (start) = 浓度 (final) × 体积 (final)
× = ×
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Help & FAQs
  • 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:
KOR agonist 4
目录号:
HY-170973
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