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

KOR agonist 1 (Compound 7a) 是阿片受体的选择性激动剂,对 KORMORDOREC50 分别为 3.4、701.2 和 1649 nM。KOR agonist 1 与 KOR、MOR 和 DOR 结合,Ki 分别为 3.9、1053 和 4196 nM。KOR agonist 1 在 ICR 小鼠模型中表现出抗伤害作用 (热板试验中的 ED50 为 0.3 mg/kg,腹部收缩试验中的 ED50 为 0.2 mg/kg)。

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KOR agonist 1 Chemical Structure

KOR agonist 1 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 1 (Compound 7a) is a selective agonist for opioid receptor, with EC50s of 3.4, 701.2 and 1649 nM, for KOR, MOR and DOR, respectively. KOR agonist 1 binds KOR, MOR and DOR, with Kis of 3.9, 1053 and 4196 nM, respectively. KOR agonist 1 exhibits antinociceptive effect in ICR mouse model (ED50 in hot plate test is 0.3 mg/kg, in abdominal constriction test is 0.2 mg/kg)[1].

IC50 & Target

κ Opioid Receptor/KOR

3.4 nM (EC50)

μ Opioid Receptor/MOR

701.2 nM (EC50)

δ Opioid Receptor/DOR

1649 nM (EC50)

分子量

562.74

Formula

C37H42N2O3

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

The molarity calculator equation

Mass (g) = Concentration (mol/L) × Volume (L) × Molecular Weight (g/mol)

质量   浓度   体积   分子量 *
= × ×

The dilution calculator equation

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)
× = ×
C1   V1   C2   V2
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 1
目录号:
HY-161539
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