1. GPCR/G Protein Neuronal Signaling
  2. Opioid Receptor
  3. BU72

BU72 是一种高效、长效的 μ 和 κ 阿片受体 激动剂,同时对 δ 阿片受体也有部分激动作用 (EC50 值分别为 0.054、0.033 和 0.58 nM)。BU72 具有强效且持久的镇痛作用,主要通过 μ 阿片受体介导。BU72 的活性持续时间长,且能部分逆转吗啡的镇痛效果。BU72 可用于阿片依赖的研究。

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BU72 Chemical Structure

BU72 Chemical Structure

CAS No. : 173265-76-4

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  • 生物活性

  • 纯度 & 产品资料

  • 参考文献

生物活性

BU72 is a highly potent and long-acting agonist of μ and κ opioid receptors, and also has a partial agonist effect on δ opioid receptors (EC50 values are 0.054, 0.033, and 0.58 nM, respectively). BU72 has a strong and long-lasting analgesic effect, which is mainly mediated by μ opioid receptors. BU72 has a long-lasting activity and can partially reverse the analgesic effect of morphine. BU72 can be used in the study of opioid dependence[1].

IC50 & Target[1]

μ Opioid Receptor/MOR

0.054 nM (EC50)

κ Opioid Receptor/KOR

0.033 nM (EC50)

δ Opioid Receptor/DOR

0.58 nM (EC50)

分子量

428.57

Formula

C28H32N2O2

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
  • 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:
BU72
目录号:
HY-171758
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