1. GPCR/G Protein
  2. Adenosine Receptor
  3. AMP-579

AMP-579 是一种腺苷受体激动剂,主要靶向腺苷 A1A2A 受体 (对大鼠大脑和脂肪细胞的 A1 受体的 Ki 为 1.7 和 4.5 nM,对大鼠大脑 A2A 受体的 Ki 为 56 nM)。AMP-579 通过激活 A1 受体来抑制脂肪分解、恢复胰岛素依赖的葡萄糖转运,并降低心率,而通过激活 A2A 受体来刺激血管舒张,特别是在冠状动脉中起到明显作用 (对猪冠状动脉环 IC50 为 0.3 μM)。AMP 579 在心脏保护和急性心肌梗死领域具有应用潜力。

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AMP-579 Chemical Structure

AMP-579 Chemical Structure

CAS No. : 213453-89-5

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  • 生物活性

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  • 参考文献

生物活性

AMP-579 is an adenosine receptor agonist that primarily targets adenosine A1 and A2A receptors (with Ki values of 1.7 and 4.5 nM for the A1 receptor in rat brain and adipocytes, and a Ki value of 56 nM for the A2A receptor in rat brain). AMP-579 inhibits lipolysis, restores insulin-dependent glucose transport, and reduces heart rate through the activation of A1 receptors, while it induces vasodilation, particularly in coronary arteries, through the activation of A2A receptors (with an IC50 of 0.3 μM in porcine coronary arterial rings). AMP 579 shows potential for application in cardioprotection and the treatment of acute myocardial infarction[1].

分子量

478.01

Formula

C22H28ClN5O3S

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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  • 稀释计算器

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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:
AMP-579
目录号:
HY-19310
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