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  4. U-51605

U-51605 是一种血小板聚集抑制剂，并抑制血栓烷合成。U-51605 也是前列腺素 I2 合酶抑制剂，能够对 NO供体 (如 NOR3) 诱导的视网膜血管舒张反应起抑制作用。

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U-51605 Chemical Structure

U-51605 Chemical Structure

CAS No. : 64192-56-9

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U-51605 相关抗体

Top Publications Citing Use of Products

  • 生物活性

  • 纯度 & 产品资料

  • 参考文献

生物活性

U-51605 is a platelet aggregation inhibitor and inhibits thromboxane synthesis. U-51605 is also a prostaglandin I2 synthase inhibitor and can inhibit the retinal vasodilation response induced by NO donors (such as NOR3)[1][2].

IC50 & Target

Prostaglandin I2 synthase inhibitor 9α[2]
体外研究
(In Vitro)

U-51605 (3 μM) 抑制乙酰胆碱诱导的内皮依赖性收缩[1]。
U-51605 (0.5, 1, 3, 10 μM) 增加乙酰胆碱诱导的 PGE2 和 PGF2α 释放[1]。

MCE has not independently confirmed the accuracy of these methods. They are for reference only.

U-51605 相关抗体:
分子量

332.48

Formula

C20H32N2O2
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

U-51605 相关分类

  • 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.

Keywords:

U-5160564192-56-9U51605U 51605OthersInhibitorinhibitorinhibit

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产品名称：
U-51605
目录号：
HY-129199
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