2. GPCR/G Protein Neuronal Signaling
  3. Adrenergic Receptor
  4. CP59430

CP59430 是 α-肾上腺素受体 (adrenergic receptor) 拮抗剂 Prazosin (HY-B0193) 的叠氮化物类似物。P59430 在光解前表现为 α1-肾上腺素受体 (α1-adrenaline receptor) 竞争性拮抗剂，在光解后特异性且不可逆地标记 α1-肾上腺素受体 (α1-adrenaline receptor)，并表现为非竞争性拮抗剂活性。CP59430 可用于受体分子表征的研究。

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CP59430 Chemical Structure

CP59430 Chemical Structure

CAS No. : 86329-06-8

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CP59430 相关抗体

Top Publications Citing Use of Products

查看 Adrenergic Receptor 亚型特异性产品:

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α adrenergic receptor β adrenergic receptor

  • 生物活性

  • 纯度 & 产品资料

  • 参考文献

生物活性

CP59430 is an azide analog of the α-adrenaline receptor antagonist Prazosin (HY-B0193). P59430 behaves as a competitive antagonist of α1-adrenaline receptor before photolysis. After photolysis, it specifically and irreversibly labels α1-adrenaline receptor and exhibits non-competitive antagonist activity. CP59430 can be used for the study of receptor molecular characterization[1].

分子量

434.45

Formula

C21H22N8O3
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

CP59430 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:

CP5943086329-06-8CP 59430CP-59430Adrenergic ReceptorBeta ReceptorAdrenaline receptorsanalogsantagonistsphotolysismolecular characterizationInhibitorinhibitorinhibit

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目录号：
HY-123311
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