1. Others Neuronal Signaling GPCR/G Protein Membrane Transporter/Ion Channel
  2. Isotope-Labeled Compounds Adrenergic Receptor Calcium Channel
  3. Bevantolol-d7 hydrochloride

Bevantolol-d7 hydrochloride  (Synonyms: 贝凡洛尔盐酸盐-d7)

目录号: HY-121186S
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Bevantolol-d7 hydrochloride 是氘代标记的 Bevantolol hydrochloride (HY-121186)。 Bevantolol hydrochloride 是一种选择性的 β1/α1-肾上腺素受体 (β1/α1-adrenergic receptor) 拮抗剂,在大鼠大脑皮层中的 pKi 值分别为 7.83、6.9。Bevantolol hydrochloride 是有效的 Ca2+ 拮抗剂。

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Bevantolol-d<sub>7</sub> hydrochloride

Bevantolol-d7 hydrochloride Chemical Structure

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Other Forms of Bevantolol-d7 hydrochloride:

  • 生物活性

  • 纯度 & 产品资料

  • 参考文献

生物活性

Bevantolol-d7 hydrochloride is the deuterium labeled Bevantolol hydrochloride (HY-121186). Bevantolol hydrochloride is a selective β1 and α1-adrenergic receptor antagonist with pKi values of 7.83, 6.9 in rat cerebral cortex, respectively. Bevantolol hydrochloride is a potent Ca2+ antagonist[1][2].

产品应用

1. 该化合物可作为示踪剂。
2. 该化合物可作为 NMR、GC-MS 或 LC-MS 分析中的内标品,用于定量分析。

体外研究
(In Vitro)

氢、碳和其他元素的稳定重同位素已被掺入药物分子中,主要用作药物开发过程中定量的示踪剂。氘化因其可能影响药物的药代动力学和代谢特征而受到关注。

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

分子量

388.94

Formula

C20H21D7ClNO4

非标记 CAS
中文名称

贝凡洛尔盐酸盐-d7

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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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)
× = ×
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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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