1. Membrane Transporter/Ion Channel Anti-infection
  2. Sodium Channel Parasite
  3. Quinidine

Quinidine 是 Quinine (HY-D0143) 的一种立体异构体,是从南美金鸡纳树的树皮中提取的天然化合物。Quinidine 是已知最早的抗心律失常剂之一,可作为 1a 类抗心律失常药物和抗疟剂。Quinidine 抑制快速向内的钠电流,导致动作电位 0 期的抑制。这种机制抑制了心肌的兴奋性,最终导致动作电位持续时间延长和自动性降低。Quinidine 对快速向内的钠电流表现出 “使用依赖性阻断” 效应,这意味着试剂的影响在较高的心率时增加,在较低的心率时减少。Quinidine 可用于恶性疟原虫疟疾和室性心律失常的研究。

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Quinidine Chemical Structure

Quinidine Chemical Structure

CAS No. : 56-54-2

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生物活性

Quinidine is a stereoisomer of Quinine (HY-D0143), a natural compound derived from the bark of the South American cinchona tree. Quinidine is one of the earliest known antiarrhythmic agents and is available as a Class 1a antiarrhythmic and antimalarial drug. Quinidine inhibits the rapid inward sodium current, resulting in the suppression of action potential phase 0. This mechanism suppresses the excitability of the heart muscle, ultimately leading to longer duration of action potentials and reduced automaticity. Quinidine shows a "use-dependent blocking" effect on the rapidly inward sodium current, meaning that the drug's effects increases at higher heart rates and decreases at lower heart rates.Quinidine can be used in the study of Plasmodium falciparum malaria and ventricular arrhythmias[1].

分子量

324.42

Formula

C20H24N2O2

CAS 号
结构分类
初始来源
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.

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参考文献
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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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产品名称:
Quinidine
目录号:
HY-B1751H
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