2. GPCR/G Protein Neuronal Signaling Immunology/Inflammation
  3. Histamine Receptor
  4. Clemastine

Clemastine  (Synonyms: HS-592; Meclastine)

目录号: HY-B0298
产品使用指南

摩尔计算器

Clemastine (HS-592) 是一种口服有效的组胺受体 H1 拮抗剂。Clemastine 是一种抗组胺药，主要通过与组胺竞争结合 H1 受体来缓解过敏反应症状。具有抗炎作用。

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Clemastine Chemical Structure

Clemastine Chemical Structure

CAS No. : 15686-51-8

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规格 是否有货
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100 mg   询价  
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Clemastine 的其他形式现货产品:

Other Forms of Clemastine:

Clemastine 相关抗体

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查看 Histamine Receptor 亚型特异性产品:

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H1 Receptor H2 Receptor H3 Receptor H4 Receptor Histamine Receptor

  • 生物活性

  • 纯度 & 产品资料

  • 参考文献

生物活性

Clemastine (HS-592) is a potent and orally active histamine receptor H1 antagonist. Clemastine is an antihistamine mainly used for relieving symptoms of allergic reactions primarily by competing with histamine to bind H1 receptors. Anti-inflammatory effects[1][2].

Clinical Trial
分子量

343.89

Formula

C21H26ClNO
CAS 号
性状

固体

颜色

White to off-white

中文名称

氯马斯丁
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

Clemastine 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:

Clemastine15686-51-8HS-592 Meclastine氯马斯丁HS592HS 592Histamine ReceptorantihistamineH1 receptoranti-inflammatoryoralallergic reactionsInhibitorinhibitorinhibit

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