美索曲明水合物,Methoctramine tetrahydrochloride,≥98%

产品编号:Bellancom-116294A| CAS NO:104807-46-7| 分子式:C36H66Cl4N4O2| 分子量:728.75

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货号 包装 价格 库存与货期 购买量 操作
Bellancom-116294A
2300.00 杭州 北京(现货)
Bellancom-116294A
4800.00 杭州 北京(现货)

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美索曲明水合物

产品介绍 Methoctramine tetrahydrochloride 是一种有效的心脏选择性 M2 毒蕈碱受体拮抗剂。Methoctramine tetrahydrochloride 在体内能抑制毒蕈碱引起的心动过缓。
生物活性

Methoctramine tetrahydrochloride is a potent and cardioselectivity antagonist of M2 muscarinic receptor. Methoctramine tetrahydrochloride can inhibit Muscarine-induced bradycardia in vivo.

体外研究

Methoctramine tetrahydrochloride attenuates Acetylcholine (ACh)- and Arecaidine propargyl ester (APE)-induced increases in PG synthesis in a concentration-dependent manner.
Methoctramine (0.01-1 μM) tetrahydrochloride causes facilitation of contractions induced by both pre- and postganglionic nerve stimulation in the guinea-pig isolated, innervated tracheal tube preparation.
Methoctramine (≥10 μM) tetrahydrochloride reduces responses to both nerve stimulation and exogenous ACh.

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

体内研究

Methoctramine (300 µg/kg; i.v.) tetrahydrochloride strongly inhibits the Methacholine- and Muscarine-induced bradycardia in the anaesthetized rat, respectively.

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

体内研究

Methoctramine (300 µg/kg; i.v.) tetrahydrochloride strongly inhibits the Methacholine- and Muscarine-induced bradycardia in the anaesthetized rat, respectively.

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

性状Solid
溶解性数据
运输条件

Room temperature in continental US; may vary elsewhere.

储存方式

-20°C, sealed storage, away from moisture

*In solvent : -80°C, 6 months; -20°C, 1 month (sealed storage, away from moisture)

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