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Gallopamil hydrochloride
本产品不向个人销售,仅用作科学研究,不用于任何人体实验及非科研性质的动物实验。
Gallopamil hydrochloride图片
CAS NO:16662-46-7
包装与价格:
包装价格(元)
2 mg电议
5 mg电议
10 mg电议
25 mg电议
50 mg电议
100 mg电议
200 mg电议
500 mg电议
1 mL*10 mM(in DMSO)电议

产品名称
Methoxyverapamil hydrochloride
产品介绍
Gallopamil hydrochloride 是苯烷基胺钙的拮抗剂。Gallopamil hydrochloride 可用于抗心律失常和血管扩张剂研究。

产品描述

Gallopamil hydrochloride is an antagonist of phenylalkylamine calcium. Gallopamil hydrochloride can be used in antiarrhythmic and vasodilator studies.

体外活性

Gallopamil hydrochloride inhibits acid secretion in a concentration-dependent manner with an IC50 of 10.9 μM[1].

体内活性

In male Wistar rats, Gallopamil hydrochloride (0.2 mg/kg; i.v. for 5 min) markedly reduces ventricular tachycardia and totally prevents fibrillation. Gallopamil hydrochloride significantly reduces systolic and diastolic blood pressure measured 5 min after injection without markedly influencing heart rate[2].

Cas No.

16662-46-7

分子式

C28H41ClN2O5

分子量

521.09

别名

Methoxyverapamil hydrochloride

储存和溶解度

DMSO:95 mg/mL?(182.31 mM),Need ultrasonic
Powder: -20°C for 3 years
In solvent: -80°C for 2 years