您好,欢迎来到试剂仪器网! [登录] [免费注册]
试剂仪器网
位置:首页 > 产品库 > Norverapamil D7 hydrochloride
立即咨询
咨询类型:
     
*姓名:
*电话:
*单位:
Email:
*留言内容:
请详细说明您的需求。
*验证码:
 
Norverapamil D7 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。
Norverapamil D7 hydrochloride图片
规格:98%
分子量:484.08
包装与价格:
包装价格(元)
1mg电议
5mg电议

产品介绍
Norverapamil D7 ((±)-Norverapamil D7) hydrochloride 是一种 Norverapamil 氘代物。Norverapamil ((±)-Norverapamil) 是 Verapamil 的 N-去甲基代谢物,也是一种L型钙通道阻滞剂和 P-糖蛋白 (P-gp) 功能抑制剂。
货号:ajcx35050
CAS:1216413-74-9
分子式:C26H30D7ClN2O4
分子量:484.08
溶解度:N/A
纯度:98%
存储:Store at -20°C
库存:现货

Background:

Norverapamil D7 ((±)-Norverapamil D7) hydrochloride is a deuterium labeled Norverapamil. Norverapamil ((±)-Norverapamil), an N-demethylated metabolite of Verapamil, is a L-type calcium channel blocker and a P-glycoprotein (P-gp) function inhibitor[1][2].

Stable heavy isotopes of hydrogen, carbon, and other elements have been incorporated into drug molecules, largely as tracers for quantitation during the drug development process[3].

[1]. Adams KN, et al. Verapamil, and its metabolite norverapamil, inhibit macrophage-induced, bacterial efflux pump-mediated tolerance to multiple anti-tubercular drugs. J Infect Dis. 2014 Aug 1;210(3):456-66.
[2]. Pauli-Magnus C, et al. Characterization of the major metabolites of verapamil as substrates and inhibitors of P-glycoprotein. J Pharmacol Exp Ther. 2000 May;293(2):376-82.
[3]. Russak EM, et al. Impact of Deuterium Substitution on the Pharmacokinetics of Pharmaceuticals. Ann Pharmacother. 2019;53(2):211-216.