(R)-Verapamil D7 hydrochloride(Synonyms: (R)-(+)-Verapamil D7 hydrochloride)

发表于由

上海金畔生物科技有限公司为生命科学和医药研发人员提供生物活性分子抑制剂、激动剂、特异性抑制剂、化合物库、重组蛋白，专注于信号通路和疾病研究领域。

(R)-Verapamil D7 hydrochloride (Synonyms: (R)-(+)-Verapamil D7 hydrochloride)

(R)-Verapamil D7 hydrochloride ((R)-(+)-Verapamil D7 hydrochloride) 是 (R)-Verapamil hydrochloride 的一种氘代化合物。(R)-Verapamil hydrochloride ((R)-(+)-Verapamil hydrochloride) 是一种 P-糖蛋白抑制剂。(R)-Verapamil hydrochloride 抑制 MRP1 介导的转运，导致 MRP1 过表达细胞对抗癌药产生化学敏感性。

(R)-Verapamil D7 hydrochloride(Synonyms: (R)-(+)-Verapamil D7 hydrochloride)

(R)-Verapamil D7 hydrochloride Chemical Structure

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生物活性

(R)-Verapamil D7 hydrochloride ((R)-(+)-Verapamil D7 hydrochloride) is a deuterium labeled (R)-Verapamil hydrochloride. (R)-Verapamil hydrochloride ((R)-(+)-Verapamil hydrochloride) is a P-Glycoprotein inhibitor. (R)-Verapamil hydrochloride blocks MRP1 mediated transport, resulting in chemosensitization of MRP1-overexpressing cells to anticancer drugs[1][2].

分子量

498.11

Formula

C27H32D7ClN2O4
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.
参考文献

  • [1]. Plumb JA, et al. The activity of verapamil as a resistance modifier in vitro in drug resistant human tumour cell lines is not stereospecific. Biochem Pharmacol. 1990 Feb 15;39(4):787-92.

    [2]. Perrotton T, et al. (R)- and (S)-verapamil differentially modulate the multidrug-resistant protein MRP1. J Biol Chem. 2007 Oct 26;282(43):31542-8. Epub 2007 Jul 22.

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