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「同位素标记抑制剂」(R)-Verapamil-d7 hydrochloride
- 产品货号：E-T202508210001
- 发布时间：2025-08-22
- 产品CAS ：N/A
- 产品规格：mg
- 产品纯度：≥95%
- 产品货期：现货下单后48小时内发货，定制产品4-8周。
- 运输条件：顺丰常规运输
产品详情
货号：E-T202508210001
CAS：N/A
规格：mg
纯度：≥95%
生产商：试剂家
生物活性：(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 agents[1][2].
分子量：498.11
Formula：C27H32D7ClN2O4
非标记 CAS：38176-02-2
中文名称：盐酸维拉帕米杂质22-d7
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
Data Sheet (526 KB)
产品使用指南 (1538 KB)
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.
[Content Brief]
[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.
[Content Brief]
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