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「同位素标记抑制剂」(S)-Verapamil-d7 hydrochloride
- 产品货号：E-T202508210001
- 发布时间：2025-08-21
- 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：(S)-Verapamil-d7 (hydrochloride) is a deuterium labeled (S)-Verapamil hydrochloride. (S)-Verapamil hydrochloride (S(-)-Verapamil hydrochloride) inhibits leukotriene C4 (LTC4) and calcein transport by MRP1. (S)-Verapamil hydrochloride leads to the death of potentially resistant tumor cells[1][2].
分子量：498.11
Formula：C27H32D7ClN2O4
非标记 CAS：36622-28-3
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]. 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]
[2]. Tannergren C, et al. St John's wort decreases the bioavailability of R- and S-verapamil through induction of the first-pass metabolism. Clin Pharmacol Ther. 2004 Apr;75(4):298-309.
[Content Brief]
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