Verapamil-d6 hydrochloride

Modify Date: 2024-01-24 17:58:23

Verapamil-d6 hydrochloride Structure
Verapamil-d6 hydrochloride structure
Common Name Verapamil-d6 hydrochloride
CAS Number 1185032-80-7 Molecular Weight 497.10
Density N/A Boiling Point N/A
Molecular Formula C27H33D6ClN2O4 Melting Point 142°C dec.
MSDS N/A Flash Point N/A

 Use of Verapamil-d6 hydrochloride


Verapamil-d6 (CP-16533-1-d6) hydrochloride is the deuterium labled Verapamil (hydrochloride) (HY-A0064). Verapamil hydrochloride ((±)-Verapamil hydrochloride) is a calcium channel blocker and a potent and orally active first-generation P-glycoprotein (P-gp) inhibitor. Verapamil hydrochloride also inhibits CYP3A4. Verapamil hydrochloride has the potential for high blood pressure, heart arrhythmias and angina research[1][2][3].

 Names

Name VERAPAMIL-D6, HYDROCHLORIDE

 Verapamil-d6 hydrochloride Biological Activity

Description Verapamil-d6 (CP-16533-1-d6) hydrochloride is the deuterium labled Verapamil (hydrochloride) (HY-A0064). Verapamil hydrochloride ((±)-Verapamil hydrochloride) is a calcium channel blocker and a potent and orally active first-generation P-glycoprotein (P-gp) inhibitor. Verapamil hydrochloride also inhibits CYP3A4. Verapamil hydrochloride has the potential for high blood pressure, heart arrhythmias and angina research[1][2][3].
Related Catalog
References

[1]. Krikler DM. Verapamil in arrhythmia. Br J Clin Pharmacol. 1986;21 Suppl 2:183S-189S.  

[2]. Zhou P, et al. Anti-arrhythmic effect of Verapamil is accompanied by preservation of cx43 protein in rat heart. PLoS One. 2013 Aug 12;8(8):e71567.  

[3]. Gowarty JL, et al. Verapamil as a culprit of palbociclib toxicity. J Oncol Pharm Pract. 2019 Apr;25(3):743-746.  

[4]. Russak EM, et al. Impact of Deuterium Substitution on the Pharmacokinetics of Pharmaceuticals. Ann Pharmacother. 2019 Feb;53(2):211-216.  

 Chemical & Physical Properties

Melting Point 142°C dec.
Molecular Formula C27H33D6ClN2O4
Molecular Weight 497.10
Storage condition Refrigerator
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