![]() Verapamil-d3-1 hydrochloride structure
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Common Name | Verapamil-d3-1 hydrochloride | ||
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CAS Number | 2714485-49-9 | Molecular Weight | 494.08 | |
Density | N/A | Boiling Point | N/A | |
Molecular Formula | C27H36D3ClN2O4 | Melting Point | N/A | |
MSDS | N/A | Flash Point | N/A |
Use of Verapamil-d3-1 hydrochlorideVerapamil-d3-1 (hydrochloride) is the deuterium labeled Verapamil hydrochloride[1]. 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[2][3][4]. |
Name | Verapamil-d3-1 hydrochloride |
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Description | Verapamil-d3-1 (hydrochloride) is the deuterium labeled Verapamil hydrochloride[1]. 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[2][3][4]. |
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Related Catalog | |
In Vitro | 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. Deuteration has gained attention because of its potential to affect the pharmacokinetic and metabolic profiles of drugs[1]. |
References |
[3]. Krikler DM. Verapamil in arrhythmia. Br J Clin Pharmacol. 198621 Suppl 2:183S-189S. |
Molecular Formula | C27H36D3ClN2O4 |
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Molecular Weight | 494.08 |