Verapamil-d3
Verapamil-d3 ((±) -Verapamil-d3) is deuterium labeled Verapamil. Verapamil ((±) -Verapamil) is a calcium channel blocker and a potent and orally active first-generation P-glycoprotein (P-gp) inhibitor. Verapamil also inhibits CYP3A4. Verapamil has the potential for high blood pressure, heart arrhythmias and angina research[1][2][3].
Product Specifications
CAS Number
152561-91-6
Product Name Alternative
(±) -Verapamil-d3; CP-16533-1-d3
UNSPSC
12352005
Target
Calcium Channel; Cytochrome P450; Isotope-Labeled Compounds; P-glycoprotein
Related Pathways
Membrane Transporter/Ion Channel; Metabolic Enzyme/Protease; Neuronal Signaling; Others
Applications
Metabolism-sugar/lipid metabolism
Field of Research
Metabolic Disease; Cancer; Cardiovascular Disease
Smiles
COC(C=C1CCN(C([2H])([2H])[2H])CCCC(C#N)(C2=CC(OC)=C(C=C2)OC)C(C)C)=C(C=C1)OC
Molecular Formula
C27H35D3N2O4
Molecular Weight
457.62
References & Citations
Shipping Conditions
Room temperature
Scientific Category
Isotope-Labeled Compounds
Clinical Information
No Development Reported
Frequently Asked Questions
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