Verapamil (hydrochloride)
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].
Product Specifications
CAS Number
[152-11-4]
Product Name Alternative
(±) -Verapamil (hydrochloride) ; CP-16533-1 (hydrochloride)
UNSPSC
12352005
Hazard Statement
H301
Target
Calcium Channel; Cytochrome P450; P-glycoprotein
Type
Reference compound
Related Pathways
Membrane Transporter/Ion Channel; Metabolic Enzyme/Protease; Neuronal Signaling
Applications
COVID-19-immunoregulation
Field of Research
Cardiovascular Disease; Cancer
Assay Protocol
https://www.medchemexpress.com/Verapamil-hydrochloride.html
Purity
99.98
Solubility
DMSO : 58.33 mg/mL (ultrasonic) |H2O : 50 mg/mL (ultrasonic)
Smiles
[H]Cl.COC1=CC=C(C(C#N)(C(C)C)CCCN(CCC2=CC=C(OC)C(OC)=C2)C)C=C1OC
Molecular Formula
C27H39ClN2O4
Molecular Weight
491.06
Precautions
H301
References & Citations
Shipping Conditions
Room Temperature
Storage Conditions
4°C (Powder, sealed storage, away from moisture and light)
Scientific Category
Reference compound1
Clinical Information
Launched
Isoform
CYP3
Citation 01
Available Sizes
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