Gallopamil (hydrochloride)
Gallopamil hydrochloride (Methoxyverapamil hydrochloride), a methoxy derivative of Verapamil, is a phenylalkylamine calcium antagonist[1]. Gallopamil hydrochloride inhibits acid secretion in a concentration-dependent manner with an IC50 of 10.9 μM[2]. Gallopamil hydrochloride is a potent antiarrhythmic and vasodilator agent[3].
Product Specifications
CAS Number
16662-46-7
Product Name Alternative
Methoxyverapamil (hydrochloride)
UNSPSC
12352005
Hazard Statement
H302, H315, H319, H332, H335
Target
Calcium Channel
Type
Reference compound
Related Pathways
Membrane Transporter/Ion Channel; Neuronal Signaling
Applications
COVID-19-immunoregulation
Field of Research
Cardiovascular Disease
Assay Protocol
https://www.medchemexpress.com/gallopamil-hydrochloride.html
Concentration
10mM
Purity
99.15
Solubility
DMSO : 100 mg/mL (ultrasonic)
Smiles
COC1=C(OC)C(OC)=CC(C(CCCN(C)CCC2=CC(OC)=C(OC)C=C2)(C#N)C(C)C)=C1.[H]Cl
Molecular Formula
C28H41ClN2O5
Molecular Weight
521.09
Precautions
H302, H315, H319, H332, H335
References & Citations
Shipping Conditions
Room Temperature
Storage Conditions
4°C (Powder, sealed storage, away from moisture)
Scientific Category
Reference compound1
Clinical Information
Phase 2
Isoform
Calcium Channel
Available Sizes
Frequently Asked Questions
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