Powder: -20°C for 3 years | In solvent: -80°C for 1 year
Gallopamil (Methoxyverapamil) inhibits acid secretion in a concentration-dependent manner with an IC50 of 10.9 μM. Gallopamil is a potent antiarrhythmic and vasodilator agent. Gallopamil (Methoxyverapamil), a methoxy derivative of Verapamil, is a phenylalkylamine calcium antagonist.
Pack Size | Availability | Price/USD | Quantity |
---|---|---|---|
1 mg | In stock | $ 32.00 | |
5 mg | In stock | $ 72.00 | |
10 mg | In stock | $ 122.00 | |
25 mg | In stock | $ 198.00 | |
50 mg | In stock | $ 297.00 | |
100 mg | In stock | $ 453.00 | |
500 mg | In stock | $ 987.00 | |
1 mL * 10 mM (in DMSO) | In stock | $ 77.00 |
Description | Gallopamil (Methoxyverapamil) inhibits acid secretion in a concentration-dependent manner with an IC50 of 10.9 μM. Gallopamil is a potent antiarrhythmic and vasodilator agent. Gallopamil (Methoxyverapamil), a methoxy derivative of Verapamil, is a phenylalkylamine calcium antagonist. |
In vivo | Gallopamil(5 min) significantly reduces systolic and diastolic blood pressure measured without markedly influencing heart rate. Gallopamil (0.2 mg/kg;i.v.) markedly reduces ventricular tachycardia (VT) and totally prevents fibrillation (VF)[2]. |
Synonyms | Methoxyverapamil |
Molecular Weight | 484.63 |
Formula | C28H40N2O5 |
CAS No. | 16662-47-8 |
Powder: -20°C for 3 years | In solvent: -80°C for 1 year
DMSO: 95 mg/mL (196.03 mM), Sonification is recommended.
You can also refer to dose conversion for different animals. More
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Gallopamil 16662-47-8 Membrane transporter/Ion channel Metabolism Calcium Channel Ca channels Inhibitor inhibit Verapamil phenylalkylamine Methoxyverapamil antiarrhythmic calcium vasodilator Ca2+ channels inhibitor