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Tocainide hydrochloride, a sodium channel blocker, inhibits the sodium channels in the pain-producing foci in nerve membranes. It is an orally effective antiarrhythmic agent, structurally and pharmacologically similar to lidocaine [1][2].
Pack Size | Price | Availability | Quantity |
---|---|---|---|
2 mg | $52 | 5 days | |
1 mL x 10 mM (in DMSO) | $98 | 5 days |
Description | Tocainide hydrochloride, a sodium channel blocker, inhibits the sodium channels in the pain-producing foci in nerve membranes. It is an orally effective antiarrhythmic agent, structurally and pharmacologically similar to lidocaine [1][2]. |
Targets&IC50 | Na+ channel: |
In vivo | Tocainide (100 mg/kg) effectively reduces ventricular ectopic activity in unanesthetized dogs with coronary occlusion. Cessation of tocainide in models of digitalis toxicity and coronary occlusion rapidly causes a resurgence of ventricular ectopic activity [1]. |
Molecular Weight | 228.718 |
Formula | C11H17ClN2O |
Cas No. | 71395-14-7 |
Relative Density. | 1.31g/cm3 |
Storage | Powder: -20°C for 3 years | In solvent: -80°C for 1 year | Shipping with blue ice. |
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