All AbMole products are for research use only, cannot be used for human consumption.

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.
| Molecular Weight | 454.6 |
| CAS Number | 52-53-9 |
| Solubility (25°C) | DMSO 90 mg/mL |
| Storage | 2-8°C, protect from light |
[1] D M Krikler. Verapamil in arrhythmia
[3] N X Nguyen, et al. Verapamil and ventricular tachyarrhythmias
[4] Jasmine L Gowarty, et al. Verapamil as a culprit of palbociclib toxicity
| Best-selling Calcium Channel Products |
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| Ionomycin
Ionomycin is a calcium ionophor and an antibiotic produced by Streptomyces conglobatus. |
| Ionomycin (Calcium salt)
Ionomycin is a calcium ionophor and an antibiotic produced by Streptomyces conglobatus. |
| (R)-(+)-BAY K 8644
(R)-(+)-BAY K 8644 is a calcium channel inhibitor, inhibits Ba2+ currents (IBa) with IC50 of 975 nM. |
| Thapsigargin
Thapsigargin is an endoplasmic reticulum (ER) stress inducer, it is also an inhibitor of microsomal Ca2+-ATPase. |
| Other Calcium Channel Products |
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| KB-R7943 mesylate
KB-R7943 mesylate is a potent, selective inhibitor of the reverse mode of the Na+/Ca2+ exchanger (IC50 = 0.7 mM). |
| Cilnidipine
Cilnidipine is a dual L- and N-type calcium channel blocker that displays antihypertensive, sympatholytic and neuroprotective activity. |
| Azelnidipine
Azelnidipine is a novel dihydropyridine derivative, a L-type calcium channel blocker, and an antihypertensive. Azelnidipine inhibits the intracellular calcium ion flow and lower blood pressure by selectively blocking L-type calcium channel on the membrane of vascular smooth muscle. Azelnidipine inhibits esophageal squamous cell carcinoma proliferation by targeting MEK1/2. Azelnidipine also has anti-inflammatory, antioxidant and neuroprotective effects. |
| Catharanthine
Catharanthine inhibits nicotinic receptor mediated diaphragm contractions with IC50 of 59.6 μM |
| Cinepazide maleate
Cinepazide maleate is a maleate salt form of cinepazide which is a vasodilator. |
| Lomerizine dihydrochloride
Lomerizine dihydrochloride is a relatively new L- and T-type calcium channel blocker used in the treatment of migraine. |
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