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Formula | C27H38N2O4.HCl |
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Molecular Weight | 491.06 | CAS No. | 152-11-4 | |
Solubility (25°C)* | In vitro | DMSO | 98 mg/mL (199.56 mM) | |
Water | 98 mg/mL (199.56 mM) | |||
Ethanol | 98 mg/mL (199.56 mM) | |||
* <1 mg/ml means slightly soluble or insoluble. * Please note that Selleck tests the solubility of all compounds in-house, and the actual solubility may differ slightly from published values. This is normal and is due to slight batch-to-batch variations. * Room temperature shipping (Stability testing shows this product can be shipped without any cooling measures.) |
Description | Verapamil HCl is an L-type calcium channel blocker that is a class IV anti-arrhythmia agent. Verapamil inhibits both permeability-glycoprotein (P-gp) and CYP3A4. | |
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In vitro | The enzyme hydrolase activity of recombinant CES2 is substantially inhibited by diltiazem and verapamil (Ki = 0.25 ± 0.02 and 3.84 ± 0.99μM, respectively). |
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In vivo | Verapamil confers an anti-arrhythmic effect via calcium influx inhibition, inhibition of oxygen consumption and accompanied by preservation of Cx43 protein in rat heart. |
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Data from [Data independently produced by , , Front Pharmacol, 2018, 9:1298]
Data from [Data independently produced by , , BMC Cancer, 2015, 15:553.]
Data from [Data independently produced by , , Exp Hematol, 2017, 2.436]
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RETURN POLICY
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SHIPPING AND STORAGE
Selleck products are transported at room temperature. If you receive the product at room temperature, please rest assured, the Selleck Quality Inspection Department has conducted experiments to verify that the normal temperature placement of one month will not affect the biological activity of powder products. After collecting, please store the product according to the requirements described in the datasheet. Most Selleck products are stable under the recommended conditions.
NOT FOR HUMAN, VETERINARY DIAGNOSTIC OR THERAPEUTIC USE.