GALLOPAMIL
Gallopamil is a calcium channel blocker reducing cardiac workload and arrhythmias. Side effects include hypotension, bradycardia, and dizziness.
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Product Description
Mechanism of Action
Gallopamil is a phenylalkylamine calcium-channel blocker that inhibits L-type Ca²⁺ channels in cardiac and smooth-muscle cells, reducing contractility, slowing AV conduction and promoting vasodilation.
Benefits and Advantages
Used in electrophysiology research, cardiovascular modelling, calcium-channel studies and vasomodulation assays.
Side Effects and Risks
Bradycardia, hypotension, dizziness and constipation may occur. Handle with cardiovascular drug precautions.
Datasheet
| Molecular Formula | C28H40N2O5 |
|---|---|
| Molecular Weight | 484.6 g/mol |
| CAS Number | 16662-47-8 |
| Storage Condition | Store in a cool, dry place. Keep container tightly closed. Protect from moisture and light. |
| Solubility | Solubility depends on solvent and conditions (e.g., pH). Please contact us for solvent-specific guidance. |
| Purity | Purity information is available upon request (COA). |
| Synonym | Gallopamil; 16662-47-8; Galopamilo; Gallopamillum; D600 |
| IUPAC/Chemical Name | 5-[2-(3,4-dimethoxyphenyl)ethyl-methylamino]-2-propan-2-yl-2-(3,4,5-trimethoxyphenyl)pentanenitrile |
| InChl Key | XQLWNAFCTODIRK-UHFFFAOYSA-N |
| InChl Code | InChI=1S/C28H40N2O5/c1-20(2)28(19-29,22-17-25(33-6)27(35-8)26(18-22)34-7)13-9-14-30(3)15-12-21-10-11-23(31-4)24(16-21)32-5/h10-11,16-18,20H,9,12-15H2,1-8H3 |
| References |
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