Clentiazem
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| Names | |
|---|---|
| IUPAC name
acetic acid [(2S,3S)-8-chloro-5-(2-dimethylaminoethyl)-2-(4-methoxyphenyl)-4-oxo-2,3-dihydro-1,5-benzothiazepin-3-yl] ester | |
| Identifiers | |
| 111659-76-8 | |
| ChemSpider | 51418 |
| Jmol interactive 3D | Image |
| PubChem | 57026 |
| UNII | 40DK034DRC |
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| Properties | |
| C22H25ClN2O4S | |
| Molar mass | 448.9629 |
| Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa). | |
| | |
| Infobox references | |
Clentiazem is a calcium channel blocker.[1]
It is a chloride derivative of diltiazem.[2]
References
- ↑ Giasson S, Garceau D, Homsy W, Dumont L (October 1995). "Pharmacodynamics and pharmacokinetics of clentiazem and diltiazem in closed-chest anesthetized dogs". Cardiovasc Drugs Ther 9 (5): 685–92. doi:10.1007/BF00878551. PMID 8573551.
- ↑ Dagenais F, Hollmann C, Buluran J, Cartier R (October 1995). "Clentiazem and diltiazem preserve endothelium-dependent relaxation following global rat heart ischemia". Can J Cardiol 11 (9): 816–22. PMID 7585280.
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