Bevantolol
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| Systematic (IUPAC) name | |
|---|---|
|
(RS)-[2-(3,4-dimethoxyphenyl)ethyl][2-hydroxy-3-(3-methylphenoxy)propyl]amine | |
| Clinical data | |
| AHFS/Drugs.com | International Drug Names |
| Routes of administration | Oral |
| Legal status |
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| Identifiers | |
| CAS Number |
59170-23-9 |
| ATC code | C07AB06 (WHO) |
| PubChem | CID 2372 |
| DrugBank |
DB01295 |
| ChemSpider |
2282 |
| UNII |
34ZXW6ZV21 |
| ChEBI |
CHEBI:238698 |
| ChEMBL |
CHEMBL314010 |
| Chemical data | |
| Formula | C20H27NO4 |
| Molar mass | 345.43 g/mol |
| Chirality | Racemic mixture |
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| (verify) | |
Bevantolol (INN) is a drug that acts as both a beta blocker and a calcium channel blocker.[1]
References
- ↑ Warltier DC, Gross GJ, Jesmok GJ, Brooks HL, Hardman HF (1980). "Protection of Ischemic Myocardium: Comparison of Effects of Propranolol, Bevantolol and N-Dimethyl Propranolol on Infarct Size Following Coronary Artery Occlusion in Anesthetized Dogs". Cardiology 66.
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