Bevantolol
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Systematic (IUPAC) name | |
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(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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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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