| Weight | 345.439 g/mol |
|---|---|
| Formula | C20H27NO4 |
| Hydrogen Acceptors | 5 |
| Hydrogen Donors | 2 |
| Aromatic Rings | 2 |
| Rotatable Bonds | 10 |
Bevantolol (59170-23-9)
bevantolol hydrochloride · CI 775 · CI-775
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- Melting point phase diagrams of free base and hydrochloride salts of bevantolol, pindolol and propranolol (International Journal of Pharmaceutics, 1993)
- Assessment of bronchial beta blockade after oral bevantolol. (Clinical Pharmacology & Therapeutics, 1981)
- Respiratory and cardiac effects of metoprolol and bevantolol in patients with asthma. (Clinical Pharmacology & Therapeutics, 1986)
- Beneficial actions of bevantolol on subendocardial blood flow and contractile function in ischemic myocardium. (Journal of Cardiovascular Pharmacology, 1979)
- Cardiovascular effects of bevantolol, a selective 1-adrenoceptor antagonist with a novel pharmacological profile (British Journal of Pharmacology, 1985)
- Direct enantioselective separation of bevantolol by high-performance liquid chromatography on normal and reverse cellulose chiral stationary phases (Biomedical Chromatography, 1994)
-
Predict GHS Hazards for Any Chemical in silico.
Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. - bevantolol hydrochloride
- CI 775
- CI-775
-
SMILESCC1=CC(=CC=C1)OCC(CNCCC2=CC(=C(C=C2)OC)OC)O
-
InChIKeyHXLAFSUPPDYFEO-UHFFFAOYSA-N
- Pubchem - Bevantolol
- Wikipedia - bevantolol
Bevantolol (INN) was a drug candidate for angina and hypertension that acted as both a beta blocker and a calcium channel blocker. It was discovered and developed by Warner-Lambert but in January 1989 the company announced that it had withdrawn the New Drug Application; the company's chairman said: "Who needs the 30th beta blocker?" As of 2016 it wasn't marketed in the US, UK, or Europe and the authors of a Cochrane review could find no product monograph for it.
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Synthesis
1-amino-3-(3-methylphenoxy)propan-2-ol
+
4-(2-Chloroethyl)-1,2-dimethoxybenzene
(Alkylation of primary amines)
1,2-Dimethoxybenzene
+
Reactant
(Friedel-Crafts alkylation)
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