Chemistry:Bevantolol
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Short description: Chemical compound
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AHFS/Drugs.com | International Drug Names |
Routes of administration | Oral |
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Formula | C20H27NO4 |
Molar mass | 345.439 g·mol−1 |
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Chirality | Racemic mixture |
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Bevantolol (INN) was a drug candidate for angina and hypertension that acted as both a beta blocker and a calcium channel blocker.[1][2] It was discovered and developed by Warner-Lambert[3] but in January 1989 the company announced that it had withdrawn the New Drug Application; the company's chairman said: "Who needs the 30th beta blocker?"[4] (As of 2016) it wasn't marketed in the US, UK, or Europe and the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.[5]
References
- ↑ "Bevantolol. A preliminary review of its pharmacodynamic and pharmacokinetic properties, and therapeutic efficacy in hypertension and angina pectoris". Drugs 35 (1): 1–21. January 1988. doi:10.2165/00003495-198835010-00001. PMID 2894292.
- ↑ "Bevantolol: a beta-1 adrenoceptor antagonist with unique additional actions". Journal of Clinical Pharmacology 27 (7): 450–60. July 1987. doi:10.1002/j.1552-4604.1987.tb03049.x. PMID 2888789.
- ↑ McPherson, Edwin M. (2007). Pharmaceutical Manufacturing Encyclopedia. (3rd ed.). Burlington: Elsevier. pp. 618–619. ISBN 9780815518563. https://books.google.com/books?id=_J2ti4EkYpkC&pg=PA618.
- ↑ "Warner-Lambert Pipeline Narrowed to 40 Active Research Compounds". Pink Sheet. 30 January 1989. https://pink.pharmamedtechbi.com/PS015015/WARNERLAMBERT-PIPELINE-NARROWED-TO-40-ACTIVE-RESEARCH-COMPOUNDS-ACCUPRIL-QUINAPRIL-NDA-SUBMITTED-JAN-25-80-MIL-BUDGETTED-FOR-CV-WORK-IN-1989.
- ↑ "Blood pressure lowering efficacy of beta-1 selective beta blockers for primary hypertension". The Cochrane Database of Systematic Reviews 3 (4): CD007451. March 2016. doi:10.1002/14651858.CD007451.pub2. PMID 26961574.
Original source: https://en.wikipedia.org/wiki/Bevantolol.
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