Chemistry:Pronethalol
From HandWiki
Short description: Chemical compound
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| Routes of administration | Oral |
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| Formula | C15H19NO |
| Molar mass | 229.323 g·mol−1 |
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| Chirality | Racemic mixture |
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Pronethalol (also known as nethalide or compound 38,174; trade name Alderlin) was an early non-selective beta blocker clinical candidate. It was the first beta blocker to be developed by James Black and associates at Imperial Chemical Industries, and the first to enter clinical use, in November 1963.[1]
However, it was never used widely due to carcinogenicity in mice, which was thought to result from formation of a carcinogenic naphthalene epoxide metabolite,[2] and was superseded by propranolol from 1965 onward.[1]
See also
References
- ↑ 1.0 1.1 "Putting theory into practice: James Black, receptor theory and the development of the beta-blockers at ICI, 1958-1978". Med Hist 50 (1): 69–92. January 2006. doi:10.1017/s0025727300009455. PMID 16502872.
- ↑ "Sir James Black and propranolol. The role of the basic sciences in the history of cardiovascular pharmacology". Texas Heart Institute Journal 24 (4): 336–42. 1997. PMID 9456487.
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