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Pronethalol

From Wikipedia, the free encyclopedia
Chemical compound
Pharmaceutical compound
Pronethalol
Clinical data
Routes of
administration
Oral
ATC code
  • none
Legal status
Legal status
  • Withdrawn
Identifiers
  • 1-(naphthalen-2-yl)-2-(propan-2-ylamino)ethanol
CAS Number
PubChemCID
ChemSpider
UNII
ChEMBL
CompTox Dashboard(EPA)
Chemical and physical data
FormulaC15H19NO
Molar mass229.323 g·mol−1
3D model (JSmol)
ChiralityRacemic mixture
  • CC(C)NCC(C1=CC2=CC=CC=C2C=C1)O

Pronethalol (also known asnethalide orcompound 38,174; trade nameAlderlin) was an early non-selectivebeta blocker clinical candidate. It was the first beta blocker to be developed byJames Black and associates atImperial Chemical Industries, and the first to enter clinical use, in November 1963.[1]

However, it was never used widely due tocarcinogenicity in mice, which was thought to result from formation of a carcinogenicnaphthalene epoxide metabolite,[2] and was superseded bypropranolol from 1965 onward.[1]

See also

[edit]

References

[edit]
  1. ^abQuirke V (January 2006)."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.doi:10.1017/s0025727300009455.PMC 1369014.PMID 16502872.
  2. ^Stapleton MP (1997)."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.PMC 325477.PMID 9456487.
α1
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α2
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Antagonists
β
Agonists
Antagonists
Phenethylamines
Amphetamines
Phentermines
Cathinones
Phenylisobutylamines
(and further-extended)
Catecholamines
(and close relatives)
Cyclized
phenethylamines
Phenylalkylpyrrolidines
2-Benzylpiperidines
(phenidates)
Phenylmorpholines
(phenmetrazines)
Phenyloxazolamines
(aminorexes)
Isoquinolines and
tetrahydroisoquinolines
2-Aminoindanes
2-Aminotetralins
Others / unsorted
Related compounds
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