Ethylnorepinephrine

Chemical compound
  • None
Legal statusLegal status
  • In general: ℞ (Prescription only)
Identifiers
  • 4-(2-amino-1-hydroxybutyl)benzene-1,2-diol
CAS Number
  • 536-24-3 ☒N
PubChem CID
  • 18538
ChemSpider
  • 17508 checkY
UNII
  • M6AY4VCZ0A
ChEMBL
  • ChEMBL31159 checkY
CompTox Dashboard (EPA)
  • DTXSID10968369 Edit this at Wikidata
Chemical and physical dataFormulaC10H15NO3Molar mass197.234 g·mol−13D model (JSmol)
  • Interactive image
  • Oc1ccc(cc1O)C(O)C(N)CC
InChI
  • InChI=1S/C10H15NO3/c1-2-7(11)10(14)6-3-4-8(12)9(13)5-6/h3-5,7,10,12-14H,2,11H2,1H3 checkY
  • Key:LENNRXOJHWNHSD-UHFFFAOYSA-N checkY
 ☒NcheckY (what is this?)  (verify)

Ethylnorepinephrine (Etanor, Bronkephrine, Butanefrine) is a sympathomimetic and bronchodilator related to norepinephrine.[1][2][3] It activates both α and β adrenergic receptors.[4]

See also

  • Norepinephrine

References

  1. ^ David J. Triggle (1996). Dictionary of Pharmacological Agents. Boca Raton: Chapman & Hall/CRC. ISBN 0-412-46630-9.
  2. ^ KORNEL L (1958). "A case of calcified ventricular aneurysm with progressive heart block; observations on the effect of ethylnorepinephrine". Cardiologia. 32 (2): 101–9. doi:10.1159/000165806. PMID 13500349.
  3. ^ CHRISTENSEN JM, VALASEK FE, TAINTER ML (June 1958). "Ethylnorepinephrine; a unique bronchodilator". American Practitioner and Digest of Treatment. 9 (6): 916–21. PMID 13533786.
  4. ^ Turner, Robert A. (1965). "12. Sympatholytic Agents. VI. The Two Kinds of Receptors". Screening Methods in Pharmacology. New York: Academic Press Inc. p. 150. ISBN 1483255913.
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Stimulants: Phenylethanolamine

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