Ethylnorepinephrine

Ethylnorepinephrine
Clinical data
Other namesβ,3,4-trihydroxy-N-ethyl-2-phenylethylamine
ATC code
  • None
Legal status
Legal status
  • In general: ℞ (Prescription only)
Identifiers
IUPAC name
  • 4-(2-amino-1-hydroxybutyl)benzene-1,2-diol
CAS Number
PubChem CID
ChemSpider
UNII
ChEMBL
CompTox Dashboard (EPA)
Chemical and physical data
FormulaC10H15NO3
Molar mass197.234 g·mol−1
3D model (JSmol)
SMILES
  • 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

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. 111 Fifth Avenue, New York, New York 10003: Academic Press Inc. p. 150. ISBN 1483255913.{{cite book}}: CS1 maint: location (link)


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