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Ethylnorepinephrine

From Wikipedia, the free encyclopedia
Chemical compound
Pharmaceutical compound
Ethylnorepinephrine
Clinical data
Other namesβ,3,4-Trihydroxy-α-ethyl-2-phenylethylamine
ATC code
  • None
Legal status
Legal status
  • In general: ℞ (Prescription only)
Identifiers
  • 4-(2-amino-1-hydroxybutyl)benzene-1,2-diol
CAS Number
PubChemCID
ChemSpider
UNII
ChEMBL
CompTox Dashboard(EPA)
Chemical and physical data
FormulaC10H15NO3
Molar mass197.234 g·mol−1
3D model (JSmol)
  • Oc1ccc(cc1O)C(O)C(N)CC
  • 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, sold under the brand namesEtanor,Bronkephrine, andButanefrine, is asympathomimetic andbronchodilatormedication related tonorepinephrine.[1][2][3] It activates both α and βadrenergic receptors.[4]

Patent:[5]

See also

[edit]

References

[edit]
  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.
  5. ^Suter Chester Merle & Ruddy Arlo Wayne,U.S. patent 2,431,285 (1947 to Winthrop Stearns Inc).
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