Ethylnorepinephrine

Ethylnorepinephrine
Clinical data
Other names	β,3,4-Trihydroxy-α-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	536-24-3 ;
PubChem CID	18538;
ChemSpider	17508 ;
UNII	M6AY4VCZ0A;
ChEMBL	ChEMBL31159 ;
CompTox Dashboard (EPA)	DTXSID10968369 ;
Chemical and physical data
Formula	C10H15NO3
Molar mass	197.234 g·mol−1
3D model (JSmol)	Interactive image;
	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 ; Key:LENNRXOJHWNHSD-UHFFFAOYSA-N ;
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Ethylnorepinephrine, sold under the brand names Etanor, Bronkephrine, and Butanefrine, is a sympathomimetic and bronchodilator medication related to norepinephrine.^[1]^[2]^[3] It activates both α and β adrenergic receptors.^[4]

Patent:^[5]

References

^ David J. Triggle (1996). Dictionary of Pharmacological Agents. Boca Raton: Chapman & Hall/CRC. ISBN 0-412-46630-9.
^ 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.
^ CHRISTENSEN JM, VALASEK FE, TAINTER ML (June 1958). "Ethylnorepinephrine; a unique bronchodilator". American Practitioner and Digest of Treatment. 9 (6): 916–21. PMID 13533786.
^ 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.
^ Suter Chester Merle & Ruddy Arlo Wayne, U.S. patent 2,431,285 (1947 to Winthrop Stearns Inc).

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