Quinprenaline

Quinprenaline
Clinical data
Other namesQuinterenol
Drug classβ-Adrenergic receptor agonist; Sympathomimetic; Bronchodilator
Identifiers
  • 5-[1-hydroxy-2-(propan-2-ylamino)ethyl]quinolin-8-ol
CAS Number
PubChem CID
ChemSpider
UNII
ChEMBL
CompTox Dashboard (EPA)
Chemical and physical data
FormulaC14H18N2O2
Molar mass246.310 g·mol−1
3D model (JSmol)
  • CC(C)NCC(C1=C2C=CC=NC2=C(C=C1)O)O
  • InChI=1S/C14H18N2O2/c1-9(2)16-8-13(18)10-5-6-12(17)14-11(10)4-3-7-15-14/h3-7,9,13,16-18H,8H2,1-2H3
  • Key:RSDQHEMTUCMUPQ-UHFFFAOYSA-N

Quinprenaline (INNTooltip International Nonproprietary Name; also known as quinterenol) is a sympathomimetic, long-acting β-adrenergic receptor agonist, and bronchodilator of the phenethylamine family which was never marketed.[1][2][3][4][5] It was first described by the 1960s.[2][4]

References

  1. ^ Elks J (2014). The Dictionary of Drugs: Chemical Data: Chemical Data, Structures and Bibliographies. Springer US. p. 1060. ISBN 978-1-4757-2085-3. Retrieved 27 February 2025.
  2. ^ a b Cain CK (1965). Annual Reports in Medicinal Chemistry. Academic Press. p. 87. ISBN 978-0-08-058347-1. Retrieved 27 February 2025.
  3. ^ Broadley KJ (2017). Autonomic Pharmacology. CRC Press. p. 193. ISBN 978-1-135-74138-9. Retrieved 27 February 2025.
  4. ^ a b Aviado DM, Bowman WC, Burnstock G, Greven J, Hannappel J, Juul P, et al. (2012). Adrenergic Activators and Inhibitors: Part II. Handbook of Experimental Pharmacology. Springer Berlin Heidelberg. p. 81. ISBN 978-3-642-67584-3. Retrieved 27 February 2025.
  5. ^ Milne G (2018). Drugs: Synonyms and Properties. Routledge Revivals. Taylor & Francis. p. 518. ISBN 978-1-351-78990-5. Retrieved 27 February 2025.



This article is issued from Wikipedia. The text is available under Creative Commons Attribution-Share Alike 4.0 unless otherwise noted. Additional terms may apply for the media files.