Levisoprenaline

Levisoprenaline
Clinical data
Other namesl-Isoprenaline; l-Isoproterenol; (-)-Isoproterenol; (R)-Isoprenaline; (-)-Isoprenaline; (R)-Isoproterenol; L-(-)-Isoproterenol
Drug classSympathomimetic; β-Adrenergic receptor agonist; Bronchodilator
Identifiers
  • 4-[(1R)-1-hydroxy-2-(propan-2-ylamino)ethyl]benzene-1,2-diol
CAS Number
PubChem CID
ChemSpider
UNII
KEGG
ChEBI
ChEMBL
PDB ligand
CompTox Dashboard (EPA)
ECHA InfoCard100.161.507
Chemical and physical data
FormulaC11H17NO3
Molar mass211.261 g·mol−1
3D model (JSmol)
  • CC(C)NC[C@@H](C1=CC(=C(C=C1)O)O)O
  • InChI=1S/C11H17NO3/c1-7(2)12-6-11(15)8-3-4-9(13)10(14)5-8/h3-5,7,11-15H,6H2,1-2H3/t11-/m0/s1
  • Key:JWZZKOKVBUJMES-NSHDSACASA-N

Levisoprenaline (INNTooltip International Nonproprietary Name) is a sympathomimetic, β-adrenergic receptor agonist, and bronchodilator which was never marketed.[1][2][3] It is the levorotatory or (R)-enantiomer of isoprenaline.[3]

References

  1. ^ Elks J (2014). The Dictionary of Drugs: Chemical Data: Chemical Data, Structures and Bibliographies. Springer US. p. 710. ISBN 978-1-4757-2085-3. Retrieved 27 February 2025.
  2. ^ Buckingham J (1996). Dictionary of Organic Compounds. Chapman & Hall. p. 3994. ISBN 978-0-412-54090-5. Retrieved 27 February 2025.
  3. ^ a b Morton IK, Hall JM (2012). Concise Dictionary of Pharmacological Agents: Properties and Synonyms. Springer Netherlands. p. 164. ISBN 978-94-011-4439-1. Retrieved 27 February 2025.



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