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Levomoprolol

From Wikipedia, the free encyclopedia
Levomoprolol
Names
Preferred IUPAC name
(2S)-1-(2-Methoxyphenoxy)-3-[(propan-2-yl)amino]propan-2-ol
Other names
(−)-Moprolol; l-Moprolol
Identifiers
3D model (JSmol)
ChemSpider
UNII
  • InChI=1S/C13H21NO3/c1-10(2)14-8-11(15)9-17-13-7-5-4-6-12(13)16-3/h4-7,10-11,14-15H,8-9H2,1-3H3/t11-/m0/s1
    Key: LFTFGCDECFPSQD-NSHDSACASA-N
  • InChI=1/C13H21NO3/c1-10(2)14-8-11(15)9-17-13-7-5-4-6-12(13)16-3/h4-7,10-11,14-15H,8-9H2,1-3H3/t11-/m0/s1
    Key: LFTFGCDECFPSQD-NSHDSACABP
  • CC(C)NC[C@@H](COC1=CC=CC=C1OC)O
Properties
C13H21NO3
Molar mass239.315 g·mol−1
Except where otherwise noted, data are given for materials in theirstandard state (at 25 °C [77 °F], 100 kPa).
Chemical compound

Levomoprolol is abeta adrenergic antagonist.[1] It is the (S)-enantiomer ofmoprolol.

References

[edit]
  1. ^Gianesello, V; Brenn, E; Figini, G; Gazzaniga, A (1989). "Determination by coupled high-performance liquid chromatography-gas chromatography of the beta-blocker levomoprolol in plasma following ophthalmic administration".Journal of Chromatography.473 (2):343–52.doi:10.1016/s0021-9673(00)91318-9.PMID 2570078.
α1
Agonists
Antagonists
α2
Agonists
Antagonists
β
Agonists
Antagonists
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