Levomoprolol

Levomoprolol
	200px
colspan=2 style="background:#f8eaba; border-top:2px solid transparent; border-bottom:2px solid transparent; text-align:center;" #REDIRECTmw:Help:Magic words#Other; This page is a soft redirect. Names #REDIRECTmw:Help:Magic words#Other; This page is a soft redirect.-	IUPAC name (2S)-1-(2-Methoxyphenoxy)-3-(propan-2-ylamino)propan-2-ol
	Other names (−)-Moprolol; l-Moprolol
ChemSpider	2298561
	InChI 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;
Jmol-3D images	Image
PubChem	Template:Chembox PubChem/format
	SMILES Template:Chembox SMILES/format;
Molar mass	Lua error in Module:Math at line 495: attempt to index field 'ParserFunctions' (a nil value). g·mol−1
	Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
	Infobox references

Levomoprolol is a beta adrenergic antagonist.^[1] It is the (S)-enantiomer of moprolol.

References

^ 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. PMID 2570078. doi:10.1016/s0021-9673(00)91318-9.

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