Exaprolol

Exaprolol
	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 1-(2-Cyclohexylphenoxy)-3-(propan-2-ylamino)propan-2-ol
	Other names Esprolol
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. Identifiers#REDIRECTmw:Help:Magic words#Other; This page is a soft redirect.- ; ; ; ; ; ;	InChI InChI=1S/C18H29NO2/c1-14(2)19-12-16(20)13-21-18-11-7-6-10-17(18)15-8-4-3-5-9-15/h6-7,10-11,14-16,19-20H,3-5,8-9,12-13H2,1-2H3; Key: ABXHHEZNIJUQFM-UHFFFAOYSA-N;
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

Exaprolol is a beta-adrenoceptor antagonist.^[1]

References

^ Van Waarde, A; Doorduin, J; De Jong, JR; Dierckx, RA; Elsinga, PH (2008). "Synthesis and preliminary evaluation of (S)-11C-exaprolol, a novel beta-adrenoceptor ligand for PET". Neurochemistry international 52 (4–5): 729–33. PMID 17961850. doi:10.1016/j.neuint.2007.09.009.

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