Indenolol

Indenolol
	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-(1H-Inden-4-yloxy)-3-(propan-2-ylamino)propan-2-ol
ChemSpider	64962
DrugBank	DB08952 7px
EC number	262-323-5
	InChI InChI=1S/C15H21NO2/c1-11(2)16-9-13(17)10-18-15-8-4-6-12-5-3-7-14(12)15/h3-4,6-8,11,13,16-17H,5,9-10H2,1-2H3; Key: MPGBPFMOOXKQRX-UHFFFAOYSA-N; InChI=1/C15H21NO2/c1-11(2)16-9-13(17)10-18-15-8-4-6-12-5-3-7-14(12)15/h3-4,6-8,11,13,16-17H,5,9-10H2,1-2H3; Key: MPGBPFMOOXKQRX-UHFFFAOYAY;
Jmol-3D images	Image
KEGG	D08078
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

Indenolol is a beta-adrenergic blocker.^[1]

References

^ Ali, I; Gaitonde, VD; Aboul-Enein, HY; Hussain, A (2009). "Chiral separation of beta-adrenergic blockers on CelluCoat column by HPLC". Talanta 78 (2): 458–63. PMID 19203609. doi:10.1016/j.talanta.2008.11.043.

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