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Levobunolol

Clinical data
Trade names	Betagan
AHFS/Drugs.com	Monograph
MedlinePlus	a686011
Pregnancy category	C
Routes of administration	Topical (eye drops)
ATC code	S01ED03 (WHO)
Legal status
Legal status	US: ℞-only
Pharmacokinetic data
Elimination half-life	20 hours
Identifiers
IUPAC name (S)-5-{oxy}-3,4-dihydronaphthalen-1(2H)-one
CAS Number	47141-42-4
PubChem CID	39468
DrugBank	APRD00165
ChemSpider	36089
UNII	G6317AOI7K
KEGG	D08115
ChEBI	CHEBI:6438
ChEMBL	ChEMBL1201237
CompTox Dashboard (EPA)	DTXSID1043833
Chemical and physical data
Formula	C17H25NO3
Molar mass	291.385 g/mol g·mol
3D model (JSmol)	Interactive image
SMILES O=C2c1cccc(OC(O)CNC(C)(C)C)c1CCC2
InChI InChI=1S/C17H25NO3/c1-17(2,3)18-10-12(19)11-21-16-9-5-6-13-14(16)7-4-8-15(13)20/h5-6,9,12,18-19H,4,7-8,10-11H2,1-3H3/t12-/m0/s1 Key:IXHBTMCLRNMKHZ-LBPRGKRZSA-N
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Levobunolol (AK-Beta, Liquifilm, Betegan) is a non-selective beta blocker. It is used topically to manage glaucoma.

References

External links

• Ishibashi T, Yokoi N, Kinoshita S (2003). "Comparison of the effects of topical levobunolol and timolol solution on the human ocular surface". Cornea. 22 (8): 709–15. doi:10.1097/00003226-200311000-00001. PMID 14576520.{{cite journal}}: CS1 maint: multiple names: authors list (link)
• Ogasawara H, Yoshida A, Fujio N, Konno S, Ishiko S (1999). "". Nippon Ganka Gakkai Zasshi. 103 (7): 544–50. PMID 10443129.{{cite journal}}: CS1 maint: multiple names: authors list (link)
• Leung M, Grunwald J (1997). "Short-term effects of topical levobunolol on the human retinal circulation". Eye. 11 ( Pt 3): 371–6. PMID 9373479.

• Beta blockers
• Ketones
• Phenol ethers
• Alcohols
• Tetralins