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PubChem
Name: Levobunolol
PubChem Compound ID: 34060
Description: A nonselective beta-adrenoceptor antagonist used in the treatment of glaucoma.
Molecular formula: C17H26ClNO3
Molecular weight: 327.846 g/mol
Synonyms:
Betagan; (-)-5-(3-(tert-Butylamino)-2-hydroxypropoxy)-3,4-dihydro-1(2H)-naphthalenone hydrochloride; l-Bunolol hydrochloride; 27912-14-7; Vistagan; W 7000A; 1(2H)-Naphthalenone, 5-(3-((1,1-dimethylethyl)amino)-2-hydroxypropoxy)-3,4-dihydro-, hydrochloride, (-)-; EINECS 248-725-3; Levobunolol hydrochloride; Levobunolol hydrochloride [USAN].
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DrugBank
Identification
Name: Levobunolol
Name (isomeric): DB01210
Drug Type: small molecule
Description: A nonselective beta-adrenoceptor antagonist used in the treatment of glaucoma.
Synonyms:
Levobunololum [INN-Latin]; Levobunolol HCl
Brand: Akbeta, Betagan
Category: Sympatholytics, Adrenergic beta-Antagonists, EENT Drugs
CAS number: 47141-42-4
Pharmacology
Indication: For lowering intraocular pressure (IOP) and may be used in patients with chronic open-angle glaucoma or ocular hypertension.
Pharmacology:
Levobunolol is an ophthalmic beta-blocker, equally effective at β(1)- and β(2)-receptor sites. Levobunolol reduces both elevated and normal IOP in patients with or without glaucoma. In patients with elevated IOP, levobunolol reduces mean IOP by approximately 25-40% from baseline. As the drug is a nonselective &beta-adrenergic blocking age...
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Mechanism of Action: Levobunolol's mechanism of action in reducing IOP is not clearly defined, but is believed to be due to a reduction of the production of aqueous humor via blockage of endogenous catecholamine-stimulated increases in cyclic adenosine monophosphate (AMP) concentrations within the ciliary processes.
Absorption: 80%
Biotransformation: Hepatic
Half Life: 20 hours
Toxicity: Bradycardia, hypotension, bronchospasm, and acute cardiac failure, LD50=700 mg/kg (orally in rat).
Affected organisms: Humans and other mammals
Interactions
Drug interaction:
TreprostinilAdditive hypotensive effect. Monitor antihypertensive therapy during concomitant use.

Targets