Name: | Levobunolol |
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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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Name: | Levobunolol |
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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
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Brand: | Akbeta, Betagan |
Category: | Sympatholytics, Adrenergic beta-Antagonists, EENT Drugs |
CAS number: | 47141-42-4 |
Indication: | For lowering intraocular pressure (IOP) and may be used in patients with chronic open-angle glaucoma or ocular hypertension. |
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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 |
Drug interaction: |
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