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Betaxolol

产品号 DB00195 公司名称 DrugBank
CAS号 63659-18-7 公司网站 http://www.ualberta.ca/
分子式 C18H29NO3 电 话 (780) 492-3111
分子量 307.42776 传 真
纯 度 电子邮件 david.wishart@ualberta.ca
保 存 Chembase数据库ID: 80

产品价格信息

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产品别名

标题
Betaxolol
IUPAC标准名
(3-{4-[2-(cyclopropylmethoxy)ethyl]phenoxy}-2-hydroxypropyl)(propan-2-yl)amine
IUPAC传统名
betaxolol
商标名
Betoptic
Betaxon
Betoptic S
Kerlone
别名
Betaxololum [INN-Latin]
Betazolol
Betaxolol HCL

产品登记号

PubChem CID 2369
CAS号 63659-18-7
PubChem SID 46506041

产品性质

疏水性(logP) 2.4
溶解度 451 mg/L

产品详细信息

详细说明 (English)
Item Information
Drug Groups approved
Description A cardioselective beta-1-adrenergic antagonist with no partial agonist activity. [PubChem]
Indication For the management of hypertension.
Pharmacology Betaxolol is a competitive, beta(1)-selective (cardioselective) adrenergic antagonist. Betaxolol is used to treat hypertension, arrhythmias, coronary heart disease, glaucoma, and is also used to reduce non-fatal cardiac events in patients with heart failure. Activation of beta(1)-receptors (located mainly in the heart) by epinephrine increases the heart rate and the blood pressure, and the heart consumes more oxygen. Drugs such as betaxolol that block these receptors therefore have the reverse effect: they lower the heart rate and blood pressure and hence are used in conditions when the heart itself is deprived of oxygen. They are routinely prescribed in patients with ischemic heart disease. In addition, beta(1)-selective blockers prevent the release of renin, which is a hormone produced by the kidneys which leads to constriction of blood vessels. Betaxolol is lipophilic and exhibits no intrinsic sympathomimetic activity (ISA) or membrane stabilizing activity.
Toxicity Oral LD50s are 350 to 400 mg betaxolol/kg in mice and 860 to 980 mg/kg in rats. Predicted symptoms of overdose include bradycardia, congestive heart failure, hypotension, bronchospasm, and hypoglycemia.
Affected Organisms
Humans and other mammals
Biotransformation Primarily hepatic. Approximately 15% of the dose administered is excreted as unchanged drug, the remainder being metabolites whose contribution to the clinical effect is negligible.
Absorption Absorption of an oral dose is complete. There is a small and consistent first-pass effect resulting in an absolute bioavailability of 89% ± 5% that is unaffected by the concomitant ingestion of food or alcohol.
Half Life 14-22 hours
Protein Binding 50%
References
Canotilho J, Castro RA: The structure of betaxolol studied by infrared spectroscopy and natural bond orbital theory. Spectrochim Acta A Mol Biomol Spectrosc. 2010 Aug;76(3-4):395-400. Epub 2010 Apr 4. [Pubmed]
External Links
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参考文献

  • Canotilho J, Castro RA: The structure of betaxolol studied by infrared spectroscopy and natural bond orbital theory. Spectrochim Acta A Mol Biomol Spectrosc. 2010 Aug;76(3-4):395-400. Epub 2010 Apr 4. Pubmed