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Orciprenaline

产品号 DB00816 公司名称 DrugBank
CAS号 586-06-1 公司网站 http://www.ualberta.ca/
分子式 C11H17NO3 电 话 (780) 492-3111
分子量 211.25758 传 真
纯 度 电子邮件 david.wishart@ualberta.ca
保 存 Chembase数据库ID: 695

产品价格信息

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产品别名

标题
Orciprenaline
IUPAC标准名
5-{1-hydroxy-2-[(propan-2-yl)amino]ethyl}benzene-1,3-diol
IUPAC传统名
orciprenaline
商标名
Novasmasol
Prometa
Alotec
Alupent
Metaprel
Metaproterenol Polistirex
别名
Metaproterenol Sulfate
Metaproterenol
Orciprenalina [INN-Spanish]
Orciprenalinum [INN-Latin]
Orciprenaline Sulfate

产品登记号

PubChem SID 46504464
CAS号 586-06-1
PubChem CID 4086

产品性质

疏水性(logP) 1
溶解度 9.7mg/L

产品详细信息

详细说明 (English)
Item Information
Drug Groups approved
Description A beta-adrenergic agonist used in the treatment of asthma and bronchospasms. [PubChem]
Indication For the treatment of bronchospasm, chronic bronchitis, asthma, and emphysema.
Pharmacology Orciprenaline (also known as metaproterenol), a synthetic amine, is structurally and pharmacologically similar to isoproterenol. Orciprenaline is used exclusively as a bronchodilator. The pharmacologic effects of beta adrenergic agonist drugs, such as orciprenaline, are at least in part attributable to stimulation through beta adrenergic receptors of intracellular adenyl cyclase, the enzyme which catalyzes the conversion of adenosine triphosphate (ATP) to cyclic- 3',5'- adenosine monophosphate (c-AMP). Increased c-AMP levels are associated with relaxation of bronchial smooth muscle and inhibition of release of mediators of immediate hypersensitivity from cells, especially from mast cells.
Toxicity Symptoms of overdose include angina, hypertension or hypotension, arrhythmias, nervousness, headache, tremor, dry mouth, palpitation, nausea, dizziness, fatigue, malaise and insomnia. LD50=42 mg/kg (orally in rat).
Affected Organisms
Humans and other mammals
Biotransformation Hepatic and gastric. The major metabolite, orciprenaline-3-0-sulfate, is produced in the gastrointestinal tract. Orciprenaline is not metabolized by catechol-0-methyltransferase nor have glucuronide conjugates been isolated to date.
Absorption 3% (oral bioavailability of 40%)
Half Life 6 hours
External Links
Wikipedia
RxList

参考文献