您当前所在的位置:首页 > 产品中心 > 产品信息
Ibutilide_分子结构_CAS_122647-32-9)
点击图片或这里关闭

Ibutilide

产品号 DB00308 公司名称 DrugBank
CAS号 122647-32-9 公司网站 http://www.ualberta.ca/
分子式 C20H36N2O3S 电 话 (780) 492-3111
分子量 384.57644 传 真
纯 度 电子邮件 david.wishart@ualberta.ca
保 存 Chembase数据库ID: 193

产品价格信息

请登录

产品别名

标题
Ibutilide
IUPAC标准名
N-(4-{4-[ethyl(heptyl)amino]-1-hydroxybutyl}phenyl)methanesulfonamide
IUPAC传统名
@ibutilide
商标名
Corvert
别名
Ibutilide Fumarate
Ibutilidum [INN-Latin]
Ibutilida [INN-Spanish]
Ibutilide

产品登记号

PubChem SID 46507904
CAS号 122647-32-9
PubChem CID 60753

产品性质

疏水性(logP) 4.6
溶解度 100 mg/mL

产品详细信息

详细说明 (English)
Item Information
Drug Groups approved
Description Ibutilide is a Class III antiarrhythmic agent that is indicated for acute cardioconversion of atrial fibrillation and atrial flutter of a recent onset to sinus rhythm. [Wikipedia]
Indication Indicated for the rapid conversion of atrial fibrillation or atrial flutter of recent onset to sinus rhythm.
Pharmacology Ibutilide prolongs the action potential duration and increases both atrial and ventricular refractoriness in vivo, i.e., class III electrophysiologic effects. Voltage clamp studies indicate that ibutilide, at nanomolar concentrations, delays repolarization by activation of a slow, inward current (predominantly sodium), rather than by blocking outward potassium currents, which is the mechanism by which most other class III antiarrhythmics act.
Toxicity Acute overdose in animals results in CNS toxicity; notably, CNS depression, rapid gasping breathing, and convulsions. The intravenous median lethal dose in the rat was more than 50 mg/kg which is, on a mg/m2 basis, at least 250 times the maximum recommended human dose.
Affected Organisms
Humans and other mammals
Biotransformation Primarily hepatic. Eight metabolites of ibutilide were detected in metabolic profiling of urine. These metabolites are thought to be formed primarily by o-oxidation followed by sequential b-oxidation of the heptyl side chain of ibutilide. Of the eight metabolites, only the o-hydroxy metabolite possesses class III electrophysiologic properties similar to that of ibutilide in an in vitro isolated rabbit myocardium model.
Absorption Rapid after intravenous injection
Half Life 6 hours (ranges from 2-12 hours)
Protein Binding 40%
Elimination In healthy male volunteers, about 82% of a 0.01 mg/kg dose of [14C] ibutilide fumarate was excreted in the urine (about 7% of the dose as unchanged ibutilide) and the remainder (about 19%) was recovered in the feces.
Distribution * 11 L/kg
Clearance * 29 mL/min/kg
External Links
Wikipedia
RxList
Drugs.com

参考文献