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Modafinil

产品号 DB00745 公司名称 DrugBank
CAS号 68693-11-8 公司网站 http://www.ualberta.ca/
分子式 C15H15NO2S 电 话 (780) 492-3111
分子量 273.3501 传 真
纯 度 电子邮件 david.wishart@ualberta.ca
保 存 Chembase数据库ID: 625

产品价格信息

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产品别名

标题
Modafinil
IUPAC标准名
2-diphenylmethanesulfinylacetamide
IUPAC传统名
2-diphenylmethanesulfinylacetamide
商标名
Sparlon
Modiodal
Provigil
别名
Moderateafinil
Modafinilum [Latin]
Modafinil [USAN:INN]
Modafinilo [Spanish]

产品登记号

PubChem SID 46504648
PubChem CID 4236
CAS号 68693-11-8

产品性质

疏水性(logP) 0.6
溶解度 Slightly soluble

产品详细信息

详细说明 (English)
Item Information
Drug Groups approved; investigational
Description Modafinil is a stimulant drug marketed as a 'wakefulness promoting agent' and is one of the stimulants used in the treatment of narcolepsy. Narcolepsy is caused by dysfunction of a family of wakefulness-promoting and sleep-suppressing peptides, the orexins, whose neurons are activated by modafinil. The prexin neuron activation is associated with psychoactivation and euphoria. The exact mechanism of action is unclear, although in vitro studies have shown it to inhibit the reuptake of dopamine by binding to the dopamine reuptake pump, and lead to an increase in extracellular dopamine. Modafinil activates glutamatergic circuits while inhibiting GABA.
Indication To improve wakefulness in patients with excessive daytime sleepiness (EDS) associated with narcolepsy.
Pharmacology Modafinil is a stimulant drug marketed as a 'wakefulness promoting agent' and is one of the stimulants used in the treatment of narcolepsy. Narcolepsy is caused by dysfunction of a family of wakefulness-promoting and sleep-suppressing peptides, the orexins, whose neurons are activated by modafinil. The prexin neuron activation is associated with psychoactivation and euphoria. Modafinil is not indicated for complaints of lack of energy or fatigue; but it appears to be very helpful for some patients. Also, it has been used in the treatment of hypersomnia, a disorder in which patients lack the capacity for meaningful sleep and may require ten or more hours per day. Recent studies have have found that modafinil may help recovering cocaine addicts fight their addiction.
Affected Organisms
Humans and other mammals
Biotransformation Hepatic
Absorption Rapid following oral administration.
Half Life 23-215 hours
Protein Binding 60%
Elimination The major route of elimination is metabolism (~90%), primarily by the liver, with subsequent renal elimination of the metabolites.
Distribution * 0.9 L/kg
References
Lindsay SE, Gudelsky GA, Heaton PC: Use of modafinil for the treatment of attention deficit/hyperactivity disorder. Ann Pharmacother. 2006 Oct;40(10):1829-33. Epub 2006 Sep 5. [Pubmed]
Ishizuka T, Sakamoto Y, Sakurai T, Yamatodani A: Modafinil increases histamine release in the anterior hypothalamus of rats. Neurosci Lett. 2003 Mar 20;339(2):143-6. [Pubmed]
External Links
Wikipedia
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PDRhealth
Drugs.com

参考文献

  • Lindsay SE, Gudelsky GA, Heaton PC: Use of modafinil for the treatment of attention deficit/hyperactivity disorder. Ann Pharmacother. 2006 Oct;40(10):1829-33. Epub 2006 Sep 5. Pubmed
  • Ishizuka T, Sakamoto Y, Sakurai T, Yamatodani A: Modafinil increases histamine release in the anterior hypothalamus of rats. Neurosci Lett. 2003 Mar 20;339(2):143-6. Pubmed