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Cinitapride

产品号 DB08810 公司名称 DrugBank
CAS号 66564-14-5 公司网站 http://www.ualberta.ca/
分子式 C21H30N4O4 电 话 (780) 492-3111
分子量 402.4873 传 真
纯 度 电子邮件 david.wishart@ualberta.ca
保 存 Chembase数据库ID: 6410

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产品别名

标题
Cinitapride
IUPAC标准名
4-amino-N-[1-(cyclohex-3-en-1-ylmethyl)piperidin-4-yl]-2-ethoxy-5-nitrobenzamide
IUPAC传统名
4-amino-N-[1-(cyclohex-3-en-1-ylmethyl)piperidin-4-yl]-2-ethoxy-5-nitrobenzamide
商标名
Cinmove
Pemix
Blaston
Paxapride
Cintapro
Cidine

产品登记号

CAS号 66564-14-5

产品性质

产品详细信息

详细说明 (English)
Item Information
Drug Groups approved
Description Cinitapride is a gastroprokinetic agent and antiulcer agent of the benzamide class which is marketed in Spain and Mexico. It acts as an agonist of the 5-HT1 and 5-HT4 receptors and as an antagonist of the 5-HT2 receptors.
Indication For the treatment of gastrointestinal disorders associated with motility disturbances such as gastroesophageal reflux disease, non-ulcer dyspepsia and delayed gastric emptying.
Toxicity The symptoms of overdose include drowsiness, confusion and extrapyramidal effects.
Affected Organisms
• Humans and other mammals
Absorption The absorption of cinitapride (12mg) following oral administration was rapid, with peak levels being achieved 2 h after dosing; absorption following intramuscular administration (4mg) was even more rapid, with peak levels (50% more that oral levels) being achieved 1 h after dosing.
Half Life 3-5 h during the first 8 h and a residual half-life greater than 15 h thereafter.
References
• Alarcon-de-la-Lastra Romero C, Lopez A, Martin MJ, la Casa C, Motilva V: Cinitapride protects against ethanol-induced gastric mucosal injury in rats: role of 5-hydroxytryptamine, prostaglandins and sulfhydryl compounds. Pharmacology. 1997 Apr;54(4):193-202. [Pubmed]
External Links
• Wikipedia

参考文献

  • Alarcon-de-la-Lastra Romero C, Lopez A, Martin MJ, la Casa C, Motilva V: Cinitapride protects against ethanol-induced gastric mucosal injury in rats: role of 5-hydroxytryptamine, prostaglandins and sulfhydryl compounds. Pharmacology. 1997 Apr;54(4):193-202. Pubmed