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Mosapride

    
99.94%

4-Amino-5-chloro-2-ethoxy-N-((4-(4-fluorobenzyl)-2-morpholinyl)methyl)benzamide

源叶(MedMol)
S80109 一键复制产品信息
112885-41-3
C21H25ClFN3O3
421.893
MFCD00867430
莫沙必利;4-氨基-5-氯-2-乙氧基-N-[[4-(4-氟苄基)-2-吗啉基]甲基]苯甲酰胺/莫沙必利;莫沙比利;MOSAPRIDE;4-AMINO-5-CHLORO-2-ETHOXY-N-((4-(4-FLUOROBENZYL)-2-MORPHOLINYL)METHYL)BENZAMIDE;4-AMINO-5
货号 规格 价格 上海 北京 珠海 重庆 武汉 购买数量
S80109-10mg买3赠1
99.94%

¥210.00

6 - - - -
S80109-50mg买3赠1
99.94%

¥640.00

3 - - - -
S80109-250mg买3赠1
≥98%

¥1440.00

货期:2-3天 - - - -
产品介绍 参考文献 质检证书(COA) 摩尔浓度计算器 相关产品
产品描述: Mosapride是胃动力药,是选择性的5HT4激动剂
靶点: 5HT4;5-HTReceptor
体外研究: Mosapride facilitates acetylcholine release from the enteric cholinergic neurons. It does not block K+ channels or D2 dopaminergic receptors. Mosapride is a selective 5-HT4 receptor agonist with no affinity for 5-HT1, 5-HT2, adrenalineα1, adrenalineα2 or dopamine D2 receptors
体内研究: Mosapride augmented lower gastrointestinal motility in animal models and in patients with lower gastrointestinal disorders. It enhanced defecation responses in animal models. In human, after oral administration of single doses of mosapride 5-40 mg, peak mosapride concentrations (Cmax) were reached after about 1 hour. Both the Cmax and area under the concentration-time curve from time zero to infinity (AUC∞) increased in a dose-proportional manner. There were no significant differences in the pharmacokinetic profiles of mosapride administered as single or multiple doses. Mosapride is excreted in the urine and faeces. It is primarily metabolized in the liver by cytochrome P450 3A4 to the active metabolite, a des-4-fluorobenzyl compound
动物实验: Animal Models: Male Hartley guinea pigs Dosages: 3, 10 and 30 mg/kg Administration: i.g.
参考文献: 1. Inui A, et al. Effects of mosapride citrate, a 5-HT4 receptor agonist, on colonic motility in conscious guinea pigs. Jpn J Pharmacol. 2002, 90(4):313-20. 2. Liu Z, et al. Mosapride citrate, a novel 5-HT4 agonist and partial 5-HT3 antagonist, ameliorates constipation in parkinsonian patients. Mov Disord. 2005, 20(6):680-6. 3. Monique P. Curran, et al. Mosapride. Drugs (2008) 68: 981.
溶解性: soluble  in  DMSO
保存条件: -20℃
备注: Mosapride is a gastroprokinetic agent that acts as a selective 5HT4 agonist. Target: 5HT4 Mosapride is a gastroprokinetic agent that acts as a selective 5HT4 agonist. The major active metabolite of mosapride, known as M1, additionally acts as a 5HT3 antagonist, which accelerates gastric emptying throughout the whole of the gastrointestinal tract in humans, and is used for the treatment of gastritis, gastro-oesophageal reflux disease, functional dyspepsia and irritable bowel syndrome. It is recommended to be
配置溶液浓度参考:
1mg 5mg 10mg
1 mM 2.37 ml 11.851 ml 23.703 ml
5 mM 0.474 ml 2.37 ml 4.741 ml
10 mM 0.237 ml 1.185 ml 2.37 ml
50 mM 0.047 ml 0.237 ml 0.474 ml
注意: 部分产品我司仅能提供部分信息,我司不保证所提供信息的权威性,仅供客户参考交流研究之用。

参考文献

质检证书(COA)

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摩尔浓度计算器

质量 (mg) = 浓度 (mM) x 体积 (mL) x 分子摩尔量 (g/mol)

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