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详细介绍
 
       
              
          l  基本信息  | 
产品名称  | Rebamipide(瑞巴派特)  | 
一般描述  | Rebamipide is a cholecystokinin type 1 (CCK1) receptor inhibitor for inhibiting [125I]BH-CCK-8S with IC50 of 37.7 μM.  | 
别 称  | OPC-12759; 2-[(4-chlorobenzoyl)amino]-3-(2-oxo-1H-quinolin-4-yl)propanoic acid  | 
纯 度  | ≥98.0%(HPLC)  | CAS NO.  | 90098-04-7  | 
分子式  | C19H15ClN2O4  | 分子量  | 370.789  | 
适用范围  | 生物试剂,适用于细胞培养等  | 
l  理化信息  | 
外 观  | 白色粉末
   | 
溶解性(25°C)  | DMSO  | ≥50mg/mL  | 
乙醇  | Insoluble  | 
水  | Insoluble  | 
l  生物学信息  | 
生物活性/药理作用  | Rebamipide is a quinolinone derivative with anti-ulcer and anti-inflammatory activities. Rebamipide induces cyclooxygenase 2 (COX2) synthesis which results in an increase in endogenous prostaglandin synthesis in the gastric mucosa. This agent also inhibits H. pylori-induced production of tumor necrosis factor (TNF) alpha and subsequent inflammation of the gastric mucosa. In addition, rebamipide scavenges oxygen-derived free radicals that potentially cause mucosal injury, and stimulates prostaglandin EP4 receptor gene  followed by mucous secretion, thereby enhancing the gastric mucosal defense.  | 
l  存储  | 
存储温度  | -20°C  | 
l  注意事项及免责声明  | 
本产品仅用于实验研究,不得作为药物使用,不得用于家用或其它用途。  | 
l  参考文献  | 
1.    http://www.drugbank.ca 2.    https://ncit.nci.nih.gov 3.    https://www.ncbi.nlm.nih.gov  |