备注:
 如需更大包装,请联系销售人员,大包装有极大的折扣优惠!
          
       
       
       
       
        
        
详细介绍
 
       
              
          l  基本信息  | 
产品名称  | Selexipag  | 
一般描述  | Selexipag is an orally active, first-in-class, selective prostacyclin IP receptor agonist with Ki value of 260 nM for human IP, whereas Ki values >10,000 nM are measured at the other human G-protein-coupled prostanoid receptors (EP1-4, DP, FP and TP).  | 
别 称  | NS-304, ACT-293987; 2-[4-[(5,6-diphenylpyrazin-2-yl)-propan-2-ylamino]butoxy]-N-methylsulfonylacetamide  | 
纯 度  | ≥98.0%(HPLC)  | CAS NO.  | 475086-01-2  | 
分子式  | C26H32N4O4S  | 分子量  | 496.626  | 
适用范围  | 生物试剂,适用于细胞培养等  | 
l  理化信息  | 
外 观  | 固体  | 
溶解性(25°C)  | DMSO  | ≥50mg/mL  | 
乙醇  | ≥5mg/mL  | 
水  | Insoluble  | 
l  生物学信息  | 
生物活性/药理作用  | Selexipag is used for the treatment of pulmonary arterial hypertension. It is a prodrug for ACT-333679 (the free carboxylic acid). It has a role as an orphan drug, a prostacyclin receptor agonist, a platelet aggregation inhibitor, a vasodilator agent and a prodrug. It is a monocarboxylic acid amide, an ether, a member of pyrazines, an aromatic amine, a tertiary amino compound and a N-sulfonylcarboxamide. It derives from an ACT-333679.  | 
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  |