Phenytoin Sodium is a sodium channel protein inhibitor. Phenytoin Sodium stabilizes excitable membranes the its effects on sodium, potassium and calcium channels.
            
         Phenytoin Sodium is a sodium channel protein inhibitor. Phenytoin Sodium stabilizes excitable membranes the its effects on sodium, potassium and calcium channels.
| 					 						 动物 A (mg/kg) = 动物 B (mg/kg)×动物 B的Km系数/动物 A的Km系数  | 									 | 			
例如,已知某工具药用于小鼠的剂量为88 mg/kg , 则用于大鼠的剂量换算方法:将88 mg/kg 乘以小鼠的Km系数(3),再除以大鼠的Km系数(6),得到该药物用于大鼠的等效剂量44 mg/kg。
	
                      
                              [1] Morimoto, K., et al., BW1003C87, phenytoin and carbamazepine elevate seizure threshold in the rat amygdala-kindling model of epilepsy. Eur. J. Pharmacol. 339, 11-15, (1997).
                          
                      
                              [2] Todorovic, S.M., Lingle, C.J., Pharmacological properties of T-type Ca2+ current in adult rat sensory neurons: effects of anticonvulsant and anesthetic agents. J. Neurophysiol. 79, 240, (1998).
                          
                      
                              [3] Rush, A.M., and Elliott, J.R., Phenytoin and carbamazepine: differential inhibition of sodium currents in small cells from adult rat dorsal root ganglia. Neurosci. Lett. 226, 95-98, (1997).
                          
                      
                              [4] Soroush Ardekani et. al. Nanoliposomal Nitroglycerin Exerts Potent Anti-Inflammatory Effects. Scientific reports, 5, 16258 (2015).
                          
                      
                      
                      
                      
                      
                      
                   
| 分子式  C15H11N2NaO2  | 
                        分子量 274.25  | 
                        CAS号 630-93-3  | 
                        储存方式 ﹣20 ℃冷藏长期储存。冰袋运输  | 
                     
| 溶剂(常温) | 
                        DMSO 100 mM  | 
                        Water | 
                        Ethanol | 
                     
体内溶解度 
注:以上所有数据均来自公开文献,并不保证对所有实验均有效,数据仅供参考。
相关化合物库 
使用AMQUAR产品发表文献后请联系我们