(R)-(+)-Bay K 8644是Ca2+-通道阻断剂 (L-type)。
| 					 						 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] Franckowiak et al (1985) The optical isomers of the 1,4-dihydropyridine BAY K 8644 show opposite effects on Ca channels. Eur.J.Pharmacol. 114 223. PMID: 2412855.
                          
                      
                              [2] O'Neill and Bolger (1988) Enantiomer selectivity and the development of tolerance to the behavioral effects of the calcium channel activator BAY K 8644. Brain Res.Bull. 21 865. PMID: 2465070.
                          
                      
                              [3]Ravens and Schopper (1990) Opposite cardiac actions of the enantiomers of Bay K 8644 at different membrane potentials in guinea-pig papillary muscles. Naunyn Schmiedebergs Arch.Pharmacol. 341 232. PMID: 1692975.
                          
                      
                              [4] Shi et al (2008) Induction of pluripotent stem cells from mouse embryonic fibroblasts by Oct4 and Klf4 with small-molecule compounds. Cell Stem Cell. 3 568. PMID: 18983970.
                          
                      
                      
                      
                      
                      
                      
                   
| 分子式  C16H15F3N2O4  | 
                        分子量 356.3  | 
                        CAS号 98791-67-4  | 
                        储存方式 ﹣20 ℃长期储存。冰袋运输  | 
                     
| 溶剂(常温) | 
                        DMSO 100 mM  | 
                        Water | 
                        Ethanol 100 mM  | 
                     
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。
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