(R)-(+)-Bay-K-8644,98.53%
产品编号:Bellancom-15125| CAS NO:98791-67-4| 分子式:C16H15F3N2O4| 分子量:356.30
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(R)-(+)-Bay-K-8644
| 产品介绍 | (R)-(+)-Bay-K-8644 是钙离子通道抑制剂。(R)-(+)-Bay-K-8644 抑制 Ba2+电流 (IBa),IC50 为 975 nM。 | ||||||||||||||||
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| 生物活性 | (R)-(+)-Bay-K-8644 is a calcium channel inhibitor. (R)-(+)-Bay-K-8644 inhibits Ba2+ currents (IBa) (IC50=975 nM).  | ||||||||||||||||
| 体外研究 |                                         
                                        
                                             (R)-(+)-Bay-K-8644, a conventional racemic mixture of Bay K 8644, is widely used as an L-type Ca2+ channel agonist. Each optical isomer possesses opposite effects on IBa, (R)-(+)-Bay-K-8644 as an antagonist and S(-)-Bay K 8644 as an agonist. (R)-(+)-Bay-K-8644 inhibits Ba2+ currents (IBa) (IC50=975 nM). When (R)-(+)-Bay-K-8644 (0.5 μM) is applied, IBa is suppressed to 71±10% of control. In the presence of (R)-(+)-Bay-K-8644IBa. (R)-(+)-Bay-K-8644 is a calcium channel inhibitor. 西域 has not independently confirmed the accuracy of these methods. They are for reference only.  | ||||||||||||||||
| 体内研究 | |||||||||||||||||
| 体内研究 | |||||||||||||||||
| 性状 | Solid | ||||||||||||||||
| 溶解性数据 | 
                                        
                                             In Vitro:  
                                            DMSO : ≥ 300 mg/mL (841.99 mM) * "≥" means soluble, but saturation unknown. 配制储备液 
                                                
 
 
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                                            请根据您的实验动物和给药方式选择适当的溶解方案。以下溶解方案都请先按照 In Vitro 方式配制澄清的储备液,再依次添加助溶剂: 
                                                    ——为保证实验结果的可靠性,澄清的储备液可以根据储存条件,适当保存;体内实验的工作液,建议您现用现配,当天使用;
                                                        以下溶剂前显示的百 
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| 运输条件 | Room temperature in continental US; may vary elsewhere.  | ||||||||||||||||
| 储存方式 | 
                                
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| 参考文献 | 
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