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Vanoxerine is an antagonist of dopamine transporter (Ki: 16.9nM).
Vanoxerine is an antagonist of dopamine transporter (Ki: 16.9nM).
规格 | 价格 | 库存 | 数量 |
---|---|---|---|
25 mg | ¥ 10,600 | 待询 |
Vanoxerine 相关产品
产品描述 | Vanoxerine is an antagonist of dopamine transporter (Ki: 16.9nM). |
靶点活性 | Dopamine reuptake:1 nM (Ki) |
体外活性 | As an antagonist of DAT, vanoxerine is developed for treatment of Parkinson's disease and depression but has no effect on these diseases. Vanoxerine is also found to have desirable cardiac antiarrhythmic properties. It is a blocker of cardiac hERG (IC50:0.84nM). It also blocks the ICa,L and hNav1.5 channel (IC50: 320nM and 830nM, respectively). Vanoxerine does not significantly prolong Purkinje fiber APD60 and APD90 and has no significant effect on QT or TDR. |
分子量 | 450.56 |
分子式 | C28H32F2N2O |
CAS No. | 67469-69-6 |
密度 | 1.135 g/cm3 (Predicted) |
存储 | Powder: -20°C for 3 years | In solvent: -80°C for 1 year | Shipping with blue ice/Shipping at ambient temperature. |
溶解度信息 | DMSO: Soluble |
以上为“体内实验配液计算器”的使用方法举例,并不是具体某个化合物的推荐配制方式,请根据您的实验动物和给药方式选择适当的溶解方案。
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