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Peucedanol acts as a non-competitive inhibitor of CYP3A4 with a K i value of 4.07 μM, while serving as a competitive inhibitor for CYP1A2 and CYP2D6 with K i values of 3.39 μM and 6.77 μM, respectively [1].
Peucedanol acts as a non-competitive inhibitor of CYP3A4 with a K i value of 4.07 μM, while serving as a competitive inhibitor for CYP1A2 and CYP2D6 with K i values of 3.39 μM and 6.77 μM, respectively [1].
规格 | 价格 | 库存 | 数量 |
---|---|---|---|
10 mg | 待询 | 待询 | |
50 mg | 待询 | 待询 |
Peucedanol 相关产品
产品描述 | Peucedanol acts as a non-competitive inhibitor of CYP3A4 with a K i value of 4.07 μM, while serving as a competitive inhibitor for CYP1A2 and CYP2D6 with K i values of 3.39 μM and 6.77 μM, respectively [1]. |
别名 | 前胡醇 |
分子量 | 264.27 |
分子式 | C14H16O5 |
CAS No. | 46992-81-8 |
存储 | Powder: -20°C for 3 years | In solvent: -80°C for 1 year | Shipping with blue ice. |
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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