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AAK1-IN-3 是一种喹啉类似物,可用于研究神经病理性疼痛。AAK1-IN-3 是衔接蛋白 2 相关激酶 1 (AAK1) 抑制剂,IC50为 11 nM,具有脑渗透性。

AAK1-IN-3 是一种喹啉类似物,可用于研究神经病理性疼痛。AAK1-IN-3 是衔接蛋白 2 相关激酶 1 (AAK1) 抑制剂,IC50为 11 nM,具有脑渗透性。
| 规格 | 价格 | 库存 | 数量 |
|---|---|---|---|
| 25 mg | ¥ 10,600 | 8-10周 | |
| 50 mg | ¥ 13,800 | 8-10周 | |
| 100 mg | ¥ 17,500 | 8-10周 |
| 产品描述 | AAK1-IN-3 is a quinoline analogue that can be used in the research of neuropathic pain. AAK1-IN-3 is a brain-penetrant inhibitor of adaptor protein 2-associated kinase 1 (AAK1) (IC 50 = 11 nM) [1]. |
| 体外活性 | AAK1-IN-3 (compound (R)-31) is brain-penetrant kinase inhibitors with a B/P ratio of 1.3 [1]. AAK1-IN-3 inhibits AAK1 in HEK293 cells (IC50=108 nM) [1]. |
| 体内活性 | AAK1-IN-3 (compound (R)-31; 30 mg/kg; sc; signle dose) causes a 46% reduction of μ2 phosphorylation in C57BL6 mice [1]. |
| 分子量 | 316.4 |
| 分子式 | C20H20N4 |
| CAS No. | 1802703-20-3 |
| Smiles | C(#N)C=1C2=C(N=C([C@@H](CC(C)C)N)C1)C=CC(=C2)C=3C=CN=CC3 |
| 存储 | Powder: -20°C for 3 years | In solvent: -80°C for 1 year | Shipping with blue ice/Shipping at ambient temperature. |
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。
对于不同动物的给药剂量换算,您也可以参考 更多