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Topo I/II-IN-2 (Compound 3g) 是一种针对Topo I和Topo II的抑制剂。其对NCI-H446细胞和NCI-H1048细胞的IC50值分别为1.30 μM和1.42 μM。Topo I/II-IN-2 通过诱导线粒体凋亡 (Apoptosis) 和导致线粒体功能紊乱来促进活性生成,且可抑制PI3K/Akt/mTOR通路,从而在体外抑制小细胞肺癌 (SCLC) 细胞的增殖、侵袭和迁移。
Topo I/II-IN-2 (Compound 3g) 是一种针对Topo I和Topo II的抑制剂。其对NCI-H446细胞和NCI-H1048细胞的IC50值分别为1.30 μM和1.42 μM。Topo I/II-IN-2 通过诱导线粒体凋亡 (Apoptosis) 和导致线粒体功能紊乱来促进活性生成,且可抑制PI3K/Akt/mTOR通路,从而在体外抑制小细胞肺癌 (SCLC) 细胞的增殖、侵袭和迁移。
规格 | 价格 | 库存 | 数量 |
---|---|---|---|
10 mg | 待询 | 期货 | |
50 mg | 待询 | 期货 |
产品描述 | Topo I/II-IN-2 (Compound 3g) is an inhibitor of both Topo I and Topo II. It exhibits inhibitory activity against NCI-H446 and NCI-H1048 cells with IC50 values of 1.30 μM and 1.42 μM, respectively. Topo I/II-IN-2 induces mitochondrial apoptosis, disrupts mitochondrial function, and stimulates activity generation. Additionally, it inhibits the PI3K/Akt/mTOR pathway, effectively preventing the proliferation, invasion, and migration of small cell lung cancer (SCLC) cells in vitro. |
分子量 | 418.48 |
分子式 | C25H26N2O4 |
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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