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c-Fos-IN-1 (Compound P16) 是一种c-Jun抑制剂,能够降低c-Fos的mRNA和蛋白质水平,同时抑制ERK的磷酸化及AP-1的转录活性。它通过抑制ERK/c-Fos/Jun通路展现抗癌效果,减缓胃癌细胞(MGC-803)的增殖和迁移(IC50 2.31 μM),并使细胞周期停滞于G2/M期,诱导癌细胞凋亡,抑制胃癌肿瘤的生长。
c-Fos-IN-1 (Compound P16) 是一种c-Jun抑制剂,能够降低c-Fos的mRNA和蛋白质水平,同时抑制ERK的磷酸化及AP-1的转录活性。它通过抑制ERK/c-Fos/Jun通路展现抗癌效果,减缓胃癌细胞(MGC-803)的增殖和迁移(IC50 2.31 μM),并使细胞周期停滞于G2/M期,诱导癌细胞凋亡,抑制胃癌肿瘤的生长。
规格 | 价格 | 库存 | 数量 |
---|---|---|---|
10 mg | 待询 | 期货 | |
50 mg | 待询 | 期货 |
产品描述 | c-Fos-IN-1 (Compound P16) acts as a c-Jun inhibitor, effectively reducing the mRNA and protein levels of c-Fos. It also inhibits the phosphorylation activity of ERK and the transcriptional activity of AP-1. This compound demonstrates anticancer properties through the inhibition of the ERK/c-Fos/Jun pathway. c-Fos-IN-1 curbs the proliferation and migration of gastric cancer cells, with an IC50 of 2.31 μM for MGC-803 cells, causing cell cycle arrest at the G2/M phase and inducing apoptosis in cancer cells. Additionally, c-Fos-IN-1 hampers the growth of gastric cancer tumors. |
分子量 | 433.582 |
分子式 | C28H35NO3 |
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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