Powder: -20°C for 3 years | In solvent: -80°C for 1 year
Anticancer agent 71 (Compound 4b) 是有效的抗癌剂。Anticancer agent 71 将细胞周期阻滞在 G2/M 期。Anticancer agent 71通过上调 Bax、Ikb-α 和切割 PARP 并下调 Bcl-2 表达水平诱导细胞凋亡。
规格 | 价格/CNY | 货期 | 数量 | |
---|---|---|---|---|
25 mg | ¥ 10,600 | 6-8周 | ||
50 mg | ¥ 13,800 | 6-8周 | ||
100 mg | ¥ 17,500 | 6-8周 |
产品描述 | Anticancer agent 71 (Compound 4b) is a potent anticancer agent. Anticancer agent 71 arrests cell cycle at G2/M phase. Anticancer agent 71 induces apoptosis through upregulating Bax, Ikb-α and cleaved PARP and downregulating Bcl-2 expression levels. |
体外活性 | Anticancer agent 71 (Compound 4b) (0.1-50 μM, 24 hours; SW480 and PC3 cells) increases the cytotoxicity and exerts potent antitumor activities against SW480 and PC3 cells [1]. Anticancer agent 71 (Compound 4b) (11.08 μM, 24 hours; SW480 cells) induces a significant G2/M phase arrest [1]. Anticancer agent 71 (Compound 4b) (11.08 μM, 24 hours) induces apoptosis in SW480 cells by upregulating Bax, Ikb-α and cleaved PARP and downregulating Bcl-2 expression [1]. Cell Cytotoxicity Assay [1] Cell Line: SW480 and PC3 cells Concentration: 0.1, 1, 12.5, 25 and 50 μM Incubation Time: 24 hours Result: Inhibited with IC 50 values of 11.08 and 17.39 μM for SW480 and PC3 cells, respectively. Cell Cycle Analysis [1] Cell Line: SW480 cells Concentration: 11.08 μM Incubation Time: 24 hours Result: The cell population percent at G2/M phase increased to 45.3%. Apoptosis Analysis [1] Cell Line: SW480 cells Concentration: 11.08 μM Incubation Time: 24 hours Result: The percentage of cells in early and late apoptosis was recorded as 5.69% and 3.52%, respectively. Western Blot Analysis [1] Cell Line: SW480 cells Concentration: 11.08 μM Incubation Time: 24 hours Result: The expression of antiapoptotic protein Bcl-2 decreased and the expression of Pro apoptotic Bax increased. |
分子量 | 407.78 |
分子式 | C18H13ClF3N5O |
CAS No. | 2453228-45-8 |
Powder: -20°C for 3 years | In solvent: -80°C for 1 year
对于不同动物的给药剂量换算,您也可以参考 更多...
请在以下方框中输入您的动物实验信息后点击计算,可以得到母液配置方法和体内配方的制备方法: 比如您的给药剂量是10 mg/kg,每只动物体重20 g,给药体积100 μL,一共给药动物10 只,您使用的配方为5% DMSO+30% PEG300+5% Tween 80+60% ddH2O。那么您的工作液浓度为2 mg/mL。
母液配置方法:2 mg 药物溶于 50 μL DMSO (母液浓度为 40 mg/mL), 如您需要配置的浓度超过该产品的溶解度,请先与我们联系。
体内配方的制备方法:取 50 μL DMSO 主液,加入 300 μL PEG300, 混匀澄清,再加 50 μL Tween 80,混匀澄清,再加 600 μL ddH2O, 混匀澄清。
您可能有的问题的答案可以在抑制剂处理说明中找到,包括如何准备库存溶液,如何存储产品,以及基于细胞的分析和动物实验需要特别注意的问题。
Anticancer agent 71 2453228-45-8 Inhibitor inhibitor inhibit