Powder: -20°C for 3 years | In solvent: -80°C for 1 year
Millepachine 是分离自中草药Millettia pachycarpaBenth 的查尔酮,在体内外对多种人类癌细胞均显示出强大的抗增殖作用。
规格 | 价格/CNY | 货期 | 数量 | |
---|---|---|---|---|
1 mg | ¥ 835 | 现货 | ||
5 mg | ¥ 1,980 | 现货 | ||
10 mg | ¥ 3,310 | 现货 | ||
25 mg | ¥ 5,390 | 现货 | ||
50 mg | ¥ 7,590 | 现货 | ||
100 mg | ¥ 9,870 | 现货 | ||
1 mL * 10 mM (in DMSO) | ¥ 2,150 | 现货 |
产品描述 | Millepachine is a natural product found in the Chinese herbal medicine with strong antitumor effects against numerous human cancer cells. |
靶点活性 | Proliferation:4 μM(A2780CP cells) |
体外活性 | Millepachine (2-8 μM; 24 h) inhibits ATP-binding cassette transporter activity in A2780CP cells. Millepachine (2-8 μM; 24 or 48 h) induces significant G2/M arrest and apoptosis of cisplatin-sensitive A2780S and cisplatin-resistant A2780CP cells. The percentage of cells in the G2/M fraction increased from 15.99% in vehicle cells to 24.93%, 60.67%, and 77.31% at dose of 2, 4, and 8 μM in A2780S cells, respectively. Millepachine (2-8 μM; 24 h) decreases topoisomerase II levels in A2780S and A2780CP cells. Millepachine (1.25-20 μM; 48 h) remarkably inhibits the proliferation of cisplatin-resistant A2780CP cells with an IC50 of 4 μM[1]. |
体内活性 | Millepachine(20 mg/kg; i.v.)在A2780S和A2780CP异种移植模型中分别降低了肿瘤体积和肿瘤重量,抑制率达73.21%和65.58%。在切除的A2780S异种移植模型中,Millepachine未引发获得性药物抗性[1]。 |
分子量 | 350.41 |
分子式 | C22H22O4 |
CAS No. | 1393922-01-4 |
Powder: -20°C for 3 years | In solvent: -80°C for 1 year
DMSO: 100 mg/mL (285.38 mM), Sonication is recommended.
可选溶剂 | 浓度 体积 质量 | 1 mg | 5 mg | 10 mg | 25 mg |
DMSO | 1 mM | 2.8538 mL | 14.269 mL | 28.538 mL | 71.345 mL |
5 mM | 0.5708 mL | 2.8538 mL | 5.7076 mL | 14.269 mL | |
10 mM | 0.2854 mL | 1.4269 mL | 2.8538 mL | 7.1345 mL | |
20 mM | 0.1427 mL | 0.7134 mL | 1.4269 mL | 3.5672 mL | |
50 mM | 0.0571 mL | 0.2854 mL | 0.5708 mL | 1.4269 mL | |
100 mM | 0.0285 mL | 0.1427 mL | 0.2854 mL | 0.7134 mL |
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。
Millepachine 1393922-01-4 Apoptosis Chinese Millettia bioactive chalcone medicine natural Inhibitor pachycarpa inhibit antitumor herbal Benth cancer inhibitor