Powder: -20°C for 3 years | In solvent: -80°C for 1 year
6-Methoxydihydrosanguinarine 是一种从M. cordata 果实中分离出的生物碱,它对 MCF-7 细胞系(IC50:0.61 μM)和 SF-268 细胞系(IC50:0.54 μM)具有强的细胞毒性。
规格 | 价格/CNY | 货期 | 数量 | |
---|---|---|---|---|
1 mg | ¥ 953 | 现货 | ||
5 mg | ¥ 1,930 | 现货 | ||
10 mg | ¥ 2,880 | 现货 | ||
25 mg | ¥ 4,690 | 现货 | ||
50 mg | ¥ 6,570 | 现货 | ||
100 mg | ¥ 8,860 | 现货 |
产品描述 | 6-Methoxydihydrosanguinarine is a natural product. 6-Methoxydihydrosanguinarine shows strong cytotoxicity against MCF-7 and SF-268 cell lines with IC50 values of 0.61 μM and 0.54 μM, respectively.It has antibacterial activity against Methicillin-resistant Staphylococcus aureus (MRSA) strains with minimum inhibitory concentrations (MICs) ranging from1.9 to 3.9 microg/ml |
靶点活性 | SF-268 cells:0.54 μM (IC50), MCF-7 cells:0.61 μM (IC50) |
体内活性 | 6-methoxydihydrosanguinarine (6ME), a benzophenanthridine alkaloid isolated from Hylomecon species, may have potential as a chemotherapeutic agent.??6ME inhibits the growth of HepG2 cells in a concentration- and time-dependent manner (IC50=3.8+/-0.2 microM following 6 h incubation).?Treatment of HepG2 cells with 6ME resulted in the release of mitochondrial cytochrome c followed by the activation of caspase proteases, and subsequent proteolytic cleavage of poly(ADP-ribose) polymerase.?6ME increased the expression of p53 and bax and decreased the expression of bcl-2.?The cytotoxic effect of 6ME is mediated by the time-dependent generation of reactive oxygen species.?Preincubation of HepG2 cells with vitamin C decreased the expression of p53 and bax and inhibited the release of cytochrome c, activation of downstream caspase and the cleavage of poly(ADP-ribose) polymerase, thus inhibiting the apoptosis inducing effect of 6ME |
分子量 | 363.36 |
分子式 | C21H17NO5 |
CAS No. | 72401-54-8 |
Powder: -20°C for 3 years | In solvent: -80°C for 1 year
DMSO: 50 mg/mL (137.6 mM)
可选溶剂 | 浓度 体积 质量 | 1 mg | 5 mg | 10 mg | 25 mg |
DMSO | 1 mM | 2.7521 mL | 13.7605 mL | 27.5209 mL | 68.8023 mL |
5 mM | 0.5504 mL | 2.7521 mL | 5.5042 mL | 13.7605 mL | |
10 mM | 0.2752 mL | 1.376 mL | 2.7521 mL | 6.8802 mL | |
20 mM | 0.1376 mL | 0.688 mL | 1.376 mL | 3.4401 mL | |
50 mM | 0.055 mL | 0.2752 mL | 0.5504 mL | 1.376 mL | |
100 mM | 0.0275 mL | 0.1376 mL | 0.2752 mL | 0.688 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。
6-Methoxydihydrosanguinarine 72401-54-8 Others cancer SF-268 6 Methoxydihydrosanguinarine inhibit Inhibitor lkaloid 6Methoxydihydrosanguinarine MCF-7 inhibitor