Powder: -20°C for 3 years | In solvent: -80°C for 1 year
BIX-01294 trihydrochloride 是可逆且高度选择性的G9a 和GLP 组蛋白甲基转移酶抑制剂,IC50分别为 1.9 μM 和 0.7 μM。它可诱导坏死性凋亡和自噬,具有抗肿瘤活性。它通过与底物赖氨酸残基 N 端的氨基酸竞争结合来抑制 G9a/GLP。
规格 | 价格/CNY | 货期 | 数量 | |
---|---|---|---|---|
1 mg | ¥ 257 | 现货 | ||
2 mg | ¥ 360 | 现货 | ||
5 mg | ¥ 640 | 现货 | ||
10 mg | ¥ 987 | 现货 | ||
25 mg | ¥ 1,780 | 现货 | ||
50 mg | ¥ 2,790 | 现货 | ||
100 mg | ¥ 4,130 | 现货 | ||
500 mg | ¥ 8,730 | 现货 | ||
1 mL * 10 mM (in DMSO) | ¥ 1,280 | 现货 |
产品描述 | BIX-01294 trihydrochloride is an inhibitor of G9a histone methyltransferase.In a cell-free assay, the IC50=2.7 μM for G9a histone methyltransferase. |
靶点活性 | G9a:2.7 μM |
体内活性 | 在野生型ES细胞,小鼠胚胎成纤维细胞和HeLa细胞中, BIX-01294(4.1 μM )降低H3K9me2水平。BIX-01294能够特异性抑制G9a(IC50=1.7 μM ) 和GLP(IC50=38 μM)。 |
激酶实验 | ATR for use in the in vitro enzyme assay is obtained from HeLa nuclear extract by immunoprecipitation with rabbit polyclonal antiserum raised to amino acids 400-480 of ATR contained in the following buffer: 25 mM HEPES (pH 7.4), 2 mM MgCl2, 250 mM NaCl, 0.5 mM EDTA, 0.1 mM Na3VO4, 10% v/v glycerol, and 0.01% v/v Tween 20. ATR-antibody complexes are isolated from nuclear extract by incubating with protein A-Sepharose beads for 1 h and then through centrifugation to recover the beads. In the well of a 96-well plate, 10 μL ATR-containing Sepharose beads are incubated with 1 μg of substrate glutathione?S-transferase-p53N66 (NH2-terminal 66 amino acids of p53 fused to glutathione?S-transferase are expressed in?E. coli) in ATR assay buffer (50 mM HEPES (pH 7.4), 150 mM NaCl, 6 mM MgCl2, 4 mM MnCl2, 0.1 mM Na3VO4, 0.1 mM DTT, and 10% (v/v) glycerol) at 37°C in the presence or absence of inhibitor. After 10 min with gentle shaking, ATP is added to a final concentration of 3 μM and the reaction continued at 37°C for an additional 1 h. The reaction is stopped by addition of 100 μL of PBS, and the reaction is transferred to a white opaque glutathione coated 96-well plate and incubated overnight at 4°C. This plate is then washed with PBS/0.05% (v/v) Tween 20, blotted dry, and analyzed by a standard ELISA technique with a phosphoserine 15 p53 antibody. The detection of phosphorylated glutathione?S-transferase-p53N66 substrate is performed in combination with a goat anti-mouse horseradish peroxidase-conjugated secondary antibody. Enhanced chemiluminescence solution is used to produce a signal, and chemiluminescent detection is carried out via a TopCount plate reader. The resulting calculated % enzyme activity is then used to determine the IC50?values for the compounds (IC50?taken as the concentration at which 50% of the enzyme activity is inhibited). |
别名 | BIX 01294 |
分子量 | 600.02 |
分子式 | C28H38N6O2·3HCl |
CAS No. | 1392399-03-9 |
Powder: -20°C for 3 years | In solvent: -80°C for 1 year
H2O: 60 mg/mL (100 mM)
DMSO: 60 mg/mL (100 mM)
可选溶剂 | 浓度 体积 质量 | 1 mg | 5 mg | 10 mg | 25 mg |
H2O / DMSO | 1 mM | 1.6666 mL | 8.3331 mL | 16.6661 mL | 41.6653 mL |
5 mM | 0.3333 mL | 1.6666 mL | 3.3332 mL | 8.3331 mL | |
10 mM | 0.1667 mL | 0.8333 mL | 1.6666 mL | 4.1665 mL | |
20 mM | 0.0833 mL | 0.4167 mL | 0.8333 mL | 2.0833 mL | |
50 mM | 0.0333 mL | 0.1667 mL | 0.3333 mL | 0.8333 mL | |
100 mM | 0.0167 mL | 0.0833 mL | 0.1667 mL | 0.4167 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。
BIX-01294 trihydrochloride 1392399-03-9 Autophagy Chromatin/Epigenetic Histone Methyltransferase SUV39H1(H320R) p21 recurrent BIX-01294 Trihydrochloride Cdkn1a MLKL H3K9me3 inhibit PRMT1 p53 Inhibitor H3K9me2 BIX01294 BIX 01294 trihydrochloride BIX-01294 BIX 01294 Trihydrochloride BIX01294 Trihydrochloride BIX 01294 Gadd45a BIX01294 trihydrochloride inhibitor