化合物 U0126-EtOH,U0126-EtOH
  • 化合物 U0126-EtOH,U0126-EtOH
  • 化合物 U0126-EtOH,U0126-EtOH

化合物 U0126-EtOH|T6223|TargetMol

7篇文献
价格 167 383 617
包装 1mg 5mg 10mg
最小起订量 1mg
发货地 上海
更新日期 2025-11-17
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产品详情

中文名称:化合物 U0126-EtOH英文名称:U0126-EtOH
CAS:1173097-76-1品牌: TargetMol
产地: 美国保存条件: Powder: -20°C for 3 years | In solvent: -80°C for 1 year | Shipping with blue ice/Shipping at ambient temperature.
纯度规格: 99.88%产品类别: 抑制剂
货号: T6223
2025-11-17 化合物 U0126-EtOH U0126-EtOH 1mg/167RMB;5mg/383RMB;10mg/617RMB 167 TargetMol 美国 Powder: -20°C for 3 years | In solvent: -80°C for 1 year | Shipping with blue ice/Shipping at ambient temperature. 99.88% 抑制剂

Product Introduction

Bioactivity

名称U0126-EtOH
描述U0126-etoh (U0126 Ethanol) is a non-ATP competitive inhibitor of MEK1 (IC50=72 nM) and MEK2 (IC50=58 nM) with selectivity. U0126-EtOH inhibited autophagy and mitophagy.
细胞实验HEK293 cells were maintained in Dulbecco's modification of Eagle's medium (low glucose) plus 10% foetal bovine serum. HeLa cells stably expressing wild type or kinase-dead LKB1 have been described. AMPK activity was determined by immunoprecipitate kinase assays using anti-AMPK-a1 and -a2 antibodies. Antibodies recognising AMPK phosphorylated on Thr-172 (anti-pT172), AMPK-α1 and -α2 and acetyl-CoA carboxylase-1 (ACC1) phosphorylated on Ser-80 [16] were described previously. Quantification of ratios of signals from phosphorylated and total protein using these antibodies was performed by dual labelling using the LI-COR Odyssey IR imager as described. Contents of ATP and ADP were determined for cells in 6 cm culture dishes by quickly pouring off the medium, adding 350 μl of ice-cold 5% perchloric acid, scraping the cells off with a plastic scraper, and centrifuging (14 000 · g; 3 min, 4 °C) to remove insoluble material. The perchloric acid was then extracted from the supernatant and nucleotides analysed by capillary electrophoresis of perchloric acid extracts as described previously. All incubations of cells were performed in triplicate and results are expressed as means ± S.E.M [3].
激酶实验The amount of immunoprecipitated wild type MEK used in these assays was adjusted to give a similar amount of activity units as obtained with 10 nM recombinant MEK. All other assays were performed with a recombinant, constitutively activated mutant MEK-1 (ΔN3-S218E/S222D) or constitutively active MEK-2(S222E/S226D). Reaction velocities were measured using a 96-well nitrocellulose filter apparatus as described below. Unless otherwise noted, reactions were carried out at an enzyme concentration of 10 nM, in 20 mM Hepes, 10 mM MgCl2, 5 mM β-mercaptoethanol, 0.1 mg/ml BSA, pH 7.4, at room temperature. Reactions were initiated by the addition of [γ-33P]ATP into the premixed MEK/ERK/inhibitor reaction mixture, and an aliquot of 100 μl was taken every 6 min and transferred to the 96-well nitrocellulose membrane plate which had 50 mM EDTA to stop the reaction. The membrane plate was drawn and washed 4 times with buffer under vacuum. Wells were then filled with 30 μl of Microscint-20 scintillation fluid, and the radioactivity of33P-phosphorylated ERK was counted with a Top Count scintillation counter. Velocities were obtained from the slopes of radioactivity versus time plots. Concentrations of ERK and ATP were 400 nM and 40 μM, respectively, unless otherwise indicated [2].
动物实验Prior to injection, FI cells were labeled with a stable fluorescent dye molecule, DiA at 10 μg/ml for 5 h at 37 1C. After washing to remove free DiA, cells were trypsinized for inoculation (U0126 experiments) or transfection (RNAi experiments). Biliary epithelial cells were injected subcutaneously, at the indicated times, into the tibia of nude mice. In the chemical experiments, 3h after inoculation, mice were treated with U0126 (10.5 mg/kg) daily by intraperitoneal injection. The length and width of each tumor were measured every day by using a caliper. The following formula was used to calculate tumor volumes ? width2 length/2. Mice were killed at the end of experiment. Tumors were immediately frozen in liquid nitrogen [5].
体外活性方法:COS-7细胞用U0126-EtOH处理后检测AP-1转录活性。 结果:U0126-EtOH抑制AP-1转录活性(IC50=1 μM)。[1] 方法:HCT116细胞用U0126-EtOH处理后使用软琼脂生长实验检测克隆形成,HeLa细胞用U0126-EtOH处理后检测Elk1-荧光素酶报告基因。 结果:U0126-EtOH抑制贴壁非依赖性集落形成(IC50=19.4 μM),U0126-EtOH抑制EGF刺激的Elk1荧光素酶报告基因(IC50=0.29 μM)。[2] 方法:小鼠RAS-3T3细胞用U0126-EtOH处理后使用ELISA方法检测ERK1/2磷酸化水平。 结果:10-40 μM的U0126-EtOH抑制MEK介导的ERK1/2磷酸化。[3]
体内活性方法:为研究U0126-EtOH的抗肿瘤活性,每天将U0126-EtOH(10.5 mg/kg)腹腔注射给小鼠治疗。 结果:U0126-EtOH导致肿瘤植入和早期生长显著减少,注射9天后的肿瘤体积减少了60-70%,此后一直保持这种状态。[4] 方法:为研究U0126-EtOH对血管收缩的影响,大鼠接受120分钟的暂时性中脑动脉阻塞(tMCAO),再将U0126-EtOH(30 mg/kg)腹腔注射给大鼠。 结果:用U0126-EtOH处理后,对S6c的血管收缩显著减少。[5]
存储条件Powder: -20°C for 3 years | In solvent: -80°C for 1 year | Shipping with blue ice/Shipping at ambient temperature.
溶解度10% DMSO+40% PEG300+5% Tween 80+45% Saline : 7.9 mg/mL (18.52 mM), Solution.
Ethanol : < 1 mg/mL (insoluble or slightly soluble)
DMSO : 255 mg/mL (597.75 mM), Sonication is recommended.
关键字virus | U0126-EtOH | U-0126-EtOH | U0126EtOH | U0126 EtOH | U-0126 | U 0126 | progeny | non-ATP | Mitophagy | Mitogen-activated protein kinase kinase | Mitochondrial Autophagy | MEK2 | MEK1 | MEK | MAPKK | MAP2K | Inhibitor | inhibit | InfluenzaVirus | Influenza Virus | competitive | Autophagy
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关键字: U0126 Ethanol|||U0126|TargetMol

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TargetMol Chemicals Inc. 总部位于马萨诸塞州波士顿,致力于为全球生化领域科学家的研究提供专业的产品和服务。TargetMol?品牌的客户群分布于40多个国家和地区,已发展成为全球知名的化合物库和小分子化合物研究供应商。 TargetMol?可提供160多种满足不同需求的化合物库,以及多种类型的生化试剂产品,包括12000多种抑制剂、16000多种天然产物和各类多肽、抗体、生命科学试剂盒等,此外,我们还建设有CADD(计算机辅助药物设计)研究中心、药理实验室、药化合成平台三大技术中心,全方位满足客户的定制需求。 凭借我们优质的产品和服务、快速高效的全球供应链和专业的技术支持,我们将有效帮助您缩短研发周期,取得更成功的结果。
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