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化合物 AZ20,AZ20

化合物 AZ20|T1958|TargetMol

價格 313 488 747
包裝 2mg 5mg 10mg
最小起訂量 2mg
發(fā)貨地 上海
更新日期 2026-04-02
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產品詳情

中文名稱:化合物 AZ20英文名稱:AZ20
CAS:1233339-22-4品牌: TargetMol
產地: 美國保存條件: Powder: -20°C for 3 years | In solvent: -80°C for 1 year Shipping with blue ice/Shipping at ambient temperature.
純度規(guī)格: 99.69%產品類別: 抑制劑
貨號: T1958
2026-04-02 化合物 AZ20 AZ20 2mg/313RMB;5mg/488RMB;10mg/747RMB 313 TargetMol 美國 Powder: -20°C for 3 years | In solvent: -80°C for 1 year Shipping with blue ice/Shipping at ambient temperature. 99.69% 抑制劑

Product Introduction

Bioactivity

名稱AZ20
描述AZ20 is an effective and specific inhibitor of ATR kinase (IC50: 5 nM, in a cell-free assay), 8-fold selectivity over mTOR.
細胞實驗AZ20 is dissolved in 100% DMSO. Compound dose ranges are created by diluting in 100% DMSO and then further into assay medium (EMEM, 10% FCS, 1% glutamine) using a Labcyte Echo acoustic dispensing instrument. Cells are plated in 384-well Costar plates at 9×104?cells per mL in 40 μL of EMEM, 10% FCS, 1% glutamine and grown for 24 h. Following addition of compound the cells are incubated for 60 min. A final concentration of 3 μM?4NQO?(prepared in 100% DMSO) is then added using the Labcyte Echo, and the cells are incubated for a further 60 min. The cells are fixed by adding 40 μL of 3.7% v/v formaldehyde solution for 20 min. After removal of fix, cells are washed with PBS and permeabilized in 40 μL of PBS containing 0.1% Triton X-100. The cells are then washed, and 15 μL primary antibody solution (pChk1 Ser345) is added. The plates are incubated at 4°C overnight. The primary antibody is then washed off, and 20 μL of secondary antibody solution and 1 μM Hoechst 33258 added for 90 min at room temperature. The plates are washed and left in 40 μL of PBS. Plates are then read on an ArrayScan VTI instrument to determine staining intensities, and dose responses are obtained and used to determine the IC50?values for the compounds.
激酶實驗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).
體外活性AZ20(10 μM)可使CYP3A4介導的咪達唑侖代謝的50%被抑制.LoVo腫瘤的雌性裸鼠中,服用13天AZ20(25 mg/kg,2次/天,p.o.;50 mg/kg/day,p.o. )可使腫瘤生長受到顯著抑制,這與異種移植組織中γH2AX核染色的持續(xù)廣泛升高有關.
體內活性在體外,AZ20濃度依賴性地降低pChk1 Ser345/317/296水平。延長AZ20的處理時間可增加γH2AX核染色,這是因為存在復制壓力,且與S期阻滯和組蛋白H3的磷酸化水平增加有關。AZ20對體外生長抑制和細胞死亡的誘導作用是完全不同于其它細胞毒性藥物的。AZ2與ATM 抑制劑KU-60019聯用會增加細胞毒性。
存儲條件Powder: -20°C for 3 years | In solvent: -80°C for 1 year Shipping with blue ice/Shipping at ambient temperature.
溶解度Ethanol : 3 mg/mL (7.27 mM), Sonication is recommended.
H2O : < 1 mg/mL (insoluble or slightly soluble)
DMSO : 50 mg/mL (121.21 mM), Sonication is recommended.
10% DMSO+40% PEG300+5% Tween 80+45% Saline : 2 mg/mL (4.85 mM), Sonication is recommended.
關鍵字mTOR | Inhibitor | inhibit | AZ-20 | AZ20 | AZ 20 | ATR | ATM/ATR | ATM and RAD3 related | ATM | Ataxia telangiectasia mutated
相關產品L-Proline | Metformin | Rapamycin | Resveratrol | Methyl eugenol | L-Leucine | (E/Z)-10-Hydroxy-2-decenoic acid | Dihydromyricetin | N-Hydroxyphthalimide | Metformin hydrochloride | Stearamide | 4-Vinylcyclohexene Dioxide
相關庫抑制劑庫 | 血管生成庫 | 經典已知活性庫 | 已知活性化合物庫 | 抗癌細胞代謝庫 | 代謝化合物庫 | 自噬庫 | 激酶抑制劑庫 | 抗糖尿病庫 | 抗衰老化合物庫 | 糖代謝化合物庫 | 免疫/炎癥分子化合物庫
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關鍵字: AZ20|TargetMol

公司簡介

TargetMol Chemicals Inc. 總部位于馬薩諸塞州波士頓,致力于為全球生化領域科學家的研究提供專業(yè)的產品和服務。TargetMol?品牌的客戶群分布于40多個國家和地區(qū),已發(fā)展成為全球知名的化合物庫和小分子化合物研究供應商。 TargetMol?可提供160多種滿足不同需求的化合物庫,以及多種類型的生化試劑產品,包括12000多種抑制劑、16000多種天然產物和各類多肽、抗體、生命科學試劑盒等,此外,我們還建設有CADD(計算機輔助藥物設計)研究中心、藥理實驗室、藥化合成平臺三大技術中心,全方位滿足客戶的定制需求。 憑借我們優(yōu)質的產品和服務、快速高效的全球供應鏈和專業(yè)的技術支持,我們將有效幫助您縮短研發(fā)周期,取得更成功的結果。
成立日期 2013-04-18 (14年) 注冊資本 566.265100萬人民幣
員工人數 100-500人 年營業(yè)額 ¥ 1億以上
主營行業(yè) 天然產物,生化試劑,分子生物學,分子砌塊,生物技術服務 經營模式 貿易,工廠,試劑,定制,服務
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  • 公司成立:14年
  • 注冊資本:566.265100萬人民幣
  • 企業(yè)類型:有限責任公司(自然人投資或控股)
  • 主營產品:小分子抑制劑、藥物篩選化合物庫、藥物篩選等
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