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Onatasertib

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产品编号 T3351Cas号 1228013-30-6
别名 CC-223, CC223, CC 223

Onatasertib (CC223) 是一种口服有效的mTOR 激酶抑制剂,抑制mTOR 激酶,IC50为 16 nM。它抑制mTORC1和mTORC2。

Onatasertib
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Onatasertib

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纯度: 99.91%
产品编号 T3351 别名 CC-223, CC223, CC 223Cas号 1228013-30-6

Onatasertib (CC223) 是一种口服有效的mTOR 激酶抑制剂,抑制mTOR 激酶,IC50为 16 nM。它抑制mTORC1和mTORC2。

规格价格库存数量
1 mg¥ 338现货
2 mg¥ 488现货
5 mg¥ 793现货
10 mg¥ 1,320现货
25 mg¥ 2,360现货
50 mg¥ 3,650现货
100 mg¥ 5,130现货
500 mg¥ 10,500现货
1 mL x 10 mM (in DMSO)¥ 869现货
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产品介绍

生物活性
产品描述
Onatasertib (CC223) is an orally available mTOR inhibitor with potential antitumor activity. Onatasertib inhibits the activity of mTOR, which may result in the induction of tumor cell apoptosis and a decrease in tumor cell proliferation. Onatasertib is a potent mTOR kinase inhibitor (IC50: 16 nM), with >150-fold sensitivity than the related lipid kinase PI3Kα (IC50: 4 μM).
靶点活性
mTOR:16 nM
体外活性
在PC-3肿瘤移植的小鼠中,CC-223 (25 mg/kg,p.o.)抑制了mTORC1和mTORC2的活性.CC-223 (25 mg/kg, p.o.)还抑制了许多肿瘤模型的肿瘤生长,包括前列腺癌,神经胶质瘤,乳腺癌,肺癌以及结肠癌模型(47%-95%).
体内活性
在许多的细胞系中,CC-223对mTORC1 (S6RP and 4EBP1)和mTORC2 [AKT(S473)]标记物均有抑制作用,其IC50为pAKT(S473,11-150 nM),pS6RP(27-184 nM),p4EBP1(120-1050 nM)。CC-223还对许多癌细胞系的生长有抑制作用并诱导它们凋亡。
激酶实验
Kinase assays mTOR.: Reagents are prepared as follows:"Simple Tor buffer": 10 mM Tris pH 7.4, 100 mM NaCl, 0.1% Tween-20, 1 mM DTT. Recombinant mTOR is diluted in this buffer to an assay concentration of 0.200ug/mL. ATP/Substrate solution: 0.075 mM ATP, 12.5 mM MnCl2, 50 mM Hepes, pH 7.4, 50 mM β-GOP, 250 nM Microcystin LR, 0.25 mM EDTA, 5 mM DTT, and 3.5 μg/mL GST-p70S6. Dilution Curve: A 10-point, 1:3 dilution of compounds are prepared in neat DMSO at 50 times the final assay concentration. Detection reagent mix: 50 mM HEPES, pH 7.4 0.01% Triton X-100, 0.01% BSA, 0.1 mM EDTA, 12.7 ug/mL Cy5-anti-GST antibody, 9 ng/ml anti-phospho p70S6 antibody (Thr389), 627ng/mL anti-mouse IgG labeled with Lance Eu. To 20 uL of the Simple Tor buffer is added 0.5 uL of the compound Dilution Curve in DMSO. The final concentration range for compound is 30 to 0.0015 μM. To initiate the reaction, 5 μL of the ATP/substrate solution is added to the above. The reaction is allowed to run for 60 minutes. The assay is stopped by adding 5 μL of 60 mM EDTA. Ten (10) μL of detection reagent mix is then added, and the mixture is allowed to sit at least 2 hours before reading on a Perkin Elmer Envision microplate reader set to detect Europium-based TR-FRET.
细胞实验
Compound is spotted via an acoustic dispenser (EDC ATS-100) into an empty 384-well plate. Cells are diluted to desired densities and added directly to the compound-spotted plates. Cells are allowed to grow for 72 hours. Viability is assessed via Cell Titer-Glo. All data are normalized and represented as a percentage of the DMSO-treated cells. Results are then expressed as GI50 and/or IC50 values.(Only for Reference)
别名CC-223, CC223, CC 223
化学信息
分子量397.47
分子式C21H27N5O3
CAS No.1228013-30-6
SmilesCO[C@H]1CC[C@@H](CC1)N1C(=O)CNc2ncc(nc12)-c1ccc(nc1)C(C)(C)O
密度1.37 g/cm3 (Predicted)
储存&溶解度
存储Powder: -20°C for 3 years | In solvent: -80°C for 1 year | Shipping with blue ice.
溶解度信息
DMSO: 70 mg/mL (176.11 mM), Sonication is recommended.
Ethanol: 73 mg/mL (183.7 mM)
H2O: < 1 mg/mL (insoluble or slightly soluble)
溶液配制表
DMSO/Ethanol
1mg5mg10mg50mg
1 mM2.5159 mL12.5796 mL25.1591 mL125.7957 mL
5 mM0.5032 mL2.5159 mL5.0318 mL25.1591 mL
10 mM0.2516 mL1.2580 mL2.5159 mL12.5796 mL
20 mM0.1258 mL0.6290 mL1.2580 mL6.2898 mL
50 mM0.0503 mL0.2516 mL0.5032 mL2.5159 mL
100 mM0.0252 mL0.1258 mL0.2516 mL1.2580 mL

计算器

  • 摩尔浓度 计算器
  • 稀释 计算器
  • 配液 计算器
  • 分子量 计算器

体内实验配液计算器

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:
TargetMol | Animal experiments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 μLTargetMol | Animal experiments 一共给药动物 10 只 ,您使用的配方为 5% TargetMol | reagent 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 μLDMSOTargetMol | reagent ( 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:50μLDMSOTargetMol | reagent 母液,添加 300 μLPEG300TargetMol | reagent 混匀澄清,再加 50μLTween 80, 混匀澄清,再加 600μLddH2OTargetMol | reagent 混匀澄清

以上为“体内实验配液计算器”的使用方法举例,并不是具体某个化合物的推荐配制方式,请根据您的实验动物和给药方式选择适当的溶解方案。

1 请输入动物实验的基本信息
mg/kg
g
μL
2 请输入动物体内配方组成,不同的产品配方组成不同,如有配方需求,可先联系我们提供正确的体内配方。
% DMSO
%
%Tween 80
%ddH2O

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