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TG100-115 是 PI3Kγ/PI3Kδ 的选择性抑制剂,IC50分别为 83 和 235 nM。


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TG100-115 是 PI3Kγ/PI3Kδ 的选择性抑制剂,IC50分别为 83 和 235 nM。
| 规格 | 价格 | 库存 | 数量 | 
|---|---|---|---|
| 1 mg | ¥ 273 | In stock | |
| 5 mg | ¥ 678 | In stock | |
| 10 mg | ¥ 987 | In stock | |
| 25 mg | ¥ 1,980 | In stock | |
| 50 mg | ¥ 3,460 | In stock | |
| 100 mg | ¥ 4,930 | In stock | |
| 200 mg | ¥ 6,830 | In stock | |
| 1 mL x 10 mM (in DMSO) | ¥ 738 | In stock | 
TG100-115 相关产品
| 产品描述 | TG100-115 is a PI3Kγ/δ inhibitor (IC50: 83/235 nM), with fewer effects on PI3Kα/β. | 
| 靶点活性 |  PI3Kγ:83 nM, PI3Kδ:235 nM | 
| 体外活性 | 在患心肌梗塞的啮齿目动物和猪模型中,TG100-115(0.5-5 mg/kg)具有有效的心脏保护功能,阻止梗塞恶化,保存心机功能.在Miles实验模型中,TG100-115(1-5 mg/kg)使大鼠的水肿和炎症降低.TG100-115(5 mg/kg)可使小鼠体内Sema3A或血管内皮生长因子相关的血管通透性显著降低,表明这两种因子对血管通透性的诱导作用可能依赖于PI3Kγ/δ.在患哮喘鼠模型,TG100-115可使肺嗜酸性粒细胞增多症显著减弱,并使白细胞介素13和粘蛋白积累受到抑制. | 
| 体内活性 | 在人脐静脉内皮细胞中,TG100-115(10 μM)不影响细胞增殖和VEGF刺激的ERK磷酸化,但会阻断其他血管内皮生长因子信号通路, 如VE-钙粘蛋白磷酸化,从而抑制血管内皮生长因子诱导的VE钙粘蛋白整体水平提高。 TG100-115(0.125-10 μM)对FGF刺激的Akt磷酸化也有抑制作用。TG100-115对PI3Kα/β的抑制效果很弱(IC50:1.2/1.3 mM)。TG100-115对血管内皮生长因子调节的p70S6和mTOR激酶磷酸化有抑制作用。 | 
| 激酶实验 | PI3K assays: Forty mL of reaction buffer (20 mM Tris/4 mM MgCl2/10 mM NaCl, pH 7.4) containing 50 mM D-myo-phosphatidylinositol 4,5-bisphosphate substrate and the desired PI3K isoform are aliquoted to 96-well plates; kinase concentrations are 250-500 ng/well, such that linear kinetics are achieved over 90 min. TG100-115 is then added as 2.5 mL of a DMSO stock to final concentration range of 100 mM to 1 nM. Reactions are initiated by addition of 10 mL of ATP to a final concentration of 3 mM, and after 90 min, 50 mL of Kinase-Glo reagent added to quantify residual ATP levels; luminosity is measured using an Ultra 384 instrument. Control reactions omitting either TG100-115 or substrate are also performed. IC50 values are derived from experimental data by nonlinear curve fitting using Prism Version 4. | 
| 细胞实验 | Cells plated in 96-well cluster plates (5 × 103 cells/well) are cultured in assay medium (containing 0.5% serum and 50 ng/ml VEGF) in the presence or absence of TG100-115, and cell numbers are quantified by XTT assay 24, 48, or 72 hours late(Only for Reference) | 
| 分子量 | 346.34 | 
| 分子式 | C18H14N6O2 | 
| CAS No. | 677297-51-7 | 
| Smiles | Nc1nc(N)c2nc(-c3cccc(O)c3)c(nc2n1)-c1cccc(O)c1 | 
| 密度 | 1.516 g/cm3 (Predicted) | 
| 存储 | Powder: -20°C for 3 years | In solvent: -80°C for 1 year | Shipping with blue ice/Shipping at ambient temperature. | |||||||||||||||||||||||||||||||||||
| 溶解度信息 | H2O: < 1 mg/mL (insoluble or slightly soluble)  DMSO: 40 mg/mL (115.49 mM), Sonication is recommended.   Ethanol: < 1 mg/mL (insoluble or slightly soluble)  | |||||||||||||||||||||||||||||||||||
| 溶液配制表 | ||||||||||||||||||||||||||||||||||||
| DMSO 
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 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 ,
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%
 一共给药动物 10 只 ,您使用的配方为 5%  DMSO+ 30%PEG300+ 5%Tween 80 + 60%Saline/PBS/ddH2O, 那么您的工作液浓度为 2 mg/mL 。
DMSO+ 30%PEG300+ 5%Tween 80 + 60%Saline/PBS/ddH2O, 那么您的工作液浓度为 2 mg/mL 。 
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