- 全部删除
 您的购物车当前为空 您的购物车当前为空
PD-166866是一种选择性FGFR1酪氨酸激酶抑制剂,IC50值为52.4 nM。


为众多的药物研发团队赋能,
让新药发现更简单!
PD-166866是一种选择性FGFR1酪氨酸激酶抑制剂,IC50值为52.4 nM。
| 规格 | 价格 | 库存 | 数量 | 
|---|---|---|---|
| 1 mg | ¥ 215 | In stock | |
| 5 mg | ¥ 496 | In stock | |
| 10 mg | ¥ 728 | In stock | |
| 25 mg | ¥ 1,450 | In stock | |
| 50 mg | ¥ 2,330 | In stock | |
| 100 mg | ¥ 3,730 | In stock | |
| 200 mg | ¥ 5,320 | In stock | |
| 1 mL x 10 mM (in DMSO) | ¥ 496 | In stock | 
PD-166866 相关产品
| 产品描述 | PD-166866 is a selective FGFR tyrosine kinase inhibitor. | 
| 靶点活性 |  FGFR1:52.4 nM | 
| 体外活性 | PD166866显著导致线粒体缺陷和氧化应激[1]。PD 166866以52.4 ± 0.1 nM的IC50值抑制人源全长FGFR-1酪氨酸激酶,但对c-Src、血小板衍生生长因子受体β、表皮生长因子受体或胰岛素受体酪氨酸激酶、丝裂原活化蛋白激酶、蛋白激酶C和CDK4在高达50 μM的浓度下无效。PD 166866强效抑制在NIH 3T3细胞中表达内源性FGFR-1和在L6细胞过表达人FGFR-1酪氨酸激酶的基础成纤维生长因子(bFGF)介导的受体自磷酸化。PD 166866不抑制在血管平滑肌、A431或NIHIR细胞中由血小板衍生生长因子、表皮生长因子或胰岛素刺激的受体自磷酸化,进一步支持其对FGFR-1的特异性。此外,PD 166866是一种强效的抑制人胎盘培养动脉碎片中的微血管生长(血管生成)的抑制剂。在L6细胞中,被PD 166866抑制的磷酸化44-和42-kDa MAPK亚型的IC50值分别为4.3和7.9 nM[2]。PD166866通过抑制Akt/mTOR信号路径诱导自噬[3]。 | 
| 细胞实验 | HeLa cells are treated with PD166866 for 24 hours, the growth medium is removed, the cells are washed with PBS and fixed for 1 hour at 25°C adding a freshly made paraformaldheyde solution (4% in PBS). Samples are washed again with PBS and the endogenous oxidases were blocked for 2 minutes in the dark. Further washes with PBS followed and blocking the unspecific sites is done for 1 hour at 25℃. PARP is evidenced by immunolocalization utilizing a polyclonal antibody, directed against the N-terminal proteolytic fragment. Immuno-reaction is revealed by a secondary anti-rabbit antibody after incubation for 16 hours at 4°C. After exhaustive washing with PBS the samples are incubated for 30 minutes in solution ABC. Eventually, DAB (3,3'-Diaminobenzidine) is added and the samples are incubated for 10 minutes in the dark. The samples are washed again the plates are sealed and ready for microscopic observation.(Only for Reference) | 
| 别名 | PD166866 | 
| 分子量 | 396.44 | 
| 分子式 | C20H24N6O3 | 
| CAS No. | 192705-79-6 | 
| Smiles | COc1cc(OC)cc(c1)-c1cc2cnc(N)nc2nc1NC(=O)NC(C)(C)C | 
| 密度 | 1.277g/cm3 | 
| 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 | DMSO: 12 mg/mL (30.27 mM), Sonication is recommended.   H2O: < 1 mg/mL (insoluble or slightly soluble)  Ethanol: 3 mg/mL (7.57 mM), Sonication is recommended.  | ||||||||||||||||||||||||||||||
| 溶液配制表 | |||||||||||||||||||||||||||||||
| Ethanol/DMSO 
 DMSO 
 | |||||||||||||||||||||||||||||||
 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 。 
评论内容