半岛bd体育手机客户端 说明
一般描述
A potent, cell-permeable, reversible, ATP-competitive inhibitor of the EGFR tyrosine kinase activity (IC50= 8 pM). Also inhibits heregulin-stimulated autophosphorylation in SK-BR-3 (IC50= 49 nM) and MDA-MB-453 (IC50= 52 nM) breast carcinomas. The inhibition is competitive and results from binding of the inhibitor at the ATP site of the enzymes. Inhibits the LPA-stimulated MAP kinase kinase ? (MKK?) activation and EGFR tyrosine phosphorylation in HeLa and NIH3T3 cells.
A potent, cell-permeable, reversible, ATP-competitive inhibitor of the EGFR tyrosine kinase activity (IC50= 8 pM). Also inhibits heregulin-stimulated autophosphorylation in SK-BR-3 (IC50= 49 nM) and MDA-MB-453 (IC50= 52 nM) breast carcinomas. The inhibition is competitive and results from binding of the inhibitor at the ATP site of the enzymes. Inhibits the LPA-stimulated MAP kinase kinase 1/2 (MKK1/2) activation and EGFR tyrosine phosphorylation in HeLa and NIH 3T3 cells. A 10 mM (500 ?g/151 ?l) solution of PD 158780 (Cat. No. 513036) in DMSO is also available.
包装
500 μg in Plastic ampoule
Packaged under inert gas
生化/生理作用
Cell permeable: yes
Target IC50: 8 pM against EGFR tyrosine kinase activity; 49 nM, 52 nm, against heregulin-stimulated autophosphorylation in SK-BR-3 and MDA-MB-453 breast carcinomas, respectively
Primary Target
EGFR tyrosine kinase
Product competes with ATP.
Reversible: yes
警告
Toxicity: Standard Handling (A)
重悬
Following reconstitution, aliquot and freeze at -20°C. Stock solutions are stable for up to 6 months at -20°C.
其他说明
Cunnick, J.M., et al. 1998.J. Biol. Chem.273,14468.
Rewcastle, G.W., et al. 1998.J. Med. Chem.41,742.
法律信息
CALBIOCHEM is a registered trademark of Merck KGaA, Darmstadt, Germany
基本信息
经验(实验)分子式 | C14H12BrN5 |
分子量 | 330.18 |
MDL编号 | MFCD00942160 |
半岛bd体育手机客户端 性质
质量水平 | 100 |
测定 | ≥95% (HPLC) |
形式 | solid |
manufacturer/tradename | Calbiochem? |
储存条件 | OK to freeze protect from light |
颜色 | yellow |
溶解性 | DMSO: 5 mg/mL |
运输 | ambient |
储存温度 | ?20℃ |
安全信息
储存分类代码 | 11 - Combustible Solids |
WGK | WGK 3 |
Sigma-Aldrich