| 产品描述: | AEE788 is an inhibitor of the EGFR and ErbB2 with IC50 values of 2 and 6 nM, respectively. |
| 靶点: |
EGFR:2 nM (IC50);ErbB2:6 nM (IC50);Apoptosis;EGFR;c-Fms;FLT;Bcr-Abl |
| 体内研究: |
AEE788 efficiently inhibits growth factor-induced EGFR and ErbB2 phosphorylation in tumors for >72 h. AEE788 also inhibits VEGF-induced angiogenesis in a murine implant model. In mice treated with AEE788, tumor growth is inhibited by 54% at 21 days after the start of treatment compared with control mice |
| 参考文献: |
1. Traxler P, et al. AEE788: a dual family epidermal growth factor receptor/ErbB2 and vascular endothelial growth factor receptor tyrosine kinase inhibitor with antitumor and antiangiogenic activity. Cancer Res. 2004 Jul 15;64(14):4931-4941. 2. Park et al. AEE788, a dual tyrosine kinase receptor inhibitor, induces endothelial cell apoptosis in human cutaneous squamous cell carcinoma xenografts in nude mice. Clin Cancer Res. 2005 Mar 1;11(5):1963-1973. |
| 溶解性: |
DMSO : 50 mg/mL (113.49 mM; Need ultrasonic) |
| 保存条件: |
-20℃ |
| 配置溶液浓度参考: |
|
1mg |
5mg |
10mg |
| 1 mM |
2.27 ml |
11.349 ml |
22.697 ml |
| 5 mM |
0.454 ml |
2.27 ml |
4.539 ml |
| 10 mM |
0.227 ml |
1.135 ml |
2.27 ml |
| 50 mM |
0.045 ml |
0.227 ml |
0.454 ml |
|
| 注意: |
部分产品我司仅能提供部分信息,我司不保证所提供信息的权威性,仅供客户参考交流研究之用。 |