| 靶点: |
IC50: 5.7 nM (ATX) |
| 参考文献: |
1. Albers HM, et al. Chemical Evolution of Autotaxin Inhibitors. Chem Rev. 2012 May 9;112(5):2593-603. 2. Albers HM, et al. Structure-based design of novel boronic acid-based inhibitors of autotaxin. J Med Chem. 2011 Jul 14;54(13):4619-26. 3. Fulkerson Z, et al. Binding of autotaxin to integrins localizes lysophosphatidic acid production to platelets and mammalian cells. J Biol Chem. 2011 Oct 7;286(40):34654-63. |
| 溶解性: |
DMSO: soluble10mg/mL, clear |
| 保存条件: |
-80℃(运输条件:冰袋低温运输) |
| 配置溶液浓度参考: |
|
1mg |
5mg |
10mg |
| 1 mM |
2.158 ml |
10.792 ml |
21.585 ml |
| 5 mM |
0.432 ml |
2.158 ml |
4.317 ml |
| 10 mM |
0.216 ml |
1.079 ml |
2.158 ml |
| 50 mM |
0.043 ml |
0.216 ml |
0.432 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。 |