BX517(PDK1 inhibitor2) - Names and Identifiers
BX517(PDK1 inhibitor2) - Physico-chemical Properties
Molecular Formula | C15H14N4O2
|
Molar Mass | 282.3 |
Solubility | DMSO: ≥ 27 mg/mL |
Storage Condition | -20℃ |
In vitro study | BX-517 blocks activation of Akt in tumor cells, is potent with IC 50 of 0.1-1.0 μM. BX-517 blocks AKT2 activation in cells with submicromolar potency. BX-517 is 100-fold selective or better against a panel of seven additional Ser/Thr and Tyr kinases. |
BX517(PDK1 inhibitor2) - Preparation solution concentration reference
| 1mg | 5mg | 10mg |
---|
1 mM | 3.542 ml | 17.712 ml | 35.424 ml |
5 mM | 0.708 ml | 3.542 ml | 7.085 ml |
10 mM | 0.354 ml | 1.771 ml | 3.542 ml |
5 mM | 0.071 ml | 0.354 ml | 0.708 ml |
Last Update:2024-01-02 23:10:35
BX517(PDK1 inhibitor2) - Reference Information
biological activity | BX517 is a potent, selective PDK1 inhibitor with an IC50 value of 6 nM. |
Target | IC50: 6 nM (PDK1) |
Last Update:2024-04-09 02:00:14