Substituted quinoxalines as kinase inhibitors
Disclosed herein are compounds of formula (I) and methods of inhibiting IKKβ and the NF-κB signaling and mTOR pathways.
1. A compound having a structure selected from:
or a salt thereof.
2. The compound of claim 1 , having a structure
or a salt thereof.
3. The compound of claim 1 , having a structure
or a salt thereof.
4. The compound of claim 1 , having a structure
or a salt thereof.
5. The compound of claim 1 , having a structure
or a salt thereof.
6. The compound of claim 1 , having a structure
or a salt thereof.
7. The compound of claim 1 , having a structure
or a salt thereof.
8. A method of decreasing the inhibitor of kappa B kinase β activity in a cell, comprising contacting the cell with an effective amount of the compound of claim 1 .
9. The method of claim 8 , wherein the inhibitor of kappa B kinase β is hyperphosphorylated.
10. A method of inhibiting the nuclear factor kappaB signaling pathway in a cell, comprising contacting the cell with an effective amount of the compound of claim 1 .
11. A method of inhibiting the mammalian target of rapamycin signaling pathway in a cell, comprising contacting the cell with an effective amount of the compound of claim 1 .