Inhibitors of protein tyrosine kinase activity
This invention relates to compounds that inhibit protein tyrosine kinase activity. In particular the invention relates to compounds that inhibit the protein tyrosine kinase activity of growth factor receptors, resulting in the inhibition of receptor signaling, for example, the inhibition of VEGF receptor signaling and HGF receptor signaling. More particularly, the invention relates to compounds, compositions and methods for the inhibition of VEGF receptor signaling and HGF receptor signaling. The invention also provides compositions and methods for treating cell proliferative diseases and conditions.
1. A method of inhibiting solid tumor growth in a patient in need thereof, the method comprising administering to said patient a therapeutically effective amount of a compound having the structure:
or a composition, pharmaceutically acceptable salt, racemic mixture , scalemic mixture, diastereomer or enantiomer thereof.
2. The method according to claim 1 , wherein the compound has the structure:
3. The method according to claim 1 , wherein the compound has the structure:
4. The method according to claim 1 , wherein the compound has the structure:
5. The method according to claim 1 , wherein the compound has the structure:
6. The method according to claim 1 , wherein the compound has the structure:
7. The method according to claim 1 , wherein the compound has the structure:
8. The method according to claim 1 , wherein the compound has the structure:
9. The method according to claim 1 , wherein the compound has the structure:
10. The method according to claim 1 , wherein the compound has the structure:
11. The method according to claim 1 , wherein the compound has the structure:
12. The method according to claim 1 , wherein the compound has the structure:
13. The method according to claim 1 , wherein the compound has the structure:
14. The method according to claim 1 , wherein the compound has the structure:
15. The method according to claim 1 , wherein the compound has the structure: