Use of ATR and Chk1 inhibitor compounds
The invention relates to kinase inhibitor compounds and methods of identifying and using them. The invention further relates to pharmaceutical compositions and methods for treating or preventing herpesvirus infection and/or herpesvirus-associated diseases and disorders.
1. A method of treating or preventing a herpesvirus infection in a subject comprising administering to the subject identified as in need thereof VE-822:
or salt, hydrate or solvate thereof.
2. The method of claim 1 , wherein the subject is administered PF-00477736:
3. The method of claim 2 , wherein VE-822 or salt, hydrate or solvate thereof and PF-00477736 are administered simultaneously.
4. The method of claim 2 , wherein VE-822 or salt, hydrate or solvate thereof and PF-00477736 are administered sequentially.
5. The method of claim 1 , wherein the herpesvirus is HSV-1 or HSV-2.
6. The method of claim 1 , wherein VE-822 or salt, hydrate or solvate thereof inhibits ATR-mediated DNA-damage-checkpoint pathway.
7. The method of claim 1 , wherein VE-822 or salt, hydrate or solvate thereof does not inhibit ATM.
8. The method of claim 1 , wherein the herpesvirus is HSV-1, HSV-2, Varicella zoster virus, Epstein-Barr virus, human herpesvirus 6, human herpesvirus 7, Kaposi's sarcoma-associated herpesvirus, Pseudorabies virus, gaHV-2, BHV-1, or EHV-1.
9. A method for reducing HSV viral replication comprising contacting a cell with VE-822:
or salt, hydrate or solvate thereof.
10. A method of inhibiting HSV in a subject identified as in need of such treatment, comprising administering VE-822:
or salt, hydrate or solvate thereof.