IP Library Granted Patent US 9,156,867
Granted Patent B2
US 9,156,867 · App. 14/463,908 · Granted Oct 13, 2015

Acyclic nucleoside phosphonate diesters

Inventors: Karl Y. Hostetler (Del Mar, CA); James R. Beadle (San Diego, CA); Nadejda Valiaeva (San Diego, CA)
Assignee: The Regents of the University of California
C07F9/65616C07F9/6561C07F9/65121C07F9/65583
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Quick Facts
Patent No.
US 9,156,867
App. No.
14/463,908
Granted
Oct 13, 2015
Kind
B2
Abstract

The present disclosure relates, inter alia, to compositions and methods for treating viral diseases and cancer. There are disclosed lipophilic antiviral and anticancer acyclic nucleoside phosphonate diesters, preparation thereof, and methods of using the compounds to treat viral diseases and cancer.

Claims (53)

1. A method for treating a viral infection comprising administering an effective amount of a compound selected from the group consisting of:

or a pharmaceutically acceptable salt of any of the foregoing, to a subject in need thereof, wherein the viral infection is selected from the group consisting of a human papilloma viral infection selected from the group consisting of a HPV 11 infection, a HPV 16 infection and a HPV 18 infection, human HIV viral infection, hepatitis B viral infection, vaccinia viral infection, an adenovirus viral infection, a cytomegalovirus viral infection, herpes simplex virus 1 infection, herpes simplex virus 2 infection, BK viral infection and JC viral infection.

2. The method of claim 1 , wherein the compound is:

or a pharmaceutically acceptable salt thereof.

3. The method of claim 1 , wherein the compound is:

or a pharmaceutically acceptable salt thereof.

4. The method of claim 1 , wherein the compound is:

or a pharmaceutically acceptable salt thereof.

5. The method of claim 1 , wherein the compound is:

or a pharmaceutically acceptable salt thereof.

6. The method of claim 1 , wherein the compound is:

or a pharmaceutically acceptable salt thereof.

7. The method of claim 1 , wherein the compound is:

or a pharmaceutically acceptable salt thereof.

8. The method of claim 1 , wherein the compound is:

or a pharmaceutically acceptable salt thereof.

9. The method of claim 1 , wherein the compound is:

or a pharmaceutically acceptable salt thereof.

10. The method of claim 1 , wherein the compound is:

or a pharmaceutically acceptable salt thereof.

11. The method of claim 1 , wherein the compound is:

or a pharmaceutically acceptable salt thereof.

12. The method of claim 1 , wherein the compound is:

or a pharmaceutically acceptable salt thereof.

13. The method of claim 1 , wherein the compound is:

or a pharmaceutically acceptable salt thereof.

14. The method of claim 1 , wherein the compound is:

or a pharmaceutically acceptable salt thereof.

15. The method of claim 1 , wherein the compound is:

or a pharmaceutically acceptable salt thereof.

16. The method of claim 1 , wherein the compound is:

or a pharmaceutically acceptable salt thereof.

17. The method of claim 1 , wherein the compound is:

or a pharmaceutically acceptable salt thereof.

18. The method of claim 1 , wherein the viral infection is a human papilloma viral infection selected from the group consisting of HPV 11 infection, HPV 16 infection and HPV 18 infection.

19. The method of claim 18 , wherein the compound, or a pharmaceutically acceptable salt thereof, treats a plurality of types of human papilloma virus.

20. The method of claim 18 , wherein the human papilloma viral infection is HPV 11 infection.

21. The method of claim 1 , wherein the viral infection is human HIV infection.

22. The method of claim 1 , wherein the viral infection is hepatitis B viral infection.

23. The method of claim 18 , wherein the human papilloma viral infection is HPV 16 infection.

24. The method of claim 18 , wherein the human papilloma viral infection is HPV 18 infection.

25. The method of claim 1 , wherein the viral infection is vaccinia viral infection.

26. The method of claim 1 , wherein the viral infection is an adenovirus infection.

27. The method of claim 1 , wherein the viral infection is a cytomegalovirus infection.

28. The method of claim 1 , wherein the viral infection is herpes simplex virus 1 infection.

29. The method of claim 1 , wherein the viral infection is herpes simplex virus 2 infection.

30. The method of claim 1 , wherein the viral infection is BK virus infection.

31. The method of claim 1 , wherein the viral infection is JC virus infection.

32. A method for inhibiting growth of a cell transformed by a virus comprising contacting the cell with an effective amount of,

or a pharmaceutically acceptable salt of any of the foregoing,

wherein the virus is selected from the group consisting of a human papilloma virus selected from the group consisting of HPV 11, HPV 16, HPV 18, human HIV, hepatitis B virus, vaccinia virus, an adenovirus, a cytomegalovirus, herpes simplex virus 1, herpes simplex virus 2, BK virus and JC virus.

33. A method for treating cancer of the cervix comprising administering an effective amount of

or a pharmaceutically acceptable salt of any of the foregoing, to a subject in need thereof.

Assignments (1)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Aug 20, 2014
From: HOSTETLER, KARL Y.; BEADLE, JAMES R.; VALIAEVA, NADEJDA
To: THE REGENTS OF THE UNIVERSITY OF CALIFORNIA, A CALIFORNIA CORPORATION
Reel/Frame 033575/0690 →
Continuity (3)
Continuation 14211235 · Mar 14, 2014
Provisional Application 61793993 · Mar 15, 2013
Related Publication 20140364397A1 · Dec 11, 2014