IP Library Granted Patent US 8,309,565
Granted Patent B2
US 8,309,565 · App. 13/220,548 · Granted Nov 13, 2012

Phosphonate compounds

Assignee: The Regents of the University of California
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Quick Facts
Patent No.
US 8,309,565
App. No.
13/220,548
Granted
Nov 13, 2012
Kind
B2
Abstract

The present invention relates to phosphonate compounds, compositions containing them, processes for obtaining them, and their use for treating a variety of medical disorders, e.g., osteoporosis and other disorders of bone metabolism, cancer, viral infections, and the like.

Claims (42)

1. An antiviral compound having the structure of Formula I:

wherein

R 2 , R 2 ′, R 1′ are each independently hydrogen;

R 1 is —O—(C 1 -C 24 )alkyl;

m is an integer from 0 to 6;

n is 0; and

or a pharmaceutically acceptable salt or a stereochemically isomeric form thereof.

2. The compound of claim 1 , wherein m is 2 or 3.

3. The compound of claim 1 , wherein R 1 is —O(C 15 )alkyl or —O(C 17 )alkyl.

4. The compound of claim 1 , wherein the compound is selected from the group consisting of

or a pharmaceutically acceptable salt thereof.

5. A pharmaceutical composition comprising an effective amount of an antiviral compound of Formula I

wherein

R 2 , R 2 ′, R 1′ are each independently hydrogen;

R 1 is —O—(C 1 -C 24 )alkyl;

m is an integer from 0 to 6;

n is 0; and

or a pharmaceutically acceptable salt thereof;

in combination with a pharmaceutically acceptable carrier.

6. The pharmaceutical composition of claim 5 , wherein the composition is in a solid dosage form, capsule, tablet, aerosol, solution, suspension, or in a topical formulation.

7. The pharmaceutical composition of claim 5 , wherein the compound is selected from the group consisting of

or a pharmaceutically acceptable salt thereof.

8. A method for the treatment of a viral disease comprising administering an effective amount of an antiviral compound of Formula I

wherein

R 2 , R 2 ′, R 1′ are each independently hydrogen;

R 1 is —O—(C 1 -C 24 )alkyl;

m is an integer from 0 to 6;

n is 0; and

or a pharmaceutically acceptable salt thereof;

optionally in a pharmaceutically acceptable carrier.

9. The method of claim 8 , wherein the viral disease is selected from the group consisting of human immunodeficiency virus, influenza, herpes simplex virus, human herpes virus, cytomegalovirus, hepatitis B and C virus, Epstein-Barr virus, varicella zoster virus, orthopox virus, ebola virus and papilloma virus.

10. The method of claim 9 , wherein the orthopox is selected from variola major and minor, vaccinia, smallpox, cowpox, camelpox and monkeypox.

11. The method of claim 8 , wherein the virus is HIV.

12. The method of claim 8 , wherein the virus is influenza.

13. The method of claim 8 , wherein the virus is herpes.

14. The method of claim 8 , wherein the virus is cytomegalovirus.

15. The method of claim 8 , wherein the virus is hepatitis B or hepatitis C.

16. The method of claim 8 , wherein the virus is Epstein-Barr virus.

17. The method of claim 8 , wherein the virus is varicella zoster virus.

18. The method of claim 8 , wherein the virus is papilloma.

19. The method of claim 8 , wherein the compound is selected from the group consisting of

or a pharmaceutically acceptable salt thereof.

Assignments (1)
CONFIRMATORY LICENSE Recorded Dec 13, 2018
From: UNIVERSITY OF CALIFORNIA, SAN DIEGO
To: NATIONAL INSTITUTES OF HEALTH (NIH), U.S. DEPT. OF HEALTH AND HUMAN SERVICES (DHHS), U.S. GOVERNMENT
Reel/Frame 047819/0585 →
Continuity (10)
Continuation 12701410 · Feb 5, 2010
Continuation 11925309 · Oct 26, 2007
Continuation 11715604 · Mar 7, 2007
Continuation 11506292 · Aug 17, 2006
Continuation 11100882 · Apr 6, 2005
Continuation 10759345 · Jan 15, 2004
Continuation 10148374
Provisional Application 60205179 · May 17, 2000
Provisional Application 60168813 · Dec 3, 1999
Related Publication 20120058975A1 · Mar 8, 2012