Phosphonate compounds
View Patent ↗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.
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.