Combinations of a caspase inhibitor and an antiviral agent
View Patent ↗A compound is provided which has a structure I: A-B-C and a method for administering the compound is also provided for use in the prophylaxis and/or treatment of a viral infection, and in particular for preventing and/or inhibiting viral replication, in which A is a quinoline or quinoline-like group, B is a sole amino acid or a peptide or polypeptide having a given amino acid sequence, and C is an O-phenoxy group. According to one embodiment, the compound is a protease inhibitor such as a caspase inhibitor, and the inhibitor can be Q-VD-OPh (N-(2-(quinolyl)valylaspartyl-(2,6-difluorophenoxyl)methyl ketone), optionally in an O-methylated form. Antiviral compositions and kits are also provided.
1. A combination comprising:
a) a caspase inhibitor having the structure:
wherein:
B is a single amino acid or a peptide or polypeptide having a given amino acid sequence,
R1 and R2 are selected from a hydrogen, an alkyl, an alkoxy, a fluoro, a chloro, a carboxy, a carbonyl, an arylcarbonyl, and an amino, and
R3 and R4 are selected from hydrogen, an alkyl, an alkoxy, a fluoro, a chloro, a carboxy, a carbonyl, an arylcarbonyl, and an amino; and
b) an anti-HIV agent comprising at least one HIV reverse transcriptase inhibitor or HIV protease inhibitor.
2. The combination according to claim 1 , wherein B is a peptide or polypeptide.
3. The combination according to claim 1 , wherein the single amino acid is an aspartic acid (D) or the peptide or polypeptide comprises at least one aspartic acid.
4. The combination according to claim 3 , wherein the peptide or polypeptide comprises an aspartic acid (D) and a valine (V).
5. The combination according to claim 3 , wherein the amino acid sequence of the peptide is valine-aspartic acid (VD) or the sequence valine-alanine-aspartic acid.
6. The combination according to claim 1 , wherein the single amino acid or at least one of the amino acids of said peptide or polypeptide is O-methylated.
7. The combination according to claim 1 , wherein said caspase inhibitor is O-methylated on the single aspartic acid or on at least one of the aspartic acids of said peptide or polypeptide.
8. The combination according to claim 1 , wherein the single amino acid or the amino acid sequence of said peptide or polypeptide is not O-methylated.
9. The combination according to claim 1 , wherein R1 or R2 is a hydrogen.
10. The combination according to claim 1 , wherein R1 and R2 are a hydrogen.
11. The combination according to claim 1 , wherein R3 or R4 is a fluoro.
12. The combination according to claim 1 , wherein R3 and R4 are a fluoro.
13. The combination according to claim 1 , wherein the caspase inhibitor is N-(2-quinolyl)valyl-O-methyl-aspartyl-(2,6-difluorophenoxy)methyl ketone or N-(2-quinolyl)valyl-aspartyl-(2,6-difluorophenoxy)methyl ketone.
14. The combination according to claim 13 , wherein the caspase inhibitor is N-(2-quinolyl)valyl-aspartyl-(2,6-difluorophenoxy)methyl ketone.
15. The combination according to claim 1 , wherein the anti-HIV agent comprises at least one HIV reverse transcriptase inhibitor.
16. The combination according to claim 15 , wherein the HIV reverse transcriptase inhibitor is selected from the group consisting of zidovudine or azidothymidine (AZT), didanosine or ddl, zalcitabine or ddC, stavudine or d4T, lamivudine or 3TC, abacavir or ABC, emtricitabine or FTC, nevirapine, efavirenz, delavirdine and tenofovir or bis-POC-PMPA.
17. The combination according to claim 16 , wherein the HIV reverse transcriptase inhibitor is AZT.
18. The combination according to claim 1 , wherein the anti-HIV agent comprises at least one HIV protease inhibitor.
19. The combination according to claim 18 , wherein the HIV protease inhibitor is selected from the group constituted by the following peptidomimetic molecules: Indinavir or IDV, Nelfinavir or NLFN, Saquinavir or SQN, Ritonavir or RTN, Amprenavir, Lopinavir.
20. The combination according to claim 19 , wherein the HIV protease inhibitor is Indinavir.
21. The combination according to claim 13 , wherein the anti-HIV agent comprises at least one HIV reverse transcriptase inhibitor.
22. The combination according to claim 21 , wherein the HIV reverse transcriptase inhibitor is selected from the group consisting of zidovudine or azidothymidine (AZT), didanosine or ddl, zalcitabine or ddC, stavudine or d4T, lamivudine or 3TC, abacavir or ABC, emtricitabine or FTC, nevirapine, efavirenz, delavirdine and tenofovir or bis-POC-PMPA.
23. The combination according to claim 22 , wherein the HIV reverse transcriptase inhibitor is AZT.
24. The combination according to claim 13 , wherein the anti-HIV agent comprises at least one HIV protease inhibitor.
25. The combination according to claim 24 , wherein the HIV protease inhibitor is selected from the group constituted by the following peptidomimetic molecules: Indinavir or IDV, Nelfinavir or NLFN, Saquinavir or SQN, Ritonavir or RTN, Amprenavir, Lopinavir.
26. The combination according to claim 25 , wherein the HIV protease inhibitor is Indinavir.