Nucleic acid-based compounds and methods of use thereof
View Patent ↗The invention provides compounds capable of treating against hepatitis infections, particularly hepatitis B viral infections. Compounds of the invention are nucleic acid-based and preferably comprise 2, 3, 4, 5 or 6 nucleoside units.
1. A compound having the structure of any one of compounds 1, 2, 4, 7-11, 13, 14 or 16-62, or a pharmaceutically acceptable salt thereof, wherein compounds 1, 2, 4, 7-11, 13, 14, and 16-62 have the following structures:
2. A pharmaceutical composition comprising the compound of claim 1 in combination with a pharmaceutically acceptable carrier.
3. The pharmaceutical composition of claim 2 wherein the pharmaceutically acceptable carrier comprises a lipid.
4. A pharmaceutical composition for treating a viral infection comprising a therapeutically effective amount of a compound of claim 1 in combination with a pharmaceutically acceptable carrier.
5. A pharmaceutical composition for treating an HBV infection comprising a therapeutically effective amount of a compound of claim 1 in combination with a pharmaceutically acceptable carrier.
6. A pharmaceutical composition for treating a viral infection comprising a therapeutically effective amount of a compound of claim 1 in combination with a therapeutically effective amount of a reverse transcriptase inhibitor and a pharmaceutically acceptable carrier.
7. A pharmaceutical composition of claim 6 wherein the reverse transcriptase inhibitor is 3TC.
8. A pharmaceutical composition of claim 5 wherein the HBV infection is a drug resistant HBV infection.
9. A compound selected from the group consisting of compounds 1-11, 13, 14, 16-18, 20-23, 25-28, 31-36, 38-42, 44, 46, 49-53, 56, 58, and 60-62, or a pharmaceutically acceptable salt thereof, wherein the compound is modified by the replacement of the internucleotide linkage with a different linkage selected from the group consisting of alkylphosphonate, phosphorothioate, phosphorodithioate, alkylphosphonothioate, phosphoroamidate, carbamate, carbonate, phosphate trimester, acetamidate, carboxymethyl ester linkages, and combinations thereof wherein the structures of compounds 3, 5, and 6 are as follows and wherein the structures of compounds 1, 2, 4, 7-11, 13, 14, 16-18, 20-23, 25-28, 31-36, 38-42, 44, 46, 49-53, 56, 58, and 60-62 are as set forth in claim 1 :
10. A compound selected from the group consisting of compounds 1-11, 13, 14 and 16-62 as set forth in claim 1 or claim 9 or a pharmaceutically acceptable salt thereof, wherein the compound is modified by replacement of the moiety at the 2′ position of the sugar group with a different moiety selected from the group consisting of H, —OH, an amino group, a halogen group, a substituted or unsubstituted —O-lower alkyl group containing 1 to 6 saturated or unsaturated carbon atoms, a substituted or unsubstituted —O-aryl group having 2 to 6 carbons and a substituted or unsubstituted —O-allyl group having 2 to 6 carbon atoms.
11. A pharmaceutical composition comprising at least one compound selected from compounds 1, 2, and 4-11, 13, 14, 16-62 as set forth in claim 1 or claim 9 as specified above.
12. A pharmaceutical composition comprising a compound of claim 9 and a pharmaceutically acceptable carrier.
13. A pharmaceutical composition comprising a compound of claim 10 and a pharmaceutically acceptable carrier.
14. A method for treating a viral infection comprising administering to a patient an effective amount of a pharmaceutical composition of claim 11 .
15. A method for treating an HBV infection comprising administering to a patient an effective amount of a pharmaceutical composition of claim 11 .
16. A method for treating a viral infection comprising administering to a patient an effective amount of a pharmaceutical composition of claim 12 .
17. A method for treating an HBV infection comprising administering to a patient an effective amount of a pharmaceutical composition of claim 12 .
18. A method for treating a viral infection comprising administering to a patient an effective amount of a pharmaceutical composition of claim 13 .
19. A method for treating an HBV infection comprising administering to a patient an effective amount of a pharmaceutical composition of claim 13 .
20. A compound of claim 1 selected from compounds 18, 20, 31, 39, 50, 52, 60, or 61 having the structures as set forth in claim 1 .
21. A pharmaceutical composition comprising at least one compound selected from compounds 19, 30, 45, 47, 54, or 57 having the structures as set forth in claim 1 , or a pharmaceutically acceptable salt thereof, wherein the compound is modified by the replacement of the internucleotide linkage with a different linkage selected from the group consisting of alkylphosphonate, phosphorothioate, phosphorodithioate, alkylphosphonothioate, phosphoroamidate, carbamate, carbonate, phosphate trimester, acetamidate, carboxymethyl ester linkages, and combinations thereof.
22. A method for treating a viral infection comprising administering to a patient an effective amount of a pharmaceutical composition of claim 21 .
23. A method for treating an HBV infection comprising administering to a patient an effective amount of a pharmaceutical composition of claim 21 .
24. A compound selected from the group consisting of compounds 24, 29, 37, 43, 48, 55, and 59 having the structures as previously set forth in claim 1 , or a pharmaceutically acceptable salt thereof, wherein the compound is modified by the replacement of the internucleotide linkage with a different linkage selected from the group consisting of alkylphosphonate, phosphorodithioate, alkylphosphonothioate, phosphoroamidate, carbamate, carbonate, phosphate trimester, acetamidate, carboxymethyl ester linkages, and combinations thereof.