Claims for Patent: 8,951,985
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Summary for Patent: 8,951,985
Title: | Compounds and pharmaceutical compositions for the treatment of viral infections |
Abstract: | Provided herein are compounds, compositions and methods for the treatment of liver disorders, including HCV infections. In one embodiment, compounds and compositions of nucleoside derivatives are disclosed, which can be administered either alone or in combination with other anti-viral agents. |
Inventor(s): | Surleraux; Dominique (Wauthier-Braine, BE), Dousson; Cyril B. (Canet, FR), Dukhan; David (Saint Gely du Fesc, FR), Pierra; Claire (Montarnaud, FR) |
Assignee: | Idenix Pharmaceuticals, Inc. (Cambridge, MA) |
Application Number: | 13/610,574 |
Patent Claims: | 1. A compound of Formula I: ##STR00056## or a pharmaceutically acceptable salt, solvate, a tautomeric or polymorphic form thereof, wherein Base is heterocyclyl; A is
(CH.sub.2).sub.n, cycloalkylene, heterocyclylene or heteroarylene; n is 1 to 3; each X is independently O or S; R.sup.1 is OH, alkoxy, O-acyl or F; R.sup.2 is NH.sub.2, NH(alkyl), N(alkyl).sub.2, O-alkyl, O-aryl, O-aralkyl, S-alkyl, S-aryl or
S-aralkyl; R.sup.3 is OR.sup.5, SR.sup.5,NR.sup.6R.sup.7 or an .alpha.- or .beta.-amino acid ester; R.sup.4 is H or acyl; or R.sup.3 and R.sup.4 together form a 6-8 membered heterocyclic ring; R.sup.5 is hydrogen, alkyl, alkenyl, alkynyl, aryl,
aralkyl, cycloalkyl or cycloalkenyl; R.sup.6 and R.sup.7 are selected as follows: i) R.sup.6 and R.sup.7 are each independently hydrogen, alkyl, alkenyl, alkynyl, aryl, aralkyl, cycloalkyl or cycloalkenyl; or ii) R.sup.6 and R.sup.7 together with the
nitrogen atom on which they are substituted form a 3-7 membered heterocyclic or heteroaryl ring; and R.sup.10 and R.sup.11 are each independently hydrogen, alkyl or aryl.
2. The compound of claim 1, wherein each R.sup.10 and R.sup.11 is hydrogen. 3. The compound of claim 1, wherein each X is O. 4. The compound of claim 1, wherein Base is adenine, cytosine, guanine, hypoxanthine, thymine or uridine. 5. The compound of claim 1, wherein Base is selected from one of formulae (i) to (xxvi): ##STR00057## ##STR00058## ##STR00059## ##STR00060## ##STR00061## wherein each R.sup.L is independently hydrogen, alkyl, cycloalkyl, acyl, carbamyl, CO-alkyl, CO-aryl, CO-alkoxyalkyl, CO-aryloxyalkyl, CO-substituted aryl, sulfonate ester, alkyl sulfonyl, aryl sulfonyl, arylalkyl sulfonyl, a lipid, a phospholipid, an amino acid or a carbohydrate; and each R.sup.M and R.sup.N is independently hydrogen or alkyl; or R.sup.L and R.sup.M together with the N atom to which they are attached from heterocyclyl. 6. The compound of claim 1, or a pharmaceutically acceptable salt, a tautomeric or polymorphic form thereof, of the formula: ##STR00062## wherein each X is independently O or S; R.sup.1 is OH, alkoxy, O-acyl or F; R.sup.2 is NH.sub.2, N(alkyl).sub.2, O-alkyl, O-aryl, O-- aralkyl, S-alkyl, S-aryl or S-aralkyl; R.sup.3 is OR.sup.S, SR.sup.5,NR.sup.6R.sup.7 or an .alpha.- or .beta.-amino acid ester; R.sup.4 is H or acyl; or R.sup.3 and R.sup.4 together for a 6-8 membered heterocyclic ring; R.sup.5 is hydrogen, alkyl, alkenyl, alkynyl, aryl, aralkyl, cycloalkyl or cycloalkenyl; R.sup.6 and R.sup.7 are selected as follows: i) R.sup.6 and R.sup.7 are each independently hydrogen, alkyl, alkenyl, alkynyl, aryl, aralkyl, cycloalkyl or cycloalkenyl; or ii) R.sup.6 and R.sup.7 together with the nitrogen atom on which they are substituted form a 3-7 membered heterocyclic or heteroaryl ring. each R.sup.M and R.sup.N is independently hydrogen or alkyl; or R.sup.L and R.sup.M together with the N atom to which they are attached from heterocyclyl. 7. The compound of claim 1, or a pharmaceutically acceptable salt, a tautomeric or polymorphic form thereof, of the formula: ##STR00063## wherein A is (CH.sub.2).sub.n; n is 1 to 2; R.sup.2 is NH.sub.2, N(alkyl).sub.2, O-alkyl, O-aryl, O-- aralkyl, S-alkyl, S-aryl or S-aralkyl; R.sup.3 is NR.sup.6R.sup.7 or an .alpha.- or .beta.-amino acid ester; and R.sup.6 and R.sup.7 are selected as follows: i) R.sup.6 and R.sup.7 are each independently hydrogen, alkyl, alkenyl, alkynyl, aryl, aralkyl, cycloalkyl or cycloalkenyl; or ii) R.sup.6 and R.sup.7 together with the nitrogen atom on which they are substituted form a 3-7 membered heterocyclic or heteroaryl ring; and R.sup.L is methyl or ethyl. 8. The compound of claim 1, or a pharmaceutically acceptable salt, a tautomeric or polymorphic form thereof, of the formula Ia: ##STR00064## wherein R.sup.1 is OH, alkoxy, O-acyl or F; R.sup.2 is O-alkyl or O-benzyl; R.sup.8 is hydrogen, alkyl, aryl or aralkyl; R.sup.9 is alkyl or benzyl; and R.sup.L is methyl or ethyl. 9. A compound of claim 8, wherein R.sup.1 is OH or F; and R.sup.8 is hydrogen, alkyl or benzyl. 10. A compound of claim 8, wherein R.sup.8 is methyl, isopropyl, isobutyl or benzyl. 11. A compound of claim 8, wherein R.sup.2 is methoxy, ethoxy or isopropoxy. 12. A compound of claim 11, wherein R.sup.8 is methyl, isopropyl, isobutyl or benzyl. 13. A compound of claim 12, wherein R.sup.8 is isobutyl. 14. A compound of claim 13, wherein R.sup.9 is methyl, ethyl or isopropyl. 15. A compound of claim 1, or a pharmaceutically acceptable salt, a tautomeric or polymorphic form thereof, wherein the compound is selected from the group consisting of: ##STR00065## ##STR00066## ##STR00067## ##STR00068## ##STR00069## ##STR00070## ##STR00071## ##STR00072## ##STR00073## ##STR00074## ##STR00075## ##STR00076## ##STR00077## ##STR00078## ##STR00079## 16. A pharmaceutical composition comprising a compound of claim 1 and a pharmaceutically acceptable excipient, carrier or diluent. 17. The pharmaceutical composition of claim 16, wherein the composition is an oral formulation. 18. A method for the treatment of a host infected with a hepatitis C virus, comprising the administration of an effective treatment amount of a compound or composition of claim 1. 19. The method of claim 18, wherein the host is a human. 20. The method of claim 18, wherein said administration directs a substantial amount of said compound or pharmaceutically acceptable salt or stereoisomer thereof to the liver of said host. 21. The method of claim 18, wherein said compound or composition is administered in combination or alternation with a second anti-viral agent optionally selected from the group consisting of an interferon, a ribavirin, an interleukin, a NS3 protease inhibitor, a cysteine protease inhibitor, a phenanthrenequinone, a thiazolidine derivative, a thiazolidine, a benzanilide, a helicase inhibitor, a polymerase inhibitor, a nucleotide analogue, a gliotoxin, a cerulenin, an antisense phosphorothioate oligodeoxynucleotide, an inhibitor of IRES-dependent translation, and a ribozyme. 22. The method of claim 21, wherein the second agent is selected from the group consisting of pegylated interferon alpha 2a, interferon alphacon-1, natural interferon, albuferon, interferon beta-1a, omega interferon, interferon alpha, interferon gamma, interferon tau, interferon delta and interferon .gamma.-1b. |
Details for Patent 8,951,985
Applicant | Tradename | Biologic Ingredient | Dosage Form | BLA | Approval Date | Patent No. | Expiredate |
---|---|---|---|---|---|---|---|
Biogen Inc. | AVONEX | interferon beta-1a | For Injection | 103628 | 05/17/1996 | ⤷ Try a Trial | 2031-09-12 |
Biogen Inc. | AVONEX | interferon beta-1a | Injection | 103628 | 05/28/2003 | ⤷ Try a Trial | 2031-09-12 |
Biogen Inc. | AVONEX | interferon beta-1a | Injection | 103628 | 02/27/2012 | ⤷ Try a Trial | 2031-09-12 |
Emd Serono, Inc. | REBIF | interferon beta-1a | Injection | 103780 | 03/07/2002 | ⤷ Try a Trial | 2031-09-12 |
Emd Serono, Inc. | REBIF | interferon beta-1a | Injection | 103780 | 12/17/2004 | ⤷ Try a Trial | 2031-09-12 |
Emd Serono, Inc. | REBIF | interferon beta-1a | Injection | 103780 | 12/21/2012 | ⤷ Try a Trial | 2031-09-12 |
>Applicant | >Tradename | >Biologic Ingredient | >Dosage Form | >BLA | >Approval Date | >Patent No. | >Expiredate |
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