IP Library Granted Patent US 44,613
Granted Patent E1
US 44,613 · App. 13/281,965 · Granted Nov 26, 2013

N-substituted glycine derivatives: hydroxylase inhibitors

Inventors: Kevin J. Duffy (Collegeville, PA); William Henry Miller (Collegeville, PA); Andrea K. Myers (Collegeville, PA); Antony N. Shaw (King of Prussia, PA); Michael N. Zimmerman (Collegeville, PA)
Assignee: GlaxoSmithKline LLC
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Quick Facts
Patent No.
US 44,613
App. No.
13/281,965
Granted
Nov 26, 2013
Kind
E1
Abstract

The invention described herein relates to certain pyridazinedione N-substituted glycine derivatives of formula (I) which are antagonists of HIF prolyl hydroxylases and are useful for treating diseases benefiting from the inhibition of this enzyme, anemia being one example.

Claims (34)

1. A compound which is N-{[2-[(4-bromo-2-fluorophenyl)methyl]-5-hydroxy-6-(1 -methylethyl)-3-oxo-2,3-dihydro-4-pyridazinyl]carbonyl}glycine or a salt thereof.

2. A compound according to claim 1 which is N-{[2-[(4-bromo-2-fluorophenyl)methyl]-5-hydroxy-6-(1-methylethyl)-3-oxo-2,3-dihydro-4-pyridazinyl]carbonyl}glycine.

3. A compound according to claim 1 which is Na, K, Li, Ca, or Mg salt of N-{[2-[(4-bromo-2-fluorophenyl)methyl]-5-hydroxy-6-(1-methylethyl)-3-oxo-2,3-dihydro-4-pyridazinyl]carbonyl}glycine.

4. A method for treating anemia in a mammal, which method comprises administering an effective amount of N-{[2-[(4-bromo-2-fluorophenyl)methyl]-5-hydroxy-6-(1-methylethyl)-3-oxo-2,3-dihydro-4-pyridazinyl]carbonyl}glycine or a salt thereof to a mammal suffering from anemia which can be treated by inhibiting HIF prolyl hydroxylases.

5. A pharmaceutical composition comprising N-{[2-[(4-bromo-2-fluorophenyl)methyl]-5-hydroxy-6-(1-methylethyl)-3-oxo-2,3-dihydro-4-pyridazinyl]carbonyl}glycine or a salt thereof and one or more of pharmaceutically acceptable carriers, diluents and excipients.

6. A compound which is N-{[2-[(3,4′-difluoro-4-biphenylyl)methyl]-5-hydroxy-6-(1-methylethyl)-3-oxo-2,3-dihydro-4-pyridazinyl]carbonyl}glycine or a pharmaceutically acceptable salt thereof.

7. A compound according to claim 6 which is N-{[2-[(3,4′-difluoro-4-biphenylyl)methyl]-5-hydroxy-6-(1 -methylethyl)-3-oxo-2,3-dihydro-4-pyridazinyl]carbonyl}glycine.

8. A compound according to claim 6 which is the Na, K, Li, Ca, or Mg salt of N-{[2-[(3,4′-difluoro-4-biphenylyl)methyl]-5-hydroxy-6-(1-methylethyl)-3-oxo-2,3-dihydro-4-pyridazinyl]carbonyl}glycine.

9. A method for treating anemia in a mammal, which method comprises administering an effective amount of N-{[2-[(3,4′-difluoro-4-biphenylyl)methyl]-5-hydroxy-6-(1-methylethyl)-3-oxo-2,3-dihydro-4-pyridazinyl]carbonyl}glycine or a salt thereof to a mammal suffering from anemia which can be treated by inhibiting HIF prolyl hydroxylases.

10. A pharmaceutical composition comprising N-{[2-[(3,4′-difluoro-4-biphenylyl)methyl]-5-hydroxy-6-(1 -methylethyl)-3-oxo-2,3-dihydro-4-pyridazinyl]carbonyl}glycine or a salt thereof and one or more of pharmaceutically acceptable carriers, diluents and excipients.

11. A compound of Formula (I)

wherein

R 1 is 2-fluoro-4-bromobenzyl, 4-bromobenzyl, 4-(halophenyl)benzyl, 2-fluoro-4-(halophenyl)benzyl, 2-fluoro-4-trifluoromethylbenzyl, 4-trifluoromethylbenzyl, or 2-fluoro-4-(C 1 -C 4 alkoxyphenyl)benzyl;

R 2 is OH;

R 3 is H; and

R 4 is isopropyl, t-butyl or cyclohexyl; or

a pharmaceutically acceptable salt thereof.

12. A pharmaceutical composition comprising a compound of claim 11, or a salt thereof and one or more of pharmaceutically acceptable carriers, diluents or excipients.

13. The compound:

or a salt thereof.

14. The compound:

15. A pharmaceutical composition comprising a compound according to claim 13, and one or more of pharmaceutically acceptable carriers, diluents or excipients.

16. The compound:

or a salt thereof.

17. The compound:

18. A pharmaceutical composition comprising a compound of claim 16, and one or more of pharmaceutically acceptable carriers, diluents or excipients.

19. A method for treating anemia associated with renal disease in a human, said method comprising administering a compound according to claim 13.

20. A method for treating anemia associated with renal disease in a human, said method comprising administering a compound according to claim 16.

21. A method for treating anemia associated with cancer chemotherapy in a human, said method comprising administering a compound according to claim 13.

22. A method for treating anemia associated with cancer chemotherapy in a human, said method comprising administering a compound according to claim 16.

23. A method for treating anemia associated with reduced erythropoietin production in a human, said method comprising administering a compound according to claim 13.

24. A method for treating anemia associated with reduced erythropoietin production in a human, said method comprising administering a compound according to claim 16.

25. A method for increasing erythropoietin production in a human, said method comprising administering a compound according to claim 13.

26. A method for increasing erythropoietin production in a human, said method comprising administering a compound according to claim 16.

Assignments (3)
CHANGE OF NAME Recorded Aug 2, 2013
From: SMITHKLINE BEECHAM CORPORATION
To: GLAXOSMITHKLINE LLC
Reel/Frame 030934/0620 →
CORRECTIVE ASSIGNMENT TO CORRECT THE ASSIGNOR PREVIOUSLY RECORDED ON REEL 030847 FRAME 0443. ASSIGNOR(S) HEREBY CONFIRMS THE ASSIGNOR (SMITHKLINEBEECHAM CORPORATION) SHOULD BE LISTED AS THE ASSIGNEE. Recorded Aug 2, 2013
From: DUFFY, KEVIN J.; SHAW, ANTONY N.; MILLER, WILLIAM HENRY; MYERS, ANDREA K.; ZIMMERMAN, MICHAEL N.
To: SMITHKLINE BEECHAM CORPORATION
Reel/Frame 030949/0358 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jul 22, 2013
From: DUFFY, KEVIN J.; SHAW, ANTONY N.; MILLER, WILLIAM HENRY; MYERS, ANDREA K.; ZIMMERMAN, MICHAEL N.; SMITHKLINE BEECHAM CORPORATION
To: GLAXOSMITHKLINE LLC
Reel/Frame 030847/0443 →
Continuity (2)
Reissue 11972702 · Jan 11, 2008
Provisional Application 60884710 · Jan 12, 2007