IP Library › Granted Patent US 11,918,569
Granted Patent B2
US 11,918,569 · App. 17/401,522 · Granted Mar 5, 2024

5-deutero-2,4-thiazolidinedione derivatives and compositions comprising and methods of using the same

Inventors: Sheila DeWitt (Auburn, NH); Vincent Jacques (Somerville, MA); Leonardus van der Ploeg (Newton, MA)
Assignee: Poxel SA
A61K31/4439C07B59/002C07D277/34C07D417/12
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Quick Facts
Patent No.
US 11,918,569
App. No.
17/401,522
Granted
Mar 5, 2024
Kind
B2
Abstract

The invention provides 5-deuterium-enriched 2,4-thiazolidinediones (e.g., 5-[4-[2-(5-ethyl-2-pyridyl)-2-oxoethoxy]benzyl]-5-deutero-thiazolidine-2,4-dione), deuterated derivatives thereof, stereoisomers thereof, pharmaceutically acceptable salt forms thereof, and methods of treatment using the same.

Claims (38)

1. A method of treating a disorder selected from the group consisting of adrenoleukodystrophy (ALD), nonalcoholic fatty liver disease (NAFLD) and nonalcoholic steatohepatitis (NASH), the method comprising administering to a patient in need thereof a therapeutically effective amount of a deuterium-enriched compound of formula IIa or IIb or a pharmaceutically acceptable salt form thereof:

wherein:

R 2 , R 3 , R 4 , R 5 , R 6 , R 7 , R 8 , R 9 , R 12 , R 13 , and R 14 are H;

R 1 is H or D, provided that the abundance of deuterium in R 1 is at least 90%;

Z is H or D, provided that the abundance of deuterium in Z is at least 30%;

R 10 is H and R 11 is OH or OD; or

R 10 and R 11 are taken together with the carbon to which they are attached to form a carbonyl;

R A is ethyl;

wherein the compound has an enantiomeric excess, with respect to the C—Z carbon, of at least 5%.

2. The method of claim 1 , wherein R 10 is H and R 11 is OH.

3. The method of claim 1 , wherein R 10 and R 11 are taken together with the carbon to which they are attached to form a carbonyl.

4. The method of claim 3 , wherein the abundance of deuterium in Z is at least 50%.

5. The method of claim 3 , wherein the abundance of deuterium in Z is at least 80%.

6. The method of claim 3 , wherein the abundance of deuterium in Z is at least 90%.

7. The method of claim 3 , wherein the abundance of deuterium in Z is at least 95%.

8. The method of claim 3 , wherein the compound has an enantiomeric excess, with respect to the C—Z carbon, of at least 80%, and Z is H or D, provided that the abundance of deuterium in Z is at least 50%.

9. The method of claim 8 , wherein the abundance of deuterium in Z is at least 80%.

10. The method of claim 8 , wherein the abundance of deuterium in Z is at least 90%.

11. The method of claim 8 , wherein the abundance of deuterium in Z is at least 95%.

12. The method of claim 1 , wherein the compound is of formula IIa,

R 10 and R 11 are taken together with the carbon to which they are attached to form a carbonyl, the compound has an enantiomeric excess, with respect to the C—Z carbon, of at least 80%, and that the abundance of deuterium in Z is at least 50%.

13. The method of claim 12 , wherein the abundance of deuterium in Z is at least 80%.

14. The method of claim 12 , wherein the abundance of deuterium in Z is at least 90%.

15. The method of claim 12 , wherein the abundance of deuterium in Z is at least 95%.

16. The method of claim 14 , wherein the compound has an enantiomeric excess, with respect to the C—Z carbon, of at least 90%.

17. The method of claim 14 , wherein the compound has an enantiomeric excess, with respect to the C—Z carbon, of at least 95%.

18. The method of claim 1 , wherein the compound is of formula IIb,

R 10 and R 11 are taken together with the carbon to which they are attached to form a carbonyl, the compound has an enantiomeric excess, with respect to the C—Z carbon, of at least 80%, and that the abundance of deuterium in Z is at least 50%.

19. The method of claim 18 , wherein the abundance of deuterium in Z is at least 80%.

20. The method of claim 18 , wherein the abundance of deuterium in Z is at least 90%.

21. The method of claim 18 , wherein the abundance of deuterium in Z is at least 95%.

22. The method of claim 20 , wherein the compound has an enantiomeric excess, with respect to the C—Z carbon, of at least 90%.

23. The method of claim 20 , wherein the compound has an enantiomeric excess, with respect to the C—Z carbon, of at least 95%.

24. The method of claim 1 , wherein the abundance of deuterium in Z is at least 80%.

25. The method of claim 1 , wherein the compound is in a pharmaceutical composition, comprising a pharmaceutically acceptable carrier.

26. The method of claim 3 , wherein the compound is in a pharmaceutical composition, comprising a pharmaceutically acceptable carrier.

27. The method of claim 12 , wherein the compound is in a pharmaceutical composition, comprising a pharmaceutically acceptable carrier.

28. The method of claim 18 , wherein the compound is in a pharmaceutical composition, comprising a pharmaceutically acceptable carrier.

Assignments (2)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Dec 22, 2021
From: DEUTERX, LLC
To: POXEL SA
Reel/Frame 058464/0474 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Dec 22, 2021
From: DEWITT, SHEILA; JACQUES, VINCENT; VAN DER PLOEG, LEONARDUS
To: DEUTERX, LLC
Reel/Frame 058464/0494 →
Continuity (7)
Continuation 16292600 · Mar 5, 2019
Continuation 15805330 · Nov 7, 2017
Continuation 15226240 · Aug 2, 2016
Continuation 14616317 · Feb 6, 2015
Continuation 14211905 · Mar 14, 2014
Provisional Application 61786118 · Mar 14, 2013
Related Publication 20220211682A1 · Jul 7, 2022