IP Library › Patent Application 12206223
Patent Application
App. No. 12/206,223

DEUTERIUM-ENRICHED APIXABAN

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Patent No.
US None
App. No.
12/206,223
Abstract

The present application describes deuterium-enriched apixaban, pharmaceutically acceptable salt forms thereof, and methods of treating using the same.

Claims (26)

1 . A deuterium-enriched compound of formula I or a pharmaceutically acceptable salt thereof:

wherein R 1 -R 25 are independently selected from H and D; and

the abundance of deuterium in R 1 -R 25 is at least 4%.

2 . A deuterium-enriched compound of claim 1 , wherein the abundance of deuterium in R 1 -R 25 is selected from at least 4%, at least 6%, at least 14%, at least 19%, at least 26%, at least 32%, at least 39%, at least 45%, at least 52%, at least 58%, at least 65%, at least 71%, at least 77%, at least 84%, at least 90%, at least 97%, and 100%.

3 . A deuterium-enriched compound of claim 1 , wherein the abundance of deuterium in R 1 -R 2 is selected from at least 50% and 100%.

4 . A deuterium-enriched compound of claim 1 , wherein the abundance of deuterium in R 1 -R 12 is selected from at least 50% and 100%.

5 . A deuterium-enriched compound of claim 1 , wherein the abundance of deuterium in R 1 -R 2 and R 1 -R 12 is selected from at least 25%, at least 50%, at least 75%, and 100%.

6 . A deuterium-enriched compound of claim 1 , wherein the abundance of deuterium in R 3 -R 6 is selected from at least 25%, at least 50%, at least 75%, and 100%.

7 . A deuterium-enriched compound of claim 1 , wherein the abundance of deuterium in R 7 -R 10 is selected from at least 25%, at least 50%, at least 75%, and 100%.

8 . A deuterium-enriched compound of claim 1 , wherein the abundance of deuterium in R 11 -R 18 is selected from at least 13%, at least 25%, at least 38%, at least 50%, at least 63%, at least 75%, at least 88%, and 100%.

9 . A deuterium-enriched compound of claim 1 , wherein the abundance of deuterium in R 19 -R 22 is selected from at least 25%, at least 50%, at least 75%, and 100%.

10 . A deuterium-enriched compound of claim 1 , wherein the abundance of deuterium in R 23 -R 25 is selected from at least 33%, at least 67%, and 100%.

11 . A deuterium-enriched compound of claim 1 , wherein the compound is selected from compounds 1-9 of Table 1.

12 . A deuterium-enriched compound of claim 1 , wherein the compound is selected from compounds 10-18 of Table 2.

13 . An isolated deuterium-enriched compound of formula I or a pharmaceutically acceptable salt thereof:

wherein R 1 -R 25 are independently selected from H and D; and

the abundance of deuterium in R 1 -R 25 is at least 4%.

14 . An isolated deuterium-enriched compound of claim 13 , wherein the compound is selected from compounds 1-9 of Table 1.

15 . An isolated deuterium-enriched compound of claim 13 , wherein the compound is selected from compounds 10-18 of Table 2.

16 . A mixture of deuterium-enriched compounds of formula I or a pharmaceutically acceptable salt thereof:

wherein R 1 -R 25 are independently selected from H and D; and

the abundance of deuterium in R 1 -R 25 is at least 4%.

17 . A mixture of deuterium-enriched compound of claim 16 , wherein the compound is selected from compounds 1-9 of Table 1.

18 . A mixture of deuterium-enriched compound of claim 16 , wherein the compound is selected from compounds 10-18 of Table 2.

19 . A pharmaceutical composition, comprising: a pharmaceutically acceptable carrier and a therapeutically effective amount of a compound of claim 1 or a pharmaceutically acceptable salt form thereof.

20 . A method for treating venous thromboembolism comprising: administering, to a patient in need thereof, a therapeutically effective amount of a compound of claim 1 or a pharmaceutically acceptable salt form thereof.

Assignments (1)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Oct 24, 2008
From: CZARNIK, ANTHONY W
To: PROTIA, LLC
Reel/Frame 021733/0840 →