IP Library › Patent Application 12195517
Patent Application
App. No. 12/195,517

DEUTERIUM-ENRICHED AMLODIPINE

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Patent No.
US None
App. No.
12/195,517
Abstract

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

Claims (27)

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 8%, at least 12%, at least 16%, at least 20%, at least 24%, at least 28%, at least 32%, at least 36%, at least 40%, at least 44%, at least 48%, at least 52%, at least 56%, at least 60%, at least 64%, at least 68%, at least 72%, at least 76%, at least 80%, at least 84%, at least 88%, at least 92%, at least 96%, and 100%.

3 . A deuterium-enriched compound of claim 1 , wherein the abundance of deuterium in R 1 -R 3 is selected from at least 33%, at least 67%, and 100%.

4 . A deuterium-enriched compound of claim 1 , wherein the abundance of deuterium in R 11 -R 13 , and R 18 -R 19 is selected from at least 20%, at least 40%, at least 60%, at least 80%, and 100%.

5 . A deuterium-enriched compound of claim 1 , wherein the abundance of deuterium in R 4 -R 10 , R 14 -R 17 , and R 20 -R 25 is selected from at least 6%, at least 12%, at least 18%, at least 24%, at least 29%, at least 35%, at least 41%, at least 47%, at least 53%, at least 59%, at least 65%, at least 71%, at least 76%, at least 82%, at least 88%, at least 94%, and 100%.

6 . A deuterium-enriched compound of claim 1 , wherein the abundance of deuterium in R 1 -R 3 , R 11 -R 13 , and R 18 -R 19 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%.

7 . A deuterium-enriched compound of claim 1 , wherein the abundance of deuterium in R 1 -R 3 , R 4 -R 10 , R 14 -R 17 , and R 20 -R 25 is selected from at least 5%, least 10%, at least 15%, at least 20%, at least 25%, at least 30%, at least 35%, at least 40%, at least 45%, at least 50%, at least 55%, at least 60%, at least 65%, at least 70%, at least 75%, at least 80%, at least 85%, at least 90%, at least 95%, and 100%.

8 . A deuterium-enriched compound of claim 1 , wherein the abundance of deuterium in R 11 -R 13 , R 18 -R 19 , R 4 -R 10 , R 14 -R 17 , and R 20 -R 25 is selected from at least 5%, at least 9%, at least 14%, at least 18%, at least 23%, at least 27%, at least 32%, at least 36%, at least 41%, at least 45%, at least 50%, at least 55%, at least 59%, at least 64%, at least 68%, at least 73%, at least 77%, at least 82%, at least 86%, at least 91%, at least 95%, and 100%.

9 . A deuterium-enriched compound of claim 1 , wherein the compound is selected from compounds 1-7 of Table 1:

10 . A deuterium-enriched compound of claim 1 , wherein the compound is selected from compounds 8-14 of Table 2:

11 . 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%.

12 . An isolated deuterium-enriched compound of claim 11 , wherein the abundance of deuterium in R 1 -R 25 is selected from at least 4%, at least 8%, at least 12%, at least 16%, at least 20%, at least 24%, at least 28%, at least 32%, at least 36%, at least 40%, at least 44%, at least 48%, at least 52%, at least 56%, at least 60%, at least 64%, at least 68%, at least 72%, at least 76%, at least 80%, at least 84%, at least 88%, at least 92%, at least 96%, and 100%.

13 . An isolated deuterium-enriched compound of claim 11 , wherein the abundance of deuterium in R 1 -R 3 is selected from at least 33%, at least 67%, and 100%.

14 . An isolated deuterium-enriched compound of claim 11 , wherein the compound is selected from compounds 1-7 of Table 1:

15 . An isolated deuterium-enriched compound of claim 11 , wherein the compound is selected from compounds 8-14 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 compounds of claim 16 , wherein the compounds are selected from compounds 1-7 of Table 1:

18 . A mixture of deuterium-enriched compounds of claim 16 , wherein the compounds are selected from compounds 8-14 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 hypertension and prophylaxis of angina 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 →