IP Library › Patent Application 12198088
Patent Application
App. No. 12/198,088

DEUTERIUM-ENRICHED DALBAVANCIN

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Patent No.
US None
App. No.
12/198,088
Abstract

The present application describes deuterium-enriched dalbavancin, 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 99 are independently selected from H and D; and

the abundance of deuterium in R 1 -R 99 .

2 . A deuterium-enriched compound of claim 1 , wherein the abundance of deuterium in R 1 -R 99 is selected from at least 1%, at least 5%, at 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%, (k) 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%.

3 . A deuterium-enriched compound of claim 1 , wherein the abundance of deuterium in R 1 -R 21 is selected from at least 5%, at least 10%, at least 14%, at least 19%, at least 24%, at least 29%, at least 33%, at least 38%, at least 43%, at least 48%, at least 52%, (k) at least 57%, at least 62%, at least 67%, at least 71%, at least 76%, at least 81%, at least 86%, at least 90%, at least 95%, and 100%.

4 . A deuterium-enriched compound of claim 1 , wherein the abundance of deuterium in R 22 -R 27 is selected from at least 17%, at least 33%, at least 50%, at least 67%, at least 83%, and 100%.

5 . A deuterium-enriched compound of claim 1 , wherein the abundance of deuterium in R 22 -R 33 is selected from at least 8%, at least 17%, at least 25%, at least 33%, at least 42%, at least 50%, at least 58%, at least 67%, at least 75%, at least 83%, at least 92%, and 100%.

6 . A deuterium-enriched compound of claim 1 , wherein the abundance of deuterium in R 28 -R 33 is selected from at least 17%, at least 33%, at least 50%, at least 67%, at least 83%, and 100%.

7 . A deuterium-enriched compound of claim 1 , wherein the compound is selected from compounds 1-5 of Table 1.

8 . A deuterium-enriched compound of claim 1 , wherein the compound is selected from compounds 6-10 of Table 2.

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

wherein R 1 -R 99 are independently selected from H and D; and

the abundance of deuterium in R 1 -R 99 .

10 . An isolated deuterium-enriched compound of claim 9 , wherein the abundance of deuterium in R 1 -R 99 is selected from at least 1%, at least 5%, at 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%, (k) 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%.

11 . An isolated deuterium-enriched compound of claim 9 , wherein the abundance of deuterium in R 1 -R 21 is selected from at least 5%, at least 10%, at least 14%, at least 19%, at least 24%, at least 29%, at least 33%, at least 38%, at least 43%, at least 48%, at least 52%, (k) at least 57%, at least 62%, at least 67%, at least 71%, at least 76%, at least 81%, at least 86%, at least 90%, at least 95%, and 100%.

12 . An isolated deuterium-enriched compound of claim 9 , wherein the abundance of deuterium in R 22 -R 27 is selected from at least 17%, at least 33%, at least 50%, at least 67%, at least 83%, and 100%.

13 . An isolated deuterium-enriched compound of claim 9 , wherein the abundance of deuterium in R 22 -R 33 is selected from at least 8%, at least 17%, at least 25%, at least 33%, at least 42%, at least 50%, at least 58%, at least 67%, at least 75%, at least 83%, at least 92%, and 100%.

14 . An isolated deuterium-enriched compound of claim 9 , wherein the compound is selected from compounds 1-5 of Table 1.

15 . An isolated deuterium-enriched compound of claim 9 , wherein the compound is selected from compounds 6-10 of Table 2.

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

wherein R 1 -R 99 are independently selected from H and D; and

the abundance of deuterium in R 1 -R 99 .

17 . A mixture of deuterium-enriched compound of claim 16 , wherein the compound is selected from compounds 1-5 of Table 1.

18 . A mixture of deuterium-enriched compound of claim 16 , wherein the compound is selected from compounds 6-10 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 complicated skin and soft tissue infections 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 (2)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jul 18, 2011
From: PROTIA, LLC
To: DEUTERIA PHARMACEUTICALS INCE
Reel/Frame 026609/0689 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Oct 24, 2008
From: CZARNIK, ANTHONY W
To: PROTIA, LLC
Reel/Frame 021733/0840 →