IP Library Granted Patent US 10,479,781
Granted Patent B2
US 10,479,781 · App. 15/554,514 · Granted Nov 19, 2019

Peptidyl nitril compounds as dipeptidyl peptidase I inhibitors

Inventors: Conni Lauritzen (Rødovre, DK); John Pedersen (Nivå, DK)
Assignee: Neuprozyme Therapeutics APS
C07D405/12C07D309/14
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Quick Facts
Patent No.
US 10,479,781
App. No.
15/554,514
Granted
Nov 19, 2019
Kind
B2
Abstract

The invention relates to compounds of Formula (I) and their use as selective dipeptidyl peptidase I inhibitors, as well as pharmaceutical compositions comprising said compounds, and methods of treatment involving said compounds.

Claims (29)

1. A compound of the formula (I)

wherein n is 0, 1 or 2 and m is 0, 1 or 2; such that the sum of m and n is 1, 2, 3 or 4;

F is fluoro;

X 1 represents

wherein y represents 0, 1, 2, 3, 4, 5, 6, 7 or 8;

wherein Z represents O (oxygen);

when y is 1 or 2, then R 1 independently represents deuterium; halogen; hydroxyl; cyano;

oxo (═0); mercapto; or C 1-3 -alkyl; which C 1-3 -alkyl is optionally substituted with at least one substituent selected from halogen, hydroxyl, cyano and mercapto;

or when y represents 3, 4, 5, 6, 7 or 8, then R 1 represents deuterium;

wherein R 2 represents —C 3-6 -cycloalkyl, —C 1-3 -alkyl-C 3-6 -cycloalkyl or —C 1-6 -alkyl, which —C 1-6 -alkyl is optionally substituted with at least one substituent selected from hydroxyl, cyano or amino; as well as pharmaceutically-acceptable salts, solvates and hydrates thereof.

2. The compound of claim 1 , wherein the compound is:

3. The compound of claim 1 , wherein R 2 is —C 1-6 -alkyl, which —C 1-6 -alkyl is optionally substituted with at least one substituent selected from hydroxyl, cyano or amino.

4. The compound of claim 1 , wherein R 2 is —C 1-6 -alkyl.

5. The compound of claim 1 , wherein y represents 0, 1, 2, 3 or 4.

6. The compound of claim 1 , wherein m+n=1.

7. The compound of claim 1 , wherein m=2.

8. A pharmaceutical composition comprising the compound of formula (I) of claim 1 , or a pharmaceutically acceptable salt thereof, and at least one pharmaceutically-acceptable adjuvant, carrier or diluent.

9. The compound of claim 1 for use as a medicament.

10. The compound of claim 1 for treating asthma, chronic obstructive pulmonary disease, bronchiectasis, cystic fibrosis, alpha-1 antitrypsin deficiency, idiopathic pulmonary fibrosis, acute lung injury, acute respiratory distress syndrome, congestive heart failure, atherosclerosis, myocardial infarction, reperfusion injury, abdominal aortic aneurysms, diabetic cardiomyopathy, gout, pseudogout, respiratory syncytial virus infection, inflammatory bowel diseases, psoriasis, rheumatoid arthritis, multiple sclerosis, malaria, Alzheimer's disease or sepsis.

11. The compound of claim 1 for treating asthma, chronic obstructive pulmonary disease, bronchiectasis, cystic fibrosis, alpha-1 antitrypsin deficiency, idiopathic pulmonary fibrosis, congestive heart failure, myocardial infarction, reperfusion injury, abdominal aortic aneurysms, diabetic cardiomyopathy, gout, pseudogout, respiratory syncytial virus infection, psoriasis, rheumatoid arthritis or sepsis.

12. A method for treatment of a medical condition selected from the group consisting of asthma, chronic obstructive pulmonary disease, bronchiectasis, cystic fibrosis, alpha-1 antitrypsin deficiency, idiopathic pulmonary fibrosis, acute lung injury, acute respiratory distress syndrome, congestive heart failure, atherosclerosis, myocardial infarction, reperfusion injury, abdominal aortic aneurysms, diabetic cardiomyopathy, gout, pseudogout, respiratory syncytial virus infection, inflammatory bowel diseases, psoriasis, rheumatoid arthritis, multiple sclerosis, malaria, Alzheimer's disease or sepsis, said method comprising administration of a pharmaceutically effective amount of the compound of claim 1 .

13. The method of claim 12 , wherein the medical condition is selected from the group consisting of asthma, chronic obstructive pulmonary disease, bronchiectasis, cystic fibrosis, alpha-1 antitrypsin deficiency, idiopathic pulmonary fibrosis, congestive heart failure, myocardial infarction, reperfusion injury, abdominal aortic aneurysms, diabetic cardiomyopathy, gout, pseudogout, respiratory syncytial virus infection, psoriasis, rheumatoid arthritis or sepsis.

14. The compound of claim 1 , wherein R 2 is —C 1-3 -alkyl.

15. The compound of claim 1 , wherein R 2 is methyl-, ethyl- or propyl-.

16. The compound of claim 1 , wherein y represents 0 or 1.

17. The compound of claim 1 , wherein y represents 0.

18. The compound of claim 1 , wherein m=1.

19. The compound of claim 1 for treating cystic fibrosis.

20. The method of claim 12 , wherein the medical condition is cystic fibrosis.

Assignments (3)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Sep 25, 2019
From: PROZYMEX APS
To: NEUPROZYME THERAPEUTICS APS
Reel/Frame 050488/0626 →
CHANGE OF NAME Recorded Jun 25, 2019
From: PROZYMEX A/S
To: PROZYMEX APS
Reel/Frame 049577/0052 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Nov 27, 2017
From: LAURITZEN, CONNI; PEDERSEN, JOHN
To: PROZYMEX A/S
Reel/Frame 044225/0345 →
Priority Claims (1)
EP 15157811 · Mar 5, 2015 · regional
Continuity (1)
Related Publication 20180044328A1 · Feb 15, 2018
Cited By (3)
US 12,201,638 US 12,479,837 US 12,679,815