IP Library Granted Patent US 7,166,579
Granted Patent B2
US 7,166,579 · App. 10/735,582 · Granted Jan 23, 2007

Prodrugs of DP IV-inhibitors

Assignee: Prosidion Limited
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Quick Facts
Patent No.
US 7,166,579
App. No.
10/735,582
Granted
Jan 23, 2007
Kind
B2
Abstract

Prodrug compounds of unstable inhibitors of the serine peptidase dipeptidyl peptidase IV, are used in the treatment of various disorders, especially of metabolic disorders. The Prodrug compounds can be used in the treatment of impaired glucose tolerance, glucosuria, hyperlipidaemia, metabolic acidoses, diabetes mellitus, diabetic neuropathy and nephropathy.

Claims (15)

1. A prodrug compound that is an inhibitor of the enzymatic activity of dipeptidyl peptidase IV (DP IV), which compound has the general formula A–B–C, wherein

A is an amino acid,

B is a chemical bond between A and C or is an amino acid, and

C is a stable inhibitor of DP IV, selected from the group consisting of isoleucyl thiazolidine, isoleucyl pyrrolidine, L-allo-isoleucyl thiazolidine, L-allo-isoleucyl pyrrolidine, valyl thiazolidine and valyl pyrrolidine.

2. The prodrug compound according to claim 1 wherein said stable inhibitor is present in a salt form.

3. The prodrug compound according to claim 1 having the general formula A–B–C, wherein said compound is selected from the group consisting of glycyl-prolyl-isoleucyl thiazolidine (Gly-Pro-Ile-Thia), glycyl-isoleucyl thiazolidine (H-Gly-Ile-Thia), alanyl-isoleucyl thiazolidine (Ala-Ile-Thia), prolyl-isoleucyl thiazolidine (Pro-Ile-Thia), pyroglutamyl-isoleucyl thiazolidine (pGlu-Ile-Thia), glycyl-prolyl-isoleucyl pyrrolidine (Gly-Pro-Ile-Pyr), glycyl-isoleucyl pyrrolidine (H-Gly-Ile-Pyr), alanyl-isoleucyl pyrrolidine (Ala-Ile-Pyr), prolyl-isoleucyl pyrrolidine (Pro-Ile-Pyr), and pyroglutamyl-isoleucyl pyrrolidine (pGlu-Ile-Pyr).

4. The prodrug compound according to claim 3 wherein said compound is present in pharmaceutical acceptable salts thereof.

5. The prodrug compound according to claim 1 having the general formula A–B–C wherein said compound is selected from the group consisting of glycyl-prolyl-valyl thiazolidine (Gly-Pro-Val-Thia), glycyl-valyl thiazolidine (H-Gly-Val-Thia), alanyl-valyl thiazolidine (Ala-Val-Thia), prolyl-valyl thiazolidine (Pro-Val-Thia), pyroglutamyl-valyl thiazolidine (pGlu-Val-Thia), glycyl-prolyl-valyl pyrrolidine (Gly-Pro-Val-Pyr), glycyl-valyl pyrrolidine (H-Gly-Val-Pyr), alanyl-valyl pyrrolidine (Ala-Val-Pyr), prolyl-valyl pyrrolidine (Pro-Val-Pyr), and pyroglutamyl-valyl pyrrolidine (pGlu-Val-Pyr), and pharmaceutical acceptable salts thereof.

6. The prodrug compound according to claim 4 wherein said compound is present in pharmaceutical acceptable salts thereof.

7. A pharmaceutical composition for oral administration containing the prodrug compound of claim 1 in combination with one or more pharmaceutical carriers or excipients.

8. A pharmaceutical composition for oral administration containing at least one prodrug compound of claim 3 in combination with one or more pharmaceutical carriers or excipients.

9. A pharmaceutical composition for oral administration containing at least one prodrug compound of claim 5 in combination with one or more pharmaceutical carriers or excipients.

10. A method of treating impaired glucose tolerance, glucosuria, hyperlipidaemia, metabolic acidoses, diabetes mellitus, diabetic neuropathy, obesity and nephropathy and sequelae of diabetes mellitus in mammals, which method comprises administering a therapeutically effective amount of the compound of claim 1 .

11. A method of treating impaired glucose tolerance, glucosuria, hyperlipidaemia, metabolic acidoses, diabetes mellitus, diabetic neuropathy, obesity and nephropathy and sequelae of diabetes mellitus in mammals, which method comprises administering a therapeutically effective amount of a compound of claim 3 .

12. A method of treating impaired glucose tolerance, glucosuria, hyperlipidaemia, metabolic acidoses, diabetes mellitus, diabetic neuropathy, obesity and nephropathy and sequelae of diabetes mellitus in mammals, which method comprises administering a therapeutically effective amount of a compound of claim 5 .

Assignments (7)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Nov 22, 2011
From: DEMUTH, HANS-ULRICH; HOFFMANN, TORSTEN; SCHLENZIG, DAGMAR; MANHART, SUSANNE
To: PROBIODRUG
Reel/Frame 027265/0491 →
CHANGE OF NAME Recorded Nov 22, 2011
From: PROBIODRUG GESELLSCHAFT FUR ARZNEIMITTELFORSCHUNG MBH
To: PROBIODRUG AG
Reel/Frame 027265/0501 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded May 9, 2005
From: PROBIODRUG AG
To: PROSIDION LIMITED
Reel/Frame 016536/0621 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded May 9, 2005
From: PROBIODRUG AG
To: PROSIDION LIMITED
Reel/Frame 017045/0252 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded May 9, 2005
From: PROBIODRUG AG
To: PROSIDION LIMITED
Reel/Frame 016547/0581 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded May 9, 2005
From: PROBIODRUG AG
To: PROSIDION LIMITED
Reel/Frame 016561/0783 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Apr 14, 2005
From: PROBIODRUG AG
To: PROSIDION LIMITED
Reel/Frame 016536/0107 →
Priority Claims (2)
DE 198 28 113 · Jun 24, 1998 · national
EP PCT/EP99/04382 · Jun 24, 1999 · regional
Continuity (2)
Continuation 0974577600 · Dec 22, 2000
Related Publication 20040171555A1 · Sep 2, 2004