IP Library Granted Patent US 7,601,691
Granted Patent B2
US 7,601,691 · App. 11/067,556 · Granted Oct 13, 2009

Anti-obesity agents

View Patent ↗
Loading inventors, assignments & file history…
Monitor This Case
Get email alerts when status or documents change.
Order Certified Copies
Most orders are placed with the USPTO same day — all within 24 business hours.
Order via The Patent Place →
Pre-filled with this patent's details
Quick Facts
Patent No.
US 7,601,691
App. No.
11/067,556
Granted
Oct 13, 2009
Kind
B2
Abstract

The present invention relates to a compound comprising a PYY peptide or a functional derivative thereof, which is coupled to a reactive group. Such a reactive group is capable of reacting on a blood component so as to form a stable covalent bond therewith. The present invention also relates to a conjugate comprising such a compound which is covalently bonded to a blood component. Moreover, the invention also relates to a method of enhancing, in a patient, the anti-obesity activity of a PYY peptide or functional derivative thereof.

Claims (60)

1. A compound comprising a peptide moiety and a Michael acceptor (MA) moiety, the MA moiety being capable of reacting with an amino group, a hydroxyl group or a thiol group on a blood protein so as to form a stable covalent bond, therewith, wherein the compound is of the formula:

X 1 -X 2 Pro Glu Ala Pro Gly Glu Asp Ala Ser Pro Glu Glu Leu Asn Arg Tyr Tyr Ala Ser Leu Arg His Tyr Leu Asn Leu Val Thr Arg Gln Arg X 3 (SEQ ID NO:22)

wherein

X 1 is ile, ile(N-MA) or ile(N-linking group-MA);

X 2 is lys or lys(N ε -linking group-MA);

X 3 is tyr or a tyr derivative of formula

where

R 1 is H, a protecting group (PG), a C 1 -C 10 branched, linear or cyclic alkyl, a phosphate or a sulfate;

R 2 and R 3 are same or different and selected from the group consisting of H, D and I; and

R 4 is OH, OPG, OR 5 , SH, SPG (sulfur protecting group), SR 5 , NH 2 , NHPG, N(PG) 2 , N(R 5 ) 2 ,NR 5 PG, or NHR 6 , where R 5 is a C 1 -C 10 branched, linear or cyclic alkyl, and R 6 is a solid phase support; and wherein

X 1 is ile(N-MA) or ile(N-linking group-MA) when X 2 is lys; and X 2 is lys(N ε -linking group-MA) when X 1 is ile.

2. The compound of claim 1 , wherein X 1 is ile (N-MA) and X 2 is lys.

3. The compound of claim 1 , wherein X 1 is ile (N-linking group-MA) and X 2 is lys.

4. The compound of claim 1 , wherein X 1 is ile and X 2 is lys(N ε -linking group-MA).

5. The compound of any one of claims 1 - 4 , wherein said Michael acceptor is a maleimido-containing group.

6. The compound of claim 5 , wherein said maleimido-containing group is maleimidopropionic acid.

7. The compound of any one of claims 1 - 4 , wherein said blood protein is albumin.

8. The compound of any one of claims 1 , 3 and 4 , wherein said linking group is selected from the group consisting of (2-amino) ethoxy acetic acid (AEA), ethylenediamine (EDA), amino ethoxy ethoxy succinimic acid (AEES), 2-[2-(2-amino)ethoxy] ethoxy acetic acid (AEEA), AEEA-AEEA, —NH 2 —(CH 2 ) n -COOH where n is an integer from 1 to 20; one or more alkyl chains (C 1 -C 10 ) saturated or unsaturated which optionally comprises oxygen, nitrogen or sulfur atoms motifs, glycine, 3-aminopropionic acid (APA), 8-aminooctanoic acid (OA), 4-aminobenzoic acid (APhA), and combinations thereof.

9. A conjugate formed by the reaction of a compound with a blood protein under conditions sufficient to form a stable covalent bond therewith, wherein the compound comprises a peptide moiety and a Michael acceptor (MA) moiety, wherein the MA moiety is coupled to an amino group, a hydroxyl group or a thiol group on said blood protein, and wherein the compound is of the formula:

X 1 -X 2 Pro Glu Ala Pro Gly Glu Asp Ala Ser Pro Glu Glu Leu Asn Arg Tyr Tyr Ala Ser Leu Arg His Tyr Leu Asn Leu Val Thr Arg Gln Arg X 3 (SEQ ID NO:22)

wherein

X 1 is ile, ile(N-MA) or ile(N-linking group-MA);

X 2 is lys or lys(N ε -linking group-MA);

X 3 is tyr or a tyr derivative of formula

where

R 1 is H, a protecting group (PG), a C 1 -C 10 branched, linear or cyclic alkyl, a phosphate or a sulfate;

R 2 and R 3 are same or different and selected from the group consisting of H, D and I; and

R 4 is OH, OPG, OR 5 , SH, SPG (sulfur protecting group), SR 5 , NH 2 , NHPG, N(PG) 2 , N(R 5 ) 2 , NR 5 PG, or NHR 6 , where R 5 is a C 1 -C 10 branched, linear or cyclic alkyl, and R 6 is a solid phase support;

X 1 is ile(N-MA) or ile(N-linking group-MA) when X 2 is lys; and

X 2 is lys(N ε -linking group-MA) when X 1 is ile.

10. The conjugate of claim 9 , wherein X 1 is ile(N-MA) and X 2 is lys.

11. The conjugate of claim 9 , wherein X 1 is ile(N-linking group-MA) and X 2 is lys.

12. The conjugate of claim 9 , wherein X 1 is ile and X 2 is lys(N ε -linking group-MA).

13. The conjugate of any one of claims 9 - 12 , wherein said Michael acceptor is a maleimido-containing.

14. The conjugate of claim 13 , wherein said maleimido-containing group is maleimidopropionic acid (MPA).

15. The conjugate of any one of claims 9 - 12 , wherein said blood protein is albumin.

16. The conjugate of claim 9 , 11 , or 12 , wherein said linking group is selected from the group consisting of (2-amino) ethoxy acetic acid (AEA), ethylenediamine (EDA), amino ethoxy ethoxy succinimic acid (AEES), 2-[2-(2-amino)ethoxy] ethoxy acetic acid (AEEA), AEEA-AEEA, —NH 2 —(CH 2 ) n —COOH where n is an integer from 1 to 20; one or more alkyl chains (C 1 -C 10 ) saturated or unsaturated which optionally comprises oxygen, nitrogen or sulfur atoms motifs, glycine, 3-aminopropionic acid (APA), 8-aminooctanoic acid (OA), 4-aminobenzoic acid (APhA), and combinations thereof.

17. The compound of any one of claims 1 - 4 wherein X 3 is tyr-CONH 2 .

18. The conjugate of any one of claims 9 - 12 wherein X 3 is tyr-CONH 2 .

19. The conjugate of claim 13 , wherein said blood protein is albumin, X 3 is tyr-CONH 2 , and said linking group is selected from the group consisting of (2-amino)ethoxy acetic acid (AEA), ethylenediamine (EDA), amino ethoxy ethoxy succinimic acid (AEES), 2-[2-(2-amino)ethoxy] ethoxy acetic acid (AEEA), AEEA-AEEA, —NH 2 —(CH 2 ) n —COOH where n is an integer from 1 to 20; one or more alkyl chains (C 1 -C 10 ) saturated or unsaturated which optionally comprises oxygen, nitrogen or sulfur atoms motifs, glycine, 3-aminopropionic acid (APA), 8-aminooxtanoic acid (OA), 4-aminobenzoic acid (APhA), and combinations thereof.

20. The conjugate of claim 14 , wherein said blood protein is albumin, X 3 is tyr-CONH 2 , and said linking group is selected from the group consisting of (2-amino)ethoxy acetic acid (AEA), ethylenediamine (EDA), amino ethoxy ethoxy succinimic acid (AEES), 2-[2-(2-amino)ethoxy] ethoxy acetic acid (AEEA), AEEA-AEEA, —NH 2 —(CH 2 ) n —COOH where n is an integer from 1 to 20; one or more alkyl chains (C 1 -C 10 ) saturated or unsaturated which optionally comprises oxygen, nitrogen or sulfur atoms motifs, glycine, 3-aminopropionic acid (APA), 8-aminooxtanoic acid (OA), 4-aminobenzoic acid (APhA), and combinations thereof.

21. The conjugate of claim 10 , wherein said blood protein is albumin, X 3 is tyr-CONH 2 , and said Michael acceptor is maleimidopropionic acid (MPA).

22. The conjugate of claim 11 , wherein said blood protein is albumin, X 3 is tyr-CONH 2 , and said Michael acceptor is maleimidopropionic acid (MPA), and said linking group is 8-aminooctanoic acid (OA).

23. The conjugate of claim 12 , wherein said blood protein is albumin, X 3 is tyr-CONH 2 , said Michael acceptor is maleimidopropionic acid (MPA), and said linking group is 8-aminooxtanoic acid (OA).

24. The compound of claim 6 , wherein said blood protein is albumin.

25. The compound of claim 7 , wherein said blood protein is albumin.

26. The compound of claim 10 , wherein the Michael acceptor is capable of being covalently linked to a thiol group at amino acid residue 34 (Cys34) on albumin.

27. The compound of claim 17 , wherein said blood protein is albumin.

28. The compound of claim 6 , wherein X 3 is tyr-CONH 2 .

29. The compound of claim 7 , wherein X 3 is tyr-CONH 2 .

30. The compound of claim 28 , wherein the blood protein is albumin.

31. The compound of claim 29 , wherein the blood protein is albumin.

32. The compound of claim 27 , wherein the Michael acceptor is capable of being covalently linked to a thiol group at amino acid residue 34 (Cys34) on albumin.

33. The conjugate of claim 13 , the blood protein is albumin.

34. The conjugate of claim 14 , the blood protein is albumin.

35. The conjugate of claim 15 , wherein the Michael acceptor moiety is covalently linked to a thiol group at amino acid residue 34 (Cys34) on albumin.

36. The compound of claim 1 , wherein the blood protein is a recombinant protein.

37. The compound of claim 7 , wherein the albumin is a recombinant protein.

38. The conjugate of claim 9 , wherein the blood protein is a recombinant protein.

39. The conjugate of claim 15 , wherein the albumin is a recombinant protein.

Assignments (6)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Apr 20, 2011
From: ADVANCED DIAGNOSTICS AND DISCOVERY
To: CONJUCHEM, LLC
Reel/Frame 026157/0022 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Oct 26, 2010
From: CONJUCHEM BIOTECHNOLOGIES INC.
To: ADVANCED DIAGNOSTICS AND DISCOVERY
Reel/Frame 025198/0735 →
CHANGE OF NAME Recorded Dec 11, 2009
From: 4523482 CANADA INC.
To: CONJUCHEM BIOTECHNOLOGIES, INC.
Reel/Frame 023639/0162 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Dec 2, 2009
From: CONJUCHEM BIOTECHNOLOGIES INC.
To: 4523482 CANADA INC.
Reel/Frame 023594/0067 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Aug 1, 2006
From: CONJUCHEM INC.
To: CONJUCHEM BIOTECHNOLOGIES INC.
Reel/Frame 018039/0669 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Apr 8, 2005
From: BRIDON, DOMINIQUE P.; LEGER, ROGER; HUANG, XICAI; THIBAUDEAU, KAREN; ROBITAILLE, MARTIN; MILNER, PETER G.
To: CONJUCHEM, INC.
Reel/Frame 016056/0225 →