IP Library Granted Patent US 7,994,121
Granted Patent B2
US 7,994,121 · App. 11/842,518 · Granted Aug 9, 2011

Stable analogs of peptide and polypeptide therapeutics

Assignee: Trustees of Tufts College
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 7,994,121
App. No.
11/842,518
Granted
Aug 9, 2011
Kind
B2
Abstract

The present invention relates to compositions of peptide and polypeptide analogs that are resistant to proteolysis, pharmaceutical uses thereof, and methods of preparation thereof.

Claims (62)

1. A DPP IV-resistant analog of a biologically active peptide or polypeptide factor, wherein

the peptide or polypeptide factor is capable of binding a GLP-1-receptor;

the analog of the peptide or polypeptide factor is capable of binding a GLP-1 receptor;

the analog of the peptide or polypeptide factor is represented by Xaa-Ala-Yaa-R or Xaa-Pro-Yaa-R;

Xaa is an N-terminal amino acid residue;

R is

GTFTSDVSSYLEGQAAKEFIAWLVKGR (SEQ ID NO: 19),

GTFTSDVSSYLEGQAAKEFIAWLVKGRPSSGAPPPS-NH2

(SEQ ID NO: 20),

GTFTSDVSSYLEGQAAKEFIAWLVKGR-NH2 (SEQ ID NO: 21),

GSFSDEMNTILDNLAARDFINWLIQTKITD (SEQ ID NO: 22),

GTFISDYSIAMDKIHQQDFVNWLLAQKGKKNDWKHNITQ

(SEQ ID NO: 23),

KPDNPGEDAPAEDMARYYSALRHYINLITRQRY

(SEQ ID NO: 24),

EPVYPGDNATPEQMAQYAADLRRY (SEQ ID NO: 25) or

KPEAPGEDASPEELNRYYASLRHYLNLVTRQRY

(SEQ ID NO: 26);

Yaa is an amino acid residue represented by Formula I:

R 1 and R 2 are, independently for each occurrence, lower alkyl, heteroalkyl, cycloalkyl, heterocycloalkyl, aryl, heteroaryl, alkoxyl, carboxyl, carboxamide, carbonyl, halogen, hydroxyl, amine, or cyano; or R 1 and R 2 taken together form a ring of 4-7 atoms;

R 3 is lower alkyl, heteroalkyl, cycloalkyl, heterocycloalkyl, aryl, heteroaryl, amino, alkoxyl, halogen, carboxyl, carboxamide, carbonyl, cyano, thioalkyl, acylamino, amido, cyano, nitro, azido, sulfate, sulfonate,

sulfonamido, —(CH 2 ) m R 4 , —(CH 2 ) m OH, —(CH 2 ) m COOH, —(CH 2 ) m O-lower alkyl, —(CH 2 ) m O-lower alkenyl, —(CH 2 ) n O(CH 2 ) m R 4 , —(CH 2 ) m SH, —(CH 2 ) m S-lower alkyl, —(CH 2 ) m S-lower alkenyl, —(CH 2 ) n S(CH 2 ) m R 4 , —(CH 2 ) m NH 2 , —(CH 2 ) m NC(═NH)NH 2 , —(CH 2 ) m C(═O)NH 2 , or —(CH 2 ) m NH 2 ;

R 4 is, independently for each occurrence, aryl, aralkyl, cycloalkyl, cycloalkenyl, or heterocyclyl;

m is 0, 1, or 2; and

n is 0, 1, or 2.

2. The DPP IV-resistant analog of claim 1 , wherein the analog of the peptide or polypeptide factor is represented by Xaa-Ala-Yaa-R.

3. The DPP IV-resistant analog of claim 1 , wherein the analog of the peptide or polypeptide factor is represented by Xaa-Pro-Yaa-R.

4. The DPP IV-resistant analog of claim 1 , wherein n is 0.

5. The DPP IV-resistant analog of claim 1 , wherein R is

(SEQ ID NO: 19)

GTFTSDVSSYLEGQAAKEFIAWLVKGR,

(SEQ ID NO: 20)

GTFTSDVSSYLEGQAAKEFIAWLVKGRPSSGAPPPS-NH2,

(SEQ ID NO: 21)

GTFTSDVSSYLEGQAAKEFIAWLVKGR-NH2,

(SEQ ID NO: 22)

GSFSDEMNTILDNLAARDFINWLIQTKITD,

or

(SEQ ID NO: 23)

GTFISDYSIAMDKIHQQDFVNWLLAQKGKKNDWKHNITQ.

6. The DPP IV-resistant analog of claim 1 , wherein R is

(SEQ ID NO: 24)

KPDNPGEDAPAEDMARYYSALRHYINLITRQRY,

(SEQ ID NO: 25)

EPVYPGDNATPEQMAQYAADLRRY,

or

(SEQ ID NO: 26)

KPEAPGEDASPEELNRYYASLRHYLNLVTRQRY.

7. The DPP IV-resistant analog of claim 1 , wherein R 1 and R 2 are independently selected from the group consisting of methyl, ethyl, and propyl.

8. The DPP IV-resistant analog of claim 1 , wherein R 1 and R 2 are both methyl.

9. The DPP IV-resistant analog of claim 1 , wherein R 3 is selected from the group consisting of lower alkyl, phenyl, hydroxyphenyl, indole, imidazole,

hydroxyl, —COOH, —CH 2 COOH, —CH 2 CH 2 NC(═NH)NH 2 , —CH 2 C(═O)NH 2 , —CH 2 CH 2 C(═O)NH 2 , —SH, and —CH 2 SCH 3 .

10. The DPP IV-resistant analog of claim 1 , wherein R 1 and R 2 are independently selected from the group consisting of methyl, ethyl, and propyl; and R 3 is selected from the group consisting of lower alkyl, phenyl, hydroxyphenyl, indole, imidazole,

hydroxyl, —COOH, —CH 2 COOH, —CH 2 CH 2 NC(═NH)NH 2 , —CH 2 C(═O)NH 2 , —CH 2 CH 2 C(═O)NH 2 , —SH, and —CH 2 SCH 3 .

11. The DPP IV-resistant analog of claim 1 , wherein R 1 and R 2 are both methyl; and R 3 is selected from the group consisting of lower alkyl, phenyl, hydroxyphenyl, indole, imidazole,

hydroxyl, —COOH, —CH 2 COOH, —CH 2 CH 2 NC(═NH)NH 2 , —CH 2 C(═O)NH 2 , —CH 2 CH 2 C(═O)NH 2 , —SH, and —CH 2 SCH 3 .

12. The DPP IV-resistant analog of claim 1 , wherein R 1 and R 2 are both methyl; and R 3 is —COOH or —CH 2 COOH.

13. The DPP IV-resistant analog of claim 2 , wherein R 1 and R 2 are both methyl; and R 3 is —COOH or —CH 2 COOH.

14. The DPP IV-resistant analog of claim 3 , wherein R 1 and R 2 are both methyl; and R 3 is —COOH or —CH 2 COOH.

15. The DPP IV-resistant analog of claim 4 , wherein R 1 and R 2 are both methyl; and R 3 is —COOH or —CH 2 COOH.

16. The DPP IV-resistant analog of claim 5 , wherein R 1 and R 2 are both methyl; and R 3 is —COOH or —CH 2 COOH.

17. The DPP IV-resistant analog of claim 6 , wherein R 1 and R 2 are both methyl; and R 3 is —COOH or —CH 2 COOH.

Assignments (2)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded May 4, 2018
From: TRUSTEES OF TUFTS COLLEGE
To: BACH BIOSCIENCES, LLC
Reel/Frame 046098/0709 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jul 18, 2011
From: BACHOVCHIN, WILLIAM W.; LAI, HUNG-SEN; SANFORD, DAVID GEORGE
To: TRUSTEES OF TUFTS COLLEGE
Reel/Frame 026606/0461 →
Continuity (3)
Continuation 10847220 · May 17, 2004
Provisional Application 60471411 · May 15, 2003
Related Publication 20080051557A1 · Feb 28, 2008