IP Library Granted Patent US 7,803,774
Granted Patent B2
US 7,803,774 · App. 10/989,763 · Granted Sep 28, 2010

Modulators of β-amyloid peptide aggregation

Assignee: Praecis Pharmaceuticals, Inc.
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Quick Facts
Patent No.
US 7,803,774
App. No.
10/989,763
Granted
Sep 28, 2010
Kind
B2
Abstract

Compounds that modulate natural β amyloid peptide aggregation are provided. The modulators of the invention comprise a peptide, preferably based on a β amyloid peptide, that is comprised entirely of D-amino acids. Preferably, the peptide comprises 3-5 D-amino acid residues and includes at least two D-amino acid residues independently selected from the group consisting of D-leucine, D-phenylalanine and D-valine. In a particularly preferred embodiment, the peptide is a retro-inverso isomer of a β amyloid peptide, preferably a retro-inverso isomer of Aβ 17-21 . In certain embodiments, the peptide is modified at the amino-terminus, the carboxy-terminus, or both. Preferred amino-terminal modifying groups alkyl groups. Preferred carboxy-terminal modifying groups include an amide group, an acetate group, an alkyl amide group, an aryl amide group or a hydroxy group. Pharmaceutical compositions comprising the compounds of the invention, and diagnostic and treatment methods for amyloidogenic diseases using the compounds of the invention, are also disclosed.

Claims (34)

1. A compound comprising the structure:

wherein Xaa 1 and Xaa 2 are each D-amino acid structures and are independently selected from the group consisting of a D-leucine structure, a D-phenylalanine structure, a D-tyrosine structure, a D-iodotyrosine structure, a D-lysine structure, and a D-valine structure;

NH—NH is a hydrazine structure;

Y, which may or may not be present, is a structure having the formula (Xaa) a , wherein Xaa is any D-amino acid structure and a is an integer from 1 to 15;

Xaa 1 ′, Xaa 2 ′, and Xaa 3 ′which may or may not be present, are each D-amino acid or L-amino acid structures and at least two of Xaa 1 ′, Xaa 2 ′, and Xaa 3 ′are, independently, selected from the group consisting of a D- or L-leucine structure, a D- or L-phenylalanine structure, a D- or L-tyrosine structure, a D- or L-iodotyrosine structure, a D- or L-lysine structure, and a D- or L-valine structure;

Z is a structure having the formula (Xaa) b , wherein Xaa is any D-amino acid structure and b is an integer from 1 to 15;

A, which may or may not be present, is a modifying group covalently attached to the compound; and

n is an integer from 1 to 15;

wherein the compound binds to natural β-amyloid peptides or inhibits the aggregation or the neurotoxicity of natural β-amyloid peptides when contacted with the natural β-amyloid peptides.

2. A pharmaceutical composition comprising a therapeutically effective amount of the compound of claim 1 and a pharmaceutically acceptable carrier.

3. An in vitro method for inhibiting aggregation of natural β-amyloid peptides, comprising contacting the natural β-amyloid peptides with the compound of claim 1 such that aggregation of the natural β-amyloid peptides is inhibited.

4. An in vitro method for detecting the presence or absence of natural β-amyloid peptides in a biological sample, comprising:

contacting a biological sample with the compound of claim 1 , wherein the compound is labeled with a detectable substance; and

detecting the compound bound to natural β-amyloid peptides to thereby detect the presence or absence of natural β-amyloid peptides in the biological sample.

5. The method of claim 4 , wherein the compound is labeled with radioactive technetium or radioactive iodine.

6. A compound having a structure selected from the group consisting of: H-D-Leu-D-Val-D-Phe-NH—(H-D-Leu-D-Val-D-Phe-)NH; H-D-Leu-D-Val-D-Phe-NH—NH—COCH 3 ; H-D-Leu-D-Val-D-Phe-NH—NH 2 ; H-Leu-Val-Phe-NH—NH-Phe-Val-Leu-H; and H-Leu-Val-Phe-NH—NH-D-Phe-D-Val-D-Leu-H, wherein H is hydrogen.

7. A pharmaceutical composition comprising a pharmaceutically acceptable cater and a therapeutically effective amount of a compound comprising the structure:

wherein Xaa 1 and Xaa 2 are each D-amino acid structures and are independently selected from the group consisting of a D-leucine structure, a D-phenylalanine structure, a D-tyrosine structure, a D-iodotyrosine structure, a D-lysine structure, and a D-valine structure;

NH—NH is a hydrazine structure;

Y, which may or may not be present, is a structure having the formula (Xaa) a , wherein Xaa is any D-amino acid structure and a is an integer from 1 to 15;

Xaa 1 ′, Xaa 2 ′, and Xaa 3 ′ which may or may not be present, are each D-amino acid or L-amino acid structures and at least two of Xaa 1 ′, Xaa 2 ′, and Xaa 3 ′ are, independently, selected from the group consisting of a D- or L-leucine structure, a D- or L-phenylalanine structure, a D- or L-tyrosine structure, a D- or L-iodotyrosine structure, a D- or L-lysine structure, and a D- or L-valine structure;

Z, which may or may not be present, is a structure having the formula (Xaa) b , wherein Xaa is any D-amino acid structure and b is an integer from 1 to 15;

A, which may or may not be present, is a modifying group covalently attached to the compound; and

n is an integer from 1 to 15;

wherein the compound binds to natural β-amyloid peptides or inhibits the aggregation or the neurotoxicity of natural β-amyloid peptides when contacted with the natural β-amyloid peptides.

8. A compound comprising the structure:

wherein Xaa 1 and Xaa 2 are each D-amino acid structures and are independently selected from the group consisting of a D-leucine structure, a D-phenylalanine structure, a D-tyrosine structure, a D-iodotyrosine structure, a D-lysine structure, and a D-valine structure;

NH—NH is a hydrazine structure;

Y, which may or may not be present, is a structure having the formula (Xaa) a , wherein Xaa is any D-amino acid structure and a is an integer from 1 to 15;

Xaa 1 ′, Xaa 2 ′, and Xaa 3 ′ are each D-amino acid or L-amino acid structures and at least two of Xaa 1 ′, Xaa 2 ′, and Xaa 3 ′ are, independently, selected from the group consisting of a D- or L-leucine structure, a D- or L-phenylalanine structure, a D- or L-tyrosine structure, a D- or L-iodotyrosine structure, a D- or L-lysine structure, and a D- or L-valine structure;

Z, which may or may not be present, is a structure having the formula (Xaa) b , wherein Xaa is any D-amino acid structure and b is an integer from 1 to 15;

A, which may or may not be present, is a modifying group covalently attached to the compound; and

n is an integer from 1 to 15;

wherein the compound binds to natural β-amyloid peptides or inhibits the aggregation or the neurotoxicity of natural β-amyloid peptides when contacted with the natural β-amyloid peptides.

Assignments (3)
MERGER Recorded Apr 12, 2011
From: PRAECIS PHARMACEUTICALS INCORPORATED
To: GLAXOSMITHKLINE LLC
Reel/Frame 026116/0684 →
CHANGE OF NAME Recorded May 19, 2010
From: PHARMACEUTICAL PEPTIDES, INC.
To: PRAECIS PHARMACEUTICALS, INC.
Reel/Frame 024408/0904 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Apr 24, 2009
From: FINDEIS, MARK A.; PHILLIPS, KATHRYN; OLSON, GARY L.; SELF, CHRISTOPHER
To: PRAECIS PHARMACEUTICALS INCORPORATED
Reel/Frame 022594/0033 →
Continuity (4)
Continuation 1039529000 · Mar 24, 2003
Continuation 0951901900 · Mar 3, 2003
Provisional Application 6012273600 · Mar 4, 1999
Related Publication 20050137128A1 · Jun 23, 2005