US 9,753,034 B2 · Process for the identification of a compound which inhibits the binding of the first bromodomain of each of human BRD-2, BRD-3, and BRD-4

Abstract

A process for the identification of compounds with a molecular weight in the range 100 to 750 which inhibit the binding of the first and/or second bromodomains of human BRD-2 to 4 to acetylated lysine residues of their physiological partner proteins which comprises selecting those compounds which are able to: a) form a hydrogen bonding interaction in which the compound accepts a hydrogen bond from the sidechain NH2 group of the asparagine residue found at: BRD-2 BRD-2 BRD-3 BRD-3 BRD-4 BRD-4 BD1 BD2 BD1 BD2 BD1 BD2 ASN156 ASN429 ASN116 ASN391 ASN140 ASN433 or b) accept a water-mediated hydrogen bond in which the compound accepts a hydrogen bond from a water that is itself hydrogen-bonded to the sidechain hydroxyl of the tyrosine residue found at BRD-2 BRD-2 BRD-3 BRD-3 BRD-4 BRD-4 BD1 BD2 BD1 BD2 BD1 BD2 TYR113 TYR386 TYR73 TYR348 TYR97 TYR390 and c) which are also able to form a Van der Waals interaction with a lipophilic binding region of a binding pocket such that one or more heavy atoms of the said compounds lie within a 5 Å range of any of the heavy atoms of the following bromodomain residues which define the binding pocket: BRD-2 BRD-2 BRD-3 BRD-3 BRD-4 BRD-4 BD1 BD2 BD1 BD2 BD1 BD2 TRP97 TRP370 TRP57 TRP332 TRP81 TRP374 PRO98 PRO371 PRO58 PRO333 PRO82 PRO375 ASP161 ASP434 ASP121 GLU396 ASP145 GLU438 ILE162 VAL435 ILE122 VAL397 ILE146 VAL439 MET165 MET438 MET125 MET400 MET149 MET442 pharmaceutical compositions containing such compounds, and their use in therapy.

Claims8

Dependent claims

A process for the identification of a compound which inhibits the binding of the first bromodomain of each of human BRD-2, BRD-3, and BRD-4 to acetylated lysine residues of their physiological partner proteins which process comprises the steps of:

1) selecting compounds with a molecular weight in the range 100 to 750 Da;
and
2) determining which of those selected compounds is an interacting compound, wherein an interacting compound will:
a) form a hydrogen bonding interaction in which the compound accepts a hydrogen bond from the side chain NH2 group of the asparagine residue found at:
ASN156 of BRD-2 BD1, or ASN116 of BRD-3 BD1, or ASN140 of BRD-4 BD1 and
b) form a Van der Waals interaction with a lipophilic binding region of a binding pocket such that one or more heavy atoms of the said compounds lie within a 7.5 Å range of at least one heavy atom of each of the 3 residues of the first bromodomain wherein said bromodomain residues are selected from the group consisting of:
PRO98, ASP161, and ILE162 of BRD-2 BD1;
PRO58, ASP121, and ILE122 of BRD-3 BD1;
and
PRO82, ASP145, and ILE146 of BRD-4 BD1 and
3) testing the ability of the interacting compound to inhibit the binding of the first bromodomain to a fluorescent ligand in a fluorescent anisotropy binding assay;
wherein the fluorescent ligand is a compound having the structure
conjugated with a fluorescent label at the terminal amino group (—NH2) of the compound;
and wherein the interacting compound which is able to inhibit the binding of the first bromodomain to the fluorescent ligand in the fluorescent anisotropy binding assay is identified as the compound which inhibits the binding of the first bromodomain of each of human BRD-2, BRD-3 and BRD-4 to the acetylated lysine residues of their physiological partner proteins.

11 more elements

1) selecting compounds with a molecular weight in the range 100 to 750 Da;
2) determining which of those selected compounds is an interacting compound, wherein an interacting compound will:
a) form a hydrogen bonding interaction in which the compound accepts a hydrogen bond from the sidechain NH2 group of the asparagine residue found at:
ASN156 of BRD-2 BD1, or ASN116 of BRD-3 BD1, or ASN140 of BRD-4 BD1 and
b) accept a water-mediated hydrogen bond in which the compound accepts a hydrogen bond from a water that is itself hydrogen-bonded to the sidechain hydroxyl of the tyrosine residue found at the TYR113 of BRD-2 BD1, or TYR73 of BRD-3 BD1, or TYR97 of BRD-4 BD1 and
c) form a Van der Waals interaction with a lipophilic binding region of a binding pocket such that one or more heavy atoms of the said compounds lie within a 7.5 Å range of at least one heavy atom of each of the 3 residues of the first bromodomain wherein said first bromodomain residues are selected from the group consisting of:
PRO98, ASP161, and ILE162 of BRD-2 BD1;
PRO58, ASP121, and ILE122 of BRD-3 BD1;
and
PRO82, ASP145, and ILE146 of BRD-4 BD1;
and
3) testing the ability of the interacting compound to inhibit the binding of the first bromodomain to a fluorescent ligand in a fluorescent anisotropy binding assay;
wherein the fluorescent ligand is a compound having the structure
conjugated with a fluorescent label at the terminal amino group (—NH2) of the compound;
and wherein the interacting compound which is able to inhibit the binding of the first bromodomain to the fluorescent ligand in the fluorescent anisotropy binding assay is identified as the compound which inhibits the binding of the first bromodomain of each of human BRD-2, BRD-3 and BRD-4 to the acetylated lysine residues of their physiological partner proteins.

12 more elements

1) selecting compounds with a molecular weight in the range 100 to 750 Da;
and
2) determining which of those selected compounds is an interacting compound, wherein an interacting compound will:
a) form a hydrogen bonding interaction in which the compound accepts a hydrogen bond from the sidechain NH2 group of the asparagine residue found at:
ASN156 of BRD-2 BD1, or ASN116 of BRD-3 BD1, or ASN140 of BRD-4 BD1 and
b) form a Van der Waals interaction with a lipophilic binding region of a binding pocket such that one or more heavy atoms of the said compounds lie within a 7.5 Å range of at least one heavy atom of each of the 3 residues of the first bromodomain wherein said bromodomain residues are selected from the group consisting of:
PRO98, ASP161, and ILE162 of BRD-2 BD1;
PRO58, ASP121, and ILE122 of BRD-3 BD1;
and
PRO82, ASP145, and ILE146 of BRD-4 BD1;
and
3) testing the ability of the interacting compound to inhibit the binding of the first bromodomain to a fluorescent ligand in a fluorescent anisotropy binding assay, wherein the fluorescent ligand is a compound having the structure
conjugated with a fluorescent label at the terminal amino group (—NH2) of the compound wherein the first bromodomain is comprised in a human bromodomain protein that comprises a histidine tag;
and wherein the interacting compound which is able to inhibit the binding of the first bromodomain to the fluorescent ligand in the fluorescent anisotropy binding assay is identified as the compound which inhibits the binding of the first bromodomain of each of human BRD-2, BRD-3 and BRD-4 to the acetylated lysine residues of their physiological partner proteins.

11 more elements

1) selecting compounds with a molecular weight in the range 100 to 750 Da;
2) determining which of those selected compounds is an interacting compound, wherein an interacting compound will:
a) form a hydrogen bonding interaction in which the compound accepts a hydrogen bond from the sidechain NH2 group of the asparagine residue found at:
ASN156 of BRD-2 BD1, or ASN116 of BRD-3 BD1, or ASN140 of BRD-4 BD1 and
b) accept a water-mediated hydrogen bond in which the compound accepts a hydrogen bond from a water that is itself hydrogen-bonded to the sidechain hydroxyl of the tyrosine residue found at the TYR113 of BRD-2 BD1, or TYR73 of BRD-3 BD1, or TYR97 of BRD-4 BD1 and
c) form a Van der Waals interaction with a lipophilic binding region of a binding pocket such that one or more heavy atoms of the said compounds lie within a 7.5 Å range of at least one heavy atom of each of the 3 residues of the first bromodomain wherein said bromodomain residues are selected from the group consisting of:
PRO98, ASP161, and ILE162 of BRD-2 BD1;
PRO58, ASP121, and ILE122 of BRD-3 BD1;
and
PRO82, ASP145, and ILE146 of BRD-4 BD1;
and
3) testing the ability of the interacting compound to inhibit the binding of the first bromodomain to a fluorescent ligand in a fluorescent anisotropy binding assay, wherein the fluorescent ligand is a compound having the structure
conjugated with a fluorescent label at the terminal amino group (—NH2) of the compound, wherein the first bromodomain is comprised in a human bromodomain protein that comprises a histidine tag;
and wherein the interacting compound which is able to inhibit the binding of the first bromodomain to the fluorescent ligand in the fluorescent anisotropy binding assay is identified as the compound which inhibits the binding of the first bromodomain of each of human BRD-2, BRD-3 and BRD-4 to the acetylated lysine residues of their physiological partner proteins.

11 more elements

Dependencies are inferred from the claim text.

Process for the identification of a compound which inhibits the binding of the first bromodomain of each of human BRD-2, BRD-3, and BRD-4

Life of this patent

Process for the identification of a compound which inhibits the binding of the first bromodomain of each of human BRD-2, BRD-3, and BRD-4

Life of this patent

Abstract

Claims8