Systems and Methods for Developing Covalent Inhibitor Libraries for Screening Using Virtual Docking and Experimental Approaches

Patent metadata

Field	Value
Publication number	US-2019362816-A1
Application number	US-201716470021-A
Country	US
Kind code	A1
Filing date	Dec 15, 2017
Priority date	Dec 16, 2016
Publication date	Nov 28, 2019
Grant date	—

Abstract

Disclosed are methods and systems for screening covalent ligand libraries to identify potential covalent inhibitors. The methods and systems may also be used to generate a covalent inhibitor library from natural ligands. These covalent inhibitors bind to the receptor irreversibly after initial reversible binding. The covalent inhibitor identified or designed using the present methods may specifically bind to and covalently modify a receptor.

First claim

What is claimed is:

1 . A method for screening libraries of covalent inhibitors, comprising:
(a) providing a potential receptor containing at least one nucleophilic group; (b) providing a potential covalent inhibitor containing at least one electrophilic group capable of forming a covalent bond with the receptor; (c) docking the potential covalent inhibitor into the receptor; (d) ranking the docked potential covalent inhibitor based on one or more screening criteria and their combinations thereof; and (e) selecting the highly ranked potential covalent inhibitors.

2 . The method of claim 1 , wherein the one or more screening criteria are selected from the group consisting of Van der Waals radius, angle of attack, solvation effects, cone angle, bond length, bond strength, and electronic character.

3 . The method of claim 1 , wherein providing the potential receptor further comprising providing three-dimensional structure information of the potential receptor.

4 . The method of claim 1 , wherein docking the potential covalent inhibitor into the receptor further comprising docking the potential covalent inhibitor into a ligand binding region or a ligand binding pocket of the receptor.

5 . The method of claim 1 , wherein docking the potential covalent inhibitor into the receptor is performed using a docking algorithm.

6 . The method of claim 5 , wherein the docking algorithm is GLIDE or CovDock.

7 . The method of claim 1 , further comprising experimentally testing the selected covalent inhibitors.

8 . The method of claim 7 , wherein experimentally testing the selected covalent inhibitors further comprising:
measuring binding kinetics of the potential covalent inhibitor, wherein a two-step mechanism specifies a binding kinetics according to the following equation:

where R is the receptor, I is the potential covalent inhibitor, k 1 is an association constant; k −1 is a dissociation constant, and k 2 is an association constant of the receptor that is covalently modified by the potential covalent inhibitor,
wherein the potential covalent inhibitor initially binds reversibly to the receptor, then an electrophilic center of the potential covalent inhibitor binds irreversibly to a nucleophile center of an amino acid within the receptor.

9 . The method of claim 1 , wherein the potential covalent inhibitor is:
a carboxylic acid (R 1 —COOH) coupled to an electrophilic fragment terminated with an aminomethyl group; or an aminomethyl group (R 1 —CH 2 —NH 2 ) coupled to an electrophilic fragment terminated with a carboxylic acid; wherein R 1 is a drug-like fragment, or a fragment comprising 10-17 non-hydrogen atoms.

10 . The method of claim 9 , wherein R 1 does not influence a reactivity of an electrophile center of the potential covalent inhibitor with a nucleophile of the receptor.

11 . A method of generating a covalent inhibitor library, comprising:
(a) identifying a natural ligand capable of covalently binding to a receptor, wherein the natural ligand comprising a directing group and a reactive group containing an electrophilic fragment; (b) modifying the reactive group by replacing the directing group with a carboxylic acid or an amine; and (c) coupling the carboxylic acid-modified reactive group to a second directing group comprising an aminomethyl group (R 1 —CH 2 —NH 2 ); or (d) coupling the amine-modified reactive group to a third directing group comprising a carboxylic acid.

12 . The method of claim 11 , wherein the electrophilic fragment is a Michael acceptor or an alkylating agent.

13 . The method of claim 11 , wherein the electrophilic fragment is an sp 2 Michael acceptor or an sp Michael acceptor.

14 . The method of claim 11 , wherein the sp 2 electrophilic fragment is selected from the group consisting of:

15 . The method of claim 11 , wherein the sp electrophilic fragment is selected from the group consisting of:

16 . The method of claim 11 , wherein the electrophilic fragment further comprises an electron withdrawing group.

17 . The method of claim 16 , wherein the electron withdrawing group is selected from the group consisting of nitros, amides, esters, acid, nitriles, ketones, sulfones, sulfoxides, sulfonamides, nitriles, halides, lactams, lactones, oxygen heterocycles, nitrogen heterocycles, substituted or unsubstituted aromatic fragments, and epoxides.

18 . The method of claim 17 , wherein the potential covalent inhibitor is an agonist, an inverse agonist, an antagonist or a neutral antagonist.

19 . The method of claim 17 , wherein an electrophile center of the potential covalent inhibitor reacts with a nucleophile center of an amino acid in the receptor.

20 . The method of claim 19 , wherein the nucleophile center of the amino acid in the receptor is sulfur or nitrogen.

21 . The method of claim 19 , wherein the amino acid is cysteine, methionine, proline, tryptophan, asparagine, glutamine, tryptophan, or histidine.

22 . The method of claim 11 , wherein the aminomethyl-coupled electrophilic fragment is selected from the group consisting of:

wherein R 1 is a drug-like fragment, or a fragment comprising 10-17 non-hydrogen atoms.

23 . A covalent inhibitor generated from the method of claim 22 .

Assignees

• Univ Northwestern

Inventors

• Statsyuk Alexander V

Classifications

• G16C20/60

  In silico combinatorial chemistry · CPC title

• G16B15/00 Primary

  ICT specially adapted for analysing two-dimensional [2D] or three-dimensional [3D] molecular structures, e.g. structural or functional relations or structure alignment · CPC title

• G16B35/00

  ICT specially adapted for in silico combinatorial libraries of nucleic acids, proteins or peptides · CPC title

• G16C20/64 Primary

  Screening of libraries · CPC title

• G16C60/00

  Computational materials science, i.e. ICT specially adapted for investigating the physical or chemical properties of materials or phenomena associated with their design, synthesis, processing, characterisation or utilisation · CPC title