EBNA1 inhibitors and their method of use

Patent metadata

Field	Value
Publication number	US-9856214-B2
Application number	US-201415036211-A
Country	US
Kind code	B2
Filing date	Nov 14, 2014
Priority date	Nov 15, 2013
Publication date	Jan 2, 2018
Grant date	Jan 2, 2018

Abstract

The invention provides EBNA1 inhibitors, and pharmaceutical compositions comprising the same, that are useful for the treatment of diseases caused by EBNA1 activity such as, but not limited to, cancer, infectious mononucleosis, chronic fatigue syndrome, multiple sclerosis, systemic lupus erythematosus and/or rheumatoid arthritis. The compounds and compositions of the invention are further useful for the treatment of diseases caused by latent Epstein-Barr Virus (EBV) infection. The compounds and compositions of the invention are further useful for the treatment of diseases caused by lytic EBV infection.

First claim

What is claimed is:

1. A compound of formula (IX):

or a hydrate, solvate, polymorph, pharmaceutically acceptable salt, or prodrug thereof, wherein:
R 1 is selected from the group consisting of optionally substituted C 1-6 linear alkyl, optionally substituted C 3-6 branched alkyl, optionally substituted C 3-6 cyclic alkyl, optionally substituted phenyl, optionally substituted heteroaryl, optionally substituted benzyl, optionally substituted heteroaryl methyl,

R 2 is

R 3 is CO 2 R 4d ;
R 4d is selected from the group consisting of hydrogen, optionally substituted C 1-6 linear alkyl, and optionally substituted C 3-6 branched alkyl;
R 8a , R 8b , R 8c , R 8d , and R 8e are each independently selected from the group consisting of hydrogen, optionally substituted C 1-6 linear alkyl, and optionally substituted C 3-6 branched alkyl;
R 9a , R 9b , R 9c , R 9d , and R 9e are each independently selected from the group consisting of hydrogen, optionally substituted C 1-6 linear alkyl, and optionally substituted C 3-6 branched alkyl;
L 2 is (CH 2 ) m ;
and
m is 0, 1, 2, or 3.

2. A compound selected from the group consisting of:
2-(1H-indol-6-yl)-3-(2-phenylethynyl)benzoic acid;
2-(1-methyl-1H-indol-6-yl)-3-(2-phenylethynyl)benzoic acid;
2-[3-(methoxycarbonyl)-1H-indol-6-yl]-3-(2-phenylethynyl)benzoic acid;
2-(1-methyl-1H-indol-5-yl)-3-[2-(1,3-thiazol-4-yl)ethynyl]benzoic acid;
3-(4-amino-phenylethynyl)-2-(1H-indol-6-yl)-benzoic acid;
3-(4-carboxy-phenylethynyl)-2-(1H-indol-6-yl)-benzoic acid;
2-(1H-indol-6-yl)-3-(4-methoxy-phenylethynyl)-benzoic acid;
3-(4-carbamoyl-phenylethynyl)-2-(1H-indol-6-yl)-benzoic acid;
2-(1H-indol-6-yl)-3-[4-(piperazine-1-carbonyl)-phenylethynyl]-benzoic acid;
3-(4-acetylamino-phenylethynyl)-2-(1H-indol-6-yl)-benzoic acid;
2-(1H-indol-6-yl)-3-{4-[(pyridine-3-carbonyl)-amino]-phenylethynyl}-benzoic acid;
2-(1H-indol-6-yl)-3-(4-methanesulfonylamino-phenylethynyl)-benzoic acid;
2-(1H-indol-6-yl)-3-[4-(thiophene-2-sulfonylamino)-phenylethynyl]-benzoic acid;
2-(3-(Methoxycarbonyl)-1H-indol-6-yl)-3-(thiazol-4-ylethynyl)benzoic acid;
2-(1H-indol-6-yl)-3-(thiazol-4-ylethynyl)benzoic acid;
2-(3-chloro-1H-indol-6-yl)-3-((3-hydroxyphenyl)ethynyl)benzoic acid;
2-(3-(2-acetamidoethyl)-1H-indol-6-yl)-3-((3-hydroxyphenyl)ethynyl)benzoic acid;
2-(1H-indol-6-yl)-3-((4-(tetrahydro-2H-pyran-4-yloxy)phenyl)ethynyl)benzoic acid;
2-(1H-indol-6-yl)-3-((4-morpholinophenyl)ethynyl)benzoic acid;
3((3-carbamoylphenyl)ethynyl)-2-(1H-indol-6-yl)benzoic acid;
3((4-Fluorophenyl)ethynyl)-2-(1H-indol-6-yl)benzoic acid;
3((2,4-Difluorophenyl)ethynyl)-2-(1H-indol-6-yl)benzoic acid;
3((3-Acetamidophenyl)ethynyl)-2-(1H-indol-6-yl)benzoic acid;
2-(1H-indol-6-yl)-3-((3-(nicotinamido)phenyl)ethynyl)benzoic acid;
3-((3-(3-chloro-4-fluorophenylsulfonamido)phenyl)ethynyl)-2-(1H-indol-6-yl)benzoic acid;
3((3-aminophenyl)ethynyl)-2-(1H-indol-6-yl)benzoic acid;
2-(1H-indol-6-yl)-3-((3-(methylsulfonamido)phenyl)ethynyl)benzoic acid;
2-(1H-indol-6-yl)-3-((3-(thiophene-2-sulfonamido)phenyl)ethynyl)benzoic acid;
3-((3-acetamido-5-fluorophenyl)ethynyl)-2-(1H-indol-6-yl)benzoic acid;
3((6-aminopyridin-2-yl)ethynyl)-2-(1H-indol-6-yl)benzoic acid;
3((2-aminopyridin-4-yl)ethynyl)-2-(1H-indol-6-yl)benzoic acid;
3-(4-hydroxybut-1-ynyl)-2-(1H-indol-6-yl)benzoic acid;
3-(3-amino-3-methylbut-1-ynyl)-2-(1H-indol-6-yl)benzoic acid;
3-(3-hydroxy-3-phenylprop-1-ynyl)-2-(1H-indol-6-yl)benzoic acid;
3-(3-hydroxy-3-methylbut-1-ynyl)-2-(1H-indol-6-yl)benzoic acid;
3((3-(hydroxymethyl)phenyl)ethynyl)-2-(1H-indol-6-yl)benzoic acid;
2-(2-(ethoxycarbonyl)-1H-indol-6-yl)-3-(phenylethynyl)benzoic acid;
3-((3-carbamoyl-5-methoxyphenyl)ethynyl)-2-(1H-indol-6-yl)benzoic acid;
3-((4-fluoro-3-(tetrahydro-2H-pyran-4-yloxy)phenyl)ethynyl)-2-(1H-indol-6-yl)benzoic acid;
2-(1H-indol-6-yl)-3-[2-(pyridin-4-yl)ethynyl]benzoic acid; and
3-[2-(3-hydroxyphenyl)ethynyl]-2-(1H-indol-6-yl)benzoic acid;
or a pharmaceutically acceptable salt, carboxylic ester, polymorph or solvate thereof.

3. A composition comprising at least one compound of claim 1 and at least one excipient.

4. A composition comprising at least one compound of claim 2 and at least one excipient.

5. The compound of claim 1 , wherein R 4d is selected from the group consisting of hydrogen, C 1-6 linear alkyl, and C 3-6 branched alkyl.

6. The compound of claim 1 , wherein R 4d is hydrogen.

7. The compound of claim 1 , wherein R 4d is selected from the group consisting of methyl, ethyl, n-propyl, isopropyl, n-butyl, sec-butyl, iso-butyl, and tert-butyl.

8. The compound of claim 2 , wherein the carboxylic ester is selected from the group consisting of methyl, ethyl, n-propyl, isopropyl, n-butyl, sec-butyl, iso-butyl, and tert-butyl.

Assignees

• Wistar Inst

Inventors

• Messick Troy E
• Smith Garry R
• Reitz Allen B
• Lieberman Paul M
• Mcdonnell Mark E
• Zhang Yan
• Velvadapu Venkata

Classifications

• A61P37/02

  Immunomodulators · CPC title

• A61P43/00

  Drugs for specific purposes, not provided for in groups A61P1/00-A61P41/00 · CPC title

• A61P31/12

  Antivirals · CPC title

• A61P35/02

  specific for leukemia · CPC title

• A61P31/22

  for herpes viruses · CPC title