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Msg  10993 of 11719  at  3/30/2023 9:46:52 AM  by

JBWIN


Building IP: BMY Patent Appl "SUBSTITUTED INDOLE COMPOUNDS"

 

SUBSTITUTED INDOLE COMPOUNDS

DOCUMENT ID

US 20230098244 A1

DATE PUBLISHED

2023-03-30

INVENTOR INFORMATION

NAME

CITY

STATE

ZIP CODE

COUNTRY

Dyckman; Alaric J.
Lawrenceville
NJ
N/A
US
Dodd; Dharmpal S.
San Diego
CA
N/A
US
Mussari; Christopher P.
Princeton
NJ
N/A
US
Sherwood; Trevor C.
West Windsor
NJ
N/A
US
Gilmore; John L.
Yardley
PA
N/A
US
Haque; Tsair Shamsul
Yardley
PA
N/A
US
Whiteley; Brian K.
Lebanon
NJ
N/A
US
Tortolani; David R.
Skillman
NJ
N/A
US
Posy; Shoshana L.
Highland Park
NJ
N/A
US
Macor; John E.
Washington Crossing
PA
N/A
US
Lombardo; Louis J.
Belle Mead
NJ
N/A
US
Sistla; Ramesh Kumar
Bangalore
N/A
N/A
IN
Ramachandra Reddy; Anupama Kandhi
Bangalore
N/A
N/A
IN
Hegde; Subramanya
Bangalore
N/A
N/A
IN
Pasunoori; Laxman
Warangal
N/A
N/A
IN
Kumar; Sreekantha Ratna
Bangalore
N/A
N/A
IN

APPLICANT INFORMATION

NAME
Bristol-Myers Squibb Company
CITY
Princeton
STATE
NJ
ZIP CODE
N/A
COUNTRY
US
AUTHORITY
N/A
TYPE
assignee

APPLICATION NO

17/699944

DATE FILED

2022-03-21

DOMESTIC PRIORITY (CONTINUITY DATA)

parent US continuation 16763670 20200513 PENDING WO continuation PCT/US2018/060590 20181113 child US 17699944

us-provisional-application US 62585733 20171114

US CLASS CURRENT:

514/230.5

CPC CURRENT

TYPE

CPC

DATE

CPCI
2013-01-01
CPCI
2013-01-01
CPCI
2013-01-01
CPCI
2013-01-01
CPCI
2013-01-01
CPCI
2013-01-01
CPCI
2013-01-01
CPCI
2013-01-01
CPCI
2013-01-01

Abstract

Disclosed are compounds of Formula (I)

##STR00001##

or salts thereof, wherein Ring Het, R.sub.1, R.sub.2, R.sub.3, R.sub.4, R.sub.5, m, n, and p are defined herein. Also disclosed are methods of using such compounds as inhibitors of signaling through Toll-like receptor 7, or 8, or 9, and pharmaceutical compositions comprising such compounds. These compounds are useful in treating inflammatory and autoimmune diseases.

Background/Summary

CROSS REFERENCE [0001] This application claims the benefit of U.S. Provisional Application Ser. No. 62/585,733, filed Nov. 14, 2017, which is incorporated herein in its entirety.

DESCRIPTION

[0002] The present invention generally relates to substituted indole compounds useful as inhibitors of signaling through Toll-like receptor 7, 8, or 9 (TLR7, TLR8, TLR9) or combinations thereof. Provided herein are substituted indole compounds, compositions comprising such compounds, and methods of their use. The invention further pertains to pharmaceutical compositions containing at least one compound according to the invention that are useful for the treatment of conditions related to TLR modulation, such as inflammatory and autoimmune diseases, and methods of inhibiting the activity of TLRs in a mammal.

[0003] Toll/IL-1 receptor family members are important regulators of inflammation and host resistance. The Toll-like receptor family recognizes molecular patterns derived from infectious organisms including bacteria, fungi, parasites, and viruses (reviewed in Kawai, T. et al., Nature Immunol., 11:373-384 (2010)). Ligand binding to the receptor induces dimerization and recruitment of adaptor molecules to a conserved cytoplasmic motif in the receptor termed the Toll/IL-1 receptor (TIR) domain. With the exception of TLR3, all TLRs recruit the adaptor molecule MyD88. The IL-1 receptor family also contains a cytoplasmic TIR motif and recruits MyD88 upon ligand binding (reviewed in Sims, J. E. et al., Nature Rev. Immunol., 10:89-102 (2010)).

[0004] Toll-like receptors (TLRs) are a family of evolutionarily conserved, transmembrane innate immune receptors that participate in the first-line defense. As pattern recognition receptors, the TLRs protect against foreign molecules, activated by pathogen associated molecular patterns (PAMPs), or from damaged tissue, activated by danger associated molecular patterns (DAMPs). A total of 13 TLR family members have been identified, 10 in human, that span either the cell surface or the endosomal compartment. TLR7-9 are among the set that are endosomally located and respond to single-stranded RNA (TLR7 and TLR8) or unmethylated single-stranded DNA containing cytosine-phosphate-guanine (CpG) motifs (TLR9).

[0005] Activation of TLR7/8/9 can initiate a variety of inflammatory responses (cytokine production, B cell activation and IgG production, Type I interferon response). In the case of autoimmune disorders, the aberrant sustained activation of TLR7/8/9 leads to worsening of disease states. Whereas overexpression of TLR7 in mice has been shown to exacerbate autoimmune disease, knockout of TLR7 in mice was found to be protective against disease in lupus-prone MRL/lpr mice. Dual knockout of TLR7 and 9 showed further enhanced protection.

[0006] As numerous conditions may benefit by treatment involving modulation of cytokines, IFN production and B cell activity, it is immediately apparent that new compounds capable of modulating TLR7 and/or TLR8 and/or TLR9 and methods of using these compounds could provide substantial therapeutic benefits to a wide variety of patients.

[0007] The present invention relates to a new class of substituted indole compounds found to be effective inhibitors of signaling through TLR7/8/9. These compounds are provided to be useful as pharmaceuticals with desirable stability, bioavailability, therapeutic index, and toxicity values that are important to their drugability.

SUMMARY OF THE INVENTION

[0008] The present invention provides compounds of Formula (I) that are useful as inhibitors of signaling through Toll-like receptor 7, 8, or 9 and are useful for the treatment of proliferative diseases, allergic diseases, autoimmune diseases and inflammatory diseases, or stereoisomers, tautomers, pharmaceutically acceptable salts, solvates or prodrugs thereof.

[0009] The present invention also provides pharmaceutical compositions comprising a pharmaceutically acceptable carrier and at least one of the compounds of the present invention or stereoisomers, tautomers, pharmaceutically acceptable salts, solvates, or prodrugs thereof.

[0010] The present invention also provides a method for inhibition of Toll-like receptor 7, 8, or 9 comprising administering to a host in need of such treatment a therapeutically effective amount of at least one of the compounds of the present invention or stereoisomers, tautomers, pharmaceutically acceptable salts, solvates, or prodrugs thereof.

[0011] The present invention also provides a method for treating proliferative, metabolic, allergic, autoimmune and inflammatory diseases, comprising administering to a host in need of such treatment a therapeutically effective amount of at least one of the compounds of the present invention or stereoisomers, tautomers, pharmaceutically acceptable salts, solvates, or prodrugs thereof.

[0012] The present invention also provides a method of treating a disease or disorder associated with Toll-like receptor 7, 8, or 9 activity, the method comprising administering to a mammal in need thereof, at least one of the compounds of Formula (I) or salts, solvates, and prodrugs thereof.

[0013] The present invention also provides processes and intermediates for making the compounds of Formula (I) including salts, solvates, and prodrugs thereof.

[0014] The present invention also provides at least one of the compounds of Formula (I) or salts, solvates, and prodrugs thereof, for use in therapy.

[0015] The present invention also provides the use of at least one of the compounds of Formula (I) or salts, solvates, and prodrugs thereof, for the manufacture of a medicament for the treatment of prophylaxis of Toll-like receptor 7, 8, or 9 related conditions, such as allergic disease, autoimmune diseases, inflammatory diseases, and proliferative diseases.

[0016] The compound of Formula (I) and compositions comprising the compounds of Formula (I) may be used in treating, preventing, or curing various Toll-like receptor 7, 8, or 9 related conditions. Pharmaceutical compositions comprising these compounds are useful for treating, preventing, or slowing the progression of diseases or disorders in a variety of therapeutic areas, such as allergic disease, autoimmune diseases, inflammatory diseases, and proliferative diseases.

[0017] These and other features of the invention will be set forth in expanded form as the disclosure continues.

Description



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