Cysteine-dependent inverse agonists of nuclear receptors ROR-gamma/ROR-gamma-t and methods of treating diseases or disorders therewith

Patent metadata

Field	Value
Publication number	US-12060340-B2
Application number	US-201917252841-A
Country	US
Kind code	B2
Filing date	Jun 20, 2019
Priority date	Jun 20, 2018
Publication date	Aug 13, 2024
Grant date	Aug 13, 2024

Abstract

Provided herein are compounds, compositions and methods for treating and preventing diseases and disorders, comprising administering to patients therapeutically effective amounts of cysteine-dependent inverse agonists of the nuclear receptor RORγ/RORγt. In some such embodiments, the inverse agonists bind to cysteine 476 of a nuclear receptor RORγ in the patient. Also provided are methods, as well as compounds and compositions, for modulating the activity of RORγ and RORγt by binding to the allosteric binding site through a covalent bond. In some aspects, the present disclosure relates to using compounds containing Michael acceptor groups which bind to a cysteine residue in the allosteric binding site such as cysteine 476 in RORγ.

First claim

What is claimed is:

1. A method of treating a disease or disorder, wherein the disease or disorder is an autoimmune disease, in a patient in need thereof, comprising administering to the patient a therapeutically effective amount of a cysteine-dependent inverse agonist of nuclear receptor RORγ/RORγt, wherein the cysteine-dependent inverse agonist binds via the formation of a covalent bond between the inverse agonist and a cysteine of the patient's nuclear receptor RORγ/RORγt, and wherein the inverse agonist comprises a group of the formula:

wherein:
the bond between carbon atoms 4 and 5 is a single bond or a double bond;
R 1 is cyano, heteroaryl (C≤8) , substituted heteroaryl (C≤8) , —CF 3 , or —C(O)R a ; wherein:
R a is hydroxy, amino, or alkoxy (C≤8) , alkylamino (C≤8) , dialkylamino (C≤8) , alkylsulfonylamino (C≤8) , or a substituted version of any of these groups;

R 2 is hydrogen or alkyl (C≤12) , cycloalkyl (C≤12) , alkenyl (C≤12) , alkynyl (C≤12) , aryl (C≤12) , aralkyl (C≤12) , heteroaryl (C≤12) , heteroaralkyl (C≤12) , acyl (C≤12) , or a substituted version of any of these groups, or -alkanediyl (C≤8) -cycloalkyl (C≤12) or a substituted version of this group;
R 2′ is absent, hydrogen, or alkyl (C≤12) , cycloalkyl (C≤12) , alkenyl (C≤12) , alkynyl (C≤12) , aryl (C≤12) , aralkyl (C≤12) , heteroaryl (C≤12) , heteroaralkyl (C≤12) , acyl (C≤12) , or a substituted version of these groups; provided that when the bond between carbon atoms 4 and 5 is a double bond then R 2′ is absent; and
R 3 is alkyl (C≤12) , alkenyl (C≤12) , aryl (C≤12) , aralkyl (C≤12) , or a substituted version of any of these groups;
provided that when carbon atoms 4 and 5 are joined by a double bond, then R 2′ and the hydrogen atom at carbon atom 5 are absent.

2. The method of claim 1 , wherein the therapeutically effective amount is sufficient to modulate the activity of the nuclear receptor RORγ/RORγt in the patient.

3. The method of claim 1 , wherein the inverse agonist binds to cysteine 476 of the nuclear receptor RORγ in the patient.

4. The method of claim 3 , wherein the inverse agonist selectively binds to cysteine 476 of the nuclear receptor RORγ in the patient.

5. The method of claim 3 , wherein the inverse agonist preferentially binds to cysteine 476 of the nuclear receptor RORγ relative to the orthosteric binding pocket in the ligand binding domain (LBD) of RORγ/RORγt in the patient.

6. The method of claim 1 , wherein the inverse agonist does not bind to any significant extent to the orthosteric binding pocket in the ligand binding domain (LBD) of RORγ/RORγt in the patient.

7. The method of claim 1 , wherein the inverse agonist inhibits activity of the nuclear receptor RORγ/RORγt without significantly affecting activity of the nuclear receptor RORα or the nuclear receptor RORβ in the patient.

8. The method of claim 1 , wherein the method modulates the function of the nuclear receptor RORγ in the patient.

9. The method of claim 1 , wherein the method suppresses interleukin-17A production in the patient.

10. The method of claim 1 , wherein the method selectively inhibits T helper 17 (Th17) cell differentiation in the patient.

11. The method of claim 1 , wherein the inverse agonist's RORγt-LBD-GAL4 reporter assay IC 50 activity is less than 1 μM.

12. The method of claim 1 , wherein the inverse agonist's suppression of IL-17A secretion from human CD4+ T-cells assay IC 50 activity is less than 500 nM.

13. The method of claim 1 , wherein the formula is further defined as:

14. The method of claim 1 , wherein the inverse agonist is a compound of the formula:

wherein:
the bond between carbon atoms 4 and 5 is a single bond or a double bond;
a is 0, 1, or 2;
R 1 is cyano, heteroaryl (C≤8) , substituted heteroaryl (C≤8) , —CF 3 , or —C(O)R a ; wherein:
R a is hydroxy, amino, or alkoxy (C≤8) , alkylamino (C≤8) , dialkylamino (C≤8) , alkylsulfonylamino (C≤8) , or a substituted version of any of these groups;

R 2 is hydrogen or alkyl (C≤12) , cycloalkyl (C≤12) , alkenyl (C≤12) , alkynyl (C≤12) , aryl (C≤12) , aralkyl (C≤12) , heteroaryl (C≤12) , heteroaralkyl (C≤12) , acyl (C≤12) , or a substituted version of any of these groups, or -alkanediyl (C≤8) -cycloalkyl (C≤12) or a substituted version of this group;
R 2′ is absent, hydrogen, or alkyl (C≤12) , cycloalkyl (C≤12) , alkenyl (C≤12) , alkynyl (C≤12) , aryl (C≤12) , aralkyl (C≤12) , heteroaryl (C≤12) , heteroaralkyl (C≤12) , acyl (C≤12) , or a substituted version of these groups; provided that when the bond between carbon atoms 4 and 5 is a double bond then R 2′ is absent;
R 3 is alkyl (C≤12) , alkenyl (C≤12) , aryl (C≤12) , aralkyl (C≤12) , or a substituted version of any of these groups;
R 4 is hydrogen, amino, alkyl (C≤18) , substituted alkyl (C≤18) , cycloalkyl (C≤18) , substituted cycloalkyl (C≤18) , aryl (C≤18) , substituted aryl (C≤18) , aralkyl (C≤18) , substituted aralkyl (C≤18) , heteroaryl (C≤18) , substituted heteroaryl (C≤18) , heteroaralkyl (C≤18) , substituted heteroaralkyl (C≤18) , heterocycloalkyl (C≤18) , substituted heterocycloalkyl (C≤18) , amido (C≤18) , substituted amido (C≤18) , or
—X 1 —(CH 2 ) m —R 4′ ;

wherein:
X 1 is NR b , O, or S; wherein:
R b is hydrogen, alkyl (C≤6) , or substituted alkyl (C≤6) ;

m is 0, 1, 2, 3, or 4; and
R 4′ is alkyl (C≤12) , cycloalkyl (C≤12) , aryl (C≤18) , aralkyl (C≤18) , heteroaryl (C≤18) , heteroaralkyl (C≤8) , heterocycloalkyl (C≤8) , or a substituted version of any of these groups; or

wherein:
n is 0, 1, 2, 3, or 4; and
R 4″ is —H, —OH, —F, —Cl, —Br, —I, —NH 2 , —NO 2 , —CN, —SH, —S(O) 2 OH, or —S(O) 2 NH 2 , or alkyl (C≤8) , cycloalkyl (C≤8) , aryl (C≤8) , heteroaryl (C≤8) , heterocycloalkyl (C≤8) , acyl (C≤8) , amido (C≤8) , alkoxy (C≤8) , acyloxy (C≤8) , alkylamino (C≤8) , dialkylamino (C≤8) , —C(O)-alkoxy (C≤8) , —C(O)-alkylamino (C≤8) , —C(O)-dialkyl-amino (C≤8) , alkylsulfonyl (C≤8) , arylsulfonyl (C≤8) , alkoxysulfonyl (C≤8) , or a substituted version of any of these groups; or
—X 2 —(CH 2 ) p —R 4′″ ;

wherein:
X 2 is arenediyl (C≤12) , substituted arenediyl (C≤12) , heterocycloalkanediyl (C≤12) , substituted heterocycloalkanediyl (C≤12) , heteroarenediyl (C≤12) , or substituted heteroarenediyl (C≤12) ;
p is 0, 1, 2, 3, or 4; and
R 4′″ is alkyl (C≤8) , cycloalkyl (C≤8) , aryl (C≤8) , heteroaryl (C≤8) , heterocycloalkyl (C≤8) , acyl (C≤8) , amido (C≤8) , alkoxy (C≤8) , acyloxy (C≤8) , —C(O)-alkoxy (C≤8) , —C(O)-alkylamino (C≤8) , —C(O)-dialkyl-amino (C≤8) , alkylsulfonyl (C≤8) , arylsulfonyl (C≤8) , alkoxysulfonyl (C≤8) , or a substituted version of any of these groups; and

R 5 is amino, hydroxy, —OS(O) 2 C 6 H 4 CH 3 , alkyl (C≤12) , alkoxy (C≤12) , cycloalkyl (C≤12) , cycloalkoxy (C≤12) , aryl (C≤12) , aralkyl (C≤12) , heteroaryl (C≤12) , heteroaralkyl (C≤12) , heterocycloalkyl (C≤12) , acyl (C≤12) , acyloxy (C≤12) , alkylamino (C≤12) , dialkylamino (C≤12) , alkylsulfonylamino (C≤12) , or a substituted version of any of the last fourteen groups, or
—OY 1 -A 1 ;

wherein:
Y 1 is alkanediyl (C≤8) or substituted alkanediyl (C≤8) ; and
A 1 is cycloalkyl (C≤8) or substituted cycloalkyl (C≤8) ; or
—Y 2

Assignees

• Reata Pharmaceuticals Inc

Inventors

• Visnick Melean
• Jiang Xin

Classifications

• C07D403/04

  directly linked by a ring-member-to-ring-member bond · CPC title

• A61P19/02

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• A61P17/06

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• A61P37/00

  Drugs for immunological or allergic disorders · CPC title

• A61K31/4192

  1,2,3-Triazoles · CPC title