Degraders that target proteins via KEAP1
Disclosed are bifunctional compounds, pharmaceutical compositions containing them, and methods of making and using them to treat diseases and disorders characterized by aberrant protein activity wherein the protein is targeted for degradation by KEAP1 and the Cul3-based E3-ubiquitin ligase complex.
1. A bifunctional compound of formula (I):
wherein:
R is methyl or halo;
R 2 is methyl,
wherein L is a linker comprising an alkylene chain or a bivalent alkylene chain which may be interrupted by, and/or terminate at either or both termini in at least one of —O—, —S—, —N(R′)—, —C(O)—, —C(O)O—, —OC(O)—, —OC(O)O—, —C(NOR′)—, —C(O)N(R′)—, —C(O)N(R′)C(O)—, —C(O)N(R′)C(O)N(R′)—, —N(R′)C(O)—, —N(R′)C(O)N(R′)—, —N(R′)C(O)O—, —OC(O)N(R′)—, —C(NR′)—, —N(R′)C(NR′)—, —C(NR′)N(R′)—, —N(R′)C(NR′)N(R′)—, —S(O) 2 —, —OS(O)—, —S(O)O—, —S(O)—, —OS(O) 2 —, —S(O) 2 O—, —N(R′)S(O) 2 —, —S(O) 2 N(R′)—, —N(R′)S(O)—, —S(O)N(R′)—, —N(R′)S(O) 2 N(R′)—, —N(R′)S(O)N(R′)—, C 3-12 carbocyclene, 3- to 12-membered heterocyclene, 5- to 12-membered heteroarylene or any combination thereof, wherein R′ is H or C 1 -C 6 alkyl; and
TL is a targeting ligand of the structure:
wherein R 9 is methyl, or tertiary butyl, or
wherein R 3 is H or
R 4 is H, halo or
R 5 is methoxy or
R 6 is H or methyl; and
R 8 is H or ethyl,
provided that one of R 2 , R 3 , R 4 and R 5 is
or a pharmaceutically acceptable salt or stereoisomer thereof.
2. The bifunctional compound of claim 1 , wherein R is methyl;
R 1 is
R 2 is
wherein
R 3 is
R 5 is methoxy; and R 6 is methyl,
the bifunctional compound is represented by formula (Ia):
or a pharmaceutically acceptable salt or stereoisomer thereof.
3. The bifunctional compound of claim 1 , wherein R is methyl;
R 1 is
wherein
R 4 is
R 5 is methoxy; and R 8 is H,
the bifunctional compound is represented by formula (Ib):
or a pharmaceutically acceptable salt or stereoisomer thereof.
4. The bifunctional compound of claim 1 , wherein R is methyl;
R 1 is
R 2 is
R 5 is methoxy;
R 6 is H; and R 8 is H,
the bifunctional compound is represented by formula (Ic):
or a pharmaceutically acceptable salt or stereoisomer thereof.
5. The bifunctional compound of claim 1 , wherein R is Cl,
R 1 is
R 2 is
R 3 is
R 5 is methoxy;
R 6 is methyl; and R 8 is H,
the bifunctional compound is represented by formula (Id):
or a pharmaceutically acceptable salt or stereoisomer thereof.
6. The bifunctional compound of claim 1 , wherein R is Cl;
R 1 is
wherein
R 2 is
R 5 is methoxy;
R 6 is H; and R 8 is H,
the bifunctional compound is represented by formula (Ie):
or a pharmaceutically acceptable salt or stereoisomer thereof.
7. The bifunctional compound of claim 1 , wherein R is methyl;
R 1 is
R 4 is H; and
R 5 is
and R 8 is H,
the bifunctional compound is represented by formula (If):
or a pharmaceutically acceptable salt or stereoisomer thereof.
8. The bifunctional compound of claim 1 , wherein the targeting ligand binds BRD4, BRD3 and BRD2, and wherein the bifunctional compound is represented by a structure selected from the group consisting of:
or a pharmaceutically acceptable salt or stereoisomer thereof.
9. The bifunctional compound of claim 1 , wherein the targeting ligand binds BRD4, BRD3 and BRD2, and wherein the bifunctional compound is represented by a structure selected from the group consisting of:
a pharmaceutically acceptable salt or stereoisomer thereof.
10. A pharmaceutical composition comprising a therapeutically effective amount of the bifunctional compound of claim 1 , and a pharmaceutically acceptable carrier.
11. A method of treating a disease or disorder characterized by an aberrant or dysfunctional BRD4, BRD3 or BRD2, comprising administering to a subject in need thereof a therapeutically effective amount of the bifunctional compound of claim 1 .