BI-FUNCTIONAL COMPOUNDS AND METHODS FOR TARGETED UBIQUITINATION OF ANDROGEN RECEPTOR
The present invention relates to bi-functional compounds which function to recruit endogenous proteins to an E3 ubiquitin ligase for degradation, and methods for using same. More specifically, the present disclosure provides specific proteolysis targeting chimera (PROTAC) molecules which find utility as modulators of targeted ubiquitination of a variety of polypeptides and other proteins, in particular the androgen receptor of a slice variant of AR which lacks the LBD, labelled as AR-V7, which are then degraded and/or otherwise inhibited by the compounds as described herein.
1 . A compound having a chemical structure ARB-L-E3LB, wherein ARB is an AR binding moiety that does not bind to a ligand binding domain, E3LB is an E3 ligase binding moiety, and L is a linker coupling the AR binding moiety to the E3 ligase binding moiety, and wherein:
the AR binding moiety is selected from:
and
wherein the E3 ligase binding moiety is selected from:
(a) a structure selected from the group consisting of:
wherein “ ” in the above structures, represents a bond that may be stereospecific ((R) or (S)), or non-stereospecific, optionally wherein the bond is oriented to form the (R)-chiral carbon, and wherein:
R 1 is each independently H or halo (e.g., F); and
R 4 is H; or
(b)
and
wherein the linker (“L” or “Link”) comprises a chemical structure represented by -A q -, in which q is an integer greater than 1, and A is independently selected from the group consisting of a bond, CR L1 R L2 , O, NR L3 , CONR L3 , and CO; wherein R L1 , R L2 , and R L3 are each independently selected from the group consisting of H, halo, and C 1-8 alkyl.
2 . The compound of claim 1 , wherein the linker group (e.g., “L” or “Link”) is selected from:
wherein n is from 1-5;
wherein n is from 1-5;
wherein n is from 1-5;
wherein m is from 0-12;
wherein m is rom 0-12;
wherein m is from 0-12;
wherein m is from 2-4;
wherein m is from 0-12;
wherein n is from 0-10;
wherein n is from 1-5;
wherein n is from 1-5;
wherein n is from 1-5
wherein m is from 0-10;
wherein m is from 0-10;
wherein m is from 0-10;
wherein n is from 1-5;
wherein n is from 1-5;
wherein n is from 1-5;
wherein n is from 1-5;
wherein n is from 1-5;
n wherein m is from 1-12;
wherein m is from 1-12;
wherein m is from 1-12; and
wherein m is from 0-10.
3 . The compound of claim 1 , wherein the linker group (e.g., “L” or “Link”) is selected from:
wherein n is from 2-4;
wherein n is from 2-4;
wherein n is from 2-3;
wherein m is from 2-8;
wherein m is from 4-8;
wherein m is from 2-4;
wherein m is from 2-4;
wherein m is from 1-4;
wherein m is from 1-4;
wherein n is from 2-4;
wherein n is from 1-3;
wherein n is from 1-2;
wherein m is from 4-6;
wherein m is from 2-4; and
wherein m is from 2-4.
4 . The compound of claim 1 , wherein the linker group (e.g., “L” or “Link”) is selected from:
wherein n is from 0-4 (e.g., 1) and m is from 0-4 (e.g., 0);
wherein n is from 0-4 (e.g., 1) and m is
wherein n is from 0-4 (e.g., 1) and m is
wherein n is from 0-4 (e.g., 1) and m is from 0-4 (e.g., 0);
wherein n is from 0-4 (e.g., 1) and m is from 0-4 (e.g., 0);
wherein n is from 0-4 (e.g., 1) and m is from 0-4 (e.g., 0);
wherein n is from 0-4 (e.g., 1) and m is from 0-4
(e.g., 0);
wherein n is from 0-4 (e.g., 1) and m is from 0-4 (e.g., 0);
wherein n is from 0-4 (e.g., 1) and m is from 0-4 (e.g., 0);
wherein n is from 0-4 (e.g., 1) and m is from 0-4 (e.g., 0);
wherein n is from 0-4 (e.g., 1) and m is from 0-4 (e.g., 0);
wherein m 1 is from 0-6 (e.g., 0 or 1) and m 2 is from 0-4 (e.g., 0);
wherein m 1 is from 0-6 (e.g., 0 or 1) and m 2 is from 0-4 (e.g., 0);
wherein m 1 is from 0-6 (e.g., 0 or 1) and m 2 is from 0-4
wherein m 1 is from 0-6 (e.g., 0 or 1) and m 2 is from 0-4 (e.g., 0);
wherein m 1 is from 0-6 (e.g., 0 or 1) and m 2 is from 0-4 (e.g., 0);
wherein m 1 is from 0-6 (e.g., 0 or 1) and m 2 is from 0-4 (e.g., 0);
wherein m 1 is from 0-6 (e.g., 0 or 1) and m 2 is from 0-4 (e.g., 0);
wherein m 1 is from 0-6 (e.g., 0 or 1) and m 2 is from 0-4 (e.g. 0
wherein m 1 is from 0-6 (e.g., 0 or 1) and m 2 is from 0-4 (e.g., 0);
wherein m 1 is from 0-6 (e.g., 0 or 1) and m 2 is from 0-4 (e.g., 0);
wherein m 1 is from 0-6 (e.g., 0 or 1) and m 2 is from 0-4 (e.g., 0);
wherein m 1 is from 0-6 (e.g., 0 or 1) and m 2 is from 0-4 (e.g., 0).
5 . The compound of claim 1 , wherein the linker group (e.g., “L” or “Link”) is selected from:
wherein n is from 1 to 4 (e.g., 2, 3, or 4),
wherein n is from 1 to 4 (e.g., 2, 3, or 4);
wherein m is from 2 to 8 (e.g., 4, 6, or 8);
wherein m is from 2 to 8 (e.g., 4, 6, or 8);
wherein n is from 1 to 4 (e.g., 2, 3, or 4),
wherein n is from 1 to 4 (e.g., 2, 3, or 4);
wherein m is from 2 to 8 (e.g., 4, 6, or 8);
wherein m is from 2 to 8 (e.g., 4, 6, or 8);
wherein n is from 1 to 4 (e.g., 2, 3, or 4); and
wherein n is from 1 to 4 (e.g., 2, 3, or 4).
6 . The compound of claim 5 , wherein the compound comprises:
the AR binding moiety
and
wherein the compound has an E3 ligase binding moiety selected from:
optionally wherein, in each of said compounds, the “ ” bond is oriented to form the (R)-chiral carbon.
7 . The compound of claim 1 , wherein the linker group (e.g., “L” or “Link”) is selected from:
wherein m is from 0-6 (e.g., 1, 2, 3, or 4);
wherein m is from 0-6 (e.g., 1, 2, 3, or 4);
wherein m is from 0-6 (e.g., 1, 2, 3, or 4);
wherein n is from 1-5 (e.g., 1 or 2);
wherein n is from 1-5;
wherein m is from 0-6 (e.g., 2, 3, 4, or 5);
wherein n is from 1-6 (e.g., 1, 2, or 3);
wherein m 1 is from 0-6 (e.g., 1) and m 2 is from 0-4 (e.g., 0); and
wherein n is from 0-4 (e.g., 1) and m is from 0-4 (e.g., 0).
8 . The compound of claim 7 , wherein the compound comprises:
the AR binding moiety
and
wherein the compound has the E3 ligase binding moiety
9 . The compound of claim 7 , wherein the compound comprises:
the AR binding moiety
and
wherein the compound has the E3 ligase binding
10 . The compound of claim 1 , wherein the linker group (e.g., “L” or “Link”) is selected from:
wherein n is from 1 to 4 (e.g., 1, 2, or 3);
wherein m is from 2 to 8 (e.g., 2, 4, or 6);
wherein n is 1 to 4 (e.g., 2 or 3); and
wherein m is from 2 to 8 (e.g., 2, 4, or 6).
11 . The compound of claim 10 , wherein the compound comprises:
the AR binding moiety
and
wherein the compound has the E3 ligase binding moiety
12 . A compound selected from the group consisting of:
13 . A pharmaceutical composition comprising a compound according to claim 1 , and a pharmaceutically acceptable carrier, additive and/or excipient.
14 . A method of treating a disease state or condition in a patient wherein dysregulated protein activity is responsible for said disease or condition, said method comprising administering an effective amount of a compound according to claim 1 , to a patient in need thereof.
15 . A method of degrading an androgen receptor in a cell, e.g., a mutated AR such as any AR-V1 to AR-V15 splice variant, e.g., the AR-V7 splice variant, said method comprising administering an effective amount of a compound according to claim 1 , to such cell, e.g., a cancer cell.
16 . A method of inducing apoptosis in a cell, e.g., a cancer cell, said method comprising administering an effective amount of a compound according to claim 1 , to such cell.
17 . (canceled)
18 . (canceled)
19 . A method of treating a disease state or condition in a patient wherein dysregulated protein activity is responsible for said disease or condition, said method comprising administering an effective amount of a compound according to claim 12 , to a patient in need thereof.
20 . A method of degrading an androgen receptor in a cell, e.g., a mutated AR such as any AR-V1 to AR-V15 splice variant, e.g., the AR-V7 splice variant, said method comprising administering an effective amount of a compound according to claim 12 , to such cell, e.g., a cancer cell.
21 . A method of inducing apoptosis in a cell, e.g., a cancer cell, said method comprising administering an effective amount of a compound according to claim 12 , to such cell.