Substituted benzothiophene analogs as selective estrogen receptor degraders
In one aspect, the disclosure relates to relates to substituted benzothiophene analogs which are useful as selective degraders of estrogen receptor, methods of making same, pharmaceutical compositions comprising same, and methods of treating one or more clinical conditions associated with estrogen receptor, such as a cancer, including breast cancer, or osteoporosis. This abstract is intended as a scanning tool for purposes of searching in the particular art and is not intended to be limiting of the present disclosure.
1. A compound having a structure represented by a formula:
wherein m is selected from 0 and 1;
wherein p is selected from 0, 1, and 2;
wherein q is selected from 0, 1, and 2;
wherein each of Z 1 and Z 2 is independently selected from —CH— or —N—; provided Z 1 and Z 2 are not simultaneously —CH— or —N—; and provided when Z 1 is —CH— and m is 1, that p and q are not both 0;
wherein Z 10 is selected from —O— or —NH—;
wherein Z 11 is, when present, —CH 2 CH 2 —;
wherein Z 40 is —(CH 2 ) n —;
wherein each of R 10a and R 10b are independently selected from hydrogen, deuterium, halogen, and C1-C3 methyl;
wherein R is C1-C6 alkyl, C1-C6 haloalkyl, halogen, or hydroxy; and
wherein n is selected from 0, 1, 2, and 3;
or a pharmaceutically acceptable salt thereof.
2. The compound of claim 1 , wherein Z 10 is —O—.
3. The compound of claim 1 , wherein Z 40 is selected from —(CH 2 )— and —(CH 2 ) 3 —.
4. The compound of claim 1 wherein —Z 1 — is N and Z 2 is —CH—.
5. The compound of claim 1 wherein —Z 1 — is —CH— and Z 2 is —N—.
6. The compound of claim 1 , having a structure represented by a formula:
7. The compound of claim 1 , having a structure represented by a formula:
8. The compound of claim 1 , having a structure represented by a formula:
9. A pharmaceutical composition comprising a therapeutically effective amount of a compound of claim 1 , or a pharmaceutically acceptable salt thereof, and a pharmaceutically acceptable carrier.