Compounds and their use for the treatment of alpha1-antitrypsin deficiency
The invention relates to specified benzamide compounds of formula (1), and pharmaceutical compositions containing the compounds. The compounds may be inducers of α 1 -antitrypsin (A1AT), and may be used in the treatment of a disease or disorder such as α 1 -antitrypsin deficiency (A1AD or AATD).
1. A compound represented by the structure:
or a pharmaceutically acceptable salt of any one thereof.
2. The compound of claim 1 , wherein the compound is in a crystalline form.
3. A pharmaceutical composition comprising a compound represented by the structure:
or a pharmaceutically acceptable salt of any one thereof, and a pharmaceutically acceptable carrier.
4. A method of inducing Z A1AT secretion in a subject in need thereof, comprising administering to the subject a compound represented by the structure:
or a pharmaceutically acceptable salt of any one thereof.
5. The compound of claim 1 , wherein the compound is represented by:
or a pharmaceutically acceptable salt thereof.
6. The compound of claim 1 , wherein the compound is represented by:
or a pharmaceutically acceptable salt thereof.
7. The compound of claim 1 , wherein the compound is represented by:
or a pharmaceutically acceptable salt thereof.
8. The compound of claim 1 , wherein the compound is represented by:
or a pharmaceutically acceptable salt thereof.
9. The compound of claim 1 , wherein the compound is represented by:
or a pharmaceutically acceptable salt thereof.
10. The pharmaceutical composition of claim 3 , wherein the compound is represented by:
or a pharmaceutically acceptable salt thereof.
11. The pharmaceutical composition of claim 3 , wherein the compound is represented by:
or a pharmaceutically acceptable salt thereof.
12. The pharmaceutical composition of claim 3 , wherein the compound is represented by:
or a pharmaceutically acceptable salt thereof.
13. The pharmaceutical composition of claim 3 , wherein the compound is represented by:
or a pharmaceutically acceptable salt thereof.
14. The pharmaceutical composition of claim 3 , wherein the compound is represented by:
or a pharmaceutically acceptable salt thereof.
15. The method of claim 4 , wherein the structure is represented by:
or a pharmaceutically acceptable salt thereof.
16. The method of claim 4 , wherein the compound is represented by:
or a pharmaceutically acceptable salt thereof.
17. The method of claim 4 , wherein the compound is represented by:
or a pharmaceutically acceptable salt thereof.
18. The method of claim 4 , wherein the compound is represented by:
or a pharmaceutically acceptable salt thereof.
19. The method of claim 4 , wherein the compound is represented by:
or a pharmaceutically acceptable salt thereof.