Heterocyclic modulators of lipid synthesis
US-2024400552-A1 · Dec 5, 2024 · US
US9505754B2 · US · B2
| Field | Value |
|---|---|
| Publication number | US-9505754-B2 |
| Application number | US-201414451127-A |
| Country | US |
| Kind code | B2 |
| Filing date | Aug 4, 2014 |
| Priority date | Jun 26, 2009 |
| Publication date | Nov 29, 2016 |
| Grant date | Nov 29, 2016 |
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A compound is disclosed that has a formula represented by the following: This compound may be prepared as a pharmaceutical composition, and may be used for the prevention and treatment of a variety of conditions in mammals including humans, including by way of non-limiting example, inflammatory conditions, autoimmune diseases, proliferative diseases, transplantation rejection, diseases involving impairment of cartilage turnover, congenital cartilage malformations, and/or diseases associated with hypersecretion of IL6.
Opening claim text (preview).
What is claimed is: 1. A method for the treatment of an inflammatory condition selected from Crohn's disease and colitis, or a proliferative disease selected from psoriasis, said method comprising administering a therapeutically effective amount of a compound according to Formula I: or a pharmaceutically acceptable salt thereof. 2. The method according to claim 1 , comprising the administration of a pharmaceutical composition comprising a pharmaceutically acceptable carrier and a pharmaceutically effective amount of said compound, or a pharmaceutically acceptable salt thereof. 3. The method according to claim 1 , wherein the inflammatory condition is Crohn's disease. 4. The method according to claim 1 , wherein the inflammatory condition is colitis. 5. The method according to claim 1 , wherein the method is for the treatment of psoriasis. 6. The method according to claim 2 , wherein the inflammatory condition is Crohn's disease. 7. The method according to claim 2 , wherein the inflammatory condition is colitis. 8. The method according to claim 2 , wherein the method is for the treatment of psoriasis. 9. The method according to claim 1 , wherein said compound is administered in combination with a further therapeutic agent. 10. The method according to claim 2 , wherein said pharmaceutical composition is administered in combination with a further therapeutic agent. 11. The method according to claim 9 , wherein said further therapeutic agent is an agent for the treatment of Crohn's disease. 12. The method according to claim 9 , wherein said further therapeutic agent is an agent for the treatment of colitis. 13. The method according to claim 9 , wherein said further therapeutic agent is an agent for the treatment of psoriasis. 14. The method according to claim 10 , wherein said further therapeutic agent is an agent for the treatment of Crohn's disease. 15. The method according to claim 10 , wherein said further therapeutic agent is an agent for the treatment of colitis. 16. The method according to claim 10 , wherein said further therapeutic agent is an agent for the treatment of psoriasis. 17. The method according to claim 11 , wherein the further therapeutic agent is an agent selected from glucocorticoids, synthetic disease modifying, immunomodulatory agents, and biological disease modifying, immunomodulatory agents. 18. The method according to claim 17 , wherein the further therapeutic agent is selected from prednisone, budesonide, methotrexate, leflunomide, sulfasalazine, mesalazine, azathioprine, 6-mercaptopurine, cyclosporine, infliximab, adalimumab, rituximab, and abatacept. 19. The method according to claim 12 , wherein the further therapeutic agent is an agent selected from glucocorticoids, synthetic disease modifying, immunomodulatory agents, and biological disease modifying, immunomodulatory agents. 20. The method according to claim 19 , wherein the further therapeutic agent is selected from prednisone, budesonide, methotrexate, leflunomide, sulfasalazine, mesalazine, azathioprine, 6-mercaptopurine, cyclosporine, infliximab, adalimumab, rituximab, and abatacept. 21. The method according to claim 13 , wherein the further therapeutic agent is selected from topical agents selected from coal tar, dithranol, corticosteroids, vitamin D 3 analogues, and retinoids; and systemic agents selected from synthetic disease modifying, immunomodulatory agents, and biological disease modifying, immunomodulatory agents. 22. The method according to claim 21 , wherein the further therapeutic agent is selected from methotrexate, cyclosporine, retinoids, tioguanine, hydroxyurea, sulfasalazine, mycophenolate mofetil, azathioprine, tacrolimus, fumaric acid esters, and ustekinumab.
Immunosuppressants, e.g. drugs for graft rejection · CPC title
Immunomodulators · CPC title
Antineoplastic agents · CPC title
Drugs for immunological or allergic disorders · CPC title
Non-central analgesic, antipyretic or antiinflammatory agents, e.g. antirheumatic agents; Non-steroidal antiinflammatory drugs [NSAID] · CPC title
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