Gpx4 inhibitors, pharmaceutical compositions thereof, and their use for treating gpx4-mediated diseases
US-2024246901-A1 · Jul 25, 2024 · US
US9498461B2 · US · B2
| Field | Value |
|---|---|
| Publication number | US-9498461-B2 |
| Application number | US-201314533111-A |
| Country | US |
| Kind code | B2 |
| Filing date | May 15, 2013 |
| Priority date | May 23, 2012 |
| Publication date | Nov 22, 2016 |
| Grant date | Nov 22, 2016 |
A practical reading order for non-experts. Skip the full description unless you need deep technical detail.
What the patent document calls the invention.
A short plain-language summary of the technical disclosure.
Who owns or filed the patent and who is credited as inventor.
Filing, priority, publication, and grant dates set the timeline.
The legal scope of protection — read this for what is actually claimed.
Technology tags used to group this patent with similar filings.
Prior art links and similar publications in this corpus.
Official abstract text for this publication.
The invention relates to the compounds of formula I and formula II or its pharmaceutical acceptable salts, as well as polymorphs, solvates, enantiomers, stereoisomers and hydrates thereof. The pharmaceutical compositions comprising an effective amount of compounds of formula I or formula II; and methods for treating or preventing inflammatory bowel disease may be formulated for oral, buccal, rectal, topical, transdermal, transmucosal, intravenous, parenteral administration, syrup, or injection. Such compositions may be used to treatment of gastrointestinal diseases and inflammation such as inflammatory bowel disease, ulcerative colitis, mild-to-moderate Crohn's disease, rheumatoid arthritis, inflammatory arthritis, psoriatic arthritis, liver cirrhosis and idiopathic urticaria.
Opening claim text (preview).
What is claimed is: 1. A compound of: or a pharmaceutically acceptable salt, hydrate, polymorph, solvate, enantiomer, or stereoisomer thereof. 2. A compound of: or a pharmaceutically acceptable salt, hydrate, polymorph, solvate, prodrug, enantiomer, or stereoisomer thereof. 3. A pharmaceutical composition comprising a compound of claim 1 and a pharmaceutically acceptable carrier. 4. A pharmaceutical composition comprising a compound of claim 2 and a pharmaceutically acceptable carrier. 5. A pharmaceutical composition of claim 3 , further comprising a molecular conjugate of mesalazine, caprylic acid and carboxylic compounds selected form a group consisting of eicosapentaenoic acid and docosahexaenoic acid. 6. The pharmaceutical composition of claim 5 , wherein the carboxylic acid compound is eicosapentaenoic acid. 7. The pharmaceutical composition of claim 5 , wherein the carboxylic acid compound is docosahexaenoic acid. 8. A pharmaceutical composition of claim 4 , further comprising a molecular conjugate of, caprylic acid and a compound selected form a group consisting of eicosapentaenoic acid and docosahexaenoic acid. 9. The pharmaceutical composition of claim 8 , wherein the carboxylic acid compound is eicosapentaenoic acid. 10. The pharmaceutical composition of claim 8 , wherein the carboxylic acid compound is docosahexaenoic acid.
Antineoplastic agents · CPC title
Non-central analgesic, antipyretic or antiinflammatory agents, e.g. antirheumatic agents; Non-steroidal antiinflammatory drugs [NSAID] · CPC title
for ulcers, gastritis or reflux esophagitis, e.g. antacids, inhibitors of acid secretion, mucosal protectants · CPC title
Antipsoriatics · CPC title
Drugs for disorders of the alimentary tract or the digestive system · CPC title
Related publications grouped by family.
Answers are generated from the same data shown on this page.