Dipeptide Comprising a Non-Proteogenic Amino Acid
US-2019002496-A1 · Jan 3, 2019 · US
US11319337B2 · US · B2
| Field | Value |
|---|---|
| Publication number | US-11319337-B2 |
| Application number | US-202017025475-A |
| Country | US |
| Kind code | B2 |
| Filing date | Sep 18, 2020 |
| Priority date | Mar 11, 2016 |
| Publication date | May 3, 2022 |
| Grant date | May 3, 2022 |
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 present application provides Compound 1:or a pharmaceutically acceptable salt or amino acid conjugate thereof. The present invention relates to an FXR activator and to methods of making and using said compound.
Opening claim text (preview).
The invention claimed is: 1. A method for treating a chronic liver disease, comprising administering to a subject in need thereof an effective amount of compound (1) or a pharmaceutically acceptable salt or amino acid conjugate thereof. 2. The method of claim 1 , comprising administering compound (1). 3. The method of claim 1 , comprising administering a pharmaceutically acceptable salt of compound (1). 4. The method of claim 1 , comprising administering a pharmaceutically acceptable amino acid conjugate of compound (1). 5. The method of claim 4 , wherein the amino acid conjugate is glycine conjugate or sarcosine conjugate. 6. The method of claim 1 , wherein the chronic liver disease is primary biliary cirrhosis (PBC), cerebrotendinous xanthomatosis (CTX), primary sclerosing cholangitis (PSC), drug induced cholestasis, intrahepatic cholestasis of pregnancy, parenteral nutrition associated cholestasis (PNAC), bacterial overgrowth or sepsis associated cholestasis, autoimmune hepatitis, chronic viral hepatitis, alcoholic liver disease, nonalcoholic fatty liver disease (NAFLD), nonalcoholic steatohepatitis (NASH), liver transplant associated graft versus host disease, living donor transplant liver regeneration, congenital hepatic fibrosis, choledocholithiasis, granulomatous liver disease, intra- or extrahepatic malignancy, Sjogren's syndrome, Sarcoidosis, Wilson's disease, Gaucher's disease, hemochromatosis, or alphal-antitrypsin deficiency. 7. The method of claim 1 , wherein the chronic liver disease is nonalcoholic fatty liver disease (NAFLD). 8. The method of claim 1 , wherein the chronic liver disease is nonalcoholic steatohepatitis (NASH). 9. The method of claim 1 , wherein the chronic liver disease is primary biliary cirrhosis (PBC).
Drugs for specific purposes, not provided for in groups A61P1/00-A61P41/00 · CPC title
Normal steroids containing carbon, hydrogen, halogen or oxygen, not substituted in position 3 · CPC title
Drugs for disorders of the cardiovascular system · CPC title
Drugs for disorders of the metabolism (of the blood or the extracellular fluid A61P7/00) · CPC title
Anorexiants; Antiobesity agents · CPC title
Related publications grouped by family.
Answers are generated from the same data shown on this page.