US2022143029A1PendingUtilityA1

Pharmaceutical composition for preventing and treating nonalcoholic steatohepatitis, hepatic fibrosis, and liver cirrhosis, comprising adenosine derivatives

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Assignee: FUTURE MEDICINE CO LTDPriority: Oct 31, 2016Filed: Jan 26, 2022Published: May 12, 2022
Est. expiryOct 31, 2036(~10.3 yrs left)· nominal 20-yr term from priority
A61K 31/7076A61K 9/0053A61P 1/16A61K 9/48A61K 31/52A61K 47/38
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Claims

Abstract

An oral agent for preventing or treating liver disease is provided. The oral agent includes a compound represented by formula 1 below or a pharmaceutically acceptable salt of the compound as an active ingredient:where A is S, R is a linear or branched C1-C5 alkyl which is non-substituted or is independently or selectively substituted with one or more C6-C10 aryl groups, a benzyl which is non-substituted or is independently or selectively substituted with halogen or one or more linear or branched C1-C4 alkoxy groups, or a hydroxycarbonyl-substituted benzyl, and Y is H or a halogen atom.

Claims

exact text as granted — not AI-modified
What is claimed is: 
     
         1 . A method of treating a liver disease in a subject in need thereof, comprising:
 administering an oral agent comprising a compound represented by formula 1 below or a pharmaceutically acceptable salt of the compound to the subject:   
       
         
           
           
               
               
           
         
         where A is S, R is a linear or branched C 1 -C 5  alkyl which is non-substituted or is substituted with one or more C 6 -C 10  aryl groups, a benzyl which is non-substituted or is substituted with halogen or one or more linear or branched C 1 -C 4  alkoxy groups, or a hydroxycarbonyl-substituted benzyl, and Y is H or a halogen atom. 
       
     
     
         2 . The method of  claim 1 , wherein the oral agent further comprises a vehicle which comprises one or more of methyl cellulose (MC), dimethyl sulfoxide (DMSO), polyethylene glycol (PEG), and distilled water. 
     
     
         3 . The method of  claim 1 , wherein the compound represented by formula 1 or the pharmaceutically acceptable salt of the compound is filled in a powder state in a capsule. 
     
     
         4 . The method of  claim 1 , wherein the liver disease comprises one or more of NASH or NAFLD, liver fibrosis, and liver cirrhosis. 
     
     
         5 . The method of  claim 1 , wherein the formula 1 is a compound represented by formula A below:

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