US2003060506A1PendingUtilityA1

Bile secretion promoting composition

Assignee: SUCAMPO A GPriority: Apr 6, 2000Filed: Jul 18, 2002Published: Mar 27, 2003
Est. expiryApr 6, 2020(expired)· nominal 20-yr term from priority
A61P 7/08A61P 41/00A61P 1/18A61P 1/16A61K 31/5585A61K 31/5575A61K 31/558A61K 31/557
42
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Claims

Abstract

Disclosed is a method for promoting bile secretion, which comprises administering and effective amount of a certain 15-keto-prostaglandin compound to a subject having a disease or condition associated with bile secretion deficient. Also disclosed is a method for treatment of a liver to be transplanted in a liver transplantation process, which comprises contacting the liver with a liquid composition comprising the 15-keto-prostaglandin compound as above.

Claims

exact text as granted — not AI-modified
What is claimed is:  
     
         1 . A method for promoting bile secretion comprising administering an effective amount of a 15-keto-prostaglandin compound represented by the general formula (I):  
       
         
           
           
               
               
           
         
         wherein W 1 , W 2  and W 3  are carbon or oxygen atoms;  
         L, M and N are hydrogen, hydroxy, halogen, lower alkyl, lower alkoxy, hydroxy(lower)alkyl or oxo, wherein at least one of L and M is a group other than hydrogen, and the five-membered ring may have one or more double bond(s);  
         A is —CH 2 OH, —COCH 2 OH, —COOH or its functional derivative;  
         B is —CH 2 —CH 2 —, —CH═CH— or —C≡C—;  
         R 1  is a divalent saturated or unsaturated lower-medium aliphatic hydrocarbon residue, which is unsubstituted or substituted by halogen, alkyl, hydroxy, oxo, aryl or heterocyclic group; and  
         Ra is a saturated or unsaturated lower-medium aliphatic hydrocarbon residue, which is unsubstituted or substituted by halogen, oxo, hydroxy, lower alkyl, lower alkoxy, lower alkanoyloxy, cyclo(lower)alkyl, cyclo(lower)alkyloxy, aryl, aryloxy, heterocyclic group or heterocyclic-oxy group; cyclo(lower)alkyl; cyclo(lower)alkyloxy; aryl; aryloxy; heterocyclic group; or heterocyclic-oxy group, to a subject having a condition or disease associated with bile secretion deficient.  
       
     
     
         2 . The method of  claim 1 , wherein the 5-keto-prostaglandin compound is a 13,14-dihydro-15-keto-prostaglandin compound  
     
     
         3 . The method of  claim 1 , wherein the 5-keto-prostaglandin compound is a 15-keto-16-mono or di-halogen-prostaglandin compound.  
     
     
         4 . The method of  claim 1 , wherein the 5-keto-prostaglandin compound is a 13,14-dihydro-15-keto-16-mono or di-halogen-prostaglandin compound.  
     
     
         5 . The method of  claim 1 , wherein the 15-keto-prostaglandin compound is a 15-keto-16-mono or di-fluoro-prostaglandin compound.  
     
     
         6 . The method of  claim 1 , wherein the 15-keto-prostaglandin compound is a 13,14-dihydro-15-keto-16-mono or di-fluoro-prostaglandin compound.  
     
     
         7 . The method of  claim 1 , wherein the 15-keto-prostaglandin compound is a 15-keto-prostaglandin E compound.  
     
     
         8 . The method of  claim 1 , wherein the 15-keto-prostaglandin compound is 13,14-dihydro-15-keto-16,16-difluoro-18-methyl-prostaglandin E 1.    
     
     
         9 . The method of  claim 1 , wherein the 5-keto-prostaglandin compound is 13,14-dihydro-15-keto-16,16-difluoro-17-methyl-prostaglandin E 1 .  
     
     
         10 . A method for treating a liver to be transplanted in a liver transplantation process, which comprises contacting the liver with a liquid composition comprising a 15-keto-prostaglandin compound represented by the general formula (I):  
       
         
           
           
               
               
           
         
         wherein W 1 , W 2  and W 3  are carbon or oxygen atoms;  
         L, M and N are hydrogen, hydroxy, halogen, lower alkyl, lower alkoxy, hydroxy(lower)alkyl or oxo, wherein at least one of L and M is a group other than hydrogen, and the five-membered ring may have one or more double bond(s);  
         A is —CH 2 OH, —COCH 2 OH, —COOH or its functional derivative;  
         B is —CH 2 —CH 2 —, —CH═CH— or —C≡C—;  
         R 1  is a divalent saturated or unsaturated lower-medium aliphatic hydrocarbon residue, which is unsubstituted or substituted by halogen, alkyl, hydroxy, oxo, aryl or heterocyclic group; and  
         Ra is a saturated or unsaturated lower-medium aliphatic hydrocarbon residue, which is unsubstituted or substituted by halogen, oxo, hydroxy, lower alkyl, lower alkoxy, lower alkanoyloxy, cyclo(lower)alkyl, cyclo(lower)alkyloxy, aryl, aryloxy, heterocyclic group or heterocyclic-oxy group; cyclo(lower)alkyl; cyclo(lower)alkyloxy; aryl; aryloxy; heterocyclic group; or heterocyclic-oxy group.  
       
     
     
         11 . The method of  claim 10 , wherein the 15-keto-prostaglandin compound is a 13,14-dihydro-15-keto-prostaglandin compound.  
     
     
         12 . The method of  claim 10 , wherein the 15-keto-prostaglandin compound is a 15-keto-16-mono or dihalogen-prostaglandin compound.  
     
     
         13 . The method of  claim 10 , wherein the 15-keto-prostaglandin compound is a 13,14-dihydro-15-keto-16-mono or di-halogen-prostaglandin compound.  
     
     
         14 . The method of  claim 10 , wherein the 15-keto-prostaglandin compound is a 15-keto-16-mono or di-fluoro-prostaglandin compound.  
     
     
         15 . The method of  claim 10 , wherein the 15-keto-prostaglandin compound is a 13,14-dihydro-15-keto-16-mono or di-fluoro-prostaglandin compound.  
     
     
         16 . The method of  claim 10 , wherein the 15-keto-prostaglandin compound is a 15-keto-prostaglandin E compound.  
     
     
         17 . The method of  claim 10 , wherein the 15-keto-prostaglandin compound is 13,14-dihydro-15-keto-16,16-difluoro-18-methyl-prostaglandin E 1 .  
     
     
         18 . The method of  claim 10 , wherein the 15-keto-prostaglandin compound is 13,14-dihydro-15-keto-16,16-difluoro-17-methyl-prostaglandin E 1 .  
     
     
         19 . The method of  claim 10 , wherein the liquid composition is a preservation solution.  
     
     
         20 . The method of  claim 10 , wherein the liquid composition is a perfusate.  
     
     
         21 . The method of  claim 10 , wherein the liquid composition is a rinse solution.

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