US2005124646A1PendingUtilityA1

Tricyclo compounds, a process for their production and a pharmaceutical composition containing the same

Assignee: FUJISAWA PHARMACEUTICAL COPriority: Dec 3, 1984Filed: Nov 9, 2004Published: Jun 9, 2005
Est. expiryDec 3, 2004(expired)· nominal 20-yr term from priority
A61P 37/06A61P 37/00A61P 31/04A61P 31/00Y10S435/886Y02P20/55C12P 17/188C12P 19/44C07H 19/01Y10S435/898C07D 498/18C07H 17/00C12R 2001/55C12R 2001/465C12N 1/205
63
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Claims

Abstract

This invention relates to tricyclo compounds useful for treatment and prevention of resistance by transplantation, graft-versus-host diseases by medulla ossium transplantation, autoimmune diseases, infectious diseases, and the like, which can be represented by the following formula: to a process for their production, to a pharmaceutical composition containing the same and to a use thereof.

Claims

exact text as granted — not AI-modified
1 - 19 . (canceled)  
     
     
         20 . A method for suppressing Mixed Lymphocyte Reaction by using a compound of the formula:  
       
         
           
           
               
               
           
         
       
       wherein 
 R 1  is hydroxy or pharmaceutically acceptable protected hydroxy selected from the group consisting of 1-(lower alkylthio)(lower)alkyloxy, tri(lower)alkylsilyloxy, lower alkyl-diphenyl-siloxy, pharmaceutically acceptable organic carboxylic acyloxy, pharmaceutically acceptable organic sulfonic acyloxy, and pharmaceutically acceptable organic carbamic acyloxy,  
 R 2  is hydrogen or the same meanings as R 1 ,  
 R 3  is methyl, ethyl, propyl or allyl, n is an integer of 1 or 2, and  
 the symbol of a line and dotted line is a single bond or a double bond, or pharmaceutically acceptable basic salt thereof.  
 
     
     
         21 . The method of  claim 20 , wherein the compound is  
       
         
           
           
               
               
           
         
       
     
     
         22 . The method of  claim 20 , wherein the compound is  
       
         
           
           
               
               
           
         
       
     
     
         23 . The method of  claim 20 , wherein the compound is

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