Ex parte PLATT et al. - Page 4




          Appeal No. 1996-2537                                                        
          Application No. 08/102,654                                                  


          Getman, these compounds manifest glycosidase inhibition                     
          activity.  Getman illustrates the glycosidase inhibition                    
          activity of 1,4-dideoxy-4-fluoronojirimycin and N-butyl-1,4-                
          dideoxy-4-fluoronojirimycin (Table 1 at col. 14, and the                    
          accompanying text).  Getman                                                 





          discloses that “[i]t is contemplated that other N-derivatives               
          will also manifest glycosidase inhibition activity” (col. 12,               
          lines 61-66).                                                               
               D.  The examiner concludes that a person having ordinary               
          skill in the art at the time the invention was made would have              
          found it obvious to vary the length of the alkyl chain                      
          attached to the nitrogen-ring-atom of Legler's DGJ compound                 
          with the expectation that the resulting compounds would be                  
          useful in binding $-D-galactosidase from E.coli and $-D-                    
          glucosidase from almonds.  Answer, page 2, lines 18-23.                     
               E.  We agree with the examiner’s prima facie case of                   
          obviousness.  Legler’s N-heptyl-DGJ and the 1,4-dideoxy-4-                  


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