Ex Parte Nair et al - Page 3


               Appeal No. 2006-1245                                                                          Page 3                  
               Application No. 10/294,106                                                                                            

               forth therein.  However, in response to a species election requirement, Appellants                                    
               elected to prosecute claims directed to in vivo treatment methods.  Office Action of                                  
               February 10, 2003, page 4.  Moreover, on page 2 of Appendix A of the Appeal Brief,                                    
               Appellants provide the parenthetical descriptor “(non elected species)” with the                                      
               recitation of claim 4.  Thus, because claim 4 is directed to in vitro inhibition of the COX-2                         
               enzyme, which is non-elected subject matter, claim 4 is not a part of this appeal.                                    
                       Claims 1, 3, 5, 15 and 16 are therefore the subject of this appeal, and read as                               
               follows:                                                                                                              
                       1. A method for selectively inhibiting COX2 enzyme relative to COX1                                           
                       enzyme in a system containing the enzymes which comprises providing an                                        
                       effective amount of at least one withanolide selected from the group consisting of                            
                       physagulin D  (1→6)-β-D-glucopyranosyl-(1→4)-β-D-glucopyranoside; 27-O-β-D-                                   
                       glucopyranosyl physagulin D; 27-O-β-D-glucopyranosyl viscosalactone B; 4, 16-                                 
                       dihydroxy-5β, 6β-epoxyphysagulin D; and, 4-(1-hydroxy-2,2-dimethylcyclo-                                      
                       propanone)-2, 3-dihydrowithaferin A so as to produce the COX2 inhibition.                                     
                       3. A method for selectively inhibiting COX2 enzyme relative to COX1                                           
                       enzyme which comprises providing an effective amount of at least one                                          
                       withanolide selected from the group consisting of physagulin D  (1→6)-β-D-                                    
                       glucopyranosyl-(1→4)-β-D-glucopyranoside; 27-O-β-D-glucopyranosyl                                             
                       physagulin D; 27-O-β-D-glucopyranosyl viscosalactone B; 4, 16-dihydroxy-5β,                                   
                       6β-epoxyphysagulin D; and, 4-(1-hydroxy-2,2-dimethylcyclo-propanone)-2, 3-                                    
                       dihydrowithaferin A in a pharmaceutically acceptable carrier in vivo to a mammal                              
                       in need thereof so as to produce the COX2 inhibition.                                                         
                       5. The method of claim 1 wherein the inhibition is in vivo in a mammal.                                       
                       15. A method for selectively inhibiting COX2 enzyme relative to COX1                                          
                       enzyme which comprises providing an effective amount of a compound selected                                   
                       from the group consisting of compounds physagulin D  (1→6)-β-D-                                               
                       glucopyranosyl-(1→4)-β-D-glucopyranoside; 27-O-β-D-glucopyranosyl                                             
                       physagulin D; 27-O-β-D-glucopyranosyl viscosalactone B; 4, 16-dihydroxy-5β,                                   
                       6β-epoxyphysagulin D; and, 4-(1-hydroxy-2,2-dimethylcyclo-propanone)-2,3-                                     
                       dihydrowithaferin A; and, mixtures thereof and a compound selected from the                                   
                       group consisting of 2, 3-dihydrowithaferin A; viscosalactone B; 23, 24-                                       
                       dihydrowithaferin A; sitoindoside IX; physagulin D; withanoside IV; withaferin A;                             






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