US2009118323A1PendingUtilityA1

Antitumor benzoylsulfonamides

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Assignee: MADER MARY MARGARETPriority: Nov 22, 2002Filed: Sep 11, 2007Published: May 7, 2009
Est. expiryNov 22, 2022(expired)· nominal 20-yr term from priority
C07D 333/54A61P 35/00C07D 495/04C07D 319/18C07C 2602/08C07C 2602/06C07D 277/64C07C 311/51C07D 209/30C07D 317/62C07D 317/44C07D 209/08C07D 307/79
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Claims

Abstract

The present invention provides antitumor compounds of the formula (I); and antitumor methods.

Claims

exact text as granted — not AI-modified
1 . A compound of Formula I: 
     
       
         
         
             
             
         
       
     
     where:
 A is phenyl, benzofuryl, cyclopentadienyl, cyclobutyl, or a cyclopentyl that is optionally substituted at one of the two carbons adjacent to the ring fusion of the cyclopentyl with an oxo moiety; 
 R 1  and R 2  are either both halo, both trifluoromethyl, or one is halo and the other is C 1 -C 6  alkyl; or 
 a pharmaceutically acceptable base addition salt thereof. 
 
   
   
       2 . The compound of  claim 1 , wherein the compound is a pharmaceutically acceptable base addition salt. 
   
   
       3 . The compound of  claim 2 , wherein the pharmaceutically acceptable base addition salt is a sodium salt. 
   
   
       4 . A method of treating susceptible neoplasms in a mammal comprising administering to a mammal in need of such treatment an oncolytically effective amount of a compound of Formula I: 
     
       
         
         
             
             
         
       
     
     where:
 A is phenyl, benzofuryl, cyclopentadienyl, cyclobutyl, or a cyclopentyl that is optionally substituted at one of the two carbons adjacent to the ring fusion of the cyclopentyl with an oxo moiety; 
 R 1  and R 2  are either both halo, both trifluoromethyl, or one is halo and the other is C 1 -C 6  alkyl; or 
 a pharmaceutically acceptable base addition salt thereof. 
 
   
   
       5 . A pharmaceutical formulation comprising a compound of Formula I: 
     
       
         
         
             
             
         
       
     
     where:
 A is phenyl, benzofuryl, cyclopentadienyl, cyclobutyl, or a cyclopentyl that is optionally substituted at one of the two carbons adjacent to the ring fusion of the cyclopentyl with an oxo moiety; 
 R 1  and R 2  are either both halo, both trifluoromethyl, or one is halo and the other is C 1 -C 6  alkyl; or 
 a pharmaceutically acceptable base addition salt thereof, and a pharmaceutically acceptable carrier, diluent, or excipient.

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