US2007155801A1PendingUtilityA1

Advanced glycation end-product intermediaries and post-amadori inhibition

Assignee: UNIV KANSAS MEDICAL CENTERPriority: Sep 10, 1996Filed: Feb 20, 2007Published: Jul 5, 2007
Est. expirySep 10, 2016(expired)· nominal 20-yr term from priority
A61P 43/00C07C 215/50G01N 33/68A61K 38/06A61K 31/4415C07D 213/66G01N 2400/02C07K 5/0812G01N 33/6842A61K 31/435A61K 31/00A61K 38/07A61K 31/675A61K 31/506G01N 2500/04A61K 31/44A61K 38/05A61P 13/12C07K 5/06052C07K 5/06034A61K 31/04
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Claims

Abstract

The instant invention provides compositions and methods for modeling post-Amadori AGE formation and the identification and characterization of effective inhibitors of post-Amadori AGE formation, and such identified inhibitor compositions.

Claims

exact text as granted — not AI-modified
1 . A compound of the general formula:  
     
       
         
         
             
             
         
       
       wherein R 1  is CH 2 NH 2 , CH 2 SH, COOH, CH 2 CH 2 NH 2 , CH 2 CH 2 SH, or CH 2 COOH;  
       R 2  and R 6  is H, OH, SH, NH 2 , C 1-6 alkyl, alkoxy or alkene;  
       R 4  and R 5  are H, C 1-6 alkyl, alkoxy or alkene;  
       Y is N or C, such that when Y is N R 3  is nothing, and when Y is C, R 3  is NO 2  or another electron withdrawing group, and salts thereof, wherein said compound is not pyridoxamine.  
     
   
   
       2 . A pharmaceutical composition comprising a compound of  claim 1 , or salt thereof in a suitable carrier.  
   
   
       3 . A method for inhibiting post-Amadori AGE formation comprising administering an effective post-Amadori AGE inhibiting amount of a compound of  claim 1 .  
   
   
       4 . A method for treating a patient with AGE related pathology comprising administering an effective therapeutic amount of a compound of  claim 1.

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