US2015344420A1PendingUtilityA1

Paclitaxel enhancer compounds

Assignee: SYNTA PHARMACEUTICALS CORPPriority: Jul 10, 2001Filed: Aug 14, 2015Published: Dec 3, 2015
Est. expiryJul 10, 2021(expired)· nominal 20-yr term from priority
A61P 43/00A61P 35/00A61K 31/16C07D 407/12C07C 2601/08A61K 31/165C07D 209/42C07C 327/56C07D 305/14A61K 31/381C07C 2601/14C07C 2601/04C07D 333/68A61K 31/337A61K 31/505C07D 213/83C07D 261/18C07D 209/44C07D 333/38C07D 307/68A61K 31/53A61K 31/277A61K 47/58A61K 31/5377C07C 2601/02A61K 31/44C07C 2101/14A45D 8/006
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Claims

Abstract

Disclosed is a compound represented by the Structural Formula (I): Y is a covalent bond, a phenylene group or a substituted or unsubstituted straight chained hydrocarbyl group. In addition, Y, taken together with both >C═Z groups to which it is bonded, is a substituted or unsubstituted aromatic group. Preferably, Y is a covalent bond or —C(R 7 R 8 )—. R 1 and R 2 are independently an aryl group or a substituted aryl group, R 3 and R 4 are independently —H, an aliphatic group, a substituted aliphatic group, an aryl group or a substituted aryl group. R 5 -R 6 are independently —H, an aliphatic group, a substituted aliphatic group, an aryl group or a substituted aryl group. R 7 and R 8 are each independently —H, an aliphatic or substituted aliphatic group, or R 7 is —H and R 8 is a substituted or unsubstituted aryl group, or, R 7 and R 8, taken together, are a C2-C6 substituted or unsubstituted alkylene group. Z is ═O or ═S. Also disclosed are pharmaceutical compositions comprising the compound of the present invention and a pharmaceutically acceptable carrier or diluent. Also disclosed is a method of treating a subject with cancer by administering to the subject a compound of Structural Formula (I) in combination with Paclitaxel or an analog of Paclitaxel.

Claims

exact text as granted — not AI-modified
What is claimed is: 
     
         1 . A compound represented by the following structural formula: 
       
         
           
           
               
               
           
         
       
       or a pharmaceutically acceptable salt thereof, wherein:
 Y is a covalent bond, a phenylene group or a substituted or unsubstituted straight chained hydrocarbyl group, or, Y, taken together with both >C═Z groups to which it is bonded, is a substituted or unsubstituted aromatic group; 
 R 1  and R 2  are independently an aryl group or a substituted aryl group; 
 R 3  and R 4  are independently —H, an aliphatic group, a substituted aliphatic group, an aryl group or a substituted aryl group; 
 R 5 -R 6  are independently —H, an aliphatic group, a substituted aliphatic group, an aryl group or a substituted aryl group; and 
 Z is ═O or ═S; 
 provided that when Y is —CH 2 —, R 3  and R 4  are both phenyl and R 5 -R 6  are all —H, then R 1  and R 2  are not both phenyl.

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