Heterocyclic lsf inhibitors and their uses

Abstract

The present invention is directed to heterocyclic SV40 Factor (LSF) inhibitors and their uses. In some implementations, the present invention discloses small-molecule compounds of Formula (I). In some implementations, the compounds of Formula (I) are used in methods for inhibiting LSF in a subject. In some implementations, the compounds of Formula (I) are used in methods for treating cancer in a subject.

What is claimed is: 
     
         1 . A compound of Formula (I): 
       
         
           
           
               
               
           
         
         or enantiomers, prodrugs, derivatives, and pharmaceutically acceptable salts thereof, and 
         none, one, or more vicinal pairs of R 1 , R 2 , R 3 , R 4 , R 5 , R 6 , R 7 , R 8 , and R 9  each, together with the carbons to which they are attached, form a 5-8 membered cycloalkyl or heterocyle ring; and
 the remaining R 1 , R 2 , R 3 , R 4 , R 5 , R 6 , R 7 , R 8 , or R 9  are each independently selected from the group consisting of hydrogen, halogen, OR 1A , N 1A R 2A , SR 1A , SO 2 R 1A , —NO 2 , C 1 -C 6  alkyl, C 1 -C 6  haloalkyl, C 1 -C 6  heteroalkyl, C 2 -C 8 alkenyl, aryl, and heteroaryl; 
 
         R 10  is hydrogen, C 1 -C 6  alkyl, C 1 -C 6  haloalkyl, C 1 -C 6  heteroalkyl, C 2 -C 8 alkenyl, aryl, heteroaryl, or halogen; or R 10  and one of the vicinal R 11  or R 12  groups together form a double bond between the carbon atoms they are attached to; 
         none or a vicinal pair of R 11 , R 12 , R 13  and R 14  together form a double bond between the carbon atoms they are attached to and the remaining R 11 , R 12 , R 13  and R 14  are each independently selected from the group consisting of hydrogen, halogen, C 1 -C 6  alkyl, C 1 -C 6  haloalkyl, C 1 -C 6  heteroalkyl, C 2 -C 8 alkenyl, OR 3A , SR 3A , SO 2 R 3A , N 3A R 4A , heteroaryl, and aryl; or
 one or two of a germinal pair of R 11 , R 12 , R 13  and R 14  together form a carbonyl (═O) and the remaining R 11 , R 12 , R 13  and R 14  are each independently selected from the group consisting of hydrogen, halogen, C 1 -C 6  alkyl, C 1 -C 6  haloalkyl, C 1 -C 6  heteroalkyl, C 2 -C 8 alkenyl, OR 3A , SR 3A , SO 2 R 3A , N 3A R 4A , halogen, heteroaryl, and aryl; 
 
         wherein,
 R 1A , R 2A , R 3A  and R 4A  are each independently selected from the group consisting of hydrogen, C 1 -C 8  alkyl, C 2 -C 8  alkenyl, C 2 -C 8  alkynyl, cycloalkyl, heterocyclyl, C 1 -C 8  haloalkyl, C 1 -C 8  heteroalkyl, heteroaryl, and aryl, wherein the alkyl, alkenyl, alkynyl, cycloalkyl, heterocyclyl, haloalkyl, heteroalkyl, heteroaryl, and aryl can be optionally substituted with halogen, C 1 -C 4  alkyl, C 1 -C 4  haloalkyl, C 1 -C 4  heteroalkyl or C 1 -C 6  alkoxy, and 
 any of the 5-8 membered cycloalkyl, the heterocyle ring, the alkyl, the haloalkyl, the heteroalkyl, the alkenyl, the heteroaryl, and the aryl can be optionally substituted with halogen, C 1 -C 6  alkyl, C 1 -C 6  haloalkyl, C 1 -C 6  heteroalkyl, C 1 -C 6  alkoxy, C 2 -C 8  alkenyl, amino (NH 2 ), mono(C 1 -C 6  alkyl)amino or di(C 1 -C 6  alkyl)amino. 
 
       
     
     
         2 . The compound according to  claim 1 , wherein at least one germinal pair of R 11 , R 12 , R 13  and R 14  together forms a carbonyl (═O). 
     
     
         3 . The compound according to  claim 1 , wherein at least one vicinal pair of R 10  and R 12 , or R 12  and R 14  together form a double bond between the carbon atoms they are attached to. 
     
     
         4 . The compound according to  claim 1 , wherein R 7  and R 8  together with the carbons to which they are attached, form a 5-8 membered cycloalkyl or heterocycle ring. 
     
     
         5 . The compound of  claim 1 , wherein the compound is of Formula (IA): 
       
         
           
           
               
               
           
         
         wherein 
         n is 1, 2 or 3; and 
         R 7′  and R 8′  independently are hydrogen or halogen. 
       
     
     
         6 . The compound of  claim 5 , wherein n is 1 or 2. 
     
     
         7 . The compound of  claim 5 , wherein R 7′  is H or F. 
     
     
         8 . The compound of  claim 5 , wherein R 8′  is H or F. 
     
     
         9 . The compound of  claim 1 , wherein R 6  is hydrogen, halogen, OR 1A , NR 1A R 2A , SR 1A , or C 1 -C 6  alkyl. 
     
     
         10 . The compound of  claim 9 , wherein R 6  is hydrogen, halogen or OR 1A . 
     
     
         11 . The compound of  claim 1 , wherein R 9  is hydrogen, halogen, OR 1A , NR 1A R 2A , SR 1A , or C 1 -C 6  alkyl. 
     
     
         12 . The compound of  claim 11 , wherein R 9  is hydrogen, halogen or OR 1A . 
     
     
         13 . The compound of  claim 1 , wherein R 10  is hydrogen or C 1 -C 6  alkyl. 
     
     
         14 . The compound of  claim 1 , wherein R 1  is hydrogen, halogen, OR 1A , NR 1A R 2A , SR 1A , C 1 -C 6 alkyl or —NO 2 . 
     
     
         15 . The compound of  claim 14 , wherein R 1  is O(C 1 -C 6  alkyl). 
     
     
         16 . The compound of  claim 1 , wherein R 2  is hydrogen, halogen, OR 1A  NR 1A R 2A , SR 1A , C 1 -C 6 alkyl or —NO 2 . 
     
     
         17 . The compound of  claim 16 , wherein R 2  is hydrogen or halogen. 
     
     
         18 . The compound of  claim 1 , wherein R 3  is hydrogen, halogen, OR 1A , NR 1A R 2A , C 1 -C 6 alkyl, C 2 -C 8 alkenyl, or —NO 2 . 
     
     
         19 . The compound of  claim 18 , wherein R 3  is N(C 1 -C 6  alkyl) 2 , halogen or —NO 2 . 
     
     
         20 . The compound of  claim 1 , wherein R 4  is hydrogen, halogen, OR 1A  NR 1A R 2A , SR 1A , C 1 -C 6 alkyl or —NO 2 . 
     
     
         21 . The compound of  claim 20 , wherein R 4  is hydrogen or halogen. 
     
     
         22 . The compound of  claim 1 , wherein R 5  is hydrogen, halogen, OR 1A  NR 1A R 2A , SR 1A , C 1 -C 6 alkyl or —NO 2 . 
     
     
         23 . The compound of  claim 22 , wherein R 5  is hydrogen or halogen. 
     
     
         24 . The compound of  claim 1 , wherein R 1  is O(C 1 -C 6  alkyl) and R 3  is N(C 1 -C 6  alkyl) 2 . 
     
     
         25 . The compound of  claim 1 , wherein R 2 , R 4  and R 5  are hydrogen. 
     
     
         26 . The compound of  claim 1 , wherein R 11  and R 12 , or R 13  and R 14  are hydrogen. 
     
     
         27 . The compound of  claim 1 , wherein the compound is 
       
         
           
           
               
               
           
         
       
     
     
         28 . A pharmaceutical composition comprising a compound of  claim 1  and a pharmaceutically acceptable excipient or carrier. 
     
     
         29 . A method for inhibiting LSF in a subject, the method comprising administering an effective amount of a compound of  claim 1  to a subject in need thereof. 
     
     
         30 . A method for treating cancer in a subject, the method comprising administering an effective amount of a compound of  claim 1  to a subject in need thereof.