Stilbene analogs and methods of treating cancer
Stilbene analogs and pharmaceutical compositions that are useful for the treatment of various cancers, including without limitation, colorectal cancer (CRC) and breast cancer are disclosed. Such stilbene analogs include, for example, compounds of the following formula: wherein R a , R b , R 4 , R 6 , R 7 , R 9 and R 10 are all H; R 2 and R 3 are independently H, halo, amino, alkylamino, dialkylamino, N-oxides of dialkylamino, arylalkylamino, trialkylammonium, mercapto, alkylthio, alkanoyl, nitro, nitrosyl, cyano, alkoxy, alkenyloxy, aryl, heteroaryl, sulfonyl, sulfonamide, CONR 11 R 12 , NR 11 CO(R 13 ), NR 11 COO(R 13 ) or NR 11 CONR 12 R 13 ; R 11 , R 12 and R 13 , are independently, H, alkyl, aryl, heteroaryl or a fluorine; R 8 is NR C R d Z wherein R c is H, alkyl, alkoxy, aryl or heteroaryl, R d is an alkyl group, Z is a an unshared pair of electrons, H, alkyl or oxygen; and R 1 and R 5 are halogen.
1. A compound according to formula (II):
or a pharmaceutically acceptable salt thereof, wherein R a , R b , R 4 , R 6 , R 7 , R 9 , R 10 are all H; R 2 and R 3 are independently H, halo, amino, alkylamino, dialkylamino, N-oxides of dialkylamino, arylalkylamino, trialkylammonium, mercapto, alkylthio, alkanoyl, nitro, nitrosyl, cyano, alkoxy, alkenyloxy, aryl, heteroaryl, sulfonyl, sulfonamide, CONR 11 R 12 , NR 11 CO(R 13 ), NR 11 COO(R 13 ), NR 11 CONR 12 R 13 ; R 11 , R 12 and R 13 , are independently, H, alkyl, aryl, heteroaryl or a fluorine; R 8 is NR c R d Z wherein R c is H, alkyl, alkoxy, aryl, heteroaryl, R d is an alkyl group, Z is a an unshared pair of electrons, H, alkyl, oxygen; and R 1 and R 5 are halogen.
2. The compound according to claim 1 , wherein the compound is selected from the group consisting of (E)-4-(2,6-Difluorostyryl)-N,N-dimethylaniline; (E)-4-(2,6-Difluorostyryl)-N,N-diethylaniline; (E)-4-(2-chloro-6-fluorostyryl)-N,N-dimethylaniline; (E)-4-(2,6-dichlorostyryl) -N,N-dimethylaniline; (E)-4-(2,6-difluorostyryl)-N-methylaniline; (E)-4-(2-chloro-6-fluorostyryl)-N-methylaniline; (E and Z)-4-(2,6-dichlorostyryl)-N-methylaniline; (E)-4-(2,6-difluorostyryl)-N,N,N-trimethylbenzenammonium iodide; and
pharmaceutically acceptable salts thereof.
3. The compound according to claim 1 , wherein Z is O.
4. The compound according to claim 3 , wherein the compound is selected from the group consisting of (E)-4-(2,6-difluorostyryl)-N,N-dimethylaniline oxide; (E)-4-(2-chloro-6-fluorostyryl)-N,N-dimethylaniline oxide; (E)-4-(2,6-dichlorostyryl)-N,N-dimethylaniline oxide.
5. A composition comprising a compound according to formula (II):
or a pharmaceutically acceptable salt thereof, wherein R a , R b , R 4 , R 6 , R 7 R 9 , R 10 are all H; R 2 and R 3 are independently H, halo, amino, alkylamino, dialkylamino, N-oxides of dialkylamino, arylalkylamino, trialkylammonium, mercapto, alkylthio, alkanoyl, nitro, nitrosyl, cyano, alkoxy, alkenyloxy, aryl, heteroaryl, sulfonyl, sulfonamide, CONR 11 R 12 , NR 11 CO(R 13 ), NR 11 COO(R 13 ), NR 11 CONR 12 R 13 ; R 11 , R 12 and R 13 , are independently, H, alkyl, aryl, heteroaryl or a fluorine; R 8 is NR c R d Z wherein R c is H, alkyl, alkoxy, aryl, heteroaryl, R d is an alkyl group, Z is a an unshared pair of electrons, H, alkyl, oxygen; and R 1 and R 5 are halogen; and a pharmaceutically acceptable carrier.
6. The composition of claim 5 , wherein R 1 and R 5 are independently a chlorine or fluorine.
7. The composition according to claim 5 , wherein R 1 and R 5 are fluorine substituents and R d is lower alkyl group.
8. The composition of claim 5 , wherein R 1 is chlorine and R 5 is fluorine.
9. The composition of claim 5 , wherein R c is H or alkyl, R d is a lower alkyl group, and Z is a an unshared pair of electrons.
10. The compound of claim 1 , wherein R 1 and R 5 are independently a chlorine or fluorine.
11. The compound of claim 1 , wherein R 1 is chlorine and R 5 is fluorine.
12. The compound of claim 1 , wherein R c is H or alkyl, R d is a lower alkyl group, and Z is a an unshared pair of electrons.
13. The compound of claim 10 , wherein R c is H or alkyl, R d is a lower alkyl group, and Z is a an unshared pair of electrons.