Carboline derivatives useful in the inhibition of angiogenesis
View Patent ↗In accordance with the present invention, compounds that inhibit the expression of VEGF post-transcriptionally have been identified, and methods for their use provided. In one aspect of the invention, compounds useful in the inhibition of VEGF production, in the inhibition of angiogenesis, and/or in the treatment of cancer, diabetic retinopathy or exudative macular degeneration are provided. In another aspect of the invention, methods are provided for the inhibition of VEGF production, the inhibition of angiogenesis, and/or the treatment of cancer, diabetic retinopathy or exudative macular degeneration using the compounds of the invention.
1. A compound having the formula:
or a pharmaceutically acceptable salt, racemate or stereoisomer thereof, wherein,
X is halogen;
R o is halogen, substituted or unsubstituted C 1 to C 8 alkyl or OR a ;
R a is H or C 1 to C 8 alkyl optionally substituted with one or more substituents independently selected from hydroxyl and halogen; and
R d is phenyl substituted with one or more alkoxy or halogen substituents.
2. The compound of claim 1 having the formula:
or a pharmaceutically acceptable salt, racemate or stereoisomer thereof, wherein,
X is halogen;
R o is OR a ;
R a is H or C 1 to C 8 alkyl optionally substituted with one or more substituents independently selected from hydroxyl and halogen; and
R d is phenyl substituted with one or more alkoxy or halogen substituents.
3. The compound of claim 1 having the formula:
or a pharmaceutically acceptable salt, racemate or stereoisomer thereof, wherein,
X is halogen;
R a is H or C 1 to C 8 alkyl optionally substituted with one or more substituents independently selected from hydroxyl and halogen; and
R d is phenyl substituted with one or more halogen substituents.
4. The compound of claim 1 having the formula:
or a pharmaceutically acceptable salt, racemate or stereoisomer thereof, wherein,
X is halogen;
R a is C 1 to C 8 alkyl optionally substituted with one or more substituents independently selected from hydroxyl and halogen; and
R d is phenyl substituted at the para position with a halogen substituent.
5. The compound of claim 4 , or a pharmaceutically acceptable salt, racemate or stereoisomer thereof, wherein X is chloro.
6. The compound of claim 5 , or a pharmaceutically acceptable salt, racemate or stereoisomer thereof, wherein R d is phenyl substituted at the para position with chloro.
7. The compound of claim 6 , or a pharmaceutically acceptable salt, racemate or stereoisomer thereof, wherein R a is unsubstituted C 1 to C 8 alkyl.
8. The compound of claim 6 , or a pharmaceutically acceptable salt, racemate or stereoisomer thereof, wherein R a is C 1 to C 8 alkyl substituted with one or more hydroxyl substituents.
9. A pharmaceutical composition comprising a compound having the formula:
or a pharmaceutically acceptable salt, racemate or stereoisomer thereof, wherein,
X is halogen;
R o is halogen, substituted or unsubstituted C 1 to C 8 alkyl or OR a ;
R a is H or C 1 to C 8 alkyl optionally substituted with one or more substituents independently selected from hydroxyl and halogen; and
R d is phenyl substituted with one or more alkoxy or halogen substituents,
and a pharmaceutically acceptable excipient.
10. The pharmaceutical composition of claim 9 , wherein the compound has the formula:
or a pharmaceutically acceptable salt, racemate or stereoisomer thereof, wherein,
X is halogen;
R o is OR a ;
R a is H or C 1 to C 8 alkyl optionally substituted with one or more substituents independently selected from hydroxyl and halogen; and
R d is phenyl substituted with one or more alkoxy or halogen substituents.
11. The pharmaceutical composition of claim 10 , wherein the compound has the formula:
or a pharmaceutically acceptable salt, racemate or stereoisomer thereof, wherein,
X is halogen;
R a is H or C 1 to C 8 alkyl optionally substituted with one or more substituents independently selected from hydroxyl and halogen; and
R d is phenyl substituted with one or more halogen substituents.
12. The pharmaceutical composition of claim 11 , wherein the compound has the formula:
or a pharmaceutically acceptable salt, racemate or stereoisomer thereof, wherein,
X is halogen;
R a is C 1 to C 8 alkyl optionally substituted with one or more substituents independently selected from hydroxyl and halogen; and
R d is phenyl substituted at the para position with a halogen substituent.
13. The pharmaceutical composition of claim 12 , wherein X is chloro.
14. The pharmaceutical composition of claim 13 , wherein R d is phenyl substituted at the para position with chloro.
15. The pharmaceutical composition of claim 14 , wherein R a is unsubstituted C 1 to C 8 alkyl.
16. The pharmaceutical composition of claim 14 , wherein R a is C 1 to C 8 alkyl substituted with one or more hydroxyl substituents.
17. The compound of either of claim 1 or 2 , wherein said compound has a chiral carbon at the point of attachment of the R o substituted phenyl and said compound is an (S) isomer at said chiral carbon.
18. The compound of any of claims 3 - 8 wherein said compound has a chiral carbon at the point of attachment of the OR a substituted phenyl and said compound is an (S) isomer at said chiral carbon.
19. The pharmaceutical composition of either of claim 9 or 10 , wherein said compound has a chiral carbon at the point of attachment of the R o substituted phenyl and said compound is an (S) isomer at said chiral carbon.
20. The pharmaceutical composition of any of claims 11 - 16 wherein said compound has a chiral carbon at the point of attachment of the OR a substituted phenyl and said compound is an (S) isomer at said chiral carbon.
21. A compound, wherein said compound is selected from the group consisting of:
or a pharmaceutically acceptable salt thereof, wherein said compound has a chiral carbon at the point of attachment of the phenyl ring directly attached to the tricyclic core and said compound is an (S) isomer at said chiral carbon.
22. The compound of claim 21 , wherein said compound is:
or a pharmaceutically acceptable salt thereof.
23. A pharmaceutical composition comprising a compound of claim 21 or 22 or a pharmaceutically acceptable salt thereof and a pharmaceutically acceptable excipient.