Antioxidant inflammation modulators: oleanolic acid derivatives with saturation in the C-ring
This invention provides, but is not limited to, novel oleanolic acid derivatives having the formula: wherein the variables are defined herein. Also provided are pharmaceutical compositions, kits and articles of manufacture comprising such compounds, methods and intermediates useful for making the compounds, and methods of using the compounds and compositions.
1. A compound of the formula:
wherein:
Y is cyano or —C(O)R a , wherein
R a is:
hydrogen, hydroxy, halo, amino, hydroxyamino, azido or mercapto; or
alkyl (C≦12) , alkenyl (C≦12) , alkynyl (C≦12) , aryl (C≦12) , aralkyl (C≦12) , heteroaryl (C≦12) , heteroaralkyl (C≦12) , alkoxy (C≦12) , alkenyloxy (C≦12) , alkynyloxy (C≦12) , aryloxy (C≦12) , aralkoxy (C≦12) , heteroaryloxy (C≦12) , heteroaralkoxy (C≦12) , acyloxy (C≦12) , alkylamino (C≦12) , dialkylamino (C≦12) , alkoxyamino (C≦12) , alkenylamino (C≦12) , alkynylamino (C≦12) , arylamino (C≦12) , aralkylamino (C≦12) , heteroarylamino (C≦12) , heteroaralkylamino (C≦12) , alkylsulfonylamino (C≦12) , amido (C≦12) , alkylthio (C≦12) , alkenylthio (C≦12) , alkynylthio (C≦12) , arylthio (C≦12) , aralkylthio (C≦12) , heteroarylthio (C≦12) , heteroaralkylthio (C≦12) , acylthio (C≦12) , alkylammonium (C≦12) , alkylsulfonium (C≦12) , alkylsilyl (C≦12) , or a substituted version of any of these groups;
X is OR b , NR b R c , or SR b , wherein R b and R c are each independently:
hydrogen;
alkyl (C≦8) , aryl (C≦8) , aralkyl (C≦8) , acyl (C≦8) , or a substituted version of any of these groups; or
provided that R b is absent when the atom to which it is bound is part of a double bond, further provided that when R b is absent the atom to which it is bound is part of a double bond; and
R 1 is:
hydrogen, cyano, hydroxy, halo or amino; or
alkyl (C≦8) , alkenyl (C≦8) , alkynyl (C≦8) , aryl (C≦8) , aralkyl (C≦8) , heteroaryl (C≦8) , heteroaralkyl (C≦8) , acyl (C≦8) , alkoxy (C≦8) , aryloxy (C≦8) , acyloxy (C≦8) , alkylamino (C≦8) , arylamino (C≦8) , amido (C≦8) , or a substituted version of any of these groups;
or a salt or tautomer thereof.
2. A compound of the formula:
wherein:
Y is cyano or —C(O)R a , wherein
R a is:
hydrogen, hydroxy, halo, amino, hydroxyamino, azido or mercapto; or
alkyl (C≦12) , alkenyl (C≦12) , alkynyl (C≦12) , aryl (C≦12) , aralkyl (C≦12) , heteroaryl (C≦12) , heteroaralkyl (C≦12) , alkoxy (C≦12) , alkenyloxy (C≦12) , alkynyloxy (C≦12) , aryloxy (C≦12) , aralkoxy (C≦12) , heteroaryloxy (C≦12) , heteroaralkoxy (C≦12) , acyloxy (C≦12) , alkylamino (C≦12) , dialkylamino (C≦12) , alkoxyamino (C≦12) , alkenylamino (C≦12) , alkynylamino (C≦12) , arylamino (C≦12) , aralkylamino (C≦12) , heteroarylamino (C≦12) , heteroaralkylamino (C≦12) , alkylsulfonylamino (C≦12) , amido (C≦12) , alkylthio (C≦12) , alkenylthio (C≦12) , alkynylthio (C≦12) , arylthio (C≦12) , aralkylthio (C≦12) , heteroarylthio (C≦12) , heteroaralkylthio (C≦12) , acylthio (C≦12) , alkylammonium (C≦12) , alkylsulfonium (C≦12) , alkylsilyl (C≦12) , or a substituted version of any of these groups;
X is OR b , NR b R c , or SR b , wherein R b and R c are each independently:
hydrogen;
alkyl (C≦8) , aryl (C≦8) , aralkyl (C≦8) , acyl (C≦8) , or a substituted version of any of these groups; or
provided that R b is absent when the atom to which it is bound is part of a double bond, further provided that when R b is absent the atom to which it is bound is part of a double bond; and
R 1 is:
hydrogen, cyano, hydroxy, halo or amino; or
alkyl (C≦8) , alkenyl (C≦8) , alkynyl (C≦8) , aryl (C≦8) , aralkyl (C≦8) , heteroaryl (C≦8) , heteroaralkyl (C≦8) , acyl (C≦8) , alkoxy (C≦8) , aryloxy (C≦8) , acyloxy (C≦8) , alkylamino (C≦8) , arylamino (C≦8) , amido (C≦8) , or a substituted version of any of these groups;
R′ is hydroxy, alkoxy (C≦12) , substituted alkoxy (C≦12) , aryloxy (C≦12) , substituted aryloxy (C≦12) , aralkoxy (C≦12) , substituted aralkoxy (C≦12) , acyloxy (C≦12) , or substituted acyloxy (C≦12) ;
or a salt or tautomer thereof.
3. The compound of claim 1 , wherein Y is cyano.
4. The compound of claim 1 , wherein Y is —C(O)R a .
5. The compound of claim 1 , wherein X is OR b .
6. The compound of claim 5 , wherein R b is absent.
7. The compound of claim 5 , wherein R b is hydrogen.
8. The compound of claim 4 , wherein R a is hydroxy.
9. The compound of claim 4 , wherein R a is alkoxy (C≦6) , aryloxy (C≦8) , aralkyloxy (C≦8) , or a substituted version of any of these groups.
10. The compound of claim 9 , wherein R a is alkoxy (C1-2) or substituted alkoxy (C1-2) .
11. The compound of claim 10 , wherein R a is methoxy.
12. The compound of claim 4 , wherein R a is amino.
13. The compound of claim 4 , wherein R a is alkylamino (C1-6) , alkoxyamino (C1-6) , arylamino (C1-8) , aralkylamino (C1-8) , dialkylamino (C2-8) , or a substituted version of any of these groups.
14. The compound of claim 13 , wherein R a is substituted alkylamino (C1-3) .
15. The compound of claim 14 , wherein R a is 2,2,2-trifluoroethylamino.
16. The compound of claim 1 , wherein R 1 is —H.
17. The compound of claim 2 , wherein R′ is acetyloxy.
18. The compound of claim 2 , wherein R′ is hydroxy.
19. The compound of claim 1 , further defined as:
substantially free from other optical isomers thereof.
20. The compound of claim 1 , further defined as:
Or a salt or tautomer thereof.
21. The compound of claim 2 , further defined as:
substantially free from other optical isomers thereof.