Heterocyclic containing cyclopropyl FXR modulators
The present technology is directed to compounds of formula (II) as well as compositions thereof and methods related to modulation of FXR. In particular, the present compounds and compositions may be used to treat FXR-mediated disorders and conditions, including, e.g., liver disease, hyperlipidemia, hypercholesteremia, obesity, metabolic syndrome, cardiovascular disease, gastrointestinal disease, and atherosclerosis, and renal disease.
1. A compound according to formula (II):
stereoisomers, and/or salts thereof; wherein
W is
X is a substituted or unsubstituted aryl or heteroaryl group;
Y is a substituted or unsubstituted phenyl or pyridyl group;
Z is CH or N;
R 1 and R 2 are independently H, OH, halo, CN, carboxyl, NR a R b , or a substituted or unsubstituted alkyl, alkoxy, or hydroxyalkyl group;
R 3 is a substituted or unsubstituted alkyl or cycloalkyl group;
R 4 is CN, SO 3 H, CONR a R b , SO 2 NR a R b , NHSO 2 R b , SO 2 NHCOR a , CO 2 R c , or a substituted or unsubstituted tetrazolyl or 1,2,4-oxadiazol-5(4H)-one-3-yl group;
R 5 is CN or C 1 -C 3 alkyl group and R 6 is H; R 5 is H and R 6 is CN or C 1 -C 3 alkyl group; or R 5 and R 6 are independently CN or C 1 -C 3 alkyl group;
R 10 at each occurrence is independently halo, or a substituted or unsubstituted alkyl, alkoxy, cycloalkyl, or fluorinated cycloalkyl group;
R a at each occurrence is independently H, or a substituted or unsubstituted alkyl, haloalkyl, cycloalkyl, aryl, alkylene-R d , or SO 2 -alkyl group;
R b at each occurrence is H or a substituted or unsubstituted alkyl, or haloalkyl group;
R c is H or a substituted or unsubstituted alkyl, alkenyl, alkynyl, or cycloalkyl group;
R d is CO 2 H, OH, or SO 3 H;
R g and R h at each occurrence are independently H or a substituted or unsubstituted C 1 -C 6 alkyl group; and
n is 0, 1, 2, 3, or 4.
2. The compound of claim 1 wherein W is
3. The compound of claim 1 wherein W is
4. The compound of claim 1 , wherein Z is N.
5. The compound of claim 1 , wherein W is
6. The compound of claim 1 , wherein R 4 is CO 2 H, CONH 2 , SO 2 NH 2 , or a substituted or unsubstituted CO 2 —C 1 -C 6 alkyl, CO 2 —C 3 -C 6 cycloalkyl, CONH—C 1 -C 6 alkyl, CONH—C 3 -C 6 cycloalkyl, or NH—SO 2 —C 1 -C 6 alkyl group.
7. The compound of claim 6 , wherein R 4 is CO 2 H, CONH 2 , or a substituted or unsubstituted CO 2 —C 1 -C 6 alkyl, or CONH—C 1 -C 6 alkyl group.
8. The compound of claim 6 , wherein R 4 is CO 2 H or CONH—C 1 -C 6 alkyl wherein the C1-C6 alkyl is substituted with SO 3 H.
9. The compound of claim 1 , wherein Y is a phenyl or pyridyl group substituted with one or two substituents independently selected from the group consisting of C 1 -C 6 alkyl, C 3 -C 6 cycloalkyl, C 1 -C 6 haloalkyl, and halo.
10. The compound of claim 9 , wherein Y is phenyl group substituted with one or two substituents independently selected from the group consisting of F, Cl, and CF 3 groups.
11. The compound of claim 1 , wherein R 1 and R 2 are independently H, halo, CN, CO 2 H, NR e R f , or a substituted or unsubstituted C 1 -C 6 alkyl, C 1 -C 6 alkoxy, or C 1 -C 6 hydroxyalkyl group; and wherein R e and R f at each occurrence are independently H or a substituted or unsubstituted C 1 -C 6 alkyl group.
12. The compound of claim 11 , wherein R 1 and R 2 are independently H, F, Cl, CN, NR e R f , or a substituted or unsubstituted C 1 -C 3 alkyl, C 1 -C 3 alkoxy, or C 1 -C 3 hydroxyalkyl group.
13. The compound of claim 11 , wherein R 1 and R 2 are independently H, F, Cl OCHF 2 , OCF 3 , CN, NH 2 , CH 3 , CH 2 NH 2 , or OCH 3 .
14. The compound of claim 11 , wherein R 1 and R 2 are both Cl, or R 1 is H and R 2 is Cl, OCF 3 or OCHF 2 .
15. The compound of claim 1 , wherein R 3 is a substituted or unsubstituted C 1 -C 6 alkyl or C 3 -C 6 cycloalkyl group.
16. The compound of claim 15 , wherein R 3 is CH 3 , CH 2 CH 3 , CH(CH 3 ) 2 , CH 2 CH(CH 3 ) 2 , CH(CH 2 CH 3 ) 2 , CH(CH 2 CH 3 )(CH 3 ), C(CH 3 ) 3 , or cyclopropyl.
17. The compound of claim 1 , wherein R 5 is CN or CH 3 ; and R 6 is H.
18. The compound of claim 1 , wherein R 6 is CN or CH 3 ; and R 5 is H.
19. The compound of claim 1 , wherein the compound has the structure IIIA:
20. The compound of claim 1 , wherein X is
wherein:
R 13 is H, halo, or a substituted or unsubstituted C 1 -C 6 alkyl, or O—(C 1 -C 6 alkyl) group;
R 14 at each occurrence is independently halo, CF 3 , or a substituted or unsubstituted alkyl, or alkoxy group;
R 15 is H or a substituted or unsubstituted C 1 -C 6 alkyl group;
m is 0, 1, 2, or 3;
p is 0, 1, 2, 3, or 4;
s is 0, 1, or 2; and
t is 0 or 1.
21. The compound of claim 20 , wherein R 13 is an unsubstituted O—(C 1 -C 3 alkyl) group.
22. The compound of claim 20 wherein m, p, s, or t is 0.
23. A composition comprising the compound of claim 1 and a pharmaceutically acceptable carrier.
24. A pharmaceutical composition comprising an effective amount of the compound of claim 1 for treating a liver disease selected from the group consisting of primary biliary cirrhosis (PBC), cerebrotendinous xanthomatosis (CTX), primary sclerosing cholangitis (PSC), nonalcoholic fatty liver disease (NAFLD), nonalcoholic steatohepatitis (NASH), liver fibrosis, and liver cirrhosis.
25. A method for treating a liver disease selected from the group consisting of primary biliary cirrhosis (PBC), cerebrotendinous xanthomatosis (CTX), primary sclerosing cholangitis (PSC), nonalcoholic fatty liver disease (NAFLD), nonalcoholic steatohepatitis (NASH), liver fibrosis, and liver cirrhosis comprising administering an effective amount of a compound of claim 1 , or administering a pharmaceutical composition comprising an effective amount of a compound of claim 1 , to a subject in need thereof.
26. A method for activating FXR comprising contacting FXR with an effective amount of a compound of claim 1 .
27. The compound of claim 9 , wherein the C 1 -C 6 haloalkyl substituent is CF 3 .