Inhibitors for the soluble epoxide hydrolase
Inhibitors of the soluble epoxide hydrolase (sEH) are provided that incorporate multiple pharmacophores and are useful in the treatment of diseases.
1. A compound having a formula:
and its pharmaceutically acceptable salts, wherein
R 1 is selected from the group consisting of cyclohexyl, cycloheptyl, cyclooctyl, norbornyl, adamantyl, noradamantyl, and phenyl, wherein the phenyl group is either unsubstituted or substituted with from one to three substituents selected from the group consisting of halogen, lower alkyl, lower halo alkyl, lower alkoxy, lower haloalkoxy, C 3 -C 5 cycloalkyl and cyano;
P 1 is —NHC(O)NH—;
P 2 is selected from the group consisting of —C(O)—, —O(CH 2 CH 2 O) q —, and —C(O)O—;
P 3 is —C(O)OR 2 , wherein R 2 is a member selected from the group consisting of hydrogen, methyl and ethyl;
the subscripts n and m are each 1, and the subscript q is 0 to 6;
L 1 is cyclohexylene; and
L 2 is a phenylene.
2. The compound in accordance with claim 1 , wherein R 1 is phenyl substituted with from 1 to 3 substituents selected from the group consisting of halogen, methyl, isopropyl, methoxy, trifluoromethyl, and trifluoromethoxy.
3. The compound in accordance with claim 2 , wherein R 1 is 4-substituted phenyl.
4. The compound in accordance with claim 3 , wherein the R 1 is 4-trifluoromethoxyphenyl.
5. The compound in accordance with claim 1 , wherein P 2 is —O(CH 2 CH 2 O) q —; and wherein q is 0.
6. The compound in accordance with claim 1 , wherein L 1 is trans-substituted.
7. The compound in accordance with claim 1 , wherein L 2 is a 1,2-, 1,3-, or 1,4-linked phenylene.
8. The compound in accordance with claim 7 , wherein L 2 is a 1,3- or 1,4-linked phenylene.
9. The compound in accordance with claim 1 ,
R 1 is 4-trifluoromethoxyphenyl;
P 2 is —O—;
L 1 is 1,3- or 1,4-cyclohexylene; and
L 2 is a 1,3- or 1,4-linked phenylene.