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US 2014/0371190 A1Published application
Farnesoid X receptor modulators
AssigneeIntercept Pharmaceuticals, Inc.
InventorRoberto Pellicciari
Life of this patent
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Abstract
The present invention provides a compound of formula (I): or a pharmaceutically acceptable salt, solvate, or amino acid conjugate thereof, wherein R1, R2, R3, R4, R5, and R6 are as described herein. The present invention relates generally to selective FXR agonists and to methods of making and using them.
Claims20
A compound of formula I:
- or a pharmaceutically acceptable salt, solvate, or amino acid conjugate thereof, wherein:
- R1 is hydroxyl;
- R2 is hydrogen, hydroxyl, alkyl, or halogen, wherein said alkyl is unsubstituted or substituted with one or more Ra;
- R3 is hydrogen, hydroxyl, alkyl, or halogen, wherein said alkyl is unsubstituted or substituted with one or more Rb;
- R4 is hydrogen, alkyl, alkenyl, alkynyl, or halogen, wherein said alkyl is unsubstituted or substituted with one or more Rc;
- Ra, Rb, and Rc are each independently halogen or hydroxyl;
- R5 is hydroxyl, OSO3H, OSO3−, OCOCH3, OPO3H, OPO32−, or hydrogen;
- and
- R6 is hydroxyl, OSO3H, OSO3−, OCOCH3, OPO3H, OPO32−, or hydrogen;
- or taken together R5 and R6 with the carbon atom to which they are attached form a carbonyl.
7 more elements
A compound having the following formula:
- or a pharmaceutically acceptable salt, solvate, or amino acid conjugate thereof.
Dependencies are inferred from the claim text.