Back to results
US 2021/0228599 A1Published application
Farnesoid x receptor modulators
AssigneeIntercept Pharmaceuticals, Inc.
InventorRoberto PELLICCIARI
Life of this patent
Estimating the term…
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.
Claims17
A method of treating fibrosis or one or more symptoms of intrahepatic cholestasis or extrahepatic cholestasis in a subject in need thereof, comprising administering to the subject an effective amount of 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 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, OPO3H2, OPO32−, or hydrogen;
- and
- R6 is hydroxyl, OSO3H, OSO3−, OCOCH3, OPO3H2, OPO32−, or hydrogen;
- or taken together R5 and R6 with the carbon atom to which they are attached form a carbonyl.
7 more elements
Dependencies are inferred from the claim text.