Beyond Bile Acids: Targeting Farnesoid X Receptor (FXR) with Natural and Synthetic Ligands

Author(s): Andrea Carotti, Maura Marinozzi, Chiara Custodi, Bruno Cerra, Roberto Pellicciari, Antimo Gioiello, Antonio Macchiarulo

Journal Name: Current Topics in Medicinal Chemistry

Volume 14 , Issue 19 , 2014

Become EABM
Become Reviewer
Call for Editor

Graphical Abstract:


The modulation of FXR receptor remains an attractive area in drug discovery to develop novel therapeutic opportunities for liver and metabolic disorders. Despite the large variety of FXR ligands reported so far, only a very restricted number of agonists have entered in clinical settings. In this review article we provide the reader with an overview on the different classes of natural and synthetic ligands that have been developed by academic groups and pharmaceutical companies to target FXR. We discuss their structure-activity relationships, analyzing the binding modes that some of these compounds adopt to interact with the receptor.

Keywords: Bile acid homeostasis, Farnesoid X receptor, Natural ligands, Nuclear receptors, Synthetic ligands.

Rights & PermissionsPrintExport Cite as

Article Details

Year: 2014
Published on: 24 November, 2014
Page: [2129 - 2142]
Pages: 14
DOI: 10.2174/1568026614666141112094058
Price: $65

Article Metrics

PDF: 94