Recent Advances in the Medicinal Chemistry of Liver X Receptors
Document Type
Article
Publication Title
Journal of Medicinal Chemistry
Abstract
Nuclear hormone receptors represent a large family of ligand-activated transcription factors that include steroid receptors, thyroid/retinoid receptors, and orphan receptors. Among nuclear hormone receptors, the liver X receptors have emerged as very important drug targets. These receptors regulate some of the most important metabolic functions, and they were also identified as anti-inflammatory transcription factors and regulators of the immune system. The development of drugs targeting liver X receptors continues to be a challenge, but advances in our knowledge of receptor structure and function move us forward, toward achieving this goal. This review highlights the latest advances in the development of synthetic LXR modulators in the primary literature from 2013 to 2017. In this review, we place great emphasis on the structure and function of LXRs because of their essential role in the drug design process. The structure-activity relationships of the most active and promising synthetic modulators are discussed.
First Page
10935
Last Page
10956
DOI
10.1021/acs.jmedchem.8b00045
Publication Date
12-27-2018
Recommended Citation
El-Gendy, Bahaa El Dien M.; Goher, Shaimaa S.; Hegazy, Lamees S.; Arief, Mohamed M.H.; and Burris, Thomas P., "Recent Advances in the Medicinal Chemistry of Liver X Receptors" (2018). Pharmaceutical and Administrative Sciences Faculty Publications. 94.
https://doi.org/10.1021/acs.jmedchem.8b00045
https://collections.uhsp.edu/pharm-admin-sciences_pubs/94