Literature DB >> 17100573

Orphan nuclear receptors, excellent targets of drug discovery.

Yanhong Shi1.   

Abstract

To date, the pharmaceutical industry has placed a considerable amount of interest in the discovery of drug targets and diagnostics. One of the most challenging areas of drug discovery today is the search for novel receptor-ligand pairs. Nuclear receptors comprise a large superfamily of ligand-dependent transcription factors that regulate the expression of genes critical for a variety of biological processes, including development, growth, differentiation, and homeostasis. Orphan nuclear receptors, for which the ligands are not yet identified, represent the most ancient component of the nuclear receptor superfamily. Orphan nuclear receptors not only offer a unique system to uncover novel signaling pathways that impact human health, but also provide excellent targets of drug discoveries for a variety of human diseases. This review highlights advances made on ligand identification for orphan nuclear receptors using transgenic mouse models, cell-based screening, direct binding, structure-based assays, and computer-aided virtual screening. With rapid advances in combinatorial chemistry and high throughput screening, along with other modern technologies, this field promises a bountiful harvest.

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Year:  2006        PMID: 17100573     DOI: 10.2174/138620706778700125

Source DB:  PubMed          Journal:  Comb Chem High Throughput Screen        ISSN: 1386-2073            Impact factor:   1.339


  4 in total

Review 1.  Signaling through non-membrane nuclear phosphoinositide binding proteins in human health and disease.

Authors:  Jamal M Bryant; Raymond D Blind
Journal:  J Lipid Res       Date:  2018-09-10       Impact factor: 5.922

2.  Use of differential scanning fluorimetry as a high-throughput assay to identify nuclear receptor ligands.

Authors:  Kara DeSantis; Aaron Reed; Raneen Rahhal; Jeff Reinking
Journal:  Nucl Recept Signal       Date:  2012-02-27

Review 3.  In silico pharmacology for drug discovery: applications to targets and beyond.

Authors:  S Ekins; J Mestres; B Testa
Journal:  Br J Pharmacol       Date:  2007-06-04       Impact factor: 8.739

4.  Two- and three-dimensional quantitative structure-activity relationships studies on a series of liver x receptor ligands.

Authors:  Káthia M Honório; Lívia B Salum; Richard C Garratt; Igor Polikarpov; Adriano D Andricopulo
Journal:  Open Med Chem J       Date:  2008-10-07
  4 in total

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