Commentary

Subject Category: Commentary

British Journal of Pharmacology (2007) 152, 5–7; doi:10.1038/sj.bjp.0707308; published online 29 May 2007

Chemogenomic approaches to drug discovery: similar receptors bind similar ligands

T Klabunde1

1Sanofi-Aventis Pharma Deutschland GmbH, Science & Medical Affairs, Drug Design, Industriepark Hoechst, Frankfurt am Main, Germany

Correspondence: Dr T Klabunde, Sanofi-Aventis Pharma Deutschland GmbH, Science & Medical Affairs, Drug Design, Industriepark Hoechst, Germany. E-mail: Thomas.Klabunde@sanofi-aventis.com

Received 12 March 2007; Accepted 25 April 2007; Published online 29 May 2007.

Top

Abstract

Within recent years, a paradigm shift from traditional receptor-specific studies to a cross-receptor view has taken place within pharmaceutical research to increase the efficiency of modern drug discovery. Receptors are no longer viewed as single entities but grouped into sets of related proteins or receptor families that are explored in a systematic manner. This interdisciplinary approach attempting to derive predictive links between the chemical structures of bioactive molecules and the receptors with which these molecules interact is referred to as chemogenomics. Insights from chemogenomics are used for the rational compilation of screening sets and for the rational design and synthesis of directed chemical libraries to accelerate drug discovery.

Keywords:

chemogenomics, drug discovery, target hopping, lead finding, drug design

Abbreviations:

CRTH2, chemoattractant receptor-homologous molecule expressed on Th2 cells; GPCR, G-protein-coupled receptor; 3D, three-dimensional

Extra navigation

.

natureproducts


ADVERTISEMENT