Chemical genomics as an emerging paradigm for postgenomic drug discovery
- 1 May 2003
- journal article
- review article
- Published by Taylor & Francis in Pharmacogenomics
- Vol. 4 (3) , 257-267
- https://doi.org/10.1517/phgs.4.3.257.22692
Abstract
Chemical genomics approaches are evolving to overcome key problems limiting the efficiency of drug discovery in the postgenomic era. Many of these stem from the low success rates in finding drugs for novel genomics targets whose biochemical properties and therapeutic relevance is poorly understood. The fundamental objective of chemical genomics is to find and optimize chemical compounds that can be used to directly test the therapeutic relevance of new targets revealed through genome sequencing. An integrated approach to chemical genomics encompasses a diverse set of tools including quantitative affinity-based screens, computer-directed combinatorial chemistry, and structure-based drug design. The approach is most effectively applied across targets classes whose members are structurally related, and where some members are known to have bona fide therapeutic relevance.Keywords
This publication has 42 references indexed in Scilit:
- New drug approvals for 2002Nature Reviews Drug Discovery, 2003
- An Autosampling Differential Scanning Calorimeter Instrument for Studying Molecular InteractionsASSAY and Drug Development Technologies, 2002
- Applications of biomolecular interaction analysis in drug developmentTARGETS, 2002
- Minireview: Genomics Versus Orphan Nuclear Receptors--A Half-Time ReportMolecular Endocrinology, 2002
- High-Density Miniaturized Thermal Shift Assays as a General Strategy for Drug DiscoverySLAS Discovery, 2001
- Profiling Serine Hydrolase Activities in Complex ProteomesBiochemistry, 2001
- HTS in the new millenniumJournal of Pharmacological and Toxicological Methods, 2000
- Chemical ligands, genomics and drug discoveryDrug Discovery Today, 2000
- Serendipity meets precision: the integration of structure-based drug design and combinatorial chemistry for efficient drug discoveryStructure, 1997
- Discovering High-Affinity Ligands for Proteins: SAR by NMRScience, 1996