| Literature DB >> 15742383 |
Ursula Egner1, Jörn Krätzschmar, Bertolt Kreft, Hans-Dieter Pohlenz, Martin Schneider.
Abstract
In order to minimise attrition rates in drug development projects, a target discovery process is implemented to select and characterise the most suitable candidate kinase targets, before lead identification and lead optimisation are embarked upon. The process consists of 1) target selection, 2) target assessment, and 3) target validation. This rational approach to target discovery, as a prerequisite for lead discovery, ensures that new therapeutic targets fulfil a set of general criteria, as well as indication-specific, descriptive and functional ones. The approach should ultimately maximise the likelihood of achieving target-selective inhibition by small-molecule inhibitors with minimal in vivo side effects and a therapeutic effect based on a sound biological hypothesis.Mesh:
Substances:
Year: 2005 PMID: 15742383 DOI: 10.1002/cbic.200400158
Source DB: PubMed Journal: Chembiochem ISSN: 1439-4227 Impact factor: 3.164