| Literature DB >> 21554080 |
Steffen Renner1, Maxim Popov, Ansgar Schuffenhauer, Hans-Joerg Roth, Werner Breitenstein, Andreas Marzinzik, Ian Lewis, Philipp Krastel, Florian Nigsch, Jeremy Jenkins, Edgar Jacoby.
Abstract
The design of a high-quality screening collection is of utmost importance for the early drug-discovery process and provides, in combination with high-quality assay systems, the foundation of future discoveries. Herein, we review recent trends and observations to successfully expand the access to bioactive chemical space, including the feedback from hit assessment interviews of high-throughput screening campaigns; recent successes with chemogenomics target family approaches, the identification of new relevant target/domain families, diversity-oriented synthesis and new emerging compound classes, and non-classical approaches, such as fragment-based screening and DNA-encoded chemical libraries. The role of in silico library design approaches are emphasized.Mesh:
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Year: 2011 PMID: 21554080 DOI: 10.4155/fmc.11.15
Source DB: PubMed Journal: Future Med Chem ISSN: 1756-8919 Impact factor: 3.808