| Literature DB >> 19545644 |
Alison Easter1, M Elizabeth Bell, James R Damewood, William S Redfern, Jean-Pierre Valentin, Matthew J Winter, Carlos Fonck, Russell A Bialecki.
Abstract
Assessment of seizure risk traditionally occurs late in the drug discovery process using low-throughput, resource intensive in vivo assays. Such approaches do not allow sufficient time to mitigate risk by influencing chemical design. Early identification using cheaper, higher throughput assays with lower animal and compound requirements would be preferable. Here we review the current techniques available to assess this issue and describe how they may be combined in a rational step-wise cascade allowing more effective assessment of seizure risk.Entities:
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Year: 2009 PMID: 19545644 DOI: 10.1016/j.drudis.2009.06.003
Source DB: PubMed Journal: Drug Discov Today ISSN: 1359-6446 Impact factor: 7.851