© Guba and Stoffler; licensee BioMed Central Ltd. 2011
Published: 19 April 2011
Over the years a massive amount of high-throughput screening (HTS) data has been collected, however, the data are mainly utilized for providing lead generation programs with chemical entry points. The comparison of molecular structures and HTS data across many projects allows to identify and validate structural patterns of frequent hitters, i.e. compounds which generate multiple hits in various target families. The identification of frequent hitters is an important component in maintaining a high-quality screening deck and supports project teams in the triaging of HTS hit lists. In addition, frequent hitters will be contrasted with privileged motifs which are believed to show activities in specific target classes only. The talk will also address the question what causes compounds to be frequent hitters, and in-silico prediction methods will be discussed.
This article is published under license to BioMed Central Ltd. This is an open access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.