Literature DB >> 16711725

An empirical process for the design of high-throughput screening deck filters.

Bradley C Pearce1, Michael J Sofia, Andrew C Good, Dieter M Drexler, David A Stock.   

Abstract

A process for objective identification and filtering of undesirable compounds that contribute to high-throughput screening (HTS) deck promiscuity is described. Two methods of mapping hit promiscuity have been developed linking SMARTS-based structural queries with historical primary HTS data. The first compares an expected assay hit rate to actual hit rates. The second examines the propensity of an individual compound to hit multiple assays. Statistical evaluation of the data indicates a correlation between the resultant functional group filters and compound promiscuity. These data corroborate a number of commonly applied filters as well as producing some unexpected results. Application of these models to HTS collection triage reduced the number of in-house compounds considered for screening by 12%. The implications of these findings are further discussed in the context of the HTS screening set and combinatorial library design as well as compound acquisition.

Mesh:

Year:  2006        PMID: 16711725     DOI: 10.1021/ci050504m

Source DB:  PubMed          Journal:  J Chem Inf Model        ISSN: 1549-9596            Impact factor:   4.956


  23 in total

1.  Post-HTS case report and structural alert: Promiscuous 4-aroyl-1,5-disubstituted-3-hydroxy-2H-pyrrol-2-one actives verified by ALARM NMR.

Authors:  Jayme L Dahlin; J Willem M Nissink; Subhashree Francis; Jessica M Strasser; Kristen John; Zhiguo Zhang; Michael A Walters
Journal:  Bioorg Med Chem Lett       Date:  2015-08-10       Impact factor: 2.823

2.  Quantitative analyses of aggregation, autofluorescence, and reactivity artifacts in a screen for inhibitors of a thiol protease.

Authors:  Ajit Jadhav; Rafaela S Ferreira; Carleen Klumpp; Bryan T Mott; Christopher P Austin; James Inglese; Craig J Thomas; David J Maloney; Brian K Shoichet; Anton Simeonov
Journal:  J Med Chem       Date:  2010-01-14       Impact factor: 7.446

3.  High-throughput identification of promiscuous inhibitors from screening libraries with the use of a thiol-containing fluorescent probe.

Authors:  Megan M McCallum; Premchendar Nandhikonda; Jonathan J Temmer; Charles Eyermann; Anton Simeonov; Ajit Jadhav; Adam Yasgar; David Maloney; Alexander Leggy Arnold
Journal:  J Biomol Screen       Date:  2013-02-27

4.  Computational prediction and validation of an expert's evaluation of chemical probes.

Authors:  Nadia K Litterman; Christopher A Lipinski; Barry A Bunin; Sean Ekins
Journal:  J Chem Inf Model       Date:  2014-10-07       Impact factor: 4.956

5.  Development of a Novel Screening Strategy Designed to Discover a New Class of HIV Drugs.

Authors:  Nancy Cheng; Sook-Kyung Lee; P Scott Donover; Mel Reichman; Celia A Schiffer; Emily A Hull-Ryde; Ronald Swanstrom; William P Janzen
Journal:  J Lab Autom       Date:  2013-12-04

Review 6.  Computational Toxicology Methods in Chemical Library Design and High-Throughput Screening Hit Validation.

Authors:  Kirk E Hevener
Journal:  Methods Mol Biol       Date:  2018

Review 7.  Rational methods for the selection of diverse screening compounds.

Authors:  David J Huggins; Ashok R Venkitaraman; David R Spring
Journal:  ACS Chem Biol       Date:  2011-02-15       Impact factor: 5.100

8.  Antitubercular specific activity of ibuprofen and the other 2-arylpropanoic acids using the HT-SPOTi whole-cell phenotypic assay.

Authors:  Juan D Guzman; Dimitrios Evangelopoulos; Antima Gupta; Kristian Birchall; Solomon Mwaigwisya; Barbara Saxty; Timothy D McHugh; Simon Gibbons; John Malkinson; Sanjib Bhakta
Journal:  BMJ Open       Date:  2013-06-20       Impact factor: 2.692

9.  FAF-Drugs2: free ADME/tox filtering tool to assist drug discovery and chemical biology projects.

Authors:  David Lagorce; Olivier Sperandio; Hervé Galons; Maria A Miteva; Bruno O Villoutreix
Journal:  BMC Bioinformatics       Date:  2008-09-24       Impact factor: 3.169

10.  Lessons learnt from assembling screening libraries for drug discovery for neglected diseases.

Authors:  Ruth Brenk; Alessandro Schipani; Daniel James; Agata Krasowski; Ian Hugh Gilbert; Julie Frearson; Paul Graham Wyatt
Journal:  ChemMedChem       Date:  2008-03       Impact factor: 3.466

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