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Comparison of topological descriptors for similarity-based virtual screening using multiple bioactive reference structures

Organic & Biomolecular Chemistry · 2004 · Vol. 2(22) · pp. 3256–3256
Jérôme HertPeter WillettDavid J. WiltonPierre AcklinKhalil AzzaouiEdgar JacobyAnsgar Schuffenhauer

Abstract

This paper reports a detailed comparison of a range of different types of 2D fingerprints when used for similarity-based virtual screening with multiple reference structures. Experiments with the MDL Drug Data Report database demonstrate the effectiveness of fingerprints that encode circular substructure descriptors generated using the Morgan algorithm. These fingerprints are notably more effective than fingerprints based on a fragment dictionary, on hashing and on topological pharmacophores. The combination of these fingerprints with data fusion based on similarity scores provides both an effective and an efficient approach to virtual screening in lead-discovery programmes.

Computational Drug Discovery MethodsMicrobial Natural Products and BiosynthesisBioinformatics and Genomic NetworksPharmacophoreVirtual screeningSimilarity (geometry)Pattern recognition (psychology)Fingerprint (computing)Range (aeronautics)SubstructureArtificial intelligenceData miningComputer science

MeSH terms

AlgorithmsChemistry, PharmaceuticalComputer SimulationDrug Evaluation, PreclinicalPharmaceutical PreparationsDrug DesignDatabases, FactualQuantitative Structure-Activity Relationship
Citations
263
FWCI
19.90
field-weighted impact
References
34
Percentile
100%
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References
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Journal of Medicinal Chemistry · 2002 · 825 citations
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