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Effectiveness of graph-based and fingerprint-based similarity measures for virtual screening of 2D chemical structure databases \ud

By J.W. Raymond and P. Willett

Abstract

This paper reports an evaluation of both graph-based and fingerprint-based measures of structural similarity, when used for virtual screening of sets of 2D molecules drawn from the MDDR and ID Alert databases. The graph-based measures employ a new maximum common edge subgraph isomorphism algorithm, called RASCAL, with several similarity coefficients described previously for quantifying the similarity between pairs of graphs. The effectiveness of these graph-based searches is compared with that resulting from similarity searches using BCI, Daylight and Unity 2D fingerprints. Our results suggest that graph-based approaches provide an effective complement to existing fingerprint-based approaches to virtual screening.\u

Publisher: Springer Netherlands
Year: 2002
OAI identifier: oai:eprints.whiterose.ac.uk:3567

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