Atom-Atom-Path similarity and Sphere Exclusion clustering: tools for prioritizing fragment hits.

J Cheminform

Small Molecule Discovery, Discovery Chemistry, Genentech, 1 DNA Way, 94080 South San Francisco, CA USA.

Published: April 2015

Background: After performing a fragment based screen the resulting hits need to be prioritized for follow-up structure elucidation and chemistry. This paper describes a new similarity metric, Atom-Atom-Path (AAP) similarity that is used in conjunction with the Directed Sphere Exclusion (DISE) clustering method to effectively organize and prioritize the fragment hits. The AAP similarity rewards common substructures and recognizes minimal structure differences. The DISE method is order-dependent and can be used to enrich fragments with properties of interest in the first clusters.

Results: The merit of the software is demonstrated by its application to the MAP4K4 fragment screening hits using ligand efficiency (LE) as quality measure. The first clusters contain the hits with the highest LE. The clustering results can be easily visualized in a LE-over-clusters scatterplot with points colored by the members' similarity to the corresponding cluster seed. The scatterplot enables the extraction of preliminary SAR.

Conclusions: The detailed structure differentiation of the AAP similarity metric is ideal for fragment-sized molecules. The order-dependent nature of the DISE clustering method results in clusters ordered by a property of interest to the teams. The combination of both allows for efficient prioritization of fragment hit for follow-ups. Graphical abstractAAP similarity computation and DISE clustering visualization.

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http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4392110PMC
http://dx.doi.org/10.1186/s13321-015-0056-8DOI Listing

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