| Literature DB >> 17958407 |
Dimitris K Agrafiotis1, Maxim Shemanarev, Peter J Connolly, Michael Farnum, Victor S Lobanov.
Abstract
We present structure-activity relationship (SAR) maps, a new, intuitive method for visualizing SARs targeted specifically at medicinal chemists. The method renders an R-group decomposition of a chemical series as a rectangular matrix of cells, each representing a unique combination of R-groups and thus a unique compound. Color-coding the cells by chemical property or biological activity allows patterns to be easily identified and exploited. SAR maps allow the medicinal chemist to interactively analyze complicated datasets with multiple R-group dimensions, rapidly correlate substituent structure and biological activity, assess additivity of substituent effects, identify missing analogs and screening data, and create compelling graphical representations for presentation and publication. We believe that this method fills a long-standing gap in the medicinal chemist's toolset for understanding and rationalizing SAR.Mesh:
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Year: 2007 PMID: 17958407 DOI: 10.1021/jm070845m
Source DB: PubMed Journal: J Med Chem ISSN: 0022-2623 Impact factor: 7.446