SAR Maps: A New SAR Visualization Technique for Medicinal Chemists. Agrafiotis, D., Shemanarev, M., Connolly, P., Farnum, M., & Lobanov, V. J.~Med.~Chem., 50(24):5926--5937, Johnson & Johnson Pharmaceutical Research and Development, L.L.C., 665 Stockton Drive, Exton, Pennsylvania 19341., 2007. doi abstract bibtex 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.
@article{Agrafiotis:2007aa,
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.},
Address = {Johnson \& Johnson Pharmaceutical Research and Development, L.L.C., 665 Stockton Drive, Exton, Pennsylvania 19341.},
Author = {Agrafiotis, D.K. and Shemanarev, M. and Connolly, P.J. and Farnum, M. and Lobanov, V.S.},
Da = {20071025},
Date-Added = {2007-12-11 17:01:03 -0500},
Date-Modified = {2007-12-11 17:02:52 -0500},
Dep = {20071025},
Doi = {10.1021/jm070845m},
Edat = {2007/10/26 09:00},
Issn = {0022-2623 (Print)},
Jid = {9716531},
Journal = {J.~Med.~Chem.},
Keywords = {SAR; Structure-Activity Relationship; map; visualization; SALI},
Language = {ENG},
Local-Url = {file://localhost/Users/rguha/Documents/articles/jm070845m.pdf},
Mhda = {2007/10/26 09:00},
Number = {24},
Own = {NLM},
Pages = {5926--5937},
Pmid = {17958407},
Pst = {aheadofprint},
Pt = {JOURNAL ARTICLE},
Pubm = {Print-Electronic},
So = {J.~Med.~Chem.. 2007 Oct 25;.},
Stat = {Publisher},
Title = {SAR Maps: A New SAR Visualization Technique for Medicinal Chemists.},
Volume = {50},
Year = {2007},
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