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. 2017 Jul 20;7:6019. doi: 10.1038/s41598-017-06131-0

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© The Author(s) 2017

Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/.

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Molecular SAR mechanism of maslinic acid derivatives, representing different geometries of field contributions to the predicted activity. The red color circle indicates electrostatics field points, controlling the decrease in predicted activity. The purple color triangle indicates steric field points, controlling the increase in predicted activity, while blue color square indicates electrostatics field points, controlling the increase in predicted activity.