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. 2018 Jul 19;8:10923. doi: 10.1038/s41598-018-29199-8

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© The Author(s) 2018

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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Binding and interactions of compound E5 with PDGFRα, c-KIT and CSF1R. (A,C,E) The superimposition of docked E5 on native ligand co-crystallized with PDGFRα, c-KIT and CSF1R, respectively. The carbons of E5 are colored green while those of native ligand are in purple. (B,D,F) 2-D schematic diagram of docking model of E5 with PDGFRα, c-KIT and CSF1R.