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. 2019 Oct 29;9:15528. doi: 10.1038/s41598-019-52108-6

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© The Author(s) 2019

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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Effect of SM1044 on intracellular level of peroxynitrite (ONOO⁻) and hydrogen peroxide (H₂O₂). The cells treated with DMSO served as the negative control. Results were presented as relative level of ONOO− or H₂O₂, expressed as the ratio of fluorescence intensity of treated cells divided by that of negative control cells and expressed as fold increase compared with the control. Data were presented as mean ± SD of triplicate with three independent samples. *P < 0.05, **P < 0.01 vs the relative level of the control.