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. 2021 May 14;12(5):490. doi: 10.1038/s41419-021-03771-z

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© The Author(s) 2021

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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Fig. 6 — A HUVEC cell viability assay by treating with 5 μM BAY-85-3934, 25 nM CPM, 10 μM E3330, and 5 μM LW6. B HUVECs cells were cultured in normoxia and exposed to 1% O₂ and also treated with BAY-85-3934 in 1% O₂. C One percent O₂-exposed HUVECs were treated with CPM, E3330, and LW6. Scale bar, 100 μm. Data were expressed as mean ± SEM (n = 3). **P < 0.01, ***P < 0.001 compared to control groups.