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. 2019 Dec 5;10:5564. doi: 10.1038/s41467-019-13522-6

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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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Fig. 5 — Transport of [³H]adenosine via P1 and P2 transporters in the presence nucleoside analogues. Uptake of [³H]adenosine was measured in the presence of increasing concentrations of nucleoside analogues 8, 9 and 10. Inhibition plots of adenosine and its analogues versus P1- or P2-mediated [³H]adenosine transport. The graphs represent one representative out of three independent experiments (n = 3), each performed in triplicate. Error bars are SEM, which fall within the symbol when not shown. Source data are provided as a Source Data file.