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PL Paula Lindner
SC Søren Brøgger Christensen
PN Poul Nissen
JM Jesper Vuust Møller
NE Nikolai Engedal
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Thapsigargin (Tg) was purchased from Sigma (T9033). The Tg analogs 8-O-debutanoyl-8-O-N-L-Leucinoyl-12-aminododecanoylthapsigargin (Leu-8ADT) and 8-O-debutanoyl-8-O-N-L-β-aspartoyl-12-aminododecanoylthapsigargin (βAsp-8ADT) were synthesized as previously described [60]. The PERK inhibitor GSK2606414 [61] was a kind gift from Dr. Jeffrey M. Axten (GlaxoSmithKline). The JNK inhibitor JNK-IN-8 was from Sigma (SML1246). The chemical structures of Tg, Leu-8ADT, βAsp-8ADT, GSK2606414, and JNK-IN-8 are depicted in Additional file 1: Figure S1.

Copyright and License information: The Author(s). ©2020
Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided 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 Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.

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