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Ferrostatin-1 is a ferroptosis inhibitor.1 It inhibits cell death induced by the ferroptosis inducers erastin (Item No. 17754; EC50 = 60 nM) and RSL3, but not by hydrogen peroxide, rotenone, or staurosporine, in HT-1080 cells when used at a concentration of 0.5 μM. Ferrostatin-1 (0.5 μM) inhibits erastin-induced production of reactive oxygen species (ROS) and lipid peroxidation in HT-1080 cells. It increases cell survival in cell-based models of Huntington's disease, periventricular leukomalacia, and kidney proximal tubule damage in a concentration-dependent manner.2 Ferrostatin-1 (2 μM) inhibits cell death induced by L-glutamate in a rat organotypic hippocampal slice culture (OHSC) model.1 It also inhibits autooxidation of lipids by trapping peroxyl radicals.1,3
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Formation of protein adducts with hydroperoxy-
RB1-
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A non-
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Dengue virus envelope protein domain III induces Nlrp3 inflammasome-
Krüppel-
GOT1 inhibition primes pancreatic cancer for ferroptosis through the autophagic release of labile iron. bioRxiv (2020).
A novel redox modulator induces a GPX4-
The CoQ oxidoreductase FSP1 acts parallel to GPX4 to inhibit ferroptosis. Nature 575(7784), 688-692 (2019).
CD8+ T cells regulate tumour ferroptosis during cancer immunotherapy. Nature 569(7755), 270-274 (2019).