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Our meta-analyses of existing RBC proteomics and metabolomics studies revealed the abundance of GPx4 to be correlated with lipid-anchored proteins

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In addition, NSAID prodrugs with anticholinergic agents, acetylcholinesterase inhibitory activity (AChEI-NSAIDs) and chemically stable nitroxides, 2,2,6,6-tetramethyl-1-piperidinyloxy (TEMPO) and 4-hydroxy-TEMPO (TEMPOL), have also been designed and tested for their efficacy, albeit with reduced toxicity [220]