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doi: 10.1038/s41522-025-00779-7, 98 MigniniI.GalassoL.PiccirilliG.CalvezV.TermiteF.EspostoG.et al

Metabolism Selinexor is metabolized by CYP3A4, multiple UDP-glucuronosyltransferases (UGTs) and glutathione S-transferases (GSTs)

[83] The most commonly reported adverse effects are typically mild and transient, often resolving with continued use or dose adjustments

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Balachandran, S RIPK3 Activates Parallel Pathways of MLKL-Driven Necroptosis and FADD-Mediated Apoptosis to Protect against Influenza A Virus Cell Host Microbe 20 1: 13-24