glutathione reductase molecualr weight molecular structure RCSB PDB Glutathione peroxidase glutathione reductase molecular weight L-Glutathione

Smallmolecule ferroptosis inhibitors and natural compounds show efficacy but are constrained by poor pharmacokinetics and bioavailability

Short-term treatment with a novel HIF-prolyl hydroxylase inhibitor (GSK1278863) failed to improve measures of performance in subjects with claudication-limited peripheral artery disease

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Beyond monotherapies, the strategic modulation of autophagy and ferroptosis offers a powerful approach to augment the efficacy of established cancer treatments and overcome resistance to them