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The flux of cysteine and the end products are driven by how much methionine is eaten, as well as how much glutathione is needed to combat oxidative stress in cells.[ref][ref] Homocysteine thiolactone: Damaging endothelial cells, increasing inflammation Homocysteine can also become homocysteine thiolactone when a thiol group is attached

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For example, a previous study demonstrated that the ferroptosis inhibitory activity of ferrostatin-1 and liproxstatin-1 is likely driven by their reactivity as radical-trapping antioxidants rather than their potency as inhibitors of lipoxygenases (81)