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doi:10.1038/srep34427
A molecule with FDA approvals spanning all of these systems is sitting at the intersection of overlapping biological networks, not functioning as an appetite suppressant with an unusually long list of side benefits
Toxic lipid peroxides can be converted into nontoxic lipid alcohols (L-OH) in the presence of GPX4 and GSH to inhibit ferroptosis [21]
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For example, certain antimicrobial agents (i.e., clarithromycin, levofloxacin, sulfamethoxazole-trimethoprim, metronidazole, and ciprofloxacin) can interact with sulfonylureas to increase the risk of hypoglycemia [29, 30]
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