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TGR inhibitors do not react covalently with GSH, selenocysteine, or TGR, and inhibition of TGR is reversible To evaluate stability of the TGR inhibitors in the presence of GSH and selenocysteine, compound 2 and a known covalent inhibitor of TGR, TRi-1 20,45 , were incubated with GSH or the N-Boc protected methyl ester of selenocysteine, and the reaction mixtures were analyzed by LCMS (Supplementary Figs

Oral F.n translocate to the intestine by resisting the acidic environment at pH 1.5 owing to the presence of erucic acid in its cell membrane, which is regulated by FnFabM, increasing its colonization efficiency in the stomach and jejunum of mice (Li et al., 2025)

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C., & Touyz, R