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. 2009 Apr 13;76(1):163–172. doi: 10.1124/mol.109.055855

Fig. 7.

Fig. 7.

A proposed mechanism for the inhibition of TrxR by indolequinones. A, indolequinone activation by two-electron reduction to generate a reactive iminium electrophile. B, reduction of oxidized TrxR by NADPH to generate the reduced C-terminal selenocysteine. C, inhibition of TrxR via alkylation of the reduced C-terminal selenocysteine by the reactive indolequinone iminium electrophile.