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It also inhibits drug transporters (P-glycoprotein) and enzymes (CYP3A4), potentially affecting levels of anticoagulants, immunosuppressants, statins, and other medications, so always inform your healthcare team before use

The N-terminal domain of GSTs is relatively conservative, containing key specific residues for catalytic activity through the binding to the glutathione (GSH) through hydrogen bonds

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In healthy subjects, mean C max and AUC (0 t ) increased in a dose-dependent manner

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