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An efficient baseline enzymatic transformation of these molecules may yield a distinct ligand profile capable of co-activating host farnesoid X receptor (FXR) and G protein-coupled bile acid receptor TGR5 pathways, thereby synergizing with the exogenous drug to improve metabolic flexibility (80)

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It is not subject to feedback inhibition by GSH, and its substrates gamma-glutamylcysteine and glycine are rapidly ligated to form GSH

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The benzyl alcohol concentration maintains bacteriostatic properties during this period

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