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Molecular docking analysis of cardamonin, pinocembrin, and pinostrobin with P-gp. The best docking poses between P-gp and cardamonin (a), pinocembrin (d), and pinostrobin (g). Magnified view of the binding site for cardamonin (b), pinocembrin (e), and pinostrobin (h). Hydrogen and hydrophobic interaction diagram of cardamonin (c), pinocembrin (f), and pinostrobin (i). The green dotted lines show hydrogen bonds between ligands and BACE1.
