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In our screening, the isoflavone (e.g., daidzein, genistein, and glycitein) and methoxyflavone (e.g., tricin, tangeretin, and diosmetin) derivatives as well as flavone O- and C-glycosides (e.g., isoquercitrin, orientin, and vitexin) were either completely inactive or exerted low inhibition capacities against both ChEs
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