Fig. 20From: Molecular docking studies of coumarin hybrids as potential acetylcholinesterase, butyrylcholinesterase, monoamine oxidase A/B and β-amyloid inhibitors for Alzheimer’s diseaseThe relative orientation of carboxamide linker of the best docking poses of C13a and C14a. The carboxamide linker of C14a oriented to a hydrophillic pocket (red surface) of the active site [10]Back to article page