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- W4385329982 abstract "A novel series of ligustrazine derivatives was designed, synthesized, and evaluated as acetylcholinesterase (AChE) and butylcholinesterase (BuChE) inhibitors for the treatment of Alzheimer's disease (AD). In vitro studies displayed that some of the synthesized compounds revealed promising AChE and BuChE inhibitory effects. Particularly, compounds E12 and E27, indicated highly AChE inhibitory activity with IC50 values of 1.85 μM and 0.98 μM, respectively and showed noteworthy protective effects against on glutamate-induced SH-SY5Y cells damage at 1 μM and 10 μM concentrations. Furthermore, molecular simulation docking elucidates compounds E12 and E27 interacting with residues in the binding site of AChE (PDB code: 4EY7) and BuChE (PDB code: 1P0I), emphasizing the protein residues that participate in the main interactions with the two targets. Taken together, these results revealed that compounds E12 and E27 might be potential lead compounds for further structure optimization in the drug-discovery process against AD." @default.
- W4385329982 created "2023-07-29" @default.
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- W4385329982 date "2023-07-28" @default.
- W4385329982 modified "2023-10-14" @default.
- W4385329982 title "Design and synthesis of ligustrazine derivatives as potential anti-Alzheimer’s agents" @default.
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- W4385329982 doi "https://doi.org/10.1080/14786419.2023.2241155" @default.
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