Acetylcholinesterase inhibitory activity of novel chitooligosaccharide derivatives

In this study, three kinds of chitooligosaccharides (COS) with different substitution groups, including aminoethyl (AE), dimethylaminoethyl (DMEM) and diethylaminoethyl (DEAE) groups, were evaluated for their inhibitory activities against cholinesterase (acetylcholinesterase and butyrylcholinesterase). These COS derivatives were synthesized and their structures were characterized as AE-COS, DMAE-COS and DEAE-COS, respectively; the structures were elucidated via spectroscopic techniques (1H NMR). Of these, DMAE- and DEAE-COS were synthesized for the first time in this work. These COS derivatives evidenced potent acetylcholinesterase (AChE) inhibitory activities with IC50 values of 56.5 ± 0.26, 24.1 ± 0.39 and 9.2 ± 0.33 μg/ml, respectively; however, these compounds exhibited no activity against butyrylcholinesterase. These were further analyzed for their inhibitory pattern on AChE via Lineweaver–Burk plots. AE-COS showed non-competition type inhibition, and DMAE-COS and DEAE-COS exhibited competition type inhibition against AChE. In this study, we suggested that COS derivatives have potential as AChE inhibitors for preventing Alzheimer’s disease.