Tertiary amine derivatives of chlorochalcone as acetylcholinesterase (AChE) and buthylcholinesterase (BuChE) inhibitors: the influence of chlorine, alkyl amine side chain and α,β-unsaturated ketone group
Xiao-hui Gao
Chao Zhou
Hao-ran Liu
Lin-bo Liu
Jing-jing Tang
Xin-hua Xia
10.6084/m9.figshare.4159962.v1
https://tandf.figshare.com/articles/journal_contribution/Tertiary_amine_derivatives_of_chlorochalcone_as_acetylcholinesterase_AChE_and_buthylcholinesterase_BuChE_inhibitors_the_influence_of_chlorine_alkyl_amine_side_chain_and_-unsaturated_ketone_group/4159962
<p>A new series of tertiary amine derivatives of chlorochalcone (<b>4a∼4l</b>) were designed, synthesized and evaluated for the effect on acetylcholinesterase (AChE) and buthylcholinesterase (BuChE). The results indicated that all compounds revealed moderate or potent inhibitory activity against AChE, and some possessed high selectivity for AChE over BuChE. The structure–activity investigation showed that the substituted position of chlorine significantly influenced the activity and selectivity. The alteration of tertiary amine group also leads to obvious change in bioactivity. Among them, IC<sub>50</sub> of compound <b>4l</b> against AChE was 0.17 ± 0.06 µmol/L, and the selectivity was 667.2 fold for AChE over BuChE. Molecular docking and enzyme kinetic study on compound <b>4l</b> suggested that it simultaneously binds to the catalytic active site (CAS) and peripheral anionic site (PAS) of AChE. Further study showed that the pyrazoline derivatives synthesized from chlorochalcones had weaker activity and lower selectivity in inhibiting AChE compared to that of chlorochalcone derivatives.</p>
2016-11-01 13:13:44
Acetylcholinesterase inhibitors
Alzheimer’s disease
chlorochalcones
pyrazoline
structure–activity relationship