Molecular docking and receptor-specific 3D-QSAR studies of acetylcholinesterase inhibitors

PK Deb, A Sharma, P Piplani, RR Akkinepally - Molecular Diversity, 2012 - Springer
The reversible inhibition of acetylcholinesterase (AChE) has become a promising target for
the treatment of Alzheimer's disease (AD) which is mainly associated with low in vivo levels …

Release of acetylcholinesterase (AChE) from β-amyloid plaques assemblies improves the spatial memory impairments in APP-transgenic mice

MC Dinamarca, M Arrázola, E Toledo, WF Cerpa… - Chemico-biological …, 2008 - Elsevier
The major protein constituent of amyloid deposits in Alzheimer's disease (AD) is the amyloid-
β-peptide (Aβ). Amyloid deposits contain “chaperone molecules” which play critical roles in …

Multifunctional cholinesterase and amyloid beta fibrillization modulators. Synthesis and biological investigation

S Butini, M Brindisi, S Brogi, S Maramai… - ACS medicinal …, 2013 - ACS Publications
In order to identify novel Alzheimer's modifying pharmacological tools, we developed bis-
tacrines bearing a peptide moiety for specific interference with surface sites of human …

Synthesis and characterization of 1H-phenanthro [9, 10-d] imidazole derivatives as multifunctional agents for treatment of Alzheimer's disease

J Liu, J Qiu, M Wang, L Wang, L Su, J Gao, Q Gu… - … et Biophysica Acta (BBA …, 2014 - Elsevier
Background Alzheimer's disease (AD) is a progressive neurodegenerative brain disorder
that is characterized by dementia, cognitive impairment, and memory loss. Diverse factors …

Multifunctional thioxanthone derivatives with acetylcholinesterase, monoamine oxidases and β-amyloid aggregation inhibitory activities as potential agents against …

L Luo, Y Li, X Qiang, Z Cao, R Xu, X Yang… - Bioorganic & Medicinal …, 2017 - Elsevier
Abstract A series of 1-hydroxyl-3-aminoalkoxy-thioxanthone derivatives were designed,
synthesized and evaluated as potential multifunctional agents against Alzheimer's disease …

The hyperforin derivative IDN5706 occludes spatial memory impairments and neuropathological changes in a double transgenic Alzheimer's mouse model

W Cerpa, JL Hancke, P Morazzoni… - Current Alzheimer …, 2010 - ingentaconnect.com
The use of natural compounds is an interesting stratagem in the search of drugs with
therapeutic potential for the treatment of Alzheimer's disease (AD). We report here the effect …

Green Tea Seed Oil Suppressed Aβ1–42-Induced Behavioral and Cognitive Deficit via the Aβ-Related Akt Pathway

JM Kim, SK Park, JY Kang, SB Park, SK Yoo… - International Journal of …, 2019 - mdpi.com
The aim of this study was to investigate the availability of seeds, one of the byproducts of
green tea, and evaluate the physiological activity of seed oil. The ameliorating effect of …

Novel Uracil-Based Inhibitors of Acetylcholinesterase with Potency for Treating Memory Impairment in an Animal Model of Alzheimer's Disease

VE Semenov, IV Zueva, SV Lushchekina… - Molecules, 2022 - mdpi.com
Novel derivatives based on 6-methyluracil and condensed uracil, 2, 4-quinazoline-2, 4-
dione, were synthesized with terminal meta-and para-benzoate moieties in polymethylene …

Acetylcholinesterase-amyloid-β-peptide interaction: effect of Congo Red and the role of the Wnt pathway

NC Inestrosa, A Alvarez, MC Dinamarca… - Current Alzheimer …, 2005 - ingentaconnect.com
The cholinergic system impairment observed in Alzheimer's disease (AD) patients leads to
the cognitive, global and behavioral dysfunction commonly associated with dementia. The …

Kinetics of inhibition of acetylcholinesterase in the presence of acetonitrile

M Pietsch, L Christian, T Inhester, S Petzold… - The FEBS …, 2009 - Wiley Online Library
The hydrolysis of acetylthiocholine by acetylcholinesterase from Electrophorus electricus
was investigated in the presence of the inhibitors tacrine, gallamine and compound 1. The …