AChE inhibition-based multi-target-directed ligands, a novel pharmacological approach for the symptomatic and disease-modifying therapy of Alzheimer's disease

Y Wang, H Wang, H Chen - Current neuropharmacology, 2016 - ingentaconnect.com
Alzheimer's disease (AD) is the most common form of dementia in elder people,
characterised by a progressive decline in memory as a result of an impairment of cholinergic …

Synthesis, biological evaluation and molecular docking study of novel piperidine and piperazine derivatives as multi-targeted agents to treat Alzheimer's disease

P Meena, V Nemaysh, M Khatri, A Manral… - Bioorganic & medicinal …, 2015 - Elsevier
Abstract Development of Multi-Target Directed Ligands (MTDLs) has emerged as a
promising approach for targeting complex etiology of Alzheimer's disease (AD). Following …

Exploring basic tail modifications of coumarin-based dual acetylcholinesterase-monoamine oxidase B inhibitors: Identification of water-soluble, brain-permeant …

L Pisani, R Farina, M Catto, RM Iacobazzi… - Journal of Medicinal …, 2016 - ACS Publications
Aiming at modulating two key enzymatic targets for Alzheimer's disease (AD), ie,
acetylcholinesterase (AChE) and monoamine oxidase B (MAO B), a series of multitarget …

Novel Tacrine-Hydroxyphenylbenzimidazole hybrids as potential multitarget drug candidates for Alzheimer's disease

A Hiremathad, RS Keri, AR Esteves… - European journal of …, 2018 - Elsevier
Alzheimer's disease (AD) is a severe age-dependent neurodegenerative disorder affecting
millions of people, with no cure so far. The current treatments only achieve some temporary …

[HTML][HTML] Two decades of new drug discovery and development for Alzheimer's disease

Z Liu, A Zhang, H Sun, Y Han, L Kong, X Wang - RSC advances, 2017 - pubs.rsc.org
Alzheimer's disease is a progressive and irreversible neurodegenerative disease,
associated with a decreased cognitive function and severe behavioral abnormalities. Due to …

Development of chalcone-O-alkylamine derivatives as multifunctional agents against Alzheimer's disease

P Bai, K Wang, P Zhang, J Shi, X Cheng… - European journal of …, 2019 - Elsevier
A series of novel chalcone-O-alkylamine derivatives were designed, synthesized and
evaluated as multifunctional anti-Alzheimer's disease agents. Based on the experimental …

Acetylcholinesterase inhibitors with photoswitchable inhibition of β-amyloid aggregation

X Chen, S Wehle, N Kuzmanovic… - ACS Chemical …, 2014 - ACS Publications
Photochromic cholinesterase inhibitors were obtained from cis-1, 2-α-dithienylethene-based
compounds by incorporating one or two aminopolymethylene tacrine groups. All target …

Novel inhibitors of AChE and Aβ aggregation with neuroprotective properties as lead compounds for the treatment of Alzheimer's disease

Y Liu, G Uras, I Onuwaje, W Li, H Yao, S Xu, X Li… - European Journal of …, 2022 - Elsevier
A series of sulfone analogs of donepezil were designed and synthesized as novel
acetylcholinesterase (AChE) inhibitors with the potent inhibiting Aβ aggregation and …

Design, synthesis and biological evaluation of novel donepezil–coumarin hybrids as multi-target agents for the treatment of Alzheimer's disease

SS Xie, JS Lan, X Wang, ZM Wang, N Jiang, F Li… - Bioorganic & Medicinal …, 2016 - Elsevier
Combining N-benzylpiperidine moiety of donepezil and coumarin into in a single molecule,
novel hybrids with ChE and MAO-B inhibitory activity were designed and synthesized. The …

Design, synthesis and biological evaluation of novel coumarin-N-benzyl pyridinium hybrids as multi-target agents for the treatment of Alzheimer's disease

JS Lan, Y Ding, Y Liu, P Kang, JW Hou… - European Journal of …, 2017 - Elsevier
Combining N-benzyl pyridinium moiety and coumarin into in a single molecule, novel
hybrids with ChE and MAO-B inhibitory activities were designed and synthesized. The …