[引用][C] Molecular docking and design of novel heterodimers of donepezil and huperzine fragments as acetylcholinesterase inhibitors

黄初升, 涂文通, 罗敏, 施建成 - 结构化学, 2016

[HTML][HTML] 5, 6-Dimethoxybenzofuran-3-one derivatives: a novel series of dual Acetylcholinesterase/Butyrylcholinesterase inhibitors bearing benzyl pyridinium moiety

H Nadri, M Pirali-Hamedani, A Moradi… - DARU Journal of …, 2013 - Springer
Background Several studies have been focused on design and synthesis of multi-target anti
Alzheimer compounds. Utilizing of the dual Acetylcholinesterase/Butyrylcholinesterase …

Exploring indole-based-thiadiazole derivatives as potent acetylcholinesterase and butyrylcholinesterase enzyme inhibitors

M Taha, F Rahim, N Uddin, IU Khan, N Iqbal… - International Journal of …, 2021 - Elsevier
Abstract Indole based thiadiazole derivatives (1–18) were synthesized and evaluated for
their acetylcholinesterase (AChE) and butyrylcholinesterase (BChE) inhibition. The IC 50 …

Screening and identification of secondary metabolites in the bark of Bauhinia variegata to treat Alzheimer's disease by using molecular docking and molecular …

N Khare, SK Maheshwari, AK Jha - Journal of Biomolecular …, 2021 - Taylor & Francis
Abstract Acetylcholinesterase (AChE) and Butyrylcholinesterase (BChE) acts as a promising
protein targets for which drug as an inhibitor can be designed to treat Alzheimer's Disease …

7, 8-Dihydroxycoumarin derivatives: In silico molecular docking and in vitro anticholinesterase activity

M Özdemir, D Taşkın, D Ceyhan, B Köksoy… - Journal of Molecular …, 2023 - Elsevier
In this study, acetylcholinesterase enzyme (AChE) inhibition potential and antioxidant
activity of eight different coumarin derivatives together with two (5 and 8) newly synthesized …

Design, synthesis, extra-precision docking, and molecular dynamics simulation studies of pyrrolidin-2-one derivatives as potential acetylcholinesterase inhibitors

M Gupta, A Kumar, C Prasun, MS Nair… - Journal of …, 2023 - Taylor & Francis
Inhibition of acetylcholinesterase (AChE) has been widely explored to develop novel
molecules for management of Alzheimer's disease. In past research finding reported …

Synthesis, characterization, evaluation of metabolic enzyme inhibitors and in silico studies of thymol based 2-amino thiol and sulfonic acid compounds

RE Bora, HG Bilgicli, EM Üç, MA Alagöz… - Chemico-Biological …, 2022 - Elsevier
Eight new aminothiols (4a-g and 5) and three new sulfonic acid derivatives (6a-c) were
synthesized, and their structures were characterized. Inhibitory effects of the obtained …

Investigation of potent inhibitors of cholinesterase based on thiourea and pyrazoline derivatives: Synthesis, inhibition assay and molecular modeling studies

A Mumtaz, A Majeed, S Zaib, SU Rahman… - Bioorganic …, 2019 - Elsevier
Owing to the desperate need of new drugs development to treat Alzheimer's ailment the
synthesis of 1-aroyl-3-(5-(4-chlorophenyl)-1, 2, 4-triazole-3-thioneaminylthioureas (2–6) …

(⿿)-Epicatechin derivate from Orostachys japonicus as potential inhibitor of the human butyrylcholinesterase

JH Kim, SH Lee, HW Lee, YN Sun, WH Jang… - International journal of …, 2016 - Elsevier
Cholinesterase inhibitors block the bioconversion of neurotransmitters by cholinesterase in
the nervous system. Epicatechin derivatives (1, 3 and 5), polyphenols (6 and 7) from …

New azole-derived hemiaminal ethers as promising acetylcholinesterase inhibitors: synthesis, X-ray structures, in vitro and in silico studies

M Nisar, HY Gondal, ZM Cheema… - Journal of …, 2023 - Taylor & Francis
A new class of azole-derived hemiaminal ethers is designed as acetylcholinesterase (AChE)
inhibitors. The synthesized compounds exhibited remarkable inhibitory activity against …