[HTML][HTML] Pursuing the Complexity of Alzheimer's Disease: Discovery of Fluoren-9-Amines as Selective Butyrylcholinesterase Inhibitors and N-Methyl-d-Aspartate …

J Konecny, A Misiachna, M Hrabinova, L Pulkrabkova… - Biomolecules, 2020 - mdpi.com
Alzheimer's disease (AD) is a complex disorder with unknown etiology. Currently, only
symptomatic therapy of AD is available, comprising cholinesterase inhibitors and N-methyl-d …

Identification of butyrylcholinesterase and monoamine oxidase B targeted ligands and their putative application in alzheimer's treatment: a computational strategy

NR Jabir, MT Rehman, S Tabrez… - Current …, 2021 - ingentaconnect.com
Background: With the burgeoning worldwide aging population, the incidence of Alzheimer's
disease (AD) and its associated disorders is continuously rising. To appraise other relevant …

[HTML][HTML] Structure-Guided Design of N-Methylpropargylamino-Quinazoline Derivatives as Multipotent Agents for the Treatment of Alzheimer's Disease

B Svobodova, L Pulkrabkova, D Panek… - International Journal of …, 2023 - mdpi.com
Alzheimer's disease (AD) is a complex disease with an unknown etiology. Available
treatments, limited to cholinesterase inhibitors and N-methyl-d-aspartate receptor (NMDAR) …

[HTML][HTML] Novel 2-pheynlbenzofuran derivatives as selective butyrylcholinesterase inhibitors for Alzheimer's disease

A Kumar, F Pintus, A Di Petrillo, R Medda, P Caria… - Scientific reports, 2018 - nature.com
Alzheimer's disease (AD) is a neurodegenerative disorder representing the leading cause of
dementia and is affecting nearly 44 million people worldwide. AD is characterized by a …

current quest in natural bioactive compounds for Alzheimer's disease: Multi-targeted-designed-ligand based approach with preclinical and clinical based evidence

A Iqubal, SO Rahman, M Ahmed, P Bansal… - Current Drug …, 2021 - ingentaconnect.com
Alzheimer's disease is a common and most chronic neurological disorder (NDs) associated
with cognitive dysfunction. Pathologically, Alzheimer's disease (AD) is characterized by the …

Discovery, Structure-Based Modification, In Vitro, In Vivo, and In Silico Exploration of m-Sulfamoyl Benzoamide Derivatives as Selective Butyrylcholinesterase …

X Lu, Y Li, Q Guan, H Yang, Y Liu, C Du… - ACS Chemical …, 2024 - ACS Publications
For the potential therapy of Alzheimer's disease (AD), butyrylcholinesterase (BChE) has
gradually gained worldwide interest in the progression of AD. This study used a …

The Discovery of Benzylidene‐Indenone as Selective Butyrylcholinesterase Inhibitor with Choline Acetyltransferase Gene and Neurite Promoting Abilities

L Ooi, K San Tang, JBL Tan, K Yoon Yeong - ChemistrySelect, 2024 - Wiley Online Library
Alzheimer's disease (AD) is a multifactorial and progressive neurodegenerative disease,
associated with aging. A total of forty benzylidene‐indenone derivatives were synthesized in …

Pharmacophore mapping of the crucial mediators of acetylcholinesterase and butyrylcholinesterase dual inhibition in Alzheimer's disease

FY Adeowo, AA Elrashedy, MA Ejalonibu, IA Lawal… - Molecular Diversity, 2022 - Springer
Optimization and re-optimization of bioactive molecules using in silico methods have found
application in the design of more active ones. Herein, we applied a pharmacophore …

Benzofurans as Acetylcholinesterase Inhibitors for Treating Alzheimer's Disease: Synthesis, in vitro Testing, and in silico Analysis

A Coaviche‐Yoval, R Tovar‐Miranda… - …, 2024 - Wiley Online Library
Alzheimer's disease (AD) is a neurodegenerative disorder and the leading cause of
dementia worldwide. It is characterized by a progressive decline in cholinergic …

[HTML][HTML] Amino-7, 8-dihydro-4H-chromenone derivatives as potential inhibitors of acetylcholinesterase and butyrylcholinesterase for Alzheimer's disease management …

A Asadipour, Y Pourshojaei, M Mansouri… - BMC chemistry, 2024 - Springer
In this article, we present the design and synthesis of amino-7, 8-dihydro-4H-chromenone
derivatives as possible inhibitors of acetylcholinesterase (AChE) and butyrylcholinesterase …