A review on cholinesterase inhibitors for Alzheimer's disease

P Anand, B Singh - Archives of pharmacal research, 2013 - Springer
Abstract Alzheimer's disease (AD), a progressive neurodegenerative disorder, is
characterized by the deficits in the cholinergic system and deposition of beta amyloid (Aβ) in …

Acetylcholinesterase inhibitors as Alzheimer therapy: from nerve toxins to neuroprotection

M Singh, M Kaur, H Kukreja, R Chugh, O Silakari… - European journal of …, 2013 - Elsevier
Acetylcholinesterase is a member of the α/β hydrolase protein super family, with a significant
role in acetylcholine-mediated neurotransmission. Research in the modulators of AChEs …

Recent developments in cholinesterases inhibitors for Alzheimer's disease treatment

A Musial, M Bajda, B Malawska - Current medicinal chemistry, 2007 - ingentaconnect.com
Alzheimer's disease (AD) is a progressive neurodegenerative disorder of the central
nervous system (CNS) which is the most common cause of dementia in the elderly. It is …

Molecular docking of different inhibitors and activators to butyrylcholinesterase

SY Chiou, TT Weng, GZ Lin, RJ Lu… - Journal of Biomolecular …, 2015 - Taylor & Francis
There are three major active sites of butyrylcholinesterase: catalytic site, peripheral site, and
activator site. In this study, pseudosubstrate inhibitors, 1, 3, 5-alkylcarbamyloxybenzenes (1 …

Ortho Effects for Inhibition Mechanisms of Butyrylcholinesterase by o-Substituted Phenyl N-Butyl Carbamates and Comparison with Acetylcholinesterase …

G Lin, YR Lee, YC Liu, YG Wu - Chemical research in toxicology, 2005 - ACS Publications
Phenyl carbamates are used to treat Alzheimer's disease. These compounds inhibit
acetylcholinesterase and butyrylcholinesterase. The goal of this work was to determine the …

QSARs for Peripheral Anionic Site of Butyrylcholinesterase with Inhibitions by 4‐Acyloxy‐biphenyl‐4′‐N‐butylcarbamates

G Lin, GH Chen, CP Lu, SC Yeh - QSAR & Combinatorial …, 2005 - Wiley Online Library
Acyloxy‐biphenyl‐4′‐N‐butylcarbamates (1–8) are synthesized from 4, 4′‐biphenol by
two‐step reactions. Carbamates 1–7 are characterized as the pseudo‐substrate inhibitors of …

[HTML][HTML] Alzheimer's disease and its current treatments; Is there a possibility for a cure?

A Ehab, M Ibrahim, M Magdi, M Ayman… - Open journal of …, 2019 - chemisgroup.us
Alzheimer's disease (AD) is an irreversible, progressive brain disorder that slowly destroys
the memory and the thinking skills, and eventually the ability to carry out the simplest tasks …

Probing the peripheral anionic site of acetylcholinesterase with quantitative structure activity relationships for inhibition by biphenyl‐4‐acyoxylate‐4′‐N …

G Lin, GH Chen, SC Yeh, CP Lu - Journal of Biochemical and …, 2005 - Wiley Online Library
Abstract Biphenyl‐4‐acyoxylate‐4′‐N‐butylcarbamates 1–8 are synthesized from 4, 4′‐
biphenol and are characterized as the pseudosubstrate inhibitors of acetylcholinesterase. In …

Molecular modeling and docking calculations of 4-acyloxy-biphenyl-4′-N-butylcarbamates as potential inhibitors of human butyrylcholinesterase

YF Shen, GH Chen, SH Lin, G Lin - Canadian Journal of …, 2016 - cdnsciencepub.com
The kinetic studies and drug designs of butyrylcholinesterase play an important role in the
development of Alzheimer's disease therapeutics. In this research, automated docking …

Synthesis of enantiomers of exo‐2‐norbornyl‐Nn‐butylcarbamate and endo‐2‐norbornyl‐Nn‐butylcarbamate for stereoselective inhibition of …

SY Chiou, CF Huang, SJ Yeh… - … of Molecular Asymmetry, 2010 - Wiley Online Library
The acetylcholinesterase inhibition by enantiomers of exo‐and endo‐2‐norbornyl‐N‐n‐
butylcarbamates shows high stereoselelectivity. For the acetylcholinesterase inhibitions by …