The state of the art on acetylcholinesterase inhibitors in the treatment of Alzheimer's disease
Alzheimer's disease (AD) is a chronic disabling disease that affects the central nervous
system. The main consequences of AD include the decline of cognitive functions and …
system. The main consequences of AD include the decline of cognitive functions and …
[PDF][PDF] Cholinesterases, a target of pharmacology and toxicology.
M Pohanka - Biomedical Papers of the Medical Faculty of …, 2011 - pdfs.semanticscholar.org
Background. Cholinesterases are a group of serine hydrolases that split the neurotransmitter
acetylcholine (ACh) and terminate its action. Of the two types, butyrylcholinesterase and …
acetylcholine (ACh) and terminate its action. Of the two types, butyrylcholinesterase and …
Organophosphorus compounds as chemical warfare agents: a review
RT Delfino, TS Ribeiro… - Journal of the Brazilian …, 2009 - SciELO Brasil
Chemical warfare agents constitute one of the greatest threats in the modern world. Among
them, the neurotoxic agents are of special interest due to their high lethality and danger …
them, the neurotoxic agents are of special interest due to their high lethality and danger …
Structure of acetylcholinesterase complexed with the nootropic alkaloid,(–)-huperzine A
ML Raves, M Harel, YP Pang, I Silman… - Nature structural …, 1997 - nature.com
Huperzine A (HupA) is found in an extract from a club moss that has been used for centuries
in Chinese folk medicine. Its action has been attributed to its ability to strongly inhibit …
in Chinese folk medicine. Its action has been attributed to its ability to strongly inhibit …
Acetylcholinesterase: how is structure related to function?
I Silman, JL Sussman - Chemico-biological interactions, 2008 - Elsevier
In accordance with its biological role, termination of neurotransmission at cholinergic
synapses by rapid hydrolysis of the neurotransmitter, acetylcholine, acetylcholinesterase is …
synapses by rapid hydrolysis of the neurotransmitter, acetylcholine, acetylcholinesterase is …
Synthesis and pharmacology of galantamine
J Marco-Contelles, M do Carmo Carreiras… - Chemical …, 2006 - ACS Publications
(-)-Galantamine (1){(4aS, 6R, 8aS)-4a, 5, 9, 10, 11, 12-hexahydro-3-methoxy-11-methyl-6H-
benzofuro [3a, 3, 2-ef][2]-benzazepin-6-ol}(Chart 1), an alkaloid isolated from the Caucasian …
benzofuro [3a, 3, 2-ef][2]-benzazepin-6-ol}(Chart 1), an alkaloid isolated from the Caucasian …
Acetylcholinesterase inhibition by fasciculin: crystal structure of the complex
The crystal structure of the snake toxin fasciculin, bound to mouse acetylcholinesterase
(mAChE), at 3.2 Å resolution reveal sa synergistic three-point anchorage consistent with the …
(mAChE), at 3.2 Å resolution reveal sa synergistic three-point anchorage consistent with the …
A comprehensive review of cholinesterase modeling and simulation
D De Boer, N Nguyen, J Mao, J Moore, EJ Sorin - Biomolecules, 2021 - mdpi.com
The present article reviews published efforts to study acetylcholinesterase and
butyrylcholinesterase structure and function using computer-based modeling and simulation …
butyrylcholinesterase structure and function using computer-based modeling and simulation …
Open" back door" in a molecular dynamics simulation of acetylcholinesterase
MK Gilson, TP Straatsma, JA McCammon, DR Ripoll… - Science, 1994 - science.org
The enzyme acetylcholinesterase generates a strong electrostatic field that can attract the
cationic substrate acetylcholine to the active site. However, the long and narrow active site …
cationic substrate acetylcholine to the active site. However, the long and narrow active site …
Crystal structure of an acetylcholinesterase–fasciculin complex: interaction of a three-fingered toxin from snake venom with its target
M Harel, GJ Kleywegt, RBG Ravelli, I Silman… - Structure, 1995 - cell.com
Abstract Background: Fasciculin (FAS), a 61-residue polypeptide purified from mamba
venom, is a three-fingered toxin which is a powerful reversible inhibitor of …
venom, is a three-fingered toxin which is a powerful reversible inhibitor of …