[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 …

Targeting acetylcholinesterase to treat neurodegeneration

U Holzgrabe, P Kapková, V Alptüzün… - Expert opinion on …, 2007 - Taylor & Francis
Neurodegenerative disorders, such as Alzheimer's disease, are often characterised by the
degeneration of the cholinergic system. Thus, the aim of many treatment regimens is to …

Acetylcholinesterase inhibitors: pharmacology and toxicology

MB Colovic, DZ Krstic… - Current …, 2013 - ingentaconnect.com
Acetylcholinesterase is involved in the termination of impulse transmission by rapid
hydrolysis of the neurotransmitter acetylcholine in numerous cholinergic pathways in the …

Binding interaction of allethrin with esterase: bioremediation potential and mechanism

P Bhatt, ER Rene, AJ Kumar, W Zhang, S Chen - Bioresource technology, 2020 - Elsevier
The main aim of this work was to study the allethrin binding interactions with esterase and its
bioremediation potential using an isolated bacterial strain CW7, identified as Pseudomonas …

Acetylcholinesterase: a primary target for drugs and insecticides

S Thapa, M Lv, H Xu - Mini reviews in medicinal chemistry, 2017 - ingentaconnect.com
Background: Acetylcholinesterase is a serine hydrolase that terminates the action of the
neurotransmitter acetylcholine by hydrolyzing it into acetic acid and choline. Objective: The …

Multitarget drugs of plants origin acting on Alzheimer's disease

P Russo, A Frustaci, A Del Bufalo… - Current medicinal …, 2013 - ingentaconnect.com
The etiopathology of Alzheimer's disease (AD) is extremely complex and heterogeneous,
often associated with comorbidities. As a result it may be unlikely that AD may be mitigated …

Three‐dimensional structure of a complex of galanthamine (Nivalin®) with acetylcholinesterase from Torpedo californica: Implications for the design of new anti …

C Bartolucci, E Perola, C Pilger, G Fels… - Proteins: structure …, 2001 - Wiley Online Library
The 3D structure of a complex of the anti‐Alzheimer drug galanthamine with Torpedo
californica acetylcholinesterase is reported. Galanthamine, a tertiary alkaloid extracted from …

Novel chirality descriptors derived from molecular topology

A Golbraikh, D Bonchev, A Tropsha - Journal of Chemical …, 2001 - ACS Publications
Several series of novel chirality descriptors of chemical organic molecules have been
introduced. The descriptors have been developed on the basis of conventional topological …

Novel benzothiazole sulfonamides as potent α-glucosidase and cholinesterase inhibitors: design, synthesis, structural properties, biological evaluation and docking …

S Khair-ul-Bariyah, M Sarfraz, A Sharif… - Journal of Molecular …, 2024 - Elsevier
A simplified synthetic method yielded diverse 2-aminobenzothiazole variants through
sulfonylation and amino group alkylation. Extensive characterization via X-ray diffraction …

Synthesis of a series of novel 2-amino-5-substituted 1, 3, 4-oxadiazole and 1, 3, 4-thiadiazole derivatives as potential anticancer, antifungal and antibacterial agents

EC Pham, TN Truong, NH Dong, DD Vo… - Medicinal …, 2022 - ingentaconnect.com
Background: Many compounds containing a five-membered heterocyclic ring display
exceptional chemical properties and versatile biological activities. Objective: The objective …