SAR study to find optimal cholinesterase reactivator against organophosphorous nerve agents and pesticides

L Gorecki, J Korabecny, K Musilek, D Malinak… - Archives of …, 2016 - Springer
Irreversible inhibition of acetylcholinesterase (AChE) by organophosphates leads to many
failures in living organism and ultimately in death. Organophosphorus compounds …

Design, synthesis, biological evaluation, and docking study of novel dual-acting thiazole-pyridiniums inhibiting acetylcholinesterase and β-amyloid aggregation for …

G Ghotbi, M Mahdavi, Z Najafi, FH Moghadam… - Bioorganic …, 2020 - Elsevier
New compounds containing thiazole and pyridinium moieties were designed and
synthesized. The potency of the synthesized compounds as selective inhibitors of …

Advances in the development of reactivators for the treatment of organophosphorus inhibited cholinesterase

A Thakur, P Patil, A Sharma… - Current Organic …, 2020 - benthamdirect.com
Organophosphorus Compounds (OPCs) are used as pesticides to control pest, as chemical
weapons in military conflict and unfortunately in the terrorist attack. These compounds are …

Rediscovering Cyanogen Gas for Organic Synthesis: Formation of 2-Cyanothiazole Derivatives

M Prieschl, J Sedelmeier, K Püntener… - The Journal of …, 2023 - ACS Publications
The expeditious synthesis of an API building block, 2-cyanothiazole, from cyanogen gas and
a readily available dithiane is reported. A previously undisclosed partially saturated …

[PDF][PDF] SYNTHESIS OF 1, 3-THIAZOLE DERIVATIVES.

R Omar, P Koparir, M Koparir - Indian Drugs, 2021 - researchgate.net
Many heterocyclic compounds containing nitrogen atom are used in drug development.
Thiazole is one of the most important heterocyclic compounds in drug design, which …

N-Heterocycles Scaffolds as Quorum Sensing Inhibitors. Design, Synthesis, Biological and Docking Studies

A Fuentes-Gutiérrez, E Curiel-Quesada… - International Journal of …, 2020 - mdpi.com
Quorum sensing is a communication system among bacteria to sense the proper time to
express their virulence factors. Quorum sensing inhibition is a therapeutic strategy to block …

[PDF][PDF] Investigation of experimental and in silico physicochemical properties of thiazole-pyridinium anti-acetylcholinesterase derivatives with potential anti-Alzheimer's …

G Ghotbi, M Hamzeh-Mivehroud, A Taghvimi… - Pharmaceutical …, 2020 - ps.tbzmed.ac.ir
Background: Physicochemical properties play important role in fundamental issues like
absorption and distribution of pharmaceuticals to the target tissue. This is particularly …

Unveiling new thiazole‐clubbed piperazine derivatives as multitarget anti‐AD: Design, synthesis, and in silico studies

EE Nasr, SS Tawfik, MAM Massoud… - Archiv der …, 2024 - Wiley Online Library
New thiazole‐clubbed piperazine derivatives were designed, synthesized, evaluated for
their inhibitory capabilities against human acetylcholinesterase and butyrylcholinesterase …

A review of the synthesis of quaternary acetylcholinesterase reactivators

D Malinak, J Korabecny, O Soukup… - Current Organic …, 2018 - ingentaconnect.com
Acetylcholinesterase (AChE) is well-known enzyme studied in many fields of research, eg in
Alzheimer's disease, Parkinson's disease, or in eco-toxicology as a biological marker. Many …

Synthesis and in vitro kinetic study of novel mono-pyridinium oximes as reactivators of organophosphorus (OP) inhibited human acetylcholinesterase (hAChE)

AK Valiveti, UM Bhalerao, J Acharya, HN Karade… - Chemico-Biological …, 2015 - Elsevier
A series of mono pyridinium oximes linked with arenylacetamides as side chains were
synthesized and their in vitro reactivation potential was evaluated against human …