Novel thiophene Chalcones-Coumarin as acetylcholinesterase inhibitors: Design, synthesis, biological evaluation, molecular docking, ADMET prediction and …

AH Hasan, S Murugesan, SI Amran, S Chander… - Bioorganic …, 2022 - Elsevier
A series of around eight novel chalcone based coumarin derivatives (23a-h) was designed,
subjected to in-silico ADMET prediction, synthesized, characterized by IR, NMR, Mass …

Thiazole-pyrazoline hybrids as potential antimicrobial agent: Synthesis, biological evaluation, molecular docking, DFT studies and POM analysis

RHH Salih, AH Hasan, NH Hussen, FE Hawaiz… - Journal of Molecular …, 2023 - Elsevier
In this study, an efficient synthesis of new thiazole-pyrazoline hybrids was investigated and
hybrids were screened for their antimicrobial activities against four species of pathogenic …

Discovery of novel coumarin-schiff base hybrids as potential acetylcholinesterase inhibitors: design, synthesis, enzyme inhibition, and computational studies

AH Hasan, FA Abdulrahman, AJ Obaidullah… - Pharmaceuticals, 2023 - mdpi.com
To discover anti-acetylcholinesterase agents for the treatment of Alzheimer's disease (AD), a
series of novel Schiff base-coumarin hybrids was rationally designed, synthesized …

Design, synthesis, anti-acetylcholinesterase evaluation and molecular modelling studies of novel coumarin-chalcone hybrids

AH Hasan, S Shakya, FHS Hussain… - Journal of …, 2023 - Taylor & Francis
The major enzyme responsible for the hydrolytic breakdown of the neurotransmitter
acetylcholine (ACh) is acetylcholinesterase (AChE). Acetylcholinesterase inhibitors …

Design, synthesis, biological activity, molecular docking, and molecular dynamics of novel benzimidazole derivatives as potential AChE/MAO‐B dual inhibitors

D Osmaniye, AE Evren, BN Sağlık, S Levent… - Archiv der …, 2022 - Wiley Online Library
To develop new acetylcholinesterase (AChE)–monoamine oxidase‐B (MAO‐B) dual
inhibitors against Alzheimer's disease, the benzimidazole ring, which has a propargyl side …

Synthesis, biological evaluation and molecular modeling studies of modulated benzyloxychalcones as potential acetylcholinesterase inhibitors

A Abdalla Ali, SA Mhamad, AH Hasan… - Journal of …, 2024 - Taylor & Francis
Acetylcholinesterase inhibitors (AChEIs) have become a significant target in the search for
an efficient treatment of Alzheimer's disease. Chalcone-based compounds display a strong …

Design and discovery of anthranilamide derivatives as a potential treatment for neurodegenerative disorders via targeting cholinesterases and monoamine oxidases

S Zaib, I Khan, HS Ali, MT Younas, A Ibrar… - International Journal of …, 2024 - Elsevier
Neurodegenerative diseases with progressive cellular loss of the central nervous system
and elusive disease etiology provide a continuous impetus to explore drug discovery …

Coumarin–azasugar–benzyl conjugates as non-neurotoxic dual inhibitors of butyrylcholinesterase and cancer cell growth

ICV Holmgard, A González-Bakker, E Poeta… - Organic & …, 2024 - pubs.rsc.org
We have applied the copper-catalyzed azide–alkyne cycloaddition (CuAAC) reaction to
prepare a library of ten coumarin–azasugar–benzyl conjugates and two phthalimide …

Design and synthesis of novel chalcone derivatives and evaluation of their inhibitory activities against acetylcholinesterase

I Ceyhun, Ş Karaca, D Osmaniye, BN Sağlık… - Archiv der …, 2022 - Wiley Online Library
According to the cholinergic hypothesis, an increase in the acetylcholine level in Alzheimer's
disease patients relatively slows down the symptoms of the disease. The most commonly …

Benzyloxychalcone Hybrids as Prospective Acetylcholinesterase Inhibitors against Alzheimer's Disease: Rational Design, Synthesis, In Silico ADMET Prediction …

HM Al-Maqtari, AH Hasan, M Suleiman… - ACS …, 2024 - ACS Publications
Acetylcholinesterase inhibitors (AChEIs) are crucial therapeutic targets for both the early and
severe stages of Alzheimer's disease (AD). Chalcones and their chromone-based …