Biological evaluation and molecular docking studies of 4-aminobenzohydrazide derivatives as cholinesterase inhibitors

Z Almaz, A Oztekin, A Tan, H Ozdemir - Journal of Molecular Structure, 2021 - Elsevier
Nowadays, inhibition of the acetylcholinesterase (AChE) and butyrylcholinesterase (BChE)
enzymes have emerged as an encouraging approach in the treatment of dementia and …

Synthesis, in silico and in vitro studies of hydrazide‐hydrazone imine derivatives as potential cholinesterase inhibitors

SA Güngör - Chemical Biology & Drug Design, 2023 - Wiley Online Library
A series of hydrazide‐hydrazone imine derivative compounds (3a–k) were synthesized and
their structures characterized using FTIR, 1H, and 13C (NMR) spectroscopic methods. In …

A series of new hydrazone derivatives: Synthesis, molecular docking and anticholinesterase activity studies

İ Bozbey, Z Özdemir, H Uslu, AB Özçelik… - Mini reviews in …, 2020 - ingentaconnect.com
Background: Acetylcholinesterase (AChE) and butyrylcholinesterase (BChE) are known to
be serine hydrolase enzymes responsible for the hydrolysis of acetylcholine (ACh), which is …

[HTML][HTML] Synthesis and AChE-inhibitory activity of new benzimidazole derivatives

U Acar Cevik, BN Saglik, S Levent, D Osmaniye… - Molecules, 2019 - mdpi.com
Alzheimer's disease (AD), one of the main causes of aged dementia, is a progressive and
degenerative neurological disorder characterized by loss of cognition and memory …

In silico studies on 2, 3-dihydro-1, 5-benzothiazepines as cholinesterase inhibitors

FL Ansari, S Kalsoom, Z Ali, F Jabeen - Medicinal Chemistry Research, 2012 - Springer
In vitro studies on cholinesterase inhibitory potential on the three sets of 2, 3-dihydro-1, 5-
benzothiazepines have been carried out. The compounds in Set 1 were unsubstituted on …

Bioactive sulfonyl hydrazones with alkyl derivative: Characterization, ADME properties, molecular docking studies and investigation of inhibition on choline esterase …

E Bilen, ÜÖ Özmen, S Çete, S Alyar, A Yaşar - Chemico-Biological …, 2022 - Elsevier
In this work, new sulfonylhydrazone compounds with alkyl derivatives (SH1–SH4 series)
were synthesized via a green chemistry method, and their inhibition effects on …

Molecular docking and investigation of 4-(benzylideneamino)-and 4-(benzylamino)-benzenesulfonamide derivatives as potent AChE inhibitors

M Işık, Y Demir, M Durgun, C Türkeş, A Necip… - Chemical Papers, 2020 - Springer
The discovery of acetylcholinesterase inhibitors is important for the treatment of Alzheimer's
disease (AD), known as the most common type of dementia. Due to the side effects of …

Multifunctional cholinesterase inhibitors for Alzheimer's disease: Synthesis, biological evaluations, and docking studies of o/p‐propoxyphenylsubstituted‐1H …

G Sarıkaya, G Çoban, S Parlar… - Archiv der …, 2018 - Wiley Online Library
This study indicates the synthesis, cholinesterase (ChE) inhibitory activity, and molecular
modeling studies of 48 compounds as o‐and p‐(3‐substitutedethoxyphenyl)‐1H …

Design, synthesis, evaluation and molecular modeling study of 4-N-phenylaminoquinolines for Alzheimer disease treatment

J Zhu, LN Wang, R Cai, SQ Geng, YF Dong… - Bioorganic & Medicinal …, 2019 - Elsevier
Dual binding site acetylcholinesterase (AChE) inhibitors and butyrylcholinesterase (BChE)
inhibitors have recently emerged as two classes of new anti-Alzheimer agents to positively …

Synthesis, biological evaluation, theoretical investigations, docking study and ADME parameters of some 1, 4-bisphenylhydrazone derivatives as potent antioxidant …

I Amine Khodja, H Boulebd - Molecular Diversity, 2021 - Springer
Abstract Five 1, 4-bisphenylhydrazone derivatives (1–5) were successfully synthesized and
evaluated for their antioxidant and acetylcholinesterase inhibitory activities. The antioxidant …