Synthesis and biological evaluation of 1, 3, 4-thiadiazole analogues as novel AChE and BuChE inhibitors

A Skrzypek, J Matysiak, A Niewiadomy, M Bajda… - European journal of …, 2013 - Elsevier
In this paper a series of new 1, 3, 4-thiadiazole derivatives has been designed, synthesized
and evaluated as the acetyl-and butyrylcholinesterase inhibitors. Some analogues showed …

Synthesis and biological evaluation of thiazole-based derivatives as potential acetylcholinesterase inhibitors

AY Hemaida, GS Hassan, AR Maarouf, J Joubert… - ACS …, 2021 - ACS Publications
Nineteen new thiazole-based derivatives were synthesized and their structures
characterized with analytical and spectral data. The in vitro assessment of their …

[HTML][HTML] Novel triazole-quinoline derivatives as selective dual binding site acetylcholinesterase inhibitors

SP Mantoani, TPC Chierrito, AFL Vilela, CL Cardoso… - Molecules, 2016 - mdpi.com
Alzheimer's disease (AD) is the most prevalent neurodegenerative disorder worldwide.
Currently, the only strategy for palliative treatment of AD is to inhibit acetylcholinesterase …

Synthesis and anticholinesterase activities of novel 1, 3, 4-thiadiazole based compounds

A Skrzypek, J Matysiak, MM Karpińska… - Journal of Enzyme …, 2013 - Taylor & Francis
In the present study, new (1, 3, 4-thiadiazol-2-yl) benzene-1, 3-diol based compounds have
been synthesized and their potential anticholinesterases properties have been investigated …

Synthesis of novel benzimidazole and benzothiazole derivatives bearing a 1, 2, 3-triazole ring system and their acetylcholinesterase inhibitory activity

L Faraji, S Shahkarami, H Nadri… - Journal of Chemical …, 2017 - journals.sagepub.com
A series of 20 novel benzimidazole and benzothiazole derivatives linked to a 1, 2, 3-triazole
ring system was synthesised, characterised and evaluated for in vitro acetylcholinesterase …

1, 2, 3-Triazole-Isoxazole based acetylcholinesterase inhibitors: Synthesis, biological evaluation and docking study

Z Najafi, M Mahdavi, M Saeedi… - Letters in Drug …, 2017 - ingentaconnect.com
In this work, a series of derivatives containing 1, 2, 3-triazole and isoxazole were
synthesized. All of them were evaluated as novel dual AChE inhibitors. Most of synthesized …

Novel structural hybrids of pyrazolobenzothiazines with benzimidazoles as cholinesterase inhibitors

S Aslam, S Zaib, M Ahmad, JM Gardiner… - European journal of …, 2014 - Elsevier
Two series of novel pyrazolobenzothiazine-based hybrid compounds were efficiently
synthesized starting from saccharin sodium salt. Pyrazolo [4, 3-c][1, 2] benzothiazine …

Design, synthesis, and AChE inhibitory activity of new benzothiazole–piperazines

ÜD Özkay, ÖD Can, BN Sağlık, UA Çevik… - Bioorganic & medicinal …, 2016 - Elsevier
In the current study, 14 new benzothiazole–piperazine compounds were designed to meet
the structural requirements of acetylcholine esterase (AChE) inhibitors. The target …

Design and synthesis of selective acetylcholinesterase inhibitors: arylisoxazole‐phenylpiperazine derivatives

M Saeedi, D Mohtadi‐Haghighi… - Chemistry & …, 2019 - Wiley Online Library
In this work, a novel series of arylisoxazole‐phenylpiperazines were designed, synthesized,
and evaluated toward acetylcholinesterase (AChE) and butyrylcholinesterase (BChE). Our …

Novel benzisoxazole derivatives as potent and selective inhibitors of acetylcholinesterase

A Villalobos, JF Blake, CK Biggers… - Journal of medicinal …, 1994 - ACS Publications
A series of iV-benzylpiperidine benzisoxazoles has been developed as potent and selective
inhibitors of the enzyme acetylcholinesterase (AChE). The benzisoxazole heterocycle was …