Recent advance on carbamate-based cholinesterase inhibitors as potential multifunctional agents against Alzheimer's disease

H Zhang, Y Wang, Y Wang, X Li, S Wang… - European Journal of …, 2022 - Elsevier
Abstract Alzheimer's disease (AD), as the fourth leading cause of death among the elderly
worldwide, has brought enormous challenge to the society. Due to its extremely complex …

Acetylcholinesterase inhibitors as Alzheimer therapy: from nerve toxins to neuroprotection

M Singh, M Kaur, H Kukreja, R Chugh, O Silakari… - European journal of …, 2013 - Elsevier
Acetylcholinesterase is a member of the α/β hydrolase protein super family, with a significant
role in acetylcholine-mediated neurotransmission. Research in the modulators of AChEs …

Recent developments in cholinesterases inhibitors for Alzheimer's disease treatment

A Musial, M Bajda, B Malawska - Current medicinal chemistry, 2007 - ingentaconnect.com
Alzheimer's disease (AD) is a progressive neurodegenerative disorder of the central
nervous system (CNS) which is the most common cause of dementia in the elderly. It is …

Discovery of highly selective and nanomolar carbamate-based butyrylcholinesterase inhibitors by rational investigation into their inhibition mode

E Sawatzky, S Wehle, B Kling, J Wendrich… - Journal of medicinal …, 2016 - ACS Publications
Butyrylcholinesterase (BChE) is a promising target for the treatment of later stage cognitive
decline in Alzheimer's disease. A set of pseudo-irreversible BChE inhibitors with high …

Identifying possible AChE inhibitors from drug-like molecules via machine learning and experimental studies

TH Nguyen, PT Tran, NQA Pham, VH Hoang… - ACS …, 2022 - ACS Publications
Acetylcholinesterase (AChE) is one of the most important drug targets for Alzheimer's
disease (AD) treatment. In this work, a machine learning model was trained to rapidly and …

Iron-catalyzed oxidative C (3)–H functionalization of amines

N Takasu, K Oisaki, M Kanai - Organic letters, 2013 - ACS Publications
Fe-catalyzed direct dehydrogenative C (3)-functionalization of tertiary arylamines was
developed via activation of the sp3 C (3)–H bond. The reaction is applicable to both cyclic …

One-Step Synthesis of Hydropyrrolo[3,2-b]indoles via Cascade Reactions of Oxindole-Derived Nitrones with Allenoates

ML Luo, Q Hou, SJ Liu, Q Zhao, R Qin, C Peng… - Organic …, 2022 - ACS Publications
Hydropyrrolo [2, 3-b] indole is a privileged indoline motif, while its analogue, hydropyrrolo [3,
2-b] indole, has been much less explored. Herein, we developed a cascade reaction of …

Novel carbamates as orally active acetylcholinesterase inhibitors found to improve scopolamine-induced cognition impairment: pharmacophore-based virtual …

SS Chaudhaery, KK Roy, N Shakya… - Journal of Medicinal …, 2010 - ACS Publications
A systematic virtual screening (VS) experiment, consisting of the development of 3D-
pharmacophore, screening of virtual library, synthesis, and pharmacology, is reported. The …

The kinetics of inhibition of human acetylcholinesterase and butyrylcholinesterase by two series of novel carbamates

E Groner, Y Ashani, D Schorer-Apelbaum… - Molecular …, 2007 - ASPET
Controlled inhibition of brain acetyl-and butyrylcholinesterases (AChE and BChE,
respectively) and of monoamine oxidase-B (MAO-B) may slow neurodegeneration in …

Asymmetric N-oxidation catalyzed by bisguanidinium dinuclear oxodiperoxomolybdosulfate

W Wu, ECX Ang, X Xu, Q Wang, H Wang, R Lee… - Nature …, 2024 - nature.com
N-oxides play a pivotal role in natural products and emerging drug design, while also
serving as valuable ligand scaffolds in organometallic chemistry. Among heteroatom …