Tacripyrimidines, the first tacrine-dihydropyrimidine hybrids, as multi-target-directed ligands for Alzheimer's disease

M Chioua, E Buzzi, I Moraleda, I Iriepa, M Maj… - European Journal of …, 2018 - Elsevier
Notwithstanding the combination of cholinesterase (ChE) inhibition and calcium channel
blockade within a multitarget therapeutic approach is envisaged as potentially beneficial to …

Tacrines as therapeutic agents for alzheimer's disease. V. recent developments

ÓM Bautista‐Aguilera, L Ismaili, I Iriepa… - The Chemical …, 2021 - Wiley Online Library
Herein we have reviewed our recent developments for the identification of new tacrine
analogues for Alzheimer's disease (AD) therapy. Tacrine, the first cholinesterase inhibitor …

Newly developed drugs for Alzheimer's disease in relation to energy metabolism, cholinergic and monoaminergic neurotransmission

J Korábečný, E Nepovimova, T Cikankova, K Špilovská… - Neuroscience, 2018 - Elsevier
Current options for Alzheimer's disease (AD) treatment are based on administration of
cholinesterase inhibitors (donepezil, rivastigmine, galantamine) and/or memantine, acting …

Inhibition of cholinesterase activity and amyloid aggregation by berberine-phenyl-benzoheterocyclic and tacrine-phenyl-benzoheterocyclic hybrids

L Huang, T Su, W Shan, Z Luo, Y Sun, F He… - Bioorganic & medicinal …, 2012 - Elsevier
A series of berberine-phenyl-benzoheterocyclic (26–29) and tacrine-phenyl-
benzoheterocyclic hybrids (44–46) were synthesised and evaluated as multifunctional anti …

A Four‐Component Domino Reaction: An Eco‐Compatible and Highly Efficient Construction of 1,8‐Naphthyridine Derivatives, Their In Silico Molecular Docking, Drug …

A Garg, A Tadesse, R Eswaramoorthy - Journal of Chemistry, 2021 - Wiley Online Library
A multicomponent domino reaction of enaminone, malononitrile, and o‐phthalaldehyde has
been established, providing direct access to novel highly functionalized pentacyclic …

Dual inhibitors of β-amyloid aggregation and acetylcholinesterase as multi-target anti-Alzheimer drug candidates

E Viayna, R Sabate… - Current topics in medicinal …, 2013 - ingentaconnect.com
Notwithstanding the functional role that the aggregates of some amyloidogenic proteins can
play in different organisms, protein aggregation plays a pivotal role in the pathogenesis of a …

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 …

[HTML][HTML] Neuroactive multifunctional tacrine congeners with cholinesterase, anti-amyloid aggregation and neuroprotective properties

M Kozurkova, S Hamulakova, Z Gazova, H Paulikova… - Pharmaceuticals, 2011 - mdpi.com
The review summarizes research into the highly relevant topics of cholinesterase and
amyloid aggregation inhibitors connected to tacrine congeners, both of which are associated …

B(C6F5)3-Catalyzed α,β-Difunctionalization and C–N Bond Cleavage of Saturated Amines with Benzo[c]isoxazoles: Access to Quinoline Derivatives

Y He, Q Liu, Z Du, Y Xu, L Cao, X Zhang… - The Journal of Organic …, 2022 - ACS Publications
Herein, we disclose a strategy to realize α, β-difunctionalization and C–N bond cleavage of
saturated amines with benzo [c] isoxazoles via a B (C6F5) 3-catalyzed consecutive …

Searching for the multi-target-directed ligands against Alzheimer's disease: discovery of quinoxaline-based hybrid compounds with AChE, H3R and BACE 1 inhibitory …

W Huang, L Tang, Y Shi, S Huang, L Xu… - Bioorganic & medicinal …, 2011 - Elsevier
A novel series of quinoxaline derivatives, as Multi-Target-Directed Ligands (MTDLs) for AD
treatment, were designed by lending the core structural elements required for H3R …