Molecular docking and in vitro evaluation of a new hybrid molecule (JM-20) on cholinesterase activity from different sources
FDA da Silva, PA Nogara, E Ochoa-Rodriguez… - Biochimie, 2020 - Elsevier
The main function of AChE is the hydrolysis of the neurotransmitter acetylcholine (ACh) at
the neuromuscular and in cholinergic brain synapses. In some pathologies, loss of …
the neuromuscular and in cholinergic brain synapses. In some pathologies, loss of …
A facile eco-friendly one-pot five-component synthesis of novel 1, 2, 3-triazole-linked pentasubstituted 1, 4-dihydropyridines and their biological and photophysical …
H Singh, J Sindhu, JM Khurana… - Australian Journal of …, 2013 - CSIRO Publishing
An eco-friendly one-pot five-component synthesis of novel 1, 2, 3-triazole-linked
pentasubstituted 1, 4-dihydropyridines under ultrasonic and microwave irradiation in …
pentasubstituted 1, 4-dihydropyridines under ultrasonic and microwave irradiation in …
[HTML][HTML] Design and synthesis of novel 4-substituted 1, 4-dihydropyridine derivatives as hypotensive agents
PA Datar, PB Auti - Journal of Saudi Chemical Society, 2016 - Elsevier
Calcium-channel blockers have an important role in the treatment of several cardiovascular
disorders. Derivatives of 1, 4-dihydropyridines are one of the most potent calcium …
disorders. Derivatives of 1, 4-dihydropyridines are one of the most potent calcium …
Novel multipotent phenylthiazole–tacrine hybrids for the inhibition of cholinesterase activity, β-amyloid aggregation and Ca2+ overload
Y Wang, F Wang, JP Yu, FC Jiang, XL Guan… - Bioorganic & medicinal …, 2012 - Elsevier
In this study, a series of multipotent phenylthiazole–tacrine hybrids (7a–7e, 8, and 9a–9m)
were synthesized and biologically evaluated. Screening results showed that phenylthiazole …
were synthesized and biologically evaluated. Screening results showed that phenylthiazole …
Ruthenium-porphyrin-catalyzed [4+ 2] cycloaddition of α, β-unsaturated imines and aldehydes
K Maeda, T Terada, T Iwamoto, T Kurahashi… - Organic …, 2015 - ACS Publications
A new efficient synthetic route to unsymmetrically substituted dihydropyridine scaffolds via
dehydrative [4+ 2] cycloaddition of N-tosylated α, β-unsaturated imines with aldehydes has …
dehydrative [4+ 2] cycloaddition of N-tosylated α, β-unsaturated imines with aldehydes has …
Predicting targets of compounds against neurological diseases using cheminformatic methodology
K Nikolic, L Mavridis, OM Bautista-Aguilera… - Journal of computer …, 2015 - Springer
Recently developed multi-targeted ligands are novel drug candidates able to interact with
monoamine oxidase A and B; acetylcholinesterase and butyrylcholinesterase; or with …
monoamine oxidase A and B; acetylcholinesterase and butyrylcholinesterase; or with …
A novel acetylcholinesterase inhibitor and calcium channel blocker SCR-1693 improves Aβ25–35-impaired mouse cognitive function
Z Zhang, R Chen, W An, C Wang, G Liao, X Dong… - …, 2016 - Springer
Rationale The mechanism involved in AD is complex, which has prompted to develop
compounds that could simultaneously interact with several potential targets. Here, we report …
compounds that could simultaneously interact with several potential targets. Here, we report …
Novel multitarget hybrid compounds for the treatment of Alzheimer's disease
P Michalska, I Buendia, L Barrio… - Current Topics in …, 2017 - ingentaconnect.com
Alzheimer's disease (AD) is the most prevalent among the aging diseases known as
neurodegenerative disorders. Drug design programs over the last two decades were mainly …
neurodegenerative disorders. Drug design programs over the last two decades were mainly …
Synthesis of novel acridine-sulfonamide hybrid compounds as acetylcholinesterase inhibitor for the treatment of alzheimer's disease
In this study we report that amino acridine intermediates 7 and 8 were obtained from the
reduction of nitro acridine derivatives 5 and 6 that were synthesized via the condensation of …
reduction of nitro acridine derivatives 5 and 6 that were synthesized via the condensation of …
Construction of Virtual Compound Library and Screening of Acetylcholinesterase Inhibitor for the Medicinal Chemistry Laboratory
J Yang, Y Yuan, N Wang, X Liu, J Gu… - Journal of Chemical …, 2024 - ACS Publications
The utilization of virtual compound libraries and virtual screening has become a routine
method in drug discovery and has accelerated the research of pharmacy and translational …
method in drug discovery and has accelerated the research of pharmacy and translational …