Microwave-assisted copper (II)-catalyzed one-pot four-component synthesis of multifunctionalized dihydropyridines

KK Pasunooti, C Nixon Jensen, H Chai… - Journal of …, 2010 - ACS Publications
A fast and highly efficient copper-catalyzed multicomponent synthesis of 1, 4-
dihydropyridines under microwave irradiation is described. The protocol utilizes mild …

Recent highlights on molecular hybrids potentially useful in central nervous system disorders

M Matias, S Silvestre, A Falcao… - Mini Reviews in …, 2017 - ingentaconnect.com
Molecular hybridization is a recent strategy based on the covalent fusion of two or more
pharmacophores to create a single molecule with multiple mechanisms of action, which …

Tacrines as therapeutic agents for Alzheimer's disease. IV. The tacripyrines and related annulated tacrines

M Bartolini, J Marco‐Contelles - The Chemical Record, 2019 - Wiley Online Library
Notwithstanding the clinical use of tacrine was hampered by severe hepatotoxicity, tacrine
still remains a reference scaffold in the search for new efficient drugs for Alzheimer's disease …

Fused 1, 4‐Dihydropyridines and Their Corresponding Pyridines: Synthesis, Molecular Modeling and Cholinesterase Inhibition

Z Najafi, M Alaei, A Bahmani, T Akbarzadeh… - …, 2023 - Wiley Online Library
Abstract Novel series of fused 1, 4‐dihydropyridine derivatives were designed and
synthesized. Oxidized to the corresponding pyridines were these dihydropyridines. Both …

Benzothiazepine CGP37157 and its isosteric 2′-methyl analogue provide neuroprotection and block cell calcium entry

L Gonzalez-Lafuente, J Egea, R León… - ACS Chemical …, 2012 - ACS Publications
Benzothiazepine CGP37157 is widely used as tool to explore the role of mitochondria in cell
Ca2+ handling, by its blocking effect of the mitochondria Na+/Ca2+ exchanger. Recently …

Synthesis, biological assessment and molecular modeling of 14-aryl-10, 11, 12, 14-tetrahydro-9H-benzo [5, 6] chromeno [2, 3-b] quinolin-13-amines

E Maalej, F Chabchoub, A Samadi… - Bioorganic & medicinal …, 2011 - Elsevier
The synthesis and pharmacological evaluation of racemic 14-aryl-10, 11, 12, 14-tetrahydro-
9H-benzo [5, 6] chromeno [2, 3-b] quinolin-13-amines (19–28), prepared by Friedländer …

Quantitative structure and bioactivity relationship study on human acetylcholinesterase inhibitors

A Yan, K Wang - Bioorganic & Medicinal Chemistry Letters, 2012 - Elsevier
Several QSAR (Quantitative Structure–Activity Relationships) models for predicting the
inhibitory activity of 404 Acetylcholinesterase inhibitors were developed. The whole dataset …

Acetamidines and acetamidoximes containing an electron-withdrawing group at the α-carbon atom: their use in the synthesis of nitrogen heterocycles

PS Lobanov, DV Dar'in - Chemistry of Heterocyclic Compounds, 2013 - Springer
Published information on heterocyclizations involving acetamidines and acetamidoximes
substituted at the α-position with an electron-withdrawing group is reviewed, where these …

Molecular diversity from the three-component reaction of 2-hydroxy-1, 4-naphthaquinone, aldehydes and 6-aminouracils: a reaction condition dependent MCR

R Bharti, P Kumari, T Parvin, LH Choudhury - RSC advances, 2017 - pubs.rsc.org
The three-component reaction of 2-hydroxy-1, 4-naphthaquinone, aldehydes, and 6-
aminouracil derivatives in acetic acid/water (1: 1; v/v) under microwave heating conditions …

CADD modeling of multi-target drugs against Alzheimer's disease

P Ambure, K Roy - Current Drug Targets, 2017 - ingentaconnect.com
Alzheimer's disease (AD) is a neurodegenerative disorder that is described by multiple
factors linked with the progression of the disease. The currently approved drugs in the …