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Novel Arylidene Thiobarbiturate Derivatives as Selective Acetylcholinesterase, Α-Glucosidase, and Nonclassical Human Carbonic Anhydrase Inhibitors: Biological Activity and Molecular Modeling Study

https://doi.org/10.2139/ssrn.4803185
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Rapid screening and identification of α ‐glucosidase inhibitors from mulberry leaves using enzyme‐immobilized magnetic beads coupled with HPLC/MS and NMR
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Thiobarbiturates as Sirtuin Inhibitors: Virtual Screening, Free‐Energy Calculations, and Biological Testing
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MAB, a generally applicable molecular force field for structure modelling in medicinal chemistry
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Strenuous endurance training in humans reduces oxidative stress following exhausting exercise
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Antibacterial, Antiurease, and Antioxidant Activities of Some Arylidene Barbiturates
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Assay for lipid peroxides in animal tissues by thiobarbituric acid reaction
inferredcites →https://doi.org/10.1016/0006-2952(61)90145-9openalex-extracted
A new and rapid colorimetric determination of acetylcholinesterase activity
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Taurine as a green bio-organic catalyst for the preparation of bio-active barbituric and thiobarbituric acid derivatives in water media
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A new entry into the portfolio of α-glucosidase inhibitors as potent therapeutics for type 2 diabetes: Design, bioevaluation and one-pot multi-component synthesis of diamine-bridged coumarinyl oxadiazole conjugates
inferredcites →https://doi.org/10.1016/j.bioorg.2019.01.033openalex-extracted
Mechanistic investigation of anthocyanidin derivatives as α-glucosidase inhibitors
inferredcites →https://doi.org/10.1016/j.bioorg.2019.102980openalex-extracted
Synthesis of oxazolidinone from enantiomerically enriched allylic alcohols and determination of their molecular docking and biologic activities
inferredcites →https://doi.org/10.1016/j.bmc.2015.04.019openalex-extracted
Discovery of potent carbonic anhydrase and acetylcholine esterase inhibitors: Novel sulfamoylcarbamates and sulfamides derived from acetophenones
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Structure-based design of potent and selective inhibitors of collagenase-3 (MMP-13)
inferredcites →https://doi.org/10.1016/j.bmcl.2008.02.066openalex-extracted
Synthesis of barbiturate-based methionine aminopeptidase-1 inhibitors
inferredcites →https://doi.org/10.1016/j.ejmech.2009.05.023openalex-extracted
Inhibitory effects of 5-benzylidene barbiturate derivatives on mushroom tyrosinase and their antibacterial activities
inferredcites →https://doi.org/10.1016/j.ejmech.2017.11.070openalex-extracted
Trisubstituted barbiturates and thiobarbiturates: Synthesis and biological evaluation as xanthine oxidase inhibitors, antioxidants, antibacterial and anti-proliferative agents
inferredcites →https://doi.org/10.1016/j.jmgm.2011.07.001openalex-extracted
Molecular modeling-based antioxidant arylidene barbiturates as urease inhibitors
inferredcites →https://doi.org/10.1016/j.molstruc.2022.134535openalex-extracted
7,8-Dihydroxycoumarin derivatives: In silico molecular docking and in vitro anticholinesterase activity
inferredcites →https://doi.org/10.1021/acsomega.0c00468openalex-extracted
Barbiturate- and Thiobarbituarte-Based s -Triazine Hydrazone Derivatives with Promising Antiproliferative Activities
inferredcites →https://doi.org/10.1021/jf048741xopenalex-extracted
Novel Total Antioxidant Capacity Index for Dietary Polyphenols and Vitamins C and E, Using Their Cupric Ion Reducing Capability in the Presence of Neocuproine: CUPRAC Method
inferredcites →https://doi.org/10.1021/jf100853copenalex-extracted
Inhibition of Three Selected Beverage Extracts on α-Glucosidase and Rapid Identification of Their Active Compounds Using HPLC-DAD-MS/MS and Biochemical Detection
inferredcites →https://doi.org/10.1021/jm050550dopenalex-extracted
Discovery of Nonpeptidic Small-Molecule AP-1 Inhibitors: Lead Hopping Based on a Three-Dimensional Pharmacophore Model
inferredcites →https://doi.org/10.1023/a:1022869222652openalex-extracted
Cholinesterases: New Roles in Brain Function and in Alzheimer's Disease
inferredcites →https://doi.org/10.1038/nrd2467openalex-extracted
Carbonic anhydrases: novel therapeutic applications for inhibitors and activators
inferredcites →https://doi.org/10.1074/jbc.274.43.30370openalex-extracted
Conformational Flexibility of the Acetylcholinesterase Tetramer Suggested by X-ray Crystallography
inferredcites →https://doi.org/10.1080/07391102.2020.1863263openalex-extracted
Design and in silico study of the novel coumarin derivatives against SARS-CoV-2 main enzymes
inferredcites →https://doi.org/10.1080/17460441.2017.1253677openalex-extracted
Advances in structure-based drug discovery of carbonic anhydrase inhibitors
inferredcites →https://doi.org/10.1093/bja/67.5.539openalex-extracted
PROPOFOL AND MIDAZOLAM ACT SYNERGISTICALLY IN COMBINATION
inferredcites →https://doi.org/10.1093/nar/28.1.235openalex-extracted
The Protein Data Bank
inferredcites →https://doi.org/10.1093/nar/gkw1132openalex-extracted
The SWISS-MODEL Repository—new features and functionality
inferredcites →https://doi.org/10.1107/s1744309109036665openalex-extracted
High-resolution structure of human carbonic anhydrase II complexed with acetazolamide reveals insights into inhibitor drug design
inferredcites →https://doi.org/10.1124/jpet.104.071332openalex-extracted
Inhibition of Activator Protein 1 by Barbiturates Is Mediated by Differential Effects on Mitogen-Activated Protein Kinases and the Small G Proteins Ras and Rac-1
inferredcites →https://doi.org/10.1145/174462.156635openalex-extracted
Three-dimensional alpha shapes
inferredcites →https://doi.org/10.1146/annurev.arplant.45.1.369openalex-extracted
The Role of Carbonic Anhydrase in Photosynthesis
inferredcites →https://doi.org/10.3906/kim-2012-55openalex-extracted
Synthesis and molecular docking study of novel COVID-19 inhibitors
inferredcites →https://doi.org/10.1146/annurev.pp.45.060194.002101openalex-snapshot
The Role of Carbonic Anhydrase in Photosynthesis
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