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Isolation and in-silico approach of Modified Embelin derivative from Embelia ribes fruits as anti‐Alzheimer agent.
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- Natural Product Research, 2025, v. 39, n. 1, p. 208, doi. 10.1080/14786419.2023.2255920
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A Novel Galantamine–Curcumin Hybrid Inhibits Butyrylcholinesterase: A Molecular Dynamics Study.
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- Chemistry (2624-8549), 2024, v. 6, n. 6, p. 1645, doi. 10.3390/chemistry6060100
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Optimization of Culture Conditions for High Cell Productivity and Astaxanthin Accumulation in Vietnam's Green Microalgae Haematococcus pluvialis HB and a Neuroprotective Activity of Its Astaxanthin.
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- Bioengineering (Basel), 2024, v. 11, n. 12, p. 1176, doi. 10.3390/bioengineering11121176
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Anticholinesterase Activity and Bioactive Compound Profiling of Six Hop (Humulus lupulus L.) Varieties.
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- Foods, 2024, v. 13, n. 24, p. 4155, doi. 10.3390/foods13244155
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Quantification of Bioactive Compounds by HPLC-ESI-MS/MS and Evaluation of Antioxidant and Enzyme Inhibitory Activities of Acorn Flour Extracts.
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- Antioxidants, 2024, v. 13, n. 12, p. 1526, doi. 10.3390/antiox13121526
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Biological Implications of the Intrinsic Deformability of Human Acetylcholinesterase Induced by Diverse Compounds: A Computational Study.
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- Biology (2079-7737), 2024, v. 13, n. 12, p. 1065, doi. 10.3390/biology13121065
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α,β-DEHYDROPHENYLALANINE CHOLINE ESTERS: POTENT REVERSIBLE INHIBITORS OF HUMAN ACETYLCHOLINESTERASE AND BUTYRYLCHOLINESTERASE.
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- Electronic Journal of Natural Sciences, 2006, v. 6, n. 1, p. 14
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- Article
Purification of Acetylcholinesterase by 9-Amino-1,2,3,4-tetrahydroacridine from Human Erythrocytes.
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- Applied Biochemistry & Biotechnology, 2013, v. 170, n. 1, p. 198, doi. 10.1007/s12010-013-0177-3
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- Article
Acetylcholinesterase Immobilization on Polyacrylamide/Functionalized Multi-walled Carbon Nanotube Nanocomposite Nanofibrous Membrane.
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- Applied Biochemistry & Biotechnology, 2013, v. 170, n. 1, p. 91, doi. 10.1007/s12010-013-0162-x
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- Article
Purification of Soluble Acetylcholinesterase from Sheep Liver by Affinity Chromatography.
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- Applied Biochemistry & Biotechnology, 2011, v. 165, n. 1, p. 336, doi. 10.1007/s12010-011-9254-7
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Design, synthesis and cholinesterase inhibitory activity of α-mangostin derivatives.
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- Natural Product Research, 2020, v. 34, n. 10, p. 1380, doi. 10.1080/14786419.2018.1510925
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- Article
The natural phenolic compounds and their antioxidant and anticholinesterase potential of herb Leiotulus dasyanthus (K. Koch) Pimenov & Ostr.
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- Natural Product Research, 2020, v. 34, n. 9, p. 1303, doi. 10.1080/14786419.2018.1557176
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- Article
Two new prenylated C<sub>6</sub>–C<sub>3</sub> compounds from Illicium micranthum Dunn.
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- Natural Product Research, 2020, v. 34, n. 3, p. 425, doi. 10.1080/14786419.2018.1531860
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- Article
Screening of acetylcholinesterase inhibitors in marine organisms from the Caribbean Sea.
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- Natural Product Research, 2019, v. 33, n. 24, p. 3533, doi. 10.1080/14786419.2018.1481837
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Derivatization, molecular docking and in vitro acetylcholinesterase inhibitory activity of glycyrrhizin as a selective anti-Alzheimer agent.
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- Natural Product Research, 2019, v. 33, n. 18, p. 2591, doi. 10.1080/14786419.2018.1462177
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- Article
Sugammadex: A Novel Agent for the Reversal of Neuromuscular Blockade.
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- Pharmacotherapy, 2007, v. 27, n. 8, p. 1181, doi. 10.1592/phco.27.8.1181
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- Article
Monocrotophos detection with a bienzyme biosensor based on ionic-liquid-modified carbon nanotubes.
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- Analytical & Bioanalytical Chemistry, 2019, v. 411, n. 13, p. 2905, doi. 10.1007/s00216-019-01743-z
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- Article
Acetylcholinesterase-functionalized two-dimensional photonic crystal for the sensing of G-series nerve agents.
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- Analytical & Bioanalytical Chemistry, 2019, v. 411, n. 12, p. 2577, doi. 10.1007/s00216-019-01700-w
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An ultrasensitive signal-on electrochemiluminescence biosensor based on Au nanoclusters for detecting acetylthiocholine.
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- Analytical & Bioanalytical Chemistry, 2019, v. 411, n. 4, p. 905, doi. 10.1007/s00216-018-1513-9
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Screen-printed electrode modified with carbon black and chitosan: a novel platform for acetylcholinesterase biosensor development.
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- Analytical & Bioanalytical Chemistry, 2016, v. 408, n. 26, p. 7299, doi. 10.1007/s00216-016-9604-y
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A nano-silver enzyme electrode for organophosphorus pesticide detection.
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- Analytical & Bioanalytical Chemistry, 2016, v. 408, n. 21, p. 5819, doi. 10.1007/s00216-016-9694-6
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Cyclic voltammetric acetylcholinesterase biosensor for the detection of captan in apple samples with the aid of chemometrics.
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- Analytical & Bioanalytical Chemistry, 2015, v. 407, n. 16, p. 4863, doi. 10.1007/s00216-015-8687-1
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V-type nerve agents phosphonylate ubiquitin at biologically relevant lysine residues and induce intramolecular cyclization by an isopeptide bond.
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- Analytical & Bioanalytical Chemistry, 2014, v. 406, n. 21, p. 5171, doi. 10.1007/s00216-014-7706-y
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Development of a stable biosensor based on a SiO nanosheet-Nafion-modified glassy carbon electrode for sensitive detection of pesticides.
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- Analytical & Bioanalytical Chemistry, 2013, v. 405, n. 8, p. 2545, doi. 10.1007/s00216-012-6634-y
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- Article
Fluorescence biosensing micropatterned surfaces based on immobilized human acetylcholinesterase.
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- Analytical & Bioanalytical Chemistry, 2013, v. 405, n. 2/3, p. 795, doi. 10.1007/s00216-012-6237-7
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On-line immobilized acetylcholinesterase microreactor for screening of inhibitors from natural extracts by capillary electrophoresis.
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- Analytical & Bioanalytical Chemistry, 2012, v. 404, n. 8, p. 2397, doi. 10.1007/s00216-012-6333-8
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- Article
Paraoxonase Mimic by a Nanoreactor Aggregate Containing Benzimidazolium Calix and l‐Histidine: Demonstration of the Acetylcholine Esterase Activity.
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- Chemistry - A European Journal, 2021, v. 27, n. 18, p. 5737, doi. 10.1002/chem.202004944
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- Article
Chemoselective Hydrogenation of 6‐Alkynyl‐3‐fluoro‐2‐pyridinaldoximes: Access to First‐in‐Class 6‐Alkyl‐3‐Fluoro‐2‐pyridinaldoxime Scaffolds as New Reactivators of Sarin‐Inhibited Human Acetylcholinesterase with Increased Blood–Brain Barrier Permeability
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- Chemistry - A European Journal, 2020, v. 26, n. 65, p. 15035, doi. 10.1002/chem.202002012
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Frontispiece: Resurrection and Reactivation of Acetylcholinesterase and Butyrylcholinesterase.
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- Chemistry - A European Journal, 2019, v. 25, n. 21, p. N.PAG, doi. 10.1002/chem.201982161
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- Article
Resurrection and Reactivation of Acetylcholinesterase and Butyrylcholinesterase.
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- Chemistry - A European Journal, 2019, v. 25, n. 21, p. 5337, doi. 10.1002/chem.201805075
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- Article
Reversal of Tabun Toxicity Enabled by a Triazole‐Annulated Oxime Library—Reactivators of Acetylcholinesterase.
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- Chemistry - A European Journal, 2019, v. 25, n. 16, p. 4100, doi. 10.1002/chem.201805051
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- Article
Anisotropic Dual S‐Scheme Heterojunctions Mimic Natural Photosynthetic System for Boosting Photoelectric Response.
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- Angewandte Chemie, 2024, v. 136, n. 33, p. 1, doi. 10.1002/ange.202407481
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- Article
In Situ Assembly of Choline Acetyltransferase Ligands by a Hydrothiolation Reaction Reveals Key Determinants for Inhibitor Design.
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- Angewandte Chemie, 2021, v. 133, n. 2, p. 826, doi. 10.1002/ange.202011989
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Effects of sucrose and plant growth regulators on acetylcholinesterase inhibitory activity of alkaloids accumulated in shoot cultures of Amaryllidaceae.
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- Plant Cell, Tissue & Organ Culture, 2011, v. 106, n. 3, p. 381, doi. 10.1007/s11240-011-9933-7
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In silico and in vitro anti-AChE activity investigations of constituents from Mytragyna speciosa for Alzheimer's disease treatment.
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- Journal of Computer-Aided Molecular Design, 2021, v. 35, n. 3, p. 325, doi. 10.1007/s10822-020-00372-4
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An activity prediction model for steroidal and triterpenoidal inhibitors of Acetylcholinesterase enzyme.
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- Journal of Computer-Aided Molecular Design, 2020, v. 34, n. 10, p. 1079, doi. 10.1007/s10822-020-00324-y
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Computational exploration and experimental validation to identify a dual inhibitor of cholinesterase and amyloid-beta for the treatment of Alzheimer's disease.
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- Journal of Computer-Aided Molecular Design, 2020, v. 34, n. 9, p. 983, doi. 10.1007/s10822-020-00318-w
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Binding free energy calculations to rationalize the interactions of huprines with acetylcholinesterase.
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- Journal of Computer-Aided Molecular Design, 2018, v. 32, n. 5, p. 607, doi. 10.1007/s10822-018-0114-1
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- Article
Revealing the importance of linkers in K-series oxime reactivators for tabun-inhibited AChE using quantum chemical, docking and SMD studies.
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- Journal of Computer-Aided Molecular Design, 2017, v. 31, n. 8, p. 729, doi. 10.1007/s10822-017-0036-3
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Benefits of statistical molecular design, covariance analysis, and reference models in QSAR: a case study on acetylcholinesterase.
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- Journal of Computer-Aided Molecular Design, 2015, v. 29, n. 3, p. 199, doi. 10.1007/s10822-014-9808-1
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Protein and ligand preparation: parameters, protocols, and influence on virtual screening enrichments.
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- Journal of Computer-Aided Molecular Design, 2013, v. 27, n. 3, p. 221, doi. 10.1007/s10822-013-9644-8
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Mapping of the interaction sites of galanthamine: a quantitative analysis through pairwise potentials and quantum chemistry.
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- Journal of Computer-Aided Molecular Design, 2012, v. 26, n. 10, p. 1111, doi. 10.1007/s10822-012-9602-x
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- Article
Radiosynthesis of O‐(1‐[<sup>18</sup>F]fluoropropan‐2‐yl)‐O‐(4‐nitrophenyl)methylphosphonate: A novel PET tracer surrogate of sarin.
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- Journal of Labelled Compounds & Radiopharmaceuticals, 2018, v. 61, n. 14, p. 1089, doi. 10.1002/jlcr.3688
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- Article
Photodynamic inhibition of acetylcholinesterase after two-photon excitation of copper tetrasulfophthalocyanine.
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- Lasers in Medical Science, 2008, v. 23, n. 1, p. 19, doi. 10.1007/s10103-007-0446-x
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- Article
Probing O-dealkylation and deamination aging processes in tabun-conjugated AChE: a computational study.
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- Theoretical Chemistry Accounts: Theory, Computation, & Modeling, 2012, v. 131, n. 3, p. 1, doi. 10.1007/s00214-012-1175-1
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- Article
Semiempirical QM/MM potential with simple valence bond (SVB) for enzyme reactions. Application to the nucleophilic addition reaction in haloalkane dehalogenase.
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- Theoretical Chemistry Accounts: Theory, Computation, & Modeling, 2003, v. 109, n. 3, p. 133, doi. 10.1007/s00214-002-0419-x
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A charge-scaling method to treat solvent in QM/MM simulations.
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- Theoretical Chemistry Accounts: Theory, Computation, & Modeling, 2003, v. 109, n. 3, p. 118, doi. 10.1007/s00214-002-0417-z
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- Article
Quantum mechanics and mixed quantum mechanics/molecular mechanics simulations of model nerve agents with acetylcholinesterase.
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- Theoretical Chemistry Accounts: Theory, Computation, & Modeling, 2003, v. 109, n. 3, p. 160, doi. 10.1007/s00214-002-0424-0
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Immunohistochemistry for acetylcholinesterase and butyrylcholinesterase in the dorsal motor nucleus of the vagus (DMNV) of formalin-fixed, paraffin-embedded tissue: comparison with reported literature.
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- Histochemistry & Cell Biology, 2023, v. 159, n. 3, p. 247, doi. 10.1007/s00418-022-02164-3
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Modification of motor cortical excitability by an acetylcholinesterase inhibitor.
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- Experimental Brain Research, 2005, v. 164, n. 3, p. 399, doi. 10.1007/s00221-005-2326-6
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- Article