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Fine molecular tuning at position 4 of 2H-chromen-2-one derivatives in the search of potent and selective monoamine oxidase B inhibitors
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What this work says
Outgoing claims: the papers this work cites, builds on, or argues with.
inferredcites →https://doi.org/10.1002/cbdv.200690017openalex-snapshot
Lipophilicity Plays a Major Role in Modulating the Inhibition of Monoamine Oxidase B by 7‐Substituted Coumarins
inferredcites →https://doi.org/10.1002/cmdc.201100538openalex-snapshot
8‐Substituted 3‐Arylcoumarins as Potent and Selective MAO‐B Inhibitors: Synthesis, Pharmacological Evaluation, and Docking Studies
inferredcites →https://doi.org/10.1002/jhet.362openalex-snapshot
Synthesis and characterization of new 3‐acyl‐7‐hydroxy‐6,8‐substituted‐coumarin and 3‐acyl‐7‐benzyloxy‐6,8‐substituted‐coumarin derivatives
inferredcites →https://doi.org/10.1002/jhet.464openalex-snapshot
Synthesis and anti‐Helicobacter pylori activity of 4‐(coumarin‐3‐yl)thiazol‐2‐ylhydrazone derivatives
inferredcites →https://doi.org/10.1002/minf.201000126openalex-snapshot
Discovery of a Potent and Selective Hetero‐Bivalent AChE Inhibitor via Bioisosteric Replacement
inferredcites →https://doi.org/10.1002/prot.10465openalex-snapshot
Improved protein–ligand docking using GOLD
inferredcites →https://doi.org/10.1006/prep.2000.1309openalex-snapshot
High-Level Expression of Human Liver Monoamine Oxidase B in Pichia pastoris
inferredcites →https://doi.org/10.1006/prep.2001.1546openalex-snapshot
High-Level Expression of Human Liver Monoamine Oxidase A in Pichia pastoris: Comparison with the Enzyme Expressed in Saccharomyces cerevisiae
inferredcites →https://doi.org/10.1016/0006-2952(68)90066-xopenalex-snapshot
Some observations upon a new inhibitor of monoamine oxidase in brain tissue
inferredcites →https://doi.org/10.1016/0006-2952(77)90398-7openalex-snapshot
Substrate- and inhibitor-related characteristics of human platelet monoamine oxidase
inferredcites →https://doi.org/10.1016/0024-3205(96)00459-6openalex-snapshot
Localization of monoamine oxidases in human peripheral tissues
inferredcites →https://doi.org/10.1016/b978-0-12-386467-3.00001-7openalex-snapshot
Structural properties of human monoamine oxidases A and B
inferredcites →https://doi.org/10.1016/j.addr.2008.06.002openalex-snapshot
Monoamine oxidase inactivation: From pathophysiology to therapeutics
inferredcites →https://doi.org/10.1016/j.ejmech.2003.12.010openalex-snapshot
Synthesis and in vitro inhibitory activity on human platelet aggregation of novel properly substituted 4-(1-piperazinyl)coumarins
inferredcites →https://doi.org/10.1016/j.tetlet.2006.01.147openalex-snapshot
Microwave initiated reactions: Pechmann coumarin synthesis, Biginelli reaction, and acylation
inferredcites →https://doi.org/10.1016/j.tips.2004.11.007openalex-snapshot
Multi-functional drugs for various CNS targets in the treatment of neurodegenerative disorders
inferredcites →https://doi.org/10.1016/s0024-3205(01)01178-xopenalex-snapshot
Inhibition of brain monoamine oxidase activity by the generation of hydroxyl radicals Potential implications in relation to oxidative stress
inferredcites →https://doi.org/10.1016/s0024-3205(97)00114-8openalex-snapshot
Inhibition of brain monoamine oxidase by adducts of 1,2,3,4-tetrahydroisoquinoline with components of cigarette smoke
inferredcites →https://doi.org/10.1016/s0161-813x(03)00097-4openalex-snapshot
Clinical Pharmacology of MAO Inhibitors: Safety and Future
inferredcites →https://doi.org/10.1021/jm001028oopenalex-snapshot
Inhibition of Monoamine Oxidases by Functionalized Coumarin Derivatives: Biological Activities, QSARs, and 3D-QSARs
inferredcites →https://doi.org/10.1021/jm00156a031openalex-snapshot
Synthesis and rat lens aldose reductase inhibitory activity of some benzopyran-2-ones
inferredcites →https://doi.org/10.1021/jm00284a022openalex-snapshot
4-Hydroxycoumarins. Synthesis of the metabolites and some other derivatives of warfarin
inferredcites →https://doi.org/10.1021/jm058225dopenalex-snapshot
Designed Multiple Ligands. An Emerging Drug Discovery Paradigm
inferredcites →https://doi.org/10.1021/jm060183lopenalex-snapshot
Structural Insights into Monoamine Oxidase Inhibitory Potency and Selectivity of 7-Substituted Coumarins from Ligand- and Target-Based Approaches
inferredcites →https://doi.org/10.1021/jm070677yopenalex-snapshot
Structures of Human Monoamine Oxidase B Complexes with Selective Noncovalent Inhibitors: Safinamide and Coumarin Analogs
inferredcites →https://doi.org/10.1021/jm070728ropenalex-snapshot
Synthesis and Monoamine Oxidase Inhibitory Activity of New Pyridazine-, Pyrimidine- and 1,2,4-Triazine-Containing Tricyclic Derivatives
inferredcites →https://doi.org/10.1021/jm200716yopenalex-snapshot
Synthesis and Study of a Series of 3-Arylcoumarins as Potent and Selective Monoamine Oxidase B Inhibitors
inferredcites →https://doi.org/10.1021/jm4000769openalex-snapshot
Discovery, Biological Evaluation, and Structure–Activity and −Selectivity Relationships of 6′-Substituted ( E )-2-(Benzofuran-3(2 H )-ylidene)- N -methylacetamides, a Novel Class of Potent and Selective Monoamine Oxidase Inhibitors
inferredcites →https://doi.org/10.1021/jm7009364openalex-snapshot
Multi-target-Directed Ligands To Combat Neurodegenerative Diseases
inferredcites →https://doi.org/10.1021/jm801496uopenalex-snapshot
Synthesis, Molecular Modeling, and Selective Inhibitory Activity against Human Monoamine Oxidases of 3-Carboxamido-7-Substituted Coumarins
inferredcites →https://doi.org/10.1021/jm9010127openalex-snapshot
Discovery of a Novel Class of Potent Coumarin Monoamine Oxidase B Inhibitors: Development and Biopharmacological Profiling of 7-[(3-Chlorobenzyl)oxy]-4-[(methylamino)methyl]-2H-chromen-2-one Methanesulfonate (NW-1772) as a Highly Potent, Selective, Reversible, and Orally Active Monoamine Oxidase B…
inferredcites →https://doi.org/10.1021/jm981005yopenalex-snapshot
Inhibition of Monoamine Oxidase-B by Condensed Pyridazines and Pyrimidines: Effects of Lipophilicity and Structure−Activity Relationships
inferredcites →https://doi.org/10.1021/tx010073bopenalex-snapshot
Interactions of Nitrogen-Containing Xenobiotics with Monoamine Oxidase (MAO) Isozymes A and B: SAR Studies on MAO Substrates and Inhibitors
inferredcites →https://doi.org/10.1038/nrn1883openalex-snapshot
The therapeutic potential of monoamine oxidase inhibitors
inferredcites →https://doi.org/10.1038/sj.bjp.0703826openalex-snapshot
Rasagiline [N‐propargyl‐1R(+)‐aminoindan], a selective and potent inhibitor of mitochondrial monoamine oxidase B
inferredcites →https://doi.org/10.1038/sj.bjp.0706464openalex-snapshot
Monoamine oxidase: isoforms and inhibitors in Parkinson's disease and depressive illness
inferredcites →https://doi.org/10.1056/nejmoa0809335openalex-snapshot
A Double-Blind, Delayed-Start Trial of Rasagiline in Parkinson's Disease
inferredcites →https://doi.org/10.1073/pnas.0505975102openalex-snapshot
Three-dimensional structure of human monoamine oxidase A (MAO A): Relation to the structures of rat MAO A and human MAO B
inferredcites →https://doi.org/10.1073/pnas.0710626105openalex-snapshot
Structure of human monoamine oxidase A at 2.2-Å resolution: The control of opening the entry for substrates/inhibitors
inferredcites →https://doi.org/10.1073/pnas.1633804100openalex-snapshot
Insights into the mode of inhibition of human mitochondrial monoamine oxidase B from high-resolution crystal structures
inferredcites →https://doi.org/10.1073/pnas.94.10.4890openalex-snapshot
Parkinson disease: A new link between monoamine oxidase and mitochondrial electron flow
inferredcites →https://doi.org/10.1074/jbc.m100431200openalex-snapshot
Effects of Carboxyl-terminal Truncations on the Activity and Solubility of Human Monoamine Oxidase B
inferredcites →https://doi.org/10.1074/jbc.m500949200openalex-snapshot
Demonstration of Isoleucine 199 as a Structural Determinant for the Selective Inhibition of Human Monoamine Oxidase B by Specific Reversible Inhibitors
inferredcites →https://doi.org/10.1089/ars.2012.4616openalex-snapshot
Monoamine Oxidase B Prompts Mitochondrial and Cardiac Dysfunction in Pressure Overloaded Hearts
inferredcites →https://doi.org/10.1126/science.3099392openalex-snapshot
Mapping Human Brain Monoamine Oxidase A and B with11C-Labeled Suicide Inactivators and PET
inferredcites →https://doi.org/10.1161/circresaha.109.198366openalex-snapshot
Monoamine Oxidase A–Mediated Enhanced Catabolism of Norepinephrine Contributes to Adverse Remodeling and Pump Failure in Hearts With Pressure Overload
inferredcites →https://doi.org/10.1523/jneurosci.12-05-01977.1992openalex-snapshot
Quantitative enzyme radioautography with 3H-Ro 41-1049 and 3H-Ro 19- 6327 in vitro: localization and abundance of MAO-A and MAO-B in rat CNS, peripheral organs, and human brain
inferredcites →https://doi.org/10.2174/0929867043364784openalex-snapshot
Structure and Mechanism of Monoamine Oxidase
inferredcites →https://doi.org/10.2174/092986711797379302openalex-snapshot
Targeting Monoamine Oxidases with Multipotent Ligands: An Emerging Strategy in the Search of New Drugs Against Neurodegenerative Diseases
inferredcites →https://doi.org/10.2174/0929867305666220314202430openalex-snapshot
Structural Aspects of Monoamine Oxidase and its Reversible Inhibition
inferredcites →https://doi.org/10.2174/138161210793176527openalex-snapshot
Monoamine Oxidase Inhibitors as Neuroprotective Agents in Age-Dependent Neurodegenerative Disorders
inferredcites →https://doi.org/10.2174/138955712802762301openalex-snapshot
Discovery of MAO-B Inhibitors - Present Status and Future Directions Part I: Oxygen Heterocycles and Analogs
inferredcites →https://doi.org/10.4088/jcp.v64n0216openalex-snapshot
A Double-Blind, Placebo-Controlled Trial of the Safety and Efficacy of Selegiline Transdermal System Without Dietary Restrictions in Patients With Major Depressive Disorder
What points at this work
Incoming claims: where this work appears in other papers’ reference lists and arguments.
inferred← citeshttps://doi.org/10.2139/ssrn.4636655openalex-extracted
Probing the MAO Enzymes with a Novel Family of Quaternary Propargylamine Derivatives
inferred← citeshttps://doi.org/10.1002/ardp.202200084openalex-snapshot
Revealing the role of the benzyloxy pharmacophore in the design of a new class of monoamine oxidase‐B inhibitors
inferred← citeshttps://doi.org/10.1002/cbdv.201500367openalex-snapshot
Potent and Selective Monoamine Oxidase‐B Inhibitory Activity: Fluoro‐ vs . Trifluoromethyl‐4‐hydroxylated Chalcone Derivatives
inferred← citeshttps://doi.org/10.1002/cmdc.202000491openalex-snapshot
Selected 1,3‐Benzodioxine‐Containing Chalcones as Multipotent Oxidase and Acetylcholinesterase Inhibitors
inferred← citeshttps://doi.org/10.1002/slct.201600735openalex-snapshot
8‐Aminomethyl‐7‐hydroxy‐4‐methylcoumarins as Multitarget Leads for Alzheimer's Disease
inferred← citeshttps://doi.org/10.1007/s00702-018-1861-9openalex-snapshot
Kinetics, mechanism, and inhibition of monoamine oxidase
inferred← citeshttps://doi.org/10.1007/s00706-018-2260-5openalex-snapshot
Amino acid-sensitive reagents with coumarin moiety for latent prints examination
inferred← citeshttps://doi.org/10.1007/s10593-018-2281-3openalex-snapshot
4-Hydroxycoumarins as Michael donors in asymmetric routes to polycyclic coumarins (microreview)
inferred← citeshttps://doi.org/10.1007/s11164-018-3261-zopenalex-snapshot
Biological evaluation and in silico molecular docking study of a new series of thiazol-2-yl-hydrazone conglomerates
inferred← citeshttps://doi.org/10.1007/s11164-020-04081-3openalex-snapshot
Rapid and green synthesis of 4H-benzo[b]pyrans using triethanolamine as an efficient homogeneous catalyst under ambient conditions
inferred← citeshttps://doi.org/10.1007/s11224-022-02092-xopenalex-snapshot
In vitro and in silico investigation of inhibitory activities of 3-arylcoumarins and 3-phenylazo-4-hydroxycoumarin on MAO isoenzymes
inferred← citeshttps://doi.org/10.1016/b978-0-12-809593-5.00005-7openalex-snapshot
Coumarin-Based Molecules as Suitable Models for Developing New Neuroprotective Agents Through Structural Modification
inferred← citeshttps://doi.org/10.1016/j.bioorg.2019.103335openalex-snapshot
Design, synthesis and biological evaluation of oxygenated chalcones as potent and selective MAO-B inhibitors
inferred← citeshttps://doi.org/10.1016/j.bioorg.2020.104503openalex-snapshot
Accelerating the identification of subtype selective inhibitors via Three-Dimensional Biologically Relevant Spectrum (BRS-3D): The monoamine oxidase subtypes as a case study
inferred← citeshttps://doi.org/10.1016/j.bmc.2016.02.045openalex-snapshot
Novel tricyclic pyrazolo[1,5-d][1,4]benzoxazepin-5(6H)-one: Design, synthesis, model and use as hMAO-B inhibitors
inferred← citeshttps://doi.org/10.1016/j.bmcl.2022.128994openalex-snapshot
Design, synthesis, in-vitro, in-vivo and ex-vivo pharmacology of thiazolidine-2,4-dione derivatives as selective and reversible monoamine oxidase-B inhibitors
inferred← citeshttps://doi.org/10.1016/j.ejmech.2014.10.029openalex-snapshot
In silico design of novel 2H-chromen-2-one derivatives as potent and selective MAO-B inhibitors
inferred← citeshttps://doi.org/10.1016/j.ejmech.2015.08.055openalex-snapshot
Novel 2H-chromen-2-one derivatives of resveratrol: Design, synthesis, modeling and use as human monoamine oxidase inhibitors
inferred← citeshttps://doi.org/10.1016/j.ejmech.2018.10.016openalex-snapshot
Investigating alkyl nitrates as nitric oxide releasing precursors of multitarget acetylcholinesterase-monoamine oxidase B inhibitors
inferred← citeshttps://doi.org/10.1016/j.ejmech.2023.115352openalex-snapshot
Bioisosteric replacement based on 1,2,4-oxadiazoles in the discovery of 1H-indazole-bearing neuroprotective MAO B inhibitors
inferred← citeshttps://doi.org/10.1016/j.ejps.2017.02.008openalex-snapshot
A rational approach to elucidate human monoamine oxidase molecular selectivity
inferred← citeshttps://doi.org/10.1016/j.ijbiomac.2023.126158openalex-snapshot
Monoamine oxidase B inhibitors based on natural privileged scaffolds: A review of systematically structural modification
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Integrated Binary QSAR-Driven Virtual Screening and In Vitro Studies for Finding Novel hMAO-B-Selective Inhibitors
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Structure-Based Design and Optimization of Multitarget-Directed 2H-Chromen-2-one Derivatives as Potent Inhibitors of Monoamine Oxidase B and Cholinesterases
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Exploring Basic Tail Modifications of Coumarin-Based Dual Acetylcholinesterase-Monoamine Oxidase B Inhibitors: Identification of Water-Soluble, Brain-Permeant Neuroprotective Multitarget Agents
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Proposing Novel MAO-B Hit Inhibitors Using Multidimensional Molecular Modeling Approaches and Application of Binary QSAR Models for Prediction of Their Therapeutic Activity, Pharmacokinetic and Toxicity Properties
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Introduction of benzyloxy pharmacophore into aryl/heteroaryl chalcone motifs as a new class of monoamine oxidase B inhibitors
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Neuroprotective potential of synthesized coumarin-based glycinate and heterocyclic amide derivatives: an acetylcholinesterase inhibition study
inferred← citeshttps://doi.org/10.1039/c4md00437jopenalex-snapshot
Synthesis and evaluation of 6-methylcoumarin derivatives as potent and selective monoamine oxidase B inhibitors
inferred← citeshttps://doi.org/10.1186/s13065-018-0497-zopenalex-snapshot
Molecular docking studies of coumarin hybrids as potential acetylcholinesterase, butyrylcholinesterase, monoamine oxidase A/B and β-amyloid inhibitors for Alzheimer’s disease
inferred← citeshttps://doi.org/10.1515/msp-2016-0115openalex-snapshot
Quantum chemical studies on the molecular structure, spectroscopic and electronic properties of (6-Methoxy-2-oxo-2H-chromen-4-yl)-methyl pyrrolidine-1-carbodithioate
inferred← citeshttps://doi.org/10.2147/dddt.s86225openalex-snapshot
2-acetylphenol analogs as potent reversible monoamine oxidase inhibitors
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Computer-aided Drug Design Applied to Parkinson Targets
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Searching for Multi-Targeting Neurotherapeutics against Alzheimer’s: Discovery of Potent AChE-MAO B Inhibitors through the Decoration of the 2H-Chromen-2-one Structural Motif
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