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Combination of Virtual Screening Protocol by in Silico toward the Discovery of Novel 4-Hydroxyphenylpyruvate Dioxygenase Inhibitors

https://doi.org/10.3389/fchem.2018.00014
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Outgoing claims: the papers this work cites, builds on, or argues with.

inferredcites →https://doi.org/10.1002/1526-4998(200102)57:2<120::aid-ps254>3.0.co;2-eopenalex-snapshot
Mesotrione: a new selective herbicide for use in maize
inferredcites →https://doi.org/10.1002/anie.201302365openalex-snapshot
4‐Hydroxyphenylpyruvate Dioxygenase Inhibitors in Combination with Safeners: Solutions for Modern and Sustainable Agriculture
inferredcites →https://doi.org/10.1002/jcc.10128openalex-snapshot
Fast, efficient generation of high‐quality atomic charges. AM1‐BCC model: II. Parameterization and validation
inferredcites →https://doi.org/10.1002/jcc.20035openalex-snapshot
Development and testing of a general amber force field
inferredcites →https://doi.org/10.1002/jcc.20145openalex-snapshot
Junmei Wang, Romain M. Wolf, James W. Caldwell, Peter A. Kollman, and David A. Case, "Development and testing of a general amber force field" Journal of Computational Chemistry (2004) 25(9) 1157–1174
inferredcites →https://doi.org/10.1002/prot.21123openalex-snapshot
Comparison of multiple Amber force fields and development of improved protein backbone parameters
inferredcites →https://doi.org/10.1002/ps.3727openalex-snapshot
Current state of herbicides in herbicide‐resistant crops
inferredcites →https://doi.org/10.1002/ps.3894openalex-snapshot
Design, synthesis and herbicidal activity of novel quinazoline‐2,4‐diones as 4‐hydroxyphenylpyruvate dioxygenase inhibitors
inferredcites →https://doi.org/10.1002/ps.554openalex-snapshot
Activity of mesotrione on resistant weeds in maize
inferredcites →https://doi.org/10.1007/s00044-015-1436-3openalex-snapshot
Molecular insight into the inhibition mechanism of plant and rat 4-hydroxyphenylpyruvate dioxygenase by molecular docking and DFT calculations
inferredcites →https://doi.org/10.1016/0021-9991(77)90098-5openalex-snapshot
Numerical integration of the cartesian equations of motion of a system with constraints: molecular dynamics of n-alkanes
inferredcites →https://doi.org/10.1016/j.abb.2004.08.015openalex-snapshot
4-Hydroxyphenylpyruvate dioxygenase
inferredcites →https://doi.org/10.1016/j.abb.2013.10.022openalex-snapshot
4-Hydroxyphenylpyruvate dioxygenase and hydroxymandelate synthase: Exemplars of the α-keto acid dependent oxygenases
inferredcites →https://doi.org/10.1016/j.bmc.2008.11.006openalex-snapshot
Design, synthesis and herbicidal activity of new iron chelating motifs for HPPD-inhibitors
inferredcites →https://doi.org/10.1016/j.bmc.2009.03.015openalex-snapshot
Herbicidal 4-hydroxyphenylpyruvate dioxygenase inhibitors—A review of the triketone chemistry story from a Syngenta perspective
inferredcites →https://doi.org/10.1016/j.bmc.2014.08.011openalex-snapshot
Pyrazolone–quinazolone hybrids: A novel class of human 4-hydroxyphenylpyruvate dioxygenase inhibitors
inferredcites →https://doi.org/10.1016/j.bmc.2015.11.032openalex-snapshot
Discovery of (2-benzoylethen-1-ol)-containing 1,2-benzothiazine derivatives as novel 4-hydroxyphenylpyruvate dioxygenase (HPPD) inhibiting-based herbicide lead compounds
inferredcites →https://doi.org/10.1016/j.ejmech.2010.01.016openalex-snapshot
3D QSAR pharmacophore based virtual screening and molecular docking for identification of potential HSP90 inhibitors
inferredcites →https://doi.org/10.1016/j.jtbi.2016.09.016openalex-snapshot
3D pharmacophore-based virtual screening, docking and density functional theory approach towards the discovery of novel human epidermal growth factor receptor-2 (HER2) inhibitors
inferredcites →https://doi.org/10.1016/s0031-9422(02)00121-8openalex-snapshot
The inhibitory activity of natural products on plant p-hydroxyphenylpyruvate dioxygenase
inferredcites →https://doi.org/10.1016/s0960-894x(02)00432-8openalex-snapshot
3D-QSAR studies on 4-hydroxyphenylpyruvate dioxygenase inhibitors by comparative molecular field analysis (CoMFA)
inferredcites →https://doi.org/10.1017/s0043174500093218openalex-snapshot
The discovery and structural requirements of inhibitors of p-hydroxyphenylpyruvate dioxygenase
inferredcites →https://doi.org/10.1021/acs.jafc.6b04110openalex-snapshot
An Efficient One-Pot Synthesis of 2-(Aryloxyacetyl)cyclohexane-1,3-diones as Herbicidal 4-Hydroxyphenylpyruvate Dioxygenase Inhibitors
inferredcites →https://doi.org/10.1021/acs.jafc.7b03851openalex-snapshot
4-Hydroxyphenylpyruvate Dioxygenase Inhibitors: From Chemical Biology to Agrochemicals
inferredcites →https://doi.org/10.1021/bi049317sopenalex-snapshot
Structure of the Ferrous Form of (4-Hydroxyphenyl)pyruvate Dioxygenase from Streptomyces avermitilis in Complex with the Therapeutic Herbicide, NTBC,
inferredcites →https://doi.org/10.1021/bi049323oopenalex-snapshot
Structural Basis for Herbicidal Inhibitor Selectivity Revealed by Comparison of Crystal Structures of Plant and Mammalian 4-Hydroxyphenylpyruvate Dioxygenases
inferredcites →https://doi.org/10.1021/bi049503yopenalex-snapshot
4-Hydroxyphenylpyruvate Dioxygenase: A Hybrid Density Functional Study of the Catalytic Reaction Mechanism
inferredcites →https://doi.org/10.1021/bi052409copenalex-snapshot
Catalytic, NonCatalytic, and Inhibitory Phenomena: Kinetic Analysis of (4-Hydroxyphenyl)pyruvate Dioxygenase from Arabidopsis thaliana
inferredcites →https://doi.org/10.1021/ci200159gopenalex-snapshot
Molecular Dynamics Simulation and Free Energy Calculation Studies of the Binding Mechanism of Allosteric Inhibitors with p38α MAP Kinase
inferredcites →https://doi.org/10.1021/ct1002626openalex-snapshot
Structural Survey of Zinc-Containing Proteins and Development of the Zinc AMBER Force Field (ZAFF)
inferredcites →https://doi.org/10.1021/ct400751uopenalex-snapshot
Taking into Account the Ion-Induced Dipole Interaction in the Nonbonded Model of Ions
inferredcites →https://doi.org/10.1021/j100058a043openalex-snapshot
Accurate Calculation of Hydration Free Energies Using Macroscopic Solvent Models
inferredcites →https://doi.org/10.1021/jf8034385openalex-snapshot
Synthesis and Structure−Activity Relationships of Substituted Cinnamic Acids and Amide Analogues: A New Class of Herbicides
inferredcites →https://doi.org/10.1021/jf9005593openalex-snapshot
β-Triketone Inhibitors of Plant p-Hydroxyphenylpyruvate Dioxygenase: Modeling and Comparative Molecular Field Analysis of Their Interactions
inferredcites →https://doi.org/10.1021/jm010360copenalex-snapshot
Pharmacophore Mapping of a Series of 2,4-Diamino-5-deazapteridine Inhibitors of Mycobacterium avium Complex Dihydrofolate Reductase
inferredcites →https://doi.org/10.1021/jm010568yopenalex-snapshot
Mode of Action of 4-Hydroxyphenylpyruvate Dioxygenase Inhibition by Triketone-type Inhibitors
inferredcites →https://doi.org/10.1038/nchembio.71openalex-snapshot
Versatility of biological non-heme Fe(II) centers in oxygen activation reactions
inferredcites →https://doi.org/10.1063/1.464397openalex-snapshot
Particle mesh Ewald: An N ⋅log( N ) method for Ewald sums in large systems
inferredcites →https://doi.org/10.1063/1.470117openalex-snapshot
A smooth particle mesh Ewald method
inferredcites →https://doi.org/10.1073/pnas.0605067103openalex-snapshot
Spectroscopic and electronic structure studies of aromatic electrophilic attack and hydrogen-atom abstraction by non-heme iron enzymes
inferredcites →https://doi.org/10.1074/jbc.m111.227595openalex-snapshot
4-Hydroxyphenylpyruvate Dioxygenase Catalysis
inferredcites →https://doi.org/10.1104/pp.114.247205openalex-snapshot
Broad 4-Hydroxyphenylpyruvate Dioxygenase Inhibitor Herbicide Tolerance in Soybean with an Optimized Enzyme and Expression Cassette
inferredcites →https://doi.org/10.1371/journal.pone.0069733openalex-snapshot
The Interactions in the Carboxyl Terminus of Human 4-Hydroxyphenylpyruvate Dioxygenase Are Critical to Mediate the Conformation of the Final Helix and the Tail to Shield the Active Site for Catalysis
inferredcites →https://doi.org/10.1614/ws-08-175.1openalex-snapshot
Interactions of Mesotrione and Atrazine in Two Weed Species with Different Mechanisms for Atrazine Resistance
inferredcites →https://doi.org/10.2307/2970379openalex-snapshot
Algebra: 228-233
inferredcites →https://doi.org/10.3390/molecules21010001openalex-snapshot
Extended Functional Groups (EFG): An Efficient Set for Chemical Characterization and Structure-Activity Relationship Studies of Chemical Compounds
inferredcites →https://doi.org/10.3390/molecules21070927openalex-snapshot
Computational Approaches for the Discovery of Human Proteasome Inhibitors: An Overview
inferredcites →https://doi.org/10.5012/bkcs.2013.34.10.2909openalex-snapshot
The Structure-Based Three-Dimensional Pharmacophore Models for Arabidopsis thaliana HPPD inhibitors as Herbicide

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.4643141openalex-extracted
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inferred← citeshttps://doi.org/10.1002/ps.5405openalex-snapshot
Transcriptome responses to the natural phytotoxin t‐chalcone in Arabidopsis thaliana L.
inferred← citeshttps://doi.org/10.1002/ps.5591openalex-snapshot
Synthesis and herbicidal activity of novel pyrazole aromatic ketone analogs as HPPD inhibitor
inferred← citeshttps://doi.org/10.1016/b978-0-12-817903-1.00011-5openalex-snapshot
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inferred← citeshttps://doi.org/10.1016/j.aac.2023.05.001openalex-snapshot
Discovery of tetrazolium nicotinamide derivatives as novel 4-Hydroxyphenylpyruvate dioxygenase inhibiting-based herbicides
inferred← citeshttps://doi.org/10.1016/j.arabjc.2022.103919openalex-snapshot
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inferred← citeshttps://doi.org/10.1016/j.ecoenv.2022.113699openalex-snapshot
Comparison of the binding interactions of 4-hydroxyphenylpyruvate dioxygenase inhibitor herbicides with humic acid: Insights from multispectroscopic techniques, DFT and 2D-COS-FTIR
inferred← citeshttps://doi.org/10.1016/j.ecoenv.2024.116087openalex-snapshot
Physiological effects of maize stressed by HPPD inhibitor herbicides via multi-spectral technology and two-dimensional correlation spectrum technology
inferred← citeshttps://doi.org/10.1016/j.envres.2026.125808openalex-snapshot
Advancements in the absorption, metabolism, and transport mechanisms of HPPD inhibitor herbicides in soil-plant system
inferred← citeshttps://doi.org/10.1016/j.indcrop.2019.05.070openalex-snapshot
Design, synthesis, SAR and molecular docking of novel green niacin-triketone HPPD inhibitor
inferred← citeshttps://doi.org/10.1016/j.indcrop.2023.116258openalex-snapshot
Artemisia argyi essential oil exerts herbicidal activity by inhibiting photosynthesis and causing oxidative damage
inferred← citeshttps://doi.org/10.1016/j.jtice.2019.08.005openalex-snapshot
Identification of novel inhibitors of p-hydroxyphenylpyruvate dioxygenase using receptor-based virtual screening
inferred← citeshttps://doi.org/10.1016/j.jtice.2023.104711openalex-snapshot
In silico approach of novel HPPD/PDS dual target inhibitors by pharmacophore, AILDE and molecular docking
inferred← citeshttps://doi.org/10.1016/j.molliq.2022.119683openalex-snapshot
Discovery of novel HPPD inhibitors based on a combination strategy of pharmacophore, consensus docking and molecular dynamics
inferred← citeshttps://doi.org/10.1016/j.molstruc.2019.127677openalex-snapshot
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inferred← citeshttps://doi.org/10.1016/j.mtphys.2021.100501openalex-snapshot
Plateau-like magnetocaloric effect in layered intermetallic compounds activated by tripled magnetic cell
inferred← citeshttps://doi.org/10.1016/j.pestbp.2021.104811openalex-snapshot
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inferred← citeshttps://doi.org/10.1016/j.pestbp.2022.105109openalex-snapshot
Virtual screening based on pharmacophore model for developing novel HPPD inhibitors
inferred← citeshttps://doi.org/10.1016/j.pestbp.2023.105390openalex-snapshot
Discovery of novel HPPD inhibitors: Virtual screening, molecular design, structure modification and biological evaluation
inferred← citeshttps://doi.org/10.1016/j.tibs.2023.02.006openalex-snapshot
Insights into 4-hydroxyphenylpyruvate dioxygenase-inhibitor interactions from comparative structural biology
inferred← citeshttps://doi.org/10.1021/acs.jafc.1c05210openalex-snapshot
Design, Synthesis, and Herbicidal Activity of Diphenyl Ether Derivatives Containing a Five-Membered Heterocycle
inferred← citeshttps://doi.org/10.1021/acs.jafc.2c02010openalex-snapshot
Survey on the Recent Advances in 4-Hydroxyphenylpyruvate Dioxygenase (HPPD) Inhibition by Diketone and Triketone Derivatives and Congeneric Compounds: Structural Analysis of HPPD/Inhibitor Complexes and Structure–Activity Relationship Considerations
inferred← citeshttps://doi.org/10.1021/acs.jafc.3c06312openalex-snapshot
Integrated Virtual Screening and Validation toward Potential HPPD Inhibition Herbicide
inferred← citeshttps://doi.org/10.1021/acs.jafc.4c01171openalex-snapshot
4-Hydroxyphenylpyruvate Dioxygenase Inhibitors: From Molecular Design to Synthesis
inferred← citeshttps://doi.org/10.1039/d2ra02645gopenalex-snapshot
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inferred← citeshttps://doi.org/10.1515/ncrs-2019-0019openalex-snapshot
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inferred← citeshttps://doi.org/10.21203/rs.3.rs-9717193/v1openalex-snapshot
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inferred← citeshttps://doi.org/10.21577/0100-4042.20240024openalex-snapshot
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inferred← citeshttps://doi.org/10.2174/1568026619666190816101948openalex-snapshot
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inferred← citeshttps://doi.org/10.3389/fchem.2019.00002openalex-snapshot
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inferred← citeshttps://doi.org/10.3389/fchem.2019.00381openalex-snapshot
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inferred← citeshttps://doi.org/10.3389/fchem.2019.00556openalex-snapshot
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inferred← citeshttps://doi.org/10.3389/fchem.2020.00167openalex-snapshot
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inferred← citeshttps://doi.org/10.3389/fphar.2021.728354openalex-snapshot
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inferred← citeshttps://doi.org/10.3390/books978-3-03897-615-8openalex-snapshot
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inferred← citeshttps://doi.org/10.3390/ijms21155546openalex-snapshot
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inferred← citeshttps://doi.org/10.3390/molecules23051040openalex-snapshot
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inferred← citeshttps://doi.org/10.4155/fmc-2019-0349openalex-snapshot
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inferred← citeshttps://doi.org/10.53879/id.61.01.13346openalex-snapshot
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inferred← citeshttps://doi.org/10.61751/bmbr/4.2023openalex-snapshot
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