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Design, Synthesis, and Structure–Activity Relationship of Novel Aryl-Substituted Formyl Oxazolidine Derivatives as Herbicide Safeners

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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/(sici)1526-4998(200003)56:3<218::aid-ps116>3.0.co;2-9openalex-snapshot
Design, synthesis and structure-activity relationships of novel ALS inhibitors
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/etc.1889openalex-snapshot
Using in situ pore water concentrations to estimate the phytotoxicity of nicosulfuron in soils to corn (Zea mays L.)
inferredcites →https://doi.org/10.1002/j.1460-2075.1988.tb02937.xopenalex-snapshot
The molecular basis of sulfonylurea herbicide resistance in tobacco
inferredcites →https://doi.org/10.1002/ps.1917openalex-snapshot
Residues of the herbicide fenoxaprop‐P‐ethyl, its agronomic safener isoxadifen‐ethyl and their metabolites in rice after field application
inferredcites →https://doi.org/10.1002/ps.4190openalex-snapshot
Progress of modern agricultural chemistry and future prospects
inferredcites →https://doi.org/10.1002/ps.6005openalex-snapshot
Protective efficacy of phenoxyacetyl oxazolidine derivatives as safeners against nicosulfuron toxicity in maize
inferredcites →https://doi.org/10.1002/ps.6193openalex-snapshot
Fragments recombination, design, synthesis, safener activity and CoMFA model of novel substituted dichloroacetylphenyl sulfonamide derivatives
inferredcites →https://doi.org/10.1002/ps.6851openalex-snapshot
The safener isoxadifen‐ethyl confers fenoxaprop‐p‐ethyl resistance on a biotype of Echinochloa crus‐galli
inferredcites →https://doi.org/10.1016/0048-3575(91)90076-xopenalex-snapshot
Role of glutathione and glutathione S-transferase in the selectivity of acetochlor in maize and wheat
inferredcites →https://doi.org/10.1016/j.bmcl.2018.12.061openalex-snapshot
Fragment splicing-based design, synthesis and safener activity of novel substituted phenyl oxazole derivatives
inferredcites →https://doi.org/10.1016/j.ecoenv.2020.111576openalex-snapshot
Assessing the toxicity of three “inert” herbicide safeners toward Danio rerio: Effects on embryos development
inferredcites →https://doi.org/10.1016/j.indcrop.2019.05.070openalex-snapshot
Design, synthesis, SAR and molecular docking of novel green niacin-triketone HPPD inhibitor
inferredcites →https://doi.org/10.1016/j.molstruc.2010.04.033openalex-snapshot
Complex of nicosulfuron with human serum albumin: A biophysical study
inferredcites →https://doi.org/10.1016/j.pestbp.2018.01.015openalex-snapshot
Effects of nicosulfuron on growth, oxidative damage, and the ascorbate-glutathione pathway in paired nearly isogenic lines of waxy maize (Zea mays L.)
inferredcites →https://doi.org/10.1016/j.pestbp.2019.03.003openalex-snapshot
Rational design, synthesis and structure-activity relationship of novel substituted oxazole isoxazole carboxamides as herbicide safener
inferredcites →https://doi.org/10.1016/j.pestbp.2021.104958openalex-snapshot
Quinoxaline derivatives as herbicide safeners by improving Zea mays tolerance
inferredcites →https://doi.org/10.1016/j.pestbp.2022.105185openalex-snapshot
Diazabicyclo derivatives as safeners protect cotton from injury caused by flumioxazin
inferredcites →https://doi.org/10.1016/j.plaphy.2018.05.025openalex-snapshot
The expression of detoxification genes in two maize cultivars by interaction of isoxadifen-ethyl and nicosulfuron
inferredcites →https://doi.org/10.1016/j.scitotenv.2020.143273openalex-snapshot
Developmental toxicity and transcriptome analysis of zebrafish (Danio rerio) embryos following exposure to chiral herbicide safener benoxacor
inferredcites →https://doi.org/10.1016/s0045-6535(02)00185-6openalex-snapshot
Herbicide safeners: uses, limitations, metabolism, and mechanisms of action
inferredcites →https://doi.org/10.1021/acs.jafc.0c01867openalex-snapshot
Design, Synthesis, and Bioevaluation of Substituted Phenyl Isoxazole Analogues as Herbicide Safeners
inferredcites →https://doi.org/10.1021/acs.jafc.0c04436openalex-snapshot
Design, Synthesis, and SAR of Novel 1,3-Disubstituted Imidazolidine or Hexahydropyrimidine Derivatives as Herbicide Safeners
inferredcites →https://doi.org/10.1021/acs.jafc.1c02221openalex-snapshot
Fragmenlt Recombination Design, Synthesis, and Safener Activity of Novel Ester-Substituted Pyrazole Derivatives
inferredcites →https://doi.org/10.1021/acs.jafc.1c04621openalex-snapshot
Design, Synthesis, Structure–Activity Relationship, Molecular Docking, and Herbicidal Evaluation of 2-Cinnamoyl-3-Hydroxycyclohex-2-en-1-one Derivatives as Novel 4-Hydroxyphenylpyruvate Dioxygenase Inhibitors
inferredcites →https://doi.org/10.1021/acs.jafc.1c05210openalex-snapshot
Design, Synthesis, and Herbicidal Activity of Diphenyl Ether Derivatives Containing a Five-Membered Heterocycle
inferredcites →https://doi.org/10.1021/acs.jafc.2c01565openalex-snapshot
Research Progress in the Design and Synthesis of Herbicide Safeners: A Review
inferredcites →https://doi.org/10.1021/acs.jafc.2c08815openalex-snapshot
Research Progress on the Action Mechanism of Herbicide Safeners: A Review
inferredcites →https://doi.org/10.1021/acs.jafc.7b01813openalex-snapshot
Pesticide Interactions: Mechanisms, Benefits, and Risks
inferredcites →https://doi.org/10.1021/acs.jafc.8b00665openalex-snapshot
Design, Synthesis, and Herbicidal Activity of Pyrimidine–Biphenyl Hybrids as Novel Acetohydroxyacid Synthase Inhibitors
inferredcites →https://doi.org/10.1021/acs.jafc.8b02449openalex-snapshot
Pesticide Detox by Design
inferredcites →https://doi.org/10.1021/acs.jafc.9b03587openalex-snapshot
Safeners Improve Maize Tolerance under Herbicide Toxicity Stress by Increasing the Activity of Enzymes in Vivo
inferredcites →https://doi.org/10.1021/acs.jafc.9b07449openalex-snapshot
Design, Synthesis, and Biological Activity of Novel Diazabicyclo Derivatives as Safeners
inferredcites →https://doi.org/10.1021/jo00213a037openalex-snapshot
Synthesis of 2,2-disubstituted N-nitrosooxazolidines with nitrosyl chloride
inferredcites →https://doi.org/10.1073/pnas.83.12.4418openalex-snapshot
Single amino acid substitutions in the enzyme acetolactate synthase confer resistance to the herbicide sulfometuron methyl
inferredcites →https://doi.org/10.1080/00498250802651976openalex-snapshot
2-ABT-S-oxide detoxification by glutathioneS-transferases A1-1, M1-1 and P1-1: Implications for toxicity associated with zileuton
inferredcites →https://doi.org/10.1107/s2053229614024218openalex-snapshot
Crystal structure refinement with SHELXL
inferredcites →https://doi.org/10.1111/j.1742-4658.2009.06863.xopenalex-snapshot
Crystal structures of two novel sulfonylurea herbicides in complex with Arabidopsis thaliana acetohydroxyacid synthase
inferredcites →https://doi.org/10.1111/wre.12146openalex-snapshot
Computational analysis of mutated AHAS in response to sulfonylurea herbicides
inferredcites →https://doi.org/10.1371/journal.pone.0173502openalex-snapshot
Physiological basis for isoxadifen-ethyl induction of nicosulfuron detoxification in maize hybrids
inferredcites →https://doi.org/10.1614/p2002-168copenalex-snapshot
Metabolism-based herbicide resistance: regulationby safeners
inferredcites →https://doi.org/10.1614/ws-06-217.1openalex-snapshot
Mechanism of Antagonism of Mesotrione on Sulfonylurea Herbicides
inferredcites →https://doi.org/10.2165/00003088-199500292-00007openalex-snapshot
The Pharmacokinetics of Zileuton in Healthy Young and Elderly Volunteers
inferredcites →https://doi.org/10.3390/ijms23147822openalex-snapshot
Computer-Aided and AILDE Approaches to Design Novel 4-Hydroxyphenylpyruvate Dioxygenase Inhibitors

What points at this work

Incoming claims: where this work appears in other papers’ reference lists and arguments.

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inferred← citeshttps://doi.org/10.1002/cbdv.202301867openalex-snapshot
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Five-membered ring systems with O and N atoms
inferred← citeshttps://doi.org/10.1016/j.aac.2026.05.001openalex-snapshot
Advancing herbicide safeners: Integrating structure-guided design, pathway mechanism elucidation, and smart delivery
inferred← citeshttps://doi.org/10.1016/j.heliyon.2023.e21313openalex-snapshot
A new series of acylhydrazones derived from metribuzin with modulated herbicidal activity
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Electrospinning for producing antifungal nanofibers consisting of prochloraz/hydroxypropyl-γ-cyclodextrin inclusion complex
inferred← citeshttps://doi.org/10.1016/j.indcrop.2025.122462openalex-snapshot
Xanthanolide sesquiterpenes from stems and leaves of Xanthium sibiricum and their herbicidal and ALS inhibitory activities against invasive plants
inferred← citeshttps://doi.org/10.1016/j.molstruc.2023.136325openalex-snapshot
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Discovery of novel five-membered heterocycle-containing phenoxypyridine protoporphyrinogen oxidase inhibitors with herbicidal activity
inferred← citeshttps://doi.org/10.1016/j.pestbp.2023.105493openalex-snapshot
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inferred← citeshttps://doi.org/10.1016/j.pestbp.2023.105588openalex-snapshot
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inferred← citeshttps://doi.org/10.1016/j.pestbp.2025.106312openalex-snapshot
Re-exploration of phenolic compounds from natural waste rice husks: Combined synthesis of novel herbicide and evaluation of herbicidal activity
inferred← citeshttps://doi.org/10.1016/j.plaphy.2024.109309openalex-snapshot
Developing fluorescence hyperspectral imaging methods for non-invasive detection of herbicide safeners action mechanism and effectiveness
inferred← citeshttps://doi.org/10.1021/acs.jafc.3c03585openalex-snapshot
Review on the Discovery of Novel Natural Herbicide Safeners
inferred← citeshttps://doi.org/10.1021/acs.jafc.3c03593openalex-snapshot
Synthesis and Biological Activity Evaluation of Benzoxazinone-Pyrimidinedione Hybrids as Potent Protoporphyrinogen IX Oxidase Inhibitor
inferred← citeshttps://doi.org/10.1021/acs.jafc.3c04651openalex-snapshot
Design, Synthesis, and Bioactivity of Novel 2-(Arylformyl)cyclohexane-1,3-dione Derivatives as HPPD Inhibitors
inferred← citeshttps://doi.org/10.1021/acs.jafc.3c07411openalex-snapshot
Design, Synthesis, and Biological Activity of Novel Phenyltriazolinone PPO Inhibitors Containing Five-Membered Heterocycles
inferred← citeshttps://doi.org/10.1021/acs.jafc.3c08138openalex-snapshot
Design, Synthesis, and Biological Evaluation of Novel Purine Derivatives as Herbicide Safeners
inferred← citeshttps://doi.org/10.1021/acs.jafc.3c08705openalex-snapshot
Design, Synthesis, and Biological Activity of Novel Triketone-Containing Phenoxy Nicotinyl Inhibitors of HPPD
inferred← citeshttps://doi.org/10.1021/acs.jafc.4c02889openalex-snapshot
Design, Synthesis and Proteomics-Based Analysis of Novel Triazinone Derivatives Containing Amide Structures as Safer Protoporphyrinogen IX Oxidase Inhibitors
inferred← citeshttps://doi.org/10.1021/acs.jafc.4c07027openalex-snapshot
Pharmacophore Recombination Design, Synthesis, and Bioactivity of Ester-Substituted Pyrazole Purine Derivatives as Herbicide Safeners
inferred← citeshttps://doi.org/10.1021/acs.jafc.4c09757openalex-snapshot
Design, Synthesis, and Biological Activity Evaluation of Novel Phenoxypyridine Derivatives Containing Acylthiourea Fragments as Protoporphyrinogen Oxidase Inhibitor Herbicides
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Pharmacophore Reorganization-Based Design, Synthesis, and Safener Activity of Novel Isoxazole–Piperazinone Derivatives
inferred← citeshttps://doi.org/10.1021/acs.jafc.5c17631openalex-snapshot
Design, Synthesis, and Herbicidal Activity of Novel Diketonitrile Derivatives as HPPD Inhibitors
inferred← citeshttps://doi.org/10.1021/acs.jafc.6c03719openalex-snapshot
Design, Synthesis, and Activity Evaluation of Novel Herbicide Safeners Derived from the Natural Product Quinine
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Developing Fluorescence Hyperspectral Imaging Models for Non-Invasive Detection of Herbicide Safeners Action Mechanism in Wheat Crop
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