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3D-quantitative structure-activity relationship study of organophosphate compounds

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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/ange.19640761603openalex-snapshot

Phosphorylierungsmittel — Bauprinzip und Reaktionsweise

inferredcites →https://doi.org/10.1002/ps.2780290402openalex-snapshot

Use of gas chromatographic retention indices for quantitative structure activity relationship studies of dialkyl phenyl phosphates

inferredcites →https://doi.org/10.1006/toxs.1997.2431openalex-snapshot

Common Mechanism of Toxicity: A Case Study of Organophosphorus Pesticides

inferredcites →https://doi.org/10.1016/s0300-483x(00)00219-5openalex-snapshot

Occupational exposure limits for 30 organophosphate pesticides based on inhibition of red blood cell acetylcholinesterase

inferredcites →https://doi.org/10.1016/s1093-3263(01)00123-1openalex-snapshot

Beware of q2!

inferredcites →https://doi.org/10.1021/cr0000067openalex-snapshot

Chem-Bioinformatics and QSAR: A Review of QSAR Lacking Positive Hydrophobic Terms

inferredcites →https://doi.org/10.1021/ja00226a005openalex-snapshot

Comparative molecular field analysis (CoMFA). 1. Effect of shape on binding of steroids to carrier proteins

inferredcites →https://doi.org/10.1021/ja01511a025openalex-snapshot

The Effect of Structure on the Reactivity of Alkylphosphonate Esters1,2

inferredcites →https://doi.org/10.1021/jm00050a010openalex-snapshot

Molecular Similarity Indices in a Comparative Analysis (CoMSIA) of Drug Molecules to Correlate and Predict Their Biological Activity

inferredcites →https://doi.org/10.1023/a:1008047919606openalex-snapshot

Comparative Molecular Similarity Index Analysis (CoMSIA) to study hydrogen-bonding properties and to score combinatorial libraries

inferredcites →https://doi.org/10.1080/109374099281205openalex-snapshot

ORGANOPHOSPHORUS PESTICIDES: DO THEY ALL HAVE THE SAME MECHANISM OF TOXICITY?

inferredcites →https://doi.org/10.1093/toxsci/63.2.223openalex-snapshot

Prediction of Organophosphorus Acetylcholinesterase Inhibition Using Three-Dimensional Quantitative Structure-Activity Relationship (3D-QSAR) Methods

What points at this work

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inferred← citeshttps://doi.org/10.1016/j.bioorg.2022.106098openalex-snapshot

Facile synthesis, larvicidal activity, biological effects, and molecular docking of sulfonamide-incorporating quaternary ammonium iodides as acetylcholinesterase inhibitors against Culex pipiens L

inferred← citeshttps://doi.org/10.1016/j.ecoenv.2021.112342openalex-snapshot

New insights into the mechanism of hepatocyte apoptosis induced by typical organophosphate ester: An integrated in vitro and in silico approach

inferred← citeshttps://doi.org/10.1016/j.etap.2012.11.018openalex-snapshot

Quantitative structure–activity relationship of organophosphate compounds based on molecular interaction fields descriptors

inferred← citeshttps://doi.org/10.1016/j.jhazmat.2020.123724openalex-snapshot

Quantitative structure-toxicity relationship model for acute toxicity of organophosphates via multiple administration routes in rats and mice

inferred← citeshttps://doi.org/10.1016/j.tet.2006.02.049openalex-snapshot

What are the pKa values of organophosphorus compounds?

inferred← citeshttps://doi.org/10.1080/1062936x.2024.2389818openalex-snapshot

Combining QSAR and SSD to predict aquatic toxicity and species sensitivity of pyrethroid and organophosphate pesticides

inferred← citeshttps://doi.org/10.1080/15287394.2010.501716openalex-snapshot

Quantitative Structure–Activity Relationships for Organophosphates Binding to Trypsin and Chymotrypsin

inferred← citeshttps://doi.org/10.1360/03wb0173openalex-snapshot

Relationship between toxicity and molecular volume of dioxins, organic phosphorous compounds and n-alkanols

inferred← citeshttps://doi.org/10.2174/138955712802762365openalex-snapshot

QSAR Applications During Last Decade on Inhibitors of Acetylcholinesterase in Alzheimer’s Disease

inferred← citeshttps://doi.org/10.7598/cst2014.719openalex-snapshot

Computer Aided Pesticide Design: A Rational Tool for Supplementing DDT Lacunae

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