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Nitrobenzene toxicity: QSAR correlations and mechanistic interpretations

https://doi.org/10.1002/poc.643
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Outgoing claims: the papers this work cites, builds on, or argues with.

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A Comprehensive QSAR Treatment of the Genotoxicity of Heteroaromatic and Aromatic Amines
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QSAR Study of the Toxicity of Nitrobenzenes to Tetrahymena pyriformis
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Oxidative DNA Damage by a Metabolite of Carcinogenic and Reproductive Toxic Nitrobenzene in the Presence of NADH and Cu(II)
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Biochemical responses of skin to allergenic and non-allergenic nitrohalobenzenes
inferredcites →https://doi.org/10.1007/s002040050505openalex-snapshot
Involvement of apoptosis in the rat germ cell degeneration induced by nitrobenzene
inferredcites →https://doi.org/10.1016/0048-9697(91)90210-6openalex-snapshot
QSARs for monosubstituted anilines eliciting the polar narcosis mechanism of action
inferredcites →https://doi.org/10.1016/s0045-6535(99)00049-1openalex-snapshot
Quantitative structure-toxicity relationships for halogenated substituted-benzenes to Vibrio fischeri, using atom-based semi-empirical molecular-orbital descriptors
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Acute immunotoxicity of p-chloronitrobenzene in mice: II. Effect of p-chloronitrobenzene on the immunophenotype of murine splenocytes determined by flow cytometry
inferredcites →https://doi.org/10.1016/s0968-0896(01)00211-5openalex-snapshot
QSAR prediction of toxicity of nitrobenzenes
inferredcites →https://doi.org/10.1021/ac00220a013openalex-snapshot
Development and use of charged partial surface area structural descriptors in computer-assisted quantitative structure-property relationship studies
inferredcites →https://doi.org/10.1021/ci000134wopenalex-snapshot
Interpretation of Quantitative Structure−Property and −Activity Relationships
inferredcites →https://doi.org/10.1021/ci010011ropenalex-snapshot
Theoretical Descriptors for the Correlation of Aquatic Toxicity of Environmental Pollutants by Quantitative Structure-Toxicity Relationships
inferredcites →https://doi.org/10.1021/ci9903206openalex-snapshot
Structurally Diverse Quantitative Structure−Property Relationship Correlations of Technologically Relevant Physical Properties
inferredcites →https://doi.org/10.1021/cr950202ropenalex-snapshot
Quantum-Chemical Descriptors in QSAR/QSPR Studies
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Development and use of quantum mechanical molecular models. 76. AM1: a new general purpose quantum mechanical molecular model
inferredcites →https://doi.org/10.1021/tx0155202openalex-snapshot
Development of Quantitative Structure−Activity Relationships for the Toxicity of Aromatic Compounds to Tetrahymena pyriformis: Comparative Assessment of the Methodologies
inferredcites →https://doi.org/10.1021/tx960104gopenalex-snapshot
Molecular Orbital Parameters as Predictors of Skin Sensitization Potential of Halo- and Pseudohalobenzenes Acting as SNAr Electrophiles
inferredcites →https://doi.org/10.1021/tx970166mopenalex-snapshot
Quantitative Structure−Activity Analyses of Nitrobenzene Toxicity to Tetrahymena pyriformis
inferredcites →https://doi.org/10.1021/tx9901635openalex-snapshot
Quantitative Structure−Activity Analysis of the Algae Toxicity of Nitroaromatic Compounds
inferredcites →https://doi.org/10.1080/10629360108032919openalex-snapshot
Quantitative Structure–Toxicity Relationships Using Tops-Mode. 1. Nitrobenzene Toxicity toTetrahymena Pyriformis
inferredcites →https://doi.org/10.1080/10629369808039153openalex-snapshot
Comparison of Tetrahymena and Pimephales Toxicity Based on Mechanism of Action
inferredcites →https://doi.org/10.1080/10915810050202097openalex-snapshot
In Vitro Inhibition of Mammalian Glutathione Transferases by Selected Nitrobenzenes

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

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In vivo toxicity of nitroaromatics: A comprehensive quantitative structure–activity relationship study
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The role of intramolecular self‐destruction of reactive metabolic intermediates in determining toxicity
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Recent Advances in QSAR Studies
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New Advances in QSPR/QSAR Analysis of Nitrocompounds: Solubility, Lipophilicity, and Toxicity
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QSTR based on Monte Carlo approach using SMILES and graph features for toxicity toward Tetrahymena pyriformis
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