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Theoretical Descriptors for the Correlation of Aquatic Toxicity of Environmental Pollutants by Quantitative Structure-Toxicity Relationships

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What this work says

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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COMPARISON OF FISH TOXICITY SCREENING DATA FOR 55 ALCOHOLS WITH THE QUANTITATIVE STRUCTURE-ACTIVITY RELATIONSHIP PREDICTIONS OF MINIMUM TOXICITY FOR NONREACTIVE NONELECTROLYTE ORGANIC COMPOUNDS
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An algorithm for the location of transition states
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Calculation of the nonlinear optical properties of molecules
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A QSAR Approach for Estimating the Aquatic Toxicity of Soft Electrophiles [QSAR for Soft Electrophiles]
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Quantum‐chemical Descriptors for Estimating the Acute Toxicity of Substituted Benzenes to the Guppy (Poecilia reticulata) and Fathead Minnow (Pimephales promelas)
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Future Events
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Structure–Toxicity Relationships for Three Mechanisms of Action of Toxicity toVibrio fischeri
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Quantitative Structure-Activity Relationships of Environmental Pollutants
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Theory of Orientation and Stereoselection
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QSAR in Environmental Toxicology - II
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Structure-toxicity relationships for Tetrahymena: Aliphatic aldehydes
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Classifying environmental pollutants
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Quantitative structure-toxicity relationships for 80 chlorinated compounds using quantum chemical descriptors
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Modeling and prediction by using whim descriptors in QSAR studies: toxicity of heterogeneous chemicals on Daphnia magna
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The handbook of environmental chemistry
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Relation between physicochemical properties of phenols and their toxicity and accumulation in fish
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Relationships of quantitative structure-activity to comparative toxicity of selected phenols in the Pimephales promelas and Tetrahymena pyriformis test systems
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Practical applications of quantitative structure-activity relationships (QSAR) in environmental chemistry and toxicology
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The acute toxicity of aldehydes to the guppy
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NEIGHBORHOOD COMPLEXITIES AND SYMMETRY OF CHEMICAL GRAPHS AND THEIR BIOLOGICAL APPLICATIONS
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Quantitative structure–activity (QSAR) relationships of mutagenic aromatic and heterocyclic amines
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The Use of Computer Based Structure−Activity Relationships in the Risk Assessment of Industrial Chemicals
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Quantitative Structure−Activity Relationships for the Aquatic Toxicity of Polar and Nonpolar Narcotic Pollutants
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Quantum-Chemical Descriptors in QSAR/QSPR Studies
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p-σ-π Analysis. A Method for the Correlation of Biological Activity and Chemical Structure
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Correlation of Boiling Points with Molecular Structure. 1. A Training Set of 298 Diverse Organics and a Test Set of 9 Simple Inorganics
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Molecular Size Based Approach To Estimate Partition Properties for Organic Solutes
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Solid Phase Microextraction as a Tool To Determine Membrane/Water Partition Coefficients and Bioavailable Concentrations in in Vitro Systems
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Quantitative Structure−Activity Analyses of Nitrobenzene Toxicity to Tetrahymena pyriformis
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Understanding and Estimating Membrane/Water Partition Coefficients: Approaches To Derive Quantitative Structure Property Relationships
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QSPR: the correlation and quantitative prediction of chemical and physical properties from structure
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Factors that influence tadpole narcosis. An LFER analysis
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Applied Regression Analysis
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Quantitative correlation studies between the acute lethal toxicity of 15 organic halides to the guppy (Poecillah Reticulata) and chemical reactivity towards 4‐nitrobenzylpyridine
inferredcites →https://doi.org/10.1080/10629369308029895openalex-snapshot
Relationships Between Descriptors for Hydrophobicity and Soft Electrophilicity in Predicting Toxicity
inferredcites →https://doi.org/10.1135/cccc19991551openalex-snapshot
QSPR and QSAR Models Derived Using Large Molecular Descriptor Spaces. A Review of CODESSA Applications
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Calculation of octanol-water partition coefficients of organic solutes from their molecular volumes
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Structure–Toxicity Relationships for the Fathead Minnow, Pimephales promelas: Narcotic Industrial Chemicals
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Applied Regression Analysis
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Mechanisms of General Anesthesia
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Rules for Distinguishing Toxicants That Cause Type I and Type II Narcosis Syndromes
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Uncouplers of Oxidative Phosphorylation
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QSPR as a means of predicting and understanding chemical and physical properties in terms of structure

What points at this work

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

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