On the public citation graph

Comparative QSAR: On the Toxicology of the Phenolic OH Moiety

https://doi.org/10.1080/20014091111686

0 signed · 96 inferred · view as graph

Inferred edges come from two machine sources: sweeps of open repository metadata (mostly SSRN and Zenodo), and a bulk OpenAlex citation snapshot. Every row below is labelled with the one it came from. Neither is a complete citation index — absence here is not evidence of absence.

Is this your work? Sign in with ORCID and put your name on the claims that are yours.

Claim with ORCID

Reference health. See whether every reference in this work resolves to a known work and none has been retracted — and get a dated CiteStamped badge you can embed.

See reference health

What this work says

Outgoing claims: the papers this work cites, builds on, or argues with.

inferredcites →https://doi.org/10.1002/em.2850110110openalex-snapshot

Responses of the L5178Y tk+/tk− mouse lymphoma cell forward mutation assay ii: 18 coded chemicals

inferredcites →https://doi.org/10.1002/em.2850140306openalex-snapshot

Chromosomal aberrations and sister chromatid exchange tests in Chinese hamster ovary cells in vitro. IV. Results with 15 chemicals

inferredcites →https://doi.org/10.1002/em.2850160409openalex-snapshot

Chromosome aberration and sister chromatid exchange tests in chinese hamster ovary cells in vitro. V: Results With 46 Chemicals

inferredcites →https://doi.org/10.1002/em.2860120111openalex-snapshot

Responses of the l5178y tk+/tk− mouse lymphoma cell forward mutation assay: III. 72 Coded chemicals

inferredcites →https://doi.org/10.1002/ijc.2910560126openalex-snapshot

Carcinogenicity of 4‐methoxyphenol and 4‐methylcatechol in F344 rats

inferredcites →https://doi.org/10.1002/qsar.19930120402openalex-snapshot

A QSAR Approach for Estimating the Aquatic Toxicity of Soft Electrophiles [QSAR for Soft Electrophiles]

inferredcites →https://doi.org/10.1002/tera.1420410106openalex-snapshot

Structure‐activity relationships in the developmental toxicity of substituted phenols: In vivo effects

inferredcites →https://doi.org/10.1002/tera.1420450103openalex-snapshot

In vitro embryotoxicity of a series of para‐substituted phenols: Structure, activity, and correlation with in vivo data

inferredcites →https://doi.org/10.1002/tera.1420480402openalex-snapshot

Toxicokinetics and structure‐activity relationships of nine para‐substituted phenols in rat embryos in vitro

inferredcites →https://doi.org/10.1006/enrs.1997.3782openalex-snapshot

Estrogenic Effects ofp-Hydroxybenzoic Acid in CD1 Mice

inferredcites →https://doi.org/10.1006/taap.1998.8544openalex-snapshot

Some Alkyl Hydroxy Benzoate Preservatives (Parabens) Are Estrogenic

inferredcites →https://doi.org/10.1007/bf01607892openalex-snapshot

Toxicities of selected phenols to fermentative and oxidative yeasts

inferredcites →https://doi.org/10.1007/bf01689453openalex-snapshot

Comparative toxicity and structure-activity inChlorella andTetrahymena: Monosubstituted phenols

inferredcites →https://doi.org/10.1016/0045-6535(96)00054-9openalex-snapshot

Structure-toxicity relationships for phenols to Tetrahymena pyriformis

inferredcites →https://doi.org/10.1016/0048-9697(91)90074-oopenalex-snapshot

The acute toxicity of pulse-dosed, para-substituted phenols to larval American flagfish (Jordanella floridae): a comparison with toxicity to photoluminescent bacteria and predicted toxicity using log Kow

inferredcites →https://doi.org/10.1016/0147-6513(87)90040-6openalex-snapshot

Effects of chlorophenols on isolated class A chloroplasts and thylakoids: A QSAR study

inferredcites →https://doi.org/10.1016/0165-1218(91)90125-6openalex-snapshot

The beneficial and hazardous effects of simple phenolic compounds

inferredcites →https://doi.org/10.1016/0891-5849(95)02227-9openalex-snapshot

Structure-antioxidant activity relationships of flavonoids and phenolic acids

inferredcites →https://doi.org/10.1016/s0009-2797(98)00027-1openalex-snapshot

Phenol toxicity in leukemia cells: a radical process?

inferredcites →https://doi.org/10.1016/s0090-6980(80)80040-2openalex-snapshot

Structure-activity relationships for inhibition of prostaglandin cyclooxygenase by phenolic compounds

inferredcites →https://doi.org/10.1016/s0968-0896(98)00039-xopenalex-snapshot

Quantitative Structure–Activity Analyses of Novel Hydroxyphenylurea Derivatives as Antioxidants

inferredcites →https://doi.org/10.1021/ar00028a003openalex-snapshot

Quantitative structure-activity relationships and the unnamed science

inferredcites →https://doi.org/10.1021/ar00132a003openalex-snapshot

Molecular graphics and QSAR in the study of enzyme-ligand interactions. On the definition of bioreceptors

inferredcites →https://doi.org/10.1021/bk-1995-0606.ch015openalex-snapshot

The QSAR of Insecticidal Uncouplers

inferredcites →https://doi.org/10.1021/cr9400976openalex-snapshot

Comparative QSAR: Toward a Deeper Understanding of Chemicobiological Interactions

inferredcites →https://doi.org/10.1021/cr9601021openalex-snapshot

Comparative QSAR: Radical Reactions of Benzene Derivatives in Chemistry and Biology

inferredcites →https://doi.org/10.1021/cr980018gopenalex-snapshot

Comparative QSAR Analysis of Estrogen Receptor Ligands

inferredcites →https://doi.org/10.1021/ja00952a044openalex-snapshot

The Role of Substituents in the Hydrophobic Bonding of Phenols by Serum and Mitochondrial Proteins

inferredcites →https://doi.org/10.1021/jm00243a002openalex-snapshot

Rm values of phenols. Their relation with log P values and activity

inferredcites →https://doi.org/10.1021/jo00279a038openalex-snapshot

The steric effect of ortho substituents on the acidic hydrolysis of benzamides

inferredcites →https://doi.org/10.1021/tx00020a005openalex-snapshot

Structure-activity study of paracetamol analogs: inhibition of replicative DNA synthesis in V79 Chinese hamster cells

inferredcites →https://doi.org/10.1038/194178b0openalex-snapshot

Correlation of Biological Activity of Phenoxyacetic Acids with Hammett Substituent Constants and Partition Coefficients

inferredcites →https://doi.org/10.1038/337285a0openalex-snapshot

Nonmutagenic carcinogens induce intrachromosomal recombination in yeast

inferredcites →https://doi.org/10.1038/39645openalex-snapshot

Molecular basis of agonism and antagonism in the oestrogen receptor

inferredcites →https://doi.org/10.1039/a801684dopenalex-snapshot

Molecular orbital parameters and comparative QSAR in the analysis of phenol toxicity to leukemia cells

inferredcites →https://doi.org/10.1039/a905764aopenalex-snapshot

On the toxicity of phenols to fast growing cells. A QSAR model for a radical-based toxicity

inferredcites →https://doi.org/10.1056/nejm197104222841604openalex-snapshot

Adenocarcinoma of the Vagina

inferredcites →https://doi.org/10.1056/nejm199506153322401openalex-snapshot

The Use of Estrogens and Progestins and the Risk of Breast Cancer in Postmenopausal Women

inferredcites →https://doi.org/10.1073/pnas.90.17.7915openalex-snapshot

Oxidants, antioxidants, and the degenerative diseases of aging.

inferredcites →https://doi.org/10.1073/pnas.95.1.288openalex-snapshot

DNA oxidation matters: The HPLC–electrochemical detection assay of 8-oxo-deoxyguanosine and 8-oxo-guanine

inferredcites →https://doi.org/10.1073/pnas.95.16.9562openalex-snapshot

Acetyl- l -carnitine fed to old rats partially restores mitochondrial function and ambulatory activity

inferredcites →https://doi.org/10.1080/00021369.1963.10858111openalex-snapshot

Effect of Chlorophenol Analogues on the Oxidative Phosphorylation in Rat Liver Mitochondria

inferredcites →https://doi.org/10.1080/00139157.1997.10544047openalex-snapshot

Our Stolen Future: Are We Threatening Our Fertility, Intelligence, and Survival?—A Scientific Detective Story

inferredcites →https://doi.org/10.1080/10629369508029905openalex-snapshot

Comparative QSAR: Radical Toxicity and Scavenging. Two Different Sides of the Same Coin

inferredcites →https://doi.org/10.1111/j.1432-1033.1971.tb01502.xopenalex-snapshot

Effects of Ring Substituents on the Activity of Phenols as Inhibitors and Uncouplers of Mitochondrial Respiration

inferredcites →https://doi.org/10.1111/j.1749-6632.1993.tb39148.xopenalex-snapshot

Oxidants in Cigarette Smoke Radicals, Hydrogen Peroxide, Peroxynitrate, and Peroxynitritea

inferredcites →https://doi.org/10.1177/00220345860650010901openalex-snapshot

Pharmacological Studies on the Anti-inflammatory Action of Phenolic Compounds

inferredcites →https://doi.org/10.1248/jhs1956.34.343openalex-snapshot

Acute toxicity and hatching inhibition of chlorophenols to Japanese Medaka, Oryzias latipes and structure-activity relationships.

inferredcites →https://doi.org/10.1289/ehp.98106167openalex-snapshot

The Estrogenicity of Bisphenol A-Related Diphenylalkanes with Various Substituents at the Central Carbon and the Hydroxy Groups

inferredcites →https://doi.org/10.3109/10408448909037471openalex-snapshot

Toward A Quantitative Comparative Toxicology of Organic Compounds

inferredcites →https://doi.org/10.3109/10408449509089887openalex-snapshot

Comparative QSAR in Toxicology: Examples from Teratology and Cancer Chemotherapy of Aniline Mustards

inferredcites →https://doi.org/10.5860/choice.33-6336openalex-snapshot

Our stolen future: are we threatening our fertility, intelligence, and survival?--a scientific detective story

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.4648546openalex-extracted

inferred← citeshttps://doi.org/10.1002/0471266949.bmc001openalex-snapshot

History of Quantitative Structure‐Activity Relationships

inferred← citeshttps://doi.org/10.1002/0471266949.bmc001.pub2openalex-snapshot

History of Quantitative Structure–Activity Relationships

inferred← citeshttps://doi.org/10.1002/etc.4740openalex-snapshot

Evaluation of Phenolic Compound Toxicity Using a Bioluminescent Assay with the Fungus Gerronema viridilucens

inferred← citeshttps://doi.org/10.1002/poc.1447openalex-snapshot

Predictive QSPR modeling of the acidic dissociation constant (pKa) of phenols in different solvents

inferred← citeshttps://doi.org/10.1002/qsar.200330816openalex-snapshot

Structure‐Activity Relationships for the Toxicity of Substituted Poly‐hydroxylated Benzenes to Tetrahymena pyriformis: Influence of Free Radical Formation

inferred← citeshttps://doi.org/10.1002/qsar.200710099openalex-snapshot

Review of (Quantitative) Structure–Activity Relationships for Acute Aquatic Toxicity

inferred← citeshttps://doi.org/10.1002/slct.202401288openalex-snapshot

Interaction between Halogenated Phenols and Thyroxine‐Binding Protein: A Multispectral and Computational Approach

inferred← citeshttps://doi.org/10.1007/978-1-4020-9783-6openalex-snapshot

Recent Advances in QSAR Studies

inferred← citeshttps://doi.org/10.1007/978-1-4020-9783-6_2openalex-snapshot

The Use of Quantum Mechanics Derived Descriptors in Computational Toxicology

inferred← citeshttps://doi.org/10.1007/978-3-030-21005-2_12openalex-snapshot

Quantitative Prediction of Toxicity of Substituted Phenols Using Deep Learning

inferred← citeshttps://doi.org/10.1007/978-3-642-32750-6_5openalex-snapshot

Biological Activity and Toxicity: A Conceptual DFT Approach

inferred← citeshttps://doi.org/10.1007/s00044-016-1532-zopenalex-snapshot

An antioxidant mechanism of morphine and related derivatives

inferred← citeshttps://doi.org/10.1007/s00894-012-1397-0openalex-snapshot

The basic antioxidant structure for flavonoid derivatives

inferred← citeshttps://doi.org/10.1007/s11030-006-9019-3openalex-snapshot

Discrimination between modes of toxic action of phenols using rule based methods

inferred← citeshttps://doi.org/10.1016/b978-0-443-13993-2.00016-5openalex-snapshot

Phytoremediation of phenolic compounds from soil

inferred← citeshttps://doi.org/10.1016/j.bmcl.2018.01.025openalex-snapshot

Synthesis of novel (−)-epicatechin derivatives as potential endothelial GPER agonists: Evaluation of biological effects

inferred← citeshttps://doi.org/10.1016/j.chemosphere.2007.04.060openalex-snapshot

Chromatographic retention–activity relationships for prediction of the toxicity pH-dependence of phenols

inferred← citeshttps://doi.org/10.1016/j.envint.2008.09.004openalex-snapshot

Mechanistic aspects regarding the direct aqueous environmental photochemistry of phenol and its simple halogenated derivatives. A review

inferred← citeshttps://doi.org/10.1016/j.watres.2013.10.010openalex-snapshot

Comparisons between abiotic nitration and biotransformation reactions of phenolic micropollutants in activated sludge

inferred← citeshttps://doi.org/10.1016/s0045-6535(02)00508-8openalex-snapshot

Comparative assessment of methods to develop QSARs for the prediction of the toxicity of phenols to Tetrahymena pyriformis

inferred← citeshttps://doi.org/10.1016/s0065-7743(06)41024-1openalex-snapshot

Structure–Activity Relationships for In vitro and In vivo Toxicity

inferred← citeshttps://doi.org/10.1016/s0166-1280(02)00623-1openalex-snapshot

QSAR models in receptor-mediated effects: the nuclear receptor superfamily

inferred← citeshttps://doi.org/10.1016/s0968-0896(02)00326-7openalex-snapshot

Quantitative structure–Activity relationships of phenolic compounds causing apoptosis

inferred← citeshttps://doi.org/10.1016/s0968-0896(03)00184-6openalex-snapshot

QSAR of apoptosis induction in various cancer cells

inferred← citeshttps://doi.org/10.1021/ci0497915openalex-snapshot

Use of Structure Descriptors To Discriminate between Modes of Toxic Action of Phenols

inferred← citeshttps://doi.org/10.1021/cr940024mopenalex-snapshot

Comparative QSAR and the Radical Toxicity of Various Functional Groups

inferred← citeshttps://doi.org/10.1021/es010307dopenalex-snapshot

Polar Fuel Constituents: Compound Identification and Equilibrium Partitioning between Nonaqueous Phase Liquids and Water

inferred← citeshttps://doi.org/10.1021/jm050567wopenalex-snapshot

Cellular Apoptosis and Cytotoxicity of Phenolic Compounds: A Quantitative Structure−Activity Relationship Study

inferred← citeshttps://doi.org/10.1039/b201478eopenalex-snapshot

QSAR for the cytotoxicity of 2-alkyl or 2,6-dialkyl, 4-X-phenols: the nature of the radical reaction

inferred← citeshttps://doi.org/10.1080/1062936031000073162openalex-snapshot

Quantitative structure-toxicity relationships using TOPS-MODE. 3. Structural factors influencing the permeability of commercial solvents through living human skin

inferred← citeshttps://doi.org/10.1080/1062936x.2013.766260openalex-snapshot

Comparative study to predict toxic modes of action of phenols from molecular structures

inferred← citeshttps://doi.org/10.1080/1062936x.2017.1376705openalex-snapshot

Machine learning-based models to predict modes of toxic action of phenols to Tetrahymena pyriformis

inferred← citeshttps://doi.org/10.1080/10803548.2004.11076620openalex-snapshot

Toxicity of Some Phenolic Derivatives—In Vitro Studies

inferred← citeshttps://doi.org/10.1109/acit54803.2022.9913174openalex-snapshot

Prediction of Toxicity of Phenols Using Artificial Neural Networks

inferred← citeshttps://doi.org/10.1109/is.2002.1044269openalex-snapshot

Neural and neuro-fuzzy models of toxic action of phenols

inferred← citeshttps://doi.org/10.1504/ijep.2006.010456openalex-snapshot

Analysis of phenols in wastewater using capillary electrophoresis and solid phase extraction

inferred← citeshttps://doi.org/10.1504/ijep.2006.010457openalex-snapshot

Removal of 2,4-dinitrophenol from wastewater by adsorption technology: a batch and column study

inferred← citeshttps://doi.org/10.1517/17425250903042318openalex-snapshot

Physicochemical drug properties associated within vivotoxicological outcomes: a review

inferred← citeshttps://doi.org/10.22059/ijer.2011.450openalex-snapshot

PREDICTION OF THE AQUATIC TOXICITY OF PHENOLS TO TETRAHYMENA PYRIFORMIS FROM MOLECULAR DESCRIPTORS

inferred← citeshttps://doi.org/10.2751/jcac.22.17openalex-snapshot

Extended Regression Modeling of the Toxicity of Phenol Derivatives to Tetrahymena pyriformis Using the Electronic-Structure Informatics Descriptor

inferred← citeshttps://doi.org/10.3390/analytica5040043openalex-snapshot

Refinement of Retention Indices in Gas Chromatography for a Number of Substituted Phenols

inferred← citeshttps://doi.org/10.4028/www.scientific.net/amr.610-613.607openalex-snapshot

3D-QSAR Study on Toxicities of Substituted Phenols against Vibrio Qinghaiensis(Q67)

inferred← citeshttps://doi.org/10.47749/t/unicamp.2007.408805openalex-snapshot

Metodos quimiometricos em estudos eletroquimicos de fenois sobre filmes de diamante dopado com boro

Editorial review for independent work. ICSAC — the Institute for Complexity Science and Advanced Computing — runs a structured editorial panel for researchers publishing outside journals, and publishes on CiteStamp rails. Submission is free and goes through ORCID: icsacinstitute.org/submit.