On the public citation graph
Formation of Categories from Structure−Activity Relationships To Allow Read-Across for Risk Assessment: Toxicity of α,β-Unsaturated Carbonyl Compounds
0 signed · 137 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.
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known work and none has been retracted — and get a dated CiteStamped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.
What this work says
Outgoing claims: the papers this work cites, builds on, or argues with.
inferredcites →https://doi.org/10.1002/em.1039openalex-snapshot
Mutagenicity of 2‐alkylpropenals in Salmonella typhimurium strain TA 100: Structural influences
inferredcites →https://doi.org/10.1002/em.20158openalex-snapshot
Simple and α,β-unsaturated aldehydes: Correct prediction of genotoxic activity through structure-activity relationship models
inferredcites →https://doi.org/10.1002/em.2850190413openalex-snapshot
Mutagenicity of β‐alkyl substituted acrolein congeners in the Salmonella typhimurium strain TA100 and genotoxicity testing in the SOS chromotest
inferredcites →https://doi.org/10.1002/em.2860080802openalex-snapshot
Salmonella mutagenicity tests: II. Results from the testing of 270 chemicals
inferredcites →https://doi.org/10.1002/etc.5620160514openalex-snapshot
Predicting modes of toxic action from chemical structure: Acute toxicity in the fathead minnow ( Pimephales promelas )
inferredcites →https://doi.org/10.1002/qsar.200630020openalex-snapshot
Assessing Applicability Domains of Toxicological QSARs: Definition, Confidence in Predicted Values, and the Role of Mechanisms of Action
inferredcites →https://doi.org/10.1002/qsar.200710119openalex-snapshot
The Integrated Use of Models for the Properties and Effects of Chemicals by means of a Structured Workflow
inferredcites →https://doi.org/10.1002/qsar.200730016openalex-snapshot
Structure–Activity Relationships for Aldehyde Categories
inferredcites →https://doi.org/10.1007/978-1-4020-6102-8_11openalex-snapshot
Intelligent Testing Strategies
inferredcites →https://doi.org/10.1016/0045-6535(92)90280-5openalex-snapshot
Classifying environmental pollutants
inferredcites →https://doi.org/10.1016/0048-9697(91)90175-eopenalex-snapshot
Outliers: their origin and use in the classification of molecular mechanisms of toxicity
inferredcites →https://doi.org/10.1016/0165-1218(78)90090-3openalex-snapshot
Mutagenicity of some commercially available nitro compounds for Salmonella typhimurium
inferredcites →https://doi.org/10.1016/0165-1218(86)90077-7openalex-snapshot
Mutagenicity of mono-nitrobenzene derivatives in the Ames test and rec assay
inferredcites →https://doi.org/10.1016/0165-1218(87)90003-6openalex-snapshot
Mutagenic potency of some conjugated nitroaromatic compounds and its relationship to structure
inferredcites →https://doi.org/10.1016/0165-1218(91)90128-9openalex-snapshot
Aldehydes: occurrence, carcinogenic potential, mechanism of action and risk assessment
inferredcites →https://doi.org/10.1016/0165-1218(94)90108-2openalex-snapshot
Genotoxicity of 2-halosubstituted enals and 2-chloroacrylonitrile in the Ames test and the SOS-chromotest
inferredcites →https://doi.org/10.1016/0165-7992(87)90120-5openalex-snapshot
Mutagenicity of nitrofurans in Salmonella typhimurium TA98, TA98NR and TA98/1,8-DNP6
inferredcites →https://doi.org/10.1016/0300-483x(81)90130-xopenalex-snapshot
Quantitative structure-activity relationships in fish toxicity studies Part 1: Relationship for 50 industrial pollutants
inferredcites →https://doi.org/10.1016/0378-4274(93)90048-3openalex-snapshot
The possible role of α,β-unsaturated carbonyl compounds in mutagenesis and carcinogenesis
inferredcites →https://doi.org/10.1016/0887-2333(94)90048-5openalex-snapshot
Risk assessment for mutagenic and carcinogenic activities of α,β-unsaturated carbonyl compounds by a screening strategy based on structure-activity relationships
inferredcites →https://doi.org/10.1016/0891-5849(89)90137-8openalex-snapshot
Biological interactions of α,β-unsaturated aldehydes
inferredcites →https://doi.org/10.1016/j.mrfmmm.2006.08.006openalex-snapshot
Inhibition of spontaneous mutagenesis by vanillin and cinnamaldehyde in Escherichia coli: Dependence on recombinational repair
inferredcites →https://doi.org/10.1016/j.mrfmmm.2006.11.022openalex-snapshot
Antimutagenicity of cinnamaldehyde and vanillin in human cells: Global gene expression and possible role of DNA damage and repair
inferredcites →https://doi.org/10.1016/s0278-6915(03)00223-0openalex-snapshot
Classification of contact allergens according to potency: proposals
inferredcites →https://doi.org/10.1016/s1383-5718(00)00078-4openalex-snapshot
The role of alcohols as solvents in the genotoxicity testing of α,β-unsaturated ketones in the SOS chromotest
inferredcites →https://doi.org/10.1021/ar700246xopenalex-snapshot
Interstrand DNA Cross-Links Induced by α,β-Unsaturated Aldehydes Derived from Lipid Peroxidation and Environmental Sources
inferredcites →https://doi.org/10.1021/jm040835aopenalex-snapshot
Derivation and Validation of Toxicophores for Mutagenicity Prediction
inferredcites →https://doi.org/10.1021/jo00236a004openalex-snapshot
Study of reactions of .alpha.,.beta.-unsaturated carbonyl compounds with deoxyguanosine
inferredcites →https://doi.org/10.1021/tx049833jopenalex-snapshot
Structure−Toxicity Relationships for the Effects to Tetrahymena pyriformis of Aliphatic, Carbonyl-Containing, α,β-Unsaturated Chemicals
inferredcites →https://doi.org/10.1021/tx0601004openalex-snapshot
Mechanistic Applicability Domains for Nonanimal-Based Prediction of Toxicological End Points: General Principles and Application to Reactive Toxicity
inferredcites →https://doi.org/10.1021/tx060102oopenalex-snapshot
Mechanistic Applicability Domains for Non-Animal Based Prediction of Toxicological Endpoints. QSAR Analysis of the Schiff Base Applicability Domain for Skin Sensitization
inferredcites →https://doi.org/10.1021/tx700024wopenalex-snapshot
Mechanistic Applicability Domain Classification of a Local Lymph Node Assay Dataset for Skin Sensitization
inferredcites →https://doi.org/10.1021/tx700322gopenalex-snapshot
Quantitative and Mechanistic Read Across for Predicting the Skin Sensitization Potential of Alkenes Acting via Michael Addition
inferredcites →https://doi.org/10.1034/j.1600-0536.2001.044006331.xopenalex-snapshot
Skin‐sensitization structure‐activity relationships for aldehydes
inferredcites →https://doi.org/10.1080/105172397243079openalex-snapshot
TETRATOX: TETRAHYMENA PYRIFORMIS POPULATION GROWTH IMPAIRMENT ENDPOINTA SURROGATE FOR FISH LETHALITY
inferredcites →https://doi.org/10.1080/10629360008033237openalex-snapshot
Structure-Toxicity Relationships for Aliphatic Compounds Encompassing a Variety of Mechanisms of Toxic Action toVibrio fischeri
inferredcites →https://doi.org/10.1080/10629360600884371openalex-snapshot
A conceptual framework for predicting the toxicity of reactive chemicals: modeling soft electrophilicity
inferredcites →https://doi.org/10.1080/10629360601054354openalex-snapshot
Discriminating toxicant classes by mode of action: 3. Substructure indicators
inferredcites →https://doi.org/10.1080/10629360701306050openalex-snapshot
How can structural similarity analysis help in category formation?§
inferredcites →https://doi.org/10.1080/10629360802083848openalex-snapshot
Toxmatch–a new software tool to aid in the development and evaluation of chemically similar groups
inferredcites →https://doi.org/10.1080/10629360802085033openalex-snapshot
Characterisation of the chemical and biological properties of molecules with QSAR/QSPR and chemical grouping, and its application to a group of alkyl ethers
inferredcites →https://doi.org/10.1080/10629360802550366openalex-snapshot
Definition of the structural domain of the baseline non-polar narcosis model for Tetrahymena pyriformis
inferredcites →https://doi.org/10.1093/mutage/13.1.19openalex-snapshot
The effectiveness of Salmonella strains TA100, TA102 and TA104 for detecting mutagenicity of some aldehydes and peroxides
inferredcites →https://doi.org/10.1093/mutage/6.4.261openalex-snapshot
Genotoxicity of P-nitrocinnamaldehyde and related α,β-unsaturated carbonyl compounds in two bacterial assays
inferredcites →https://doi.org/10.1093/mutage/9.5.473openalex-snapshot
Genotoxicity of 2-halocinnamaldehydes in two bacterial assays. Induction of SOS repair and frame-shift mutation
inferredcites →https://doi.org/10.1289/ehp.908899openalex-snapshot
Molecular mechanisms of DNA damage initiated by alpha, beta-unsaturated carbonyl compounds as criteria for genotoxicity and mutagenicity.
inferredcites →https://doi.org/10.1289/ehp.9399245openalex-snapshot
Biomonitoring Studies and Susceptibility Markers for Acrolein Congeners and Allylic and Benzyl Compounds
inferredcites →https://doi.org/10.1897/02-579openalex-snapshot
Interspecies quantitative structure-activity relationship model for aldehydes: Aquatic toxicity
inferredcites →https://doi.org/10.2310/6620.2005.05040openalex-snapshot
Compilation of Historical Local Lymph Node Data for Evaluation of Skin Sensitization Alternative Methods
What points at this work
Incoming claims: where this work appears in other papers’ reference lists and arguments.
inferred← citeshttps://doi.org/10.1002/9781119650034.ch18openalex-snapshot
In Silico Modeling as a Tool to Predict and Characterize Plant Toxicity
inferred← citeshttps://doi.org/10.1002/cbdv.201800269openalex-snapshot
Inhibition of Pro‐Inflammatory Functions of Human Neutrophils by Constituents of Melodorum fruticosum Leaves
inferred← citeshttps://doi.org/10.1002/cbdv.202501277openalex-snapshot
Toxic Evaluations of Calea phyllolepis Extracts Standardized on 6‐ epi ‐β‐Verbesinol Coumarate and Its In Silico Prediction of the Toxicity
inferred← citeshttps://doi.org/10.1002/cmdc.200900499openalex-snapshot
The Tunable Functionality of α,β‐Unsaturated Carbonyl Compounds Enables Their Differential Application in Biological Systems
inferred← citeshttps://doi.org/10.1002/ejoc.201001119openalex-snapshot
Exploitation of Furanoid 5‐Azido‐3‐ C ‐Branched‐Chain Sugars Towards Highly Functionalized Nitrogen‐Containing Carbohydrate Derivatives
inferred← citeshttps://doi.org/10.1002/jsfa.9132openalex-snapshot
Cinnamaldehyde and related phenylpropanoids, natural repellents, and insecticides against Sitophilus zeamais (Motsch.). A chemical structure‐bioactivity relationship
inferred← citeshttps://doi.org/10.1002/minf.201200085openalex-snapshot
Read‐Across Prediction of the Acute Toxicity of Organic Compounds toward the Water Flea Daphnia magna
inferred← citeshttps://doi.org/10.1002/minf.201800084openalex-snapshot
Interpretation of QSAR Models: Mining Structural Patterns Taking into Account Molecular Context
inferred← citeshttps://doi.org/10.1002/minf.201800121openalex-snapshot
Filling Data Gaps by Read‐across: A Mini Review on its Application, Developments and Challenges
inferred← citeshttps://doi.org/10.1002/wcms.1240openalex-snapshot
In silico toxicology: computational methods for the prediction of chemical toxicity
inferred← citeshttps://doi.org/10.1007/978-1-4020-9783-6_11openalex-snapshot
Prediction of Harmful Human Health Effects of Chemicals from Structure
inferred← citeshttps://doi.org/10.1007/978-1-4020-9783-6_7openalex-snapshot
Chemical Category Formation and Read-Across for the Prediction of Toxicity
inferred← citeshttps://doi.org/10.1007/978-3-032-01098-8_9openalex-snapshot
Marine Microbial Natural Products Research in the East Sea Region
inferred← citeshttps://doi.org/10.1007/s11356-024-35290-7openalex-snapshot
Biomarker and adverse outcome pathway responses of Tubifex tubifex (sludge worm) exposed to environmentally-relevant levels of acenaphthene: insights from behavioral, physiological, and chemical structure–activity analyses
inferred← citeshttps://doi.org/10.1007/s12678-015-0278-6openalex-snapshot
Photoelectrochemical Treatment of α,β-Unsaturated Ketones on TiO2-RuO2/Ti Electrode
inferred← citeshttps://doi.org/10.1016/b978-0-444-59603-1.00012-6openalex-snapshot
Oleuropeic and Menthiafolic Acid Glucose Esters from Plants
inferred← citeshttps://doi.org/10.1016/j.bbadis.2021.166144openalex-snapshot
Association of metabolites with obesity based on two gene variants, MC4R rs17782313 and BDNF rs6265
inferred← citeshttps://doi.org/10.1016/j.bbrc.2023.149167openalex-snapshot
Lipid peroxidation: Reactive carbonyl species, protein/DNA adducts, and signaling switches in oxidative stress and cancer
inferred← citeshttps://doi.org/10.1016/j.biopha.2021.112378openalex-snapshot
Neoechinulins: Molecular, cellular, and functional attributes as promising therapeutics against cancer and other human diseases
inferred← citeshttps://doi.org/10.1016/j.bmc.2010.11.060openalex-snapshot
Synthesis of sugars embodying conjugated carbonyl systems and related triazole derivatives from carboxymethyl glycoside lactones. Evaluation of their antimicrobial activity and toxicity
inferred← citeshttps://doi.org/10.1016/j.chemosphere.2011.07.037openalex-snapshot
Application of a computational model for Michael addition reactivity in the prediction of toxicity to Tetrahymena pyriformis
inferred← citeshttps://doi.org/10.1016/j.chemosphere.2015.06.009openalex-snapshot
Investigation of the Verhaar scheme for predicting acute aquatic toxicity: Improving predictions obtained from Toxtree ver. 2.6
inferred← citeshttps://doi.org/10.1016/j.comtox.2022.100213openalex-snapshot
A review of in silico toxicology approaches to support the safety assessment of cosmetics-related materials
inferred← citeshttps://doi.org/10.1016/j.comtox.2022.100220openalex-snapshot
A strategy to define applicability domains for read-across
inferred← citeshttps://doi.org/10.1016/j.dental.2009.11.158openalex-snapshot
QSAR models to predict mutagenicity of acrylates, methacrylates and α , β -unsaturated carbonyl compounds
inferred← citeshttps://doi.org/10.1016/j.ejmech.2013.03.065openalex-snapshot
2-Arylpaullones are selective antitrypanosomal agents
inferred← citeshttps://doi.org/10.1016/j.ejmech.2024.116704openalex-snapshot
Covalent small-molecule inhibitors of SARS-CoV-2 Mpro: Insights into their design, classification, biological activity, and binding interactions
inferred← citeshttps://doi.org/10.1016/j.foodchem.2025.146795openalex-snapshot
Development, validation and application of an SFC-ESI-QqQ-MS/MS method for simultaneous analysis of malondialdehyde and typical α,β-unsaturated aldehydes in edible oils and oil-containing foods
inferred← citeshttps://doi.org/10.1016/j.fufo.2025.100606openalex-snapshot
Advancements and challenges in the bioproduction of raspberry ketone by precision fermentation
inferred← citeshttps://doi.org/10.1016/j.jhazmat.2009.12.038openalex-snapshot
QSAR modeling of toxicity of diverse organic chemicals to Daphnia magna using 2D and 3D descriptors
inferred← citeshttps://doi.org/10.1016/j.jpha.2026.101638openalex-snapshot
Novel strategy for characterizing the metabolism of GSH–enal adducts in myocardial ischemia rat model using UHPLC–MS
inferred← citeshttps://doi.org/10.1016/j.molstruc.2014.01.063openalex-snapshot
Synthesis, DFT and antimicrobial activity assays in vitro for novel cis/trans-but-2-enedioic acid esters
inferred← citeshttps://doi.org/10.1016/j.phrs.2026.108132openalex-snapshot
Pathophysiological significance of the TRPM2 ion channel as a potential target in cancer, neurological disorders, and ischemia/reperfusion injury
inferred← citeshttps://doi.org/10.1016/j.phytochem.2011.08.026openalex-snapshot
α,β-Unsaturated monoterpene acid glucose esters: Structural diversity, bioactivities and functional roles
inferred← citeshttps://doi.org/10.1016/j.rechem.2026.103614openalex-snapshot
Probing the solvation and activity behavior of acrylate- based monomers for potential dental polymer applications: DFT and molecular simulation approach
inferred← citeshttps://doi.org/10.1016/j.tiv.2011.04.015openalex-snapshot
Modelling acute oral mammalian toxicity. 1. Definition of a quantifiable baseline effect
inferred← citeshttps://doi.org/10.1016/j.tox.2009.11.023openalex-snapshot
A topological substructural molecular design approach for predicting mutagenesis end-points of α , β -unsaturated carbonyl compounds
inferred← citeshttps://doi.org/10.1016/j.yrtph.2017.05.016openalex-snapshot
Utility of published DNA reactivity alerts
inferred← citeshttps://doi.org/10.1021/acs.chemrestox.4c00402openalex-snapshot
Chemical Transformation of Vaping Emissions under Indoor Atmospheric Aging Processes
inferred← citeshttps://doi.org/10.1021/acs.chemrestox.5b00287openalex-snapshot
Characterization of a Hemoglobin Adduct from Ethyl Vinyl Ketone Detected in Human Blood Samples
inferred← citeshttps://doi.org/10.1021/acs.chemrestox.5b00308openalex-snapshot
Reactivity of Biliatresone, a Natural Biliary Toxin, with Glutathione, Histamine, and Amino Acids
inferred← citeshttps://doi.org/10.1021/acs.chemrev.8b00138openalex-snapshot
Development of Multifunctional Molecules as Potential Therapeutic Candidates for Alzheimer’s Disease, Parkinson’s Disease, and Amyotrophic Lateral Sclerosis in the Last Decade
inferred← citeshttps://doi.org/10.1021/acs.est.0c06551openalex-snapshot
Development of an Enhanced Mechanistically Driven Mode of Action Classification Scheme for Adverse Effects on Environmental Species
inferred← citeshttps://doi.org/10.1021/acs.jafc.4c01043openalex-snapshot
Occurrence and Synthesis Pathways of (Suspected) Genotoxic α,β-Unsaturated Carbonyls in Chocolate and Other Commercial Sweet Snacks
inferred← citeshttps://doi.org/10.1021/acs.jcim.5b00139openalex-snapshot
Predicting Toxicities of Diverse Chemical Pesticides in Multiple Avian Species Using Tree-Based QSAR Approaches for Regulatory Purposes
inferred← citeshttps://doi.org/10.1021/acsenvironau.4c00025openalex-snapshot
Solid-Phase Reactivity-Directed Extraction (SPREx): An Alternative Approach for Simultaneous Extraction, Identification, and Prioritization of Toxic Electrophiles Produced in Water Treatment Applications
inferred← citeshttps://doi.org/10.1021/acsmedchemlett.0c00153openalex-snapshot
Design and Synthesis of 1,2-Deoxy-pyranose Derivatives of Spliceostatin A toward Prostate Cancer Treatment
inferred← citeshttps://doi.org/10.1021/ar500152xopenalex-snapshot
The Ongoing Search for Small Molecules to Study Metal-Associated Amyloid-β Species in Alzheimer’s Disease
inferred← citeshttps://doi.org/10.1021/cr100098nopenalex-snapshot
Measurement and Estimation of Electrophilic Reactivity for Predictive Toxicology
inferred← citeshttps://doi.org/10.1021/cr100222qopenalex-snapshot
Mechanisms of Chemical Carcinogenicity and Mutagenicity: A Review with Implications for Predictive Toxicology
inferred← citeshttps://doi.org/10.1021/es200361ropenalex-snapshot
Quantitative Read-Across for Predicting the Acute Fish Toxicity of Organic Compounds
inferred← citeshttps://doi.org/10.1021/ic400851wopenalex-snapshot
Tuning Reactivity of Diphenylpropynone Derivatives with Metal-Associated Amyloid-β Species via Structural Modifications
inferred← citeshttps://doi.org/10.1021/om2010222openalex-snapshot
Nickel-Catalyzed Alkylation and Transfer Hydrogenation of α,β-Unsaturated Enones with Methanol
inferred← citeshttps://doi.org/10.1021/tx100172xopenalex-snapshot
Prediction of Michael-Type Acceptor Reactivity toward Glutathione
inferred← citeshttps://doi.org/10.1021/tx2003257openalex-snapshot
Application of the Hard and Soft, Acids and Bases (HSAB) Theory to Toxicant–Target Interactions
inferred← citeshttps://doi.org/10.1039/9781849732093-00606openalex-snapshot
Using In Silico Toxicity Predictions: Case Studies for Skin Sensitisation
inferred← citeshttps://doi.org/10.1039/9781849734400-00001openalex-snapshot
An Introduction to Chemical Grouping, Categories and Read-Across to Predict Toxicity
inferred← citeshttps://doi.org/10.1039/c1ob05298eopenalex-snapshot
Alkylating potential of α,β-unsaturated compounds
inferred← citeshttps://doi.org/10.1039/c1ob06065aopenalex-snapshot
Predicting Michael-acceptor reactivity and toxicity through quantum chemical transition-state calculations
inferred← citeshttps://doi.org/10.1039/c5dt01516bopenalex-snapshot
Bond and small-molecule activation with low-valent nickel complexes
inferred← citeshttps://doi.org/10.1039/c7en00102aopenalex-snapshot
Development of valuable predictive read-across models based on “real-life” (sparse) nanotoxicity data
inferred← citeshttps://doi.org/10.1039/d2sc04331aopenalex-snapshot
Intramolecular tetrazine-acryloyl cycloaddition: chemistry and applications
inferred← citeshttps://doi.org/10.1039/d3cp04204aopenalex-snapshot
Conformational diversity and environmental implications of trans -2-pentenal
inferred← citeshttps://doi.org/10.1039/d5cp03603hopenalex-snapshot
Resolving s- trans -dominant ionization dynamics in tiglic aldehyde using VUV-MATI spectroscopy and PES analysis
inferred← citeshttps://doi.org/10.1080/1062936x.2010.528943openalex-snapshot
Examination of Michael addition reactivity towards glutathione by transition-state calculations
inferred← citeshttps://doi.org/10.1089/aivt.2017.0021openalex-snapshot
Relationship Between Adverse Outcome Pathways and Chemistry-Based In Silico Models to Predict Toxicity
inferred← citeshttps://doi.org/10.1111/cbdd.12963openalex-snapshot
Biological screening of cucurbitacin inspired estrone analogs targeting mitogen‐activated protein kinase (MAPK) pathway
inferred← citeshttps://doi.org/10.1136/tobaccocontrol-2018-054321openalex-snapshot
IQOS: examination of Philip Morris International’s claim of reduced exposure
inferred← citeshttps://doi.org/10.1155/2024/3229770openalex-snapshot
In Vitro Proinflammatory and Cytotoxic Activity of Chicken‐and Turkey‐Based Würstels: A Preliminary Report
inferred← citeshttps://doi.org/10.1177/026119290903700508openalex-snapshot
The In Chemico–In Silico Interface: Challenges for Integrating Experimental and Computational Chemistry to Identify Toxicity
inferred← citeshttps://doi.org/10.1177/17475198231214490openalex-snapshot
An alternative method for the preparation of vismodegib: A tool for an undergraduate laboratory course
inferred← citeshttps://doi.org/10.1186/s41021-020-00171-1openalex-snapshot
Screening for Ames mutagenicity of food flavor chemicals by (quantitative) structure-activity relationship
inferred← citeshttps://doi.org/10.1186/s41021-021-00182-6openalex-snapshot
Development of a new quantitative structure–activity relationship model for predicting Ames mutagenicity of food flavor chemicals using StarDrop™ auto-Modeller™
inferred← citeshttps://doi.org/10.1186/s41021-021-00204-3openalex-snapshot
In vivo and in vitro mutagenicity of perillaldehyde and cinnamaldehyde
inferred← citeshttps://doi.org/10.1289/ehp3614openalex-snapshot
Nonanimal Models for Acute Toxicity Evaluations: Applying Data-Driven Profiling and Read-Across
inferred← citeshttps://doi.org/10.14573/altex.1601251openalex-snapshot
Toward Good Read-Across Practice (GRAP) guidance
inferred← citeshttps://doi.org/10.25082/jpbr.2021.01.005openalex-snapshot
In vitro and in vivo evaluation of genotoxicity, cytotoxicity, and protective effects of synthetic chalcones (E)-3-(4-chlorophenyl)-1-phenyl-2-propen-1-one (4-CL) and (E)-3-(3,4-dimethoxyphenyl)-1- phenyl-2-propen-1-one (DMF)
inferred← citeshttps://doi.org/10.2788/26123openalex-snapshot
Review of QSAR Models and Software Tools for Predicting of Genotoxicity and Carcinogenicity
inferred← citeshttps://doi.org/10.3390/ijms13010758openalex-snapshot
Mechanisms of Action of (Meth)acrylates in Hemolytic Activity, in Vivo Toxicity and Dipalmitoylphosphatidylcholine (DPPC) Liposomes Determined Using NMR Spectroscopy
inferred← citeshttps://doi.org/10.3390/ijms27135941openalex-snapshot
Organocatalytic Thioesterification of a Conjugated α,β-Unsaturated Dialdehyde
inferred← citeshttps://doi.org/10.3390/molecules181113245openalex-snapshot
Anti-Inflammatory Effect of Neoechinulin A from the Marine Fungus Eurotium sp. SF-5989 through the Suppression of NF-кB and p38 MAPK Pathways in Lipopolysaccharide-Stimulated RAW264.7 Macrophages
inferred← citeshttps://doi.org/10.3390/molecules25010061openalex-snapshot
Biologically Active Echinulin-Related Indolediketopiperazines from the Marine Sediment-Derived Fungus Aspergillus niveoglaucus
inferred← citeshttps://doi.org/10.3390/toxics12120931openalex-snapshot
Development of a Predictive Model for N-Dealkylation of Amine Contaminants Based on Machine Learning Methods
inferred← citeshttps://doi.org/10.4028/www.scientific.net/amr.726-731.175openalex-snapshot
QSAR Study on Toxic Effects of Reactive Organic Compounds
inferred← citeshttps://doi.org/10.6084/m9.figshare.13311010openalex-snapshot
Additional file 1 of Screening for Ames mutagenicity of food flavor chemicals by (quantitative) structure-activity relationship
inferred← citeshttps://doi.org/10.70675/39fa17a6z86efz466dza1b5zf90c5c888194openalex-snapshot
Etude de la réactivité et de la toxicité des particules de méthoxyphénols : analyse de leur action in vivo chez le rat en atmosphère contrôlée sur la fonction cardiaque et les paramètres du stress oxydant.
inferred← citeshttps://doi.org/10.70675/e9db0006zb00dz46abz98a6zc7c06e53ba03openalex-snapshot
Synthesis of new sugar derivatives containing an α,β -unsaturated carbonyl system in their structure and biological evaluation
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.