On the public citation graph
Predicting the Genotoxicity of Thiophene Derivatives from Molecular Structure
0 signed · 75 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known work and none has been retracted — and get a dated CiteStamped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/(sici)1099-1263(199611)16:6<539::aid-jat375>3.0.co;2-kopenalex-snapshot
Patty's Industrial Hygiene and Toxicology
inferredcites →https://doi.org/10.1002/9783527610907.scardopenalex-snapshot
Methods and Principles in Medicinal Chemistry
inferredcites →https://doi.org/10.1002/9783906390406openalex-snapshot
Computer‐Assisted Lead Finding and Optimization
inferredcites →https://doi.org/10.1002/jps.2600690652openalex-snapshot
Computer assisted studies of chemical structure and biological function
inferredcites →https://doi.org/10.1002/jps.2600760325openalex-snapshot
Molecular Connectivity in Structure–activity Analysis
inferredcites →https://doi.org/10.1007/bf00128336openalex-snapshot
MOPAC: A semiempirical molecular orbital program
inferredcites →https://doi.org/10.1016/0009-2614(82)80009-2openalex-snapshot
Highly discriminating distance-based topological index
inferredcites →https://doi.org/10.1016/s0165-6147(96)90278-3openalex-snapshot
Chemometric methods in molecular design
inferredcites →https://doi.org/10.1016/s0169-409x(02)00012-1openalex-snapshot
Computer systems for the prediction of toxicity: an update
inferredcites →https://doi.org/10.1021/ci00043a009openalex-snapshot
On molecular identification numbers
inferredcites →https://doi.org/10.1021/ci00049a002openalex-snapshot
A simple method for the representation, quantification, and comparison of the volumes and shapes of chemical compounds
inferredcites →https://doi.org/10.1021/ci020366qopenalex-snapshot
Rule Extraction from a Mutagenicity Data Set Using Adaptively Grown Phylogenetic-like Trees
inferredcites →https://doi.org/10.1021/ci960049hopenalex-snapshot
Eccentric Connectivity Index: A Novel Highly Discriminating Topological Descriptor for Structure−Property and Structure−Activity Studies
inferredcites →https://doi.org/10.1021/ja00336a004openalex-snapshot
Artificial intelligence approach to structure-activity studies. Computer automated structure evaluation of biological activity of organic molecules
inferredcites →https://doi.org/10.1021/ja00856a001openalex-snapshot
Characterization of molecular branching
inferredcites →https://doi.org/10.1021/jm000244uopenalex-snapshot
Classification of Multidrug-Resistance Reversal Agents Using Structure-Based Descriptors and Linear Discriminant Analysis
inferredcites →https://doi.org/10.1021/jm00135a003openalex-snapshot
Computer-assisted structure-activity studies of chemical carcinogens. Aromatic amines
inferredcites →https://doi.org/10.1021/jm00196a017openalex-snapshot
Chance factors in studies of quantitative structure-activity relationships
inferredcites →https://doi.org/10.1021/tx00014a002openalex-snapshot
Synthesis and mutagenicity of trans-dihydrodiol metabolites of benzo[b]naphtho[2,1-d]thiophene
inferredcites →https://doi.org/10.1023/a:1015092201811openalex-snapshot
Prediction of the Intestinal Absorption of Endothelin Receptor Antagonists Using Three Theoretical Methods of Increasing Complexity
inferredcites →https://doi.org/10.1080/10629369908039170openalex-snapshot
Prediction of Acute Mammalian Toxicity of Organophosphorus Pesticide Compounds from Molecular Structure
inferredcites →https://doi.org/10.1146/annurev.genet.34.1.479openalex-snapshot
THE SOS RESPONSE: Recent Insights into umuDC -Dependent Mutagenesis and DNA Damage Tolerance
inferredcites →https://doi.org/10.2307/1403797openalex-snapshot
Discriminatory Analysis. Nonparametric Discrimination: Consistency Properties
inferredcites →https://doi.org/10.2307/2005713openalex-snapshot
Algorithms for Minimization Without Derivatives
inferredcites →https://doi.org/10.5860/choice.30-5638openalex-snapshot
Numerical recipes in C: the art of scientific computing
What points at this work
Incoming claims: where this work appears in other papers’ reference lists and arguments.
inferred← citeshttps://doi.org/10.1002/cbdv.202400473openalex-snapshot
Anticancer Potential of the S ‐Heterocyclic Ring Containing Drugs and its Bioactivation to Reactive Metabolites
inferred← citeshttps://doi.org/10.1002/chin.200444297openalex-snapshot
Quantum Chemical Descriptors in Structure—Activity Relationships: Calculation, Interpretation, and Comparison of Methods
inferred← citeshttps://doi.org/10.1002/em.20589openalex-snapshot
Reflections on the origins and evolution of genetic toxicology and the environmental mutagen society
inferred← citeshttps://doi.org/10.1002/jccs.201100417openalex-snapshot
Bayesian Regularized Artificial Neural Network Modeling of the Anti‐protozoal Activities of 1‐Methylbenzimidazole Derivatives AgainstT. VaginalisInfection
inferred← citeshttps://doi.org/10.1002/jps.20232openalex-snapshot
Quantitative Structure-Pharmacokinetic Relationships for Drug Distribution Properties by Using General Regression Neural Network
inferred← citeshttps://doi.org/10.1002/qsar.200860090openalex-snapshot
Predicting the Androgenicity of Structurally Diverse Compounds from Molecular Structure Using Different Classifiers
inferred← citeshttps://doi.org/10.1007/978-0-387-44961-6_14openalex-snapshot
Elementary Predictive Toxicology for Advanced Applications
inferred← citeshttps://doi.org/10.1007/978-1-0716-4976-3_27openalex-snapshot
Artificial Intelligence and Machine Learning-Based Approaches for Genetic Damage Prediction
inferred← citeshttps://doi.org/10.1007/978-1-4419-0197-2_2openalex-snapshot
(Q)SAR Models for Genotoxicity Assessment
inferred← citeshttps://doi.org/10.1016/b0-08-045044-x/00259-5openalex-snapshot
Quantum Mechanical Calculations in Medicinal Chemistry: Relevant Method or a Quantum Leap Too Far?
inferred← citeshttps://doi.org/10.1016/b978-0-12-381290-2.00001-xopenalex-snapshot
Designing Drugs to Avoid Toxicity
inferred← citeshttps://doi.org/10.1016/j.apcatb.2016.07.037openalex-snapshot
Preparation of wrapped carbon nanotubes poly(4-vinylpyridine)/MTO based heterogeneous catalysts for the oxidative desulfurization (ODS) of model and synthetic diesel fuel
inferred← citeshttps://doi.org/10.1016/j.bmc.2007.08.057openalex-snapshot
A novel QSAR model for prediction of apoptosis-inducing activity of 4-aryl-4-H-chromenes based on support vector machine
inferred← citeshttps://doi.org/10.1016/j.bmcl.2005.02.002openalex-snapshot
Novel cyclopentane dicarboxamide sodium channel blockers as a potential treatment for chronic pain
inferred← citeshttps://doi.org/10.1016/j.ejmech.2010.07.056openalex-snapshot
QSAR prediction of D2 receptor antagonistic activity of 6-methoxy benzamides
inferred← citeshttps://doi.org/10.1016/j.jmgm.2005.10.004openalex-snapshot
Quantitative structure–pharmacokinetic relationships for drug clearance by using statistical learning methods
inferred← citeshttps://doi.org/10.1016/j.psep.2020.07.022openalex-snapshot
A new method for identifying persistent, bioaccumulative, and toxic organic pollutants in coking wastewater
inferred← citeshttps://doi.org/10.1016/j.taap.2009.08.022openalex-snapshot
In silico toxicology for the pharmaceutical sciences☆
inferred← citeshttps://doi.org/10.1016/j.toxlet.2005.11.017openalex-snapshot
In silico search of putative adverse drug reaction related proteins as a potential tool for facilitating drug adverse effect prediction
inferred← citeshttps://doi.org/10.1016/j.toxlet.2007.12.005openalex-snapshot
Classification structure–activity relationship (CSAR) studies for prediction of genotoxicity of thiophene derivatives
inferred← citeshttps://doi.org/10.1016/s1359-6446(05)03505-1openalex-snapshot
Computational prediction of genotoxicity: room for improvement
inferred← citeshttps://doi.org/10.1021/ci050049uopenalex-snapshot
Application of the Random Forest Method in Studies of Local Lymph Node Assay Based Skin Sensitization Data
inferred← citeshttps://doi.org/10.1021/cr100098nopenalex-snapshot
Measurement and Estimation of Electrophilic Reactivity for Predictive Toxicology
inferred← citeshttps://doi.org/10.1021/jm200825uopenalex-snapshot
Ethionamide Boosters. 2. Combining Bioisosteric Replacement and Structure-Based Drug Design To Solve Pharmacokinetic Issues in a Series of Potent 1,2,4-Oxadiazole EthR Inhibitors
inferred← citeshttps://doi.org/10.1021/tx049652hopenalex-snapshot
Prediction of Genotoxicity of Chemical Compounds by Statistical Learning Methods
inferred← citeshttps://doi.org/10.1039/9781788018982-00533openalex-snapshot
Discovery Toxicology in Lead Optimization
inferred← citeshttps://doi.org/10.1080/10406630490472473openalex-snapshot
GENOTOXIC ACTIVITY OF THIOPHENES ON LIVER HUMAN CELL LINE (HepG2)
inferred← citeshttps://doi.org/10.1093/bib/bbs021openalex-snapshot
Bioinformatics opportunities for identification and study of medicinal plants
inferred← citeshttps://doi.org/10.1111/j.1747-0285.2009.00790.xopenalex-snapshot
Modelling of Cytotoxicity Data (CC50) of Anti‐HIV 1‐[5‐Chlorophenyl) Sulfonyl]‐1H‐Pyrrole Derivatives Using Calculated Molecular Descriptors and Levenberg–Marquardt Artificial Neural Network
inferred← citeshttps://doi.org/10.1177/0748233710369125openalex-snapshot
High-altitude medicines: A short-term genotoxicity study
inferred← citeshttps://doi.org/10.1201/9780203642627.ch6openalex-snapshot
Quantum Chemical Descriptors in Structure-Activity Relationships — Calculation, Interpretation, and Comparison of Methods
inferred← citeshttps://doi.org/10.1517/17460441.2012.668182openalex-snapshot
Decision tree models for data mining in hit discovery
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/10.2903/j.efsa.2008.455openalex-snapshot
Flavouring Group Evaluation 21: Thiazoles, thiophene, thiazoline and thienyl derivatives from chemical group 29. Miscellaneous substances from chemical group 30. (Commission Regulation (EC) No 1565/2000 of 18 July 2000) ‐ Opinion of the Scientific Panel on Food Additives, Flavourings, Processing…
inferred← citeshttps://doi.org/10.2903/j.efsa.2008.875openalex-snapshot
Flavouring Group Evaluation 76, (FGE.76) - Consideration of sulphur-containing heterocyclic compounds evaluated by JECFA (59th meeting) structurally related to thiazoles, thiophene, thiazoline and thienyl derivatives from chemical group 29, miscellaneous
inferred← citeshttps://doi.org/10.2903/j.efsa.2009.1023openalex-snapshot
Flavouring Group Evaluation 21, Revision 1 (FGE.21Rev1): Thiazoles, thiophene, thiazoline and thienyl derivatives from chemical group 29 Miscellaneous substances from chemical group 30
inferred← citeshttps://doi.org/10.2903/j.efsa.2009.1206openalex-snapshot
Flavouring Group Evaluation 93 (FGE.93): Consideration of sulphur containing heterocyclic compounds evaluated by JECFA (68th meeting) structurally related to thiazoles, thiophene, thiazoline and thienyl derivatives evaluated by EFSA in FGE.21Rev1 (2009)
inferred← citeshttps://doi.org/10.2903/j.efsa.2011.1989openalex-snapshot
Scientific Opinion on Flavouring Group Evaluation 21, Revision 2 (FGE.21Rev2): Thiazoles, thiophene, thiazoline and thienyl derivatives from chemical group 29. Miscellaneous substances from chemical group 30
inferred← citeshttps://doi.org/10.2903/j.efsa.2012.2457openalex-snapshot
Scientific Opinion on Flavouring Group Evaluation 21, Revision 3 (FGE.21Rev3): Thiazoles, thiophenes, thiazoline and thienyl derivatives from chemical groups 29 and 30
inferred← citeshttps://doi.org/10.2903/j.efsa.2013.3451openalex-snapshot
Scientific Opinion on Flavouring Group Evaluation 21, Revision 4 (FGE.21Rev4): Thiazoles, thiophenes, thiazoline and thienyl derivatives from chemical groups 29 and 30
inferred← citeshttps://doi.org/10.2903/j.efsa.2013.3452openalex-snapshot
Scientific Opinion on Flavouring Group Evaluation 93, Revision 1 (FGE.93Rev1): Consideration of sulphur containing heterocyclic compounds evaluated by JECFA (68th meeting) structurally related to thiazoles, thiophene, thiazoline and thienyl derivatives evaluated by EFSA in FGE.21Rev3
inferred← citeshttps://doi.org/10.2903/j.efsa.2013.3455openalex-snapshot
Scientific Opinion on Flavouring Group Evaluation 76, Revision 1 (FGE.76Rev1): Consideration of sulphur‐containing heterocyclic compounds evaluated by JECFA (59th meeting) structurally related to thiazoles, thiophene, thiazoline and thienyl derivatives from chemical group 29 and miscellaneous…
inferred← citeshttps://doi.org/10.2903/j.efsa.2015.4066openalex-snapshot
Scientific Opinion on Flavouring Group Evaluation 21, Revision 5 (FGE.21Rev5): Thiazoles, thiophenes, thiazoline and thienyl derivatives from chemical groups 29 and 30
inferred← citeshttps://doi.org/10.3109/10408444.2010.494175openalex-snapshot
A review of the electrophilic reaction chemistry involved in covalent DNA binding
inferred← citeshttps://doi.org/10.3390/ijms10073237openalex-snapshot
Prediction of Skin Sensitization with a Particle Swarm Optimized Support Vector Machine
inferred← citeshttps://doi.org/10.51847/4anibsrliwopenalex-snapshot
Interaction of Thiophene and Their Derivatives with BRCA-1 Using a Theoretical Model
inferred← citeshttps://doi.org/10.51847/rheeej44vtopenalex-snapshot
Theoretical Model of Thiophene and Its Derivatives Interaction with BRCA-1
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.