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Quantitative structure-activity relationships for human health effects: Commonalities with other endpoints
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Outgoing claims: the papers this work cites, builds on, or argues with.
inferredcites →https://doi.org/10.1002/(sici)1096-9063(199901)55:1<78::aid-ps853>3.0.co;2-7openalex-snapshot
Hydrogen bonding part 46: a review of the correlation and prediction of transport properties by an lfer method: physicochemical properties, brain penetration and skin permeability
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Quantitative structure-activity relationship (QSAR) studies of mutagens and carcinogens
inferredcites →https://doi.org/10.1002/(sici)1098-2280(1996)27:4<314::aid-em6>3.0.co;2-copenalex-snapshot
Structural and quantum chemical factors affecting mutagenic potency of aminoimidazo-azaarenes
inferredcites →https://doi.org/10.1002/(sici)1098-2280(1996)28:1<31::aid-em7>3.0.co;2-hopenalex-snapshot
A computerized connectivity approach for analyzing the structural basis of mutagenicity in Salmonella and its relationship with rodent carcinogenicity
inferredcites →https://doi.org/10.1002/(sici)1099-1263(199607)16:4<355::aid-jat357>3.0.co;2-zopenalex-snapshot
‘Dynamic’ QSAR For Semicarbazide-induced Mortality in Frog Embryos
inferredcites →https://doi.org/10.1002/(sici)1520-6866(1996)16:2<109::aid-tcm5>3.0.co;2-mopenalex-snapshot
Developmental toxicity of carboxylic acids to Xenopus embryos: A quantitative structure‐activity relationship and computer‐automated structure evaluation
inferredcites →https://doi.org/10.1002/1521-3838(200010)19:4<356::aid-qsar356>3.0.co;2-iopenalex-snapshot
Exploring the Potential for Allergic Contact Dermatitisvia Computed Heats of Reaction of Haptens with Protein End-groups Heats of Reaction of Haptens with Protein End-groups by Computation
inferredcites →https://doi.org/10.1002/1526-4998(200101)57:1<3::aid-ps269>3.0.co;2-6openalex-snapshot
Selecting the right compounds for screening: does Lipinski's Rule of 5 for pharmaceuticals apply to agrochemicals?
inferredcites →https://doi.org/10.1002/9783906390406openalex-snapshot
Computer‐Assisted Lead Finding and Optimization
inferredcites →https://doi.org/10.1002/9783906390406.ch2openalex-snapshot
Prediction of Acute Mammalian Toxicity from Molecular Structure for a Diverse Set of Substituted Anilines Using Regression Analysis and Computational Neural Networks
inferredcites →https://doi.org/10.1002/em.2850190108openalex-snapshot
Quantitative structure‐activity relationship investigation of the role of hydrophobicity in regulating mutagenicity in the Ames test: 2. Mutagenicity of aromatic and heteroaromatic nitro compounds in Salmonella typhimurium TA100
inferredcites →https://doi.org/10.1002/etc.5620070303openalex-snapshot
STRUCTURE-ACTIVITY RELATIONSHIPS OF SPECIES-SELECTIVITY IN ACUTE CHEMICAL TOXICITY BETWEEN FISH AND RODENTS
inferredcites →https://doi.org/10.1002/etc.5620100405openalex-snapshot
Structure-activity relationships for osteolathyrism: IV. Para-substituted benzoic acid hydrazides and alkyl carbazates
inferredcites →https://doi.org/10.1002/etc.5620131008openalex-snapshot
Interspecies toxicity correlations of rat, mouse and Photobacterium phosphoreum
inferredcites →https://doi.org/10.1002/jat.2550100111openalex-snapshot
Structure–activity relationships for osteolathyrism. III. Substituted thiosemicarbazides
inferredcites →https://doi.org/10.1002/jps.2600621213openalex-snapshot
Structure–Side-Effect Sorting of Drugs II: Skin Sensitization
inferredcites →https://doi.org/10.1002/qsar.19910100404openalex-snapshot
A QSAR Model of Teratogenesis
inferredcites →https://doi.org/10.1002/qsar.19920110208openalex-snapshot
MULTICASE 1. A Hierarchical Computer Automated Structure Evaluation Program
inferredcites →https://doi.org/10.1002/qsar.19940130106openalex-snapshot
A Classification Model for Allergic Contact Dermatitis
inferredcites →https://doi.org/10.1002/qsar.19950140202openalex-snapshot
QSAR in Toxicology. 2. Prediction of Acute Mammalian Toxicity and Interspecies Correlations
inferredcites →https://doi.org/10.1002/qsar.19950140402openalex-snapshot
QSAR in Toxicology. 3. Prediction of Chronic Toxicities
inferredcites →https://doi.org/10.1002/qsar.19960150307openalex-snapshot
QSAR for Allergic Contact Dermatitis
inferredcites →https://doi.org/10.1002/qsar.19970160106openalex-snapshot
Correspondence Analysis of the Skin Sensitization Potential of Organic Chemicals
inferredcites →https://doi.org/10.1006/eesa.1993.1027openalex-snapshot
Commonalities in the Structural Determinants of Toxicity in Fish and Mammals
inferredcites →https://doi.org/10.1006/eesa.1997.1626openalex-snapshot
Comparisons of Acute Toxicity of Selected Chemicals to Rainbow Trout and Rats
inferredcites →https://doi.org/10.1006/faat.1996.0077openalex-snapshot
An Analysis of Nasal Irritation Thresholds Using a New Solvation Equation
inferredcites →https://doi.org/10.1006/meth.1998.0583openalex-snapshot
Quantitative Structure-Based Modeling Applied to Characterization and Prediction of Chemical Toxicity
inferredcites →https://doi.org/10.1006/rtph.1998.1259openalex-snapshot
A New Highly Specific Method for Predicting the Carcinogenic Potential of Pharmaceuticals in Rodents Using EnhancedMCASEQSAR-ES Software
inferredcites →https://doi.org/10.1006/taap.1995.1172openalex-snapshot
Physicochemical Properties of Nonreactive Volatile Organic Chemicals to Estimate RD50: Alternatives to Animal Studies
inferredcites →https://doi.org/10.1007/s001280000141openalex-snapshot
Interspecies Modeling of Narcotics Toxicity to Aquatic Animals
inferredcites →https://doi.org/10.1007/s001289900898openalex-snapshot
StructureToxicity Relationships for Selected Lactones to Tetrahymena pyriformis
inferredcites →https://doi.org/10.1007/s002040050479openalex-snapshot
Structure-activity relationships of volatile organic chemicals as sensory irritants
inferredcites →https://doi.org/10.1007/s0089490050252openalex-snapshot
Data Mining of Toxic Chemicals: Structure Patterns and QSAR
inferredcites →https://doi.org/10.1016/0009-2797(92)90032-gopenalex-snapshot
The structure-activity relationship of skin carcinogenicity of aromatic hydrocarbons and heterocycles
inferredcites →https://doi.org/10.1016/0009-2797(95)03609-xopenalex-snapshot
Molecular fragments associated with non-genotoxic carcinogens, as detected using a software program based on graph theory: their usefulness to predict carcinogenicity
inferredcites →https://doi.org/10.1016/0027-5107(94)90122-8openalex-snapshot
Two million rodent carcinogens? The role of SAR and QSAR in their detection
inferredcites →https://doi.org/10.1016/0027-5107(94)90124-4openalex-snapshot
Approaches to SAR in carcinogenesis and mutagenesis. Prediction of carcinogenicity/mutagenicity using MULTI-CASE
inferredcites →https://doi.org/10.1016/0027-5107(94)90125-2openalex-snapshot
Use of SAR in computer-assited prediction of carcinogenicity and mutagenicity of chemicals by the TOPKAT program
inferredcites →https://doi.org/10.1016/0027-5107(94)90126-0openalex-snapshot
The importance of the hydrophobic interaction in the mutagenicity of organic compounds
inferredcites →https://doi.org/10.1016/0027-5107(94)90127-9openalex-snapshot
Application of SAR methods to non-congeneric data bases assocated with carcinogenicity and mutagenicity: Issues and approachs
inferredcites →https://doi.org/10.1016/0048-9697(91)90198-nopenalex-snapshot
QSAR studies of comparative toxicity in aquatic organisms
inferredcites →https://doi.org/10.1016/0165-1218(88)90114-0openalex-snapshot
Chemical structure, Salmonella mutagenicity and extent of carcinogenicity as indicators of genotoxic carcinogenesis among 222 chemicals tested in rodents by the U.S. NCI/NTP
inferredcites →https://doi.org/10.1016/0166-1280(93)85009-nopenalex-snapshot
Binding of some dioxins and dibenzofurans to the Ah receptor. A QSAR model based on comparative molecular field analysis (CoMFA)
inferredcites →https://doi.org/10.1016/0166-1280(94)80022-7openalex-snapshot
Modelling of molecular mutagenicity with comparative molecular field analysis (CoMFA). Structural and electronic properties of MX compounds related to TA 100 mutagenicity
inferredcites →https://doi.org/10.1016/0166-445x(88)90052-5openalex-snapshot
A quantitative structure-activity relationship for the acute toxicity of some epoxy compounds to the guppy
inferredcites →https://doi.org/10.1016/0278-6915(86)90188-2openalex-snapshot
Structure-activity relationships in allergic contact dermatitis
inferredcites →https://doi.org/10.1016/0300-483x(88)90243-0openalex-snapshot
Structure-activity relationships for osteolathyrism: II. Effects of alkyl-substituted acid hydrazides
inferredcites →https://doi.org/10.1016/0300-483x(92)90190-popenalex-snapshot
Multivariate quantitative structure-toxicity relationships in a series of dopamine mimetics
inferredcites →https://doi.org/10.1016/0300-483x(95)03132-yopenalex-snapshot
Structure activity relationships in skin sensitization using the murine local lymph node assay
inferredcites →https://doi.org/10.1016/0378-4274(92)90238-fopenalex-snapshot
Prediction of non-genotoxic carcinogenesis
inferredcites →https://doi.org/10.1016/0378-4274(95)03373-sopenalex-snapshot
Development of structure-activity relationship rules for predicting carcinogenic potential of chemicals
inferredcites →https://doi.org/10.1016/0378-4274(96)03689-2openalex-snapshot
Structure-activity relationships and computer-assisted analysis of respiratory sensitization potential
inferredcites →https://doi.org/10.1016/0887-2333(94)90204-6openalex-snapshot
A quantitative structure-activity relationship (QSAR) investigation of a Draize eye irritation database
inferredcites →https://doi.org/10.1016/0887-2333(94)90244-5openalex-snapshot
An expert system rulebase for identifying contact allergens
inferredcites →https://doi.org/10.1016/0887-2333(96)00014-8openalex-snapshot
The use of in vitro cytotoxicity measurements in QSAR methods for the prediction of the skin corrosivity potential of acids
inferredcites →https://doi.org/10.1016/s0002-9378(97)70603-3openalex-snapshot
Structural determinants associated with risk of human developmental toxicity
inferredcites →https://doi.org/10.1016/s0003-2670(00)00963-6openalex-snapshot
Prediction of drug transfer into human milk from theoretically derived descriptors
inferredcites →https://doi.org/10.1016/s0027-5107(97)00202-9openalex-snapshot
Identification of `genotoxic' and `non-genotoxic' alerts for cancer in mice: the carcinogenic potency database
inferredcites →https://doi.org/10.1016/s0027-5107(98)00068-2openalex-snapshot
Structure-based methods for predicting mutagenicity and carcinogenicity: are we there yet?
inferredcites →https://doi.org/10.1016/s0045-6535(98)00503-7openalex-snapshot
Frontier orbital energies, hydrophobicity and steric factors as physical qsar descriptors of molecular mutagenicity. A review with a case study: MX compounds
inferredcites →https://doi.org/10.1016/s0045-6535(99)00525-1openalex-snapshot
Electronic eigenvalue (EEVA): a new QSAR/QSPR descriptor for electronic substituent effects based on molecular orbital energies. A QSAR approach to the Ah receptor binding affinity of polychlorinated biphenyls (PCBs), dibenzo-p-dioxins (PCDDs) and dibenzofurans (PCDFs)
inferredcites →https://doi.org/10.1016/s0165-1218(96)90023-3openalex-snapshot
A validation study of the COMPACT and HazardExpert techniques with 40 chemicals
inferredcites →https://doi.org/10.1016/s0165-1218(97)00026-8openalex-snapshot
Methods for predicting carcinogenic hazards: new opportunities coming from recent developments in molecular oncology and SAR studies
inferredcites →https://doi.org/10.1016/s0169-409x(00)00129-0openalex-snapshot
Experimental and computational approaches to estimate solubility and permeability in drug discovery and development settings 1PII of original article: S0169-409X(96)00423-1. The article was originally published in Advanced Drug Delivery Reviews 23 (1997) 3–25. 1
inferredcites →https://doi.org/10.1016/s0169-409x(96)00423-1openalex-snapshot
Experimental and computational approaches to estimate solubility and permeability in drug discovery and development settings
inferredcites →https://doi.org/10.1016/s0278-6915(97)87277-8openalex-snapshot
A quantitative structure-toxicity relationships model for the dermal sensitization guinea pig maximization assay
inferredcites →https://doi.org/10.1016/s0300-483x(02)00022-7openalex-snapshot
Web resources for drug toxicity
inferredcites →https://doi.org/10.1016/s0300-483x(02)00026-4openalex-snapshot
Genetic toxicology: web resources
inferredcites →https://doi.org/10.1016/s0300-483x(97)03631-7openalex-snapshot
Computational predictive programs (expert systems) in toxicology
inferredcites →https://doi.org/10.1016/s0887-2333(01)00007-8openalex-snapshot
Establishment of an in vitro reporter gene assay for developmental cardiac toxicity
inferredcites →https://doi.org/10.1016/s0887-2333(96)00063-xopenalex-snapshot
QSARS for the eye irritation potential of neutral organic chemicals
inferredcites →https://doi.org/10.1016/s0887-2333(97)00044-1openalex-snapshot
Skin irritant-induced cytotoxicity and prostaglandin E2 release in human skin keratinocyte cultures
inferredcites →https://doi.org/10.1016/s0887-2333(97)00117-3openalex-snapshot
A Quantitative Structure–Activity Relationship (QSAR) for a Draize Eye Irritation Database
inferredcites →https://doi.org/10.1016/s0887-2333(98)00010-1openalex-snapshot
Draize Eye Scores and Eye Irritation Thresholds in Man Combined into one Quantitative Structure–Activity Relationship
inferredcites →https://doi.org/10.1016/s0887-2333(98)00056-3openalex-snapshot
Molecular modelling of the rat peroxisome proliferator-activated receptor -α (rPPARα) by homology with the human retinoic acid X receptor α (hRXRα) and investigation of ligand binding interactions I: QSARs
inferredcites →https://doi.org/10.1016/s0887-2333(99)00086-7openalex-snapshot
A QSAR model for the eye irritation of cationic surfactants
inferredcites →https://doi.org/10.1016/s0928-0987(98)00041-4openalex-snapshot
Investigation of the mechanism of flux across human skin in vitro by quantitative structure–permeability relationships
inferredcites →https://doi.org/10.1016/s1011-1344(00)00100-7openalex-snapshot
Development of an expert system rulebase for the prospective identification of photoallergens
inferredcites →https://doi.org/10.1016/s1383-5742(97)00019-7openalex-snapshot
Review of mutagenicity of monocyclic aromatic amines: quantitative structure–activity relationships
inferredcites →https://doi.org/10.1016/s1383-5742(97)00021-5openalex-snapshot
The first US National Toxicology Program exercise on the prediction of rodent carcinogenicity: definitive results
inferredcites →https://doi.org/10.1021/bk-1989-0413.ch024openalex-snapshot
Correlations and Mechanisms of Chemical Toxicity in Animals
inferredcites →https://doi.org/10.1021/ci00017a019openalex-snapshot
Structure-activity relationships for skin sensitization potential: Development of structural alerts for use in knowledge-based toxicity prediction systems
inferredcites →https://doi.org/10.1021/ci9800965openalex-snapshot
Response-Surface Analyses for Toxicity to Tetrahymena pyriformis: Reactive Carbonyl-Containing Aliphatic Chemicals
inferredcites →https://doi.org/10.1021/ci980204nopenalex-snapshot
Validation and Subsequent Development of the Derek Skin Sensitization Rulebase by Analysis of the BgVV List of Contact Allergens
inferredcites →https://doi.org/10.1021/cr9901079openalex-snapshot
Quantitative Structure−Activity Relationships of Mutagenic and Carcinogenic Aromatic Amines
inferredcites →https://doi.org/10.1021/ja00226a005openalex-snapshot
Comparative molecular field analysis (CoMFA). 1. Effect of shape on binding of steroids to carrier proteins
inferredcites →https://doi.org/10.1021/tx00039a006openalex-snapshot
Structure-Activity Relationships for Contact Allergenic Potential of .gamma.,.gamma.-Dimethyl-.gamma.-butyrolactone Derivatives. 2. Quantitative Structure-Skin Sensitization Relationships for .alpha.-Substituted-.alpha.-methyl-.gamma.,.gamma.-dimethyl-.gamma.-butyrolactones
inferredcites →https://doi.org/10.1021/tx015502kopenalex-snapshot
Parametrization of Electrophilicity for the Prediction of the Toxicity of Aromatic Compounds
inferredcites →https://doi.org/10.1021/tx970166mopenalex-snapshot
Quantitative Structure−Activity Analyses of Nitrobenzene Toxicity to Tetrahymena pyriformis
inferredcites →https://doi.org/10.1023/a:1007543708522openalex-snapshot
Estimation of Molecular Linear Free Energy Relationship Descriptors. 4. Correlation and Prediction of Cell Permeation
inferredcites →https://doi.org/10.1023/a:1008192010023openalex-snapshot
Lipophilicity in PK design: methyl, ethyl, futile
inferredcites →https://doi.org/10.1034/j.1600-0536.2000.042003154.xopenalex-snapshot
Quantitative structure‐activity relationships: sulfonate esters in the local lymph node assay
inferredcites →https://doi.org/10.1080/10590508509373329openalex-snapshot
Effects of carcinogenic agents on aquatic animals: An environmental and experimental overview
inferredcites →https://doi.org/10.1080/10590509609373485openalex-snapshot
α,β‐unsaturated ketones class study: Development of chemical nominations for carcinogenicity testing
inferredcites →https://doi.org/10.1080/10590509909373507openalex-snapshot
Tumor profiles and carcinogenic potency in rodents and humans: Value for cancer risk assessment
inferredcites →https://doi.org/10.1080/1062936021000020062openalex-snapshot
Global Government applications of analogues, SAR s and QSAR s to predict aquatic toxicity, chemical or physical properties, environmental fate parameters and health effects of organic chemicals
inferredcites →https://doi.org/10.1080/10629360290002316openalex-snapshot
The importance of hydrophobicity and electrophilicity descriptors in mechanistically-based QSARs for toxicological endpoints
inferredcites →https://doi.org/10.1080/10629369408029901openalex-snapshot
Multivariate Qsar Analysis of a Skin Sensitization Database
inferredcites →https://doi.org/10.1080/10629369608032987openalex-snapshot
The Use of Cluster Significance Analysis to Identify Asymmetric QSAR Data Sets in Toxicology. An Example With Eye Irritation Data
inferredcites →https://doi.org/10.1080/10629369808039150openalex-snapshot
Enhancing the Flexibility and Adaptability of the Darc Structural Representation for Computer-Aided Drug Design
inferredcites →https://doi.org/10.1080/10629369908039164openalex-snapshot
EEVA (Electronic Eigenvalue): A New QSAR/QSPR Descriptor for Electronic Substituent Effects Based on Molecular Orbital Energies
inferredcites →https://doi.org/10.1080/10629369908039181openalex-snapshot
Development, Characterization and Application of Predictive-Toxicology Models
inferredcites →https://doi.org/10.1080/10629369908039182openalex-snapshot
Knowledge-Based Expert Systems for Toxicity and Metabolism Prediction: DEREK, StAR and METEOR
inferredcites →https://doi.org/10.1080/109158199225486openalex-snapshot
Does Photosensitivity Predict Photococarcinogenicity?
inferredcites →https://doi.org/10.1093/mutage/5.1.3openalex-snapshot
Prediction of the outcome of rodent carcinogenicity bioassays currently being conducted on 44 chemicals by the National Toxicology Program
inferredcites →https://doi.org/10.1093/mutage/9.1.7openalex-snapshot
Prediction of rodent carcinogenicity for 44 chemicals: results
inferredcites →https://doi.org/10.1111/j.1600-0536.1987.tb01478.xopenalex-snapshot
Structure‐activity relationships for skin sensitisation potential of diacrylates and dimethacrylates
inferredcites →https://doi.org/10.1111/j.1600-0536.1992.tb05241.xopenalex-snapshot
The value of the local lymph node assay in quantitative structure‐activity investigations
inferredcites →https://doi.org/10.1111/j.1600-0536.1995.tb00440.xopenalex-snapshot
Structure‐activity relationships in allergic contact dermatitis
inferredcites →https://doi.org/10.1111/j.1600-0536.1999.tb05971.xopenalex-snapshot
Structure‐activity relationships in allergic contact dermatitis induced by methacrylates
inferredcites →https://doi.org/10.1111/j.1600-0773.1998.tb01481.xopenalex-snapshot
A Theoretical Approach to the Ferguson Principle and its Use with Non‐Reactive and Reactive Airborne Chemicals
inferredcites →https://doi.org/10.1111/j.2042-7158.1998.tb06169.xopenalex-snapshot
An Investigation of the Mechanism of Flux Across Polydimethylsiloxane Membranes by use of Quantitative Structure-Permeability Relationships
inferredcites →https://doi.org/10.1177/019262339602400511openalex-snapshot
Review Article: Experimental Chemical Carcinogenesis in Fish
inferredcites →https://doi.org/10.1177/026119290002800106openalex-snapshot
Development of a Decision Support System for the Introduction of Alternative Methods into Local Irritancy/Corrosivity Testing Strategies. Development of a Relational Database
inferredcites →https://doi.org/10.1177/026119290002800108openalex-snapshot
Local Irritation/Corrosion Testing Strategies: Development of a Decision Support System for the Introduction of Alternative Methods
inferredcites →https://doi.org/10.1177/026119290002800318openalex-snapshot
Structure–permeability Relationships for Transcorneal Penetration
inferredcites →https://doi.org/10.1177/026119299302100104openalex-snapshot
Multiple Computer Automated Structure Evaluation Methodology as an Alternative to In Vivo Eye Irritation Testing
inferredcites →https://doi.org/10.1177/026119299802600512openalex-snapshot
An Evaluation of the Proposed OECD Testing Strategy for Skin Corrosion
inferredcites →https://doi.org/10.1177/074823378800400407openalex-snapshot
An Overview of Structure-Activity Relationships as an Alternative To Testing in Animals for Carcinogenicity, Mutagenicity, Dermal and Eye Irritation, and Acute Oral Toxicity
inferredcites →https://doi.org/10.1177/096032719101000405openalex-snapshot
Computer Prediction of Possible Toxic Action from Chemical Structure; The DEREK System
inferredcites →https://doi.org/10.1289/ehp.9310065openalex-snapshot
The Fifth Plot of the Carcinogenic Potency Database: Results of Animal Bioassays Published in the General Literature through 1988 and by the National Toxicology Program through 1989
inferredcites →https://doi.org/10.1289/ehp.9310162openalex-snapshot
Mechanistic Relationship among Mutagenicity, Skin Sensitization, and Skin Carcinogenicity
inferredcites →https://doi.org/10.1289/ehp.96104s51031openalex-snapshot
Prediction of rodent carcinogenicity bioassays from molecular structure using inductive logic programming.
inferredcites →https://doi.org/10.1289/ehp.96104s51085openalex-snapshot
A Mechanism-Mediated Model for Carcinogenicity: Model Content and Prediction of the Outcome of Rodent Carcinogenicity Bioassays Currently Being Conducted on 25 Organic Chemicals
inferredcites →https://doi.org/10.1289/ehp.97105940openalex-snapshot
Allergic Contact Sensitizing Chemicals as Environmental Carcinogens
inferredcites →https://doi.org/10.1289/ehp.99107129openalex-snapshot
Relationship between Allergic Contact Dermatitis and Electrophilicity
inferredcites →https://doi.org/10.1897/01-234openalex-snapshot
Overview of data and conceptual approaches for derivation of quantitative structure-activity relationships for ecotoxicological effects of organic chemicals
inferredcites →https://doi.org/10.1897/01-363openalex-snapshot
Quantitative structure-property relationships for prediction of boiling point, vapor pressure, and melting point
inferredcites →https://doi.org/10.1897/01-605openalex-snapshot
Quantitative structure-property relationships for predicting henry's law constant from molecular structure
inferredcites →https://doi.org/10.1897/1552-8618(1994)13[1599:itcorm]2.0.co;2openalex-snapshot
INTERSPECIES TOXICITY CORRELATIONS OF RAT, MOUSE AND PHOTOBACTERIUM PHOSPHOREUM
inferredcites →https://doi.org/10.2131/jts.16.111openalex-snapshot
Studies on eye irritation caused by chemicals in rabbits. II. Structure-activity relationships and in vitro approach to primary eye irritation of salicylates in rabbits.
inferredcites →https://doi.org/10.2165/00003088-199528030-00005openalex-snapshot
Placental Transfer of Drugs Administered to the Mother
inferredcites →https://doi.org/10.2307/3226453openalex-snapshot
Structure-Activity Relationships for Osteolathyrism. I. Effects of Altering the Semicarbazide Structure
inferredcites →https://doi.org/10.3109/03602539808996328openalex-snapshot
An Improved and Updated Version of the Compact Procedure for the Evaluation of P450-Mediated Chemical Activation
inferredcites →https://doi.org/10.3109/09273949709085057openalex-snapshot
Trauma and alkali burns induce distinct patterns of cytokine gene expression in the rat cornea
inferredcites →https://doi.org/10.3109/09273949709085060openalex-snapshot
Secretion of proinflammatory cytokines by human conjunctival epithelial cells
inferredcites →https://doi.org/10.3109/10408449109089879openalex-snapshot
Mechanisms of Activation of the Sensory Irritant Receptor by Airborne Chemicals
inferredcites →https://doi.org/10.4049/jimmunol.99.2.370openalex-snapshot
Delayed Contact Sensitivity to Catechols
inferredcites →https://doi.org/10.5107/sccj.28.344openalex-snapshot
Quantitative Structure-activity Relationship of Surfactants on Eye Irritation Predicted by Hemoglobin Denaturation.
What points at this work
Incoming claims: where this work appears in other papers’ reference lists and arguments.
inferred← citeshttps://doi.org/10.1002/jat.1466openalex-snapshot
Application of quantitative structure–activity relationships for modeling drug and chemical transport across the human placenta barrier: a multivariate data analysis approach
inferred← citeshttps://doi.org/10.1002/qsar.200710103openalex-snapshot
A Review of (Q)SAR Models for Skin and Eye Irritation and Corrosion
inferred← citeshttps://doi.org/10.1002/qsar.200710107openalex-snapshot
A Mini Review of Mammalian Toxicity (Q)SAR Models
inferred← citeshttps://doi.org/10.1002/qsar.200710118openalex-snapshot
(Q)SARs for Predicting Effects Relating to Reproductive Toxicity
inferred← citeshttps://doi.org/10.1007/978-94-007-0923-2_8openalex-snapshot
New Advances in QSPR/QSAR Analysis of Nitrocompounds: Solubility, Lipophilicity, and Toxicity
inferred← citeshttps://doi.org/10.1007/s00044-012-0134-7openalex-snapshot
Simple and reliable prediction of toxicological activities of benzoic acid derivatives without using any experimental data or computer codes
inferred← citeshttps://doi.org/10.1007/s00204-010-0532-xopenalex-snapshot
Chronic oral LOAEL prediction by using a commercially available computational QSAR tool
inferred← citeshttps://doi.org/10.1007/s00204-023-03642-wopenalex-snapshot
Exposure limits for indoor volatile substances concerning the general population: The role of population-based differences in sensory irritation of the eyes and airways for assessment factors
inferred← citeshttps://doi.org/10.1016/b0-12-369400-0/00970-4openalex-snapshot
Toxicity Testing, Modeling
inferred← citeshttps://doi.org/10.1016/b978-0-12-373593-5.00069-0openalex-snapshot
Software Tools for Toxicology and Risk Assessment
inferred← citeshttps://doi.org/10.1016/b978-0-444-63299-9.00017-xopenalex-snapshot
QSARs on the Thyroid Hormone Effects of Polybrominated Diphenyl Ether (PBDE) Derivatives
inferred← citeshttps://doi.org/10.1016/j.jhazmat.2012.07.048openalex-snapshot
Accurate prediction of the toxicity of benzoic acid compounds in mice via oral without using any computer codes
inferred← citeshttps://doi.org/10.1016/j.taap.2012.03.018openalex-snapshot
VirtualToxLab — A platform for estimating the toxic potential of drugs, chemicals and natural products
inferred← citeshttps://doi.org/10.1016/j.toxlet.2014.09.004openalex-snapshot
OpenVirtualToxLab—A platform for generating and exchanging in silico toxicity data
inferred← citeshttps://doi.org/10.1016/j.yrtph.2011.02.002openalex-snapshot
Predictive models for nanotoxicology: Current challenges and future opportunities
inferred← citeshttps://doi.org/10.1016/j.yrtph.2011.06.007openalex-snapshot
Evaluation of research activities and research needs to increase the impact and applicability of alternative testing strategies in risk assessment practice
inferred← citeshttps://doi.org/10.1016/j.yrtph.2022.105311openalex-snapshot
Understanding and overcoming the technical challenges in using in silico predictions in regulatory decisions of complex toxicological endpoints – A pesticide perspective for regulatory toxicologists with a focus on machine learning models
inferred← citeshttps://doi.org/10.1080/10408398.2012.726661openalex-snapshot
Assessing Herbal Products with Health Claims
inferred← citeshttps://doi.org/10.1080/1062936x.2018.1518261openalex-snapshot
Evaluation and improvement of QSAR predictions of skin sensitization for pesticides
inferred← citeshttps://doi.org/10.1109/cec.2005.1554695openalex-snapshot
Derivation of Quantitative Structure-Toxicity Relationships for Ecotoxicological Effects of Organic Chemicals: Evolving Neural Networks and Evolving Rules
inferred← citeshttps://doi.org/10.1177/026119290503301s08openalex-snapshot
3.2. Skin Irritation and Corrosion
inferred← citeshttps://doi.org/10.1177/026119290603400119openalex-snapshot
Animal Carcinogenicity Studies: 3. Alternatives to the Bioassay
inferred← citeshttps://doi.org/10.1177/026119290903700506openalex-snapshot
In Silico Toxicology in Drug Discovery — Concepts Based on Three-dimensional Models
inferred← citeshttps://doi.org/10.1177/2397847320971259openalex-snapshot
Development of cardiotoxicity model using ligand-centric and receptor-centric descriptors
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/10.1289/ehp.11811openalex-snapshot
Efficacy of Simple Short-Term in Vitro Assays for Predicting the Potential of Metal Oxide Nanoparticles to Cause Pulmonary Inflammation
inferred← citeshttps://doi.org/10.14573/altex.2008.3.213openalex-snapshot
Non-animal methodologies within biomedical research and toxicity testing
inferred← citeshttps://doi.org/10.2760/925662openalex-snapshot
[A needle for performing a water load and cholangiography during the intraoperative revision of the extrahepatic bile ducts].
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/molecules18089061openalex-snapshot
Determining Chemical Reactivity Driving Biological Activity from SMILES Transformations: The Bonding Mechanism of Anti-HIV Pyrimidines
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
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