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Probabilistic Neural Network Multiple Classifier System for Predicting the Genotoxicity of Quinolone and Quinoline Derivatives

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What this work says

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

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Highly discriminating distance-based topological index
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DNA synthesis inhibition and the induction of protein X in Escherichia coli
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Molecular connectivity in structure-activity analysis
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Delayed and prolonged cholestatic hepatitis with ductopenia after long-term ciprofloxacin therapy for Crohn's disease
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The fluoroquinolone antibacterials: past, present and future perspectives
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Antibacterial activity of quinolone–Macrocycle conjugates
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Novel quinolone derivatives as potent antibacterials
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Quinolone antibacterials: A new class of photochemical carcinogens
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Computer-assisted study of the relationship between molecular structure and Henry's law constant
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Computer-Assisted Drug Design
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Automated Descriptor Selection for Quantitative Structure-Activity Relationships Using Generalized Simulated Annealing
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A simple method for the representation, quantification, and comparison of the volumes and shapes of chemical compounds
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Development of Quantitative Structure−Activity Relationship and Classification Models for a Set of Carbonic Anhydrase Inhibitors
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Prediction of Glycine/NMDA Receptor Antagonist Inhibition from Molecular Structure
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Eccentric Connectivity Index: A Novel Highly Discriminating Topological Descriptor for Structure−Property and Structure−Activity Studies
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Future Papers
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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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Random Forests
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Genotoxicity of fluoroquinolines and methyiquinolines
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PENNSYLVANIA STATE UNIVERSITY
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Effects of norfloxacin on DNA metabolism in Pseudomonas aeruginosa
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Differential effects of antibiotics inhibiting gyrase
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THE EVOLUTION OF FLUORINATED QUINOLONES: Pharmacology, Microbiological Activity, Clinical Uses, and Toxicities
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Deprivation of the mutagenic property of quinoline. Inhibition of mutagenic metabolism by fluorine substitution.

What points at this work

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

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Electrotopological State Indices
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Bibliography
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One for Many: A Universal Reagent for Acylation Processes
inferred← citeshttps://doi.org/10.1002/tox.21905openalex-snapshot
Genotoxicity risk assessment of diversely substituted quinolines using the SOS chromotest
inferred← citeshttps://doi.org/10.1007/978-0-387-30440-3_134openalex-snapshot
Drug Design with Artificial Neural Networks
inferred← citeshttps://doi.org/10.1007/springerreference_60306openalex-snapshot
Drug Design with Artificial Neural Networks
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Risk Assessment
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Risk Assessment
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Biotransformation kinetics of pharmaceutical and industrial micropollutants in groundwaters by a laccase cocktail from Pycnoporus sanguineus CS43 fungi
inferred← citeshttps://doi.org/10.1016/j.surfin.2021.101019openalex-snapshot
Dual-mode electrochemical evaluation of 8‑hydroxy-5-nitroquinoline in industrial sewage
inferred← citeshttps://doi.org/10.1021/es061500gopenalex-snapshot
Isolation and Identification of Xenobiotic Aryl Hydrocarbon Receptor Ligands in Dyeing Wastewater
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Discovery of Novel and Cardioselective Diltiazem-like Calcium Channel Blockers via Virtual Screening
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