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Group Philicity and Electrophilicity as Possible Descriptors for Modeling Ecotoxicity Applied to Chlorophenols
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Outgoing claims: the papers this work cites, builds on, or argues with.
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Radical toxicity of phenols: A reference point for obtaining perspective in the formulation of QSAR
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Wiley Series in Probability and Statistics
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The fungitoxicity of chlorophenols to the pathogenic fungi, Fusarium oxysporum and Rhizoctonia solani: A structure‐activity relationship study
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The Toxicity of Substituted Phenols in the Nitrification Inhibition Test and Luminescent Bacteria Test
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Applicability of CoMFA in Ecotoxicology: A Critical Study on Chlorophenols
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Density Functional Theory of Atoms and Molecules
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Phytotoxicity of Low-Molecular-Weight Phenols from Olive Mill Waste Waters
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Analyzing Toxicity Through Electrophilicity
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Electrophilicity as a possible descriptor for toxicity prediction
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Intermolecular reactivity through the generalized philicity concept
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Chemical Reactivity Profiles of Two Selected Polychlorinated Biphenyls
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An Oxygen-Bonded C8-Deoxyguanosine Nucleoside Adduct of Pentachlorophenol by Peroxidase Activation: Evidence for Ambident C8 Reactivity by Phenoxyl Radicals
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Role of Phenoxyl Radicals in DNA Adduction by Chlorophenol Xenobiotics Following Peroxidase Activation
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A Novel Tri-Coordination Zinc Complex Functionalized Silicotungstate with ROS Catalytic Ability and Anti-Tumor Cells Activity
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/10.3390/molecules26113365openalex-snapshot
Detecting and Quantifying Polyhaloaromatic Environmental Pollutants by Chemiluminescence-Based Analytical Method
inferred← citeshttps://doi.org/10.3390/ph15111383openalex-snapshot
Quantitative Structure–Toxicity Relationship in Bioactive Molecules from a Conceptual DFT Perspective
inferred← citeshttps://doi.org/10.3390/ph16101339openalex-snapshot
Design of β-Keto Esters with Antibacterial Activity: Synthesis, In Vitro Evaluation, and Theoretical Assessment of Their Reactivity and Quorum-Sensing Inhibition Capacity
inferred← citeshttps://doi.org/10.4018/978-1-4666-4010-8.ch005openalex-snapshot
Toxicity of Halogen, Sulfur and Chlorinated Aromatic Compounds
inferred← citeshttps://doi.org/10.4018/978-1-4666-8136-1.ch004openalex-snapshot
Quantitative Structure-Activity/Property/Toxicity Relationships through Conceptual Density Functional Theory-Based Reactivity Descriptors
inferred← citeshttps://doi.org/10.4018/978-1-5225-1762-7.ch058openalex-snapshot
Quantitative Structure-Activity/Property/Toxicity Relationships through Conceptual Density Functional Theory-Based Reactivity Descriptors
inferred← citeshttps://doi.org/10.4018/978-1-60960-860-6.ch001openalex-snapshot
Modeling Ecotoxicity as Applied to some Selected Aromatic Compounds
inferred← citeshttps://doi.org/10.4018/ijcce.2011010105openalex-snapshot
Toxicity of Halogen, Sulfur and Chlorinated Aromatic Compounds
inferred← citeshttps://doi.org/10.4028/p-4dwjyfopenalex-snapshot
Adsorption Energies of X-Doped Fullerene (X = Si, Sn, BN): A First-Principles Study
inferred← citeshttps://doi.org/10.4067/s0718-07642014000100017openalex-snapshot
DISEÑO DE FÁRMACOS ANTICANCEROSOS DERIVADOS DE CIS-PLATINO(II) MEDIANTE LA TÉCNICA QSAR, BASADA EN EL FUNCIONAL DE LA DENSIDAD
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.