verified SJR 0,957 · Q1 • database Scopus / SJR & Web of Science indexed

United States · American Chemical Society

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Chemical Research in Toxicology

Chemical Research in Toxicology is a journal indexed in SJR in Medicine (miscellaneous) and Toxicology with an H index of 183. It has a price of 3678 €. It has an SJR impact factor of 0,957 and it has a best quartile of Q1. It is published in English. It has an SJR impact factor of 0,957.

Chemical Research in Toxicology focuses its scope in these topics and keywords: human, reactive, dna, urinary, cell, induced, liver, transcription, protein, polymerases, ...

ISSN: 0893-228X

Editorial: American Chemical Society

Category: Medicine (miscellaneous)

Indexation: verifiedScopus / SJR verifiedWeb of Science

Unclaimed profile — some fields may be incomplete.

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SJR Impact Factor trending_up

0,957 Q1

H-index 183

Tasa de Aceptación pie_chart

21% Selectiva

Fuente Acceptance_Rate

Tiempo a publicación hourglass_top

NPD

Campo Sin dato

Coste de Publicación (APC) payments

3.678 € Open Access

Ruta Non-OA 0 €

Metrics

Campos Scimago / CoP — sin series inventadas

Scopus / SJR Web of Science

SJR Impact

0,957

H-index

183

Docs (year)

180

Docs 3y

659

Total refs

10936

Cites 3y

2573

Citable 3y

622

Cites/Doc 2y

3.65

Ref/Doc

60.76

Immediate OA

3678 €

Embargoed OA

1839 €

Non OA / Submission

0 €

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Best articles by citations

Bone as Target Organ for Metals: The Case of f-Elements

What Happens after Activation of Ascaridole? Reactive Compounds and Their Implications for Skin Sensitization

Cytotoxicity of Tirapazamine (3-Amino-1,2,4-benzotriazine-1,4-dioxide)-Induced DNA Damage in Chicken DT40 Cells

Cytolethal Distending Toxin: A Bacterial Toxin Which Disrupts the Eukaryotic Cell Cycle

Contrasting Effects of Metal Ions onS-Nitrosoglutathione, Related to Coordination Equilibria: GSNO Decomposition Assisted by Ni(II) vs Stability Increase in the Presence of Zn(II) and Cd(II)

Computational Study of the Radical Mediated Mechanism of the Formation of C8, C5, and C4 Guanine:Lysine Adducts in the Presence of the Benzophenone Photosensitizer

Computational Study of the Oxidation of Guanine To Form 5-Carboxyamido-5-formamido-2-iminohydantoin (2Ih)

Computational Models for Predicting the Binding Affinities of Ligands for the Wild-Type Androgen Receptor and a Mutated Variant Associated with Human Prostate Cancer

Computational Investigation of Drug Phototoxicity: Photosafety Assessment, Photo-Toxophore Identification, and Machine Learning

Comparative Toxicity and Metabolism of N-Acyl Homologues of Acetaminophen and Its Isomer 3'-Hydroxyacetanilide

Chromatographic Separation and Identification of Products from the Reaction of Dimethylarsinic Acid with Hydrogen Sulfide

Carbamate Insecticides Target Human Melatonin Receptors

SHOW MORE ARTICLES

Bypass of Mutagenic O6-Carboxymethylguanine DNA Adducts by Human Y- and B-Family Polymerases

2,6-Diarylaminotetrahydropyrans from Reactions of Glutaraldehyde with Anilines: Models for Biomolecule Cross-Linking

Bioactive 4-Oxoheptanedioic Monoamide Derivatives of Proteins and Ethanolaminephospholipids: Products of Docosahexaenoate Oxidation

Bioactivation of GPR40 Agonist MK-8666: Formation of Protein Adducts in Vitro from Reactive Acyl Glucuronide and Acyl CoA Thioester

Binding of Pollutants to Biomolecules: A Simulation Study

Analysis of 3'-Phosphoglycolaldehyde Residues in Oxidized DNA by Gas Chromatography/Negative Chemical Ionization/Mass Spectrometry

Air Pollution Particles Mediated Oxidative DNA Base Damage in a Cell Free System and in Human Airway Epithelial Cells in Relation to Particulate Metal Content and Bioreactivity

Acute Gene Expression Profile of Lung Tissue Following Sulfur Mustard Inhalation Exposure in Large Anesthetized Swine

Abstracts, American Chemical Society Division of Chemical Toxicology, 226th ACS National Meeting, New York, New York, September 7-11, 2003

A Planar Catechin Analogue Having a More Negative Oxidation Potential than (+)-Catechin as an Electron Transfer Antioxidant against a Peroxyl Radical

A Novel Approach for Predicting Acyl Glucuronide Reactivity via Schiff Base Formation: Development of Rapidly Formed Peptide Adducts for LC/MS/MS Measurements

A Modified Immuno-Enriched32P-Postlabeling Method for Analyzing the Malondialdehyde-Deoxyguanosine Adduct, 3-(2-Deoxy-beta-d-erythro-pentofuranosyl)- pyrimido[1,2-a]purin-10(3H)one in Human Tissue Samples

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