ISSN: 0893-228X

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Chemical Research in Toxicology Q1 Unclaimed

American Chemical Society United States

Unfortunately this journal has not been claimed yet. For this reason, some information may be unavailable.

Chemical Research in Toxicology is a journal indexed in SJR in Medicine (miscellaneous) and Toxicology with an H index of 177. It has a price of 3678 €. It has an SJR impact factor of 0,981 and it has a best quartile of Q1. It is published in English. It has an SJR impact factor of 0,981.

Chemical Research in Toxicology focuses its scope in these topics and keywords: dna, reactive, human, cell, induced, urinary, nitrogen, species, radical, receptor, ...

Type: Journal

Type of Copyright:

Languages: English

Open Access Policy: Open Choice

Type of publications:

Publication frecuency: -

Categories: Medicine (miscellaneous) (Q1) Toxicology (Q1)

Price

3678 €

Inmediate OA

1839 €

Embargoed OA

0 €

Non OA

Metrics

0,981

SJR Impact factor

177

H Index

198

Total Docs (Last Year)

757

Total Docs (3 years)

10649

Total Refs

2927

Total Cites (3 years)

716

Citable Docs (3 years)

3.65

Cites/Doc (2 years)

53.78

Ref/Doc

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Aims and Scope

Best articles by citations

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

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

Quantitative Analysis and Chronic Dosimetry of the Aflatoxin B1Plasma Albumin Adduct Lys-AFB1in Rats by Isotope Dilution Mass Spectrometry

Exploration of Unimolecular Gas-Phase Detoxication Pathways of Sarin and Soman: A Computational Study from the Perspective of Reaction Energetics and Kinetics

O6-2'-Deoxyguanosine-butylene-O6-2'-deoxyguanosine DNA Interstrand Cross-Links Are Replication-Blocking and Mutagenic DNA Lesions

Carbamate Insecticides Target Human Melatonin Receptors

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

N-Nitroso Products from the Reaction of Indoles with Angeli's Salt

Identification of Metabolites of the Fungicide Penconazole in Human Urine

Fast-Flow EPR Spectroscopic Observation of the Isoniazid, Iproniazid, and Phenylhydrazine Hydrazyl Radicals

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

Dihydromethysticin (DHM) Blocks Tobacco Carcinogen 4-(Methylnitrosamino)-1-(3-pyridyl)-1-butanone (NNK)-Induced O6-Methylguanine in a Manner Independent of the Aryl Hydrocarbon Receptor (AhR) Pathway in C57BL/6 Female Mice

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Tolerogenic Role of Kupffer Cells in Allergic Reactions

d-Amino Acid Oxidase Generates Agonists of the Aryl Hydrocarbon Receptor fromd-Tryptophan

Genomics and Proteomics

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

Mutagenicity of a Model DNA-Peptide Cross-Link in Human Cells: Roles of Translesion Synthesis DNA Polymerases

Multidrug Resistance-Associated Protein 2 (MRP2) Enhances 4-Hydroxynonenal-Induced Toxicity in Madin-Darby Canine Kidney II Cells

Exposure to Inorganic Arsenic and Lead and Autism Spectrum Disorder in Children: A Systematic Review and Meta-Analysis

Structure-Activity Relationships for the Toxicity of Polychlorinated Dibenzofurans: Approach through Density Functional Theory-Based Descriptors

Preparation and Antiproliferative Activity of Liposomes Containing a Combination of Cisplatin and Procainamide Hydrochloride

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

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

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