(Q50181937)

English

Structure-activity relationship of genotoxic polycyclic aromatic nitro compounds: further evidence for the importance of hydrophobicity and molecular orbital energies in genetic toxicity.

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Europe PubMed Central

PubMed publication ID

26 February 2018

http://europepmc.org/abstract/MED/1505530

Structure-activity relationship of genotoxic polycyclic aromatic nitro compounds: further evidence for the importance of hydrophobicity and molecular orbital energies in genetic toxicity. (English)

1 reference

Europe PubMed Central

PubMed publication ID

26 February 2018

http://europepmc.org/abstract/MED/1505530

1 reference

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inferred from title

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author name string

Debnath AK

1

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Europe PubMed Central

PubMed publication ID

26 February 2018

http://europepmc.org/abstract/MED/1505530

Hansch C

2

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Europe PubMed Central

PubMed publication ID

26 February 2018

http://europepmc.org/abstract/MED/1505530

publication date

1 January 1992

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Europe PubMed Central

PubMed publication ID

26 February 2018

http://europepmc.org/abstract/MED/1505530

Environmental and Molecular Mutagenesis

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Europe PubMed Central

PubMed publication ID

26 February 2018

http://europepmc.org/abstract/MED/1505530

20

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Europe PubMed Central

PubMed publication ID

26 February 2018

http://europepmc.org/abstract/MED/1505530

2

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Europe PubMed Central

PubMed publication ID

26 February 2018

http://europepmc.org/abstract/MED/1505530

140-144

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Europe PubMed Central

PubMed publication ID

26 February 2018

http://europepmc.org/abstract/MED/1505530

The SOS Chromotest, a colorimetric bacterial assay for genotoxins: procedures

1 reference

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LUMO energies and hydrophobicity as determinants of mutagenicity by nitroaromatic compounds in Salmonella typhimurium

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Structure-activity relationship of mutagenic aromatic and heteroaromatic nitro compounds. Correlation with molecular orbital energies and hydrophobicity

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A QSAR investigation of the role of hydrophobicity in regulating mutagenicity in the Ames test: 1. Mutagenicity of aromatic and heteroaromatic amines in Salmonella typhimurium TA98 and TA100.

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7 January 2021

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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 inSalmonella typhimurium TA100

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Evaluation of the mutagenic and genotoxic activities of 48 nitroimidazoles and related imidazole derivatives by the Ames test and the SOS chromotest.

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Development and use of quantum mechanical molecular models. 76. AM1: a new general purpose quantum mechanical molecular model

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Genotoxicity of nitrated polycyclic aromatic hydrocarbons and related structures onEscherichia coli PQ37 (SOS chromotest)

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SOS chromotest, a direct assay of induction of an SOS function in Escherichia coli K-12 to measure genotoxicity

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Sampling of vehicle emissions for chemical analysis and biological testing

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Mutagenicity and carcinogenicity of nitroarenes and their sources in the environment

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The structure-activity relationship of skin carcinogenicity of aromatic hydrocarbons and heterocycles

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Identifiers

10.1002/EM.2850200210

1 reference

Europe PubMed Central

PubMed publication ID

26 February 2018

http://europepmc.org/abstract/MED/1505530

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

26 February 2018

http://europepmc.org/abstract/MED/1505530

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