(Q44104976)

English

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.

scientific article published in January 1992

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scholarly article

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Europe PubMed Central

PubMed publication ID

29 November 2017

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. (English)

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Europe PubMed Central

PubMed publication ID

29 November 2017

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Salmonella Typhimurium

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author name string

Debnath AK

1

1 reference

Europe PubMed Central

PubMed publication ID

29 November 2017

Debnath G

2

1 reference

Europe PubMed Central

PubMed publication ID

29 November 2017

Shusterman AJ

3

1 reference

Europe PubMed Central

PubMed publication ID

29 November 2017

Hansch C

4

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Europe PubMed Central

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29 November 2017

publication date

1 January 1992

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Europe PubMed Central

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29 November 2017

Environmental and Molecular Mutagenesis

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Europe PubMed Central

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29 November 2017

19

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Europe PubMed Central

PubMed publication ID

29 November 2017

1

1 reference

Europe PubMed Central

PubMed publication ID

29 November 2017

37-52

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Europe PubMed Central

PubMed publication ID

29 November 2017

Relationship between mutagenic potency in Salmonella typhimurium and chemical structure of amino- and nitro-substituted biphenyls

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

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The evaluation of mutagenicities of 19 structurally related aromatic amines and acetamides in Salmonella typhimurium TA98 and TA100

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

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Toward a quantitative comparative toxicology of organic compounds.

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Enzyme-catalyzed reactions of the carcinogen N-hydroxy-2-fluorenylacetamide with nucleic acid

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Computer analysis of toxicological data bases: mutagenicity of aromatic amines in Salmonella tester strains

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Microbial mutagenicity of isomeric two-, three-, and four-ring amino polycyclic aromatic hydrocarbons

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Mutagenicity of aminocarbazoles and nitrocarbazoles

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Structure-activity correlations for antibacterial agents on gram-positive and gram-negative cells.

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The basis of the insensitivity of Salmonella typhimurium strain TA98/1,8-DNP6 to the mutagenic action of nitroarenes

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Esterification of arylhydroxylamines: evidence for a specific gene product in mutagenesis

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Salmonella mutagenicity tests: II. Results from the testing of 270 chemicals

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Mutagenicity of 4,4'-methylenedianiline derivatives in the Salmonella histidine reversion assay

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Structure-activity relationship within a series of m-diaminobenzene derivatives

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Disubstituted amino-, nitroso-, and nitrofluorenes: a physicochemical basis for structure-activity relationships in Salmonella typhimurium

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Mutagenicity of nitro- and amino-substituted phenazines in Salmonella typhimurium

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Salmonella mutagenicity tests: III. Results from the testing of 255 chemicals

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Bacterial mutagenicity and mammalian cell DNA damage by several substituted anilines

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Identifiers

10.1002/EM.2850190107

1 reference

Europe PubMed Central

PubMed publication ID

29 November 2017

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

29 November 2017

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