Literature DB >> 1730146

Relative stabilities of nitrenium ions derived from heterocyclic amine food carcinogens: relationship to mutagenicity.

G P Ford1, G R Griffin.   

Abstract

The bacterial mutagenicities of a wide variety of complex heteroaromatic amine mutagens and carcinogens present in cooked foods are approximately related to the stabilities of the corresponding nitrenium ions through equations of the kind: log(m) = a delta delta H + b. The stabilities of the nitrenium ions (delta delta H) were computed using the semiempirical AM1 molecular orbital procedure. Parallel calculations of the energies, charge distributions and geometries of simple model compounds provides a qualitative framework within which the stabilities of the nitrenium ions derived from the food carcinogens can be easily understood.

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Year:  1992        PMID: 1730146     DOI: 10.1016/0009-2797(92)90024-f

Source DB:  PubMed          Journal:  Chem Biol Interact        ISSN: 0009-2797            Impact factor:   5.192


  5 in total

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Review 3.  Genetic toxicology in the 21st century: reflections and future directions.

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Journal:  Environ Mol Mutagen       Date:  2011-04-28       Impact factor: 3.216

4.  A local QSAR model based on the stability of nitrenium ions to support the ICH M7 expert review on the mutagenicity of primary aromatic amines.

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5.  Hemoglobin binding of arylamines and nitroarenes: molecular dosimetry and quantitative structure-activity relationships.

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Journal:  Environ Health Perspect       Date:  1994-10       Impact factor: 9.031

  5 in total

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