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dc.creatorBraga, R.S.-
dc.creatorBarone, Paulo Monteiro Vieira Braga-
dc.creatorGalvão, D.S.-
dc.date.accessioned2019-02-22T13:27:50Z-
dc.date.available2019-02-21-
dc.date.available2019-02-22T13:27:50Z-
dc.date.issued2000-
dc.citation.volume30pt_BR
dc.citation.issue3pt_BR
dc.citation.spage560pt_BR
dc.citation.epage568pt_BR
dc.identifier.doihttp://dx.doi.org/10.1590/S0103-97332000000300013pt_BR
dc.identifier.urihttps://repositorio.ufjf.br/jspui/handle/ufjf/9170-
dc.description.abstractPolycyclic aromatic hydrocarbons (PAHs) are a class of planar molecules, abundant in urban environment, which can induce chemical carcinogenesis. Their carcinogenic power varies in a large range, from very strong carcinogens to inactive ones. In a previous study, we proposed a methodology to identify the PAHs carcinogenic activity exploring electronic and topological indices. In the present work, we show that it is possible to simplify that methodology and expand its applicability to include methylated PAHs compounds. Using very simple rules, we can predict their carcinogenic activity with high accuracy (» 89%).pt_BR
dc.description.resumo-pt_BR
dc.languageengpt_BR
dc.publisher-pt_BR
dc.publisher.countryBrasilpt_BR
dc.publisher.initials-pt_BR
dc.relation.ispartofBrazilian Journal of Physicspt_BR
dc.rightsAcesso Abertopt_BR
dc.subject-pt_BR
dc.subject.cnpq-pt_BR
dc.titleIdentifying carcinogenic activity of methylated and non-methylated polycyclic aromatic hydrocarbons (PAHs) through electronic and topological indicespt_BR
dc.typeArtigo de Periódicopt_BR
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