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dc.creatorNunes, Cleiton A.-
dc.creatorFreitas, Matheus P.-
dc.date.accessioned2014-12-10T19:56:15Z-
dc.date.available2014-12-10T19:56:15Z-
dc.date.issued2013-05-25-
dc.identifier.citationNUNES, C. A.; FREITAS, M.P. aug-MIA-QSPR study of guanidine derivative sweeteners. European Food Research & Technology, Berlin, v. 237, n. 4, p. 565-570, Oct. 2013.pt_BR
dc.identifier.urihttp://link.springer.com/article/10.1007%2Fs00217-013-2032-8pt_BR
dc.identifier.urihttp://repositorio.ufla.br/jspui/handle/1/4828-
dc.description.abstractThe sweetness values relative to sucrose (RS) of a series of sweet-tasting guanidine derivatives have been modeled using augmented multivariate image analysis applied to quantitative structure–property relationship (aug-MIA-QSPR). This QSPR approach is based on 2D molecular shape, as well as atomic sizes and colors to encode chemical, physical and biological properties. A 2 predictive model with r 2 = 0.955, q 2 = 0.731 and r test 1⁄4 0:571 was used to estimate log(RS) of two novel sweet- tasting guanidine derivatives, which were built from the combination of substructures of the sweetest derivatives along the series. Given the synergistic effect of different substituents to provide new molecules, promising guani- dine sweeteners are proposed for further synthesis.pt_BR
dc.languageenpt_BR
dc.publisherFederation of European Chemical Societiespt_BR
dc.rightsacesso abertopt_BR
dc.sourceEuropean Food Research & Technologypt_BR
dc.subjectGuanidine derivativespt_BR
dc.subjectSweetenerspt_BR
dc.subjectaug-MIA-QSPRpt_BR
dc.subjectChemometricspt_BR
dc.titleaug-MIA-QSPR study of guanidine derivative sweetenerspt_BR
dc.typeArtigopt_BR
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