Brazilian Journal of Pharmaceutical Sciences · 2011 · 24 citations · 22 references
PharmacyBiochemistryMedicinal ChemistryDrug DesignDrug DiscoveryStructure-activity RelationshipsAntioxidant DefenseChemical Space ExplorationMolecular DescriptorsQuantitative Structure-activity RelationshipsStructure-activity Relationship AnalysisAntioxidant Activity AssaysChemical Structure-activity RelationshipsComputational Structure-activity ModelingDescriptor-based ModelingExperimental Data CollectionMolecular Weight DescriptorsSelf-organizing MapsStructure - Activity Relationship Mapping
Tissue damage due to oxidative stress is directly linked to development of many, if not all, human morbidity factors and chronic diseases. In this context, the search for dietary natural occurring molecules with antioxidant activity, such as flavonoids, has become essential. In this study, we investigated a set of 41 flavonoids (23 flavones and 18 flavonols) analyzing their structures and biological antioxidant activity. The experimental data were submitted to a QSAR (quantitative structure-activity relationships) study. NMR 13C data were used to perform a Kohonen self-organizing map study, analyzing the weight that each carbon has in the activity. Additionally, we performed MLR (multilinear regression) using GA (genetic algorithms) and molecular descriptors to analyze the role that specific carbons and substitutions play in the activity.
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Free radicals in biology and medicine
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