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Structure-radical scavenging activity relationships of flavonoids 2003 2026 2010 2018 452
  1. Structure-radical scavenging activity relationships of flavonoids (2003)
    Dragan Amić, Dušanka Davidović-Amić et al. Croatica Chemica Acta

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Works of Dragan Amić being referenced

Structure-radical scavenging activity relationships of flavonoids
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1997
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2000
4-Carboxyflavylium Salts: Stable Red Dyes?
1994
PM6 and DFT study of free radical scavenging activity of morin
2012
Antiradical activity of delphinidin, pelargonidin and malvin towards hydroxyl and nitric oxide radicals: The energy requirements calculations as a prediction of the possible antiradical mechanisms
2016
Reliability of bond dissociation enthalpy calculated by the PM6 method and experimental TEAC values in antiradical QSAR of flavonoids
2009
Selected Attributes of Polyphenols in Targeting Oxidative Stress in Cancer
2015
Free radical scavenging potency of quercetin catecholic colonic metabolites: Thermodynamics of 2H+/2e− processes
2016
SAR and QSAR of the Antioxidant Activity of Flavonoids
2007
Bond dissociation free energy as a general parameter for flavonoid radical scavenging activity
2013
Synthesis and theoretical investigation of some new 4-substituted flavylium salts
2017
The Laplacian matrix in chemistry
1994
The 2H+/2e− free radical scavenging mechanisms of uric acid: thermodynamics of NH bond cleavage
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Structure-Activity Correlation of Flavone Derivatives for Inhibition of cAMP Phosphodiesterase
1995
The Use of the Ordered Orthogonalized Multivariate Linear Regression in a Structure−Activity Study of Coumarin and Flavonoid Derivatives as Inhibitors of Aldose Reductase
1997
The Detour Matrix in Chemistry
1997
The distance matrix in chemistry
1992
Structural transformations of apigeninidin-type flavylium salts
1990
Application of topological indices to chromatographic data
1993
QSAR of Flavylium Salts as Inhibitors of Xanthine Oxidase
1998
Reactivity of some flavylium cations and corresponding anhydrobases
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Calculation of Retention Times of Anthocyanins with Orthogonalized Topological Indices
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Activation Hardness as an Index for Predicting the Orientation of Nucleophilic Aromatic Substitution: Application to Flavylium Salts
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