Reactivity of flavonoids toward superoxide radical: An electrochemical approach
暂无分享,去创建一个
[1] I. Jovanović,et al. The relationship between the first oxidation potential and changes in electronic structures upon the electrochemical oxidation of flavonoids: Approach to O-glycosyl, galloyl and methoxy substituents , 2021 .
[2] G. Miletić,et al. Electrochemical oxidation of flavonoids: PM6 and DFT for elucidating electronic changes and modelling oxidation potential (part II) , 2019 .
[3] G. Miletić,et al. Electrochemical oxidation of flavonoids: PM6 and DFT for elucidating electronic changes and modelling oxidation potential , 2019, Journal of Molecular Liquids.
[4] S. Anwar,et al. Electrochemical reactivity of bulky-phenols with superoxide anion radical , 2019, Electrochimica Acta.
[5] C. Gahn,et al. Effective and Novel Application of Hydrodynamic Voltammetry to the Study of Superoxide Radical Scavenging by Natural Phenolic Antioxidants , 2019, Antioxidants.
[6] G. Miletić,et al. Changes in electronic structures of flavonoids upon electrochemical oxidation and a theoretical model for the estimation of the first oxidation potential , 2018, Electrochimica Acta.
[7] R. Webster,et al. Comparing the Relative Reactivities of Structurally Varied Alcohols toward Electrochemically Generated Superoxide , 2018 .
[8] Safeer Ahmed,et al. Antioxidant Activity Coefficient, Mechanism, and Kinetics of Different Derivatives of Flavones and Flavanones Towards Superoxide Radical , 2018 .
[9] R. Webster,et al. Comparing the Relative Reactivities of Food and Vitamin Molecules Toward Electrochemically Generated Superoxide in Dimethylformamide , 2017 .
[10] I. A. Tahiri,et al. A comprehensive heterogeneous electron transfer rate constant evaluation of dissolved oxygen in DMSO at glassy carbon electrode measured by different electrochemical methods , 2016 .
[11] B. Uno,et al. Concerted two-proton–coupled electron transfer from catechols to superoxide via hydrogen bonds , 2016 .
[12] B. Uno,et al. Importance of Proton-Coupled Electron Transfer from Natural Phenolic Compounds in Superoxide Scavenging. , 2015, Chemical & pharmaceutical bulletin.
[13] Shu Liu,et al. Rapid assay for testing superoxide anion radical scavenging activities to natural pigments by ultra-high performance liquid chromatography-diode-array detection method , 2015 .
[14] M. Tamura,et al. A mitochondrial superoxide theory for oxidative stress diseases and aging , 2014, Journal of clinical biochemistry and nutrition.
[15] Zhihong Cheng,et al. High-throughput superoxide anion radical scavenging capacity assay. , 2014, Journal of agricultural and food chemistry.
[16] Libuse Trnkova,et al. eL-Chem Viewer: A Freeware Package for the Analysis of Electroanalytical Data and Their Post-Acquisition Processing , 2014, Sensors.
[17] I. Novak,et al. Abrasive stripping voltammetry of myricetin and dihydromyricetin , 2013 .
[18] B. Ji,et al. Analysis of the antioxidant capacities of flavonoids under different spectrophotometric assays using cyclic voltammetry and density functional theory. , 2011, Journal of agricultural and food chemistry.
[19] R. Salazar,et al. Study on the oxidation of C4-phenolic-1,4-dihydropyridines and its reactivity towards superoxide radical anion in dimethylsulfoxide , 2010 .
[20] P. Hapiot,et al. How do phenolic compounds react toward superoxide ion? A simple electrochemical method for evaluating antioxidant capacity. , 2010, Analytical chemistry.
[21] B. Uno,et al. Quinone–Hydroquinone π-Conjugated Redox Reaction Involving Proton-coupled Electron Transfer Plays an Important Role in Scavenging Superoxide by Polyphenolic Antioxidants , 2010 .
[22] M. Šeruga,et al. Square-wave and cyclic voltammetry of epicatechin gallate on glassy carbon electrode , 2009 .
[23] M. Šeruga,et al. Electrochemical Characterization of Epigallocatechin Gallate Using Square-Wave Voltammetry , 2009 .
[24] D. Hauchard,et al. Validation of a new method using the reactivity of electrogenerated superoxide radical in the antioxidant capacity determination of flavonoids. , 2008, Talanta.
[25] N. Trinajstic,et al. Bond dissociation enthalpies calculated by the PM3 method confirm activity cliffs in radical scavenging of flavonoids , 2008, Molecular diversity.
[26] I. Afanas’ev. Signaling Functions of Free Radicals Superoxide & Nitric Oxide under Physiological & Pathological Conditions , 2007, Molecular biotechnology.
[27] S. Paik,et al. Cyclooxygenase-2-dependent neuronal death proceeds via superoxide anion generation. , 2006, Free radical biology & medicine.
[28] L. Yu,et al. ESR determination of the reactions between selected phenolic acids and free radicals or transition metals , 2006 .
[29] G. K. Budnikov,et al. Reactions of superoxide anion radical with antioxidants and their use in voltammetry , 2005 .
[30] Ludmil Benov. How superoxide radical damages the cell , 2005, Protoplasma.
[31] N. Sugihara,et al. The contribution of the pyrogallol moiety to the superoxide radical scavenging activity of flavonoids. , 2002, Biological & pharmaceutical bulletin.
[32] Special issue: Lars Ernster commemorative issue. , 2000, Free Radical Biology & Medicine.
[33] F. Muller. The nature and mechanism of superoxide production by the electron transport chain: Its relevance to aging , 2000, Journal of the American Aging Association.
[34] K. Cimanga,et al. Structure-activity relationship and classification of flavonoids as inhibitors of xanthine oxidase and superoxide scavengers. , 1998, Journal of natural products.
[35] S. Roy,et al. Superoxide generation by lipoxygenase in the presence of NADH and NADPH. , 1994, Biochimica et biophysica acta.
[36] M. Alcaraz,et al. Superoxide Scavenging Properties of Flavonoids in a Non-Enzymic System , 1990, Zeitschrift fur Naturforschung. C, Journal of biosciences.
[37] M. Tilset,et al. Anionic nucleophile–cation radical combination reactions. The super‐electrophilic properties of cation radicals in solution , 1989 .
[38] J. Zweier,et al. Characterization of free radical generation by xanthine oxidase. Evidence for hydroxyl radical generation. , 1989, The Journal of biological chemistry.
[39] J. Gladysz,et al. New mechanistic probes of hydride abstraction from rhenium-alkyl complexes (.eta.5-C5H5)Re(NO)(PPh3)(R) by Ph3C+ PF6-. Evidence for initial electron transfer , 1987 .
[40] G. Bontempelli,et al. Digital simulation of electrochemical processes involving very fast chemical reactions : Part 2. A new criterion for determining rate constants of consecutive second-order irreversible chemical reactions , 1985 .
[41] D. T. Sawyer,et al. Effects of media and electrode materials on the electrochemical reduction of dioxygen , 1982 .
[42] V. Parker,et al. On the origin of voltammetric pre-peaks and cathodic potential shifts during anodic substitution reactions , 1973 .
[43] Julian L. Roberts,et al. Electrochemistry of oxygen and superoxide ion in dimethylsulfoxide at platinum, gold and mercury electrodes , 1966 .
[44] Ralfaele Lattes,et al. Annals New York Academy of Sciences: Discussion , 1966 .
[45] D. Maricle,et al. Reducion of Oxygen to Superoxide Anion in Aprotic Solvents. , 1965 .