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Volumn 15, Issue 4, 2016, Pages 720-738

Flavonoids as Potent Scavengers of Hydroxyl Radicals

Author keywords

Fenton reaction; flavonoids; hydroxyl radical; scavenging; structure activity relationship

Indexed keywords

ANTIOXIDANTS; HYDROXYLATION; MOLECULES; NEURODEGENERATIVE DISEASES; NUCLEIC ACIDS; OXIDATION; OXIDATIVE STRESS; OXYGEN; PATHOLOGY; SCAVENGING;

EID: 84979723220     PISSN: None     EISSN: 15414337     Source Type: Journal    
DOI: 10.1111/1541-4337.12204     Document Type: Review
Times cited : (322)

References (125)
  • 2
    • 84865331553 scopus 로고    scopus 로고
    • HPLC-DAD-MS/MS profiling of antioxidant flavonoid glycosides in sea buckthorn (Hippophae rhamnoides L.) seeds
    • Arimboor R, Arumughan C. 2012. HPLC-DAD-MS/MS profiling of antioxidant flavonoid glycosides in sea buckthorn (Hippophae rhamnoides L.) seeds. Intl J Food Sci Nutr 63:730–8. doi: 10.3109/09637486.2011.652075.
    • (2012) Intl J Food Sci Nutr , vol.63 , pp. 730-738
    • Arimboor, R.1    Arumughan, C.2
  • 3
    • 0000348721 scopus 로고
    • The role of iron in ascorbate-dependent deoxyribose degradation. Evidence consistent with a site-specific hydroxyl radical generation caused by deoxyribose molecule
    • Arouma OI, Grootveld M, Halliwell B. 1987. The role of iron in ascorbate-dependent deoxyribose degradation. Evidence consistent with a site-specific hydroxyl radical generation caused by deoxyribose molecule. J Inorg Biochem 29:289–99. doi:10.1016/0162-0134(87)80035-1.
    • (1987) J Inorg Biochem , vol.29 , pp. 289-299
    • Arouma, O.I.1    Grootveld, M.2    Halliwell, B.3
  • 4
    • 0141922800 scopus 로고    scopus 로고
    • A new model of tropospheric hydroxyl radical concentrations
    • Bahm K, Khalil MAK. 2004. A new model of tropospheric hydroxyl radical concentrations. Chemosphere 54:143–66. doi:10.1016/j.chemosphere.2003.08.006.
    • (2004) Chemosphere , vol.54 , pp. 143-166
    • Bahm, K.1    Khalil, M.A.K.2
  • 5
    • 79954705723 scopus 로고    scopus 로고
    • Fenton reaction—controversy concerning the chemistry
    • Barbusiński K. 2009. Fenton reaction—controversy concerning the chemistry. Ecol Chem Eng S 16:347–56.
    • (2009) Ecol Chem Eng S , vol.16 , pp. 347-356
    • Barbusiński, K.1
  • 6
    • 33746561383 scopus 로고    scopus 로고
    • Novel hydroxyl radical scavenging antioxidant assay for water-soluble antioxidants using a modified CUPRAC method
    • Bektaşoğlu B, Çelik SE, Özyürek M, Güçlü K, Apak R. 2006. Novel hydroxyl radical scavenging antioxidant assay for water-soluble antioxidants using a modified CUPRAC method. Biochem Biophys Res Commun 345:1194–200. doi:10.1016/j.bbrc.2006.05.038.
    • (2006) Biochem Biophys Res Commun , vol.345 , pp. 1194-1200
    • Bektaşoğlu, B.1    Çelik, S.E.2    Özyürek, M.3    Güçlü, K.4    Apak, R.5
  • 7
    • 0030841350 scopus 로고    scopus 로고
    • Protein oxidation in aging, disease and oxidative stress
    • Berlett BS, Stadtmann ER. 1997. Protein oxidation in aging, disease and oxidative stress. J Biol Chem 272:20313–6. doi:10.1074/jbc.272.33.20313.
    • (1997) J Biol Chem , vol.272 , pp. 20313-20316
    • Berlett, B.S.1    Stadtmann, E.R.2
  • 8
    • 35649005931 scopus 로고    scopus 로고
    • Chemical composition and in vitro antioxidant studies on Syzygium cumini fruit
    • Benherlal PS, Arumughan C. 2007. Chemical composition and in vitro antioxidant studies on Syzygium cumini fruit. J Sci Food Agric 87:2560–9. doi:10.1002/jsfa.2957.
    • (2007) J Sci Food Agric , vol.87 , pp. 2560-2569
    • Benherlal, P.S.1    Arumughan, C.2
  • 9
    • 56349118018 scopus 로고    scopus 로고
    • Studies on modulation of DNA integrity in Fenton's system by phytochemicals
    • Benherlal PS, Arumughan C. 2008. Studies on modulation of DNA integrity in Fenton's system by phytochemicals. Mutat Res, Fundam Mol Mech Mutagen 648:1–8. doi:10.1016/j.mrfmmm.2008.09.001.
    • (2008) Mutat Res, Fundam Mol Mech Mutagen , vol.648 , pp. 1-8
    • Benherlal, P.S.1    Arumughan, C.2
  • 10
    • 0033951258 scopus 로고    scopus 로고
    • What is oxidative stress?
    • Betteridge DJ. 2000. What is oxidative stress? Metabolism 49:3–8. doi:10.1016/S0026-0495(00)80077-3.
    • (2000) Metabolism , vol.49 , pp. 3-8
    • Betteridge, D.J.1
  • 11
    • 0030901059 scopus 로고    scopus 로고
    • Quantitation of hydroxyl radicals produced by radiation and copper-linked oxidation of ascorbate by 2-deoxy-D-ribose method
    • Biaglow JE, Manevich Y, Uckun F, Held KD. 1997. Quantitation of hydroxyl radicals produced by radiation and copper-linked oxidation of ascorbate by 2-deoxy-D-ribose method. Free Rad Biol Med 22:1129–38. doi:10.1016/S0891-5849(96)00527-8.
    • (1997) Free Rad Biol Med , vol.22 , pp. 1129-1138
    • Biaglow, J.E.1    Manevich, Y.2    Uckun, F.3    Held, K.D.4
  • 12
    • 0038464586 scopus 로고    scopus 로고
    • Main flavonoids in the root of Scutellaria baicalensis cultivated in Europe and their comparative antiradical properties
    • Bochořáková H, Paulová H, Slanina J, Musil P, Táborská E. 2003. Main flavonoids in the root of Scutellaria baicalensis cultivated in Europe and their comparative antiradical properties. Phytother Res 17:640–4. doi:10.1002/ptr.1216.
    • (2003) Phytother Res , vol.17 , pp. 640-644
    • Bochořáková, H.1    Paulová, H.2    Slanina, J.3    Musil, P.4    Táborská, E.5
  • 13
    • 0033043969 scopus 로고    scopus 로고
    • Regulation of HepG2 cell apolipoprotein B metabolism by citrus flavonones hesperetin and naringenin
    • Borradaile NM, Carroll KK, Kurowska EM. 1999. Regulation of HepG2 cell apolipoprotein B metabolism by citrus flavonones hesperetin and naringenin. Lipids 34:591–8. doi:10.1007/s11745-999-0403-7.
    • (1999) Lipids , vol.34 , pp. 591-598
    • Borradaile, N.M.1    Carroll, K.K.2    Kurowska, E.M.3
  • 14
    • 0033405864 scopus 로고    scopus 로고
    • Antioxidant capacity of flavanols and gallate esters: pulse radiolysis studies
    • Bors W, Michel C. 1999. Antioxidant capacity of flavanols and gallate esters: pulse radiolysis studies. Free Rad Biol Med 27:1413–26. doi:10.1016/S0891-5849(99)00187-2.
    • (1999) Free Rad Biol Med , vol.27 , pp. 1413-1426
    • Bors, W.1    Michel, C.2
  • 15
    • 33947348085 scopus 로고
    • Ferryl ion, a compound of tetravalent iron
    • Bray WC, Gorin MH. 1932. Ferryl ion, a compound of tetravalent iron. J Am Chem Soc 54:2124–5. doi:10.1021/ja01344a505.
    • (1932) J Am Chem Soc , vol.54 , pp. 2124-2125
    • Bray, W.C.1    Gorin, M.H.2
  • 16
    • 84939623751 scopus 로고    scopus 로고
    • Development and validation of an in vitro experimental gastrointestinal dialysis model with colon phase to study the availability and colonic metabolisation of polyphenolic compounds
    • Breynaert A, Bosscher D, Kahnt A, Claeys M, Cos P, Pieters L, Hermans Nina. 2015. Development and validation of an in vitro experimental gastrointestinal dialysis model with colon phase to study the availability and colonic metabolisation of polyphenolic compounds. Planta Med 81(12/13):1075–83
    • (2015) Planta Med , vol.81 , Issue.12-13 , pp. 1075-1083
    • Breynaert, A.1    Bosscher, D.2    Kahnt, A.3    Claeys, M.4    Cos, P.5    Pieters, L.6    Nina, H.7
  • 17
    • 0027251053 scopus 로고
    • The pecking order of free radicals and antioxidants lipid peroxidation alpha-tocopherol and ascorbate
    • Buettner GR. 1993. The pecking order of free radicals and antioxidants lipid peroxidation alpha-tocopherol and ascorbate. Arch Biochem Biophys 300:535–43. doi:10.1006/abbi.1993.1074.
    • (1993) Arch Biochem Biophys , vol.300 , pp. 535-543
    • Buettner, G.R.1
  • 19
    • 0034152767 scopus 로고    scopus 로고
    • Oxidative damage to bacteria and protein damage by reactive oxygen species
    • Cabiscol E, Tamarit J, Ros J. 2000. Oxidative damage to bacteria and protein damage by reactive oxygen species. Intl Microbiol 3:3–8.
    • (2000) Intl Microbiol , vol.3 , pp. 3-8
    • Cabiscol, E.1    Tamarit, J.2    Ros, J.3
  • 20
    • 0031020195 scopus 로고    scopus 로고
    • Antioxidant and prooxidant behavior of flavonoids: structure-activity relationship
    • Cao G, Sofic E, Prior RL. 1997. Antioxidant and prooxidant behavior of flavonoids: structure-activity relationship. Free Rad Biol Med 22:749–60. doi:10.1016/S0891-5849(96)00351-6.
    • (1997) Free Rad Biol Med , vol.22 , pp. 749-760
    • Cao, G.1    Sofic, E.2    Prior, R.L.3
  • 21
    • 84867029857 scopus 로고    scopus 로고
    • A review on antioxidants, prooxidants and related controversy: natural and synthetic compounds, screening and analysis methodologies and future perspectives
    • Carocho M, Ferreira ICFR. 2013. A review on antioxidants, prooxidants and related controversy: natural and synthetic compounds, screening and analysis methodologies and future perspectives. Food Chemical Toxicol 51:15–25. doi:10.1016/j.fct.2012.09.021.
    • (2013) Food Chemical Toxicol , vol.51 , pp. 15-25
    • Carocho, M.1    Ferreira, I.C.F.R.2
  • 22
    • 77956180789 scopus 로고    scopus 로고
    • A synopsis of the process of lipid peroxidation since the discovery of essential fatty acids
    • Catalá A. 2010. A synopsis of the process of lipid peroxidation since the discovery of essential fatty acids. Biochem Biophys Res Commun 399:318–23. doi:10.1016/j.bbrc.2010.07.087.
    • (2010) Biochem Biophys Res Commun , vol.399 , pp. 318-323
    • Catalá, A.1
  • 23
    • 77951071565 scopus 로고    scopus 로고
    • Antioxidant properties, radical scavenging activity and biomolecule protection capacity of flavonoid naringenin and its glycoside naringin: a comparative study
    • Cavia-Saiz M, Busto MD, Pilar-Izquierdo MC, Ortega N, Perez-Mateos M, Muñiz P. 2010. Antioxidant properties, radical scavenging activity and biomolecule protection capacity of flavonoid naringenin and its glycoside naringin: a comparative study. J Sci Food Agric 90:1238–44. doi:10.1002/jsfa.3959.
    • (2010) J Sci Food Agric , vol.90 , pp. 1238-1244
    • Cavia-Saiz, M.1    Busto, M.D.2    Pilar-Izquierdo, M.C.3    Ortega, N.4    Perez-Mateos, M.5    Muñiz, P.6
  • 25
  • 26
    • 0036307556 scopus 로고    scopus 로고
    • Structure-activity relationship of natural flavonoids in hydroxyl radical-scavenging effects
    • Chen J-W, Zhu Z-Q, Hu T-X, Zhu D-Y. 2002. Structure-activity relationship of natural flavonoids in hydroxyl radical-scavenging effects. Acta Pharmacol Sin 23:667–72.
    • (2002) Acta Pharmacol Sin , vol.23 , pp. 667-672
    • Chen, J.-W.1    Zhu, Z.-Q.2    Hu, T.-X.3    Zhu, D.-Y.4
  • 27
    • 0023916221 scopus 로고
    • Hydroxyl-radical-induced iron-catalyzed degradation of 2-deoxyribose
    • Cheeseman KH, Beavis A, Esterbauer H. 1988. Hydroxyl-radical-induced iron-catalyzed degradation of 2-deoxyribose. Biochem J 252:649–53.
    • (1988) Biochem J , vol.252 , pp. 649-653
    • Cheeseman, K.H.1    Beavis, A.2    Esterbauer, H.3
  • 28
    • 78649631235 scopus 로고    scopus 로고
    • Bioavailability of dietary flavonoids and phenolic compounds
    • Crozier A, Del Rio D, Clifford MN. 2010. Bioavailability of dietary flavonoids and phenolic compounds. Mol Aspects Med 31:446–67. doi: 10.1016/j.mam.2010.09.007.
    • (2010) Mol Aspects Med , vol.31 , pp. 446-467
    • Crozier, A.1    Del Rio, D.2    Clifford, M.N.3
  • 29
    • 0026093901 scopus 로고
    • Synthesis and evaluation of hydroxylated flavones and related compounds as potential inhibitors of the protein-tyrosine kinase p56Ick
    • Cushman M, Nagarathnam D, Geahlen RL. 1991. Synthesis and evaluation of hydroxylated flavones and related compounds as potential inhibitors of the protein-tyrosine kinase p56Ick. J Natl Prod 54:1345–52. doi: 10.1021/np50077a018.
    • (1991) J Natl Prod , vol.54 , pp. 1345-1352
    • Cushman, M.1    Nagarathnam, D.2    Geahlen, R.L.3
  • 31
    • 34447309103 scopus 로고    scopus 로고
    • Polyphenolic grape extract inhibits platelet activation through PECAM-1: an explanation for the French paradox
    • De Lange DW, Verhoef S, Gorter G, Kraaijenhagen RJ, van de Wiel A, Akkerman J-WN. 2007. Polyphenolic grape extract inhibits platelet activation through PECAM-1: an explanation for the French paradox. Alcohol Clin Exp Res 31:1308–14. doi:10.1111/j.1530-0277.2007.00439.x.
    • (2007) Alcohol Clin Exp Res , vol.31 , pp. 1308-1314
    • De Lange, D.W.1    Verhoef, S.2    Gorter, G.3    Kraaijenhagen, R.J.4    van de Wiel, A.5    Akkerman, J.-W.N.6
  • 32
    • 77951891625 scopus 로고    scopus 로고
    • Flavanols and anthocyanins in cardiovascular health: a review of current evidence
    • De Pascual-Teresa S, Moreno D A, García-Viguera C. 2010. Flavanols and anthocyanins in cardiovascular health: a review of current evidence. Intl J Mol Sci 11:1679–703. doi: 10.3390/ijms11041679.
    • (2010) Intl J Mol Sci , vol.11 , pp. 1679-1703
    • De Pascual-Teresa, S.1    Moreno, D.A.2    García-Viguera, C.3
  • 33
    • 0035813490 scopus 로고    scopus 로고
    • High-performance liquid chromatographic assay of hydroxyl free radical using salicylic acid hydroxylation during in vitro experiments involving thiols
    • Diez L, Livertoux M-H, Stark A-A, Wellman-Rousseau M, Leroy P. 2001. High-performance liquid chromatographic assay of hydroxyl free radical using salicylic acid hydroxylation during in vitro experiments involving thiols. J Chromatogr B 763:185–93. doi:10.1016/S0378-4347(01)00396-6.
    • (2001) J Chromatogr B , vol.763 , pp. 185-193
    • Diez, L.1    Livertoux, M.-H.2    Stark, A.-A.3    Wellman-Rousseau, M.4    Leroy, P.5
  • 34
    • 70349796201 scopus 로고    scopus 로고
    • Antioxidant evaluation of O-methylated metabolites of catechin, epicatechin and quercetin
    • Dueñas M, González-Manzano S, González-Paramás A, Santos-Buelga C. 2010. Antioxidant evaluation of O-methylated metabolites of catechin, epicatechin and quercetin. J Pharm Biomed Anal 51:443–9. doi:10.1016/j.jpba.2009.04.007.
    • (2010) J Pharm Biomed Anal , vol.51 , pp. 443-449
    • Dueñas, M.1    González-Manzano, S.2    González-Paramás, A.3    Santos-Buelga, C.4
  • 36
    • 4444339833 scopus 로고    scopus 로고
    • Oxidative DNA damage and disease: induction, repair and significance
    • Evans MD, Dizdaroglu M, Cooke MS. 2004. Oxidative DNA damage and disease: induction, repair and significance. Mutat Res 567:1–61. doi:10.1016/j.mrrev.2003.11.001
    • (2004) Mutat Res , vol.567 , pp. 1-61
    • Evans, M.D.1    Dizdaroglu, M.2    Cooke, M.S.3
  • 37
    • 18544384019 scopus 로고
    • Oxidation of tartaric acid in presence of iron
    • Fenton HJH. 1894. Oxidation of tartaric acid in presence of iron. J Chem Soc Trans 65:899–910. doi:10.1039/CT89465FP001
    • (1894) J Chem Soc Trans , vol.65 , pp. 899-910
    • Fenton, H.J.H.1
  • 39
    • 84860418682 scopus 로고    scopus 로고
    • Free-radical scavenging activities of silybin and its analogues: a pulse radiolysis study
    • Fu H, Lin M, Katsumura Y, Muroya Y. 2011. Free-radical scavenging activities of silybin and its analogues: a pulse radiolysis study. Intl J Chem Kinet 43:590–7. doi:10.1002/kin.20589.
    • (2011) Intl J Chem Kinet , vol.43 , pp. 590-597
    • Fu, H.1    Lin, M.2    Katsumura, Y.3    Muroya, Y.4
  • 40
    • 3042574709 scopus 로고    scopus 로고
    • Potential toxicity of flavonoids and other dietary phenolics: significance for their chemopreventive and anticancer properties
    • Galati G, O'Brien PJ. 2004. Potential toxicity of flavonoids and other dietary phenolics: significance for their chemopreventive and anticancer properties. Free Rad Biol Med 37:287–303. doi:10.1016/j.freeradbiomed.2004.04.034.
    • (2004) Free Rad Biol Med , vol.37 , pp. 287-303
    • Galati, G.1    O'Brien, P.J.2
  • 41
    • 0034375614 scopus 로고    scopus 로고
    • Free-radical scavenging and mechanism study of flavonoids extracted from the radix of Scutellaria baicalensis Georgi
    • Gao Z, Yang X, Huang K, Xu H. 2000. Free-radical scavenging and mechanism study of flavonoids extracted from the radix of Scutellaria baicalensis Georgi. Appl Magnet Reson 19:35–44. doi:10.1007/BF03162259.
    • (2000) Appl Magnet Reson , vol.19 , pp. 35-44
    • Gao, Z.1    Yang, X.2    Huang, K.3    Xu, H.4
  • 42
  • 43
    • 29244444522 scopus 로고    scopus 로고
    • Fluorescence probes used for detection of reactive oxygen species
    • Gomes A, Fernandes E, Lima JLFC. 2005. Fluorescence probes used for detection of reactive oxygen species. J Biochem Biophys Meth 65:45–80. doi:10.1016/j.jbbm.2005.10.003.
    • (2005) J Biochem Biophys Meth , vol.65 , pp. 45-80
    • Gomes, A.1    Fernandes, E.2    Lima, J.L.F.C.3
  • 44
    • 0027201746 scopus 로고
    • Accumulation of aldehydic lipid peroxidation products during postanoxic reoxygenation of isolated rat hepatocytes
    • Grune T, Siems WG, Schneider W. 1993. Accumulation of aldehydic lipid peroxidation products during postanoxic reoxygenation of isolated rat hepatocytes. Free Rad Biol Med 15:125–31. doi:10.1016/0891-5849(93)90051-U.
    • (1993) Free Rad Biol Med , vol.15 , pp. 125-131
    • Grune, T.1    Siems, W.G.2    Schneider, W.3
  • 45
    • 0023338482 scopus 로고
    • Ferrous-salt-promoted damage to deoxyribose and benzoate
    • Gutteridge JMC. 1987. Ferrous-salt-promoted damage to deoxyribose and benzoate. Biochem J 243:709–14.
    • (1987) Biochem J , vol.243 , pp. 709-714
    • Gutteridge, J.M.C.1
  • 46
    • 0029030073 scopus 로고
    • Antioxidant characterization: methodology and mechanism
    • Halliwell B. 1995. Antioxidant characterization: methodology and mechanism. Biochem Pharmacol 49:1341–8. doi:10.1016/0006-2952(95)00088-H.
    • (1995) Biochem Pharmacol , vol.49 , pp. 1341-1348
    • Halliwell, B.1
  • 48
    • 0023219256 scopus 로고
    • The deoxyribose method: a simple “test-tube“assay for determination of rate constants for reactions of hydroxyl radicals
    • Halliwell B, Gutteridge JMC, Arouma OI. 1987 The deoxyribose method: a simple “test-tube“assay for determination of rate constants for reactions of hydroxyl radicals. Anal Biochem 165:215–9. doi:10.1016/0003-2697(87)90222-3.
    • (1987) Anal Biochem , vol.165 , pp. 215-219
    • Halliwell, B.1    Gutteridge, J.M.C.2    Arouma, O.I.3
  • 49
    • 0000595998 scopus 로고
    • An electron spin resonance study of the spin adducts of OH and HO2 radicals with nitrones in the ultraviolet photolysis of aqueous hydrogen peroxide solutions
    • Harbour JR, Chow V, Bolton JR. 1974. An electron spin resonance study of the spin adducts of OH and HO2 radicals with nitrones in the ultraviolet photolysis of aqueous hydrogen peroxide solutions. Can J Chem 52:3549–53. doi:10.1139/v74-527.
    • (1974) Can J Chem , vol.52 , pp. 3549-3553
    • Harbour, J.R.1    Chow, V.2    Bolton, J.R.3
  • 50
    • 77049308856 scopus 로고
    • Aging: a theory based on free radical and radiation chemistry
    • Harman D. 1956. Aging: a theory based on free radical and radiation chemistry. J Gerontol 11:298–300. doi:10.1093/geronj/11.3.298.
    • (1956) J Gerontol , vol.11 , pp. 298-300
    • Harman, D.1
  • 51
    • 33646759971 scopus 로고    scopus 로고
    • Luteolin and chrysin differentially inhibit cyclooxygenase-2 expression and scavenge reactive oxygen species but similarly inhibit prostaglandin-E2 formation in RAW 264.7 cells
    • Harris GK, Qian Y, Leonard SS, Sbarra DC, Shi X. 2006. Luteolin and chrysin differentially inhibit cyclooxygenase-2 expression and scavenge reactive oxygen species but similarly inhibit prostaglandin-E2 formation in RAW 264.7 cells. J Nutr 136:1517–21.
    • (2006) J Nutr , vol.136 , pp. 1517-1521
    • Harris, G.K.1    Qian, Y.2    Leonard, S.S.3    Sbarra, D.C.4    Shi, X.5
  • 52
    • 84887057164 scopus 로고    scopus 로고
    • Protein tyrosine kinase (PTK) as a novel target for some natural anti-cancer molecules extracted from plants
    • Hashemi M, Behrangi N, Borna H, Entezari M. 2012. Protein tyrosine kinase (PTK) as a novel target for some natural anti-cancer molecules extracted from plants. J Med Plants Res 6:64375–8. doi:10.5897/JMPR11.1005.
    • (2012) J Med Plants Res , vol.6 , pp. 64375-64378
    • Hashemi, M.1    Behrangi, N.2    Borna, H.3    Entezari, M.4
  • 53
    • 0036774226 scopus 로고    scopus 로고
    • Flavonoid antioxidants: chemistry, metabolism and structure-activity relationship
    • Heim KE, Tagliaferro AR, Bobilya DJ. 2002. Flavonoid antioxidants: chemistry, metabolism and structure-activity relationship. J Nutr Biochem 13:572–84. doi:10.1016/S0955-2863(02)00208-5.
    • (2002) J Nutr Biochem , vol.13 , pp. 572-584
    • Heim, K.E.1    Tagliaferro, A.R.2    Bobilya, D.J.3
  • 55
    • 0027291905 scopus 로고
    • Intake of potentially anticarcinogenic flavonoids and their determinants in adults in the Netherlands
    • Hertog MG, Hollman PCH, Katan MB. 1993. Intake of potentially anticarcinogenic flavonoids and their determinants in adults in the Netherlands. Nutr Cancer 20:21–29.
    • (1993) Nutr Cancer , vol.20 , pp. 21-29
    • Hertog, M.G.1    Hollman, P.C.H.2    Katan, M.B.3
  • 56
    • 77649181729 scopus 로고    scopus 로고
    • Flavonoid-flavonoid interaction and its effect on their antioxidant activity
    • Hidalgo M, Sánchez-Moreno C, De Pascual-Teresa S. 2010. Flavonoid-flavonoid interaction and its effect on their antioxidant activity. Food Chem 121:691–6. doi:10.1016/j.foodchem.2009.12.097.
    • (2010) Food Chem , vol.121 , pp. 691-696
    • Hidalgo, M.1    Sánchez-Moreno, C.2    De Pascual-Teresa, S.3
  • 58
    • 84886951999 scopus 로고    scopus 로고
    • The use of methods of radiolysis to explore the mechanisms of free radical modifications in proteins
    • Houée-Levin C, Bobrowski K. 2013. The use of methods of radiolysis to explore the mechanisms of free radical modifications in proteins. J Proteomics 92:51–62. doi:10.1016/j.jprot.2013.02.014.
    • (2013) J Proteomics , vol.92 , pp. 51-62
    • Houée-Levin, C.1    Bobrowski, K.2
  • 59
    • 84861569514 scopus 로고    scopus 로고
    • Evaluation of antioxidant and free radical scavenging capacities of polyphenolics from pods of Caesalpinia pulcherrima
    • Hsu F-L, Huang W-J, Wu T-H, Lee M-H, Chen L-C, Lu H-J, Hou W-C, Lin M-H. 2012. Evaluation of antioxidant and free radical scavenging capacities of polyphenolics from pods of Caesalpinia pulcherrima. Intl J Mol Sci 13:6073–88. doi:10.3390/ijms13056073.
    • (2012) Intl J Mol Sci , vol.13 , pp. 6073-6088
    • Hsu, F.-L.1    Huang, W.-J.2    Wu, T.-H.3    Lee, M.-H.4    Chen, L.-C.5    Lu, H.-J.6    Hou, W.-C.7    Lin, M.-H.8
  • 60
    • 0009538299 scopus 로고
    • Hydroxyl radical scavenging activity of flavonoids
    • Husain SR, Cillard J, Cillard P. 1987. Hydroxyl radical scavenging activity of flavonoids. Phytochemistry 26:2489–91. doi:10.1016/S0031-9422(00)83860-1.
    • (1987) Phytochemistry , vol.26 , pp. 2489-2491
    • Husain, S.R.1    Cillard, J.2    Cillard, P.3
  • 61
    • 50949102839 scopus 로고    scopus 로고
    • Catechin, epicatechin, quercetin, rutin and resveratrol in red grape: content, in vitro antioxidant activity and interactions
    • Iacopini P, Baldi M, Storchi P, Sebastiani L. 2008. Catechin, epicatechin, quercetin, rutin and resveratrol in red grape: content, in vitro antioxidant activity and interactions. J Food Compost Anal 21:589–98. doi:10.1016/j.jfca.2008.03.011.
    • (2008) J Food Compost Anal , vol.21 , pp. 589-598
    • Iacopini, P.1    Baldi, M.2    Storchi, P.3    Sebastiani, L.4
  • 63
    • 84942822566 scopus 로고    scopus 로고
    • Effects of phenolic acid metabolites formed after chlorogenic acid consumption on retinal degeneration in vivo
    • Jang H, Choi Y, Ahn HR, Jung SH, Lee CY. 2015. Effects of phenolic acid metabolites formed after chlorogenic acid consumption on retinal degeneration in vivo. Mol Nutr Food Res 59(10):1918–29.
    • (2015) Mol Nutr Food Res , vol.59 , Issue.10 , pp. 1918-1929
    • Jang, H.1    Choi, Y.2    Ahn, H.R.3    Jung, S.H.4    Lee, C.Y.5
  • 64
    • 84880975570 scopus 로고    scopus 로고
    • Phenolic profiles and antioxidant and anticarcinogenic activities of Greek herbal infusions; balancing delight and chemoprevention?
    • Kaliora AC, Kogiannou DAA, Kefalas P, Papassideri IS, Kalogeropoulos N. 2014. Phenolic profiles and antioxidant and anticarcinogenic activities of Greek herbal infusions; balancing delight and chemoprevention? Food Chem 142:233-41
    • (2014) Food Chem , vol.142 , pp. 233-241
    • Kaliora, A.C.1    Kogiannou, D.A.A.2    Kefalas, P.3    Papassideri, I.S.4    Kalogeropoulos, N.5
  • 65
    • 77953464864 scopus 로고    scopus 로고
    • Attenuation of free radical by an aqueous extract of peels of safed musli tubes (Chlorophytum borivilianum Sant et Fernand)
    • Kaur R, Thukral AK, Arora S. 2010. Attenuation of free radical by an aqueous extract of peels of safed musli tubes (Chlorophytum borivilianum Sant et Fernand). J Chin Clin Med 5:7–11.
    • (2010) J Chin Clin Med , vol.5 , pp. 7-11
    • Kaur, R.1    Thukral, A.K.2    Arora, S.3
  • 66
    • 0037246317 scopus 로고    scopus 로고
    • Anti- and pro-oxidant activity of rutin and quercetin derivatives
    • Kessler M, Ubeaud G, Jung L. 2003. Anti- and pro-oxidant activity of rutin and quercetin derivatives. J Pharm Pharmacol 55:131–42. doi:10.1211/002235702559.
    • (2003) J Pharm Pharmacol , vol.55 , pp. 131-142
    • Kessler, M.1    Ubeaud, G.2    Jung, L.3
  • 67
    • 33847774008 scopus 로고    scopus 로고
    • Improved quantitative structure-activity relationship models to predict antioxidant activity of flavonoids in chemical, enzymatic, and cellular systems
    • Khlebnikov AI, Schepetkin IA, Domina NG, Kirpotina LN, Quinn MT. 2006. Improved quantitative structure-activity relationship models to predict antioxidant activity of flavonoids in chemical, enzymatic, and cellular systems. Bioorg Med Chem 15:1749–70. doi: 10.1016/j.bmc.2006.11.037.
    • (2006) Bioorg Med Chem , vol.15 , pp. 1749-1770
    • Khlebnikov, A.I.1    Schepetkin, I.A.2    Domina, N.G.3    Kirpotina, L.N.4    Quinn, M.T.5
  • 68
    • 79961119820 scopus 로고    scopus 로고
    • Flavonol content in water extract of mulberry (Morus alba L.) leaf and their antioxidant capacities
    • Kim G-N, Jang H-D. 2011. Flavonol content in water extract of mulberry (Morus alba L.) leaf and their antioxidant capacities. J Food Sci 76:869–73. doi:10.1111/j.1750-3841.2011.02262.x.
    • (2011) J Food Sci , vol.76 , pp. 869-873
    • Kim, G.-N.1    Jang, H.-D.2
  • 69
    • 0019776866 scopus 로고
    • Production of formaldehyde during metabolism of dimethyl sulfoxide by hydroxyl radical generating systems
    • Klein SM, Cohen G, Cederbaum AI. 1981. Production of formaldehyde during metabolism of dimethyl sulfoxide by hydroxyl radical generating systems. Biochemistry 20:6006–12. doi:10.1021/bi00524a013.
    • (1981) Biochemistry , vol.20 , pp. 6006-6012
    • Klein, S.M.1    Cohen, G.2    Cederbaum, A.I.3
  • 70
    • 84888846558 scopus 로고    scopus 로고
    • Herbal infusions; their phenolic profile, antioxidant and anti-inflammatory effects in HT29 and PC3 cells
    • Kogiannou DAA, Kalogeropoulos N, Kefalas P, Polissiou MG, Kaliora AC. 2013. Herbal infusions; their phenolic profile, antioxidant and anti-inflammatory effects in HT29 and PC3 cells. Food Chem Toxicol 61:152–9.
    • (2013) Food Chem Toxicol , vol.61 , pp. 152-159
    • Kogiannou, D.A.A.1    Kalogeropoulos, N.2    Kefalas, P.3    Polissiou, M.G.4    Kaliora, A.C.5
  • 71
    • 84871547129 scopus 로고    scopus 로고
    • Synthesis and antiradical/antioxidant activities of caffeic acid phenethyl ester and its related propionic, acetic and benzoic acid analogs
    • LeBlanc LM, Pare AF, Jean-Francois J, Hebert MJG, Surette ME, Touaibia M. 2012. Synthesis and antiradical/antioxidant activities of caffeic acid phenethyl ester and its related propionic, acetic and benzoic acid analogs. Molecules 17:14637–50.
    • (2012) Molecules , vol.17 , pp. 14637-14650
    • LeBlanc, L.M.1    Pare, A.F.2    Jean-Francois, J.3    Hebert, M.J.G.4    Surette, M.E.5    Touaibia, M.6
  • 72
    • 33344479129 scopus 로고    scopus 로고
    • Selective ABTS radical-scavenging activity of prenylated flavonoids from Cudrania tricuspidata
    • Lee BW, Lee JH, Gal SW, Moon YH, Park KH. 2006. Selective ABTS radical-scavenging activity of prenylated flavonoids from Cudrania tricuspidata. Biosci Biotechnol Biochem 70:427–32. doi:0.1271/bbb.70.427.
    • (2006) Biosci Biotechnol Biochem , vol.70 , pp. 427-432
    • Lee, B.W.1    Lee, J.H.2    Gal, S.W.3    Moon, Y.H.4    Park, K.H.5
  • 74
    • 38949207932 scopus 로고    scopus 로고
    • Metabolic transformation has a profound effect on anti-inflammatory activity of flavonoids such as quercetin: lack of association between antioxidant and lipoxygenase inhibitory activity
    • Loke WM, Proudfoot JM, Stewart S, McKinley AJ, Needs PW, Kroon PA, Hodgson JM, Croft KD. 2008. Metabolic transformation has a profound effect on anti-inflammatory activity of flavonoids such as quercetin: lack of association between antioxidant and lipoxygenase inhibitory activity. Biochem Pharmacol 75:1045–53. doi:10.1016/j.bcp.2007.11.002.
    • (2008) Biochem Pharmacol , vol.75 , pp. 1045-1053
    • Loke, W.M.1    Proudfoot, J.M.2    Stewart, S.3    McKinley, A.J.4    Needs, P.W.5    Kroon, P.A.6    Hodgson, J.M.7    Croft, K.D.8
  • 75
    • 55549140534 scopus 로고    scopus 로고
    • Antioxidant activity of the medicinal plant Phyllanthus amarus Linn
    • Londhe JS, Devasagayam TPA, Foo LY, Ghaskadbi SS. 2008. Antioxidant activity of the medicinal plant Phyllanthus amarus Linn. Redox Rep 13:199–207. doi:10.1179/135100008×308984.
    • (2008) Redox Rep , vol.13 , pp. 199-207
    • Londhe, J.S.1    Devasagayam, T.P.A.2    Foo, L.Y.3    Ghaskadbi, S.S.4
  • 76
    • 70149090133 scopus 로고    scopus 로고
    • Radioprotective properties of polyphenols from Phyllanthus amarus Linn
    • Londhe JS, Devasagayam TPA, Foo LY, Ghaskadbi SS. 2009. Radioprotective properties of polyphenols from Phyllanthus amarus Linn. J Rad Res 50:303–9. doi:10.1269/jrr.08096.
    • (2009) J Rad Res , vol.50 , pp. 303-309
    • Londhe, J.S.1    Devasagayam, T.P.A.2    Foo, L.Y.3    Ghaskadbi, S.S.4
  • 77
    • 79959329656 scopus 로고    scopus 로고
    • Metabolic conversion of dietary flavonoids alters their anti-inflammatory and antioxidant properties
    • Lotito SB, Zhang W-J, Yang CS, Crozier A, Frei B. 2011. Metabolic conversion of dietary flavonoids alters their anti-inflammatory and antioxidant properties. Free Rad Biol Med 51:454–63. doi:10.1016/j.freeradbiomed.2011.04.032.
    • (2011) Free Rad Biol Med , vol.51 , pp. 454-463
    • Lotito, S.B.1    Zhang, W.-J.2    Yang, C.S.3    Crozier, A.4    Frei, B.5
  • 78
    • 77049114949 scopus 로고    scopus 로고
    • Transcriptional responses to oxidative stress: pathological and toxicological implications
    • Ma Q. 2010. Transcriptional responses to oxidative stress: pathological and toxicological implications. Pharmacol Ther 125:376–93. doi:10.1016/j.pharmthera.2009.11.004.
    • (2010) Pharmacol Ther , vol.125 , pp. 376-393
    • Ma, Q.1
  • 80
    • 84899773000 scopus 로고    scopus 로고
    • Hexanoyl-lysine as an oxidative-injured marker—application of development of functional food
    • Minato K-I, Miyake Y. 2014. Hexanoyl-lysine as an oxidative-injured marker—application of development of functional food. Subcell Biochem 77:163–74
    • (2014) Subcell Biochem , vol.77 , pp. 163-174
    • Minato, K.-I.1    Miyake, Y.2
  • 81
    • 84887968690 scopus 로고    scopus 로고
    • A quantitative assessment of the production of •OH and additional oxidants in the dark Fenton reaction: Fenton degradation of aromatic amines
    • Minero C, Lucchiari M, Maurino V, Vione D. 2013. A quantitative assessment of the production of •OH and additional oxidants in the dark Fenton reaction: Fenton degradation of aromatic amines. RSC Adv 3:26443–50. doi:10.1039/C3RA44585B.
    • (2013) RSC Adv , vol.3 , pp. 26443-26450
    • Minero, C.1    Lucchiari, M.2    Maurino, V.3    Vione, D.4
  • 82
    • 0033858161 scopus 로고    scopus 로고
    • Identification and antioxidant activity of flavonoid metabolites in plasma and urine of eriocitrin-treated rats
    • Miyake Y, Shimoi K, Kumazawa S, Yamamoto K, Kinae N, Osawa T. 2000. Identification and antioxidant activity of flavonoid metabolites in plasma and urine of eriocitrin-treated rats. J Agric Food Chem 48(8):3217–24.
    • (2000) J Agric Food Chem , vol.48 , Issue.8 , pp. 3217-3224
    • Miyake, Y.1    Shimoi, K.2    Kumazawa, S.3    Yamamoto, K.4    Kinae, N.5    Osawa, T.6
  • 83
    • 33746589458 scopus 로고    scopus 로고
    • Antioxidant galloylated flavonol glycosides from Calliandra haematocephala
    • Moharram FA, Marzouk MSA, Ibrahim MT, Mabry TJ. 2006. Antioxidant galloylated flavonol glycosides from Calliandra haematocephala. Natl Prod Res 20:927–34. doi:10.1080/14786410500378494.
    • (2006) Natl Prod Res , vol.20 , pp. 927-934
    • Moharram, F.A.1    Marzouk, M.S.A.2    Ibrahim, M.T.3    Mabry, T.J.4
  • 84
    • 77049138167 scopus 로고
    • The colorimetric estimation of formaldehyde by means of the Hantzsch reaction
    • Nash T. 1953. The colorimetric estimation of formaldehyde by means of the Hantzsch reaction. Biochem J 55:416–21.
    • (1953) Biochem J , vol.55 , pp. 416-421
    • Nash, T.1
  • 85
    • 77954536067 scopus 로고    scopus 로고
    • Assessment of antioxidant capacity in vitro and in vivo
    • Niki E. 2010. Assessment of antioxidant capacity in vitro and in vivo. Free Rad Biol Med 49:503–15. doi:10.1016/j.freeradbiomed.2010.04.016.
    • (2010) Free Rad Biol Med , vol.49 , pp. 503-515
    • Niki, E.1
  • 86
    • 84919731525 scopus 로고    scopus 로고
    • Synergism effect between phenolic metabolites and endogenous antioxidants in terms of antioxidant activity
    • Noguer M, Cerezo AB, Moya ML, Troncoso AM, Garcia-Parrilla M. 2014. Synergism effect between phenolic metabolites and endogenous antioxidants in terms of antioxidant activity. Adv Chem Eng Sci 4(2):258–65
    • (2014) Adv Chem Eng Sci , vol.4 , Issue.2 , pp. 258-265
    • Noguer, M.1    Cerezo, A.B.2    Moya, M.L.3    Troncoso, A.M.4    Garcia-Parrilla, M.5
  • 87
    • 0037977138 scopus 로고    scopus 로고
    • Chlorogenic acid, quercetin-3-rutinoside and black tea phenols are extensively metabolized in humans
    • Olthof MR, Hollman PCH, Buijsman MNCP, van Amelsvoort JMM, Katan MB. 2003. Chlorogenic acid, quercetin-3-rutinoside and black tea phenols are extensively metabolized in humans. J Nutr 133(6):1806–14.
    • (2003) J Nutr , vol.133 , Issue.6 , pp. 1806-1814
    • Olthof, M.R.1    Hollman, P.C.H.2    Buijsman, M.N.C.P.3    van Amelsvoort, J.M.M.4    Katan, M.B.5
  • 88
    • 0036241543 scopus 로고    scopus 로고
    • Glucuronidation versus oxidation of the flavonoid galangin by human liver microsomes and hepatocytes
    • Otake Y, Hsieh F, Walle T. 2002. Glucuronidation versus oxidation of the flavonoid galangin by human liver microsomes and hepatocytes. Drug Metab Dispos 30:576–81. doi:10.1124/dmd.30.5.576.
    • (2002) Drug Metab Dispos , vol.30 , pp. 576-581
    • Otake, Y.1    Hsieh, F.2    Walle, T.3
  • 89
    • 0037041909 scopus 로고    scopus 로고
    • Novel fluorometric assay for hydroxyl radical prevention capacity using fluorescein as the probe
    • Ou B, Hampsch-Woodill M, Flanagan J, Deemer EK, Prior RL, Huang D. 2002. Novel fluorometric assay for hydroxyl radical prevention capacity using fluorescein as the probe. J Agric Food Chem 50:2772–7. doi:10.1021/jf011480w.
    • (2002) J Agric Food Chem , vol.50 , pp. 2772-2777
    • Ou, B.1    Hampsch-Woodill, M.2    Flanagan, J.3    Deemer, E.K.4    Prior, R.L.5    Huang, D.6
  • 90
    • 0141628930 scopus 로고    scopus 로고
    • Different antioxidant effects of polyphenols on lipid peroxidation and hydroxyl radicals in the NADPH-, Fe-ascorbate- and Fe-microsomal systems
    • Ozgová Š, Heřmánek J, Gut I. 2003. Different antioxidant effects of polyphenols on lipid peroxidation and hydroxyl radicals in the NADPH-, Fe-ascorbate- and Fe-microsomal systems. Biochem Pharmacol 66:1127–37. doi:10.1016/S0006-2952(03)00425-8.
    • (2003) Biochem Pharmacol , vol.66 , pp. 1127-1137
    • Ozgová, Š.1    Heřmánek, J.2    Gut, I.3
  • 91
    • 43049161032 scopus 로고    scopus 로고
    • Hydroxyl radical scavenging assay of phenolics and flavonoids with a modified cupric reducing antioxidant capacity (CUPRAC) method using catalase for hydrogen peroxide degradation
    • Özyürek M, Bektaşoğlu B, Güçlü K, Apak R. 2008. Hydroxyl radical scavenging assay of phenolics and flavonoids with a modified cupric reducing antioxidant capacity (CUPRAC) method using catalase for hydrogen peroxide degradation. Anal Chim Acta 616:196–206. doi:10.1016/j.aca.2008.04.033.
    • (2008) Anal Chim Acta , vol.616 , pp. 196-206
    • Özyürek, M.1    Bektaşoğlu, B.2    Güçlü, K.3    Apak, R.4
  • 94
    • 0032400815 scopus 로고    scopus 로고
    • Flavonoids: dietary occurrence and biochemical activity
    • Peterson J, Dwyer J. 1998. Flavonoids: dietary occurrence and biochemical activity. Nutr Res 18:1995–2018. doi: http://dx.doi.org/10.1016/S0271-5317(98)00169-9.
    • (1998) Nutr Res , vol.18 , pp. 1995-2018
    • Peterson, J.1    Dwyer, J.2
  • 95
    • 79955473013 scopus 로고    scopus 로고
    • Antioxidant and prooxidant properties of flavonoids
    • Procházková D, Boušová I, Wilhelmová N. 2011. Antioxidant and prooxidant properties of flavonoids. Fitoterapia 82:513–23. doi:10.1016/j.fitote.2011.01.018.
    • (2011) Fitoterapia , vol.82 , pp. 513-523
    • Procházková, D.1    Boušová, I.2    Wilhelmová, N.3
  • 96
    • 44949279890 scopus 로고
    • Effect of flavonoids on hydroxyl radical formation by Fenton-type reactions; influence of the iron chelator
    • Puppo A. 1992. Effect of flavonoids on hydroxyl radical formation by Fenton-type reactions; influence of the iron chelator. Phytochemistry 31:85–8. doi:10.1016/0031-9422(91)83011-9.
    • (1992) Phytochemistry , vol.31 , pp. 85-88
    • Puppo, A.1
  • 97
    • 0025083680 scopus 로고
    • Complexes involving quercetin, DNA and Cu(II)
    • Rahman A, Shahabuddin A, Hadi SM, Parish JH. 1990. Complexes involving quercetin, DNA and Cu(II). Carcinogenesis 11:2001–3. doi: 10.1093/carcin/11.11.2001.
    • (1990) Carcinogenesis , vol.11 , pp. 2001-2003
    • Rahman, A.1    Shahabuddin, A.2    Hadi, S.M.3    Parish, J.H.4
  • 99
    • 0029888128 scopus 로고    scopus 로고
    • Structure-antioxidant activity of flavonoids and phenolic acids
    • Rice-Evans CA, Miller NJ, Paganga G. 1996. Structure-antioxidant activity of flavonoids and phenolic acids. Free Rad Biol Med 20:933–56. doi:10.1016/0891-5849(95)02227-9.
    • (1996) Free Rad Biol Med , vol.20 , pp. 933-956
    • Rice-Evans, C.A.1    Miller, N.J.2    Paganga, G.3
  • 101
    • 84856998207 scopus 로고    scopus 로고
    • New phenolic compounds hydrothermally extracted from the olive oil byproduct alperujo and their antioxidative activities
    • Rubio-Senent F, Rodriguez-Gutierrez G, Lama-Munoz A, Fernandez-Bolanos J. 2012. New phenolic compounds hydrothermally extracted from the olive oil byproduct alperujo and their antioxidative activities. J Agric Food Chem 60(5):1175–86.
    • (2012) J Agric Food Chem , vol.60 , Issue.5 , pp. 1175-1186
    • Rubio-Senent, F.1    Rodriguez-Gutierrez, G.2    Lama-Munoz, A.3    Fernandez-Bolanos, J.4
  • 102
    • 33144460053 scopus 로고    scopus 로고
    • Total antioxidant capacity evaluation: critical steps for assaying berry antioxidant features
    • Scalzo J, Mezzetti B, Battino M. 2008. Total antioxidant capacity evaluation: critical steps for assaying berry antioxidant features. BioFactors 23:221–7. doi:10.1002/biof.5520230407.
    • (2008) BioFactors , vol.23 , pp. 221-227
    • Scalzo, J.1    Mezzetti, B.2    Battino, M.3
  • 103
    • 0034937284 scopus 로고    scopus 로고
    • Quercetin glucuronides but not glucosides are present in human plasma after consumption of quercetin-3-glucoside or quercetin-4´-glucoside
    • Sesnik ALA, O'Leary KA, Hollman PCH. 2001. Quercetin glucuronides but not glucosides are present in human plasma after consumption of quercetin-3-glucoside or quercetin-4´-glucoside. J Nutr 131:1938–41.
    • (2001) J Nutr , vol.131 , pp. 1938-1941
    • Sesnik, A.L.A.1    O'Leary, K.A.2    Hollman, P.C.H.3
  • 105
    • 80054081662 scopus 로고    scopus 로고
    • Antioxidative low molecular weight extractives from triploid Populus tomentosa xylem
    • Si C-L, Lu Y-Y, Zhang Y, Xu J, Qin P-P, Sun R-C, Ni Y-H. 2011. Antioxidative low molecular weight extractives from triploid Populus tomentosa xylem. Bioresources 6:232–42.
    • (2011) Bioresources , vol.6 , pp. 232-242
    • Si, C.-L.1    Lu, Y.-Y.2    Zhang, Y.3    Xu, J.4    Qin, P.-P.5    Sun, R.-C.6    Ni, Y.-H.7
  • 106
    • 0024287763 scopus 로고
    • Colorimetric detection of the hydroxyl radical: comparison of the hydroxyl-radical-generating ability of various iron complexes
    • Singh S, Hider RC. 1988. Colorimetric detection of the hydroxyl radical: comparison of the hydroxyl-radical-generating ability of various iron complexes. Anal Biochem 171:47–54. doi:10.1016/0003-2697(88)90123-6.
    • (1988) Anal Biochem , vol.171 , pp. 47-54
    • Singh, S.1    Hider, R.C.2
  • 107
    • 33644774555 scopus 로고    scopus 로고
    • Antioxidant profile of dihydroxy- and trihydroxyphenolic acids—a structure-activity relationship study
    • Siquet C, Paiva-Martins F, Lima JLFC, Reis S, Borges F. 2006. Antioxidant profile of dihydroxy- and trihydroxyphenolic acids—a structure-activity relationship study. Free Rad Res 40(4):433–42.
    • (2006) Free Rad Res , vol.40 , Issue.4 , pp. 433-442
    • Siquet, C.1    Paiva-Martins, F.2    Lima, J.L.F.C.3    Reis, S.4    Borges, F.5
  • 108
    • 0037120770 scopus 로고    scopus 로고
    • A new simple and sensitive fluorimetric method for the determination of hydroxyl radical and its application
    • Tai C, Gu X, Zou H, Guo Q. 2002. A new simple and sensitive fluorimetric method for the determination of hydroxyl radical and its application. Talanta 58:661–7. doi:10.1016/S0039-9140(02)00370-3.
    • (2002) Talanta , vol.58 , pp. 661-667
    • Tai, C.1    Gu, X.2    Zou, H.3    Guo, Q.4
  • 109
    • 77953979658 scopus 로고    scopus 로고
    • Determination of antiradical and antioxidant activity: basic principles and new insights
    • Tirzitis G, Bartosz G. 2010. Determination of antiradical and antioxidant activity: basic principles and new insights. Acta Biochim Pol 57:139–42.
    • (2010) Acta Biochim Pol , vol.57 , pp. 139-142
    • Tirzitis, G.1    Bartosz, G.2
  • 110
    • 84879686850 scopus 로고    scopus 로고
    • Determination of antioxidant activity using oxidative damage to plasmid DNA—pursuit of solvent optimization
    • Treml J, Šmejkal K, Hošek J, Žemlička M. 2013. Determination of antioxidant activity using oxidative damage to plasmid DNA—pursuit of solvent optimization. Chem Pap 67:484–9. doi:10.2478/s11696-013-0334-8.
    • (2013) Chem Pap , vol.67 , pp. 484-489
    • Treml, J.1    Šmejkal, K.2    Hošek, J.3    Žemlička, M.4
  • 111
    • 0034857944 scopus 로고    scopus 로고
    • Rapid and specific detection of hydroxyl radical using an ultraweak chemoluminescence analyzer and a low-level chemoluminescence emitter: application to hydroxyl radical-scavenging ability of aqueous extracts of food constituents
    • Tsai C-H, Stern A, Chiou J-F, Chern C-L, Liu T-Z. 2001. Rapid and specific detection of hydroxyl radical using an ultraweak chemoluminescence analyzer and a low-level chemoluminescence emitter: application to hydroxyl radical-scavenging ability of aqueous extracts of food constituents. J Agric Food Chem 49:2137–41. doi:10.1021/jf001071k.
    • (2001) J Agric Food Chem , vol.49 , pp. 2137-2141
    • Tsai, C.-H.1    Stern, A.2    Chiou, J.-F.3    Chern, C.-L.4    Liu, T.-Z.5
  • 112
    • 0030580038 scopus 로고    scopus 로고
    • Inhibition of lipid peroxidation and active oxygen radical scavenging effect of anthocyanin pigments isolated from Phaseolus vulgaris L
    • Tsuda T, Shiga K, Ohshima K, Kawakishi S, Osawa T. 1996. Inhibition of lipid peroxidation and active oxygen radical scavenging effect of anthocyanin pigments isolated from Phaseolus vulgaris L. Biochem Pharmacol 52:1033–9. doi:10.1016/0006-2952(96)00421-2.
    • (1996) Biochem Pharmacol , vol.52 , pp. 1033-1039
    • Tsuda, T.1    Shiga, K.2    Ohshima, K.3    Kawakishi, S.4    Osawa, T.5
  • 113
    • 0028268359 scopus 로고
    • Isozyme- and species-specific suspectibility of cDNA-expressed CYP1A P-450s to different flavonoids
    • Tsyrlov IB, Mikhailenko VM, Gelboin HV. 1994. Isozyme- and species-specific suspectibility of cDNA-expressed CYP1A P-450s to different flavonoids. Biochim Biophys Acta 205:325–35. doi:10.1016/0167-4838(94)90252-6.
    • (1994) Biochim Biophys Acta , vol.205 , pp. 325-335
    • Tsyrlov, I.B.1    Mikhailenko, V.M.2    Gelboin, H.V.3
  • 115
  • 116
    • 0034664115 scopus 로고    scopus 로고
    • The predictive value of the antioxidant capacity of structurally related flavonoids using the Trolox equivalent antioxidant capacity (TEAC) assay
    • Van den Berg R, Haenen GRMM, van den Berg H, van der Vijgh W, Bast A. 2000. The predictive value of the antioxidant capacity of structurally related flavonoids using the Trolox equivalent antioxidant capacity (TEAC) assay. Food Chem 70:391–5. doi:10.1016/S0308-8146(00)00092-3.
    • (2000) Food Chem , vol.70 , pp. 391-395
    • Van den Berg, R.1    Haenen, G.R.M.M.2    van den Berg, H.3    van der Vijgh, W.4    Bast, A.5
  • 117
    • 1642528478 scopus 로고    scopus 로고
    • Absorption and metabolism of flavonoids
    • Walle T. 2004. Absorption and metabolism of flavonoids. Free Rad Biol Med 36:829–37. doi:10.1016/j.freeradbiomed.2004.01.002.
    • (2004) Free Rad Biol Med , vol.36 , pp. 829-837
    • Walle, T.1
  • 118
    • 0034979805 scopus 로고    scopus 로고
    • Flavonoid biosynthesis. A colorful model for genetics, biochemistry, cell biology, and biotechnology
    • Winkel-Shirley B. 2001. Flavonoid biosynthesis. A colorful model for genetics, biochemistry, cell biology, and biotechnology. Plant Physiol 126:485–93. doi: http://dx.doi.org/10.1104/pp.126.2.485.
    • (2001) Plant Physiol , vol.126 , pp. 485-493
    • Winkel-Shirley, B.1
  • 119
    • 0005955494 scopus 로고
    • EPR spin-trapping study on the oxidizing species formed in the reaction of the ferrous ion with hydrogen peroxide
    • Yamazaki I, Piette LH. 1991. EPR spin-trapping study on the oxidizing species formed in the reaction of the ferrous ion with hydrogen peroxide. J Am Chem Soc 113:7588–93. doi:10.1021/ja00020a021.
    • (1991) J Am Chem Soc , vol.113 , pp. 7588-7593
    • Yamazaki, I.1    Piette, L.H.2
  • 120
    • 84873711404 scopus 로고    scopus 로고
    • Biotransformation of 4,5-O-dicaffeoylquinic acid methyl ester by human intestinal flora and evaluation on their inhibition of NO production and antioxidant activity of the products
    • Yang X-W, Wang N, Li W, Xu W, Wu S. 2013. Biotransformation of 4,5-O-dicaffeoylquinic acid methyl ester by human intestinal flora and evaluation on their inhibition of NO production and antioxidant activity of the products. Food Chem Toxicol 55:297–303.
    • (2013) Food Chem Toxicol , vol.55 , pp. 297-303
    • Yang, X.-W.1    Wang, N.2    Li, W.3    Xu, W.4    Wu, S.5
  • 122
    • 0029137536 scopus 로고
    • Chemiluminescence of benzoic and cinnamic acids, and flavonoids in the presence of aldehyde and hydrogen peroxide or hydroxyl radical by Fenton reaction
    • Yoshiki Y, Okubo K, Onuma M, Igarashi K. 1995. Chemiluminescence of benzoic and cinnamic acids, and flavonoids in the presence of aldehyde and hydrogen peroxide or hydroxyl radical by Fenton reaction. Phytochemistry 39:225–9. doi:10.1016/0031-9422(94)00896-2.
    • (1995) Phytochemistry , vol.39 , pp. 225-229
    • Yoshiki, Y.1    Okubo, K.2    Onuma, M.3    Igarashi, K.4
  • 123
    • 33645243967 scopus 로고    scopus 로고
    • Identification of the major flavonoids from pericarp tissues of lychee fruit in relation to their antioxidant activities
    • Zhao M, Yang B, Wang J, Li B, Jiang Y. 2006. Identification of the major flavonoids from pericarp tissues of lychee fruit in relation to their antioxidant activities. Food Chem 98:539–44. doi:10.1016/j.foodchem.2005.06.028.
    • (2006) Food Chem , vol.98 , pp. 539-544
    • Zhao, M.1    Yang, B.2    Wang, J.3    Li, B.4    Jiang, Y.5
  • 124
    • 0028085081 scopus 로고
    • Catechol-O-methyltransferase-catalyzed rapid O-methylation of mutagenic flavonoids, Metabolic inactivation as a possible reason for their lack of carcinogenicity in vivo
    • Zhu BT, Ezell EL, Liehr JG. 1994. Catechol-O-methyltransferase-catalyzed rapid O-methylation of mutagenic flavonoids. Metabolic inactivation as a possible reason for their lack of carcinogenicity in vivo. J Biol Chem 269:292–9.
    • (1994) J Biol Chem , vol.269 , pp. 292-299
    • Zhu, B.T.1    Ezell, E.L.2    Liehr, J.G.3
  • 125
    • 77957302774 scopus 로고    scopus 로고
    • Antiradical and cytoprotective activities of several C-geranyl-substituted flavanones from Paulownia tomentosa fruit
    • Zima A, Hošek J, Treml J, Muselík J, Suchý P, Pražanová G, Lopes A, Žemlička M. 2010. Antiradical and cytoprotective activities of several C-geranyl-substituted flavanones from Paulownia tomentosa fruit. Molecules 15:6035–49. doi:10.3390/molecules15096035.
    • (2010) Molecules , vol.15 , pp. 6035-6049
    • Zima, A.1    Hošek, J.2    Treml, J.3    Muselík, J.4    Suchý, p.5    Pražanová, G.6    Lopes, A.7    Žemlička, M.8


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