Solvent effects are important in elucidating radical-scavenging mechanisms of antioxidants. A case study on genistein

被引:9
作者
Zhang, HY [1 ]
Wang, LF [1 ]
机构
[1] Shandong Univ Technol, Lab Computat Biol, Shandong Prov Res Ctr Bioinformat Engn & Tech, Zibo 255049, Peoples R China
基金
中国国家自然科学基金;
关键词
antioxidants; flavonoids; isoflavonoids; genistein; radical; solvent effect; density functional theory;
D O I
10.1080/07391102.2005.10507019
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
In two recent researches on antioxidant mechanisms of flavonoids and isoflavonoids, quantum chemical method was employed to calculate the proton dissociation energies. the bond dissociation energies and the ionization potentials for the phenols and derived radicals to help determine the radical-scavenging mechanisms. As the solvent effect was left out of consideration, the conclusion drawn from the calculation incurred some controversies. In the current study, we re-calculated the parameters for genistein and its anion by employing a B3LYP/6-311+G(d,p)H6-31G(d,p) method with solvent effect. Accordingly. a more reasonable explanation on the experimentally observed behavior of genistein as a radical scavenger was obtained. Therefore, solvent effect should be considered in the investigation of radical-scavenging mechanisms of antioxidants in polar solvents.
引用
收藏
页码:483 / 486
页数:4
相关论文
共 18 条
  • [1] AUTOXIDATION OF BIOLOGICAL MOLECULES .4. MAXIMIZING THE ANTIOXIDANT ACTIVITY OF PHENOLS
    BURTON, GW
    DOBA, T
    GABE, EJ
    HUGHES, L
    LEE, FL
    PRASAD, L
    INGOLD, KU
    [J]. JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 1985, 107 (24) : 7053 - 7065
  • [2] THE DEVELOPMENT AND USE OF QUANTUM-MECHANICAL MOLECULAR-MODELS .76. AM1 - A NEW GENERAL-PURPOSE QUANTUM-MECHANICAL MOLECULAR-MODEL
    DEWAR, MJS
    ZOEBISCH, EG
    HEALY, EF
    STEWART, JJP
    [J]. JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 1985, 107 (13) : 3902 - 3909
  • [3] Naphthalene diols: A new class of antioxidants intramolecular hydrogen bonding in catechols, naphthalene diols, and their aryloxyl radicals
    Foti, MC
    Johnson, ER
    Vinqvist, MR
    Wright, JS
    Barclay, LRC
    Ingold, KU
    [J]. JOURNAL OF ORGANIC CHEMISTRY, 2002, 67 (15) : 5190 - 5196
  • [4] FRISCH MJ, 2001, GAUSSIAN 98 REVISION
  • [5] Development of novel antioxidants: Design, synthesis, and reactivity
    Hussain, HH
    Babic, G
    Durst, T
    Wright, JS
    Flueraru, M
    Chichirau, A
    Chepelev, LL
    [J]. JOURNAL OF ORGANIC CHEMISTRY, 2003, 68 (18) : 7023 - 7032
  • [6] FLAVONOIDS AS ANTIOXIDANTS
    JOVANOVIC, SV
    STEENKEN, S
    TOSIC, M
    MARJANOVIC, B
    SIMIC, MG
    [J]. JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 1994, 116 (11) : 4846 - 4851
  • [7] Theoretical elucidation of the radical-scavenging-activity difference of hydroxycinnamic acid derivatives
    Kong, L
    Sun, ZL
    Wang, LF
    Zhang, HY
    Yao, SD
    [J]. HELVETICA CHIMICA ACTA, 2004, 87 (02) : 511 - 515
  • [8] The influence of pH on antioxidant properties and the mechanism of antioxidant action of hydroxyflavones
    Lemanska, K
    Szymusiak, H
    Tyrakowska, B
    Zielinski, R
    Soffers, AEMF
    Rietjens, IMCM
    [J]. FREE RADICAL BIOLOGY AND MEDICINE, 2001, 31 (07) : 869 - 881
  • [9] Abnormal solvent effects on hydrogen atom abstractions.: 1.: The reactions of phenols with 2,2-diphenyl-1-picrylhydrazyl (dpph•) in alcohols
    Litwinienko, G
    Ingold, KU
    [J]. JOURNAL OF ORGANIC CHEMISTRY, 2003, 68 (09) : 3433 - 3438
  • [10] Effects of metal ions distinguishing between one-step hydrogen- and electron-transfer mechanisms for the radical-scavenging reaction of (+)-catechin
    Nakanishi, I
    Miyazaki, K
    Shimada, T
    Ohkubo, K
    Urano, S
    Ikota, N
    Ozawa, T
    Fukuzumi, S
    Fukuhara, K
    [J]. JOURNAL OF PHYSICAL CHEMISTRY A, 2002, 106 (46) : 11123 - 11126