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10967/165 - QDB Compounds

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Lien, E. J.; Ren, S.; Bui, H.-H.; Wang, R. Quantitative structure-activity relationship analysis of phenolic antioxidants. Free Radic. Biol. Med. 1999, 26, 285–294.

44 compounds | Property E7: Redox potential [V] i

ID Name E7 Details
Tab1-1 4-Nitrophenol 1.23 View
Tab1-2 4-Cyanophenol 1.17 View
Tab1-3 4-Iodophenol 1.09 View
Tab1-4 1-(4-Hydroxyphenyl)ethanone 1.06 View
Tab1-5 4-Carboxyphenol 1.04 View
Tab1-6 Phenol 0.97 View
Tab1-7 4-Bromophenol 0.96 View
Tab1-8 4-Chlorophenol 0.94 View
Tab1-9 4-Fluorophenol 0.93 View
Tab1-10 Tyrosine 0.89 View
Tab1-11 1-(2,4-Dihydroxyphenyl)ethanone 0.89 View
Tab1-12 4-Methylphenol 0.87 View
Tab1-13 3,5-Dimethoxyphenol 0.85 View
Tab1-14 5-Methoxybenzene-1,3-diol 0.84 View
Tab1-15 Benzene-1,3-diol 0.81 View
Tab1-16 4-Methoxyphenol 0.73 View
Tab1-17 2-Methoxy-4-methylphenol 0.68 View
Tab1-18 3,4-Dimethoxyphenol 0.67 View
Tab1-19 3,4,5-Trimethoxyphenol 0.66 View
Tab1-20 Sesamol 0.62 View
Tab1-21 3,4-Dihydroxybenzoic acid 0.6 View
Tab1-22 2,6-Dimethoxyphenol 0.58 View
Tab1-23 ​Benzene-1,​2,​3-triol 0.58 View
Tab1-24 Methyl 3,4,5-trihydroxybenzoate 0.56 View
Tab1-25 3,4-Dihydroxycinnamic acid 0.54 View
Tab1-26 Benzene-1,2-diol 0.53 View
Tab1-27 4-Methylbenzene-1,2-diol 0.52 View
Tab1-28 alpha-Tocopherol 0.48 View
Tab1-29 Benzene-1,4-diol 0.46 View
Tab1-30 4-Aminophenol 0.41 View
Tab1-31 4-Dimethylaminophenol 0.36 View
Tab2-1 3,5-Dichlorophenol 1.15 View
Tab2-2 4-(Trifluoromethy)lphenol 1.13 View
Tab2-3 3-Nitrophenol 1.13 View
Tab2-4 (4-Hydroxyphenyl)-phenylmethanone 1.12 View
Tab2-5 3-Cyanophenol 1.11 View
Tab2-6 1-(3-hydroxyphenyl)ethanone 0.98 View
Tab2-7 3-Methylphenol 0.85 View
Tab2-8 3,5-Dimethylphenol 0.84 View
Tab2-9 4-Phenylphenol 0.84 View
Tab2-10 2-Methylphenol 0.82 View
Tab2-11 4-tert-Butylphenol 0.8 View
Tab2-12 2-Methoxyphenol 0.77 View
Tab2-13 2,6-Dimethylphenol 0.77 View

Bibliography

  1. Lien, E. J.; Ren, S.; Bui, H.-H.; Wang, R. Quantitative structure-activity relationship analysis of phenolic antioxidants. Free Radical Biology and Medicine 1999, 26, 285–294. http://dx.doi.org/10.1016/s0891-5849(98)00190-7

  2. Jovanovic, S. V.; Tosic, M.; Simic, M. G. Use of the Hammett correlation and .delta.+ for calculation of one-electron redox potentials of antioxidants. The Journal of Physical Chemistry 1991, 95, 10824–10827. http://dx.doi.org/10.1021/j100179a054

  3. Jovanovic, S. V.; Steenken, S.; Simic, M. G.; Hara, Y. Antioxidant properties of flavonoids: Reduction potentials and electron transfer reductions of flavonoid radicals. In Flavonoids in health and disease; Rice-Evans, C.A.; Packers, L., Eds.; Marcel Dekker, Inc, New York; 1998.