10967/165 - QDB Compounds

QsarDB Repository

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

IDNameE7Details
Tab1-14-Nitrophenol1.23View
Tab1-24-Cyanophenol1.17View
Tab1-34-Iodophenol1.09View
Tab1-41-(4-Hydroxyphenyl)ethanone1.06View
Tab1-54-Carboxyphenol1.04View
Tab1-6Phenol0.97View
Tab1-74-Bromophenol0.96View
Tab1-84-Chlorophenol0.94View
Tab1-94-Fluorophenol0.93View
Tab1-10Tyrosine0.89View
Tab1-111-(2,4-Dihydroxyphenyl)ethanone0.89View
Tab1-124-Methylphenol0.87View
Tab1-133,5-Dimethoxyphenol0.85View
Tab1-145-Methoxybenzene-1,3-diol0.84View
Tab1-15Benzene-1,3-diol0.81View
Tab1-164-Methoxyphenol0.73View
Tab1-172-Methoxy-4-methylphenol0.68View
Tab1-183,4-Dimethoxyphenol0.67View
Tab1-193,4,5-Trimethoxyphenol0.66View
Tab1-20Sesamol0.62View
Tab1-213,4-Dihydroxybenzoic acid0.6View
Tab1-222,6-Dimethoxyphenol0.58View
Tab1-23​Benzene-1,​2,​3-triol0.58View
Tab1-24Methyl 3,4,5-trihydroxybenzoate0.56View
Tab1-253,4-Dihydroxycinnamic acid0.54View
Tab1-26Benzene-1,2-diol0.53View
Tab1-274-Methylbenzene-1,2-diol0.52View
Tab1-28alpha-Tocopherol0.48View
Tab1-29Benzene-1,4-diol0.46View
Tab1-304-Aminophenol0.41View
Tab1-314-Dimethylaminophenol0.36View
Tab2-13,5-Dichlorophenol1.15View
Tab2-24-(Trifluoromethy)lphenol1.13View
Tab2-33-Nitrophenol1.13View
Tab2-4(4-Hydroxyphenyl)-phenylmethanone1.12View
Tab2-53-Cyanophenol1.11View
Tab2-61-(3-hydroxyphenyl)ethanone0.98View
Tab2-73-Methylphenol0.85View
Tab2-83,5-Dimethylphenol0.84View
Tab2-94-Phenylphenol0.84View
Tab2-102-Methylphenol0.82View
Tab2-114-tert-Butylphenol0.8View
Tab2-122-Methoxyphenol0.77View
Tab2-132,6-Dimethylphenol0.77View

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. https://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. https://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.