2,2,5,7,8-pentamethyl-1-hydroxychroman has been researched along with phenoxy radical in 4 studies
Timeframe | Studies, this research(%) | All Research% |
---|---|---|
pre-1990 | 0 (0.00) | 18.7374 |
1990's | 1 (25.00) | 18.2507 |
2000's | 3 (75.00) | 29.6817 |
2010's | 0 (0.00) | 24.3611 |
2020's | 0 (0.00) | 2.80 |
Authors | Studies |
---|---|
Goldman, R; Grogan, J; Kagan, VE; Tsyrlov, IB | 1 |
Kagan, VE; Kisin, ER; Kuzmenko, AI; Shvedova, AA; Tyurina, YY; Yalowich, JC | 1 |
Kagan, VE; Kisin, ER; Kuzmenko, AI; Li, R; Martin, I; Quinn, PJ; Shvedova, AA; Tyurin, VA; Tyurina, YY; Yalowich, JC | 1 |
Gill, PM; Lee, SB; Lin, CY; Webster, RD | 1 |
4 other study(ies) available for 2,2,5,7,8-pentamethyl-1-hydroxychroman and phenoxy radical
Article | Year |
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Reactions of phenoxyl radicals with NADPH-cytochrome P-450 oxidoreductase and NADPH: reduction of the radicals and inhibition of the enzyme.
Topics: Animals; Antioxidants; Binding Sites; Chromans; Dithionitrobenzoic Acid; Electron Spin Resonance Spectroscopy; Etoposide; Free Radicals; Humans; Kinetics; NADP; NADPH-Ferrihemoprotein Reductase; Oxidation-Reduction; Phenol; Phenols; Recombinant Proteins; Spodoptera; Transfection | 1997 |
Myeloperoxidase-catalyzed phenoxyl radicals of vitamin E homologue, 2,2,5,7,8-pentamethyl- 6-hydroxychromane, do not induce oxidative stress in live HL-60 cells.
Topics: Cell Survival; Chromans; Electron Spin Resonance Spectroscopy; Free Radicals; Glutathione; HL-60 Cells; Humans; Hydrogen Peroxide; Kinetics; Oxidative Stress; Peroxidase; Phenols | 2000 |
Direct evidence for recycling of myeloperoxidase-catalyzed phenoxyl radicals of a vitamin E homologue, 2,2,5,7,8-pentamethyl-6-hydroxy chromane, by ascorbate/dihydrolipoate in living HL-60 cells.
Topics: Antioxidants; Ascorbic Acid; Cell Survival; Chromans; Chromatography, High Pressure Liquid; Electron Spin Resonance Spectroscopy; Free Radicals; HL-60 Cells; Humans; Hydrogen Peroxide; Oxidation-Reduction; Peroxidase; Phenols; Spectrophotometry; Substrate Cycling; Thioctic Acid | 2003 |
Transformation of alpha-tocopherol (vitamin E) and related chromanol model compounds into their phenoxonium ions by chemical oxidation with the nitrosonium cation.
Topics: Antioxidants; Chromans; Electrochemistry; Nitric Oxide; Oxidation-Reduction; Phenols; Spectroscopy, Fourier Transform Infrared; Vitamin E | 2005 |