Every reference with a DOI in the deposited reference list resolved to a known
work in Crossref or DataCite at the dated check, and none carried a retraction,
withdrawal, or removal notice.
The 128 checked references that resolve
resolves10.1002/rcm.1291Assignment of quinone derivatives as the main compound class composing ‘interstellar’ grains based on both polarity ions detected by the ‘Cometary and Interstellar Dust Analyser’ (CIDA) onboard the spacecraft STARDUST
resolves10.1016/S0021-9258(19)38410-8The protonmotive Q cycle. Energy transduction by coupling of proton translocation to electron transfer by the cytochrome bc1 complex.
resolves10.1073/pnas.88.5.1646Ubiquinol-10 protects human low density lipoprotein more efficiently against lipid peroxidation than does alpha-tocopherol.
resolves10.1126/science.877547Adriamycin: The Role of Lipid Peroxidation in Cardiac Toxicity and Tumor Response
resolves10.1016/0003-9861(91)90023-CAn electron paramagnetic resonance study of the interactions between the adriamycin semiquinone, hydrogen peroxide, iron-chelators, and radical scavengers
resolves10.1016/0005-2728(80)90095-XThe kinetics and thermodynamics of the reduction of cytochrome c by substituted p-benzoquinols in solution
resolves10.1021/j100638a003Ionization constants and spectral characteristics of some semiquinone radicals in aqueous solution
resolves10.1039/c29710001249Semiquinone free radicals: determination of acid dissociation constants by pulse radiolysis
resolves10.1021/ol901188qCyclization Reactions through DDQ-Mediated Vinyl Oxazolidinone Oxidation
resolves10.2174/0929867013372959Electron Transfer and Oxidative Stress as Key Factors in the Design of Drugs Selectively Active in Hypoxia.
resolves10.1063/1.555843Reduction Potentials of One-Electron Couples Involving Free Radicals in Aqueous Solution
resolves10.1016/S0891-5849(01)00480-4Redox environment of the cell as viewed through the redox state of the glutathione disulfide/glutathione couple
resolves10.1021/tx8000175Semiquinone Radicals from Oxygenated Polychlorinated Biphenyls: Electron Paramagnetic Resonance Studies
resolves10.1021/jo801397gChlorination Increases the Persistence of Semiquinone Free Radicals Derived from Polychlorinated Biphenyl Hydroquinones and Quinones
resolves10.1021/j100582a004One-electron transfer equilibriums and redox potentials of radicals studied by pulse radiolysis
resolves10.1006/abbi.1993.1074The Pecking Order of Free Radicals and Antioxidants: Lipid Peroxidation, α-Tocopherol, and Ascorbate
resolves10.3109/10715769109088942The Reduction Potential of Benzyl Viologen: An Important Reference Compound for Oxidant/Radical Redox Couples
resolves10.1042/bj1390049The mechanism of action of superoxide dismutase from pulse radiolysis and electron paramagnetic resonance. Evidence that only half the active sites function in catalysis
resolves10.1016/0009-2614(75)85269-9Free energy correlation of rate constants for electron transfer between organic systems in aqueous solutions
resolves10.1083/jcb.107.6.2169Molecular immunocytochemistry of the CuZn superoxide dismutase in rat hepatocytes.
resolves10.1042/bj1470493Polarographic assay and intracellular distribution of superoxide dismutase in rat liver.
resolves10.1042/bj2030155Reactions of Adriamycin with haemoglobin. Superoxide dismutase indirectly inhibits reactions of the Adriamycin semiquinone
resolves10.1021/j100472a005Electron transfer rates and equilibriums between substituted phenoxide ions and phenoxyl radicals
resolves10.1021/tx9001463Electrophilic Reaction Chemistry of Low Molecular Weight Respiratory Sensitizers
resolves10.1021/ja01199a005Oxidation Processes. XIX.<sup>1</sup> Quinone Catalysis in the Autoxidation of Hydroquinones
resolves10.1039/b000538jKinetics of oxidation of hydroquinones by molecular oxygen. Effect of superoxide dismutase
resolves10.1021/ja01666a030THE INFLUENCE OF HYDROGEN CONCENTRATION ON THE AUTO-OXIDATION OF HYDROQUINONE. A NOTE ON THE STABILITY OF THE QUINHYDRONE ELECTRODE
resolves10.1021/ja01268a032Oxidation Processes. XI.<sup>1</sup> The Autoxidation of Durohydroquinone
resolves10.1021/ja01276a020Oxidation Processes. XII.<sup>1</sup> The Autoxidation of Hydroquinone and of the Mono-, Di- and Trimethylhydroquinones
resolves10.1021/ja01871a064Oxidation Processes. XIII.<sup>1</sup> The Inhibitory Action of Sulfite and other Compounds in the Autoxidation of Hydroquinone and its Homologs
resolves10.1021/ja01259a021Oxidation Processes. XIV.<sup>1</sup> The Effect of Silver on the Autoxidation of Some Photographic Developing Agents
resolves10.1021/ja01248a018Oxidation Processes. XV.<sup>1</sup> The Effect of Reducing Agents on the Autoxidation of Some Photographic Developing Agents
resolves10.1021/ja01199a077Oxidation Processes. XX.<sup>1</sup> The Mechanism of Autoxidation Reactions in the Presence of Foreign Catalysts and Inhibitors
resolves10.1071/CH9821133Outer-sphere electron-transfer reactions of ascorbate anions
resolves10.1073/pnas.0810352106Nonenzymatic displacement of chlorine and formation of free radicals upon the reaction of glutathione with PCB quinones
resolves10.1016/0009-2797(94)03326-4ESR evidence for the generation of reactive oxygen species from the copper-mediated oxidation of the benzene metabolite, hydroquinone: role in DNA damage
resolves10.1016/0009-2797(89)90006-9On the mechanism of the Mn3+-induced neurotoxicity of dopamine: Prevention of quinone-derived oxygen toxicity by DT diaphorase and superoxide dismutase
resolves10.1016/0165-022X(88)90100-5In the absence of catalytic metals ascorbate does not autoxidize at pH 7: ascorbate as a test for catalytic metals
resolves10.1016/S0026-895X(25)10137-5Sequential oxidation and glutathione addition to 1,4-benzoquinone: correlation of toxicity with increased glutathione substitution.
resolves10.1016/0009-2797(88)90021-XReductive addition of glutathione to p-benzoquinone, 2-hydroxy-p-benzoquinone, and p-benzoquinone epoxides. Effect of the hydroxy- and glutathionyl substituents on p-benzohydroquinone autoxidation
resolves10.1016/0009-2797(87)90003-2Reactivity of thiols towards derivatives of 2- and 6-methyl-1,4-naphthoquinone bioreductive alkylating agents
resolves10.1016/0006-2952(90)90294-UReaction kinetics of 4-methoxy ortho benzoquinone in relation to its mechanism of cytotoxicity: a pulse radiolysis study
resolves10.1021/tx950117eMetabolic Activation of PCBs to Quinones: Reactivity toward Nitrogen and Sulfur Nucleophiles and Influence of Superoxide Dismutase
resolves10.1016/0003-9861(87)90495-4Quinone toxicity in hepatocytes: Studies on mitochondrial Ca2+ release induced by benzoquinone derivatives
resolves10.1021/bi00398a025Location and activity of ubiquinone 10 and ubiquinone analogs in model and biological membranes
resolves10.1021/bi802282hReduction of Hydrophilic Ubiquinones by the Flavin in Mitochondrial NADH:Ubiquinone Oxidoreductase (Complex I) and Production of Reactive Oxygen Species
resolves10.1039/a807650bThe kinetics and thermodynamics of quinone–semiquinone–hydroquinone systems under physiological conditions
resolves10.1016/S0022-3565(24)34992-4Glutathione-Dependent Metabolism of cis-3-(9 H-Purin-6-ylthio)acrylic Acid to Yield the Chemotherapeutic Drug 6-Mercaptopurine: Evidence for Two Distinct Mechanisms in Rats
resolves10.1016/0891-5849(94)00175-JEnzymic- and thiol-mediated activation of halogen-substituted diaziridinylbenzoquinones: Redox transitions of the semiquinone and semiquinone-thioether species
resolves10.1016/j.tetlet.2009.07.149‘On water’: unprecedented nucleophilic substitution and addition reactions with 1,4-quinones in aqueous suspension
resolves10.1002/bio.1170040131Formation of electronically excited states during the interaction of<i>p</i>‐benzoquinone with hydrogen peroxide
resolves10.1073/pnas.0704030104Molecular mechanism for metal-independent production of hydroxyl radicals by hydrogen peroxide and halogenated quinones
resolves10.1016/0167-4838(93)90198-ZThe one-electron reduction potential of several substrates can be related to their reduction rates by cytochrome P-450 reductase
resolves10.1021/ja00440a008Electron exchange and electron transfer of semiquinones in aqueous solutions
resolves10.1021/j100004a023Equilibria and Rates of Redox Reactions Involving the 2-tert-Butyl-1,4-benzosemiquinone Radical in Aqueous Solution: An Investigation by Potentiometry, ESR, and Pulse Radiolysis
resolves10.1021/tx990064rSonochemistry of Quinones in Argon-Saturated Aqueous Solutions: Enhanced Cytochrome <i>c</i> Reduction
resolves10.1016/0003-9861(81)90263-0Pulse radiolysis studies of antitumor quinones: Radical lifetimes, reactivity with oxygen, and one-electron reduction potentials
resolves10.5344/ajev.2003.54.2.73Review of Reaction Mechanisms of Oxygen and Proposed Intermediate Reduction Products in Wine: Central Role of Iron and Copper
resolves10.1021/j100215a033One-electron redox potentials of phenols. Hydroxy- and aminophenols and related compounds of biological interest
resolves10.1021/j100264a032One-electron redox reactions in aqueous solutions of sulfite with hydroquinone and other hydroxyphenols
resolves10.1007/s001289900777StructureToxicity Relationships for Selected Naphthoquinones to Tetrahymena pyriformis
resolves10.1039/f19837900391Reduction of the naphthazarin molecule as studied by pulse radiolysis. Part 1.—Addition of a single electron
resolves10.1039/b802649cThe aza-analogues of 1,4-naphthoquinones are potent substrates and inhibitors of plasmodial thioredoxin and glutathione reductases and of human erythrocyte glutathione reductase
resolves10.1021/jm00158a010One-electron reduction of 2- and 6-methyl-1,4-naphthoquinone bioreductive alkylating agents
resolves10.1080/10629369508029908SAR Models for Futile Metabolism: One-Electron Reduction of Quinones, Phenols and Nitrobenzenes
resolves10.1016/j.abb.2005.03.015FAD semiquinone stability regulates single- and two-electron reduction of quinones by Anabaena PCC7119 ferredoxin:NADP+ reductase and its Glu301Ala mutant
resolves10.1016/0969-806X(94)90219-4One-electron reduction of 9, 10-anthraquinone, 1-amino-9, 10-anthraquinone and 1-hydroxy-9, 10-anthraquinone in aqueous-isopropanol-acetone mixed solvent: A pulse radiolysis study
resolves10.1039/ft9908601483One- and two-electron reduction of quinizarin and 5-methoxyquinizarin: a pulse radiolysis study
resolves10.1039/ft9918701109One-electron reactions of 1,5- and 1,8-dihydroxy-9, 10-anthraquinones. A pulse radiolysis study
resolves10.1021/ja00797a017Metal ion catalysis of oxygen transfer reactions. III. Transition metal chelates as catalysts in the oxidation of nitrosobenzene. Oxygen transfer from alkyl peroxy radicals
resolves10.1039/f19888402855Successive addition of electrons to sodium quinizarin-2- and -6-sulphonate in aqueous solution. a pulse and γ-radiolysis study
resolves10.2307/3576232Radiosensitization by Derivatives of Isoindole-4,7-Dione
resolves10.2307/3576006Radiation Sensitization and Chemical Studies on Isoindole-4,7-Diones
resolves10.1021/j150655a027The equilibrium reaction of the luminol radical with oxygen and the one-electron-reduction potential of 5-aminophthalazine-1,4-dione
resolves10.1021/ja01517a051Oxidation-Reduction Potentials, Ionization Constants and Semiquinone Formation of Indigo Sulfonates and their Reduction Products
resolves10.1039/b009652kControlling the rates of reductively-activated elimination from the (indol-3-yl)methyl position of indolequinones
resolves10.1016/0006-2952(87)90309-1The effect of the anthrapyrazole antitumour agent CI941 on rat liver microsome and cytochrome P-450 reductase mediated free radical processes
resolves10.1039/p29880000489One-electron redox chemistry of amsacrine, mAMSA [9-(2-methoxy-4-methylsulphonylaminoanilino)acridinium], its quinone di-imine, and an analogue. A radiolytic study
resolves10.1021/ja00144a014Antioxidant Potential of Gallocatechins. A Pulse Radiolysis and Laser Photolysis Study
resolves10.1039/f19736900814Semiquinone free radicals and oxygen. Pulse radiolysis study of one electron transfer equilibria
resolves10.1039/tf9716703020Pulse radiolysis studies of electron transfer in aqueous quinone solutions
The 12 references without a DOI — listed, not checked
no DOI — not checkedAnticarcinogenic activity of green tea polyphenols
no DOI — not checkedBioreductive activation of quinones: redox properties and thiol reactivity
no DOI — not checked10.1016/j.freeradbiomed.2010.05.009_bib40
no DOI — not checkedPhysical chemistry of semiquinones
no DOI — not checkedCovalent binding of 1, 2-dihaloalkanes to DNA and stability of the major DNA adduct, S-[2-(N7-guanyl)ethyl]glutathione
no DOI — not checkedActivation of hydrogen peroxide by organic compounds
no DOI — not checked10.1016/j.freeradbiomed.2010.05.009_bib100
no DOI — not checkedOne-electron reduction of juglone (5-hydroxy-1, 4-naphthoquinone)—a pulse-radiolysis study
no DOI — not checkedPulse radiolytic one-electron reduction of 1, 4-amino and hydroxy disubstituted 9, 10-anthraquinones, Int. J. Radiat. Appl. Instrum. C
no DOI — not checkedThe electron-affinity of some radiotherapeutic agents used in cancer-therapy
no DOI — not checkedAre reduced quinones necessarily involved in the antitumour activity of quinone drugs?
no DOI — not checkedOn the interaction of anisyl-3, 4-semiquinone with oxygen
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