Kinetics and Mechanisms of Hypochlorous Acid Reactions

Reactions of chlorine with inorganic and organic compounds during water treatment—Kinetics and mechanisms: A critical review

Deborde, M., & von Gunten, U. (2007) · Water Research · doi:10.1016/j.watres.2007.07.025 · Cited by 2,068 · see citing works

Free radical-mediated oxidation of free amino acids and amino acid residues in proteins

Stadtman, E. R., & Levine, R. L. (2003) · Amino Acids · doi:10.1007/s00726-003-0011-2 · Cited by 1,968 · see citing works

A Comprehensive Review on Lipid Oxidation in Meat and Meat Products

Domínguez, R., Pateiro, M., Gagaoua, M., Barba, F. J., Zhang, W., & Lorenzo, J. M. (2019) · Antioxidants · doi:10.3390/antiox8100429 · Cited by 1,943 · see citing works

Oxidation events and skin aging

Kammeyer, A., & Luiten, R. M. (2015) · Ageing Research Reviews · doi:10.1016/j.arr.2015.01.001 · Cited by 980 · see citing works

Long-Lived Emissive Probes for Time-Resolved Photoluminescence Bioimaging and Biosensing

Zhang, K. Y., Yu, Q., Wei, H., Liu, S., Zhao, Q., & Huang, W. (2018) · Chemical Reviews · doi:10.1021/acs.chemrev.7b00425 · Cited by 922 · see citing works

The pharmacology of the antioxidant lipoic acid

Biewenga, G. P., Haenen, G. R. M. M., & Bast, A. (1997) · General Pharmacology The Vascular System · doi:10.1016/s0306-3623(96)00474-0 · Cited by 844 · see citing works

Modeling the Reactions of Superoxide and Myeloperoxidase in the Neutrophil Phagosome

Winterbourn, C. C., Hampton, M. B., Livesey, J. H., & Kettle, A. J. (2006) · Journal of Biological Chemistry · doi:10.1074/jbc.m605898200 · Cited by 634 · see citing works

Mechanisms of Actions of Sodium Hypochlorite in Cleaning and Disinfection Processes

Fukuzaki, S. (2006) · Biocontrol Science · doi:10.4265/bio.11.147 · Cited by 626 · see citing works

Hypochlorite-induced oxidation of amino acids, peptides and proteins

Hawkins, C. L., Pattison, D. I., & Davies, M. J. (2003) · Amino Acids · doi:10.1007/s00726-003-0016-x · Cited by 599 · see citing works

Mammalian Heme Peroxidases: From Molecular Mechanisms to Health Implications

Davies, M. J., Hawkins, C. L., Pattison, D. I., & Rees, M. D. (2008) · Antioxidants and Redox Signaling · doi:10.1089/ars.2007.1927 · Cited by 560 · see citing works

Oxidative treatment of bromide-containing waters: Formation of bromine and its reactions with inorganic and organic compounds — A critical review

Heeb, M. B., Criquet, J., Zimmermann, S. G., & von Gunten, U. (2013) · Water Research · doi:10.1016/j.watres.2013.08.030 · Cited by 542 · see citing works

Sources of Vascular Nitric Oxide and Reactive Oxygen Species and Their Regulation

Tejero, J., Shiva, S., & Gladwin, M. T. (2019) · Physiological Reviews · doi:10.1152/physrev.00036.2017 · Cited by 541 · see citing works

Mechanism of Lipid Peroxidation in Meat and Meat Products -A Review

Min, B. R., & Ahn, D. U. (2005) · Food Science and Biotechnology · Cited by 460 · see citing works

Sulfenic acid chemistry, detection and cellular lifetime

Gupta, V., & Carroll, K. S. (2013) · Biochimica et Biophysica Acta (BBA) - General Subjects · doi:10.1016/j.bbagen.2013.05.040 · Cited by 427 · see citing works

Biomarkers of myeloperoxidase-derived hypochlorous acid

Winterbourn, C. C., & Kettle, A. J. (2000) · Free Radical Biology and Medicine · doi:10.1016/s0891-5849(00)00204-5 · Cited by 390 · see citing works

Aqueous Iron(IV)–Oxo Complex: An Emerging Powerful Reactive Oxidant Formed by Iron(II)-Based Advanced Oxidation Processes for Oxidative Water Treatment

Wang, Z., Qiu, W., Pang, S., Guo, Q., Guan, C., & Jiang, J. (2022) · Environmental Science & Technology · doi:10.1021/acs.est.1c04530 · Cited by 385 · see citing works

Kinetics of the reactions of hypochlorous acid and amino acid chloramines with thiols, methionine, and ascorbate

Peskin, A. V., & Winterbourn, C. C. (2001) · Free Radical Biology and Medicine · doi:10.1016/s0891-5849(00)00506-2 · Cited by 338 · see citing works

The Role of Myeloperoxidase in Biomolecule Modification, Chronic Inflammation, and Disease

Davies, M. J., & Hawkins, C. L. (2020) · Antioxidants & Redox Signaling · doi:10.1089/ars.2020.8030 · Cited by 332 · see citing works

Living with a Killer: The Effects of Hypochlorous Acid on Mammalian Cells

Pullar, J. M., Vissers, M. C. M., & Winterbourn, C. C. (2000) · IUBMB Life · doi:10.1080/713803731 · Cited by 315 · see citing works

Hypochlorite-induced damage to proteins: formation of nitrogen-centred radicals from lysine residues and their role in protein fragmentation

Hawkins, C. L., & Davies, M. J. (1998) · Biochemical Journal · doi:10.1042/bj3320617 · Cited by 305 · see citing works

Mechanisms of Oxidative Processes in Meat and Toxicity Induced by Postprandial Degradation Products: A Review

Papuc, C. P., GORAN, G. V., Predescu, N. C., & Nicorescu, V. (2016) · Comprehensive Reviews in Food Science and Food Safety · doi:10.1111/1541-4337.12241 · Cited by 304 · see citing works

Myeloperoxidase

Winterbourn, C. C., Vissers, M. C. M., & Kettle, A. J. (2000) · Current Opinion in Hematology · doi:10.1097/00062752-200001000-00010 · Cited by 279 · see citing works

Myeloperoxidase and its contributory role in inflammatory vascular disease

Lau, D., & Baldus, S. E. (2006) · Pharmacology & Therapeutics · doi:10.1016/j.pharmthera.2005.06.023 · Cited by 277 · see citing works

Inactivation efficiency of plasmid-encoded antibiotic resistance genes during water treatment with chlorine, UV, and UV/H2O2

Yoon, Y., Chung, H. J., Di, D. Y. W., Dodd, M. C., Hur, H., & Lee, Y. (2017) · Water Research · doi:10.1016/j.watres.2017.06.056 · Cited by 267 · see citing works

Heme-thiolate haloperoxidases: versatile biocatalysts with biotechnological and environmental significance

Hofrichter, M., & Ullrich, R. (2006) · Applied Microbiology and Biotechnology · doi:10.1007/s00253-006-0417-3 · Cited by 260 · see citing works

Singlet-oxygen-mediated amino acid and protein oxidation: Formation of tryptophan peroxides and decomposition products

Gracanin, M., Hawkins, C. L., Pattison, D. I., & Davies, M. J. (2009) · Free Radical Biology and Medicine · doi:10.1016/j.freeradbiomed.2009.04.015 · Cited by 252 · see citing works

Boronate Probes as Diagnostic Tools for Real Time Monitoring of Peroxynitrite and Hydroperoxides

Zielonka, J., Sikora, A., Hardy, M., Joseph, J., Dranka, B. P., & Kalyanaraman, B. (2012) · Chemical Research in Toxicology · doi:10.1021/tx300164j · Cited by 241 · see citing works

Bioavailability and Antioxidant Activity of Black Chokeberry ( Aronia melanocarpa ) Polyphenols: in vitro and in vivo Evidences and Possible Mechanisms of Action: A Review

Denev, P. N., Kratchanov, C. G., Čı́ž, M., Lojek, A., & Kratchanova, M. G. (2012) · Comprehensive Reviews in Food Science and Food Safety · doi:10.1111/j.1541-4337.2012.00198.x · Cited by 237 · see citing works

Reactivity of hydrogen sulfide with peroxynitrite and other oxidants of biological interest

Carballal, S., Trujillo, M., Cuevasanta, E., Bartesaghi, S., Möller, M. N., Folkes, L. K., García-Bereguiain, M. Á., Gutiérrez‐Merino, C., Wardman, P., Denicola, A., et al. (2010) · Free Radical Biology and Medicine · doi:10.1016/j.freeradbiomed.2010.10.705 · Cited by 219 · see citing works

Applications of Electrolyzed Water in Agriculture & Food Industries

Al‐Haq, M. I., Sugiyama, J., & Isobe, S. (2005) · Food Science and Technology Research · doi:10.3136/fstr.11.135 · Cited by 219 · see citing works

Oxidative damage to extracellular matrix and its role in human pathologies

Rees, M. D., Kennett, E. C., Whitelock, J. M., & Davies, M. J. (2008) · Free Radical Biology and Medicine · doi:10.1016/j.freeradbiomed.2008.03.016 · Cited by 206 · see citing works

Pathophysiology of nitric oxide and related species: free radical reactions and modification of biomolecules

Eiserich, J. P., Patel, R. P., & O’Donnell, V. B. (1998) · Molecular Aspects of Medicine · doi:10.1016/s0098-2997(99)00002-3 · Cited by 210 · see citing works

Abnormal glutathione transport in cystic fibrosis airway epithelia

Gao, L., Kim, K. J., Yankaskas, J. R., & Forman, H. J. (1999) · American Journal of Physiology-Lung Cellular and Molecular Physiology · doi:10.1152/ajplung.1999.277.1.l113 · Cited by 204 · see citing works

Biochemical and spectrophotometric significance of advanced oxidized protein products

Capeillère‐Blandin, C., Gausson, V., Descamps‐Latscha, B., & Witko‐Sarsat, V. (2004) · Biochimica et Biophysica Acta (BBA) - Molecular Basis of Disease · doi:10.1016/j.bbadis.2004.02.008 · Cited by 203 · see citing works

Hypochlorite-induced oxidation of proteins in plasma: formation of chloramines and nitrogen-centred radicals and their role in protein fragmentation

Hawkins, C. L., & Davies, M. J. (1999) · Biochemical Journal · doi:10.1042/bj3400539 · Cited by 201 · see citing works

The roles of myeloperoxidase in coronary artery disease and its potential implication in plaque rupture

Teng, N., Maghzal, G. J., Talib, J., Rashid, I., Lau, A. K., & Stocker, R. (2016) · Redox Report · doi:10.1080/13510002.2016.1256119 · Cited by 191 · see citing works

Modification of low-density lipoprotein by myeloperoxidase-derived oxidants and reagent hypochlorous acid

Malle, E., Marsche, G., Arnhold, J., & Davies, M. J. (2006) · Biochimica et Biophysica Acta (BBA) - Molecular and Cell Biology of Lipids · doi:10.1016/j.bbalip.2006.03.024 · Cited by 184 · see citing works

Reactions and reactivity of myeloperoxidase-derived oxidants: Differential biological effects of hypochlorous and hypothiocyanous acids

Pattison, D. I., Davies, M. J., & Hawkins, C. L. (2012) · Free Radical Research · doi:10.3109/10715762.2012.667566 · Cited by 176 · see citing works

Unraveling oxidation behaviors for intracellular and extracellular from different oxidants (HOCl vs. H2O2) catalyzed by ferrous iron in waste activated sludge dewatering

Yu, W., Wen, Q., Yang, J., Xiao, K., Zhu, Y., Tao, S., Lv, Y., Liang, S., Fan, W., Zhu, S., et al. (2018) · Water Research · doi:10.1016/j.watres.2018.10.033 · Cited by 175 · see citing works

Hypochlorous Acid Chemistry in Mammalian Cells—Influence on Infection and Role in Various Pathologies

Andrés, C. M. C., Pérez de la Lastra, J. M., Juan, C. A., Plou, F. J., & Pérez-Lebeña, E. (2022) · International Journal of Molecular Sciences · doi:10.3390/ijms231810735 · Cited by 166 · see citing works

Reevaluation of the rate constants for the reaction of hypochlorous acid (HOCl) with cysteine, methionine, and peptide derivatives using a new competition kinetic approach

Storkey, C., Davies, M. J., & Pattison, D. I. (2014) · Free Radical Biology and Medicine · doi:10.1016/j.freeradbiomed.2014.04.024 · Cited by 165 · see citing works

Hypochlorous acid as a precursor of free radicals in living systems

Panasenko, O. M., Gorudko, I. V., & Av, S. (2013) · Biochemistry (Moscow) · doi:10.1134/s0006297913130075 · Cited by 155 · see citing works

Characterization of the oxidation products of the reaction between reduced glutathione and hypochlorous acid

Winterbourn, C. C., & Brennan, S. O. (1997) · Biochemical Journal · doi:10.1042/bj3260087 · Cited by 146 · see citing works

The synergistic effect between hydrogen peroxide and nitrite, two long-lived molecular species from cold atmospheric plasma, triggers tumor cells to induce their own cell death

Bauer, G. (2019) · Redox Biology · doi:10.1016/j.redox.2019.101291 · Cited by 145 · see citing works

Activation of the NF-κB transcription factor in a T-lymphocytic cell line by hypochlorous acid

Schoonbroodt, S., Legrand-Poels, S., Best‐Belpomme, M., & Piette, J. G. (1997) · Biochemical Journal · doi:10.1042/bj3210777 · Cited by 143 · see citing works

Nitrite as a Substrate and Inhibitor of Myeloperoxidase

van Dalen, C. J., Winterbourn, C. C., Senthilmohan, R., & Kettle, A. J. (2000) · Journal of Biological Chemistry · doi:10.1074/jbc.275.16.11638 · Cited by 139 · see citing works

Linoleic Acid Hydroperoxide Reacts With Hypochlorous Acid, Generating Peroxyl Radical Intermediates and Singlet Molecular Oxygen

Miyamoto, S., Martinez, G. R., Rettori, D., Augusto, O., Medeiros, M. H. G., & Di Mascio, P. (2006) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0508170103 · Cited by 137 · see citing works

Neutrophil-generated oxidative stress and protein damage in Staphylococcus aureus

Beavers, W. N., & Skaar, E. P. (2016) · Pathogens and Disease · doi:10.1093/femspd/ftw060 · Cited by 126 · see citing works

Measuring chlorine bleach in biology and medicine

Kettle, A. J., Albrett, A. M., Chapman, A., Dickerhof, N., Forbes, L. V., Khalilova, I. S., & Turner, R. (2013) · Biochimica et Biophysica Acta (BBA) - General Subjects · doi:10.1016/j.bbagen.2013.07.004 · Cited by 124 · see citing works

What Are the Plasma Targets of the Oxidant Hypochlorous Acid? A Kinetic Modeling Approach

Pattison, D. I., Hawkins, C. L., & Davies, M. J. (2009) · Chemical Research in Toxicology · doi:10.1021/tx800372d · Cited by 124 · see citing works

Rapid catalytic degradation of refractory textile dyes in Fe(II)/chlorine system at near neutral pH: Radical mechanism involving chlorine radical anion (Cl2−)-mediated transformation pathways and impact of environmental matrices

Meghlaoui, F. Z., Merouani, S., Hamdaoui, O., Bouhelassa, M., & Ashokkumar, M. (2019) · Separation and Purification Technology · doi:10.1016/j.seppur.2019.115685 · Cited by 123 · see citing works

Degradation of Hyaluronic Acid, Poly- and Mono-Saccharides, and Model Compounds by Hypochlorite: Evidence for Radical Intermediates and Fragmentation

Hawkins, C. L., & Davies, M. J. (1998) · Free Radical Biology and Medicine · doi:10.1016/s0891-5849(98)00009-4 · Cited by 122 · see citing works

Sodium hypochlorite as an alternative to hydrogen peroxide in Fenton process for industrial scale

Behin, J., Akbari, A., Mahmoudi, M., & Khajeh, M. (2017) · Water Research · doi:10.1016/j.watres.2017.05.015 · Cited by 121 · see citing works

Interactions of Hypochlorous Acid with Pyrimidine Nucleotides, and Secondary Reactions of Chlorinated Pyrimidines with GSH, NADH, and Other Substrates

Prütz, W. A. (1998) · Archives of Biochemistry and Biophysics · doi:10.1006/abbi.1997.0440 · Cited by 121 · see citing works

Employment of reactive oxygen species to enhance astaxanthin formation in Chlorella zofingiensis in heterotrophic culture

Ip, P.-F., & Chen, F. (2005) · Process Biochemistry · doi:10.1016/j.procbio.2005.02.014 · Cited by 117 · see citing works

Mitigation of chlorine-induced lung injury by low-molecular-weight antioxidants

Leustik, M., Doran, S. F., Bracher, A., Williams, S., Squadrito, G. L., Schoeb, T. R., Postlethwait, E. M., & Matalon, S. (2008) · American Journal of Physiology-Lung Cellular and Molecular Physiology · doi:10.1152/ajplung.90240.2008 · Cited by 114 · see citing works

Reaction of HOCl with amino acids and peptides: EPR evidence for rapid rearrangement and fragmentation reactions of nitrogen-centred radicals

Hawkins, C. L., & Davies, M. J. (1998) · Journal of the Chemical Society Perkin Transactions 2 · doi:10.1039/a802949k · Cited by 113 · see citing works

Formation, Reactivity, and Detection of Protein Sulfenic Acids

Kettenhofen, N. J., & Wood, M. J. A. (2010) · Chemical Research in Toxicology · doi:10.1021/tx100237w · Cited by 110 · see citing works

Oxidation of neutrophil glutathione and protein thiols by myeloperoxidase-derived hypochlorous acid

Carr, A. C., & Winterbourn, C. C. (1997) · Biochemical Journal · doi:10.1042/bj3270275 · Cited by 108 · see citing works

Effect of Washing with or without Antioxidants on Quality Retention of Mackerel Fillets during Refrigerated and Frozen Storage

Richards, M. P., Kelleher, S. D., & Hultin, H. O. (1998) · Journal of Agricultural and Food Chemistry · doi:10.1021/jf980311h · Cited by 106 · see citing works

Myeloperoxidase and superoxide dismutase 2 polymorphisms comodulate the risk of hepatocellular carcinoma and death in alcoholic cirrhosis #

Nahon, P., Sutton, A., Rufat, P., Ziol, M., Akouche, H., Laguillier, C., Charnaux, N., Ganne‐Carrié, N., Grando–Lemaire, V., Nkontchou, G., et al. (2009) · Hepatology · doi:10.1002/hep.23187 · Cited by 106 · see citing works

Vitamin C protects against and reverses specific hypochlorous acid- and chloramine-dependent modifications of low-density lipoprotein

Carr, A. C., TIJERINA, T., & Frei, B. B. (2000) · Biochemical Journal · doi:10.1042/bj3460491 · Cited by 103 · see citing works

Ageing of polysulfone membranes in contact with bleach solution: Role of radical oxidation and of some dissolved metal ions

Causserand, C., Rouaix, S., Lafaille, J.-P., & Aimar, P. (2007) · Chemical Engineering and Processing - Process Intensification · doi:10.1016/j.cep.2007.08.013 · Cited by 103 · see citing works

Loss of GSH and thiol enzymes in endothelial cells exposed to sublethal concentrations of hypochlorous acid

Pullar, J. M., Winterbourn, C. C., & Vissers, M. C. M. (1999) · American Journal of Physiology-Heart and Circulatory Physiology · doi:10.1152/ajpheart.1999.277.4.h1505 · Cited by 102 · see citing works

Taurine chloramine is more selective than hypochlorous acid at targeting critical cysteines and inactivating creatine kinase and glyceraldehyde-3-phosphate dehydrogenase

Peskin, A. V., & Winterbourn, C. C. (2005) · Free Radical Biology and Medicine · doi:10.1016/j.freeradbiomed.2005.08.019 · Cited by 99 · see citing works

Elucidating mechanisms of chlorine toxicity: reaction kinetics, thermodynamics, and physiological implications

Squadrito, G. L., Postlethwait, E. M., & Matalon, S. (2010) · American Journal of Physiology-Lung Cellular and Molecular Physiology · doi:10.1152/ajplung.00077.2010 · Cited by 99 · see citing works

Role of reactive oxygen species in atherosclerosis: Lessons from murine genetic models

Nègre‐Salvayre, A., Guerby, P., Gayral, S., Laffargue, M., & Salvayre, R. (2019) · Free Radical Biology and Medicine · doi:10.1016/j.freeradbiomed.2019.10.011 · Cited by 98 · see citing works

Singlet oxygen treatment of tumor cells triggers extracellular singlet oxygen generation, catalase inactivation and reactivation of intercellular apoptosis-inducing signaling

Riethmüller, M., Burger, N., & Bauer, G. (2015) · Redox Biology · doi:10.1016/j.redox.2015.07.006 · Cited by 97 · see citing works

Peroxynitrite and myeloperoxidase leave the same footprint in protein nitration

Kettle, A. J., van Dalen, C. J., & Winterbourn, C. C. (1997) · Redox Report · doi:10.1080/13510002.1997.11747120 · Cited by 97 · see citing works

Oxidative Stress in Cystic Fibrosis: Does It Occur and Does It Matter?

van der Vliet, A., Eiserich, J. P., Marelich, G. P., Halliwell, B. B., & Cross, C. E. (1996) · Advances in pharmacology · doi:10.1016/s1054-3589(08)60996-5 · Cited by 96 · see citing works

Treatment of leachate concentrate by electrocoagulation coupled with electro-Fenton-like process: Efficacy and mechanism

Ding, J., Jiang, M., Zhao, G., Wei, L., Wang, S., & Zhao, Q. (2020) · Separation and Purification Technology · doi:10.1016/j.seppur.2020.117668 · Cited by 91 · see citing works

Glutathione Oxidation by Hypochlorous Acid in Endothelial Cells Produces Glutathione Sulfonamide as a Major Product but Not Glutathione Disulfide

Pullar, J. M., Vissers, M. C. M., & Winterbourn, C. C. (2001) · Journal of Biological Chemistry · doi:10.1074/jbc.m102088200 · Cited by 91 · see citing works

Hypochlorous Acid Stimulation of the Mitogen-Activated Protein Kinase Pathway Enhances Cell Survival

Midwinter, R. G., Vissers, M. C. M., & Winterbourn, C. C. (2001) · Archives of Biochemistry and Biophysics · doi:10.1006/abbi.2001.2530 · Cited by 90 · see citing works

Target cell–derived superoxide anions cause efficiency and selectivity of intercellular induction of apoptosis

Herdener, M., Heigold, S., Sarán, M., & Bauer, G. (2000) · Free Radical Biology and Medicine · doi:10.1016/s0891-5849(00)00422-6 · Cited by 89 · see citing works

Conversion of taurine into N-chlorotaurine (taurine chloramine) and sulphoacetaldehyde in response to oxidative stress

Cunningham, C. M., TIPTON, F. K., & DIXON, B. F. H. (1998) · Biochemical Journal · doi:10.1042/bj3300939 · Cited by 88 · see citing works

Formation of active chlorine species involving the higher oxide MOx+1 on active Ti/RuO2-IrO2 anodes: A DEMS analysis

Luna-Trujillo, M., Palma‐Goyes, R. E., Vázquez-Arenas, J. G., & Manzo‐Robledo, A. (2020) · Journal of Electroanalytical Chemistry · doi:10.1016/j.jelechem.2020.114661 · Cited by 86 · see citing works

Myeloperoxidase-induced Genomic DNA-centered Radicals

Gomez-Mejiba, S., Zhai, Z., Giménez, M. S., Ashby, M. T., Chilakapati, J., Kitchin, K. T., Mason, R. P., & Ramírez, D. C. (2010) · Journal of Biological Chemistry · doi:10.1074/jbc.m109.086579 · Cited by 86 · see citing works

Kinetics and Mechanisms of Chlorine Dioxide and Chlorite Oxidations of Cysteine and Glutathione

Ison, A., Odeh, I. N., & Margerum, D. W. (2006) · Inorganic Chemistry · doi:10.1021/ic0609554 · Cited by 86 · see citing works

l-Arginine Chlorination Products Inhibit Endothelial Nitric Oxide Production

Zhang, C., Reiter, C., Eiserich, J. P., Boersma, B. J., Parks, D. A., Beckman, J. S., Barnes, S., KIRK, M. C., Baldus, S. E., Darley-Usmar, V. M., et al. (2001) · Journal of Biological Chemistry · doi:10.1074/jbc.m100191200 · Cited by 86 · see citing works

Increasing the endogenous NO level causes catalase inactivation and reactivation of intercellular apoptosis signaling specifically in tumor cells

Bauer, G. (2015) · Redox Biology · doi:10.1016/j.redox.2015.07.017 · Cited by 85 · see citing works

Production of glutathione sulfonamide and dehydroglutathione from GSH by myeloperoxidase-derived oxidants and detection using a novel LC–MS/MS method

Harwood, D. T., Kettle, A. J., & Winterbourn, C. C. (2006) · Biochemical Journal · doi:10.1042/bj20060978 · Cited by 85 · see citing works

Chlorinated lipids and fatty acids: An emerging role in pathology

Spickett, C. M. (2007) · Pharmacology & Therapeutics · doi:10.1016/j.pharmthera.2007.06.002 · Cited by 82 · see citing works

Biochemical mechanisms and therapeutic potential of pseudohalide thiocyanate in human health

Chandler, J. D., & Day, B. J. (2015) · Free Radical Research · doi:10.3109/10715762.2014.1003372 · Cited by 82 · see citing works

Selenium-containing indolyl compounds: Kinetics of reaction with inflammation-associated oxidants and protective effect against oxidation of extracellular matrix proteins

Casaril, A. M., Ignasiak, M. T., Chuang, C. Y., Vieira, B. M., Padilha, N. B., Carroll, L., Lenardao, E. J., Savegnago, L., & Davies, M. J. (2017) · Free Radical Biology and Medicine · doi:10.1016/j.freeradbiomed.2017.10.344 · Cited by 80 · see citing works

Oxidation of phosphorothioate DNA modifications leads to lethal genomic instability

Kellner, S. M., DeMott, M. S., Cheng, C. P., Russell, B. S., Cao, B., You, D., & Dedon, P. C. (2017) · Nature Chemical Biology · doi:10.1038/nchembio.2407 · Cited by 79 · see citing works

pH effect on the formation of THM and HAA disinfection byproducts and potential control strategies for food processing

Hung, Y., Waters, B. W., Yemmireddy, V. K., & Huang, C. (2017) · Journal of Integrative Agriculture · doi:10.1016/s2095-3119(17)61798-2 · Cited by 78 · see citing works

Relative reactivities ofN-chloramines and hypochlorous acid with human plasma constituents

Carr, A. C., Hawkins, C. L., Thomas, S. R., Stocker, R., & Frei, B. B. (2001) · Free Radical Biology and Medicine · doi:10.1016/s0891-5849(00)00495-0 · Cited by 77 · see citing works

Comparative investigation of diclofenac degradation by Fe2+/chlorine and Fe2+/PMS processes

Gao, Y.-Q., Rao, Y.-Y., Ning, H., Chen, J., Zeng, Q., Tian, F.-X., & Gao, N. (2022) · Separation and Purification Technology · doi:10.1016/j.seppur.2022.121555 · Cited by 74 · see citing works

Treatment of organic wastewater containing nitrogen and chlorine by combinatorial electrochemical system: Taking biologically treated landfill leachate treatment as an example

Deng, Y., Chen, N., Feng, C., Chen, F., Wang, H., Kuang, P., Feng, Z., Liu, T., Gao, Y., & Hu, W. (2019) · Chemical Engineering Journal · doi:10.1016/j.cej.2019.01.176 · Cited by 74 · see citing works

Parthenolide induces significant apoptosis and production of reactive oxygen species in high-risk pre-B leukemia cells

Zunino, S. J., Ducore, J. M., & Storms, D. H. (2007) · Cancer Letters · doi:10.1016/j.canlet.2007.03.002 · Cited by 73 · see citing works

Hypochlorous Acid-Induced DNA Base Modification: Potentiation by Nitrite: Biomarkers of DNA Damage by Reactive Oxygen Species

Whiteman, M., Spencer, J. P. E., Jenner, A. M., & Halliwell, B. B. (1999) · Biochemical and Biophysical Research Communications · doi:10.1006/bbrc.1999.0448 · Cited by 73 · see citing works

Endothelial dysfunction is induced by proinflammatory oxidant hypochlorous acid

Zhang, C., Patel, R. P., Eiserich, J. P., Zhou, F., Kelpke, S. S., Ma, W., Parks, D. A., Darley-Usmar, V. M., & White, C. R. (2001) · American Journal of Physiology-Heart and Circulatory Physiology · doi:10.1152/ajpheart.2001.281.4.h1469 · Cited by 73 · see citing works

In vitro protective effect of Rhodiola rosea extract against hypochlorous acid‐induced oxidative damage in human erythrocytes

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