Activity of thiols as singlet molecular oxygen quenchers

GLUTATHIONE

Meister, A., & Anderson, M. E. (1983) · Annual Review of Biochemistry · doi:10.1146/annurev.bi.52.070183.003431 · Cited by 5,694 · see citing works

Levels of glutathione, glutathione reductase and glutathione S-transferase activities in rat lung and liver

MORON, M., DePierre, J. W., & Mannervik, B. (1979) · Biochimica et Biophysica Acta (BBA) - General Subjects · doi:10.1016/0304-4165(79)90289-7 · Cited by 4,214 · see citing works

Lycopene as the most efficient biological carotenoid singlet oxygen quencher

Mascio, P. D., Kaiser, S., & Sies, H. (1989) · Archives of Biochemistry and Biophysics · doi:10.1016/0003-9861(89)90467-0 · Cited by 2,238 · see citing works

Biochemistry of Oxidative Stress

Sies, H. (1986) · Angewandte Chemie International Edition in English · doi:10.1002/anie.198610581 · Cited by 1,316 · see citing works

High-performance liquid chromatography analysis of nanomole levels of glutathione, glutathione disulfide, and related thiols and disulfides

Reed, D. J., Babson, J. R., Beatty, P. W., Brodie, A. E., Ellis, W. W., & Potter, D. W. (1980) · Analytical Biochemistry · doi:10.1016/0003-2697(80)90118-9 · Cited by 1,178 · see citing works

Chemistry of singlet oxygen. X. Carotenoid quenching parallels biological protection

Foote, C. S., Chang, Y. C., & Denny, R. W. (1970) · Journal of the American Chemical Society · doi:10.1021/ja00720a036 · Cited by 418 · see citing works

Solvent Deuterium Isotope Effects on Acid-Base Equilibria

Salomaa, P., Schaleger, L. L., & Long, F. A. (1964) · Journal of the American Chemical Society · doi:10.1021/ja01055a001 · Cited by 300 · see citing works

Singlet oxygen production by biological systems

Kanofsky, J. R. (1989) · Chemico-Biological Interactions · doi:10.1016/0009-2797(89)90059-8 · Cited by 259 · see citing works

Oxidation of glutathione by the superoxide radical to the disulfide and the sulfonate yielding singlet oxygen

Wefers, H., & Sies, H. (1983) · European Journal of Biochemistry · doi:10.1111/j.1432-1033.1983.tb07791.x · Cited by 229 · see citing works

[59] Glutathione disulfide (GSSG) efflux from cells and tissues

Sies, H., & Akerboom, T. P. M. (1984) · Methods in enzymology on CD-ROM/Methods in enzymology · doi:10.1016/s0076-6879(84)05062-x · Cited by 197 · see citing works

Quantification of singlet oxygen generated by thermolysis of 3,3'-(1,4-naphthylene)dipropionate endoperoxide. Monomol and dimol photoemission and the effects of 1,4-diazabicyclo[2.2.2]octane

Mascio, P. D., & Sies, H. (1989) · Journal of the American Chemical Society · doi:10.1021/ja00190a027 · Cited by 178 · see citing works

Physical and chemical scavenging of singlet molecular oxygen by tocopherols

Kaiser, S., Mascio, P. D., Murphy, M. E., & Sies, H. (1990) · Archives of Biochemistry and Biophysics · doi:10.1016/0003-9861(90)90556-e · Cited by 175 · see citing works

CHEMICAL REACTION RATES OF AMINO ACIDS WITH SINGLET OXYGEN

Matheson, I. B. C., & Lee, J. (1979) · Photochemistry and Photobiology · doi:10.1111/j.1751-1097.1979.tb07786.x · Cited by 167 · see citing works

Low Level Chemiluminescence of Liver Microsomal Fractions Initiated by tert‐Butyl Hydroperoxide

Cadenas, E., & Sies, H. (1982) · European Journal of Biochemistry · doi:10.1111/j.1432-1033.1982.tb06599.x · Cited by 162 · see citing works

DEACTIVATION OF SINGLET MOLECULAR OXYGEN BY THIOLS AND RELATED COMPOUNDS, POSSIBLE PROTECTORS AGAINST SKIN PHOTOSENSITIVITY

Rougée, M., Bensasson, R. V., Land, E. J., & Parienté, R. (1988) · Photochemistry and Photobiology · doi:10.1111/j.1751-1097.1988.tb08835.x · Cited by 160 · see citing works

CHEMISTRY OF SINGLET OXYGEN—XXV. PHOTOOXYGENATION OF METHIONINE*

Sysak, P. K., Foote, C. S., & Ching, T. (1977) · Photochemistry and Photobiology · doi:10.1111/j.1751-1097.1977.tb07443.x · Cited by 146 · see citing works

THE PRODUCTION OF SINGLET MOLECULAR OXYGEN BY ZINC(II) PHTHALOCYANINE IN ETHANOL AND IN UNILAMELLAR VESICLES. CHEMICAL QUENCHING AND PHOSPHORESCENCE STUDIES

Valduga, G., Nonell, S., Reddi, E., Jori, G., & Braslavsky, S. E. (1988) · Photochemistry and Photobiology · doi:10.1111/j.1751-1097.1988.tb02778.x · Cited by 122 · see citing works

Oxidation of glutathione by hydrogen peroxide and other oxidizing agents

Finley, J. W., Wheeler, E. L., & Witt, S. C. (1981) · Journal of Agricultural and Food Chemistry · doi:10.1021/jf00104a045 · Cited by 114 · see citing works

Singlet molecular oxygen causes loss of biological activity in plasmid and bacteriophage DNA and induces single-strand breaks

Mascio, P. D., Wefers, H., Do-Thi, H.-P., Lafleur, M. V. M., & Sies, H. (1989) · Biochimica et Biophysica Acta (BBA) - Gene Structure and Expression · doi:10.1016/0167-4781(89)90033-x · Cited by 113 · see citing works

SINGLET OXYGEN INDUCES FRANK STRAND BREAKS AS WELL AS ALKALI‐ AND PIPERIDINE‐LABILE SITES IN SUPERCOILED PLASMID DNA

Blazek, E. R., Peak, J. G., & Peak, M. J. (1989) · Photochemistry and Photobiology · doi:10.1111/j.1751-1097.1989.tb08431.x · Cited by 88 · see citing works

DNA damage by oxygen radicals and excited state species: A comparative study using enzymatic probes in vitro

Epe, B., Mützel, P., & Adam, W. (1988) · Chemico-Biological Interactions · doi:10.1016/0009-2797(88)90094-4 · Cited by 73 · see citing works

Loss of transforming activity of plasmid DNA (pBR322) in E. coli caused by singlet molecular oxygen

Wefers, H., Schulte‐Frohlinde, D., & Sies, H. (1987) · FEBS Letters · doi:10.1016/0014-5793(87)81272-3 · Cited by 61 · see citing works

Protection of DNA by thiols

Fahey, R. C. (1988) · Pharmacology & Therapeutics · doi:10.1016/0163-7258(88)90047-2 · Cited by 59 · see citing works

Zur Biochemie der Thiolgruppe: Bedeutung des Glutathions

Sies, H. (1989) · Die Naturwissenschaften · doi:10.1007/bf00396705 · Cited by 59 · see citing works

Oxidation of .alpha.-lipoic acid

Stary, F. E., Jindal, S. L., & Murray, R. W. (1975) · The Journal of Organic Chemistry · doi:10.1021/jo00889a013 · Cited by 54 · see citing works

SINGLET MOLECULAR OXYGEN INDUCED MUTAGENICITY IN A MAMMALIAN SV40‐BASED SHUTTLE VECTOR

Mascio, P. D., Menck, C. F. M., Nigro, R. G., Sarasin, A. R., & Sies, H. (1990) · Photochemistry and Photobiology · doi:10.1111/j.1751-1097.1990.tb01713.x · Cited by 47 · see citing works

Some derivatives of glutathione

CALAM, D., & Waley, S. G. (1962) · Biochemical Journal · doi:10.1042/bj0850417 · Cited by 41 · see citing works

Importance of thymol, methyl N-methylanthranilate, and monoterpene hydrocarbons to the aroma and flavor of mandarin cold-pressed oils

Wilson, C. W., & Shaw, P. E. (1981) · Journal of Agricultural and Food Chemistry · doi:10.1021/jf00105a014 · Cited by 39 · see citing works

Mutarotase. Photooxidation reactions and nature of the enzyme catalysis

Fishman, P. H., Kusiak, J. W., & Bailey, J. M. (1973) · Biochemistry · doi:10.1021/bi00737a027 · Cited by 20 · see citing works

Cytotoxic and genotoxic effects of extracellular generated singlet oxygen in human lymphocytes in vitro

Decuyper-Debergh, D., Piette, J. G., Laurent, C., & VORST, A. V. D. (1989) · Mutation Research Letters · doi:10.1016/0165-7992(89)90025-0 · Cited by 20 · see citing works

ChemInform Abstract: Photooxidation of Sulfur Compounds

ANDO, W., & Takata, T. (1986) · ChemInform · doi:10.1002/chin.198605341 · Cited by 20 · see citing works

Biological effects of singlet delta oxygen on respiratory tract epithelium

Eisenberg, W. C., Taylor, K., & Schiff, L. J. (1984) · Cellular and Molecular Life Sciences · doi:10.1007/bf01952414 · Cited by 18 · see citing works

SINGLET OXYGEN INDUCED MUTAGENESIS OF BENZO[α]PYRENE DERIVATIVES

Seed, J. L., Specht, K. G., Dahl, T. A., & Midden, W. R. (1989) · Photochemistry and Photobiology · doi:10.1111/j.1751-1097.1989.tb04318.x · Cited by 16 · see citing works

Interactions of Oxygen and Sulfhydryls with Free Radicals in Irradiated Mammalian Cells

Held, K. D. (1988) · Springer eBooks · doi:10.1007/978-1-4684-5568-7_68 · Cited by 4 · see citing works

Glutathione and its role in cellular functions

Sies, H. (1999) · Free Radical Biology and Medicine · doi:10.1016/s0891-5849(99)00177-x · Cited by 1,735 · see citing works

Antimicrobial strategies centered around reactive oxygen species – bactericidal antibiotics, photodynamic therapy, and beyond

Vatansever, F., Melo, W., Avci, P., Vecchio, D., Sadasivam, M., Gupta, A., Chandran, R., Karimi, M., Parizotto, N. A., Yin, R., et al. (2013) · FEMS Microbiology Reviews · doi:10.1111/1574-6976.12026 · Cited by 1,134 · see citing works

Vitamins E and C, beta-carotene, and other carotenoids as antioxidants

Sies, H., & Stahl, W. (1995) · American Journal of Clinical Nutrition · doi:10.1093/ajcn/62.6.1315s · Cited by 1,075 · see citing works

Antioxidant Functions of Vitamins

Sies, H., Stahl, W., & Sundquist, A. R. (1992) · Annals of the New York Academy of Sciences · doi:10.1111/j.1749-6632.1992.tb17085.x · Cited by 827 · see citing works

Antioxidant defense systems: the role of carotenoids, tocopherols, and thiols

Mascio, P. D., Murphy, M., & Sies, H. (1991) · American Journal of Clinical Nutrition · doi:10.1093/ajcn/53.1.194s · Cited by 776 · see citing works

Singlet Molecular Oxygen Reactions with Nucleic Acids, Lipids, and Proteins

Mascio, P. D., Martinez, G. R., Miyamoto, S., Ronsein, G. E., de Medeiros, M. H. G., & Cadet, J. (2019) · Chemical Reviews · doi:10.1021/acs.chemrev.8b00554 · Cited by 665 · see citing works

Redox Signaling by Reactive Electrophiles and Oxidants

Parvez, S., Long, M. J. C., Poganik, J. R., & Aye, Y. (2018) · Chemical Reviews · doi:10.1021/acs.chemrev.7b00698 · Cited by 357 · see citing works

Caffeine as an Antioxidant: Inhibition of Lipid Peroxidation Induced by Reactive Oxygen Species

Devasagayam, T. P. A., Kamat, J. P., Mohan, H., & Kesavan, P. C. (1996) · Biochimica et Biophysica Acta (BBA) - Biomembranes · doi:10.1016/0005-2736(96)00040-5 · Cited by 331 · see citing works

Chilling-enhanced photooxidation: The production, action and study of reactive oxygen species produced during chilling in the light

Wise, R. R. (1995) · Photosynthesis Research · doi:10.1007/bf00032579 · Cited by 323 · see citing works

Reactive Sulfur Species: An Emerging Concept in Oxidative Stress

Giles, G. I., & Jacob, C. (2002) · Biological Chemistry · doi:10.1515/bc.2002.042 · Cited by 314 · see citing works

Formation of 8-hydroxy(deoxy)guanosine and generation of strand breaks at guanine residues in DNA by singlet oxygen

Devasagayam, T. P. A., Steenken, S., Obendorf, M. S. W., Schulz, W. A., & Sies, H. (1991) · Biochemistry · doi:10.1021/bi00239a029 · Cited by 304 · see citing works

The biology of ergothioneine, an antioxidant nutraceutical

Borodina, I., Kenny, L. C., McCarthy, C. M., Paramasivan, K., Pretorius, E., Roberts, T. J., van der Hoek, S. A., & Kell, D. B. (2020) · Nutrition Research Reviews · doi:10.1017/s0954422419000301 · Cited by 296 · see citing works

Singlet oxygen induced DNA damage

Sies, H., & Menck, C. F. M. (1992) · Mutation Research/DNAging · doi:10.1016/0921-8734(92)90039-r · Cited by 264 · see citing works

Visible-Light-Mediated Modification and Manipulation of Biomacromolecules

Lechner, V. M., Nappi, M., Deneny, P. J., Folliet, S., Chu, J. C. K., & Gaunt, M. J. (2021) · Chemical Reviews · doi:10.1021/acs.chemrev.1c00357 · Cited by 226 · see citing works

Photosensitization Reactions of Biomolecules: Definition, Targets and Mechanisms

Baptista, M. S., Cadet, J., Greer, A., & Thomas, A. H. (2021) · Photochemistry and Photobiology · doi:10.1111/php.13470 · Cited by 205 · see citing works

Photo-oxidation of phenol and monochlorophenols in oxygen-saturated aqueous solutions by different photosensitizers

Gerdes, R., Wöhrle, D., Spiller, W., Schneider, G., Schnurpfeil, G., & Schulz‐Ekloff, G. (1997) · Journal of Photochemistry and Photobiology A Chemistry · doi:10.1016/s1010-6030(97)00209-8 · Cited by 199 · see citing works

Singlet oxygen-induced signaling effects in mammalian cells

Klotz, L., Kröncke, K., & Sies, H. (2003) · Photochemical & Photobiological Sciences · doi:10.1039/b210750c · Cited by 185 · see citing works

Elevated Carbon Dioxide Increases Contents of Antioxidant Compounds in Field-Grown Strawberries

Wang, S. Y., Bunce, J. A., & Maas, J. L. (2003) · Journal of Agricultural and Food Chemistry · doi:10.1021/jf021172d · Cited by 184 · see citing works

Metal-Free Visible-Light-Mediated Oxidative Cross-Coupling of Thiols with P(O)H Compounds Using Air as the Oxidant

Sun, J., Yang, H. Q., Li, P., & Zhang, B. (2016) · Organic Letters · doi:10.1021/acs.orglett.6b02563 · Cited by 150 · see citing works

Chemoptogenetic damage to mitochondria causes rapid telomere dysfunction

Qian, W., Kumar, N., Roginskaya, V. Y., Fouquerel, E., Opresko, P. L., Shiva, S., Watkins, S. C., Kolodieznyi, D., Bakkenist, C. J., Bruchez, M. P., et al. (2019) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1910574116 · Cited by 149 · see citing works

Singlet Oxygen Stress in Microorganisms

Glaeser, J., Nuss, A. M., Berghoff, B. A., & Klug, G. (2011) · Advances in microbial physiology/Advances in Microbial Physiology · doi:10.1016/b978-0-12-381043-4.00004-0 · Cited by 146 · see citing works

Cascading of Molecular Logic Gates for Advanced Functions: A Self‐Reporting, Activatable Photosensitizer

Erbaş-Çakmak, S., & Akkaya, E. U. (2013) · Angewandte Chemie International Edition · doi:10.1002/anie.201306177 · Cited by 145 · see citing works

Redox Mechanisms in Neurodegeneration: From Disease Outcomes to Therapeutic Opportunities

Sbodio, J. I., Snyder, S. H., & Paul, B. D. (2018) · Antioxidants and Redox Signaling · doi:10.1089/ars.2017.7321 · Cited by 143 · see citing works

Reactive oxygen species: Reactions and detection from photosynthetic tissues

Mattila, H., Khorobrykh, S. A., Havurinne, V., & Tyystjärvi, E. (2015) · Journal of Photochemistry and Photobiology B Biology · doi:10.1016/j.jphotobiol.2015.10.001 · Cited by 135 · see citing works

Contribution of culture media to oxidative stress and its effect on human oocytes

Martı́n-Romero, F. J., Miguel-Lasobras, E. M., Domínguez-Arroyo, J. A., González-Carrera, E., & Álvarez, I. S. (2008) · Reproductive BioMedicine Online · doi:10.1016/s1472-6483(10)60312-4 · Cited by 137 · see citing works

Antioxidants of Non-Enzymatic Nature: Their Function in Higher Plant Cells and the Ways of Boosting Their Biosynthesis

Rudenko, N. N., Vetoshkina, D. V., Marenkova, T. V., & Borisova‐Mubarakshina, M. M. (2023) · Antioxidants · doi:10.3390/antiox12112014 · Cited by 135 · see citing works

Characterization of Photoactivated Singlet Oxygen Damage in Single-Molecule Optical Trap Experiments

Landry, M. P., McCall, P. M., Qi, Z., & Chemla, Y. R. (2009) · Biophysical Journal · doi:10.1016/j.bpj.2009.07.048 · Cited by 133 · see citing works

Redox Chemistry of Biological Thiols

Nagy, P., & Winterbourn, C. C. (2010) · Advances in molecular toxicology · doi:10.1016/s1872-0854(10)04006-3 · Cited by 125 · see citing works

Damage to plasmid DNA by singlet oxygen and its protection

Sies, H. (1993) · Mutation Research/Genetic Toxicology · doi:10.1016/0165-1218(93)90095-u · Cited by 118 · see citing works

Degradation of Chlorophenols by Supported Co–Mg–Al Layered Double Hydrotalcite with Bicarbonate Activated Hydrogen Peroxide

Ali, J., Lu, X., Chen, Z., & Yin, G. (2014) · The Journal of Physical Chemistry A · doi:10.1021/jp5085313 · Cited by 117 · see citing works

Enabling In Vivo Photocatalytic Activation of Rapid Bioorthogonal Chemistry by Repurposing Silicon-Rhodamine Fluorophores as Cytocompatible Far-Red Photocatalysts

Wang, C., Zhang, H., Zhang, T., Zou, X., Wang, H., Rosenberger, J. E., Vannam, R., Trout, W. S., Grimm, J. B., Lavis, L. D., et al. (2021) · Journal of the American Chemical Society · doi:10.1021/jacs.1c05547 · Cited by 115 · see citing works

The Reactive Sulfur Species Concept: 15 Years On

Giles, G. I., Nasim, M. J., Ali, W., & Jacob, C. (2017) · Antioxidants · doi:10.3390/antiox6020038 · Cited by 113 · see citing works

Chemopreventive Effects of Cuminum cyminum in Chemically Induced Forestomach and Uterine Cervix Tumors in Murine Model Systems

Gagandeep, Dhanalakshmi, S., Mendiz, E., Rao, A. R., & Kale, R. K. (2003) · Nutrition and Cancer · doi:10.1207/s15327914nc4702_10 · Cited by 112 · see citing works

Reaction of phenol with singlet oxygen

Al-Nu’airat, J., Dlugogorski, B. Z., Gao, X., Zeinali, N., Skut, J., Westmoreland, P. R., Oluwoye, I., & Altarawneh, M. (2018) · Physical Chemistry Chemical Physics · doi:10.1039/c8cp04852e · Cited by 109 · see citing works

Phosphoinositide 3-kinase signaling in the cellular response to oxidative stress

Barthel, A., & Klotz, L. (2005) · Biological Chemistry · doi:10.1515/bc.2005.026 · Cited by 106 · see citing works

Regulatory Control or Oxidative Damage? Proteomic Approaches to Interrogate the Role of Cysteine Oxidation Status in Biological Processes

Held, J. M., & Gibson, B. W. (2011) · Molecular & Cellular Proteomics · doi:10.1074/mcp.r111.013037 · Cited by 103 · see citing works

Nonenzymatic Antioxidant Defense Systems

Briviba, K., & Sies, H. (1994) · Elsevier eBooks · doi:10.1016/b978-0-08-057168-3.50010-2 · Cited by 103 · see citing works

PHOTOOXIDATION OF 2‐MERCAPTOETHANOL BY VARIOUS WATER‐SOLUBLE PHTHALOCYANINES IN AQUEOUS ALKALINE SOLUTION UNDER IRRADIATION WITH VISIBLE LIGHT

Schneider, G., Wöhrle, D., Spiller, W., Stark, J., & Schulz‐Ekloff, G. (1994) · Photochemistry and Photobiology · doi:10.1111/j.1751-1097.1994.tb05112.x · Cited by 102 · see citing works

Controlled leaching with prolonged activity for Co–LDH supported catalyst during treatment of organic dyes using bicarbonate activation of hydrogen peroxide

Ali, J., Li, Y., Lu, X., Chen, Z., Liu, W., & Yin, G. (2015) · Journal of Hazardous Materials · doi:10.1016/j.jhazmat.2015.02.056 · Cited by 101 · see citing works

Nuclear and Cytoplasmic Functions of Vitamin C

Zhitkovich, A. (2020) · Chemical Research in Toxicology · doi:10.1021/acs.chemrestox.0c00348 · Cited by 106 · see citing works

Oxidant-Induced Signaling: Effects of Peroxynitrite and Singlet Oxygen

Klotz, L. (2002) · Biological Chemistry · doi:10.1515/bc.2002.047 · Cited by 99 · see citing works

Photochemical and Nonphotochemical Transformations of Cysteine with Dissolved Organic Matter

Chu, C., Erickson, P. R., Lundeen, R. A., Stamatelatos, D., Alaimo, P. J., Latch, D. E., & McNeill, K. (2016) · Environmental Science & Technology · doi:10.1021/acs.est.6b01291 · Cited by 93 · see citing works

Protective effect of dl-α-lipoic acid in cyclophosphamide induced oxidative injury in rat testis

Elangovan, S., Prahalathan, C., Mythili, Y., & Varalakshmi, P. (2004) · Reproductive Toxicology · doi:10.1016/j.reprotox.2004.06.015 · Cited by 79 · see citing works

Prevention of singlet oxygen-induced DNA damage by lipoate

Devasagayam, T. P. A., Subramanian, M., Pradhan, D. S., & Sies, H. (1993) · Chemico-Biological Interactions · doi:10.1016/0009-2797(93)90113-d · Cited by 77 · see citing works

Singlet Oxygen Signaling: From Intimate to Global

Kochevar, I. E. (2004) · Science s STKE · doi:10.1126/stke.2212004pe7 · Cited by 76 · see citing works

Singlet oxygen‐triggered chloroplast‐to‐nucleus retrograde signalling pathways: An emerging perspective

Dogra, V., Rochaix, J., & Kim, C. (2018) · Plant Cell & Environment · doi:10.1111/pce.13332 · Cited by 76 · see citing works

Reactive sulphur species: an in vitro investigation of the oxidation properties of disulphide S-oxides

Giles, G. I., Tasker, K. M., Collins, C. A., Giles, N. M., O'ROURKE, E., & Jacob, C. (2002) · Biochemical Journal · doi:10.1042/bj20011882 · Cited by 75 · see citing works

Revisiting the reactions of superoxide with glutathione and other thiols

Winterbourn, C. C. (2016) · Archives of Biochemistry and Biophysics · doi:10.1016/j.abb.2015.11.028 · Cited by 75 · see citing works

Phthalocyanine Thio‐Pyridinium Derivatives as Antibacterial Photosensitizers†

Pereira, J. B., Carvalho, E. F. A., Faustino, M. A. F., Fernandes, R., Neves, M. G. P. M. S., Cavaleiro, J. A. S., Gomes, N. C. M., Cunha, Â., Almeida, A., & Tomé, J. P. C. (2012) · Photochemistry and Photobiology · doi:10.1111/j.1751-1097.2012.01113.x · Cited by 71 · see citing works

The Ambivalent Role of Glutathione in the Protection of Dna Against Singlet Oxygen

Lafleur, M. V. M., Hoorweg, J. J., Joenje, H., Westmijze, E. J., & Retèl, J. (1994) · Free Radical Research · doi:10.3109/10715769409056550 · Cited by 68 · see citing works

Visible light photoredox catalyzed thiophosphate synthesis using methylene blue as a promoter

Zhang, H., Zhan, Z., Lin, Y., Shi, Y., Li, G., Wang, Q., Deng, Y., Hai, L., & Wu, Y. (2018) · Organic Chemistry Frontiers · doi:10.1039/c7qo01082f · Cited by 64 · see citing works

Novel Amplex Red Oxidases Based on Noncanonical DNA Structures: Property Studies and Applications in MicroRNA Detection

Wang, S., Fu, B., Wang, J., Long, Y., Zhang, X., Peng, S., Guo, P., Tian, T., & Zhou, X. (2014) · Analytical Chemistry · doi:10.1021/ac402535a · Cited by 62 · see citing works

Photo-oxidation of sodium sulfide by sulfonated phthalocyanines in oxygen-saturated aqueous solutions containing detergents or latexes

Spiller, W., Wöhrle, D., Schulz‐Ekloff, G., Ford, W. T., Schneider, G., & Stark, J. (1996) · Journal of Photochemistry and Photobiology A Chemistry · doi:10.1016/1010-6030(95)04248-2 · Cited by 62 · see citing works

Methylene blue plus light-induced lipid peroxidation in rat liver microsomes: inhibition by nicotinamide (vitamin B3) and other antioxidants

Kamat, J. P., & Devasagayam, T. P. A. (1996) · Chemico-Biological Interactions · doi:10.1016/0009-2797(95)03653-9 · Cited by 62 · see citing works

Proof-of-principle for two-stage photodynamic therapy: hypoxia triggered release of singlet oxygen

Ayan, S., Günaydın, G., Yeşilgül, N., Gedik, M. E., Seven, Ö., & Akkaya, E. U. (2020) · Chemical Communications · doi:10.1039/d0cc06031c · Cited by 60 · see citing works

Protection of plasmid pBR322 DNA by flavonoids against single-strand breaks induced by singlet molecular oxygen

Devasagayam, T. P. A., Subramanian, M., Singh, B. B., Ramanathan, R., & Das, N. P. (1995) · Journal of Photochemistry and Photobiology B Biology · doi:10.1016/1011-1344(95)07159-y · Cited by 59 · see citing works

[40] Assay of lycopene and other carotenoids as singlet oxygen quenchers

Mascio, P. D., Sundquist, A. R., Devasagayam, T. P. A., & Sies, H. (1992) · Methods in enzymology on CD-ROM/Methods in enzymology · doi:10.1016/0076-6879(92)13144-m · Cited by 59 · see citing works

Enzyme responsive luminescent ruthenium( ii ) cephalosporin probe for intracellular imaging and photoinactivation of antibiotics resistant bacteria

Shao, Q., & Xing, B. (2011) · Chemical Communications · doi:10.1039/c1cc16165b · Cited by 56 · see citing works

Cell Metabolism - Cell Homeostasis and Stress Response

Bubulya, P. A. (2012) · InTech eBooks · doi:10.5772/1081 · Cited by 56 · see citing works

Photodynamic inactivation of methicillin-resistant Staphylococcus aureus and Escherichia coli: A metalloporphyrin comparison

Skwor, T., Klemm, S., Zhang, H., Schardt, B., Blaszczyk, S. A., & Bork, M. A. (2016) · Journal of Photochemistry and Photobiology B Biology · doi:10.1016/j.jphotobiol.2016.10.016 · Cited by 56 · see citing works

New noncellular fluorescence microplate screening assay for scavenging activity against singlet oxygen

Costa, D. M., Fernandes, E. G. R., Santos, J. L. M., Pinto, D. C. G. A., Silva, A. M. S., & Lima, J. L. F. C. (2007) · Analytical and Bioanalytical Chemistry · doi:10.1007/s00216-006-0998-9 · Cited by 54 · see citing works

Ergothioneine stands out from hercynine in the reaction with singlet oxygen: Resistance to glutathione and TRIS in the generation of specific products indicates high reactivity

Stoffels, C., Oumari, M., Perrou, A., Termath, A. O., Schlundt, W., Schmalz, H., Schäfer, M., Wewer, V., Metzger, S. U., Schömig, E., et al. (2017) · Free Radical Biology and Medicine · doi:10.1016/j.freeradbiomed.2017.10.372 · Cited by 54 · see citing works

Singlet oxygen triplet energy transfer-based imaging technology for mapping protein–protein proximity in intact cells

To, T., Fadul, M. J., & Shu, X. (2014) · Nature Communications · doi:10.1038/ncomms5072 · Cited by 54 · see citing works

Multiple free-radical scavenging capacity in serum

Oowada, S., Endo, N., Kameya, H., Shimmei, M., & Kotake, Y. (2012) · Journal of Clinical Biochemistry and Nutrition · doi:10.3164/jcbn.11-113 · Cited by 52 · see citing works

Degradation of Hyaluronic Acid by Photosensitized Riboflavin In Vitro. Modulation of the Effect by Transition Metals, Radical Quenchers, and Metal Chelators

Frati, E., Khatib, A., Front, P., Panasyuk, A., Aprile, F., & Mitrovic, D. R. (1997) · Free Radical Biology and Medicine · doi:10.1016/s0891-5849(96)00525-4 · Cited by 52 · see citing works

Specific inactivation of cysteine protease-type cathepsin by singlet oxygen generated from naphthalene endoperoxides

Nagaoka, Y., Otsu, K., Okada, F., Sato, K., Ohba, Y., Kotani, N., & Fujii, J. (2005) · Biochemical and Biophysical Research Communications · doi:10.1016/j.bbrc.2005.03.146 · Cited by 50 · see citing works

Photoreactivity of Amino Acids: Tryptophan-induced Photochemical Events via Reactive Oxygen Species Generation

Igarashi, N., Onoue, S., & Tsuda, Y. (2007) · Analytical Sciences · doi:10.2116/analsci.23.943 · Cited by 49 · see citing works

Knockout of the ergothioneine transporter ETT in zebrafish results in increased 8-oxoguanine levels

Pfeiffer, C., Bach, M., Bauer, T., da Ponte, J. C., Schömig, E., & Gründemann, D. (2015) · Free Radical Biology and Medicine · doi:10.1016/j.freeradbiomed.2015.02.026 · Cited by 49 · see citing works

Protective effect of aqueous garlic extract against oxidative organ damage in a rat model of thermal injury

Şener, G., Şatýroğlu, H., Şehirli, A. Ö., & Kaçmaz, A. (2003) · Life Sciences · doi:10.1016/s0024-3205(03)00236-4 · Cited by 48 · see citing works

Ergothioneine: new functional factor in fermented foods

Xiong, K., Xue, S., Guo, H., Dai, Y., Ji, C., Dong, L., & Zhang, S. (2023) · Critical Reviews in Food Science and Nutrition · doi:10.1080/10408398.2023.2185766 · Cited by 47 · see citing works

A Photosensitized Singlet Oxygen (1O2) Toolbox for Bio-Organic Applications: Tailoring 1O2 Generation for DNA and Protein Labelling, Targeting and Biosensing

Aerssens, D., Cadoni, E., Tack, L., & Madder, A. (2022) · Molecules · doi:10.3390/molecules27030778 · Cited by 44 · see citing works

Sulfur-rich prostatic intraluminal crystalloids: A surgical pathologic and electron probe x-ray microanalytic study

del Rosario, A. D., Bui, H. X., Abdulla, M., & Ross, J. S. (1993) · Human Pathology · doi:10.1016/0046-8177(93)90210-8 · Cited by 44 · see citing works

On a heavy path – determining cold plasma-derived short-lived species chemistry using isotopic labelling

Wende, K., Bruno, G., Lalk, M., Weltmann, K., von Woedtke, T., Bekeschus, S., & Lackmann, J. (2020) · RSC Advances · doi:10.1039/c9ra08745a · Cited by 43 · see citing works

CATALASE INACTIVATION FOLLOWING PHOTOSENSITIZATION WITH TETRASULFONATEDMETALLOPHTHALOCYANINES

Gantchev, T. G., & van Lier, J. E. (1995) · Photochemistry and Photobiology · doi:10.1111/j.1751-1097.1995.tb05248.x · Cited by 43 · see citing works

Comparative in vitro oxygen radical scavenging ability of zinc methionine and selected zinc salts and antioxidants

Bagchi, D., Bagchi, M., & STOHS, S. J. (1997) · General Pharmacology The Vascular System · doi:10.1016/s0306-3623(96)00178-4 · Cited by 43 · see citing works

Characterization of Fluorescein-Based Monoboronate Probe and Its Application to the Detection of Peroxynitrite in Endothelial Cells Treated with Doxorubicin

Dębowska, K., Dębski, D., Michałowski, B., Dybała‐Defratyka, A., Wójcik, T., Michalski, R., Jakubowska, M., Selmi, A., Smulik-Izydorczyk, R., Piotrowski, Ł., et al. (2016) · Chemical Research in Toxicology · doi:10.1021/acs.chemrestox.5b00431 · Cited by 42 · see citing works

Covalent Ras Dimerization on Membrane Surfaces through Photosensitized Oxidation

Chung, J. K., Lee, Y. K., Lam, H. Y. M., & Groves, J. T. (2016) · Journal of the American Chemical Society · doi:10.1021/jacs.5b12648 · Cited by 38 · see citing works

Aquatic indirect photochemical transformations of natural peptidic thiols: impact of thiol properties, solution pH, solution salinity and metal ions

Chu, C., Stamatelatos, D., & McNeill, K. (2017) · Environmental Science Processes & Impacts · doi:10.1039/c7em00324b · Cited by 41 · see citing works

Contrasting effects of SH-compounds on oxidative DNA damage: repair and increase of damage

Lafleur, M. V. M., & Retèl, J. (1993) · Mutation Research/DNAging · doi:10.1016/0921-8734(93)90006-o · Cited by 40 · see citing works

Regeneration of ergothioneine after reaction with singlet oxygen

Oumari, M., Goldfuss, B., Stoffels, C., Schmalz, H.-G., & Gründemann, D. (2019) · Free Radical Biology and Medicine · doi:10.1016/j.freeradbiomed.2019.01.043 · Cited by 39 · see citing works

Cascading of Molecular Logic Gates for Advanced Functions: A Self‐Reporting, Activatable Photosensitizer

Erbaş-Çakmak, S., & Akkaya, E. U. (2013) · Angewandte Chemie · doi:10.1002/ange.201306177 · Cited by 39 · see citing works

Ascorbate: antioxidant and biochemical activities and their importance for in vitro models

Zhitkovich, A. (2021) · Archives of Toxicology · doi:10.1007/s00204-021-03167-0 · Cited by 35 · see citing works

Improving the Quantum Yields of Semiconductor Quantum Dots through Photoenhancement Assisted by Reducing Agents

Duncan, T. V., Polanco, M. A. M., Kim, Y., & Park, S. (2009) · The Journal of Physical Chemistry C · doi:10.1021/jp811245r · Cited by 35 · see citing works

Reaction of low-molecular-mass organoselenium compounds (and their sulphur analogues) with inflammation-associated oxidants

Carroll, L., Davies, M. J., & Pattison, D. I. (2015) · Free Radical Research · doi:10.3109/10715762.2015.1018247 · Cited by 35 · see citing works

Thiols as potential UV radiation protectors: An in vitro study

van den Broeke, L. T., & van Henegouwen, G. M. J. B. (1993) · Journal of Photochemistry and Photobiology B: Biology · doi:10.1016/1011-1344(93)80026-6 · Cited by 34 · see citing works

Indirect Antioxidant Protection Against Photooxidative Processes Initiated in Retinal Pigment Epithelial Cells by a Lipofuscin Pigment

Zhou, J., Gao, X., Cai, B., & Sparrow, J. R. (2006) · Rejuvenation Research · doi:10.1089/rej.2006.9.256 · Cited by 33 · see citing works

Facile Introduction of SH Group on Aromatic Substrates via Electrophilic Substitution Reactions

Becht, J., Wagner, A., & Mioskowski, C. (2003) · The Journal of Organic Chemistry · doi:10.1021/jo034013h · Cited by 34 · see citing works

Inactivation of cysteine and serine proteases by singlet oxygen

Suto, D., Iuchi, Y., Ikeda, Y., Sato, K., Ohba, Y., & Fujii, J. (2007) · Archives of Biochemistry and Biophysics · doi:10.1016/j.abb.2007.03.020 · Cited by 32 · see citing works

Photooxidation of the Antimicrobial, Nonribosomal Peptide Bacitracin A by Singlet Oxygen under Environmentally Relevant Conditions

Lundeen, R. A., Chu, C., Sander, M., & McNeill, K. (2016) · Environmental Science & Technology · doi:10.1021/acs.est.6b01131 · Cited by 32 · see citing works

Protective role of eicosapentaenoate-lipoate (EPA-LA) derivative in combating oxidative hepatocellular injury in hypercholesterolemic atherogenesis

Kumar, S. A., Sudhahar, V., & Varalakshmi, P. (2006) · Atherosclerosis · doi:10.1016/j.atherosclerosis.2005.11.037 · Cited by 32 · see citing works

Reactive sulphur species in oxidative signal transduction

Jacob, C., Lancaster, J. R., & Giles, G. I. (2004) · Biochemical Society Transactions · doi:10.1042/bst0321015 · Cited by 31 · see citing works

Endotoxin induces luteal cell apoptosis through the mitochondrial pathway

Mishra, D. P., & Dhali, A. (2006) · Prostaglandins & Other Lipid Mediators · doi:10.1016/j.prostaglandins.2006.10.002 · Cited by 31 · see citing works

Interaction kinetics of selenium-containing compounds with oxidants

Carroll, L., Gardiner, K. A., Ignasiak, M. T., Holmehave, J., Shimodaira, S., Breitenbach, T., Iwaoka, M., Ogilby, P. R., Pattison, D. I., & Davies, M. J. (2020) · Free Radical Biology and Medicine · doi:10.1016/j.freeradbiomed.2020.05.007 · Cited by 30 · see citing works

Research Articles: Scavenger Effect of Vitamin E and Derivatives on Free Radicals Generated by Photoirradiated Pheomelanin

Duval, C., & Poelman, M.-C. (1995) · Journal of Pharmaceutical Sciences · doi:10.1002/jps.2600840124 · Cited by 29 · see citing works

Oxidation of Hypotaurine to Taurine with Photochemically Generated Singlet Oxygen: The Effect of Azide

Pecci, L., Costa, M., Montefoschi, G., Antonucci, A. M., & Cavallini, D. (1999) · Biochemical and Biophysical Research Communications · doi:10.1006/bbrc.1998.9886 · Cited by 28 · see citing works

[58] Antioxidant action of stobadine

Horáková, Ľ., Sies, H., & Steenken, S. (1994) · Methods in enzymology on CD-ROM/Methods in enzymology · doi:10.1016/0076-6879(94)34129-x · Cited by 28 · see citing works

Oxidative Stress in Mammalian Cells Impinges on the Cysteines Redox State of Human XRCC3 Protein and on Its Cellular Localization

Girard, P.-M., Graindorge, D., Smirnova, V., Rigolet, P., Francesconi, S., Scanlon, S. E., & Sage, É. (2013) · PLoS ONE · doi:10.1371/journal.pone.0075751 · Cited by 26 · see citing works

UV Radiation Protecting Efficacy of Cysteine Derivatives, Studies with UVA-induced Binding of 8-MOP and CPZ to Rat Epidermal Biomacromoleculesin Vivo

van den Broeke, L. T., & van Henegouwen, G. M. J. B. (1995) · International Journal of Radiation Biology · doi:10.1080/09553009514550471 · Cited by 27 · see citing works

Biological Significance of Active Oxygen Species: In Vitro Studies on Singlet Oxygen-Induced DNA Damage and on the Singlet Oxygen Quenching Ability of Carotenoids, Tocopherols and Thiols

Mascio, P. D., Kaiser, S., Devasagayam, T. P. A., & Sies, H. (1991) · Advances in experimental medicine and biology · doi:10.1007/978-1-4684-5877-0_7 · Cited by 25 · see citing works

Photophysical, photodynamical, redox properties and BSA interactions of novel isomeric tetracationic peripheral palladium( ii )-bipyridyl porphyrins

Santos, F. D. S., da Silveira, C. H., Nunes, F. S., Ferreira, D. C., Victória, H. F. V., Krambrock, K., Chaves, O. A., Rodembusch, F. S., & Iglesias, B. A. (2020) · Dalton Transactions · doi:10.1039/d0dt01063d · Cited by 25 · see citing works

DEACTIVATION OF SINGLET MOLECULAR OXYGEN BY THIOLS AND RELATED COMPOUNDS, POSSIBLE PROTECTORS AGAINST SKIN PHOTOSENSITIVITY

Rougée, M., Bensasson, R. V., Land, E. J., & Parienté, R. (1988) · Photochemistry and Photobiology · doi:10.1111/j.1751-1097.1988.tb08835.x · Cited by 160 · see citing works

THE QUENCHING OF SINGLET OXYGEN BY AMINO ACIDS AND PROTEINS

Matheson, I. B. C., Etheridge, R. D., Kratowich, N., & Lee, J. (1975) · Photochemistry and Photobiology · doi:10.1111/j.1751-1097.1975.tb06647.x · Cited by 214 · see citing works

DEACTIVATION OF SINGLET MOLECULAR OXYGEN BY ORGANO‐SELENIUM COMPOUNDS EXHIBITING GLUTATHIONE PEROXIDASE ACTIVITY and BY SULFUR‐CONTAINING HOMOLOGS*

Scurlock, R. D., Rougée, M., Bensasson, R. V., Evers, M. J., & Dereu, N. L. M. (1991) · Photochemistry and Photobiology · doi:10.1111/j.1751-1097.1991.tb02082.x · Cited by 22 · see citing works

Carotenoids, tocopherols and thiols as biological singlet molecular oxygen quenchers

Mascio, P. D., Devasagayam, T. P. A., Kaiser, S., & Sies, H. (1990) · Biochemical Society Transactions · doi:10.1042/bst0181054 · Cited by 282 · see citing works

Determination of physical (kq) and chemical (kr) rate constants for singlet oxygen quenching using the thermolysis of a naphthalenic endoperoxide in H2O and D2O

Pierlot, C., Nardello‐Rataj, V., Schmidt, R., & Aubry, J. (2007) · ARKIVOC · doi:10.3998/ark.5550190.0008.819 · Cited by 5 · see citing works