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1. Full Text Organometallic anticancer complexes of lapachol: Metal centre-dependent formation of reactive oxygen species and correlation with cytotoxicity
by Kandioller, Wolfgang and Balsano, Evelyn and Meier, Samuel M and Jungwirth, Ute and Göschl, Simone and Roller, Alexander and Jakupec, Michael A and Berger, Walter and Keppler, Bernhard K and Hartinger, Christian G
Chemical Communications, ISSN 1359-7345, 04/2013, Volume 49, Issue 32, pp. 3348 - 3350
Organometallic Ru-II, Os-II and Rh-III complexes of lapachol induce apoptosis in human tumour cell lines in the low mu M range by a mode of action involving... 
CHEMISTRY, MULTIDISCIPLINARY | AGENTS | DRUGS | Rhodium - pharmacology | Cell Survival - drug effects | Osmium - pharmacology | Reactive Oxygen Species - metabolism | Guanine - analogs & derivatives | Humans | Osmium - chemistry | Amino Acids - chemistry | Antineoplastic Agents, Phytogenic - chemistry | Naphthoquinones - pharmacology | Coordination Complexes - chemistry | Ruthenium - chemistry | Ruthenium - pharmacology | Cell Line, Tumor | Coordination Complexes - pharmacology | Guanine - chemistry | Naphthoquinones - chemistry | Antineoplastic Agents, Phytogenic - pharmacology | Rhodium - chemistry | Apoptosis
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2. Full Text Placement and characterization of pairs of luminescent molecules in spatially separated regions of nanostructured thin films
by Minoofar, Payam N and Hernandez, Raquel and Chia, Shinye and Dunn, Bruce and Zink, Jeffrey I and Franville, Anne-Christine
Journal of the American Chemical Society, ISSN 0002-7863, 12/2002, Volume 124, Issue 48, pp. 14388 - 14396
Methods of making mesostructured sol-gel silicate thin films containing two different molecules deliberately placed in two different spatially separated... 
HYBRID MESOPOROUS MATERIALS | RHODAMINE 6G | ORGANIC GROUPS | SURFACTANT | FUNCTIONALITY | BEHAVIOR | CHANNEL WALLS | COMPOSITES | CHEMISTRY, MULTIDISCIPLINARY | SILICA MESOSTRUCTURES | FRAMEWORKS | Europium - chemistry | Terbium - chemistry | Cetrimonium | Nanotechnology - methods | Coumarins - chemistry | Silicates - chemistry | Luminescent Measurements | Ruthenium - chemistry | Silicone Gels - chemistry | Pyrenes - chemistry | Micelles | Hydrophobic and Hydrophilic Interactions | Naphthoquinones - chemistry | Surface-Active Agents - chemistry | Cetrimonium Compounds - chemistry | Rhodamines - chemistry | Ionic crystals | Luminescence | Research
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3. Full Text Nickel (II) complexes of naphthaquinone thiosemicarbazone and semicarbazone: Synthesis, structure, spectroscopy, and biological activity
by Afrasiabi, Zahra and Sinn, Ekk and Lin, Weisheng and Ma, Yinfa and Campana, Charles and Padhye, Subhash
Journal of Inorganic Biochemistry, ISSN 0162-0134, 07/2005, Volume 99, Issue 7, pp. 1526 - 1531
Ni(II) complexes of -naphthaquinone thiosemicarbazone and semicarbazone were synthesized and spectroscopically characterized. The X-ray crystal structure of... 
MCF-7 breast cancer cells | 1,2-Naphthaquinone | Nickel complexes | Thiosemicarbazone | Biological activity | biological activity | TRANSITION-METAL-COMPLEXES | ANTICANCER AGENTS | INVITRO | BIOCHEMISTRY & MOLECULAR BIOLOGY | 1-ACETYLISOQUINOLINE | RAY CRYSTAL-STRUCTURE | CHEMISTRY, INORGANIC & NUCLEAR | 2-ACETYLPYRIDINE | 1,2-naphthaquinone | thiosemicarbazone | INHIBITORS | nickel complexes | DERIVATIVES | 2-ACETYLQUINOLINE | CYTOTOXICITY | Magnetic Resonance Spectroscopy | Nickel - chemistry | Antineoplastic Agents - chemical synthesis | Humans | Semicarbazones - chemistry | Models, Molecular | Crystallography, X-Ray | Antineoplastic Agents - chemistry | Spectrophotometry, Ultraviolet | Thiosemicarbazones - chemistry | Spectrophotometry, Infrared | Organometallic Compounds - chemical synthesis | Cell Line, Tumor | Ligands | Naphthoquinones - chemistry | Organometallic Compounds - chemistry | Antineoplastic Agents - pharmacology | Cell Proliferation - drug effects | Molecular Structure | Organometallic Compounds - pharmacology | Drug Screening Assays, Antitumor | Cell research | Oncology, Experimental | Crystals | Nitrogen compounds | Nickel | Research | Structure | Cancer
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4. Full Text Senna singueana: Antioxidant, hepatoprotective, antiapoptotic properties and phytochemical profiling of a methanol bark extract
by Sobeh, Mansour and Mahmoud, Mona F and Hasan, Rehab A and Cheng, Haroan and El-Shazly, Assem M and Wink, Michael
Molecules, ISSN 1420-3049, 09/2017, Volume 22, Issue 9, p. 1502
Natural products are considered as an important source for the discovery of new drugs to treat aging-related degenerative diseases and liver injury. The... 
Caenorhabditis elegans | Senna singueana | Hepatoprotection | Antioxidant | HPLC-PDA-ESI-MS/MS | Proanthocyanidins | antioxidant | OXIDATIVE STRESS | proanthocyanidins | MANAGEMENT | RICH EXTRACT | CHEMISTRY, ORGANIC | FLAVONOIDS | IN-VITRO | CAENORHABDITIS-ELEGANS | D-GALACTOSAMINE | CASSIA-SINGUEANA | RESISTANCE | MEDICINAL-PLANTS | hepatoprotection | Aspartate Aminotransferases - genetics | Phenols - isolation & purification | Plant Extracts - chemistry | Oxidants - pharmacology | Antioxidants - chemistry | Proto-Oncogene Proteins c-bcl-2 - agonists | Senna Plant - chemistry | Solvents - chemistry | Caenorhabditis elegans Proteins - metabolism | Catechols - chemistry | Male | Protective Agents - chemistry | Plant Bark - chemistry | Catechols - isolation & purification | Proanthocyanidins - chemistry | Proto-Oncogene Proteins c-bcl-2 - metabolism | Biphenyl Compounds - antagonists & inhibitors | Proanthocyanidins - pharmacology | Forkhead Transcription Factors - metabolism | Protective Agents - pharmacology | Catechols - pharmacology | Chemical and Drug Induced Liver Injury - pathology | Methanol - chemistry | Phenols - pharmacology | Chemical and Drug Induced Liver Injury - prevention & control | Caenorhabditis elegans - growth & development | Caenorhabditis elegans - genetics | Naphthoquinones - antagonists & inhibitors | Rats | Naphthoquinones - pharmacology | Oxidants - antagonists & inhibitors | Protective Agents - isolation & purification | Antioxidants - pharmacology | Chemical and Drug Induced Liver Injury - genetics | Forkhead Transcription Factors - genetics | Bilirubin - blood | Picrates - antagonists & inhibitors | Animals | Caenorhabditis elegans - drug effects | Aspartate Aminotransferases - blood | Antioxidants - isolation & purification | Chemical and Drug Induced Liver Injury - metabolism | Phenols - chemistry | Caenorhabditis elegans Proteins - genetics | Proto-Oncogene Proteins c-bcl-2 - genetics | Galactosamine - toxicity | Proanthocyanidins - isolation & purification | Drugs | Reactive oxygen species | Bcl-2 protein | Juglone | Liver | Bark | Transgenic | Bilirubin | Monomers | Antioxidants | Secondary metabolites | Constituents | Metabolites | Fluorescence recovery after photobleaching | Methyl alcohol | Rodents | Aging | Methanol | Translocation | Catechin | Liver diseases | Gallic acid | Aging (artificial) | Liquid chromatography | Trimers | High-performance liquid chromatography | Phenolic compounds | Nuclear transport | Injury prevention | D-Galactosamine | Natural products | Nematodes | Phenols | In vivo methods and tests | Aspartate aminotransferase | Aging (natural) | Dimers | Drug discovery | Apoptosis | Index Medicus
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5. Full Text Transition metal-free direct C-H functionalization of quinones and naphthoquinones with diaryliodonium salts: Synthesis of aryl naphthoquinones as β-secretase inhibitors
by Wang, Dawei and Ge, Bingyang and Li, Liang and Shan, Jie and Ding, Yuqiang
Journal of Organic Chemistry, ISSN 0022-3263, 09/2014, Volume 79, Issue 18, pp. 8607 - 8613
A novel ligand-free, transition metal-free direct C-H functionalization of quinones with diaryliodonium salts has been developed for the first time. The... 
ACTIVATION | DIRECT ARYLATION | MECHANISM | ALPHA-ARYLATION | BIOSYNTHESIS | COMPLEXES | REACTIVITY | CHEMISTRY, ORGANIC | AMIDATE ANCILLARY LIGANDS | SPECTRA | DISCOVERY | Transition Elements - chemistry | Quinones - chemistry | Metals - chemistry | Naphthoquinones - chemistry | Molecular Structure | Amyloid Precursor Protein Secretases - antagonists & inhibitors | Amyloid Precursor Protein Secretases - chemistry | Onium Compounds - chemistry | Naphthoquinones - chemical synthesis | Iodine compounds | Research | Chemical properties | Chemical synthesis | Quinone
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6. Full Text Cytotoxic and antioxidant marine prenylated quinones and hydroquinones
by Sunassee, Suthananda N and Davies-Coleman, Michael T
Natural Product Reports, ISSN 0265-0568, 5/2012, Volume 29, Issue 5, pp. 513 - 535
Covering: 1972 to 2011 This review covers the literature of prenylated quinone, hydroquinone and naphthoquinone marine natural products with reported cytotoxic... 
CHEMISTRY, MEDICINAL | NATURAL-PRODUCTS | BIOCHEMISTRY & MOLECULAR BIOLOGY | CHEMISTRY, ORGANIC | CYMOPOLIA-BARBATA | ALGA SARGASSUM-MICRACANTHUM | CORAL NEPHTHEA-CHABROLII | SPONGE IRCINIA-SPINOSULA | MITOTIC CELL-DIVISION | GORGONIAN EUPLEXAURA-ANASTOMOSANS | FUNGUS PENICILLIUM SP | ZEALAND BROWN ALGA | ASCIDIAN APLIDIUM-CONICUM | Quinones - chemistry | Antioxidants - chemistry | Humans | Hydroquinones - chemistry | Quinones - isolation & purification | Naphthoquinones - pharmacology | Biological Products - pharmacology | Hydroquinones - isolation & purification | Antioxidants - pharmacology | Cytotoxins - isolation & purification | Hydroquinones - pharmacology | Biological Products - isolation & purification | Marine Biology | Biological Products - chemistry | Cytotoxins - pharmacology | Antioxidants - isolation & purification | Naphthoquinones - isolation & purification | Cytotoxins - chemistry | Naphthoquinones - chemistry | Molecular Structure | Quinones - pharmacology
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7. Full Text Aryl-free radical-mediated oxidative arylation of naphthoquinones using o-iodoxybenzoic acid and phenylhydrazines and its application toward the synthesis of benzocarbazoledione
by Patil, Pravin and Nimonkar, Abhay and Akamanchi, Krishnacharya G
Journal of Organic Chemistry, ISSN 0022-3263, 03/2014, Volume 79, Issue 5, pp. 2331 - 2336
Oxidative arylation of naphthoquinones has been developed through combination of o-iodoxybenzoic acid with arylhydrazines under mild conditions at open... 
ORGANIC-SYNTHESIS | CYCLIZATIONS | QUINONES | PALLADIUM-PROMOTED SYNTHESIS | CHEMISTRY, ORGANIC | DIMERIZATION | 1,4-NAPHTHOQUINONES | IODINE(V) REAGENTS | TETRAETHYLAMMONIUM BROMIDE | DERIVATIVES | ARYLBORONIC ACIDS | Carbazoles - chemistry | Oxidation-Reduction | Free Radicals - chemistry | Heterocyclic Compounds, 4 or More Rings - chemistry | Naphthoquinones - pharmacology | Carbazoles - chemical synthesis | Heterocyclic Compounds, 4 or More Rings - chemical synthesis | Heterocyclic Compounds, 4 or More Rings - pharmacology | Naphthoquinones - chemical synthesis | Iodobenzenes - chemistry | Naphthoquinones - chemistry | Molecular Structure | Catalysis | Carbazoles - pharmacology | Palladium - chemistry | Phenylhydrazines - chemistry | Arylation | Research | Chemical properties
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8. Full Text Et2SBr.SbCl5Br: An effective reagent for direct bromonium-induced polyene cyclizations
by Snyder, Scott A and Treitler, Daniel S
Angewandte Chemie - International Edition, ISSN 1433-7851, 10/2009, Volume 48, Issue 42, pp. 7899 - 7903
Bromine | Polyene cyclization | Terpene | Biomimetic synthesis | Isocymobarbatol | Benzopyrans - chemistry | Polyenes - chemistry | Cyclization | Stereoisomerism | Antimony - chemistry | Sulfides - chemistry | Cyclohexanes - chemistry | Naphthoquinones - chemistry | Chlorides - chemistry
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9. Full Text Renewable‐Juglone‐Based High‐Performance Sodium‐Ion Batteries
by Wang, Hua and Hu, Pengfei and Yang, Jie and Gong, Guangming and Guo, Lin and Chen, Xiaodong
Advanced Materials, ISSN 0935-9648, 04/2015, Volume 27, Issue 14, pp. 2348 - 2354
A renewable‐biomolecule‐based electrode is developed through a facile synchronous reduction and self‐assembly process, without any binder or additional... 
sodium‐ion batteries | biomolecules | graphene | renewability | self‐assembly | Renewability | Biomolecules | Self-assembly | Graphene | Sodium-ion batteries | self-assembly | sodium-ion batteries | REDUCED GRAPHENE OXIDE | PHYSICS, CONDENSED MATTER | PHYSICS, APPLIED | ELECTROCHEMICAL PROPERTIES | ANODE MATERIAL | CONVERSION | MATERIALS SCIENCE, MULTIDISCIPLINARY | CHEMISTRY, PHYSICAL | NANOSCIENCE & NANOTECHNOLOGY | CHEMISTRY, MULTIDISCIPLINARY | CATHODE MATERIAL | CARBON NANOTUBES | COMPOSITE | ENERGY-STORAGE | ELECTRODE | HIGH-CAPACITY | Electrodes | Electric Power Supplies | Green Chemistry Technology | Sodium - chemistry | Molecular Conformation | Oxides - chemistry | Models, Molecular | Naphthoquinones - chemistry | Electric Conductivity | Graphite - chemistry | Batteries | Self assembly | Synchronous | Reduction | Reagents | Devices | Binders
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10. Full Text Polyphenolic Compounds in Clove and Pimento and Their Antioxidative Activities
by YOSHIMURA, Morio and AMAKURA, Yoshiaki and YOSHIDA, Takashi
Bioscience, Biotechnology, and Biochemistry, ISSN 0916-8451, 11/2011, Volume 75, Issue 11, pp. 2207 - 2212
Two new polyphenolic glucosides, 6′-O-acetylisobiflorin (1) and (2S)-3-(4-hydroxy-3-methoxyphenyl)-propane-1,2-diol 1-O-(6′-O-galloyl)-β-D-glucoside (2), were... 
clove | antioxidant | polyphenol | oxygen radical absorbance capacity (ORAC) | pimento | Oxygen radical absorbance capacity (ORAC) | Polyphenol | Antioxidant | Pimento | Clove | GLYCOSIDES | ASSAY | BIOCHEMISTRY & MOLECULAR BIOLOGY | FOOD SCIENCE & TECHNOLOGY | TANNINS | LEAVES | PREVENTION | ELLAGITANNINS | DIOICA | DISEASES | BIOTECHNOLOGY & APPLIED MICROBIOLOGY | BERRIES | CHEMISTRY, APPLIED | LEAF EXTRACT | Gallic Acid - isolation & purification | Pimenta - chemistry | Plant Extracts - chemistry | Glucosides - pharmacology | Gallic Acid - pharmacology | Antioxidants - chemistry | Fruit - chemistry | Plant Extracts - pharmacology | Naphthoquinones - pharmacology | Plant Extracts - isolation & purification | Antioxidants - pharmacology | Flowers - chemistry | Glucosides - isolation & purification | Syzygium - chemistry | Reactive Oxygen Species - chemistry | Antioxidants - isolation & purification | Naphthoquinones - isolation & purification | Glucosides - chemistry | Naphthoquinones - chemistry | Molecular Structure | Gallic Acid - analogs & derivatives | Gallic Acid - chemistry | Biotechnology | Equivalence | Extraction plants | Plants (organisms) | Biochemistry | Spectra | Conversion | Radicals
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11. Full Text High power enzymatic biofuel cell based on naphthoquinone-mediated oxidation of glucose by glucose oxidase in a carbon nanotube 3D matrix
by Reuillard, Bertrand and Le Goff, Alan and Agnès, Charles and Holzinger, Michael and Zebda, Abdelkader and Gondran, Chantal and Elouarzaki, Kamal and Cosnier, Serge
Physical Chemistry Chemical Physics, ISSN 1463-9076, 04/2013, Volume 15, Issue 14, pp. 4892 - 4896
We report the design of a novel glucose/O-2 biofuel cell (GBFC) integrating carbon nanotube-based 3D bioelectrodes and using naphthoquinone-mediated oxidation... 
CHEMISTRY, PHYSICAL | PHYSICS, ATOMIC, MOLECULAR & CHEMICAL | Electrodes | Glucose Oxidase - chemistry | Glucose Oxidase - metabolism | Oxidation-Reduction | Nanotubes, Carbon - chemistry | Bioelectric Energy Sources | Glucose - chemistry | Oxygen - chemistry | Glucose - metabolism | Naphthoquinones - chemistry | Naphthoquinones - metabolism | Oxygen - metabolism | Chemical Sciences
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12. Full Text Baeyer-villiger C-C bond cleavage reaction in gilvocarcin and jadomycin biosynthesis
by Tibrewal, Nidhi and Pahari, Pallab and Wang, Guojun and Kharel, Madan K and Morris, Caleb and Downey, Theresa and Hou, Yanpeng and Bugni, Tim S and Rohr, Jürgen
Journal of the American Chemical Society, ISSN 0002-7863, 11/2012, Volume 134, Issue 44, pp. 18181 - 18184
GilOII has been unambiguously identified as the key enzyme performing the crucial C-C bond cleavage reaction responsible for the unique rearrangement of a... 
OXIDATION | ENZYME | ENZYMOLOGY | PATHWAY | CHEMISTRY, MULTIDISCIPLINARY | DNA | Isoquinolines - metabolism | Coumarins - metabolism | Streptomyces - chemistry | Coumarins - chemistry | Streptomyces - metabolism | Isoquinolines - chemistry | Antibiotics, Antineoplastic - chemistry | Glycosides - metabolism | Naphthoquinones - chemistry | Streptomyces - enzymology | Antibiotics, Antineoplastic - metabolism | Naphthoquinones - metabolism | Glycosides - chemistry | Analysis | Rearrangements (Chemistry) | Chemical bonds | Enzyme binding | Research | Chemical properties | Structure | Antineoplastic antibiotics | Gilvocarcin | Jadomycin | combinatorial biosynthetic enzymology | C-C bond cleavage enzyme | biosynthesis
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13. Full Text Bodipy derivatives as organic triplet photosensitizers for aerobic photoorganocatalytic oxidative coupling of amines and photooxidation of dihydroxylnaphthalenes
by Huang, Ling and Zhao, Jianzhang and Guo, Song and Zhang, Caishun and Ma, Jie
Journal of Organic Chemistry, ISSN 0022-3263, 2013, Volume 78, Issue 11, pp. 5627 - 5637
We used iodo-Bodipy derivatives that show strong absorption of visible light and long-lived triplet excited states as organic catalysts for photoredox... 
Amines - chemistry | Boron Compounds - chemistry | Naphthalenes - chemistry | Photosensitizing Agents - chemistry | Oxidation-Reduction | Singlet Oxygen - chemistry | Naphthoquinones - chemistry | Molecular Structure | Catalysis | Naphthoquinones - chemical synthesis | Photochemical Processes | Measurement | Thermal properties | Naphthalene | Analysis | Photocatalysis | Oxidation-reduction reaction | Chemical properties | Activation energy
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14. Full Text One pot synthesis of poly(5-hydroxyl-1,4-naphthoquinone) stabilized gold nanoparticles using the monomer as the reducing agent for nonenzymatic electrochemical detection of glucose
by Cooray, M.C. Dilusha and Liu, Yuping and Langford, Steven J and Bond, Alan M and Zhang, Jie
Analytica Chimica Acta, ISSN 0003-2670, 01/2015, Volume 856, pp. 27 - 34
Monodispersed and highly stable gold nanoparticles with a diameter between 8 and 9 nm were synthesized in a weakly alkaline medium by chemical reduction of... 
Polymer | Glucose | Gold nanoparticle | Naphthoquinone | Nonenzymatic | Electrochemical | CHEMISTRY, ANALYTICAL | COMPONENTS | GLASSY-CARBON | SENSORS | ELECTROCATALYTIC OXIDATION | ELECTRON-TRANSFER | FILMS | AU | DISCRIMINATION | CURRENT CYCLIC VOLTAMMETRY | ALLOY | Gold - chemistry | Limit of Detection | Chemistry Techniques, Synthetic | Oxidation-Reduction | Gold Compounds - chemistry | Drug Stability | Metal Nanoparticles - chemistry | Electric Conductivity | Electrodes | Particle Size | Glucose - chemistry | Naphthoquinones - chemistry | Polymers - chemistry | Electrochemistry - methods | Glucose - analysis | Reducing Agents - chemistry | Electrochemistry - instrumentation | Glucose metabolism | Hydroxides | Chemical properties | Dextrose | Electric properties | Index Medicus | Reduction (chemical) | Nanoparticles | Gold | Direct current | Oxidation | Nanostructure | Uric acid
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15. Full Text Scope and mechanism of allylic C-H amination of terminal alkenes by the palladium/PhI(OPiv)2 catalyst system: Insights into the effect of naphthoquinone
by Yin, Guoyin and Wu, Yichen and Liu, Guosheng
Journal of the American Chemical Society, ISSN 0002-7863, 09/2010, Volume 132, Issue 34, pp. 11978 - 11987
Palladium-catalyzed oxidative amination of unactivated alkyl olefins has been developed to produce linear (E)-allylimides with high regioselectivity. This... 
Amines - chemistry | Alkenes - chemistry | Amination | Naphthoquinones - chemistry | Molecular Structure | Amines - chemical synthesis | Catalysis | Coordination Complexes - chemistry | Palladium - chemistry
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16. Full Text Stereoselective synthesis of 1,2-annulated-C-Aryl glycosides from carbohydrate-derived terminally unsubstituted dienes and arynes: Application towards synthesis of sugar-fused- or branched- naphthalenes, and C-Aryl glycosides
by Dubbu, Sateesh and Verma, Ashish Kumar and Parasuraman, Kadigachalam and Vankar, Yashwant D
Carbohydrate Research, ISSN 0008-6215, 07/2018, Volume 465, pp. 29 - 34
Synthesis of 1,2-annulated- -aryl glycosides has been achieved in a stereoselective manner through the Diels-Alder reaction between carbohydrate-derived... 
Annulated sugars | Carbohydrates | Cycloaddition | Sugar-fused (branched) naphthalenes | C-Aryl glycosides | BRADYRHIZOSE | NATURAL-PRODUCTS | BIOCHEMISTRY & MOLECULAR BIOLOGY | ARYLATION | CHEMISTRY, ORGANIC | FUNCTIONALIZATION | NAPHTHOQUINONES | D-GALACTOSE | BERGENIN | INHIBITORS | CHEMISTRY, APPLIED | DERIVATIVES | HYBRIDS | Naphthalenes - chemical synthesis | Naphthalenes - chemistry | Sugars - chemical synthesis | Sugars - chemistry | Carbohydrates - chemistry | Stereoisomerism | Glycosides - chemical synthesis | Alkynes - chemistry | Molecular Structure | Alkadienes - chemistry | Glycosides - chemistry | Diels-Alder reaction | Chemical properties
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17. Full Text Combined chemoassay and mass spectrometric approach to study the reactive potential of electrophiles towards deoxynucleosides as model for DNA
by Schmied-Tobies, Maria I.H and Paschke, Heidrun and Reemtsma, Thorsten
Chemosphere, ISSN 0045-6535, 05/2016, Volume 151, pp. 263 - 270
The modification of DNA by adduct formation is a potential molecular initiating event of genotoxicity. A chemoassay was established to study adduct formation... 
High resolution mass spectrometry | Risk assessment | Adductomics | PARA-BENZOQUINONE | CELLS | DEOXYGUANOSINE | ENVIRONMENTAL SCIENCES | ADDUCT FORMATION | GENOTOXICITY | BENZENE METABOLITES | 3'-PHOSPHATE | P-BENZOQUINONE | HYDROQUINONE | EXPOSURE | Mutagens - chemistry | Deoxyadenosines - chemistry | Deoxycytidine - chemistry | Oxidants - chemistry | Benzoquinones - chemistry | Deoxyguanosine - chemistry | Deoxyribonucleosides - chemistry | DNA - chemistry | DNA Adducts - analysis | Chromatography, Liquid | Naphthoquinones - chemistry | DNA Damage | Tandem Mass Spectrometry - methods | Thymidine - chemistry | Liquid chromatography | Mass spectrometry | Quinone | DNA | Index Medicus
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