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  • Fonte: Chemical Research in Toxicology. Unidades: IQ, EEL, IB, FO

    Assuntos: ESTRESSE OXIDATIVO, FISIOLOGIA

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      QUEIROZ, Lucas Gonçalves et al. The toxicity of poly(acrylonitrile-styrene−butadiene) microplasticstoward Hyalella azteca Is associated with Biofragmentation and oxidative stress. Chemical Research in Toxicology, v. 38, n. 1, p. 91-101, 2025Tradução . . Disponível em: https://dx.doi.org/10.1021/acs.chemrestox.4c00300. Acesso em: 08 out. 2025.
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      Queiroz, L. G., Prado, C. C. A. do, Oliveira, P. F. M. de, Valezi, D. F., Portes, M. C., Moraes, B. R. de, et al. (2025). The toxicity of poly(acrylonitrile-styrene−butadiene) microplasticstoward Hyalella azteca Is associated with Biofragmentation and oxidative stress. Chemical Research in Toxicology, 38( 1), 91-101. doi:10.1021/acs.chemrestox.4c00300
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      Queiroz LG, Prado CCA do, Oliveira PFM de, Valezi DF, Portes MC, Moraes BR de, Ando RA, Vicente E, Paiva TCB de, Pompêo M, Borges BR. The toxicity of poly(acrylonitrile-styrene−butadiene) microplasticstoward Hyalella azteca Is associated with Biofragmentation and oxidative stress [Internet]. Chemical Research in Toxicology. 2025 ; 38( 1): 91-101.[citado 2025 out. 08 ] Available from: https://dx.doi.org/10.1021/acs.chemrestox.4c00300
    • Vancouver

      Queiroz LG, Prado CCA do, Oliveira PFM de, Valezi DF, Portes MC, Moraes BR de, Ando RA, Vicente E, Paiva TCB de, Pompêo M, Borges BR. The toxicity of poly(acrylonitrile-styrene−butadiene) microplasticstoward Hyalella azteca Is associated with Biofragmentation and oxidative stress [Internet]. Chemical Research in Toxicology. 2025 ; 38( 1): 91-101.[citado 2025 out. 08 ] Available from: https://dx.doi.org/10.1021/acs.chemrestox.4c00300
  • Fonte: Chemical Research in Toxicology. Unidades: FFCLRP, IB, FCF

    Assuntos: BACTÉRIAS PATOGÊNICAS, FÁRMACOS

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      SANTOS, Melina Cardoso dos et al. Adenanthin is an efficient inhibitor of peroxiredoxins from pathogens, inhibits bacterial growth, and potentiates antibiotic activities. Chemical Research in Toxicology, 2022Tradução . . Disponível em: https://doi.org/10.1021/acs.chemrestox.2c00049. Acesso em: 08 out. 2025.
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      Santos, M. C. dos, Tairum, C. A., Cabrera, V. I. M., Cauz, A. C. G., Ribeiro, L. F., Toledo Junior, J. C., et al. (2022). Adenanthin is an efficient inhibitor of peroxiredoxins from pathogens, inhibits bacterial growth, and potentiates antibiotic activities. Chemical Research in Toxicology. doi:10.1021/acs.chemrestox.2c00049
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      Santos MC dos, Tairum CA, Cabrera VIM, Cauz ACG, Ribeiro LF, Toledo Junior JC, Toyama MH, Lago JHG, Brocchi M. Adenanthin is an efficient inhibitor of peroxiredoxins from pathogens, inhibits bacterial growth, and potentiates antibiotic activities [Internet]. Chemical Research in Toxicology. 2022 ;[citado 2025 out. 08 ] Available from: https://doi.org/10.1021/acs.chemrestox.2c00049
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      Santos MC dos, Tairum CA, Cabrera VIM, Cauz ACG, Ribeiro LF, Toledo Junior JC, Toyama MH, Lago JHG, Brocchi M. Adenanthin is an efficient inhibitor of peroxiredoxins from pathogens, inhibits bacterial growth, and potentiates antibiotic activities [Internet]. Chemical Research in Toxicology. 2022 ;[citado 2025 out. 08 ] Available from: https://doi.org/10.1021/acs.chemrestox.2c00049
  • Fonte: Chemical Research in Toxicology. Unidade: IQ

    Assuntos: ESPECTROMETRIA DE MASSAS, ÁCIDOS GRAXOS

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      CHAVES FILHO, Adriano de Britto et al. Mass spectrometry characterization of thiol conjugates linked to polyoxygenated polyunsaturated fatty acid species. Chemical Research in Toxicology, v. 32, n. 10, p. 2028-2041, 2019Tradução . . Disponível em: https://doi.org/10.1021/acs.chemrestox.9b00199. Acesso em: 08 out. 2025.
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      Chaves Filho, A. de B., Yoshinaga, M. Y., Dantas, L. S., Diniz, L. R., Pinto, I. F. D., & Miyamoto, S. (2019). Mass spectrometry characterization of thiol conjugates linked to polyoxygenated polyunsaturated fatty acid species. Chemical Research in Toxicology, 32( 10), 2028-2041. doi:10.1021/acs.chemrestox.9b00199
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      Chaves Filho A de B, Yoshinaga MY, Dantas LS, Diniz LR, Pinto IFD, Miyamoto S. Mass spectrometry characterization of thiol conjugates linked to polyoxygenated polyunsaturated fatty acid species [Internet]. Chemical Research in Toxicology. 2019 ; 32( 10): 2028-2041.[citado 2025 out. 08 ] Available from: https://doi.org/10.1021/acs.chemrestox.9b00199
    • Vancouver

      Chaves Filho A de B, Yoshinaga MY, Dantas LS, Diniz LR, Pinto IFD, Miyamoto S. Mass spectrometry characterization of thiol conjugates linked to polyoxygenated polyunsaturated fatty acid species [Internet]. Chemical Research in Toxicology. 2019 ; 32( 10): 2028-2041.[citado 2025 out. 08 ] Available from: https://doi.org/10.1021/acs.chemrestox.9b00199
  • Fonte: Chemical Research in Toxicology. Unidade: IQ

    Assunto: CÉLULAS

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      ANGELI, José Pedro Friedmann e MIYAMOTO, Sayuri e SCHULZE, Almut. Ferroptosis: the greasy side of cell death. Chemical Research in Toxicology, v. 32, p. 362-369, 2019Tradução . . Disponível em: https://doi.org/10.1021/acs.chemrestox.8b00349. Acesso em: 08 out. 2025.
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      Angeli, J. P. F., Miyamoto, S., & Schulze, A. (2019). Ferroptosis: the greasy side of cell death. Chemical Research in Toxicology, 32, 362-369. doi:10.1021/acs.chemrestox.8b00349
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      Angeli JPF, Miyamoto S, Schulze A. Ferroptosis: the greasy side of cell death [Internet]. Chemical Research in Toxicology. 2019 ; 32 362-369.[citado 2025 out. 08 ] Available from: https://doi.org/10.1021/acs.chemrestox.8b00349
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      Angeli JPF, Miyamoto S, Schulze A. Ferroptosis: the greasy side of cell death [Internet]. Chemical Research in Toxicology. 2019 ; 32 362-369.[citado 2025 out. 08 ] Available from: https://doi.org/10.1021/acs.chemrestox.8b00349
  • Fonte: Chemical Research in Toxicology. Unidade: IQ

    Assuntos: POLUIÇÃO ATMOSFÉRICA, ADUTOS DE DNA

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      SANCHEZ, Angelica B et al. DNA adduct formation in the lungs and brain of rats exposed to low concentrations of [C-13(2)]-acetaldehyde. Chemical Research in Toxicology, v. 31, n. 5, p. 332-339, 2018Tradução . . Disponível em: https://doi.org/10.1021/acs.chemrestox.8b00016. Acesso em: 08 out. 2025.
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      Sanchez, A. B., Garcia, C. C. M., Freitas, F. P., Batista, G. L., Lopes, F. S., Carvalho, V. H., et al. (2018). DNA adduct formation in the lungs and brain of rats exposed to low concentrations of [C-13(2)]-acetaldehyde. Chemical Research in Toxicology, 31( 5), 332-339. doi:10.1021/acs.chemrestox.8b00016
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      Sanchez AB, Garcia CCM, Freitas FP, Batista GL, Lopes FS, Carvalho VH, Ronsein GE, Gutz IGR, Di Mascio P, Medeiros MHG de. DNA adduct formation in the lungs and brain of rats exposed to low concentrations of [C-13(2)]-acetaldehyde [Internet]. Chemical Research in Toxicology. 2018 ; 31( 5): 332-339.[citado 2025 out. 08 ] Available from: https://doi.org/10.1021/acs.chemrestox.8b00016
    • Vancouver

      Sanchez AB, Garcia CCM, Freitas FP, Batista GL, Lopes FS, Carvalho VH, Ronsein GE, Gutz IGR, Di Mascio P, Medeiros MHG de. DNA adduct formation in the lungs and brain of rats exposed to low concentrations of [C-13(2)]-acetaldehyde [Internet]. Chemical Research in Toxicology. 2018 ; 31( 5): 332-339.[citado 2025 out. 08 ] Available from: https://doi.org/10.1021/acs.chemrestox.8b00016
  • Fonte: Chemical Research in Toxicology. Unidade: IQ

    Assuntos: OXIDAÇÃO, INFLAMAÇÃO

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      PATRICIO, Eliziane de Souza et al. Chemical characterization of urate hydroperoxide, a pro-oxidant intermediate generated by urate oxidation in inflammatory and photoinduced processes. Chemical Research in Toxicology, v. 28, n. 8, p. 1556-1566, 2015Tradução . . Disponível em: https://doi.org/10.1021/acs.chemrestox.5b00132. Acesso em: 08 out. 2025.
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      Patricio, E. de S., Prado, F. M., Silva, R. P. da, Carvalho, L. A. da C., Prates, M. V. C., Dadamos, T. R. de L., et al. (2015). Chemical characterization of urate hydroperoxide, a pro-oxidant intermediate generated by urate oxidation in inflammatory and photoinduced processes. Chemical Research in Toxicology, 28( 8), 1556-1566. doi:10.1021/acs.chemrestox.5b00132
    • NLM

      Patricio E de S, Prado FM, Silva RP da, Carvalho LA da C, Prates MVC, Dadamos TR de L, Bertotti M, Di Mascio P, Kettle A, Meotti FC. Chemical characterization of urate hydroperoxide, a pro-oxidant intermediate generated by urate oxidation in inflammatory and photoinduced processes [Internet]. Chemical Research in Toxicology. 2015 ; 28( 8): 1556-1566.[citado 2025 out. 08 ] Available from: https://doi.org/10.1021/acs.chemrestox.5b00132
    • Vancouver

      Patricio E de S, Prado FM, Silva RP da, Carvalho LA da C, Prates MVC, Dadamos TR de L, Bertotti M, Di Mascio P, Kettle A, Meotti FC. Chemical characterization of urate hydroperoxide, a pro-oxidant intermediate generated by urate oxidation in inflammatory and photoinduced processes [Internet]. Chemical Research in Toxicology. 2015 ; 28( 8): 1556-1566.[citado 2025 out. 08 ] Available from: https://doi.org/10.1021/acs.chemrestox.5b00132
  • Fonte: Chemical Research in Toxicology. Unidade: IQ

    Assunto: MITOCÔNDRIAS

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      GENARO-MATTOS, Thiago Cardoso et al. Covalent binding and anchoring of cytochrome c to mitochondrial mimetic membranes promoted by cholesterol carboxyaldehyde. Chemical Research in Toxicology, v. 26, n. 10, p. 1536-1544, 2013Tradução . . Disponível em: https://doi.org/10.1021/tx4002385. Acesso em: 08 out. 2025.
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      Genaro-Mattos, T. C., Appolinário, P. P., Mugnol, K. C. U., Junior, C. B., Nantes, I. L., Di Mascio, P., & Miyamoto, S. (2013). Covalent binding and anchoring of cytochrome c to mitochondrial mimetic membranes promoted by cholesterol carboxyaldehyde. Chemical Research in Toxicology, 26( 10), 1536-1544. doi:10.1021/tx4002385
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      Genaro-Mattos TC, Appolinário PP, Mugnol KCU, Junior CB, Nantes IL, Di Mascio P, Miyamoto S. Covalent binding and anchoring of cytochrome c to mitochondrial mimetic membranes promoted by cholesterol carboxyaldehyde [Internet]. Chemical Research in Toxicology. 2013 ; 26( 10): 1536-1544.[citado 2025 out. 08 ] Available from: https://doi.org/10.1021/tx4002385
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      Genaro-Mattos TC, Appolinário PP, Mugnol KCU, Junior CB, Nantes IL, Di Mascio P, Miyamoto S. Covalent binding and anchoring of cytochrome c to mitochondrial mimetic membranes promoted by cholesterol carboxyaldehyde [Internet]. Chemical Research in Toxicology. 2013 ; 26( 10): 1536-1544.[citado 2025 out. 08 ] Available from: https://doi.org/10.1021/tx4002385
  • Fonte: Chemical Research in Toxicology. Unidades: FFCLRP, IQ

    Assuntos: ÓXIDO NÍTRICO, BIOQUÍMICA

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      TOLEDO JUNIOR, José Carlos e AUGUSTO, Ohara. Connecting the chemical and biological properties of nitric oxide. Chemical Research in Toxicology, v. 25, n. 5, p. 975-989, 2012Tradução . . Disponível em: https://doi.org/10.1021/tx300042g. Acesso em: 08 out. 2025.
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      Toledo Junior, J. C., & Augusto, O. (2012). Connecting the chemical and biological properties of nitric oxide. Chemical Research in Toxicology, 25( 5), 975-989. doi:10.1021/tx300042g
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      Toledo Junior JC, Augusto O. Connecting the chemical and biological properties of nitric oxide [Internet]. Chemical Research in Toxicology. 2012 ; 25( 5): 975-989.[citado 2025 out. 08 ] Available from: https://doi.org/10.1021/tx300042g
    • Vancouver

      Toledo Junior JC, Augusto O. Connecting the chemical and biological properties of nitric oxide [Internet]. Chemical Research in Toxicology. 2012 ; 25( 5): 975-989.[citado 2025 out. 08 ] Available from: https://doi.org/10.1021/tx300042g
  • Fonte: Chemical Research in Toxicology. Unidade: IQ

    Assuntos: ÁCIDO LINOLEICO, OZÔNIO, LIPÍDEOS

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      UEMI, Miriam et al. Cholesterol hydroperoxides generate singlet molecular oxygen [O IND. 2'('ANTPOT. 1 delta IND. g')]': Near-IR emission, 'ANTPOT. 18 O'-labeled hydroperoxides, and mass spectrometry. Chemical Research in Toxicology, v. 24, n. 6, p. 887-895, 2011Tradução . . Disponível em: https://doi.org/10.1021/tx200079d. Acesso em: 08 out. 2025.
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      Uemi, M., Ronsein, G. E., Prado, F. M., Motta, F. D., Miyamoto, S., Medeiros, M. H. G. de, & Di Mascio, P. (2011). Cholesterol hydroperoxides generate singlet molecular oxygen [O IND. 2'('ANTPOT. 1 delta IND. g')]': Near-IR emission, 'ANTPOT. 18 O'-labeled hydroperoxides, and mass spectrometry. Chemical Research in Toxicology, 24( 6), 887-895. doi:10.1021/tx200079d
    • NLM

      Uemi M, Ronsein GE, Prado FM, Motta FD, Miyamoto S, Medeiros MHG de, Di Mascio P. Cholesterol hydroperoxides generate singlet molecular oxygen [O IND. 2'('ANTPOT. 1 delta IND. g')]': Near-IR emission, 'ANTPOT. 18 O'-labeled hydroperoxides, and mass spectrometry [Internet]. Chemical Research in Toxicology. 2011 ; 24( 6): 887-895.[citado 2025 out. 08 ] Available from: https://doi.org/10.1021/tx200079d
    • Vancouver

      Uemi M, Ronsein GE, Prado FM, Motta FD, Miyamoto S, Medeiros MHG de, Di Mascio P. Cholesterol hydroperoxides generate singlet molecular oxygen [O IND. 2'('ANTPOT. 1 delta IND. g')]': Near-IR emission, 'ANTPOT. 18 O'-labeled hydroperoxides, and mass spectrometry [Internet]. Chemical Research in Toxicology. 2011 ; 24( 6): 887-895.[citado 2025 out. 08 ] Available from: https://doi.org/10.1021/tx200079d
  • Fonte: Chemical Research in Toxicology. Unidade: IQ

    Assuntos: AMINOÁCIDOS, BIOQUÍMICA

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      MASSARI FILHO, Júlio et al. Acetyl radical production by the methylglyoxal-peroxynitrite system: a possible route for L-lysine acetylation. Chemical Research in Toxicology, v. 23, n. 11, p. 1762-1770, 2010Tradução . . Disponível em: https://doi.org/10.1021/tx1002244. Acesso em: 08 out. 2025.
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      Massari Filho, J., Tokikawa, R., Zanolli Filho, L. A., Tavares, M. F. M., Assunção, N. A., & Bechara, E. J. H. (2010). Acetyl radical production by the methylglyoxal-peroxynitrite system: a possible route for L-lysine acetylation. Chemical Research in Toxicology, 23( 11), 1762-1770. doi:10.1021/tx1002244
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      Massari Filho J, Tokikawa R, Zanolli Filho LA, Tavares MFM, Assunção NA, Bechara EJH. Acetyl radical production by the methylglyoxal-peroxynitrite system: a possible route for L-lysine acetylation [Internet]. Chemical Research in Toxicology. 2010 ; 23( 11): 1762-1770.[citado 2025 out. 08 ] Available from: https://doi.org/10.1021/tx1002244
    • Vancouver

      Massari Filho J, Tokikawa R, Zanolli Filho LA, Tavares MFM, Assunção NA, Bechara EJH. Acetyl radical production by the methylglyoxal-peroxynitrite system: a possible route for L-lysine acetylation [Internet]. Chemical Research in Toxicology. 2010 ; 23( 11): 1762-1770.[citado 2025 out. 08 ] Available from: https://doi.org/10.1021/tx1002244
  • Fonte: Chemical Research in Toxicology. Unidade: IQ

    Assuntos: DNA, POLUIÇÃO ATMOSFÉRICA

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      GARCIA, Camila Carriao Machado et al. Ultrasensitive simultaneous quantification of 1,'N POT. 2'-Etheno-2′-deoxyguanosine and 1,'N POT. 2'-propano-2′-deoxyguanosine in DNA by an online liquid chromatography−electrospray tandem mass spectrometry assay. Chemical Research in Toxicology, v. 23, n. 7, p. 1245-1255, 2010Tradução . . Disponível em: https://doi.org/10.102/tx1001018. Acesso em: 08 out. 2025.
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      Garcia, C. C. M., Freitas, F. P., Di Mascio, P., & Medeiros, M. H. G. de. (2010). Ultrasensitive simultaneous quantification of 1,'N POT. 2'-Etheno-2′-deoxyguanosine and 1,'N POT. 2'-propano-2′-deoxyguanosine in DNA by an online liquid chromatography−electrospray tandem mass spectrometry assay. Chemical Research in Toxicology, 23( 7), 1245-1255. doi:10.102/tx1001018
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      Garcia CCM, Freitas FP, Di Mascio P, Medeiros MHG de. Ultrasensitive simultaneous quantification of 1,'N POT. 2'-Etheno-2′-deoxyguanosine and 1,'N POT. 2'-propano-2′-deoxyguanosine in DNA by an online liquid chromatography−electrospray tandem mass spectrometry assay [Internet]. Chemical Research in Toxicology. 2010 ; 23( 7): 1245-1255.[citado 2025 out. 08 ] Available from: https://doi.org/10.102/tx1001018
    • Vancouver

      Garcia CCM, Freitas FP, Di Mascio P, Medeiros MHG de. Ultrasensitive simultaneous quantification of 1,'N POT. 2'-Etheno-2′-deoxyguanosine and 1,'N POT. 2'-propano-2′-deoxyguanosine in DNA by an online liquid chromatography−electrospray tandem mass spectrometry assay [Internet]. Chemical Research in Toxicology. 2010 ; 23( 7): 1245-1255.[citado 2025 out. 08 ] Available from: https://doi.org/10.102/tx1001018
  • Fonte: Chemical Research in Toxicology. Unidade: IQ

    Assuntos: BIOMARCADORES, ESTRESSE OXIDATIVO, DANO AO DNA

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      MEDEIROS, Marisa Helena Gennari de. Exocyclic DNA adducts as biomarkers of lipid oxidation and predictors of disease: challenges in developing sensitive and specific methods for clinical studies. Chemical Research in Toxicology, v. 22, n. 3, p. 419-425, 2009Tradução . . Disponível em: http://pubs.acs.org/doi/pdf/10.1021/tx800367d. Acesso em: 08 out. 2025.
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      Medeiros, M. H. G. de. (2009). Exocyclic DNA adducts as biomarkers of lipid oxidation and predictors of disease: challenges in developing sensitive and specific methods for clinical studies. Chemical Research in Toxicology, 22( 3), 419-425. Recuperado de http://pubs.acs.org/doi/pdf/10.1021/tx800367d
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      Medeiros MHG de. Exocyclic DNA adducts as biomarkers of lipid oxidation and predictors of disease: challenges in developing sensitive and specific methods for clinical studies [Internet]. Chemical Research in Toxicology. 2009 ; 22( 3): 419-425.[citado 2025 out. 08 ] Available from: http://pubs.acs.org/doi/pdf/10.1021/tx800367d
    • Vancouver

      Medeiros MHG de. Exocyclic DNA adducts as biomarkers of lipid oxidation and predictors of disease: challenges in developing sensitive and specific methods for clinical studies [Internet]. Chemical Research in Toxicology. 2009 ; 22( 3): 419-425.[citado 2025 out. 08 ] Available from: http://pubs.acs.org/doi/pdf/10.1021/tx800367d
  • Fonte: Chemical Research in Toxicology. Unidade: IQ

    Assuntos: DOENÇA DE ALZHEIMER, ÁCIDO LINOLEICO, DANO AO DNA

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      UEMI, Miriam et al. Generation of cholesterol carboxyaldehyde by the reaction of singlet molecular oxygen ['O IND. 2' (ANTPOT. 1 delta IND. g)] as well as ozone with cholesterol. Chemical Research in Toxicology, v. 22, n. 5, p. 875-884, 2009Tradução . . Disponível em: http://pubs.acs.org/doi/pdf/10.1021/tx800447b. Acesso em: 08 out. 2025.
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      Uemi, M., Ronsein, G. E., Miyamoto, S., Medeiros, M. H. G. de, & Di Mascio, P. (2009). Generation of cholesterol carboxyaldehyde by the reaction of singlet molecular oxygen ['O IND. 2' (ANTPOT. 1 delta IND. g)] as well as ozone with cholesterol. Chemical Research in Toxicology, 22( 5), 875-884. Recuperado de http://pubs.acs.org/doi/pdf/10.1021/tx800447b
    • NLM

      Uemi M, Ronsein GE, Miyamoto S, Medeiros MHG de, Di Mascio P. Generation of cholesterol carboxyaldehyde by the reaction of singlet molecular oxygen ['O IND. 2' (ANTPOT. 1 delta IND. g)] as well as ozone with cholesterol [Internet]. Chemical Research in Toxicology. 2009 ; 22( 5): 875-884.[citado 2025 out. 08 ] Available from: http://pubs.acs.org/doi/pdf/10.1021/tx800447b
    • Vancouver

      Uemi M, Ronsein GE, Miyamoto S, Medeiros MHG de, Di Mascio P. Generation of cholesterol carboxyaldehyde by the reaction of singlet molecular oxygen ['O IND. 2' (ANTPOT. 1 delta IND. g)] as well as ozone with cholesterol [Internet]. Chemical Research in Toxicology. 2009 ; 22( 5): 875-884.[citado 2025 out. 08 ] Available from: http://pubs.acs.org/doi/pdf/10.1021/tx800447b
  • Fonte: Chemical Research in Toxicology. Unidade: IQ

    Assuntos: PEROXIDASE, BIOQUÍMICA, SUPERÓXIDO DISMUTASE

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      MEDINAS, Danilo Bilches et al. Peroxymonocarbonate and carbonate radical displace the hydroxyl-like oxidant in the Sod1 peroxidase activity under physiological conditions. Chemical Research in Toxicology, v. 22, n. 4, p. 639-648, 2009Tradução . . Disponível em: http://pubs.acs.org/doi/pdf/10.1021/tx800287m. Acesso em: 08 out. 2025.
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      Medinas, D. B., Toledo Junior, J. C., Cerchiaro, G., Amaral, A. T. do, Rezende, L. de, Malvezzi, A., & Augusto, O. (2009). Peroxymonocarbonate and carbonate radical displace the hydroxyl-like oxidant in the Sod1 peroxidase activity under physiological conditions. Chemical Research in Toxicology, 22( 4), 639-648. Recuperado de http://pubs.acs.org/doi/pdf/10.1021/tx800287m
    • NLM

      Medinas DB, Toledo Junior JC, Cerchiaro G, Amaral AT do, Rezende L de, Malvezzi A, Augusto O. Peroxymonocarbonate and carbonate radical displace the hydroxyl-like oxidant in the Sod1 peroxidase activity under physiological conditions [Internet]. Chemical Research in Toxicology. 2009 ; 22( 4): 639-648.[citado 2025 out. 08 ] Available from: http://pubs.acs.org/doi/pdf/10.1021/tx800287m
    • Vancouver

      Medinas DB, Toledo Junior JC, Cerchiaro G, Amaral AT do, Rezende L de, Malvezzi A, Augusto O. Peroxymonocarbonate and carbonate radical displace the hydroxyl-like oxidant in the Sod1 peroxidase activity under physiological conditions [Internet]. Chemical Research in Toxicology. 2009 ; 22( 4): 639-648.[citado 2025 out. 08 ] Available from: http://pubs.acs.org/doi/pdf/10.1021/tx800287m
  • Fonte: Chemical Research in Toxicology. Unidade: FCF

    Assuntos: ESPECTROMETRIA DE MASSAS (ANÁLISE), HEPATOPATIAS

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      LOUREIRO, Ana Paula de Melo et al. Mass Spectrometric Analysis of a Cyclic 7,8-Butanoguanine Adduct of N-Nitrosopyrrolidine: Comparison to Other N-Nitrosopyrrolidine Adducts in Rat Hepatic DNA. Chemical Research in Toxicology, v. 22, n. 10, p. 1728-1735, 2009Tradução . . Disponível em: https://doi.org/10.1021/tx900238t. Acesso em: 08 out. 2025.
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      Loureiro, A. P. de M., Zhang, W., Kassie, F., Zhang, S., Villalta, P. W., Wang, M., & Hecht, S. S. (2009). Mass Spectrometric Analysis of a Cyclic 7,8-Butanoguanine Adduct of N-Nitrosopyrrolidine: Comparison to Other N-Nitrosopyrrolidine Adducts in Rat Hepatic DNA. Chemical Research in Toxicology, 22( 10), 1728-1735. doi:10.1021/tx900238t
    • NLM

      Loureiro AP de M, Zhang W, Kassie F, Zhang S, Villalta PW, Wang M, Hecht SS. Mass Spectrometric Analysis of a Cyclic 7,8-Butanoguanine Adduct of N-Nitrosopyrrolidine: Comparison to Other N-Nitrosopyrrolidine Adducts in Rat Hepatic DNA [Internet]. Chemical Research in Toxicology. 2009 ; 22( 10): 1728-1735.[citado 2025 out. 08 ] Available from: https://doi.org/10.1021/tx900238t
    • Vancouver

      Loureiro AP de M, Zhang W, Kassie F, Zhang S, Villalta PW, Wang M, Hecht SS. Mass Spectrometric Analysis of a Cyclic 7,8-Butanoguanine Adduct of N-Nitrosopyrrolidine: Comparison to Other N-Nitrosopyrrolidine Adducts in Rat Hepatic DNA [Internet]. Chemical Research in Toxicology. 2009 ; 22( 10): 1728-1735.[citado 2025 out. 08 ] Available from: https://doi.org/10.1021/tx900238t
  • Fonte: Chemical Research in Toxicology. Unidade: IQ

    Assuntos: BIOQUÍMICA, ESPECTROMETRIA DE MASSAS

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    • ABNT

      RONSEIN, Graziella Eliza et al. Tryptophan oxidation by singlet molecular oxygen ['O IND. 2' ('ANTPOT. 1 Delta IND. g')]: Mechanistic studies using 'ANTPOT. 18 O'-labeled hydroperoxides, mass spectrometry, and light emission measurements. Chemical Research in Toxicology, v. 21, n. 6, p. 1271-1283, 2008Tradução . . Acesso em: 08 out. 2025.
    • APA

      Ronsein, G. E., Oliveira, M. C. B. de, Miyamoto, S., Medeiros, M. H. G. de, & Di Mascio, P. (2008). Tryptophan oxidation by singlet molecular oxygen ['O IND. 2' ('ANTPOT. 1 Delta IND. g')]: Mechanistic studies using 'ANTPOT. 18 O'-labeled hydroperoxides, mass spectrometry, and light emission measurements. Chemical Research in Toxicology, 21( 6), 1271-1283.
    • NLM

      Ronsein GE, Oliveira MCB de, Miyamoto S, Medeiros MHG de, Di Mascio P. Tryptophan oxidation by singlet molecular oxygen ['O IND. 2' ('ANTPOT. 1 Delta IND. g')]: Mechanistic studies using 'ANTPOT. 18 O'-labeled hydroperoxides, mass spectrometry, and light emission measurements. Chemical Research in Toxicology. 2008 ;21( 6): 1271-1283.[citado 2025 out. 08 ]
    • Vancouver

      Ronsein GE, Oliveira MCB de, Miyamoto S, Medeiros MHG de, Di Mascio P. Tryptophan oxidation by singlet molecular oxygen ['O IND. 2' ('ANTPOT. 1 Delta IND. g')]: Mechanistic studies using 'ANTPOT. 18 O'-labeled hydroperoxides, mass spectrometry, and light emission measurements. Chemical Research in Toxicology. 2008 ;21( 6): 1271-1283.[citado 2025 out. 08 ]
  • Fonte: Chemical Research in Toxicology. Unidade: IQ

    Assuntos: AMINOÁCIDOS, BIOQUÍMICA

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    • ABNT

      MASSARI, Júlio et al. Radical acetylation of 2'-deoxyguanosine and L-histidine coupled to the reaction of diacetyl with peroxynitrite in aerated medium. Chemical Research in Toxicology, v. 21, n. 4, p. 879-887, 2008Tradução . . Acesso em: 08 out. 2025.
    • APA

      Massari, J., Fujiy, D. E., Dutra, F., Vaz, S. M., Costa, A. C. de O., Micke, G. A., et al. (2008). Radical acetylation of 2'-deoxyguanosine and L-histidine coupled to the reaction of diacetyl with peroxynitrite in aerated medium. Chemical Research in Toxicology, 21( 4), 879-887.
    • NLM

      Massari J, Fujiy DE, Dutra F, Vaz SM, Costa AC de O, Micke GA, Tavares MFM, Tokikawa R, Assunção NA, Bechara EJH. Radical acetylation of 2'-deoxyguanosine and L-histidine coupled to the reaction of diacetyl with peroxynitrite in aerated medium. Chemical Research in Toxicology. 2008 ; 21( 4): 879-887.[citado 2025 out. 08 ]
    • Vancouver

      Massari J, Fujiy DE, Dutra F, Vaz SM, Costa AC de O, Micke GA, Tavares MFM, Tokikawa R, Assunção NA, Bechara EJH. Radical acetylation of 2'-deoxyguanosine and L-histidine coupled to the reaction of diacetyl with peroxynitrite in aerated medium. Chemical Research in Toxicology. 2008 ; 21( 4): 879-887.[citado 2025 out. 08 ]
  • Fonte: Chemical Research in Toxicology. Unidades: FCF, IQ

    Assuntos: AGENTE TÓXICO, PESTICIDAS (TOXICIDADE)

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    • ABNT

      LOUREIRO, Ana Paula de Melo e AUGUSTO, Ohara. Toxicological issues in Brazil range from long-standing problems to novel challenges.[Guest Editorial]. Chemical Research in Toxicology. Washington: Faculdade de Ciências Farmacêuticas, Universidade de São Paulo. . Acesso em: 08 out. 2025. , 2008
    • APA

      Loureiro, A. P. de M., & Augusto, O. (2008). Toxicological issues in Brazil range from long-standing problems to novel challenges.[Guest Editorial]. Chemical Research in Toxicology. Washington: Faculdade de Ciências Farmacêuticas, Universidade de São Paulo.
    • NLM

      Loureiro AP de M, Augusto O. Toxicological issues in Brazil range from long-standing problems to novel challenges.[Guest Editorial]. Chemical Research in Toxicology. 2008 ;21( 2): 267-271.[citado 2025 out. 08 ]
    • Vancouver

      Loureiro AP de M, Augusto O. Toxicological issues in Brazil range from long-standing problems to novel challenges.[Guest Editorial]. Chemical Research in Toxicology. 2008 ;21( 2): 267-271.[citado 2025 out. 08 ]
  • Fonte: Chemical Research in Toxicology. Unidades: EACH, IQ

    Assuntos: ESTRESSE OXIDATIVO, DIABETES MELLITUS, BIOQUÍMICA

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    • ABNT

      SARTORI, Adriano et al. Aminoacetone, a putative endogenous source of methylglyoxal, causes oxidative stress and death to insulin-producing RINm5f cells. Chemical Research in Toxicology, v. 21, n. 9, p. 1841-1850, 2008Tradução . . Disponível em: https://doi.org/10.1021/tx8001753. Acesso em: 08 out. 2025.
    • APA

      Sartori, A., Garay-Malpartida, H. M., Forni, M. F., Schumacher, R. I., Dutra, F., Sogayar, M. C., & Bechara, E. J. H. (2008). Aminoacetone, a putative endogenous source of methylglyoxal, causes oxidative stress and death to insulin-producing RINm5f cells. Chemical Research in Toxicology, 21( 9), 1841-1850. doi:10.1021/tx8001753
    • NLM

      Sartori A, Garay-Malpartida HM, Forni MF, Schumacher RI, Dutra F, Sogayar MC, Bechara EJH. Aminoacetone, a putative endogenous source of methylglyoxal, causes oxidative stress and death to insulin-producing RINm5f cells [Internet]. Chemical Research in Toxicology. 2008 ; 21( 9): 1841-1850.[citado 2025 out. 08 ] Available from: https://doi.org/10.1021/tx8001753
    • Vancouver

      Sartori A, Garay-Malpartida HM, Forni MF, Schumacher RI, Dutra F, Sogayar MC, Bechara EJH. Aminoacetone, a putative endogenous source of methylglyoxal, causes oxidative stress and death to insulin-producing RINm5f cells [Internet]. Chemical Research in Toxicology. 2008 ; 21( 9): 1841-1850.[citado 2025 out. 08 ] Available from: https://doi.org/10.1021/tx8001753
  • Fonte: Chemical Research in Toxicology. Unidade: IQ

    Assuntos: OXIDAÇÃO, QUÍMICA ORGÂNICA

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    • ABNT

      PESSOTO, Felipe Samuel et al. Organotellurane-promoted mitochondrial permeability transition concomitant with membrane lipid protection against oxidation. Chemical Research in Toxicology, v. 20, n. 10, p. 1453-1461, 2007Tradução . . Acesso em: 08 out. 2025.
    • APA

      Pessoto, F. S., Faria, P. A. de, Cunha, R. L. O. R., Comasseto, J. V., Rodrigues, T., & Nantes, I. L. (2007). Organotellurane-promoted mitochondrial permeability transition concomitant with membrane lipid protection against oxidation. Chemical Research in Toxicology, 20( 10), 1453-1461.
    • NLM

      Pessoto FS, Faria PA de, Cunha RLOR, Comasseto JV, Rodrigues T, Nantes IL. Organotellurane-promoted mitochondrial permeability transition concomitant with membrane lipid protection against oxidation. Chemical Research in Toxicology. 2007 ; 20( 10): 1453-1461.[citado 2025 out. 08 ]
    • Vancouver

      Pessoto FS, Faria PA de, Cunha RLOR, Comasseto JV, Rodrigues T, Nantes IL. Organotellurane-promoted mitochondrial permeability transition concomitant with membrane lipid protection against oxidation. Chemical Research in Toxicology. 2007 ; 20( 10): 1453-1461.[citado 2025 out. 08 ]

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