Filtros : "Chirality" Removido: "Indexado no Excerpta Medica" Limpar

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  • Source: Chirality. Unidade: IQSC

    Assunto: CATÁLISE

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      JIMENEZ, David et al. Enantioselective ene‐reduction of E‐2‐cyano‐3‐(furan‐2‐yl) acrylamide by marine and terrestrial fungi and absolute configuration of (R)‐2‐cyano‐3‐(furan‐2‐yl) propanamide determined by calculations of electronic circular dichroism (ECD) spectra. Chirality, v. 31, p. 534-542, 2019Tradução . . Disponível em: https://doi.org/10.1002/chir.23078. Acesso em: 12 out. 2024.
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      Jimenez, D., Barreiro, J. C., Santos Júnior, F. M. dos, Vasconcellos, S., Vasconcellos, S. P. de, Porto, A. L. M., & Batista Junior, F. M. (2019). Enantioselective ene‐reduction of E‐2‐cyano‐3‐(furan‐2‐yl) acrylamide by marine and terrestrial fungi and absolute configuration of (R)‐2‐cyano‐3‐(furan‐2‐yl) propanamide determined by calculations of electronic circular dichroism (ECD) spectra. Chirality, 31, 534-542. doi:10.1002/chir.23078
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      Jimenez D, Barreiro JC, Santos Júnior FM dos, Vasconcellos S, Vasconcellos SP de, Porto ALM, Batista Junior FM. Enantioselective ene‐reduction of E‐2‐cyano‐3‐(furan‐2‐yl) acrylamide by marine and terrestrial fungi and absolute configuration of (R)‐2‐cyano‐3‐(furan‐2‐yl) propanamide determined by calculations of electronic circular dichroism (ECD) spectra [Internet]. Chirality. 2019 ; 31 534-542.[citado 2024 out. 12 ] Available from: https://doi.org/10.1002/chir.23078
    • Vancouver

      Jimenez D, Barreiro JC, Santos Júnior FM dos, Vasconcellos S, Vasconcellos SP de, Porto ALM, Batista Junior FM. Enantioselective ene‐reduction of E‐2‐cyano‐3‐(furan‐2‐yl) acrylamide by marine and terrestrial fungi and absolute configuration of (R)‐2‐cyano‐3‐(furan‐2‐yl) propanamide determined by calculations of electronic circular dichroism (ECD) spectra [Internet]. Chirality. 2019 ; 31 534-542.[citado 2024 out. 12 ] Available from: https://doi.org/10.1002/chir.23078
  • Source: Chirality. Unidade: FCFRP

    Subjects: PRODUTOS NATURAIS, RESSONÂNCIA MAGNÉTICA NUCLEAR

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      DEMARQUE, Daniel Pecoraro et al. Revisiting empirical rules for the determination of the absolute configuration of cascarosides and other (ox-)anthrones. Chirality, v. 30, n. 4, p. 432-438, 2018Tradução . . Disponível em: https://doi.org/10.1002/chir.22803. Acesso em: 12 out. 2024.
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      Demarque, D. P., Pinho, D. R., Lopes, N. P., & Merten, C. (2018). Revisiting empirical rules for the determination of the absolute configuration of cascarosides and other (ox-)anthrones. Chirality, 30( 4), 432-438. doi:10.1002/chir.22803
    • NLM

      Demarque DP, Pinho DR, Lopes NP, Merten C. Revisiting empirical rules for the determination of the absolute configuration of cascarosides and other (ox-)anthrones [Internet]. Chirality. 2018 ; 30( 4): 432-438.[citado 2024 out. 12 ] Available from: https://doi.org/10.1002/chir.22803
    • Vancouver

      Demarque DP, Pinho DR, Lopes NP, Merten C. Revisiting empirical rules for the determination of the absolute configuration of cascarosides and other (ox-)anthrones [Internet]. Chirality. 2018 ; 30( 4): 432-438.[citado 2024 out. 12 ] Available from: https://doi.org/10.1002/chir.22803
  • Source: Chirality. Unidade: IQSC

    Subjects: CROMATOGRAFIA LÍQUIDA DE ALTA EFICIÊNCIA, CROMATOGRAFIA EM FLUÍDO SUPERCRÍTICO

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      ALVARENGA, Natália e PORTO, Andre Luiz Meleiro e BARREIRO, Juliana Cristina. Enantioselective separation of (±)‐β‐hydroxy‐1,2,3‐triazoles by supercritical fluid chromatography and high‐performance liquid chromatography. Chirality, v. 30, p. 890-899, 2018Tradução . . Disponível em: https://doi.org/10.1002/chir.22851. Acesso em: 12 out. 2024.
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      Alvarenga, N., Porto, A. L. M., & Barreiro, J. C. (2018). Enantioselective separation of (±)‐β‐hydroxy‐1,2,3‐triazoles by supercritical fluid chromatography and high‐performance liquid chromatography. Chirality, 30, 890-899. doi:10.1002/chir.22851
    • NLM

      Alvarenga N, Porto ALM, Barreiro JC. Enantioselective separation of (±)‐β‐hydroxy‐1,2,3‐triazoles by supercritical fluid chromatography and high‐performance liquid chromatography [Internet]. Chirality. 2018 ; 30 890-899.[citado 2024 out. 12 ] Available from: https://doi.org/10.1002/chir.22851
    • Vancouver

      Alvarenga N, Porto ALM, Barreiro JC. Enantioselective separation of (±)‐β‐hydroxy‐1,2,3‐triazoles by supercritical fluid chromatography and high‐performance liquid chromatography [Internet]. Chirality. 2018 ; 30 890-899.[citado 2024 out. 12 ] Available from: https://doi.org/10.1002/chir.22851
  • Source: Chirality. Unidades: FMRP, FCFRP

    Subjects: FÁRMACOS PSICOTRÓPICOS, FARMACOCINÉTICA, CROMATOGRAFIA LÍQUIDA, ESPECTROMETRIA DE MASSAS

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      ANTUNES, Natalicia de Jesus et al. Analysis of oxcarbazepine and the 10-hydroxycarbazepine enantiomers in plasma by LC-MS/MS: application in a pharmacokinetic study. Chirality, v. 25, n. 12, p. 897-903, 2013Tradução . . Disponível em: https://doi.org/10.1002/chir.22231. Acesso em: 12 out. 2024.
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      Antunes, N. de J., Wichert-Ana, L., Coelho, E. B., Pasqua, O. D., Alexandre Junior, V., Takayanagui, O. M., et al. (2013). Analysis of oxcarbazepine and the 10-hydroxycarbazepine enantiomers in plasma by LC-MS/MS: application in a pharmacokinetic study. Chirality, 25( 12), 897-903. doi:10.1002/chir.22231
    • NLM

      Antunes N de J, Wichert-Ana L, Coelho EB, Pasqua OD, Alexandre Junior V, Takayanagui OM, Tozatto E, Lanchote VL. Analysis of oxcarbazepine and the 10-hydroxycarbazepine enantiomers in plasma by LC-MS/MS: application in a pharmacokinetic study [Internet]. Chirality. 2013 ; 25( 12): 897-903.[citado 2024 out. 12 ] Available from: https://doi.org/10.1002/chir.22231
    • Vancouver

      Antunes N de J, Wichert-Ana L, Coelho EB, Pasqua OD, Alexandre Junior V, Takayanagui OM, Tozatto E, Lanchote VL. Analysis of oxcarbazepine and the 10-hydroxycarbazepine enantiomers in plasma by LC-MS/MS: application in a pharmacokinetic study [Internet]. Chirality. 2013 ; 25( 12): 897-903.[citado 2024 out. 12 ] Available from: https://doi.org/10.1002/chir.22231
  • Source: Chirality. Unidade: FCFRP

    Subjects: ANTIDEPRESSIVOS (FARMACOCINÉTICA), GASOLINA (EFEITOS ADVERSOS), CROMATOGRAFIA LÍQUIDA, ESPECTROMETRIA DE MASSAS

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      CARDOSO, Juciane Lauren Cavalcanti et al. Influence of gasoline inhalation on the enantioselective pharmacokinetics of fluoxetine in rats. Chirality, v. 25, n. 3, p. 206-210, 2013Tradução . . Disponível em: https://doi.org/10.1002/chir.22136. Acesso em: 12 out. 2024.
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      Cardoso, J. L. C., Lanchote, V. L., Pereira, M. P. M., Capela, J. M. V., & Lepera, J. S. (2013). Influence of gasoline inhalation on the enantioselective pharmacokinetics of fluoxetine in rats. Chirality, 25( 3), 206-210. doi:10.1002/chir.22136
    • NLM

      Cardoso JLC, Lanchote VL, Pereira MPM, Capela JMV, Lepera JS. Influence of gasoline inhalation on the enantioselective pharmacokinetics of fluoxetine in rats [Internet]. Chirality. 2013 ; 25( 3): 206-210.[citado 2024 out. 12 ] Available from: https://doi.org/10.1002/chir.22136
    • Vancouver

      Cardoso JLC, Lanchote VL, Pereira MPM, Capela JMV, Lepera JS. Influence of gasoline inhalation on the enantioselective pharmacokinetics of fluoxetine in rats [Internet]. Chirality. 2013 ; 25( 3): 206-210.[citado 2024 out. 12 ] Available from: https://doi.org/10.1002/chir.22136
  • Source: Chirality. Unidade: IFSC

    Subjects: FARMACOLOGIA EXPERIMENTAL, ANTI-INFLAMATÓRIOS, PLANEJAMENTO DE FÁRMACOS

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      VELOSO, Marcia P. et al. Synthesis and characterization of the atropisomeric relationships of a substituted N-Phenyl-Bipyrazole derivative with anti-inflammatory properties. Chirality, v. 24, n. 6, p. 463-470, 2012Tradução . . Disponível em: https://doi.org/10.1002/chir.22016. Acesso em: 12 out. 2024.
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      Veloso, M. P., Romeiro, N. C., Silva, G. M. S., Alves, H. de M., Doriguetto, A. C., Ellena, J., et al. (2012). Synthesis and characterization of the atropisomeric relationships of a substituted N-Phenyl-Bipyrazole derivative with anti-inflammatory properties. Chirality, 24( 6), 463-470. doi:10.1002/chir.22016
    • NLM

      Veloso MP, Romeiro NC, Silva GMS, Alves H de M, Doriguetto AC, Ellena J, Miranda ALP, Barreiro EJ, Fraga CAM. Synthesis and characterization of the atropisomeric relationships of a substituted N-Phenyl-Bipyrazole derivative with anti-inflammatory properties [Internet]. Chirality. 2012 ; 24( 6): 463-470.[citado 2024 out. 12 ] Available from: https://doi.org/10.1002/chir.22016
    • Vancouver

      Veloso MP, Romeiro NC, Silva GMS, Alves H de M, Doriguetto AC, Ellena J, Miranda ALP, Barreiro EJ, Fraga CAM. Synthesis and characterization of the atropisomeric relationships of a substituted N-Phenyl-Bipyrazole derivative with anti-inflammatory properties [Internet]. Chirality. 2012 ; 24( 6): 463-470.[citado 2024 out. 12 ] Available from: https://doi.org/10.1002/chir.22016
  • Source: Chirality. Unidades: FMRP, FCFRP

    Subjects: FÁRMACOS (SISTEMA CARDIOVASCULAR) (EFEITOS), HIPERTENSÃO, PLASMA (HUMANO), CROMATOGRAFIA LÍQUIDA, ESPECTROMETRIA DE MASSAS

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      POGGI, Josiane Cristófani et al. Analysis of carvedilol enantiomers in human plasma using chiral stationary phase column and liquid chromatography with tandem mass spectrometry. Chirality, v. 24, n. 3, p. 209-214, 2012Tradução . . Disponível em: https://doi.org/10.1002/chir.21984. Acesso em: 12 out. 2024.
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      Poggi, J. C., Silva, F. G. da, Coelho, E. B., Marques, M. P., Bertucci, C., & Lanchote, V. L. (2012). Analysis of carvedilol enantiomers in human plasma using chiral stationary phase column and liquid chromatography with tandem mass spectrometry. Chirality, 24( 3), 209-214. doi:10.1002/chir.21984
    • NLM

      Poggi JC, Silva FG da, Coelho EB, Marques MP, Bertucci C, Lanchote VL. Analysis of carvedilol enantiomers in human plasma using chiral stationary phase column and liquid chromatography with tandem mass spectrometry [Internet]. Chirality. 2012 ; 24( 3): 209-214.[citado 2024 out. 12 ] Available from: https://doi.org/10.1002/chir.21984
    • Vancouver

      Poggi JC, Silva FG da, Coelho EB, Marques MP, Bertucci C, Lanchote VL. Analysis of carvedilol enantiomers in human plasma using chiral stationary phase column and liquid chromatography with tandem mass spectrometry [Internet]. Chirality. 2012 ; 24( 3): 209-214.[citado 2024 out. 12 ] Available from: https://doi.org/10.1002/chir.21984
  • Source: Chirality. Unidades: FMRP, FCFRP

    Subjects: FARMACOCINÉTICA, HIPERTENSÃO, GRAVIDEZ, PLASMA

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      CARVALHO, Teresa Maria de Jesus Ponte et al. Stereoselective analysis of labetalol in human plasma by LC-MS/MS: application to pharmacokinetics. Chirality, v. 21, n. 8, p. 738-744, 2009Tradução . . Disponível em: https://doi.org/10.1002/chir.20673. Acesso em: 12 out. 2024.
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      Carvalho, T. M. de J. P., Cavalli, R. de C., Marques, M. P., Cunha, S. P. da, Baraldi, C. de O., & Lanchote, V. L. (2009). Stereoselective analysis of labetalol in human plasma by LC-MS/MS: application to pharmacokinetics. Chirality, 21( 8), 738-744. doi:10.1002/chir.20673
    • NLM

      Carvalho TM de JP, Cavalli R de C, Marques MP, Cunha SP da, Baraldi C de O, Lanchote VL. Stereoselective analysis of labetalol in human plasma by LC-MS/MS: application to pharmacokinetics [Internet]. Chirality. 2009 ; 21( 8): 738-744.[citado 2024 out. 12 ] Available from: https://doi.org/10.1002/chir.20673
    • Vancouver

      Carvalho TM de JP, Cavalli R de C, Marques MP, Cunha SP da, Baraldi C de O, Lanchote VL. Stereoselective analysis of labetalol in human plasma by LC-MS/MS: application to pharmacokinetics [Internet]. Chirality. 2009 ; 21( 8): 738-744.[citado 2024 out. 12 ] Available from: https://doi.org/10.1002/chir.20673
  • Source: Chirality. Unidades: FMRP, FCFRP

    Subjects: METABÓLITOS, FARMACOCINÉTICA, HIPERTENSÃO (TRATAMENTO)

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      BORALLI, Vanessa Bergamin e COELHO, Eduardo Barbosa e LANCHOTE, Vera Lúcia. Influence of quinidine, cimetidine, and ketoconazole on the enantioselective pharmacokinetics and metabolism of metoprolol in rats. Chirality, v. 21, n. 10, p. 886-893, 2009Tradução . . Disponível em: https://doi.org/10.1002/chir.20682. Acesso em: 12 out. 2024.
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      Boralli, V. B., Coelho, E. B., & Lanchote, V. L. (2009). Influence of quinidine, cimetidine, and ketoconazole on the enantioselective pharmacokinetics and metabolism of metoprolol in rats. Chirality, 21( 10), 886-893. doi:10.1002/chir.20682
    • NLM

      Boralli VB, Coelho EB, Lanchote VL. Influence of quinidine, cimetidine, and ketoconazole on the enantioselective pharmacokinetics and metabolism of metoprolol in rats [Internet]. Chirality. 2009 ; 21( 10): 886-893.[citado 2024 out. 12 ] Available from: https://doi.org/10.1002/chir.20682
    • Vancouver

      Boralli VB, Coelho EB, Lanchote VL. Influence of quinidine, cimetidine, and ketoconazole on the enantioselective pharmacokinetics and metabolism of metoprolol in rats [Internet]. Chirality. 2009 ; 21( 10): 886-893.[citado 2024 out. 12 ] Available from: https://doi.org/10.1002/chir.20682
  • Source: Chirality. Unidade: IQ

    Assunto: PRODUTOS NATURAIS (BIOSSÍNTESE)

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      BATISTA JR., João Marcos et al. Resolution and absolute configuration assignment of a natural racemic chromane from Peperomia obtusifolia (Piperaceae). Chirality, v. 21, n. 9, p. 799-801, 2009Tradução . . Disponível em: https://doi.org/10.1002/chir.20676. Acesso em: 12 out. 2024.
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      Batista Jr., J. M., López, S. N., Mota, J. da S., Vanzolini, K. L., Cass, Q. B., Rinaldo, D., et al. (2009). Resolution and absolute configuration assignment of a natural racemic chromane from Peperomia obtusifolia (Piperaceae). Chirality, 21( 9), 799-801. doi:10.1002/chir.20676
    • NLM

      Batista Jr. JM, López SN, Mota J da S, Vanzolini KL, Cass QB, Rinaldo D, Vilegas W, Bolzani V da S, Kato MJ, Furlan M. Resolution and absolute configuration assignment of a natural racemic chromane from Peperomia obtusifolia (Piperaceae) [Internet]. Chirality. 2009 ; 21( 9): 799-801.[citado 2024 out. 12 ] Available from: https://doi.org/10.1002/chir.20676
    • Vancouver

      Batista Jr. JM, López SN, Mota J da S, Vanzolini KL, Cass QB, Rinaldo D, Vilegas W, Bolzani V da S, Kato MJ, Furlan M. Resolution and absolute configuration assignment of a natural racemic chromane from Peperomia obtusifolia (Piperaceae) [Internet]. Chirality. 2009 ; 21( 9): 799-801.[citado 2024 out. 12 ] Available from: https://doi.org/10.1002/chir.20676
  • Source: Chirality. Unidades: FCFRP, FMRP

    Subjects: FARMACOCINÉTICA, CROMATOGRAFIA LÍQUIDA

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      GODOY, Ana Leonor Pardo Campos et al. Enantioselective determination of mexiletine and its metabolites p-hydroxymexiletine and hydroxymethylmexiletine in rat plasma by normal-phase liquid chromatography-tandem mass spectrometry: application to pharmacokinetics. Chirality, v. 21, n. 7, p. 648-656, 2009Tradução . . Disponível em: https://doi.org/10.1002/chir.20650. Acesso em: 12 out. 2024.
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      Godoy, A. L. P. C., Parisi, C. C., Marques, M. P., Coelho, E. B., & Lanchote, V. L. (2009). Enantioselective determination of mexiletine and its metabolites p-hydroxymexiletine and hydroxymethylmexiletine in rat plasma by normal-phase liquid chromatography-tandem mass spectrometry: application to pharmacokinetics. Chirality, 21( 7), 648-656. doi:10.1002/chir.20650
    • NLM

      Godoy ALPC, Parisi CC, Marques MP, Coelho EB, Lanchote VL. Enantioselective determination of mexiletine and its metabolites p-hydroxymexiletine and hydroxymethylmexiletine in rat plasma by normal-phase liquid chromatography-tandem mass spectrometry: application to pharmacokinetics [Internet]. Chirality. 2009 ; 21( 7): 648-656.[citado 2024 out. 12 ] Available from: https://doi.org/10.1002/chir.20650
    • Vancouver

      Godoy ALPC, Parisi CC, Marques MP, Coelho EB, Lanchote VL. Enantioselective determination of mexiletine and its metabolites p-hydroxymexiletine and hydroxymethylmexiletine in rat plasma by normal-phase liquid chromatography-tandem mass spectrometry: application to pharmacokinetics [Internet]. Chirality. 2009 ; 21( 7): 648-656.[citado 2024 out. 12 ] Available from: https://doi.org/10.1002/chir.20650
  • Source: Chirality. Unidades: FMRP, FCFRP

    Subjects: ANTIDEPRESSIVOS, FARMACOCINÉTICA, METABOLISMO

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      ROCHA, Adriana et al. Enantioselective analysis of citalopram and demethylcitalopram in human and rat plasma by chiral LC-MS/MS: application to pharmacokinetics. Chirality, v. 19, p. 793-801, 2007Tradução . . Disponível em: https://doi.org/10.1002/chir.20452. Acesso em: 12 out. 2024.
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      Rocha, A., Marques, M. P., Coelho, E. B., & Lanchote, V. L. (2007). Enantioselective analysis of citalopram and demethylcitalopram in human and rat plasma by chiral LC-MS/MS: application to pharmacokinetics. Chirality, 19, 793-801. doi:10.1002/chir.20452
    • NLM

      Rocha A, Marques MP, Coelho EB, Lanchote VL. Enantioselective analysis of citalopram and demethylcitalopram in human and rat plasma by chiral LC-MS/MS: application to pharmacokinetics [Internet]. Chirality. 2007 ; 19 793-801.[citado 2024 out. 12 ] Available from: https://doi.org/10.1002/chir.20452
    • Vancouver

      Rocha A, Marques MP, Coelho EB, Lanchote VL. Enantioselective analysis of citalopram and demethylcitalopram in human and rat plasma by chiral LC-MS/MS: application to pharmacokinetics [Internet]. Chirality. 2007 ; 19 793-801.[citado 2024 out. 12 ] Available from: https://doi.org/10.1002/chir.20452
  • Source: Chirality. Unidades: FFCLRP, FCFRP

    Subjects: FÁRMACOS (METABOLISMO HÍDRICO E MINERAL), BIOFÍSICA

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      GAITANI, Cristiane Masetto e MARTINEZ, Alexandre Souto e BONATO, Pierina Sueli. Recemization and degradation of thioridazine and thioridazine 2-sulfone in human plasma and aqueous solutions. Chirality, v. 15, p. 479-485, 2003Tradução . . Disponível em: https://doi.org/10.1002/chir.10240. Acesso em: 12 out. 2024.
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      Gaitani, C. M., Martinez, A. S., & Bonato, P. S. (2003). Recemization and degradation of thioridazine and thioridazine 2-sulfone in human plasma and aqueous solutions. Chirality, 15, 479-485. doi:10.1002/chir.10240
    • NLM

      Gaitani CM, Martinez AS, Bonato PS. Recemization and degradation of thioridazine and thioridazine 2-sulfone in human plasma and aqueous solutions [Internet]. Chirality. 2003 ; 15 479-485.[citado 2024 out. 12 ] Available from: https://doi.org/10.1002/chir.10240
    • Vancouver

      Gaitani CM, Martinez AS, Bonato PS. Recemization and degradation of thioridazine and thioridazine 2-sulfone in human plasma and aqueous solutions [Internet]. Chirality. 2003 ; 15 479-485.[citado 2024 out. 12 ] Available from: https://doi.org/10.1002/chir.10240
  • Source: Chirality. Unidades: FFCLRP, FCFRP

    Assunto: QUÍMICA ANALÍTICA

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      GAITANI, Cristiane Masetto de e MARTINEZ, Alexandre Souto e BONATO, Pierina Sueli. Racemization and degradation of thioridazine and thioridazine 2-sulfone in human plasma and aqueous solutions. Chirality, v. 15, n. 6, p. 479-485, 2003Tradução . . Disponível em: https://doi.org/10.1002/chir.10240. Acesso em: 12 out. 2024.
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      Gaitani, C. M. de, Martinez, A. S., & Bonato, P. S. (2003). Racemization and degradation of thioridazine and thioridazine 2-sulfone in human plasma and aqueous solutions. Chirality, 15( 6), 479-485. doi:10.1002/chir.10240
    • NLM

      Gaitani CM de, Martinez AS, Bonato PS. Racemization and degradation of thioridazine and thioridazine 2-sulfone in human plasma and aqueous solutions [Internet]. Chirality. 2003 ; 15( 6): 479-485.[citado 2024 out. 12 ] Available from: https://doi.org/10.1002/chir.10240
    • Vancouver

      Gaitani CM de, Martinez AS, Bonato PS. Racemization and degradation of thioridazine and thioridazine 2-sulfone in human plasma and aqueous solutions [Internet]. Chirality. 2003 ; 15( 6): 479-485.[citado 2024 out. 12 ] Available from: https://doi.org/10.1002/chir.10240
  • Source: Chirality. Unidade: FCFRP

    Assunto: FARMACOLOGIA CLÍNICA

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      CERQUEIRA, Paula Macedo et al. Stereoselective metabolism of metoprolol: enantioselectivity of 'alfa'-hydroxymetoprolol in plasma and urine. Chirality, v. 15, p. 542-549, 2003Tradução . . Disponível em: https://doi.org/10.1002/chir.10244. Acesso em: 12 out. 2024.
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      Cerqueira, P. M., Cesarino, E. J., Bertucci, C., Bonato, P. S., & Lanchote, V. L. (2003). Stereoselective metabolism of metoprolol: enantioselectivity of 'alfa'-hydroxymetoprolol in plasma and urine. Chirality, 15, 542-549. doi:10.1002/chir.10244
    • NLM

      Cerqueira PM, Cesarino EJ, Bertucci C, Bonato PS, Lanchote VL. Stereoselective metabolism of metoprolol: enantioselectivity of 'alfa'-hydroxymetoprolol in plasma and urine [Internet]. Chirality. 2003 ; 15 542-549.[citado 2024 out. 12 ] Available from: https://doi.org/10.1002/chir.10244
    • Vancouver

      Cerqueira PM, Cesarino EJ, Bertucci C, Bonato PS, Lanchote VL. Stereoselective metabolism of metoprolol: enantioselectivity of 'alfa'-hydroxymetoprolol in plasma and urine [Internet]. Chirality. 2003 ; 15 542-549.[citado 2024 out. 12 ] Available from: https://doi.org/10.1002/chir.10244
  • Source: Chirality. Unidades: FMRP, FCFRP

    Subjects: FARMACOCINÉTICA, GRAVIDEZ, HIPERTENSÃO

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      GONÇALVES, Paulo Vinícius Bernardes et al. Enantioselectivity in the steady-state pharmacokinetics and transplacental distribution of pindolol at delivery in pregnancy-induced hypertension. Chirality, v. 14, n. 8, p. 683-687, 2002Tradução . . Disponível em: https://doi.org/10.1002/chir.10124. Acesso em: 12 out. 2024.
    • APA

      Gonçalves, P. V. B., Matthes, Â. do C. S., Cunha, S. P. da, & Lanchote, V. L. (2002). Enantioselectivity in the steady-state pharmacokinetics and transplacental distribution of pindolol at delivery in pregnancy-induced hypertension. Chirality, 14( 8), 683-687. doi:10.1002/chir.10124
    • NLM

      Gonçalves PVB, Matthes  do CS, Cunha SP da, Lanchote VL. Enantioselectivity in the steady-state pharmacokinetics and transplacental distribution of pindolol at delivery in pregnancy-induced hypertension [Internet]. Chirality. 2002 ; 14( 8): 683-687.[citado 2024 out. 12 ] Available from: https://doi.org/10.1002/chir.10124
    • Vancouver

      Gonçalves PVB, Matthes  do CS, Cunha SP da, Lanchote VL. Enantioselectivity in the steady-state pharmacokinetics and transplacental distribution of pindolol at delivery in pregnancy-induced hypertension [Internet]. Chirality. 2002 ; 14( 8): 683-687.[citado 2024 out. 12 ] Available from: https://doi.org/10.1002/chir.10124
  • Source: Chirality. Unidade: IQ

    Subjects: FÍSICO-QUÍMICA, COMPOSTOS ORGÂNICOS, CRISTALIZAÇÃO

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    • ABNT

      DURAND, Daniel J. et al. Generation of molecular chiral asymmetry through stirred crystallization. Chirality, v. 14, n. 4, p. 284-287, 2002Tradução . . Disponível em: https://doi.org/10.1002/chir.10044. Acesso em: 12 out. 2024.
    • APA

      Durand, D. J., Kondepudi, D. K., Moreira Júnior, P. F., & Quina, F. H. (2002). Generation of molecular chiral asymmetry through stirred crystallization. Chirality, 14( 4), 284-287. doi:10.1002/chir.10044
    • NLM

      Durand DJ, Kondepudi DK, Moreira Júnior PF, Quina FH. Generation of molecular chiral asymmetry through stirred crystallization [Internet]. Chirality. 2002 ; 14( 4): 284-287.[citado 2024 out. 12 ] Available from: https://doi.org/10.1002/chir.10044
    • Vancouver

      Durand DJ, Kondepudi DK, Moreira Júnior PF, Quina FH. Generation of molecular chiral asymmetry through stirred crystallization [Internet]. Chirality. 2002 ; 14( 4): 284-287.[citado 2024 out. 12 ] Available from: https://doi.org/10.1002/chir.10044
  • Source: Chirality. Unidades: FCFRP, FCF

    Subjects: FARMACOLOGIA CLÍNICA, ANÁLISE TOXICOLÓGICA

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    • ABNT

      LANCHOTE, Vera Lúcia et al. Enantioselectivity in the metabolism of mexiletine by conjugation in female patients with the arrhythmic form of chronic Chagas´ heart disease. Chirality, v. 11, n. 1, p. 29-32, 1999Tradução . . Disponível em: https://doi.org/10.1002/(sici)1520-636x(1999)11:1%3C29::aid-chir5%3E3.0.co;2-u. Acesso em: 12 out. 2024.
    • APA

      Lanchote, V. L., Cesarino, E. J., Santos, V. J., Mere, Y., & Santos, S. R. C. J. (1999). Enantioselectivity in the metabolism of mexiletine by conjugation in female patients with the arrhythmic form of chronic Chagas´ heart disease. Chirality, 11( 1), 29-32. doi:10.1002/(sici)1520-636x(1999)11:1%3C29::aid-chir5%3E3.0.co;2-u
    • NLM

      Lanchote VL, Cesarino EJ, Santos VJ, Mere Y, Santos SRCJ. Enantioselectivity in the metabolism of mexiletine by conjugation in female patients with the arrhythmic form of chronic Chagas´ heart disease [Internet]. Chirality. 1999 ; 11( 1): 29-32.[citado 2024 out. 12 ] Available from: https://doi.org/10.1002/(sici)1520-636x(1999)11:1%3C29::aid-chir5%3E3.0.co;2-u
    • Vancouver

      Lanchote VL, Cesarino EJ, Santos VJ, Mere Y, Santos SRCJ. Enantioselectivity in the metabolism of mexiletine by conjugation in female patients with the arrhythmic form of chronic Chagas´ heart disease [Internet]. Chirality. 1999 ; 11( 1): 29-32.[citado 2024 out. 12 ] Available from: https://doi.org/10.1002/(sici)1520-636x(1999)11:1%3C29::aid-chir5%3E3.0.co;2-u
  • Source: Chirality. Unidades: FCFRP, FCF

    Subjects: FARMACOLOGIA, FARMACOCINÉTICA, METABOLISMO, CISTICERCOSE

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    • ABNT

      MARQUES, Maria Paula da Costa et al. Enantioselective kinetic disposition of albendazole sulfoxide in patients with neurocysticercosis. Chirality, v. 11, n. 3, p. 218-233, 1999Tradução . . Disponível em: https://doi.org/10.1002/(sici)1520-636x(1999)11:3%3C218::aid-chir8%3E3.0.co;2-g. Acesso em: 12 out. 2024.
    • APA

      Marques, M. P. da C., Takayanagui, O. M., Bonato, P. S., Santos, S. R. C. J., & Lanchote, V. L. (1999). Enantioselective kinetic disposition of albendazole sulfoxide in patients with neurocysticercosis. Chirality, 11( 3), 218-233. doi:10.1002/(sici)1520-636x(1999)11:3%3C218::aid-chir8%3E3.0.co;2-g
    • NLM

      Marques MP da C, Takayanagui OM, Bonato PS, Santos SRCJ, Lanchote VL. Enantioselective kinetic disposition of albendazole sulfoxide in patients with neurocysticercosis [Internet]. Chirality. 1999 ; 11( 3): 218-233.[citado 2024 out. 12 ] Available from: https://doi.org/10.1002/(sici)1520-636x(1999)11:3%3C218::aid-chir8%3E3.0.co;2-g
    • Vancouver

      Marques MP da C, Takayanagui OM, Bonato PS, Santos SRCJ, Lanchote VL. Enantioselective kinetic disposition of albendazole sulfoxide in patients with neurocysticercosis [Internet]. Chirality. 1999 ; 11( 3): 218-233.[citado 2024 out. 12 ] Available from: https://doi.org/10.1002/(sici)1520-636x(1999)11:3%3C218::aid-chir8%3E3.0.co;2-g
  • Source: Chirality. Unidade: FCFRP

    Subjects: QUÍMICA ANALÍTICA, MACROMOLÉCULA, MEDICAMENTO

    Acesso à fonteDOIHow to cite
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    • ABNT

      BERTUCCI, Carlo et al. Site I on human albumin: differences in the binding of (R)-and (S)-Warfarin. Chirality, v. 11, p. 675-679, 1999Tradução . . Disponível em: https://doi.org/10.1002/(sici)1520-636x(1999)11:9%3C675::aid-chir1%3E3.0.co;2-c. Acesso em: 12 out. 2024.
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      Bertucci, C., Canepa, A., Ascoli, G. A., Guimarães, L. F. L., & Felix, G. (1999). Site I on human albumin: differences in the binding of (R)-and (S)-Warfarin. Chirality, 11, 675-679. doi:10.1002/(sici)1520-636x(1999)11:9%3C675::aid-chir1%3E3.0.co;2-c
    • NLM

      Bertucci C, Canepa A, Ascoli GA, Guimarães LFL, Felix G. Site I on human albumin: differences in the binding of (R)-and (S)-Warfarin [Internet]. Chirality. 1999 ; 11 675-679.[citado 2024 out. 12 ] Available from: https://doi.org/10.1002/(sici)1520-636x(1999)11:9%3C675::aid-chir1%3E3.0.co;2-c
    • Vancouver

      Bertucci C, Canepa A, Ascoli GA, Guimarães LFL, Felix G. Site I on human albumin: differences in the binding of (R)-and (S)-Warfarin [Internet]. Chirality. 1999 ; 11 675-679.[citado 2024 out. 12 ] Available from: https://doi.org/10.1002/(sici)1520-636x(1999)11:9%3C675::aid-chir1%3E3.0.co;2-c

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