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  • Fonte: Chirality. Unidade: IQSC

    Assunto: CATÁLISE

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    • ABNT

      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: 16 nov. 2024.
    • APA

      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
    • NLM

      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 nov. 16 ] 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 nov. 16 ] Available from: https://doi.org/10.1002/chir.23078
  • Fonte: Chirality. Unidade: FCFRP

    Assuntos: 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: 16 nov. 2024.
    • APA

      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 nov. 16 ] 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 nov. 16 ] Available from: https://doi.org/10.1002/chir.22803
  • Fonte: Chirality. Unidade: IQSC

    Assuntos: 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: 16 nov. 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 nov. 16 ] 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 nov. 16 ] Available from: https://doi.org/10.1002/chir.22851
  • Fonte: Chirality. Unidades: FMRP, FCFRP

    Assuntos: 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: 16 nov. 2024.
    • APA

      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 nov. 16 ] 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 nov. 16 ] Available from: https://doi.org/10.1002/chir.22231
  • Fonte: Chirality. Unidade: FCFRP

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

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    • ABNT

      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: 16 nov. 2024.
    • APA

      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 nov. 16 ] 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 nov. 16 ] Available from: https://doi.org/10.1002/chir.22136
  • Fonte: Chirality. Unidade: IFSC

    Assuntos: 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: 16 nov. 2024.
    • APA

      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 nov. 16 ] 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 nov. 16 ] Available from: https://doi.org/10.1002/chir.22016
  • Fonte: Chirality. Unidades: FMRP, FCFRP

    Assuntos: ESPECTROMETRIA DE MASSAS, FARMACOCINÉTICA, PLASMA

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    • ABNT

      GODOY, Ana Leonor Pardo Campos et al. Simultaneous analysis of tramadol, O-desmethyltramadol, and N-desmethyltramadol enantiomers in rat plasma by high-performance liquid chromatography-tandem mass spectrometry: Application to pharmacokinetics. Chirality, v. 23, n. 4, p. 287-293, 2011Tradução . . Disponível em: https://doi.org/10.1002/chir.20914. Acesso em: 16 nov. 2024.
    • APA

      Godoy, A. L. P. C., Moraes, N. V. de, Martinez, E. Z., Carvalho, T. M. de J. P., Marques, M. P., & Lanchote, V. L. (2011). Simultaneous analysis of tramadol, O-desmethyltramadol, and N-desmethyltramadol enantiomers in rat plasma by high-performance liquid chromatography-tandem mass spectrometry: Application to pharmacokinetics. Chirality, 23( 4), 287-293. doi:10.1002/chir.20914
    • NLM

      Godoy ALPC, Moraes NV de, Martinez EZ, Carvalho TM de JP, Marques MP, Lanchote VL. Simultaneous analysis of tramadol, O-desmethyltramadol, and N-desmethyltramadol enantiomers in rat plasma by high-performance liquid chromatography-tandem mass spectrometry: Application to pharmacokinetics [Internet]. Chirality. 2011 ; 23( 4): 287-293.[citado 2024 nov. 16 ] Available from: https://doi.org/10.1002/chir.20914
    • Vancouver

      Godoy ALPC, Moraes NV de, Martinez EZ, Carvalho TM de JP, Marques MP, Lanchote VL. Simultaneous analysis of tramadol, O-desmethyltramadol, and N-desmethyltramadol enantiomers in rat plasma by high-performance liquid chromatography-tandem mass spectrometry: Application to pharmacokinetics [Internet]. Chirality. 2011 ; 23( 4): 287-293.[citado 2024 nov. 16 ] Available from: https://doi.org/10.1002/chir.20914
  • Fonte: Chirality. Unidades: FCFRP, FMRP

    Assuntos: NEOPLASIAS MAMÁRIAS, FARMACOTÉCNICA

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      SILVA, Carolina de Miranda et al. Determination of cyclophosphamide enantiomers in plasma by LC-MS/MS: application to pharmacokinetics in breast cancer and lupus nephritis patients. Chirality, v. 21, n. 3, p. 383-389, 2009Tradução . . Disponível em: https://doi.org/10.1002/chir.20596. Acesso em: 16 nov. 2024.
    • APA

      Silva, C. de M., Fernandes, B. J. D., Pereira, M. P. M., Silva, L. M. da, Donadi, E. A., Matthes, Â. do C. S., et al. (2009). Determination of cyclophosphamide enantiomers in plasma by LC-MS/MS: application to pharmacokinetics in breast cancer and lupus nephritis patients. Chirality, 21( 3), 383-389. doi:10.1002/chir.20596
    • NLM

      Silva C de M, Fernandes BJD, Pereira MPM, Silva LM da, Donadi EA, Matthes  do CS, Andrade JM de, Lanchote VL. Determination of cyclophosphamide enantiomers in plasma by LC-MS/MS: application to pharmacokinetics in breast cancer and lupus nephritis patients [Internet]. Chirality. 2009 ; 21( 3): 383-389.[citado 2024 nov. 16 ] Available from: https://doi.org/10.1002/chir.20596
    • Vancouver

      Silva C de M, Fernandes BJD, Pereira MPM, Silva LM da, Donadi EA, Matthes  do CS, Andrade JM de, Lanchote VL. Determination of cyclophosphamide enantiomers in plasma by LC-MS/MS: application to pharmacokinetics in breast cancer and lupus nephritis patients [Internet]. Chirality. 2009 ; 21( 3): 383-389.[citado 2024 nov. 16 ] Available from: https://doi.org/10.1002/chir.20596
  • Fonte: Chirality. Unidades: FMRP, FCFRP

    Assuntos: 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: 16 nov. 2024.
    • APA

      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 nov. 16 ] 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 nov. 16 ] Available from: https://doi.org/10.1002/chir.20682
  • Fonte: 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: 16 nov. 2024.
    • APA

      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 nov. 16 ] 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 nov. 16 ] Available from: https://doi.org/10.1002/chir.20676
  • Fonte: Chirality. Unidades: FCFRP, FMRP

    Assuntos: 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: 16 nov. 2024.
    • APA

      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 nov. 16 ] 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 nov. 16 ] Available from: https://doi.org/10.1002/chir.20650
  • Fonte: Chirality. Unidades: FMRP, FCFRP

    Assuntos: FARMACOCINÉTICA, ARTRITE, LÍQUIDO SINOVIAL

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      SILVA, Carolina de Miranda et al. Stereoselective disposition of fenoprofen in plasma and synovial fluid of patients with rheumathoid arthritis. Chirality, v. 19, n. 4, p. 255-263, 2007Tradução . . Disponível em: https://doi.org/10.1002/chir.20374. Acesso em: 16 nov. 2024.
    • APA

      Silva, C. de M., Marques, M. P., Barissa, G. R., Donadi, E. A., Silva, L. M. da, & Lanchote, V. L. (2007). Stereoselective disposition of fenoprofen in plasma and synovial fluid of patients with rheumathoid arthritis. Chirality, 19( 4), 255-263. doi:10.1002/chir.20374
    • NLM

      Silva C de M, Marques MP, Barissa GR, Donadi EA, Silva LM da, Lanchote VL. Stereoselective disposition of fenoprofen in plasma and synovial fluid of patients with rheumathoid arthritis [Internet]. Chirality. 2007 ; 19( 4): 255-263.[citado 2024 nov. 16 ] Available from: https://doi.org/10.1002/chir.20374
    • Vancouver

      Silva C de M, Marques MP, Barissa GR, Donadi EA, Silva LM da, Lanchote VL. Stereoselective disposition of fenoprofen in plasma and synovial fluid of patients with rheumathoid arthritis [Internet]. Chirality. 2007 ; 19( 4): 255-263.[citado 2024 nov. 16 ] Available from: https://doi.org/10.1002/chir.20374
  • Fonte: Chirality. Unidades: FMRP, FCFRP

    Assuntos: 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: 16 nov. 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 nov. 16 ] 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 nov. 16 ] Available from: https://doi.org/10.1002/chir.20452
  • Fonte: Chirality. Unidades: FCFRP, FMRP

    Assunto: FARMACOLOGIA CLÍNICA

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      PAPINI, Olga et al. Stereoselectivity in the placental transfer and kinetic disposition of racemic bupivacaine administered to parturients with or without a vasoconstrictor. Chirality, v. 16, p. 65-71, 2004Tradução . . Disponível em: https://doi.org/10.1002/chir.10308. Acesso em: 16 nov. 2024.
    • APA

      Papini, O., Mathes, Â. do C. da S., Cunha, S. P. da, & Lanchote, V. L. (2004). Stereoselectivity in the placental transfer and kinetic disposition of racemic bupivacaine administered to parturients with or without a vasoconstrictor. Chirality, 16, 65-71. doi:10.1002/chir.10308
    • NLM

      Papini O, Mathes  do C da S, Cunha SP da, Lanchote VL. Stereoselectivity in the placental transfer and kinetic disposition of racemic bupivacaine administered to parturients with or without a vasoconstrictor [Internet]. Chirality. 2004 ; 16 65-71.[citado 2024 nov. 16 ] Available from: https://doi.org/10.1002/chir.10308
    • Vancouver

      Papini O, Mathes  do C da S, Cunha SP da, Lanchote VL. Stereoselectivity in the placental transfer and kinetic disposition of racemic bupivacaine administered to parturients with or without a vasoconstrictor [Internet]. Chirality. 2004 ; 16 65-71.[citado 2024 nov. 16 ] Available from: https://doi.org/10.1002/chir.10308
  • Fonte: Chirality. Unidades: FCFRP, FMRP

    Assunto: FARMACOLOGIA CLÍNICA

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    • ABNT

      BARISSA, Giuliano Rodrigo et al. Influence of rheumatoid arthritis in the enantioselective dispositionof fenoprofen. Chirality, v. 16, p. 602-608, 2004Tradução . . Disponível em: https://doi.org/10.1002/chir.20065. Acesso em: 16 nov. 2024.
    • APA

      Barissa, G. R., Poggi, J. C., Donadi, E. A., Reis, M. L. dos, & Lanchote, V. L. (2004). Influence of rheumatoid arthritis in the enantioselective dispositionof fenoprofen. Chirality, 16, 602-608. doi:10.1002/chir.20065
    • NLM

      Barissa GR, Poggi JC, Donadi EA, Reis ML dos, Lanchote VL. Influence of rheumatoid arthritis in the enantioselective dispositionof fenoprofen [Internet]. Chirality. 2004 ; 16 602-608.[citado 2024 nov. 16 ] Available from: https://doi.org/10.1002/chir.20065
    • Vancouver

      Barissa GR, Poggi JC, Donadi EA, Reis ML dos, Lanchote VL. Influence of rheumatoid arthritis in the enantioselective dispositionof fenoprofen [Internet]. Chirality. 2004 ; 16 602-608.[citado 2024 nov. 16 ] Available from: https://doi.org/10.1002/chir.20065
  • Fonte: Chirality. Unidades: FCFRP, FMRP

    Assunto: FARMACOLOGIA CLÍNICA

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    • ABNT

      LANCHOTE, Vera Lúcia e TAKAYANAGUI, Osvaldo Massaiti e MATEUS, F H. Enantioselective renal excretion of albendazole metabolites in patients with neurocysticercosis. Chirality, v. 16, p. 520-525, 2004Tradução . . Disponível em: https://doi.org/10.1002/chir.20071. Acesso em: 16 nov. 2024.
    • APA

      Lanchote, V. L., Takayanagui, O. M., & Mateus, F. H. (2004). Enantioselective renal excretion of albendazole metabolites in patients with neurocysticercosis. Chirality, 16, 520-525. doi:10.1002/chir.20071
    • NLM

      Lanchote VL, Takayanagui OM, Mateus FH. Enantioselective renal excretion of albendazole metabolites in patients with neurocysticercosis [Internet]. Chirality. 2004 ; 16 520-525.[citado 2024 nov. 16 ] Available from: https://doi.org/10.1002/chir.20071
    • Vancouver

      Lanchote VL, Takayanagui OM, Mateus FH. Enantioselective renal excretion of albendazole metabolites in patients with neurocysticercosis [Internet]. Chirality. 2004 ; 16 520-525.[citado 2024 nov. 16 ] Available from: https://doi.org/10.1002/chir.20071
  • Fonte: Chirality. Unidades: FFCLRP, FCFRP

    Assuntos: FÁRMACOS (METABOLISMO HÍDRICO E MINERAL), BIOFÍSICA

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    • ABNT

      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: 16 nov. 2024.
    • APA

      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 nov. 16 ] 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 nov. 16 ] Available from: https://doi.org/10.1002/chir.10240
  • Fonte: Chirality. Unidades: FFCLRP, FCFRP

    Assunto: QUÍMICA ANALÍTICA

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    • ABNT

      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: 16 nov. 2024.
    • APA

      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 nov. 16 ] 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 nov. 16 ] Available from: https://doi.org/10.1002/chir.10240
  • Fonte: Chirality. Unidade: FCFRP

    Assunto: FARMACOLOGIA CLÍNICA

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    • ABNT

      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: 16 nov. 2024.
    • APA

      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 nov. 16 ] 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 nov. 16 ] Available from: https://doi.org/10.1002/chir.10244
  • Fonte: Chirality. Unidade: IQ

    Assuntos: 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: 16 nov. 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 nov. 16 ] 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 nov. 16 ] Available from: https://doi.org/10.1002/chir.10044

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