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  • Source: Chirality. Unidade: IF

    Subjects: FARMACOLOGIA, TERAPÊUTICA MÉDICA

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      CATTANI, Mauro Sergio Dorsa e BASSALO, J M F. Weak interactions and the tunneling racemization. Chirality, v. 10, p. 745-750, 1998Tradução . . Disponível em: https://doi.org/10.1002/(sici)1520-636x(1998)10:6%3C519::aid-chir3%3E3.0.co;2-z. Acesso em: 26 abr. 2024.
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      Cattani, M. S. D., & Bassalo, J. M. F. (1998). Weak interactions and the tunneling racemization. Chirality, 10, 745-750. doi:10.1002/(sici)1520-636x(1998)10:6%3C519::aid-chir3%3E3.0.co;2-z
    • NLM

      Cattani MSD, Bassalo JMF. Weak interactions and the tunneling racemization [Internet]. Chirality. 1998 ; 10 745-750.[citado 2024 abr. 26 ] Available from: https://doi.org/10.1002/(sici)1520-636x(1998)10:6%3C519::aid-chir3%3E3.0.co;2-z
    • Vancouver

      Cattani MSD, Bassalo JMF. Weak interactions and the tunneling racemization [Internet]. Chirality. 1998 ; 10 745-750.[citado 2024 abr. 26 ] Available from: https://doi.org/10.1002/(sici)1520-636x(1998)10:6%3C519::aid-chir3%3E3.0.co;2-z
  • 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: 26 abr. 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 abr. 26 ] 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 abr. 26 ] Available from: https://doi.org/10.1002/chir.22016
  • Source: 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: 26 abr. 2024.
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      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 abr. 26 ] 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 abr. 26 ] Available from: https://doi.org/10.1002/chir.10308
  • 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: 26 abr. 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 abr. 26 ] 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 abr. 26 ] Available from: https://doi.org/10.1002/chir.10244
  • Source: Chirality. Unidades: FMRP, FCFRP

    Subjects: 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: 26 abr. 2024.
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      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 abr. 26 ] 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 abr. 26 ] Available from: https://doi.org/10.1002/chir.20374
  • 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: 26 abr. 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 abr. 26 ] 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 abr. 26 ] Available from: https://doi.org/10.1002/chir.20673
  • Source: Chirality. Unidade: FCFRP

    Subjects: QUÍMICA ANALÍTICA, MACROMOLÉCULA, MEDICAMENTO

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      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: 26 abr. 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 abr. 26 ] 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 abr. 26 ] Available from: https://doi.org/10.1002/(sici)1520-636x(1999)11:9%3C675::aid-chir1%3E3.0.co;2-c
  • Source: Chirality. Unidades: FMRP, FCFRP

    Subjects: ESPECTROMETRIA DE MASSAS, FARMACOCINÉTICA, PLASMA

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      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: 26 abr. 2024.
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      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 abr. 26 ] 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 abr. 26 ] Available from: https://doi.org/10.1002/chir.20914
  • 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: 26 abr. 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 abr. 26 ] 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 abr. 26 ] Available from: https://doi.org/10.1002/chir.22803
  • 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: 26 abr. 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 abr. 26 ] 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 abr. 26 ] Available from: https://doi.org/10.1002/chir.20676
  • 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: 26 abr. 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 abr. 26 ] 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 abr. 26 ] 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: 26 abr. 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 abr. 26 ] 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 abr. 26 ] Available from: https://doi.org/10.1002/chir.10240
  • Source: Chirality. Unidades: FCFRP, FMRP

    Assunto: FARMACOLOGIA CLÍNICA

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      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: 26 abr. 2024.
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      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 abr. 26 ] 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 abr. 26 ] Available from: https://doi.org/10.1002/chir.20065
  • 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: 26 abr. 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 abr. 26 ] 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 abr. 26 ] Available from: https://doi.org/10.1002/chir.20682
  • 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: 26 abr. 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 abr. 26 ] 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 abr. 26 ] Available from: https://doi.org/10.1002/chir.22136
  • Source: Chirality. Unidade: IQ

    Subjects: FÍSICO-QUÍMICA, COMPOSTOS ORGÂNICOS, CRISTALIZAÇÃO

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      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: 26 abr. 2024.
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      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 abr. 26 ] 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 abr. 26 ] Available from: https://doi.org/10.1002/chir.10044
  • Source: Chirality. Unidades: FCF, FCFRP

    Assunto: FARMACOLOGIA CLÍNICA

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    • ABNT

      CERQUEIRA, Paula Macedo et al. Enantioselectivity in the steady-state pharmacokinetics of metoprolol in hypertensive patients. Chirality, v. 11, p. 591-597, 1999Tradução . . Disponível em: https://doi.org/10.1002/(sici)1520-636x(1999)11:7%3C591::aid-chir12%3E3.0.co;2-t. Acesso em: 26 abr. 2024.
    • APA

      Cerqueira, P. M., Cesarino, E. J., Mateus, F. H., Mere Júnior, Y., Santos, S. R. C. J., & Lanchote, V. L. (1999). Enantioselectivity in the steady-state pharmacokinetics of metoprolol in hypertensive patients. Chirality, 11, 591-597. doi:10.1002/(sici)1520-636x(1999)11:7%3C591::aid-chir12%3E3.0.co;2-t
    • NLM

      Cerqueira PM, Cesarino EJ, Mateus FH, Mere Júnior Y, Santos SRCJ, Lanchote VL. Enantioselectivity in the steady-state pharmacokinetics of metoprolol in hypertensive patients [Internet]. Chirality. 1999 ; 11 591-597.[citado 2024 abr. 26 ] Available from: https://doi.org/10.1002/(sici)1520-636x(1999)11:7%3C591::aid-chir12%3E3.0.co;2-t
    • Vancouver

      Cerqueira PM, Cesarino EJ, Mateus FH, Mere Júnior Y, Santos SRCJ, Lanchote VL. Enantioselectivity in the steady-state pharmacokinetics of metoprolol in hypertensive patients [Internet]. Chirality. 1999 ; 11 591-597.[citado 2024 abr. 26 ] Available from: https://doi.org/10.1002/(sici)1520-636x(1999)11:7%3C591::aid-chir12%3E3.0.co;2-t
  • 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: 26 abr. 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 abr. 26 ] 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 abr. 26 ] Available from: https://doi.org/10.1002/chir.10124
  • Source: Chirality. Unidades: FCFRP, FCF

    Subjects: FARMACOLOGIA CLÍNICA, ANÁLISE TOXICOLÓGICA

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      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: 26 abr. 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 abr. 26 ] 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 abr. 26 ] Available from: https://doi.org/10.1002/(sici)1520-636x(1999)11:1%3C29::aid-chir5%3E3.0.co;2-u
  • Source: Chirality. Unidade: IQSC

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

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    • ABNT

      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: 26 abr. 2024.
    • APA

      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 abr. 26 ] 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 abr. 26 ] Available from: https://doi.org/10.1002/chir.22851

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