Filtros : "Indexado no Medline" "Carvalho, Ivone" Limpar

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  • Source: Tetrahedron. Unidade: FCFRP

    Subjects: PEPTÍDEOS CÍCLICOS, QUÍMICA MÉDICA

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      MARTINS, Maristela B. e CARVALHO, Ivone. Diketopiperazines: biological activity and synthesis. Tetrahedron, v. 63, n. 40, p. 9923-9932, 2007Tradução . . Disponível em: https://doi.org/10.1016/j.tet.2007.04.105. Acesso em: 18 nov. 2024.
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      Martins, M. B., & Carvalho, I. (2007). Diketopiperazines: biological activity and synthesis. Tetrahedron, 63( 40), 9923-9932. doi:10.1016/j.tet.2007.04.105
    • NLM

      Martins MB, Carvalho I. Diketopiperazines: biological activity and synthesis [Internet]. Tetrahedron. 2007 ; 63( 40): 9923-9932.[citado 2024 nov. 18 ] Available from: https://doi.org/10.1016/j.tet.2007.04.105
    • Vancouver

      Martins MB, Carvalho I. Diketopiperazines: biological activity and synthesis [Internet]. Tetrahedron. 2007 ; 63( 40): 9923-9932.[citado 2024 nov. 18 ] Available from: https://doi.org/10.1016/j.tet.2007.04.105
  • Source: Organic and Biomolecular Chemistry. Unidade: FCFRP

    Subjects: GLICOPEPTÍDEOS, TRYPANOSOMA CRUZI

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      CAMPO, Vanessa Leiria et al. Chemical and chemoenzymatic synthesis of glycosyl-amino acids and glycopeptides related to Trypanosoma cruzi mucins. Organic and Biomolecular Chemistry, v. 5, p. 2645-2657, 2007Tradução . . Disponível em: https://doi.org/10.1039/b707772f. Acesso em: 18 nov. 2024.
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      Campo, V. L., Carvalho, I., Allman, S., Davis, B. G., & Field, R. A. (2007). Chemical and chemoenzymatic synthesis of glycosyl-amino acids and glycopeptides related to Trypanosoma cruzi mucins. Organic and Biomolecular Chemistry, 5, 2645-2657. doi:10.1039/b707772f
    • NLM

      Campo VL, Carvalho I, Allman S, Davis BG, Field RA. Chemical and chemoenzymatic synthesis of glycosyl-amino acids and glycopeptides related to Trypanosoma cruzi mucins [Internet]. Organic and Biomolecular Chemistry. 2007 ; 5 2645-2657.[citado 2024 nov. 18 ] Available from: https://doi.org/10.1039/b707772f
    • Vancouver

      Campo VL, Carvalho I, Allman S, Davis BG, Field RA. Chemical and chemoenzymatic synthesis of glycosyl-amino acids and glycopeptides related to Trypanosoma cruzi mucins [Internet]. Organic and Biomolecular Chemistry. 2007 ; 5 2645-2657.[citado 2024 nov. 18 ] Available from: https://doi.org/10.1039/b707772f
  • Source: Bioorganic and Medicinal Chemistry. Unidades: IQ, FCFRP

    Subjects: ANTIPARASITÁRIOS, PRODUTOS NATURAIS, TRYPANOSOMA CRUZI

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      BERNARDES, Lilian Sibelle Campos et al. Synthesis and trypanocidal activity of 1,4-bis(3,4,5-trimethoxy-phenyl)-1,4-butanediol and 1,4-bis-(3,4-dimethoxyphenyl)-1,4-butanediol. Bioorganic and Medicinal Chemistry, v. 14, p. 7075-7082, 2006Tradução . . Disponível em: https://doi.org/10.1016/j.bmc.2006.07.006. Acesso em: 18 nov. 2024.
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      Bernardes, L. S. C., Kato, M. J., Albuquerque, S. de, & Carvalho, I. (2006). Synthesis and trypanocidal activity of 1,4-bis(3,4,5-trimethoxy-phenyl)-1,4-butanediol and 1,4-bis-(3,4-dimethoxyphenyl)-1,4-butanediol. Bioorganic and Medicinal Chemistry, 14, 7075-7082. doi:10.1016/j.bmc.2006.07.006
    • NLM

      Bernardes LSC, Kato MJ, Albuquerque S de, Carvalho I. Synthesis and trypanocidal activity of 1,4-bis(3,4,5-trimethoxy-phenyl)-1,4-butanediol and 1,4-bis-(3,4-dimethoxyphenyl)-1,4-butanediol [Internet]. Bioorganic and Medicinal Chemistry. 2006 ; 14 7075-7082.[citado 2024 nov. 18 ] Available from: https://doi.org/10.1016/j.bmc.2006.07.006
    • Vancouver

      Bernardes LSC, Kato MJ, Albuquerque S de, Carvalho I. Synthesis and trypanocidal activity of 1,4-bis(3,4,5-trimethoxy-phenyl)-1,4-butanediol and 1,4-bis-(3,4-dimethoxyphenyl)-1,4-butanediol [Internet]. Bioorganic and Medicinal Chemistry. 2006 ; 14 7075-7082.[citado 2024 nov. 18 ] Available from: https://doi.org/10.1016/j.bmc.2006.07.006
  • Source: Journal of Molecular Graphics and Modelling. Unidade: FCFRP

    Assunto: QUÍMICA FARMACÊUTICA

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      SILVA, Carlos H. T. P. da et al. Molecular modeling, docking and ADMET studies applied to the design of a novel hybrid for treatment of Alzheimer's disease. Journal of Molecular Graphics and Modelling, v. 25, p. 169-175, 2006Tradução . . Disponível em: https://doi.org/10.1016/j.jmgm.2005.12.002. Acesso em: 18 nov. 2024.
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      Silva, C. H. T. P. da, Campo, V. L., Carvalho, I., & Taft, C. A. (2006). Molecular modeling, docking and ADMET studies applied to the design of a novel hybrid for treatment of Alzheimer's disease. Journal of Molecular Graphics and Modelling, 25, 169-175. doi:10.1016/j.jmgm.2005.12.002
    • NLM

      Silva CHTP da, Campo VL, Carvalho I, Taft CA. Molecular modeling, docking and ADMET studies applied to the design of a novel hybrid for treatment of Alzheimer's disease [Internet]. Journal of Molecular Graphics and Modelling. 2006 ; 25 169-175.[citado 2024 nov. 18 ] Available from: https://doi.org/10.1016/j.jmgm.2005.12.002
    • Vancouver

      Silva CHTP da, Campo VL, Carvalho I, Taft CA. Molecular modeling, docking and ADMET studies applied to the design of a novel hybrid for treatment of Alzheimer's disease [Internet]. Journal of Molecular Graphics and Modelling. 2006 ; 25 169-175.[citado 2024 nov. 18 ] Available from: https://doi.org/10.1016/j.jmgm.2005.12.002
  • Source: Journal of Chemical Education. Unidade: FCFRP

    Assunto: QUÍMICA FARMACÊUTICA

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      CARVALHO, Ivone e BORGES, Áurea Donizete Lanchote e BERNARDES, Lílian Sibelle Campos. Medicinal chemistry and molecular modeling:: An integration to teach drug structure-activity relationship and the molecular basis of drug action. Journal of Chemical Education, v. 82, n. 4, p. 588-596, 2005Tradução . . Acesso em: 18 nov. 2024.
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      Carvalho, I., Borges, Á. D. L., & Bernardes, L. S. C. (2005). Medicinal chemistry and molecular modeling:: An integration to teach drug structure-activity relationship and the molecular basis of drug action. Journal of Chemical Education, 82( 4), 588-596.
    • NLM

      Carvalho I, Borges ÁDL, Bernardes LSC. Medicinal chemistry and molecular modeling:: An integration to teach drug structure-activity relationship and the molecular basis of drug action. Journal of Chemical Education. 2005 ; 82( 4): 588-596.[citado 2024 nov. 18 ]
    • Vancouver

      Carvalho I, Borges ÁDL, Bernardes LSC. Medicinal chemistry and molecular modeling:: An integration to teach drug structure-activity relationship and the molecular basis of drug action. Journal of Chemical Education. 2005 ; 82( 4): 588-596.[citado 2024 nov. 18 ]
  • Source: Journal of Computer-Aided Molecular Design. Unidade: FCFRP

    Assunto: SÍNDROME DE IMUNODEFICIÊNCIA ADQUIRIDA (TRATAMENTO)

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      TOMICH, C. H. et al. Homology modeling and molecular interaction field studies of 'alfa'-glucosidases as a guide to structure-based design of novel proposed anti-HIV inhibitors. Journal of Computer-Aided Molecular Design, v. 19, p. 83-92, 2005Tradução . . Disponível em: https://doi.org/10.1007/s10822-005-1486-6. Acesso em: 18 nov. 2024.
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      Tomich, C. H., Silva, P. da, Carvalho, I., & Taft, C. A. (2005). Homology modeling and molecular interaction field studies of 'alfa'-glucosidases as a guide to structure-based design of novel proposed anti-HIV inhibitors. Journal of Computer-Aided Molecular Design, 19, 83-92. doi:10.1007/s10822-005-1486-6
    • NLM

      Tomich CH, Silva P da, Carvalho I, Taft CA. Homology modeling and molecular interaction field studies of 'alfa'-glucosidases as a guide to structure-based design of novel proposed anti-HIV inhibitors [Internet]. Journal of Computer-Aided Molecular Design. 2005 ; 19 83-92.[citado 2024 nov. 18 ] Available from: https://doi.org/10.1007/s10822-005-1486-6
    • Vancouver

      Tomich CH, Silva P da, Carvalho I, Taft CA. Homology modeling and molecular interaction field studies of 'alfa'-glucosidases as a guide to structure-based design of novel proposed anti-HIV inhibitors [Internet]. Journal of Computer-Aided Molecular Design. 2005 ; 19 83-92.[citado 2024 nov. 18 ] Available from: https://doi.org/10.1007/s10822-005-1486-6
  • Source: Carbohydrate Research. Unidade: FCFRP

    Assunto: QUÍMICA FARMACÊUTICA

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      CARVALHO, Ivone e MELO, Eduardo Borges de. Synthesis of (+)-(2R,3S,4R)-2,3,4-trihydroxycyclohehanone from D-glucose. Carbohydrate Research, v. 339, p. 361-365, 2004Tradução . . Disponível em: https://doi.org/10.1016/j.carres.2003.10.010. Acesso em: 18 nov. 2024.
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      Carvalho, I., & Melo, E. B. de. (2004). Synthesis of (+)-(2R,3S,4R)-2,3,4-trihydroxycyclohehanone from D-glucose. Carbohydrate Research, 339, 361-365. doi:10.1016/j.carres.2003.10.010
    • NLM

      Carvalho I, Melo EB de. Synthesis of (+)-(2R,3S,4R)-2,3,4-trihydroxycyclohehanone from D-glucose [Internet]. Carbohydrate Research. 2004 ; 339 361-365.[citado 2024 nov. 18 ] Available from: https://doi.org/10.1016/j.carres.2003.10.010
    • Vancouver

      Carvalho I, Melo EB de. Synthesis of (+)-(2R,3S,4R)-2,3,4-trihydroxycyclohehanone from D-glucose [Internet]. Carbohydrate Research. 2004 ; 339 361-365.[citado 2024 nov. 18 ] Available from: https://doi.org/10.1016/j.carres.2003.10.010
  • Source: Química Nova. Unidade: FCFRP

    Assunto: QUÍMICA FARMACÊUTICA

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      CARVALHO, Ivone et al. Introdução a modelagem molecular de fármacos no curso experimental de química farmacêutica. Química Nova, v. 26, n. 3, p. 428-438, 2003Tradução . . Disponível em: https://doi.org/10.1590/s0100-40422003000300023. Acesso em: 18 nov. 2024.
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      Carvalho, I., Pupo, M. T., Borges, Á. D. L., & Bernardes, L. S. C. (2003). Introdução a modelagem molecular de fármacos no curso experimental de química farmacêutica. Química Nova, 26( 3), 428-438. doi:10.1590/s0100-40422003000300023
    • NLM

      Carvalho I, Pupo MT, Borges ÁDL, Bernardes LSC. Introdução a modelagem molecular de fármacos no curso experimental de química farmacêutica [Internet]. Química Nova. 2003 ; 26( 3): 428-438.[citado 2024 nov. 18 ] Available from: https://doi.org/10.1590/s0100-40422003000300023
    • Vancouver

      Carvalho I, Pupo MT, Borges ÁDL, Bernardes LSC. Introdução a modelagem molecular de fármacos no curso experimental de química farmacêutica [Internet]. Química Nova. 2003 ; 26( 3): 428-438.[citado 2024 nov. 18 ] Available from: https://doi.org/10.1590/s0100-40422003000300023
  • Source: Carbohydrate Research. Unidade: FCFRP

    Assunto: QUÍMICA FARMACÊUTICA

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      CARVALHO, Ivone et al. Practical synthesis of the 2-acetamido-3,4,6-tri-O-acetyl-2-deoxy-'beta'-D-glucosides of Fmoc-serine and Fmoc-threonine and their benzyl esters. Carbohydrate Research, v. 338, n. 10, p. 1039-1043, 2003Tradução . . Disponível em: https://doi.org/10.1016/s0008-6215(03)00071-5. Acesso em: 18 nov. 2024.
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      Carvalho, I., Scheuerl, S. L., Kartha, K. P. R., & Field, R. A. (2003). Practical synthesis of the 2-acetamido-3,4,6-tri-O-acetyl-2-deoxy-'beta'-D-glucosides of Fmoc-serine and Fmoc-threonine and their benzyl esters. Carbohydrate Research, 338( 10), 1039-1043. doi:10.1016/s0008-6215(03)00071-5
    • NLM

      Carvalho I, Scheuerl SL, Kartha KPR, Field RA. Practical synthesis of the 2-acetamido-3,4,6-tri-O-acetyl-2-deoxy-'beta'-D-glucosides of Fmoc-serine and Fmoc-threonine and their benzyl esters [Internet]. Carbohydrate Research. 2003 ; 338( 10): 1039-1043.[citado 2024 nov. 18 ] Available from: https://doi.org/10.1016/s0008-6215(03)00071-5
    • Vancouver

      Carvalho I, Scheuerl SL, Kartha KPR, Field RA. Practical synthesis of the 2-acetamido-3,4,6-tri-O-acetyl-2-deoxy-'beta'-D-glucosides of Fmoc-serine and Fmoc-threonine and their benzyl esters [Internet]. Carbohydrate Research. 2003 ; 338( 10): 1039-1043.[citado 2024 nov. 18 ] Available from: https://doi.org/10.1016/s0008-6215(03)00071-5
  • Source: Journal of Royal Society of Chemistry. Unidade: FCFRP

    Assunto: SÍNTESE ORGÂNICA (QUÍMICA)

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      CARVALHO, Ivone e HAINES, Alan H. N-Linked carba-disaccharides as potential inhibitors of glucosidases I and II. Journal of Royal Society of Chemistry, v. 1, p. 1795-1800, 2000Tradução . . Disponível em: https://doi.org/10.1039/a902826i. Acesso em: 18 nov. 2024.
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      Carvalho, I., & Haines, A. H. (2000). N-Linked carba-disaccharides as potential inhibitors of glucosidases I and II. Journal of Royal Society of Chemistry, 1, 1795-1800. doi:10.1039/a902826i
    • NLM

      Carvalho I, Haines AH. N-Linked carba-disaccharides as potential inhibitors of glucosidases I and II [Internet]. Journal of Royal Society of Chemistry. 2000 ; 1 1795-1800.[citado 2024 nov. 18 ] Available from: https://doi.org/10.1039/a902826i
    • Vancouver

      Carvalho I, Haines AH. N-Linked carba-disaccharides as potential inhibitors of glucosidases I and II [Internet]. Journal of Royal Society of Chemistry. 2000 ; 1 1795-1800.[citado 2024 nov. 18 ] Available from: https://doi.org/10.1039/a902826i
  • Source: Bollettino Chimico Farmaceutico. Conference titles: Congress of Pharmaceutical Sciences. Unidade: FCFRP

    Assunto: SÍNTESE ORGÂNICA (QUÍMICA)

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      CARVALHO, Ivone e MIZUNO, C S e HAINES, A H. Synthesis of aminoglycosides derivatives of biological interest. Bollettino Chimico Farmaceutico. Milano: Societá Editoriale Farmaceutica. . Acesso em: 18 nov. 2024. , 1999
    • APA

      Carvalho, I., Mizuno, C. S., & Haines, A. H. (1999). Synthesis of aminoglycosides derivatives of biological interest. Bollettino Chimico Farmaceutico. Milano: Societá Editoriale Farmaceutica.
    • NLM

      Carvalho I, Mizuno CS, Haines AH. Synthesis of aminoglycosides derivatives of biological interest. Bollettino Chimico Farmaceutico. 1999 ; 132( 2): LXXXIX.[citado 2024 nov. 18 ]
    • Vancouver

      Carvalho I, Mizuno CS, Haines AH. Synthesis of aminoglycosides derivatives of biological interest. Bollettino Chimico Farmaceutico. 1999 ; 132( 2): LXXXIX.[citado 2024 nov. 18 ]

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