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  • Source: Abstracts Book. Conference titles: Congress of the International Union for Biochemistry and Molecular Biology - IUBMB. Unidade: IQ

    Assunto: INIBIDORES DE ENZIMAS

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    • ABNT

      VIVIANI, Lucas Gasparello et al. Identification of novel potential ecto-5'-nucleotidase inhibitors by pharmacophore-based screening and molecular shape matching. 2015, Anais.. São Paulo: Sociedade Brasileira de Bioquímica e Biologia Molecular (SBBq), 2015. . Acesso em: 11 nov. 2024.
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      Viviani, L. G., Cheffer, A., Piccirillo, E., Peron, L. M. de, Rezende, L., Ulrich, H., & Amaral, A. T. do. (2015). Identification of novel potential ecto-5'-nucleotidase inhibitors by pharmacophore-based screening and molecular shape matching. In Abstracts Book. São Paulo: Sociedade Brasileira de Bioquímica e Biologia Molecular (SBBq).
    • NLM

      Viviani LG, Cheffer A, Piccirillo E, Peron LM de, Rezende L, Ulrich H, Amaral AT do. Identification of novel potential ecto-5'-nucleotidase inhibitors by pharmacophore-based screening and molecular shape matching. Abstracts Book. 2015 ;[citado 2024 nov. 11 ]
    • Vancouver

      Viviani LG, Cheffer A, Piccirillo E, Peron LM de, Rezende L, Ulrich H, Amaral AT do. Identification of novel potential ecto-5'-nucleotidase inhibitors by pharmacophore-based screening and molecular shape matching. Abstracts Book. 2015 ;[citado 2024 nov. 11 ]
  • Source: Biometals. Unidade: IQ

    Subjects: PEPTÍDEOS, FERRO

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      GOSWAMI, Dibakar et al. Deferasirox-TAT(47-57) peptide conjugate as a water soluble, bifunctional iron chelator with potential use in neuromedicine. Biometals, v. 28, n. 5, p. 869-877, 2015Tradução . . Disponível em: https://doi.org/10.1007/s10534-015-9873-5. Acesso em: 11 nov. 2024.
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      Goswami, D., Vitorino, H. A., Alta, R. Y. P., Silvestre, D. M., Nomura, C. S., Machini, M. T., & Espósito, B. P. (2015). Deferasirox-TAT(47-57) peptide conjugate as a water soluble, bifunctional iron chelator with potential use in neuromedicine. Biometals, 28( 5), 869-877. doi:10.1007/s10534-015-9873-5
    • NLM

      Goswami D, Vitorino HA, Alta RYP, Silvestre DM, Nomura CS, Machini MT, Espósito BP. Deferasirox-TAT(47-57) peptide conjugate as a water soluble, bifunctional iron chelator with potential use in neuromedicine [Internet]. Biometals. 2015 ; 28( 5): 869-877.[citado 2024 nov. 11 ] Available from: https://doi.org/10.1007/s10534-015-9873-5
    • Vancouver

      Goswami D, Vitorino HA, Alta RYP, Silvestre DM, Nomura CS, Machini MT, Espósito BP. Deferasirox-TAT(47-57) peptide conjugate as a water soluble, bifunctional iron chelator with potential use in neuromedicine [Internet]. Biometals. 2015 ; 28( 5): 869-877.[citado 2024 nov. 11 ] Available from: https://doi.org/10.1007/s10534-015-9873-5
  • Source: Bioconjugate Chemistry. Unidade: IQ

    Subjects: PEPTÍDEOS, FERRO

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      GOSWAMI, Dibakar et al. Cell Penetrating Peptide (CPP)-conjugated desferrioxamine for enhanced neuroprotection: synthesis and in vitro evaluation. Bioconjugate Chemistry, v. 25, n. 11, p. 2067-2080, 2014Tradução . . Disponível em: https://doi.org/10.1021/bc5004197. Acesso em: 11 nov. 2024.
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      Goswami, D., Machini, M. T., Silvestre, D. M., Nomura, C. S., & Espósito, B. P. (2014). Cell Penetrating Peptide (CPP)-conjugated desferrioxamine for enhanced neuroprotection: synthesis and in vitro evaluation. Bioconjugate Chemistry, 25( 11), 2067-2080. doi:10.1021/bc5004197
    • NLM

      Goswami D, Machini MT, Silvestre DM, Nomura CS, Espósito BP. Cell Penetrating Peptide (CPP)-conjugated desferrioxamine for enhanced neuroprotection: synthesis and in vitro evaluation [Internet]. Bioconjugate Chemistry. 2014 ; 25( 11): 2067-2080.[citado 2024 nov. 11 ] Available from: https://doi.org/10.1021/bc5004197
    • Vancouver

      Goswami D, Machini MT, Silvestre DM, Nomura CS, Espósito BP. Cell Penetrating Peptide (CPP)-conjugated desferrioxamine for enhanced neuroprotection: synthesis and in vitro evaluation [Internet]. Bioconjugate Chemistry. 2014 ; 25( 11): 2067-2080.[citado 2024 nov. 11 ] Available from: https://doi.org/10.1021/bc5004197
  • Source: Biometals. Unidade: IQ

    Subjects: FERRO, CAFEÍNA

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      ALTA, Elizabeth Carmen Pastrana et al. Desferrioxamine-caffeine (DFCAF) as a cell permeant moderator of the oxidative stress caused by iron overload. Biometals, v. 27, n. 6, p. 1351-1360, 2014Tradução . . Disponível em: https://doi.org/10.1007/s10534-014-9795-7. Acesso em: 11 nov. 2024.
    • APA

      Alta, E. C. P., Goswami, D., Machini, M. T., Silvestre, D. M., Nomura, C. S., & Espósito, B. P. (2014). Desferrioxamine-caffeine (DFCAF) as a cell permeant moderator of the oxidative stress caused by iron overload. Biometals, 27( 6), 1351-1360. doi:10.1007/s10534-014-9795-7
    • NLM

      Alta ECP, Goswami D, Machini MT, Silvestre DM, Nomura CS, Espósito BP. Desferrioxamine-caffeine (DFCAF) as a cell permeant moderator of the oxidative stress caused by iron overload [Internet]. Biometals. 2014 ; 27( 6): 1351-1360.[citado 2024 nov. 11 ] Available from: https://doi.org/10.1007/s10534-014-9795-7
    • Vancouver

      Alta ECP, Goswami D, Machini MT, Silvestre DM, Nomura CS, Espósito BP. Desferrioxamine-caffeine (DFCAF) as a cell permeant moderator of the oxidative stress caused by iron overload [Internet]. Biometals. 2014 ; 27( 6): 1351-1360.[citado 2024 nov. 11 ] Available from: https://doi.org/10.1007/s10534-014-9795-7
  • Source: LANGMUIR. Unidades: IQ, IF, FFCLRP

    Subjects: RESSONÂNCIA MAGNÉTICA NUCLEAR, RAIOS X, FLUORESCÊNCIA

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      LIMA, Filipe da Silva et al. Effect of counterions on the shape, hydration, and degree of order at the interface of cationic micelles: the triflate case. LANGMUIR, v. 29, n. 13, p. 4193-4203 , 2013Tradução . . Disponível em: https://doi.org/10.1021/la304658e. Acesso em: 11 nov. 2024.
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      Lima, F. da S., Cuccovia, I. M., Horinek, D., Amaral, L. Q. do, Riske, K. do A., Schreier, S., et al. (2013). Effect of counterions on the shape, hydration, and degree of order at the interface of cationic micelles: the triflate case. LANGMUIR, 29( 13), 4193-4203 . doi:10.1021/la304658e
    • NLM

      Lima F da S, Cuccovia IM, Horinek D, Amaral LQ do, Riske K do A, Schreier S, Salinas RK, Bastos EL, Pires PAR, Bozelli Junior JC, Favaro DC, Rodrigues ACB, Dias LG, El Seoud OA, Chaimovich Guralnik H. Effect of counterions on the shape, hydration, and degree of order at the interface of cationic micelles: the triflate case [Internet]. LANGMUIR. 2013 ; 29( 13): 4193-4203 .[citado 2024 nov. 11 ] Available from: https://doi.org/10.1021/la304658e
    • Vancouver

      Lima F da S, Cuccovia IM, Horinek D, Amaral LQ do, Riske K do A, Schreier S, Salinas RK, Bastos EL, Pires PAR, Bozelli Junior JC, Favaro DC, Rodrigues ACB, Dias LG, El Seoud OA, Chaimovich Guralnik H. Effect of counterions on the shape, hydration, and degree of order at the interface of cationic micelles: the triflate case [Internet]. LANGMUIR. 2013 ; 29( 13): 4193-4203 .[citado 2024 nov. 11 ] Available from: https://doi.org/10.1021/la304658e
  • Source: Environmental Toxicology and Chemistry. Unidade: IQ

    Subjects: ÍONS, RHODOPHYTA

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      MENDES, Luiz Fernando et al. Prediction of mono-, bi-, and trivalent metal cation relative toxicity to the seaweed Gracilaria domingensis (Gracilariales, Rhodophyta) in synthetic seawater. Environmental Toxicology and Chemistry, v. 32, n. 11, p. 2571-2575, 2013Tradução . . Disponível em: https://doi.org/10.1002/etc.2340. Acesso em: 11 nov. 2024.
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      Mendes, L. F., Villela, L. Z., Yokoya, N. S., Bastos, E. L., Stevani, C. V., & Colepicolo, P. (2013). Prediction of mono-, bi-, and trivalent metal cation relative toxicity to the seaweed Gracilaria domingensis (Gracilariales, Rhodophyta) in synthetic seawater. Environmental Toxicology and Chemistry, 32( 11), 2571-2575. doi:10.1002/etc.2340
    • NLM

      Mendes LF, Villela LZ, Yokoya NS, Bastos EL, Stevani CV, Colepicolo P. Prediction of mono-, bi-, and trivalent metal cation relative toxicity to the seaweed Gracilaria domingensis (Gracilariales, Rhodophyta) in synthetic seawater [Internet]. Environmental Toxicology and Chemistry. 2013 ; 32( 11): 2571-2575.[citado 2024 nov. 11 ] Available from: https://doi.org/10.1002/etc.2340
    • Vancouver

      Mendes LF, Villela LZ, Yokoya NS, Bastos EL, Stevani CV, Colepicolo P. Prediction of mono-, bi-, and trivalent metal cation relative toxicity to the seaweed Gracilaria domingensis (Gracilariales, Rhodophyta) in synthetic seawater [Internet]. Environmental Toxicology and Chemistry. 2013 ; 32( 11): 2571-2575.[citado 2024 nov. 11 ] Available from: https://doi.org/10.1002/etc.2340
  • Source: Journal of Neuroscience Research. Unidade: IQ

    Subjects: RECEPTORES, RELAÇÕES QUANTITATIVAS ENTRE ESTRUTURA QUÍMICA E ATIVIDADE BIOLÓGICA

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      CHEFFER, Arquimedes et al. Lipophilicity as a determinant of binding of procaine analogs to rat `α IND. 3´`β IND. 4´ nicotinic acetylcholine receptor. Journal of Neuroscience Research, v. 90, n. 8, p. 1607-1614, 2012Tradução . . Disponível em: https://doi.org/10.1002/jnr.23047. Acesso em: 11 nov. 2024.
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      Cheffer, A., Mustafa, E. V., Amaral, A. T. do, & Ulrich, H. (2012). Lipophilicity as a determinant of binding of procaine analogs to rat `α IND. 3´`β IND. 4´ nicotinic acetylcholine receptor. Journal of Neuroscience Research, 90( 8), 1607-1614. doi:10.1002/jnr.23047
    • NLM

      Cheffer A, Mustafa EV, Amaral AT do, Ulrich H. Lipophilicity as a determinant of binding of procaine analogs to rat `α IND. 3´`β IND. 4´ nicotinic acetylcholine receptor [Internet]. Journal of Neuroscience Research. 2012 ; 90( 8): 1607-1614.[citado 2024 nov. 11 ] Available from: https://doi.org/10.1002/jnr.23047
    • Vancouver

      Cheffer A, Mustafa EV, Amaral AT do, Ulrich H. Lipophilicity as a determinant of binding of procaine analogs to rat `α IND. 3´`β IND. 4´ nicotinic acetylcholine receptor [Internet]. Journal of Neuroscience Research. 2012 ; 90( 8): 1607-1614.[citado 2024 nov. 11 ] Available from: https://doi.org/10.1002/jnr.23047
  • Source: Journal of the Brazilian Chemical Society. Unidade: IQ

    Subjects: REAÇÕES ORGÂNICAS, HIDRÓLISE

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      FIORI, Simone et al. Characterization studies of 1-(4-cyano-2-oxo-1,2-dihydro-1-pyridyl)-3-(4-cyano-1,2-dihydro-1-pyridyl)propane formed from the reaction of hydroxide ion with 1,3-bis-(4-cyano pyridinium)propane. Journal of the Brazilian Chemical Society, v. 22, n. 9, p. 1644-1648 : + Supplementary materials ( S1-S5), 2011Tradução . . Disponível em: https://doi.org/10.1590/s0103-50532011000900004. Acesso em: 11 nov. 2024.
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      Fiori, S., Schuquel, I. T. A., Silva, I. N. da, Politi, M. J., Catalani, L. H., Chaimovich Guralnik, H., et al. (2011). Characterization studies of 1-(4-cyano-2-oxo-1,2-dihydro-1-pyridyl)-3-(4-cyano-1,2-dihydro-1-pyridyl)propane formed from the reaction of hydroxide ion with 1,3-bis-(4-cyano pyridinium)propane. Journal of the Brazilian Chemical Society, 22( 9), 1644-1648 : + Supplementary materials ( S1-S5). doi:10.1590/s0103-50532011000900004
    • NLM

      Fiori S, Schuquel ITA, Silva IN da, Politi MJ, Catalani LH, Chaimovich Guralnik H, Meyer E, Hioka N. Characterization studies of 1-(4-cyano-2-oxo-1,2-dihydro-1-pyridyl)-3-(4-cyano-1,2-dihydro-1-pyridyl)propane formed from the reaction of hydroxide ion with 1,3-bis-(4-cyano pyridinium)propane [Internet]. Journal of the Brazilian Chemical Society. 2011 ; 22( 9): 1644-1648 : + Supplementary materials ( S1-S5).[citado 2024 nov. 11 ] Available from: https://doi.org/10.1590/s0103-50532011000900004
    • Vancouver

      Fiori S, Schuquel ITA, Silva IN da, Politi MJ, Catalani LH, Chaimovich Guralnik H, Meyer E, Hioka N. Characterization studies of 1-(4-cyano-2-oxo-1,2-dihydro-1-pyridyl)-3-(4-cyano-1,2-dihydro-1-pyridyl)propane formed from the reaction of hydroxide ion with 1,3-bis-(4-cyano pyridinium)propane [Internet]. Journal of the Brazilian Chemical Society. 2011 ; 22( 9): 1644-1648 : + Supplementary materials ( S1-S5).[citado 2024 nov. 11 ] Available from: https://doi.org/10.1590/s0103-50532011000900004

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