Filtros : "Brömme, Dieter" Removido: "Canadá" Limpar

Filtros



Refine with date range


  • Source: Biochemical Journal. Unidade: IFSC

    Subjects: PROTEÍNAS (PROPRIEDADES), CRISTALOGRAFIA ESTRUTURAL

    Versão PublicadaAcesso à fonteDOIHow to cite
    A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
    • ABNT

      SHARMA, Vidhu et al. Structural requirements for the collagenase and elastase activity of cathepsin K and its selective inhibition by an exosite inhibitor. Biochemical Journal, v. 465, p. 163-173, 2015Tradução . . Disponível em: https://doi.org/10.1042/BJ20140809. Acesso em: 01 nov. 2025.
    • APA

      Sharma, V., Panwar, P., O’Donoghue, A. J., Cui, H., Guido, R. V. C., S. Craik, C., & Brömme, D. (2015). Structural requirements for the collagenase and elastase activity of cathepsin K and its selective inhibition by an exosite inhibitor. Biochemical Journal, 465, 163-173. doi:10.1042/BJ20140809
    • NLM

      Sharma V, Panwar P, O’Donoghue AJ, Cui H, Guido RVC, S. Craik C, Brömme D. Structural requirements for the collagenase and elastase activity of cathepsin K and its selective inhibition by an exosite inhibitor [Internet]. Biochemical Journal. 2015 ; 465 163-173.[citado 2025 nov. 01 ] Available from: https://doi.org/10.1042/BJ20140809
    • Vancouver

      Sharma V, Panwar P, O’Donoghue AJ, Cui H, Guido RVC, S. Craik C, Brömme D. Structural requirements for the collagenase and elastase activity of cathepsin K and its selective inhibition by an exosite inhibitor [Internet]. Biochemical Journal. 2015 ; 465 163-173.[citado 2025 nov. 01 ] Available from: https://doi.org/10.1042/BJ20140809
  • Source: Brazilian Journal of Pharmaceutical Sciences. Unidade: FCF

    Subjects: ANTIOXIDANTES, LIPOPROTEÍNAS

    Acesso à fonteAcesso à fonteDOIHow to cite
    A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
    • ABNT

      COSTA-MUGICA, Ariana et al. Inhibition of LDL-oxidation and antioxidant properties related to polyphenol content of hydrophilic fractions from seaweed Halimeda Incrassata (Ellis) Lamouroux. Brazilian Journal of Pharmaceutical Sciences, v. 48, n. 1, p. 31-37, 2012Tradução . . Disponível em: https://doi.org/10.1590/s1984-82502012000100004. Acesso em: 01 nov. 2025.
    • APA

      Costa-Mugica, A., Batista-Gonzalez, A. E., Mondejar, D., Soto-López, Y., Brito-Navarro, V., Vásquez, A. M., et al. (2012). Inhibition of LDL-oxidation and antioxidant properties related to polyphenol content of hydrophilic fractions from seaweed Halimeda Incrassata (Ellis) Lamouroux. Brazilian Journal of Pharmaceutical Sciences, 48( 1), 31-37. doi:10.1590/s1984-82502012000100004
    • NLM

      Costa-Mugica A, Batista-Gonzalez AE, Mondejar D, Soto-López Y, Brito-Navarro V, Vásquez AM, Brömme D, Zaldívar-Muñoz C, Vidal-Novoa A, Silva AM de O e, Mancini-Filho J. Inhibition of LDL-oxidation and antioxidant properties related to polyphenol content of hydrophilic fractions from seaweed Halimeda Incrassata (Ellis) Lamouroux [Internet]. Brazilian Journal of Pharmaceutical Sciences. 2012 ; 48( 1): 31-37.[citado 2025 nov. 01 ] Available from: https://doi.org/10.1590/s1984-82502012000100004
    • Vancouver

      Costa-Mugica A, Batista-Gonzalez AE, Mondejar D, Soto-López Y, Brito-Navarro V, Vásquez AM, Brömme D, Zaldívar-Muñoz C, Vidal-Novoa A, Silva AM de O e, Mancini-Filho J. Inhibition of LDL-oxidation and antioxidant properties related to polyphenol content of hydrophilic fractions from seaweed Halimeda Incrassata (Ellis) Lamouroux [Internet]. Brazilian Journal of Pharmaceutical Sciences. 2012 ; 48( 1): 31-37.[citado 2025 nov. 01 ] Available from: https://doi.org/10.1590/s1984-82502012000100004
  • Source: Bioorganic & Medicinal Chemistry. Unidade: IQ

    Subjects: TELÚRIO, SELÊNIO, ADJUVANTES IMUNOLÓGICOS

    Acesso à fonteDOIHow to cite
    A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
    • ABNT

      PIOVAN, Leandro et al. Structure-activity relationships of hypervalent organochalcogenanes as inhibitors of cysteine cathepsins 'V' and 'S'. Bioorganic & Medicinal Chemistry, v. 19, n. 6, p. 2009-2014 : + supplementary data ( S1-S5), 2011Tradução . . Disponível em: https://doi.org/10.1016/j.bmc.2011.01.054. Acesso em: 01 nov. 2025.
    • APA

      Piovan, L., Alves, M. F. M., Juliano, L., Brömme, D., Cunha, R. L. O. R., & Andrade, L. H. (2011). Structure-activity relationships of hypervalent organochalcogenanes as inhibitors of cysteine cathepsins 'V' and 'S'. Bioorganic & Medicinal Chemistry, 19( 6), 2009-2014 : + supplementary data ( S1-S5). doi:10.1016/j.bmc.2011.01.054
    • NLM

      Piovan L, Alves MFM, Juliano L, Brömme D, Cunha RLOR, Andrade LH. Structure-activity relationships of hypervalent organochalcogenanes as inhibitors of cysteine cathepsins 'V' and 'S' [Internet]. Bioorganic & Medicinal Chemistry. 2011 ; 19( 6): 2009-2014 : + supplementary data ( S1-S5).[citado 2025 nov. 01 ] Available from: https://doi.org/10.1016/j.bmc.2011.01.054
    • Vancouver

      Piovan L, Alves MFM, Juliano L, Brömme D, Cunha RLOR, Andrade LH. Structure-activity relationships of hypervalent organochalcogenanes as inhibitors of cysteine cathepsins 'V' and 'S' [Internet]. Bioorganic & Medicinal Chemistry. 2011 ; 19( 6): 2009-2014 : + supplementary data ( S1-S5).[citado 2025 nov. 01 ] Available from: https://doi.org/10.1016/j.bmc.2011.01.054
  • Source: Bioorganic and Medicinal Chemistry. Unidade: IFSC

    Subjects: INIBIDORES DE ENZIMAS, PRODUTOS NATURAIS, ALCALOIDES

    Acesso à fonteDOIHow to cite
    A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
    • ABNT

      SEVERINO, Richele P. et al. Acridone alkaloids as potent inhibitors of cathepsin V. Bioorganic and Medicinal Chemistry, v. 19, n. 4, p. 1477-1481, 2011Tradução . . Disponível em: https://doi.org/10.1016/j.bmc.2010.12.056. Acesso em: 01 nov. 2025.
    • APA

      Severino, R. P., Guido, R. V. C., Marques, E. F., Brömme, D., Silva, M. F. G. F., Fernandes, J. B., et al. (2011). Acridone alkaloids as potent inhibitors of cathepsin V. Bioorganic and Medicinal Chemistry, 19( 4), 1477-1481. doi:10.1016/j.bmc.2010.12.056
    • NLM

      Severino RP, Guido RVC, Marques EF, Brömme D, Silva MFGF, Fernandes JB, Andricopulo AD, Vieira PC. Acridone alkaloids as potent inhibitors of cathepsin V [Internet]. Bioorganic and Medicinal Chemistry. 2011 ; 19( 4): 1477-1481.[citado 2025 nov. 01 ] Available from: https://doi.org/10.1016/j.bmc.2010.12.056
    • Vancouver

      Severino RP, Guido RVC, Marques EF, Brömme D, Silva MFGF, Fernandes JB, Andricopulo AD, Vieira PC. Acridone alkaloids as potent inhibitors of cathepsin V [Internet]. Bioorganic and Medicinal Chemistry. 2011 ; 19( 4): 1477-1481.[citado 2025 nov. 01 ] Available from: https://doi.org/10.1016/j.bmc.2010.12.056
  • Source: Journal of the Brazilian Chemical Society. Unidade: IQ

    Subjects: SELÊNIO, ESTEREOQUÍMICA

    Acesso à fonteAcesso à fonteDOIHow to cite
    A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
    • ABNT

      PIOVAN, Leandro et al. Chemoenzymatic synthesis of organoselenium(IV) compounds and their evaluation as cysteine protease inhibitors. Journal of the Brazilian Chemical Society, v. 21, n. 11, p. 2108-2118 : + Supplementary Information ( S1-S26), 2010Tradução . . Disponível em: https://doi.org/10.1590/s0103-50532010001100012. Acesso em: 01 nov. 2025.
    • APA

      Piovan, L., Alves, M. F. M., Juliano, L., Brömme, D., Cunha, R. L. O. R., & Andrade, L. H. (2010). Chemoenzymatic synthesis of organoselenium(IV) compounds and their evaluation as cysteine protease inhibitors. Journal of the Brazilian Chemical Society, 21( 11), 2108-2118 : + Supplementary Information ( S1-S26). doi:10.1590/s0103-50532010001100012
    • NLM

      Piovan L, Alves MFM, Juliano L, Brömme D, Cunha RLOR, Andrade LH. Chemoenzymatic synthesis of organoselenium(IV) compounds and their evaluation as cysteine protease inhibitors [Internet]. Journal of the Brazilian Chemical Society. 2010 ; 21( 11): 2108-2118 : + Supplementary Information ( S1-S26).[citado 2025 nov. 01 ] Available from: https://doi.org/10.1590/s0103-50532010001100012
    • Vancouver

      Piovan L, Alves MFM, Juliano L, Brömme D, Cunha RLOR, Andrade LH. Chemoenzymatic synthesis of organoselenium(IV) compounds and their evaluation as cysteine protease inhibitors [Internet]. Journal of the Brazilian Chemical Society. 2010 ; 21( 11): 2108-2118 : + Supplementary Information ( S1-S26).[citado 2025 nov. 01 ] Available from: https://doi.org/10.1590/s0103-50532010001100012
  • Source: Biological Chemistry. Unidade: IQ

    Subjects: SÍNTESE ORGÂNICA, TELÚRIO

    Acesso à fonteAcesso à fonteDOIHow to cite
    A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
    • ABNT

      CUNHA, Rodrigo Luiz Oliveira Rodrigues et al. Irreversible inhibition of human cathepsins B, L, S and K by hypervalent tellurium compounds. Biological Chemistry, v. 390, n. 11, p. 1205-1212, 2009Tradução . . Disponível em: https://doi.org/10.1515/bc.2009.125. Acesso em: 01 nov. 2025.
    • APA

      Cunha, R. L. O. R., Gouvêa, I. E., Feitosa, G. P. V., Alves, M. F. M., Brömme, D., Comasseto, J. V., et al. (2009). Irreversible inhibition of human cathepsins B, L, S and K by hypervalent tellurium compounds. Biological Chemistry, 390( 11), 1205-1212. doi:10.1515/bc.2009.125
    • NLM

      Cunha RLOR, Gouvêa IE, Feitosa GPV, Alves MFM, Brömme D, Comasseto JV, Tersariol IL dos S, Juliano L. Irreversible inhibition of human cathepsins B, L, S and K by hypervalent tellurium compounds [Internet]. Biological Chemistry. 2009 ; 390( 11): 1205-1212.[citado 2025 nov. 01 ] Available from: https://doi.org/10.1515/bc.2009.125
    • Vancouver

      Cunha RLOR, Gouvêa IE, Feitosa GPV, Alves MFM, Brömme D, Comasseto JV, Tersariol IL dos S, Juliano L. Irreversible inhibition of human cathepsins B, L, S and K by hypervalent tellurium compounds [Internet]. Biological Chemistry. 2009 ; 390( 11): 1205-1212.[citado 2025 nov. 01 ] Available from: https://doi.org/10.1515/bc.2009.125
  • Source: Book of abstracts. Conference titles: Brazilian Conference on Natural Products - BCNP. Unidade: IFSC

    Subjects: PRODUTOS NATURAIS, INIBIDORES DE ENZIMAS, LIGAÇÕES ESTRUTURAIS

    Acesso à fonteHow to cite
    A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
    • ABNT

      SEVERINO, Richele P. et al. Natural products as inhibitiors of cathepsin V: identification, biological activity and molecular modeling. 2007, Anais.. São Paulo: Sociedade Brasileira de Química - SBQ, 2007. Disponível em: http://dell.nossosite.com.br/bcnp2007/media/pub/abst_book.pdf. Acesso em: 01 nov. 2025.
    • APA

      Severino, R. P., Guido, R. V. C., Vieira, P. C., Fernandes, J. B., Silva, M. F. das G. F. da, Andricopulo, A. D., & Brömme, D. (2007). Natural products as inhibitiors of cathepsin V: identification, biological activity and molecular modeling. In Book of abstracts. São Paulo: Sociedade Brasileira de Química - SBQ. Recuperado de http://dell.nossosite.com.br/bcnp2007/media/pub/abst_book.pdf
    • NLM

      Severino RP, Guido RVC, Vieira PC, Fernandes JB, Silva MF das GF da, Andricopulo AD, Brömme D. Natural products as inhibitiors of cathepsin V: identification, biological activity and molecular modeling [Internet]. Book of abstracts. 2007 ;[citado 2025 nov. 01 ] Available from: http://dell.nossosite.com.br/bcnp2007/media/pub/abst_book.pdf
    • Vancouver

      Severino RP, Guido RVC, Vieira PC, Fernandes JB, Silva MF das GF da, Andricopulo AD, Brömme D. Natural products as inhibitiors of cathepsin V: identification, biological activity and molecular modeling [Internet]. Book of abstracts. 2007 ;[citado 2025 nov. 01 ] Available from: http://dell.nossosite.com.br/bcnp2007/media/pub/abst_book.pdf

Digital Library of Intellectual Production of Universidade de São Paulo     2012 - 2025