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Filtros : "Brömme, Dieter" Removido: "Guido, Rafael Victorio Carvalho" Limpar

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  • 1

1 - 5 (5 records)

  • Artigo de periodico

    Green asymmetric synthesis of epoxypeptidomimetics and evaluation as human cathepsin K inhibitors (2020)

    Silva, Taynara L.; Santos, Deborah A. dos; Jesus, Hugo C. R. de; Brömme, Dieter; Fernandes, João B.; Paixão, Marcio W.; Corrêa, Arlene G.; Vieira, Paulo Cezar

    Source: Bioorganic & Medicinal Chemistry. Unidade: FCFRP

    Subjects: GENOMAS, COLÁGENO, OSTEOPOROSE, DOENÇAS ÓSSEAS, DENSIDADE ÓSSEA

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    • ABNT

      SILVA, Taynara L. et al. Green asymmetric synthesis of epoxypeptidomimetics and evaluation as human cathepsin K inhibitors. Bioorganic & Medicinal Chemistry, v. 28, n. 15, p. 1-8, 2020Tradução . . Disponível em: https://doi.org/10.1016/j.bmc.2020.115597. Acesso em: 01 nov. 2025.

    • APA

      Silva, T. L., Santos, D. A. dos, Jesus, H. C. R. de, Brömme, D., Fernandes, J. B., Paixão, M. W., et al. (2020). Green asymmetric synthesis of epoxypeptidomimetics and evaluation as human cathepsin K inhibitors. Bioorganic & Medicinal Chemistry, 28( 15), 1-8. doi:10.1016/j.bmc.2020.115597

    • NLM

      Silva TL, Santos DA dos, Jesus HCR de, Brömme D, Fernandes JB, Paixão MW, Corrêa AG, Vieira PC. Green asymmetric synthesis of epoxypeptidomimetics and evaluation as human cathepsin K inhibitors [Internet]. Bioorganic & Medicinal Chemistry. 2020 ; 28( 15): 1-8.[citado 2025 nov. 01 ] Available from: https://doi.org/10.1016/j.bmc.2020.115597

    • Vancouver

      Silva TL, Santos DA dos, Jesus HCR de, Brömme D, Fernandes JB, Paixão MW, Corrêa AG, Vieira PC. Green asymmetric synthesis of epoxypeptidomimetics and evaluation as human cathepsin K inhibitors [Internet]. Bioorganic & Medicinal Chemistry. 2020 ; 28( 15): 1-8.[citado 2025 nov. 01 ] Available from: https://doi.org/10.1016/j.bmc.2020.115597

  • Artigo de periodico

    Inhibition of LDL-oxidation and antioxidant properties related to polyphenol content of hydrophilic fractions from seaweed Halimeda Incrassata (Ellis) Lamouroux (2012)

    Costa-Mugica, Ariana; Batista-Gonzalez, Ana Elsa; Mondejar, Diadelis; Soto-López, Yosdel; Brito-Navarro, Victor; Vásquez, Ana Maria; Brömme, Dieter; Zaldívar-Muñoz, Claudina; Vidal-Novoa, Alexis; Silva, Ana Mara de Oliveira e; Mancini-Filho, Jorge

    Source: Brazilian Journal of Pharmaceutical Sciences. Unidade: FCF

    Subjects: ANTIOXIDANTES, LIPOPROTEÍNAS

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    • 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

  • Artigo de periodico

    Structure-activity relationships of hypervalent organochalcogenanes as inhibitors of cysteine cathepsins 'V' and 'S' (2011)

    Piovan, Leandro; Alves, Márcio Fernando Madureira; Juliano, Luiz; Brömme, Dieter; Cunha, Rodrigo Luiz Oliveira Rodrigues; Andrade, Leandro Helgueira

    Source: Bioorganic & Medicinal Chemistry. Unidade: IQ

    Subjects: TELÚRIO, SELÊNIO, ADJUVANTES IMUNOLÓGICOS

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    • 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

  • Artigo de periodico

    Chemoenzymatic synthesis of organoselenium(IV) compounds and their evaluation as cysteine protease inhibitors (2010)

    Piovan, Leandro; Alves, Márcio Fernando Madureira; Juliano, Luiz; Brömme, Dieter; Cunha, Rodrigo Luiz Oliveira Rodrigues; Andrade, Leandro Helgueira

    Source: Journal of the Brazilian Chemical Society. Unidade: IQ

    Subjects: SELÊNIO, ESTEREOQUÍMICA

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    • 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

  • Artigo de periodico

    Irreversible inhibition of human cathepsins B, L, S and K by hypervalent tellurium compounds (2009)

    Cunha, Rodrigo Luiz Oliveira Rodrigues; Gouvêa, Iuri E; Feitosa, Geovana Prado Vaz; Alves, Márcio Fernando Madureira; Brömme, Dieter; Comasseto, João Valdir; Tersariol, Ivarne Luis dos Santos; Juliano, Luiz

    Source: Biological Chemistry. Unidade: IQ

    Subjects: SÍNTESE ORGÂNICA, TELÚRIO

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    • 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
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