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Filtros : "Bioorganic Chemistry" "IQSC" Removido: "Indexado na Web of Science" Limpar

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  • Artigo de periodico

    Antioxidant and anti-sickling activity of glucal-based triazoles compounds – an in vitro and in silico study (2021)

    Veloso, Rodolpho Rebello; Shamim, Anwar ; Lamarre, Yann Ives; Stefani, Hélio Alexandre ; Sciani, Juliana Mozer

    Source: Bioorganic Chemistry. Unidades: FCF, IQSC, FMRP

    Subjects: ANEMIA FALCIFORME, ANTIOXIDANTES

    PrivadoAcesso à fonteDOIHow to cite
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    • ABNT

      VELOSO, Rodolpho Rebello et al. Antioxidant and anti-sickling activity of glucal-based triazoles compounds – an in vitro and in silico study. Bioorganic Chemistry, v. 109, p. 104709, 2021Tradução . . Disponível em: https://doi.org/10.1016/j.bioorg.2021.104709. Acesso em: 14 ago. 2024.

    • APA

      Veloso, R. R., Shamim, A., Lamarre, Y. I., Stefani, H. A., & Sciani, J. M. (2021). Antioxidant and anti-sickling activity of glucal-based triazoles compounds – an in vitro and in silico study. Bioorganic Chemistry, 109, 104709. doi:10.1016/j.bioorg.2021.104709

    • NLM

      Veloso RR, Shamim A, Lamarre YI, Stefani HA, Sciani JM. Antioxidant and anti-sickling activity of glucal-based triazoles compounds – an in vitro and in silico study [Internet]. Bioorganic Chemistry. 2021 ;109 104709.[citado 2024 ago. 14 ] Available from: https://doi.org/10.1016/j.bioorg.2021.104709

    • Vancouver

      Veloso RR, Shamim A, Lamarre YI, Stefani HA, Sciani JM. Antioxidant and anti-sickling activity of glucal-based triazoles compounds – an in vitro and in silico study [Internet]. Bioorganic Chemistry. 2021 ;109 104709.[citado 2024 ago. 14 ] Available from: https://doi.org/10.1016/j.bioorg.2021.104709

  • Artigo de periodico

    Leveraging the cruzain S3 subsite to increase affinity for reversible covalent inhibitors (2018)

    Cianni, Lorenzo; Satori, Geraldo R; Rosini, Fabiana; De Vitta, Daniela; Pires, Gabriel Lino de Paula; Lopes, Bianca Rebelo; Leitão, Andrei ; Burtoloso, Antonio Carlos Bender ; Montanari, Carlos Alberto

    Source: Bioorganic Chemistry. Unidade: IQSC

    Subjects: MOLÉCULA, QUÍMICA MÉDICA

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    • ABNT

      CIANNI, Lorenzo et al. Leveraging the cruzain S3 subsite to increase affinity for reversible covalent inhibitors. Bioorganic Chemistry, p. 285-292, 2018Tradução . . Disponível em: https://doi.org/10.1016/j.bioorg.2018.04.006. Acesso em: 14 ago. 2024.

    • APA

      Cianni, L., Satori, G. R., Rosini, F., De Vitta, D., Pires, G. L. de P., Lopes, B. R., et al. (2018). Leveraging the cruzain S3 subsite to increase affinity for reversible covalent inhibitors. Bioorganic Chemistry, 285-292. doi:10.1016/j.bioorg.2018.04.006

    • NLM

      Cianni L, Satori GR, Rosini F, De Vitta D, Pires GL de P, Lopes BR, Leitão A, Burtoloso ACB, Montanari CA. Leveraging the cruzain S3 subsite to increase affinity for reversible covalent inhibitors [Internet]. Bioorganic Chemistry. 2018 ; 285-292.[citado 2024 ago. 14 ] Available from: https://doi.org/10.1016/j.bioorg.2018.04.006

    • Vancouver

      Cianni L, Satori GR, Rosini F, De Vitta D, Pires GL de P, Lopes BR, Leitão A, Burtoloso ACB, Montanari CA. Leveraging the cruzain S3 subsite to increase affinity for reversible covalent inhibitors [Internet]. Bioorganic Chemistry. 2018 ; 285-292.[citado 2024 ago. 14 ] Available from: https://doi.org/10.1016/j.bioorg.2018.04.006
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