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Filtros : "DONATE, PAULO MARCOS" "2018" Removido: "2015" Limpar

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  • Artigo de periodico

    Syntheses of non-aromatic medium and large rings synthesized via phenylnitrenium ions (2018)

    Ponte, Gino Del; Archanjo, Fernando C.; Watanabe, Lilian Y.; Donate, Paulo Marcos; Campos, Joaquín M.

    Source: Arabian Journal of Chemistry. Unidades: FCFRP, FFCLRP

    Subjects: SÍNTESE QUÍMICA, COMPOSTOS AROMÁTICOS, ANÉIS, ÍONS

    Acesso à fonteDOIHow to cite
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    • ABNT

      PONTE, Gino Del et al. Syntheses of non-aromatic medium and large rings synthesized via phenylnitrenium ions. Arabian Journal of Chemistry, v. 11, n. 3, p. 415-425, 2018Tradução . . Disponível em: https://doi.org/10.1016/j.arabjc.2016.11.001. Acesso em: 05 dez. 2025.

    • APA

      Ponte, G. D., Archanjo, F. C., Watanabe, L. Y., Donate, P. M., & Campos, J. M. (2018). Syntheses of non-aromatic medium and large rings synthesized via phenylnitrenium ions. Arabian Journal of Chemistry, 11( 3), 415-425. doi:10.1016/j.arabjc.2016.11.001

    • NLM

      Ponte GD, Archanjo FC, Watanabe LY, Donate PM, Campos JM. Syntheses of non-aromatic medium and large rings synthesized via phenylnitrenium ions [Internet]. Arabian Journal of Chemistry. 2018 ; 11( 3): 415-425.[citado 2025 dez. 05 ] Available from: https://doi.org/10.1016/j.arabjc.2016.11.001

    • Vancouver

      Ponte GD, Archanjo FC, Watanabe LY, Donate PM, Campos JM. Syntheses of non-aromatic medium and large rings synthesized via phenylnitrenium ions [Internet]. Arabian Journal of Chemistry. 2018 ; 11( 3): 415-425.[citado 2025 dez. 05 ] Available from: https://doi.org/10.1016/j.arabjc.2016.11.001

  • Artigo de periodico

    The synthesized plant metabolite 3,4,5-tri-o-galloylquinic acid methyl ester inhibits calcium oxalate crystal growth in a drosophila model, downregulates renal cell surface annexin A1 expression, and decreases crystal adhesion to cells (2018)

    Abd El-Salam, Mohamed ; Bastos, Jairo Kenupp; Han, Jing Jing; Previdi, Daniel ; Coelho, Eduardo Barbosa ; Donate, Paulo Marcos ; Romero, Michael F.; Lieske, John

    Source: Journal of Medicinal Chemistry. Unidades: FCFRP, FMRP, FFCLRP

    Subjects: FRAÇÕES SUBCELULARES, CÉLULAS, RIM, ANTIOXIDANTES, DROSOPHILA

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    • ABNT

      ABD EL-SALAM, Mohamed et al. The synthesized plant metabolite 3,4,5-tri-o-galloylquinic acid methyl ester inhibits calcium oxalate crystal growth in a drosophila model, downregulates renal cell surface annexin A1 expression, and decreases crystal adhesion to cells. Journal of Medicinal Chemistry, v. 61, n. 4, p. 1609-1621, 2018Tradução . . Disponível em: https://doi.org/10.1021/acs.jmedchem.7b01566. Acesso em: 05 dez. 2025.

    • APA

      Abd El-Salam, M., Bastos, J. K., Han, J. J., Previdi, D., Coelho, E. B., Donate, P. M., et al. (2018). The synthesized plant metabolite 3,4,5-tri-o-galloylquinic acid methyl ester inhibits calcium oxalate crystal growth in a drosophila model, downregulates renal cell surface annexin A1 expression, and decreases crystal adhesion to cells. Journal of Medicinal Chemistry, 61( 4), 1609-1621. doi:10.1021/acs.jmedchem.7b01566

    • NLM

      Abd El-Salam M, Bastos JK, Han JJ, Previdi D, Coelho EB, Donate PM, Romero MF, Lieske J. The synthesized plant metabolite 3,4,5-tri-o-galloylquinic acid methyl ester inhibits calcium oxalate crystal growth in a drosophila model, downregulates renal cell surface annexin A1 expression, and decreases crystal adhesion to cells [Internet]. Journal of Medicinal Chemistry. 2018 ; 61( 4): 1609-1621.[citado 2025 dez. 05 ] Available from: https://doi.org/10.1021/acs.jmedchem.7b01566

    • Vancouver

      Abd El-Salam M, Bastos JK, Han JJ, Previdi D, Coelho EB, Donate PM, Romero MF, Lieske J. The synthesized plant metabolite 3,4,5-tri-o-galloylquinic acid methyl ester inhibits calcium oxalate crystal growth in a drosophila model, downregulates renal cell surface annexin A1 expression, and decreases crystal adhesion to cells [Internet]. Journal of Medicinal Chemistry. 2018 ; 61( 4): 1609-1621.[citado 2025 dez. 05 ] Available from: https://doi.org/10.1021/acs.jmedchem.7b01566
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