Filtros : "Pasqualoto, Kerly Fernanda Mesquita" "Reino Unido" Limpar

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  • Source: Bioorganic & Medicinal Chemistry. Unidade: FCF

    Subjects: RESISTÊNCIA MICROBIANA ÀS DROGAS, INFECÇÕES BACTERIANAS

    Acesso à fonteDOIHow to cite
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    • ABNT

      ZORZI, Rodrigo Rocha et al. Exploring 5-nitrofuran derivatives against nosocomial pathogens: synthesis, antimicrobial activity and chemometric analysis. Bioorganic & Medicinal Chemistry, v. 22, n. 10, p. 2844-2854, 2014Tradução . . Disponível em: https://doi.org/10.1016/j.bmc.2014.03.044. Acesso em: 01 nov. 2024.
    • APA

      Zorzi, R. R., Jorge, S. D., Palace-Berl, F., Pasqualoto, K. F. M., Bortolozzo, L. de S., Siqueira, A. M. de C., & Tavares, L. C. (2014). Exploring 5-nitrofuran derivatives against nosocomial pathogens: synthesis, antimicrobial activity and chemometric analysis. Bioorganic & Medicinal Chemistry, 22( 10), 2844-2854. doi:10.1016/j.bmc.2014.03.044
    • NLM

      Zorzi RR, Jorge SD, Palace-Berl F, Pasqualoto KFM, Bortolozzo L de S, Siqueira AM de C, Tavares LC. Exploring 5-nitrofuran derivatives against nosocomial pathogens: synthesis, antimicrobial activity and chemometric analysis [Internet]. Bioorganic & Medicinal Chemistry. 2014 ; 22( 10): 2844-2854.[citado 2024 nov. 01 ] Available from: https://doi.org/10.1016/j.bmc.2014.03.044
    • Vancouver

      Zorzi RR, Jorge SD, Palace-Berl F, Pasqualoto KFM, Bortolozzo L de S, Siqueira AM de C, Tavares LC. Exploring 5-nitrofuran derivatives against nosocomial pathogens: synthesis, antimicrobial activity and chemometric analysis [Internet]. Bioorganic & Medicinal Chemistry. 2014 ; 22( 10): 2844-2854.[citado 2024 nov. 01 ] Available from: https://doi.org/10.1016/j.bmc.2014.03.044
  • Source: MedChemComm. Unidade: FCF

    Subjects: TRYPANOSOMA CRUZI, ANTIPARASITÁRIOS

    Acesso à fonteDOIHow to cite
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    • ABNT

      JORGE, Salomão Dória et al. Preliminary in vitro evaluation of N'-(benzofuroxan-5-yl)methylene benzohydrazide derivatives as potential anti-Trypanosoma cruzi agents. MedChemComm, v. 3, n. 7, p. 824-828 : + Supplementary materials ( S1-S11), 2012Tradução . . Disponível em: https://doi.org/10.1039/c2md20019h. Acesso em: 01 nov. 2024.
    • APA

      Jorge, S. D., Ishii, M., Palace-Berl, F., Ferreira, A. K., Sá Júnior, P. L. de, Oliveira, A. A. de, et al. (2012). Preliminary in vitro evaluation of N'-(benzofuroxan-5-yl)methylene benzohydrazide derivatives as potential anti-Trypanosoma cruzi agents. MedChemComm, 3( 7), 824-828 : + Supplementary materials ( S1-S11). doi:10.1039/c2md20019h
    • NLM

      Jorge SD, Ishii M, Palace-Berl F, Ferreira AK, Sá Júnior PL de, Oliveira AA de, Sonehara IY, Pasqualoto KFM, Tavares LC. Preliminary in vitro evaluation of N'-(benzofuroxan-5-yl)methylene benzohydrazide derivatives as potential anti-Trypanosoma cruzi agents [Internet]. MedChemComm. 2012 ; 3( 7): 824-828 : + Supplementary materials ( S1-S11).[citado 2024 nov. 01 ] Available from: https://doi.org/10.1039/c2md20019h
    • Vancouver

      Jorge SD, Ishii M, Palace-Berl F, Ferreira AK, Sá Júnior PL de, Oliveira AA de, Sonehara IY, Pasqualoto KFM, Tavares LC. Preliminary in vitro evaluation of N'-(benzofuroxan-5-yl)methylene benzohydrazide derivatives as potential anti-Trypanosoma cruzi agents [Internet]. MedChemComm. 2012 ; 3( 7): 824-828 : + Supplementary materials ( S1-S11).[citado 2024 nov. 01 ] Available from: https://doi.org/10.1039/c2md20019h
  • Source: Bioorganic & Medicinal Chemistry. Unidade: FCF

    Subjects: RESISTÊNCIA MICROBIANA ÀS DROGAS, STAPHYLOCOCCUS

    Acesso à fonteDOIHow to cite
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    • ABNT

      JORGE, Salomão Dória et al. Novel benzofuroxan derivatives against multidrug-resistant Staphylococcus aureus strains: design using Topliss’ decision tree, synthesis and biological assay. Bioorganic & Medicinal Chemistry, v. 19, n. 16, p. 5031-5038 : + Supplementary materials ( S1-S3), 2011Tradução . . Disponível em: https://doi.org/10.1016/j.bmc.2011.06.034. Acesso em: 01 nov. 2024.
    • APA

      Jorge, S. D., Palace-Berl, F., Masunari, A., Cechinel, C. A., Ishii, M., Pasqualoto, K. F. M., & Tavares, L. C. (2011). Novel benzofuroxan derivatives against multidrug-resistant Staphylococcus aureus strains: design using Topliss’ decision tree, synthesis and biological assay. Bioorganic & Medicinal Chemistry, 19( 16), 5031-5038 : + Supplementary materials ( S1-S3). doi:10.1016/j.bmc.2011.06.034
    • NLM

      Jorge SD, Palace-Berl F, Masunari A, Cechinel CA, Ishii M, Pasqualoto KFM, Tavares LC. Novel benzofuroxan derivatives against multidrug-resistant Staphylococcus aureus strains: design using Topliss’ decision tree, synthesis and biological assay [Internet]. Bioorganic & Medicinal Chemistry. 2011 ; 19( 16): 5031-5038 : + Supplementary materials ( S1-S3).[citado 2024 nov. 01 ] Available from: https://doi.org/10.1016/j.bmc.2011.06.034
    • Vancouver

      Jorge SD, Palace-Berl F, Masunari A, Cechinel CA, Ishii M, Pasqualoto KFM, Tavares LC. Novel benzofuroxan derivatives against multidrug-resistant Staphylococcus aureus strains: design using Topliss’ decision tree, synthesis and biological assay [Internet]. Bioorganic & Medicinal Chemistry. 2011 ; 19( 16): 5031-5038 : + Supplementary materials ( S1-S3).[citado 2024 nov. 01 ] Available from: https://doi.org/10.1016/j.bmc.2011.06.034
  • Source: Bioorganic & Medicinal Chemistry. Unidade: FCF

    Subjects: TRYPANOSOMA CRUZI, CANDIDA ALBICANS, ANTIFÚNGICOS

    Acesso à fonteDOIHow to cite
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    • ABNT

      ISHII, Marina et al. Synthesis, molecular modeling and preliminary biological evaluation of a set of 3-acetyl-2,5-disubstituted-2,3-dihydro-1,3,4-oxadiazole as potential antibacterial, anti-Trypanosoma cruzi and antifungal agents. Bioorganic & Medicinal Chemistry, v. 19, n. 21, p. 6292-6301, 2011Tradução . . Disponível em: https://doi.org/10.1016/j.bmc.2011.09.009. Acesso em: 01 nov. 2024.
    • APA

      Ishii, M., Jorge, S. D., Oliveira, A. A. de, Palace-Berl, F., Sonehara, I. Y., Pasqualoto, K. F. M., & Tavares, L. C. (2011). Synthesis, molecular modeling and preliminary biological evaluation of a set of 3-acetyl-2,5-disubstituted-2,3-dihydro-1,3,4-oxadiazole as potential antibacterial, anti-Trypanosoma cruzi and antifungal agents. Bioorganic & Medicinal Chemistry, 19( 21), 6292-6301. doi:10.1016/j.bmc.2011.09.009
    • NLM

      Ishii M, Jorge SD, Oliveira AA de, Palace-Berl F, Sonehara IY, Pasqualoto KFM, Tavares LC. Synthesis, molecular modeling and preliminary biological evaluation of a set of 3-acetyl-2,5-disubstituted-2,3-dihydro-1,3,4-oxadiazole as potential antibacterial, anti-Trypanosoma cruzi and antifungal agents [Internet]. Bioorganic & Medicinal Chemistry. 2011 ; 19( 21): 6292-6301.[citado 2024 nov. 01 ] Available from: https://doi.org/10.1016/j.bmc.2011.09.009
    • Vancouver

      Ishii M, Jorge SD, Oliveira AA de, Palace-Berl F, Sonehara IY, Pasqualoto KFM, Tavares LC. Synthesis, molecular modeling and preliminary biological evaluation of a set of 3-acetyl-2,5-disubstituted-2,3-dihydro-1,3,4-oxadiazole as potential antibacterial, anti-Trypanosoma cruzi and antifungal agents [Internet]. Bioorganic & Medicinal Chemistry. 2011 ; 19( 21): 6292-6301.[citado 2024 nov. 01 ] Available from: https://doi.org/10.1016/j.bmc.2011.09.009

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