ReP USP - Resultado da busca

Artigo de periodico
Caco-2 cells cytotoxicity of nifuroxazide derivatives with potential activity against Methicillin-resistant Staphylococcus aureus (2012)
Fernandes, Mariane Ballerini; Gonçalves, José Eduardo; Scotti, Marcus Tullius; Oliveira, Alex Alfredo de; Tavares, Leoberto Costa ; Storpirtis, Silvia
Source: Toxicology in Vitro. Unidade: FCF
Subjects: COMPOSTOS HETEROCÍCLICOS, STAPHYLOCOCCUS
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ABNT
FERNANDES, Mariane Ballerini et al. Caco-2 cells cytotoxicity of nifuroxazide derivatives with potential activity against Methicillin-resistant Staphylococcus aureus. Toxicology in Vitro, v. 28, n. 3, p. 535-540, 2012Tradução . . Disponível em: https://doi.org/10.1016/j.tiv.2012.01.018. Acesso em: 02 nov. 2024.
APA
Fernandes, M. B., Gonçalves, J. E., Scotti, M. T., Oliveira, A. A. de, Tavares, L. C., & Storpirtis, S. (2012). Caco-2 cells cytotoxicity of nifuroxazide derivatives with potential activity against Methicillin-resistant Staphylococcus aureus. Toxicology in Vitro, 28( 3), 535-540. doi:10.1016/j.tiv.2012.01.018
NLM
Fernandes MB, Gonçalves JE, Scotti MT, Oliveira AA de, Tavares LC, Storpirtis S. Caco-2 cells cytotoxicity of nifuroxazide derivatives with potential activity against Methicillin-resistant Staphylococcus aureus [Internet]. Toxicology in Vitro. 2012 ; 28( 3): 535-540.[citado 2024 nov. 02 ] Available from: https://doi.org/10.1016/j.tiv.2012.01.018
Vancouver
Fernandes MB, Gonçalves JE, Scotti MT, Oliveira AA de, Tavares LC, Storpirtis S. Caco-2 cells cytotoxicity of nifuroxazide derivatives with potential activity against Methicillin-resistant Staphylococcus aureus [Internet]. Toxicology in Vitro. 2012 ; 28( 3): 535-540.[citado 2024 nov. 02 ] Available from: https://doi.org/10.1016/j.tiv.2012.01.018
Artigo de periodico
Preliminary in vitro evaluation of N'-(benzofuroxan-5-yl)methylene benzohydrazide derivatives as potential anti-Trypanosoma cruzi agents (2012)
Jorge, Salomão Dória; Ishii, Marina ; Palace-Berl, Fanny; Ferreira, Adilson Kleber; Sá Júnior, Paulo Luiz de; Oliveira, Alex Alfredo de; Sonehara, Ieda Yuriko; Pasqualoto, Kerly Fernanda Mesquita; Tavares, Leoberto Costa
Source: MedChemComm. Unidade: FCF
Subjects: TRYPANOSOMA CRUZI, ANTIPARASITÁRIOS
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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: 02 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. 02 ] 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. 02 ] Available from: https://doi.org/10.1039/c2md20019h
Artigo de periodico
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 (2011)
Ishii, Marina ; Jorge, Salomão Dória; Oliveira, Alex Alfredo de; Palace-Berl, Fanny; Sonehara, Ieda Yuriko; Pasqualoto, Kerly Fernanda Mesquita; Tavares, Leoberto Costa
Source: Bioorganic & Medicinal Chemistry. Unidade: FCF
Subjects: TRYPANOSOMA CRUZI, CANDIDA ALBICANS, ANTIFÚNGICOS
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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: 02 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. 02 ] 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. 02 ] Available from: https://doi.org/10.1016/j.bmc.2011.09.009
Trabalho de evento-resumo periodico
Design synthesis, bioactivity evaluation and molecular modeling of potential anti-T. cruzi agents (2011)
Palace-Berl, Fanny; Jorge, Salomão Dória; Oliveira, Alex Alfredo de; Zorzi, Rodrigo Rocha; Bortolozzo, Leandro de Sá; Pasqualoto, Kerly Fernanda Mesquita; Tavares, Leoberto Costa
Source: Brazilian Journal of Pharmaceutical Sciences. Conference titles: Science and Pharmaceutical Technology Meeting of the Pharmaceutical Sciences Faculty of the University of São Paulo. Unidade: FCF
Subjects: MODELAGEM MOLECULAR, ANTIPARASITÁRIOS
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
PALACE-BERL, Fanny et al. Design synthesis, bioactivity evaluation and molecular modeling of potential anti-T. cruzi agents. Brazilian Journal of Pharmaceutical Sciences. São Paulo: Faculdade de Ciências Farmacêuticas, Universidade de São Paulo. . Acesso em: 02 nov. 2024. , 2011
APA
Palace-Berl, F., Jorge, S. D., Oliveira, A. A. de, Zorzi, R. R., Bortolozzo, L. de S., Pasqualoto, K. F. M., & Tavares, L. C. (2011). Design synthesis, bioactivity evaluation and molecular modeling of potential anti-T. cruzi agents. Brazilian Journal of Pharmaceutical Sciences. São Paulo: Faculdade de Ciências Farmacêuticas, Universidade de São Paulo.
NLM
Palace-Berl F, Jorge SD, Oliveira AA de, Zorzi RR, Bortolozzo L de S, Pasqualoto KFM, Tavares LC. Design synthesis, bioactivity evaluation and molecular modeling of potential anti-T. cruzi agents. Brazilian Journal of Pharmaceutical Sciences. 2011 ; 47 99 res. FCF193.[citado 2024 nov. 02 ]
Vancouver
Palace-Berl F, Jorge SD, Oliveira AA de, Zorzi RR, Bortolozzo L de S, Pasqualoto KFM, Tavares LC. Design synthesis, bioactivity evaluation and molecular modeling of potential anti-T. cruzi agents. Brazilian Journal of Pharmaceutical Sciences. 2011 ; 47 99 res. FCF193.[citado 2024 nov. 02 ]

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