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Artigo de periodico
Ligand-based design, synthesis, and experimental evaluation of novel benzofuroxan derivatives as anti-Trypanosoma cruzi agents (2013)
Jorge, Salomão Dória; Palace-Berl, Fanny; Pasqualoto, Kerly Fernanda Mesquita; Ishii, Marina ; Ferreira, Adilson Kleber; Berra, Carolina Maria; Bosch, Rosemary Viola; Maria, Durvanei Augusto; Tavares, Leoberto Costa
Source: European Journal of Medicinal Chemistry. Unidade: FCF
Subjects: TRYPANOSOMA CRUZI, RELAÇÕES QUANTITATIVAS ENTRE ESTRUTURA QUÍMICA E ATIVIDADE BIOLÓGICA
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
JORGE, Salomão Dória et al. Ligand-based design, synthesis, and experimental evaluation of novel benzofuroxan derivatives as anti-Trypanosoma cruzi agents. European Journal of Medicinal Chemistry, v. 64, p. 200-214, 2013Tradução . . Disponível em: https://doi.org/10.1016/j.ejmech.2013.03.053. Acesso em: 01 nov. 2024.
APA
Jorge, S. D., Palace-Berl, F., Pasqualoto, K. F. M., Ishii, M., Ferreira, A. K., Berra, C. M., et al. (2013). Ligand-based design, synthesis, and experimental evaluation of novel benzofuroxan derivatives as anti-Trypanosoma cruzi agents. European Journal of Medicinal Chemistry, 64, 200-214. doi:10.1016/j.ejmech.2013.03.053
NLM
Jorge SD, Palace-Berl F, Pasqualoto KFM, Ishii M, Ferreira AK, Berra CM, Bosch RV, Maria DA, Tavares LC. Ligand-based design, synthesis, and experimental evaluation of novel benzofuroxan derivatives as anti-Trypanosoma cruzi agents [Internet]. European Journal of Medicinal Chemistry. 2013 ; 64 200-214.[citado 2024 nov. 01 ] Available from: https://doi.org/10.1016/j.ejmech.2013.03.053
Vancouver
Jorge SD, Palace-Berl F, Pasqualoto KFM, Ishii M, Ferreira AK, Berra CM, Bosch RV, Maria DA, Tavares LC. Ligand-based design, synthesis, and experimental evaluation of novel benzofuroxan derivatives as anti-Trypanosoma cruzi agents [Internet]. European Journal of Medicinal Chemistry. 2013 ; 64 200-214.[citado 2024 nov. 01 ] Available from: https://doi.org/10.1016/j.ejmech.2013.03.053
Artigo de periodico
Design and exploratory data analysis of a second generation of dendrimer prodrugs potentially antichagasic and leishmanicide (2013)
Giarolla, Jeanine ; Pasqualoto, Kerly Fernanda Mesquita; Ferreira, Elizabeth Igne
Source: Molecular Diversity. Unidade: FCF
Subjects: MODELAGEM MOLECULAR, DOENÇA DE CHAGAS, LEISHMANIA
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
GIAROLLA, Jeanine e PASQUALOTO, Kerly Fernanda Mesquita e FERREIRA, Elizabeth Igne. Design and exploratory data analysis of a second generation of dendrimer prodrugs potentially antichagasic and leishmanicide. Molecular Diversity, v. 17, n. 4, p. 711-720, 2013Tradução . . Disponível em: https://doi.org/10.1007/s11030-013-9467-5. Acesso em: 01 nov. 2024.
APA
Giarolla, J., Pasqualoto, K. F. M., & Ferreira, E. I. (2013). Design and exploratory data analysis of a second generation of dendrimer prodrugs potentially antichagasic and leishmanicide. Molecular Diversity, 17( 4), 711-720. doi:10.1007/s11030-013-9467-5
NLM
Giarolla J, Pasqualoto KFM, Ferreira EI. Design and exploratory data analysis of a second generation of dendrimer prodrugs potentially antichagasic and leishmanicide [Internet]. Molecular Diversity. 2013 ; 17( 4): 711-720.[citado 2024 nov. 01 ] Available from: https://doi.org/10.1007/s11030-013-9467-5
Vancouver
Giarolla J, Pasqualoto KFM, Ferreira EI. Design and exploratory data analysis of a second generation of dendrimer prodrugs potentially antichagasic and leishmanicide [Internet]. Molecular Diversity. 2013 ; 17( 4): 711-720.[citado 2024 nov. 01 ] Available from: https://doi.org/10.1007/s11030-013-9467-5
Trabalho de evento-resumo periodico
Molecular properties evaluation of a second generation dendrimers pontentially antichagasic and leishmanicide (2013)
Giarolla, Jeanine ; Santos, Soraya; Pasqualoto, Kerly Fernanda Mesquita; Ferreira, Elizabeth Igne
Source: Brazilian Journal of Pharmaceutical Sciences. Conference titles: Pharmaceutical Science and Technology Meeting of the Faculty of Pharmaceutical Sciences. Unidade: FCF
Subjects: DOENÇA DE CHAGAS, PLANEJAMENTO DE FÁRMACOS
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ABNT
GIAROLLA, Jeanine et al. Molecular properties evaluation of a second generation dendrimers pontentially antichagasic and leishmanicide. Brazilian Journal of Pharmaceutical Sciences. São Paulo: Faculdade de Ciências Farmacêuticas, Universidade de São Paulo. . Acesso em: 01 nov. 2024. , 2013
APA
Giarolla, J., Santos, S., Pasqualoto, K. F. M., & Ferreira, E. I. (2013). Molecular properties evaluation of a second generation dendrimers pontentially antichagasic and leishmanicide. Brazilian Journal of Pharmaceutical Sciences. São Paulo: Faculdade de Ciências Farmacêuticas, Universidade de São Paulo.
NLM
Giarolla J, Santos S, Pasqualoto KFM, Ferreira EI. Molecular properties evaluation of a second generation dendrimers pontentially antichagasic and leishmanicide. Brazilian Journal of Pharmaceutical Sciences. 2013 ; 49 57 res. FCF110.[citado 2024 nov. 01 ]
Vancouver
Giarolla J, Santos S, Pasqualoto KFM, Ferreira EI. Molecular properties evaluation of a second generation dendrimers pontentially antichagasic and leishmanicide. Brazilian Journal of Pharmaceutical Sciences. 2013 ; 49 57 res. FCF110.[citado 2024 nov. 01 ]
Trabalho de evento-resumo periodico
Study of structure-activity relationship of 5-nitro-2-thiophylidene derivatives with antimicrobial activity (2013)
Bortolozzo, Leandro de Sá; Zorzi, Rodrigo Rocha; Jorge, Salomão Dória; Palace-Berl, Fanny; Pasqualoto, Kerly Fernanda Mesquita; Tavares, Leoberto Costa
Source: Brazilian Journal of Pharmaceutical Sciences. Conference titles: Pharmaceutical Science and Technology Meeting of the Faculty of Pharmaceutical Sciences. Unidade: FCF
Assunto: AGENTES ANTIMICROBIANOS
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ABNT
BORTOLOZZO, Leandro de Sá et al. Study of structure-activity relationship of 5-nitro-2-thiophylidene derivatives with antimicrobial activity. Brazilian Journal of Pharmaceutical Sciences. São Paulo: Faculdade de Ciências Farmacêuticas, Universidade de São Paulo. . Acesso em: 01 nov. 2024. , 2013
APA
Bortolozzo, L. de S., Zorzi, R. R., Jorge, S. D., Palace-Berl, F., Pasqualoto, K. F. M., & Tavares, L. C. (2013). Study of structure-activity relationship of 5-nitro-2-thiophylidene derivatives with antimicrobial activity. Brazilian Journal of Pharmaceutical Sciences. São Paulo: Faculdade de Ciências Farmacêuticas, Universidade de São Paulo.
NLM
Bortolozzo L de S, Zorzi RR, Jorge SD, Palace-Berl F, Pasqualoto KFM, Tavares LC. Study of structure-activity relationship of 5-nitro-2-thiophylidene derivatives with antimicrobial activity. Brazilian Journal of Pharmaceutical Sciences. 2013 ; 49 37 res. 070.[citado 2024 nov. 01 ]
Vancouver
Bortolozzo L de S, Zorzi RR, Jorge SD, Palace-Berl F, Pasqualoto KFM, Tavares LC. Study of structure-activity relationship of 5-nitro-2-thiophylidene derivatives with antimicrobial activity. Brazilian Journal of Pharmaceutical Sciences. 2013 ; 49 37 res. 070.[citado 2024 nov. 01 ]
Artigo de periodico
RPF101, a new capsaicin-like analogue, disrupts the microtubule network accompanied by arrest in the G2/M phase, inducing apoptosis and mitotic catastrophe in the MCF-7 breast cancer cells (2013)
Sá Júnior, Paulo Luiz de; Pasqualoto, Kerly Fernanda Mesquita; Ferreira, Adilson Kleber; Tavares, Maurício Temotheo; Damião, Mariana Celestina Frojuello Bernstorff; Azevedo, Ricardo Alexandre de; Câmara, Diana Aparecida Dias; Pereira, Alexandre; Souza, Dener Madeiro de; Parise Filho, Roberto
Source: Toxicology and Applied Pharmacology. Unidade: FCF
Subjects: MODELAGEM MOLECULAR, CICLO CELULAR, APOPTOSE
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
SÁ JÚNIOR, Paulo Luiz de et al. RPF101, a new capsaicin-like analogue, disrupts the microtubule network accompanied by arrest in the G2/M phase, inducing apoptosis and mitotic catastrophe in the MCF-7 breast cancer cells. Toxicology and Applied Pharmacology, v. 266, n. 3, p. 385-398, 2013Tradução . . Disponível em: https://doi.org/10.1016/j.taap.2012.11.029. Acesso em: 01 nov. 2024.
APA
Sá Júnior, P. L. de, Pasqualoto, K. F. M., Ferreira, A. K., Tavares, M. T., Damião, M. C. F. B., Azevedo, R. A. de, et al. (2013). RPF101, a new capsaicin-like analogue, disrupts the microtubule network accompanied by arrest in the G2/M phase, inducing apoptosis and mitotic catastrophe in the MCF-7 breast cancer cells. Toxicology and Applied Pharmacology, 266( 3), 385-398. doi:10.1016/j.taap.2012.11.029
NLM
Sá Júnior PL de, Pasqualoto KFM, Ferreira AK, Tavares MT, Damião MCFB, Azevedo RA de, Câmara DAD, Pereira A, Souza DM de, Parise Filho R. RPF101, a new capsaicin-like analogue, disrupts the microtubule network accompanied by arrest in the G2/M phase, inducing apoptosis and mitotic catastrophe in the MCF-7 breast cancer cells [Internet]. Toxicology and Applied Pharmacology. 2013 ; 266( 3): 385-398.[citado 2024 nov. 01 ] Available from: https://doi.org/10.1016/j.taap.2012.11.029
Vancouver
Sá Júnior PL de, Pasqualoto KFM, Ferreira AK, Tavares MT, Damião MCFB, Azevedo RA de, Câmara DAD, Pereira A, Souza DM de, Parise Filho R. RPF101, a new capsaicin-like analogue, disrupts the microtubule network accompanied by arrest in the G2/M phase, inducing apoptosis and mitotic catastrophe in the MCF-7 breast cancer cells [Internet]. Toxicology and Applied Pharmacology. 2013 ; 266( 3): 385-398.[citado 2024 nov. 01 ] Available from: https://doi.org/10.1016/j.taap.2012.11.029

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