ReP USP - Resultado da busca

Artigo de periodico
BFD-22 a new potential inhibitor of BRAF inhibits the metastasis of B16F10 melanoma cells and simultaneously increased the tumor immunogenicity (2016)
Ferreira, Adilson Kleber; Pasqualoto, Kerly Fernanda Mesquita; Kruyt, Frank A. E; Berl, Fanny Palace; Azevedo, Ricardo Alexandre de; Turra, Kely Medeiros; Rodrigues, Cecília Pessoa; Ferreira, Ana Carolina Franco; Salomon, Maria Alejandra Clavijo; Sá Júnior, Paulo Luiz de; Farias, Camyla Fernandes; Figueiredo, Carlos Rogério; Tavares, Leoberto Costa ; Barbuto, José Alexandre Marzagão ; Jorge, Salomão Dória
Source: Toxicology and Applied Pharmacology. Unidades: FCF, ICB
Subjects: MELANOMA, METÁSTASE NEOPLÁSICA, APOPTOSE
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ABNT
FERREIRA, Adilson Kleber et al. BFD-22 a new potential inhibitor of BRAF inhibits the metastasis of B16F10 melanoma cells and simultaneously increased the tumor immunogenicity. Toxicology and Applied Pharmacology, v. 295, p. 56-67, 2016Tradução . . Disponível em: https://doi.org/10.1016/j.taap.2016.02.008. Acesso em: 01 nov. 2024.
APA
Ferreira, A. K., Pasqualoto, K. F. M., Kruyt, F. A. E., Berl, F. P., Azevedo, R. A. de, Turra, K. M., et al. (2016). BFD-22 a new potential inhibitor of BRAF inhibits the metastasis of B16F10 melanoma cells and simultaneously increased the tumor immunogenicity. Toxicology and Applied Pharmacology, 295, 56-67. doi:10.1016/j.taap.2016.02.008
NLM
Ferreira AK, Pasqualoto KFM, Kruyt FAE, Berl FP, Azevedo RA de, Turra KM, Rodrigues CP, Ferreira ACF, Salomon MAC, Sá Júnior PL de, Farias CF, Figueiredo CR, Tavares LC, Barbuto JAM, Jorge SD. BFD-22 a new potential inhibitor of BRAF inhibits the metastasis of B16F10 melanoma cells and simultaneously increased the tumor immunogenicity [Internet]. Toxicology and Applied Pharmacology. 2016 ; 295 56-67.[citado 2024 nov. 01 ] Available from: https://doi.org/10.1016/j.taap.2016.02.008
Vancouver
Ferreira AK, Pasqualoto KFM, Kruyt FAE, Berl FP, Azevedo RA de, Turra KM, Rodrigues CP, Ferreira ACF, Salomon MAC, Sá Júnior PL de, Farias CF, Figueiredo CR, Tavares LC, Barbuto JAM, Jorge SD. BFD-22 a new potential inhibitor of BRAF inhibits the metastasis of B16F10 melanoma cells and simultaneously increased the tumor immunogenicity [Internet]. Toxicology and Applied Pharmacology. 2016 ; 295 56-67.[citado 2024 nov. 01 ] Available from: https://doi.org/10.1016/j.taap.2016.02.008
Artigo de periodico
Designing and exploring active N '-[(5-nitrofuran-2-yl) methylene] substituted hydrazides against three Trypanosoma cruzi strains more prevalent in Chagas disease patients (2015)
Berl, Fanny Palace; Pasqualoto, Kerly Fernanda Mesquita; Jorge, Salomão Dória; Zingales, Bianca ; Zorzi, Rodrigo Rocha; Silva, Marcelo Nunes da; Ferreira, Adilson Kleber; Azevedo, Ricardo Alexandre de; Teixeira, Sarah Fernandes; Tavares, Leoberto Costa
Source: European Journal of Medicinal Chemistry. Unidades: IQ, FCF
Subjects: DOENÇA DE CHAGAS, TRYPANOSOMA CRUZI
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ABNT
BERL, Fanny Palace et al. Designing and exploring active N '-[(5-nitrofuran-2-yl) methylene] substituted hydrazides against three Trypanosoma cruzi strains more prevalent in Chagas disease patients. European Journal of Medicinal Chemistry, v. 96, p. 330-339, 2015Tradução . . Disponível em: https://doi.org/10.1016/j.ejmech.2015.03.066. Acesso em: 01 nov. 2024.
APA
Berl, F. P., Pasqualoto, K. F. M., Jorge, S. D., Zingales, B., Zorzi, R. R., Silva, M. N. da, et al. (2015). Designing and exploring active N '-[(5-nitrofuran-2-yl) methylene] substituted hydrazides against three Trypanosoma cruzi strains more prevalent in Chagas disease patients. European Journal of Medicinal Chemistry, 96, 330-339. doi:10.1016/j.ejmech.2015.03.066
NLM
Berl FP, Pasqualoto KFM, Jorge SD, Zingales B, Zorzi RR, Silva MN da, Ferreira AK, Azevedo RA de, Teixeira SF, Tavares LC. Designing and exploring active N '-[(5-nitrofuran-2-yl) methylene] substituted hydrazides against three Trypanosoma cruzi strains more prevalent in Chagas disease patients [Internet]. European Journal of Medicinal Chemistry. 2015 ; 96 330-339.[citado 2024 nov. 01 ] Available from: https://doi.org/10.1016/j.ejmech.2015.03.066
Vancouver
Berl FP, Pasqualoto KFM, Jorge SD, Zingales B, Zorzi RR, Silva MN da, Ferreira AK, Azevedo RA de, Teixeira SF, Tavares LC. Designing and exploring active N '-[(5-nitrofuran-2-yl) methylene] substituted hydrazides against three Trypanosoma cruzi strains more prevalent in Chagas disease patients [Internet]. European Journal of Medicinal Chemistry. 2015 ; 96 330-339.[citado 2024 nov. 01 ] Available from: https://doi.org/10.1016/j.ejmech.2015.03.066
Artigo de periodico
Exploring 5-nitrofuran derivatives against nosocomial pathogens: synthesis, antimicrobial activity and chemometric analysis (2014)
Zorzi, Rodrigo Rocha; Jorge, Salomão Dória; Palace-Berl, Fanny; Pasqualoto, Kerly Fernanda Mesquita; Bortolozzo, Leandro de Sá; Siqueira, André Murillo de Castro; Tavares, Leoberto Costa
Source: Bioorganic & Medicinal Chemistry. Unidade: FCF
Subjects: RESISTÊNCIA MICROBIANA ÀS DROGAS, INFECÇÕES BACTERIANAS
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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
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
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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
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 ]
Trabalho de evento-resumo periodico
Nifuroxazide analogues against t. cruzi: Synthesis bioactivity and molecular modeling approach (2012)
Palace-Berl, Fanny; Jorge, Salomão Dória; Pasqualoto, Kerly Fernanda Mesquita; Zorzi, Rodrigo Rocha; Bortolozzo, Leandro de Sá; Petri, Simone Carolina Soares; Lindoso, José Angelo Lauletta; Tavares, Leoberto Costa
Source: Brazilian Journal of Pharmaceutical Sciences. Conference titles: Pharmaceutical Science and Technology Meeting. Unidade: FCF
Assunto: MODELAGEM MOLECULAR
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ABNT
PALACE-BERL, Fanny et al. Nifuroxazide analogues against t. cruzi: Synthesis bioactivity and molecular modeling approach. Brazilian Journal of Pharmaceutical Sciences. São Paulo: Faculdade de Ciências Farmacêuticas, Universidade de São Paulo. . Acesso em: 01 nov. 2024. , 2012
APA
Palace-Berl, F., Jorge, S. D., Pasqualoto, K. F. M., Zorzi, R. R., Bortolozzo, L. de S., Petri, S. C. S., et al. (2012). Nifuroxazide analogues against t. cruzi: Synthesis bioactivity and molecular modeling approach. Brazilian Journal of Pharmaceutical Sciences. São Paulo: Faculdade de Ciências Farmacêuticas, Universidade de São Paulo.
NLM
Palace-Berl F, Jorge SD, Pasqualoto KFM, Zorzi RR, Bortolozzo L de S, Petri SCS, Lindoso JAL, Tavares LC. Nifuroxazide analogues against t. cruzi: Synthesis bioactivity and molecular modeling approach. Brazilian Journal of Pharmaceutical Sciences. 2012 ; 48 61 res. FCF117.[citado 2024 nov. 01 ]
Vancouver
Palace-Berl F, Jorge SD, Pasqualoto KFM, Zorzi RR, Bortolozzo L de S, Petri SCS, Lindoso JAL, Tavares LC. Nifuroxazide analogues against t. cruzi: Synthesis bioactivity and molecular modeling approach. Brazilian Journal of Pharmaceutical Sciences. 2012 ; 48 61 res. FCF117.[citado 2024 nov. 01 ]
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: 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
Artigo de periodico
Novel benzofuroxan derivatives against multidrug-resistant Staphylococcus aureus strains: design using Topliss’ decision tree, synthesis and biological assay (2011)
Jorge, Salomão Dória; Palace-Berl, Fanny; Masunari, Andrea; Cechinel, Cléber André; Ishii, Marina ; Pasqualoto, Kerly Fernanda Mesquita; Tavares, Leoberto Costa
Source: Bioorganic & Medicinal Chemistry. Unidade: FCF
Subjects: RESISTÊNCIA MICROBIANA ÀS DROGAS, STAPHYLOCOCCUS
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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
Artigo de periodico
Self-organizing maps and VolSurf approach to predict aldose reductase inhibition by flavonoid compounds (2011)
Scotti, Luciana; Fernandes, Mariane Ballerini; Muramatsu, Eric; Pasqualoto, Kerly Fernanda Mesquita; Emerenciano, Vicente de Paulo; Tavares, Leoberto Costa ; Silva, Marcelo Sobral da; Scotti, Marcus Tullius
Source: Revista Brasileira de Farmacognosia. Unidades: IQ, FCF
Subjects: FLAVONÓIDES, REDES NEURAIS
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ABNT
SCOTTI, Luciana et al. Self-organizing maps and VolSurf approach to predict aldose reductase inhibition by flavonoid compounds. Revista Brasileira de Farmacognosia, v. 21, n. 1, p. 170-180, 2011Tradução . . Disponível em: https://doi.org/10.1590/S0102-695x2011005000028. Acesso em: 01 nov. 2024.
APA
Scotti, L., Fernandes, M. B., Muramatsu, E., Pasqualoto, K. F. M., Emerenciano, V. de P., Tavares, L. C., et al. (2011). Self-organizing maps and VolSurf approach to predict aldose reductase inhibition by flavonoid compounds. Revista Brasileira de Farmacognosia, 21( 1), 170-180. doi:10.1590/S0102-695x2011005000028
NLM
Scotti L, Fernandes MB, Muramatsu E, Pasqualoto KFM, Emerenciano V de P, Tavares LC, Silva MS da, Scotti MT. Self-organizing maps and VolSurf approach to predict aldose reductase inhibition by flavonoid compounds [Internet]. Revista Brasileira de Farmacognosia. 2011 ; 21( 1): 170-180.[citado 2024 nov. 01 ] Available from: https://doi.org/10.1590/S0102-695x2011005000028
Vancouver
Scotti L, Fernandes MB, Muramatsu E, Pasqualoto KFM, Emerenciano V de P, Tavares LC, Silva MS da, Scotti MT. Self-organizing maps and VolSurf approach to predict aldose reductase inhibition by flavonoid compounds [Internet]. Revista Brasileira de Farmacognosia. 2011 ; 21( 1): 170-180.[citado 2024 nov. 01 ] Available from: https://doi.org/10.1590/S0102-695x2011005000028
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: 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
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: 01 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. 01 ]
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. 01 ]

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