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Brazilian Symposium on Medicinal Chemistry - BrazMedChem, 11. . Salvador: Universidade Federal da Bahia - UFBA. . Acesso em: 07 maio 2024. , 2023
APA
Brazilian Symposium on Medicinal Chemistry - BrazMedChem, 11. (2023). Brazilian Symposium on Medicinal Chemistry - BrazMedChem, 11. Salvador: Universidade Federal da Bahia - UFBA.
NLM
Brazilian Symposium on Medicinal Chemistry - BrazMedChem, 11. 2023 ;[citado 2024 maio 07 ]
Vancouver
Brazilian Symposium on Medicinal Chemistry - BrazMedChem, 11. 2023 ;[citado 2024 maio 07 ]
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PENTEADO, André Berndt et al. Human sirtuin 2 inhibitors, their mechanisms and binding modes. Future Medicinal Chemistry, v. 15, n. 3, p. 291-311, 2023Tradução . . Disponível em: https://doi.org/10.4155/fmc-2022-0253. Acesso em: 07 maio 2024.
APA
Penteado, A. B., Hassanie, H., Gomes, R. A., Emery, F. da S., & Trossini, G. H. G. (2023). Human sirtuin 2 inhibitors, their mechanisms and binding modes. Future Medicinal Chemistry, 15( 3), 291-311. doi:10.4155/fmc-2022-0253
NLM
Penteado AB, Hassanie H, Gomes RA, Emery F da S, Trossini GHG. Human sirtuin 2 inhibitors, their mechanisms and binding modes [Internet]. Future Medicinal Chemistry. 2023 ; 15( 3): 291-311.[citado 2024 maio 07 ] Available from: https://doi.org/10.4155/fmc-2022-0253
Vancouver
Penteado AB, Hassanie H, Gomes RA, Emery F da S, Trossini GHG. Human sirtuin 2 inhibitors, their mechanisms and binding modes [Internet]. Future Medicinal Chemistry. 2023 ; 15( 3): 291-311.[citado 2024 maio 07 ] Available from: https://doi.org/10.4155/fmc-2022-0253
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FERREIRA, Glaucio Monteiro et al. Trypanosoma cruzi Sirtuin 2 as a relevant druggable target: new inhibitors developed by computer-aided drug design. Pharmaceuticals, v. 16 , p. 1-14 art. 428, 2023Tradução . . Disponível em: https://doi.org/10.3390/ph16030428. Acesso em: 07 maio 2024.
APA
Ferreira, G. M., Kronenberger, T., Maltarollo, V. G., Poso, A., Gatti, F. de M., Almeida, V. M., et al. (2023). Trypanosoma cruzi Sirtuin 2 as a relevant druggable target: new inhibitors developed by computer-aided drug design. Pharmaceuticals, 16 , 1-14 art. 428. doi:10.3390/ph16030428
NLM
Ferreira GM, Kronenberger T, Maltarollo VG, Poso A, Gatti F de M, Almeida VM, Marana SR, Lopes CD, Tezuka DY, Albuquerque S de, Emery F da S, Trossini GHG. Trypanosoma cruzi Sirtuin 2 as a relevant druggable target: new inhibitors developed by computer-aided drug design [Internet]. Pharmaceuticals. 2023 ; 16 1-14 art. 428.[citado 2024 maio 07 ] Available from: https://doi.org/10.3390/ph16030428
Vancouver
Ferreira GM, Kronenberger T, Maltarollo VG, Poso A, Gatti F de M, Almeida VM, Marana SR, Lopes CD, Tezuka DY, Albuquerque S de, Emery F da S, Trossini GHG. Trypanosoma cruzi Sirtuin 2 as a relevant druggable target: new inhibitors developed by computer-aided drug design [Internet]. Pharmaceuticals. 2023 ; 16 1-14 art. 428.[citado 2024 maio 07 ] Available from: https://doi.org/10.3390/ph16030428
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SILVA, Daniel G. et al. Synthesis and structure−activity relationships of imidazopyridine/pyrimidine- and furopyridine‐based anti‐infective agents against Trypanosomiases. ChemMedChem, v. 16, n. 6, p. 966-975, 2021Tradução . . Disponível em: https://doi.org/10.1002/cmdc.202000616. Acesso em: 07 maio 2024.
APA
Silva, D. G., Junker, A., Melo, S. M. G. de, Fumagalli, F., Gillespie, J. R., Molasky, N., et al. (2021). Synthesis and structure−activity relationships of imidazopyridine/pyrimidine- and furopyridine‐based anti‐infective agents against Trypanosomiases. ChemMedChem, 16( 6), 966-975. doi:10.1002/cmdc.202000616
NLM
Silva DG, Junker A, Melo SMG de, Fumagalli F, Gillespie JR, Molasky N, Buckner FS, Matheeussen A, Caljon G, Maes L, Emery F da S. Synthesis and structure−activity relationships of imidazopyridine/pyrimidine- and furopyridine‐based anti‐infective agents against Trypanosomiases [Internet]. ChemMedChem. 2021 ; 16( 6): 966-975.[citado 2024 maio 07 ] Available from: https://doi.org/10.1002/cmdc.202000616
Vancouver
Silva DG, Junker A, Melo SMG de, Fumagalli F, Gillespie JR, Molasky N, Buckner FS, Matheeussen A, Caljon G, Maes L, Emery F da S. Synthesis and structure−activity relationships of imidazopyridine/pyrimidine- and furopyridine‐based anti‐infective agents against Trypanosomiases [Internet]. ChemMedChem. 2021 ; 16( 6): 966-975.[citado 2024 maio 07 ] Available from: https://doi.org/10.1002/cmdc.202000616
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GOMES, Renan Augusto et al. Parasitic sirtuin 2 as an opportunity in drug discovery. Future Medicinal Chemistry, v. 13, n. 16, p. 1397-1409, 2021Tradução . . Disponível em: https://doi.org/10.4155/fmc-2021-0091. Acesso em: 07 maio 2024.
APA
Gomes, R. A., Fornari, E., Rocha, A. C. S., Tripodi, G. L., Emery, F. da S., & Trossini, G. H. G. (2021). Parasitic sirtuin 2 as an opportunity in drug discovery. Future Medicinal Chemistry, 13( 16), 1397-1409. doi:10.4155/fmc-2021-0091
NLM
Gomes RA, Fornari E, Rocha ACS, Tripodi GL, Emery F da S, Trossini GHG. Parasitic sirtuin 2 as an opportunity in drug discovery [Internet]. Future Medicinal Chemistry. 2021 ; 13( 16): 1397-1409.[citado 2024 maio 07 ] Available from: https://doi.org/10.4155/fmc-2021-0091
Vancouver
Gomes RA, Fornari E, Rocha ACS, Tripodi GL, Emery F da S, Trossini GHG. Parasitic sirtuin 2 as an opportunity in drug discovery [Internet]. Future Medicinal Chemistry. 2021 ; 13( 16): 1397-1409.[citado 2024 maio 07 ] Available from: https://doi.org/10.4155/fmc-2021-0091
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ZAMBUZI, Fabiana Albani et al. Decitabine promotes modulation in phenotype and function of monocytes and macrophages that drive immune response regulation. Cells, v. 10, n. 4, p. 1-16, 2021Tradução . . Disponível em: https://doi.org/10.3390/cells10040868. Acesso em: 07 maio 2024.
APA
Zambuzi, F. A., Silva, P. M. C., Castro, R. C., Fontanari, C., Emery, F. da S., & Frantz, F. G. (2021). Decitabine promotes modulation in phenotype and function of monocytes and macrophages that drive immune response regulation. Cells, 10( 4), 1-16. doi:10.3390/cells10040868
NLM
Zambuzi FA, Silva PMC, Castro RC, Fontanari C, Emery F da S, Frantz FG. Decitabine promotes modulation in phenotype and function of monocytes and macrophages that drive immune response regulation [Internet]. Cells. 2021 ; 10( 4): 1-16.[citado 2024 maio 07 ] Available from: https://doi.org/10.3390/cells10040868
Vancouver
Zambuzi FA, Silva PMC, Castro RC, Fontanari C, Emery F da S, Frantz FG. Decitabine promotes modulation in phenotype and function of monocytes and macrophages that drive immune response regulation [Internet]. Cells. 2021 ; 10( 4): 1-16.[citado 2024 maio 07 ] Available from: https://doi.org/10.3390/cells10040868
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LIMA, Elys Juliane Cardoso et al. Insights into newly approved drugs from a medicinal chemistry perspective. Mini-Reviews in Medicinal Chemistry, v. 21, n. 16, p. 2227-2248, 2021Tradução . . Disponível em: https://doi.org/10.2174/1389557521666210226145328. Acesso em: 07 maio 2024.
APA
Lima, E. J. C., Gomes, R. A., Fornari, E., Emery, F. da S., & Trossini, G. H. G. (2021). Insights into newly approved drugs from a medicinal chemistry perspective. Mini-Reviews in Medicinal Chemistry, 21( 16), 2227-2248. doi:10.2174/1389557521666210226145328
NLM
Lima EJC, Gomes RA, Fornari E, Emery F da S, Trossini GHG. Insights into newly approved drugs from a medicinal chemistry perspective [Internet]. Mini-Reviews in Medicinal Chemistry. 2021 ; 21( 16): 2227-2248.[citado 2024 maio 07 ] Available from: https://doi.org/10.2174/1389557521666210226145328
Vancouver
Lima EJC, Gomes RA, Fornari E, Emery F da S, Trossini GHG. Insights into newly approved drugs from a medicinal chemistry perspective [Internet]. Mini-Reviews in Medicinal Chemistry. 2021 ; 21( 16): 2227-2248.[citado 2024 maio 07 ] Available from: https://doi.org/10.2174/1389557521666210226145328
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MORI, Renan Minin de et al. Structural basis for the function and inhibition of dihydroorotate dehydrogenase from Schistosoma mansoni. The FEBS Journal, v. 288, n. 3, p. 930-944, 2021Tradução . . Disponível em: https://doi.org/10.1111/febs.15367. Acesso em: 07 maio 2024.
APA
Mori, R. M. de, Aleixo, M. A. A., Zapata, L. C. C., Calil, F. A., Emery, F. da S., & Nonato, M. C. (2021). Structural basis for the function and inhibition of dihydroorotate dehydrogenase from Schistosoma mansoni. The FEBS Journal, 288( 3), 930-944. doi:10.1111/febs.15367
NLM
Mori RM de, Aleixo MAA, Zapata LCC, Calil FA, Emery F da S, Nonato MC. Structural basis for the function and inhibition of dihydroorotate dehydrogenase from Schistosoma mansoni [Internet]. The FEBS Journal. 2021 ; 288( 3): 930-944.[citado 2024 maio 07 ] Available from: https://doi.org/10.1111/febs.15367
Vancouver
Mori RM de, Aleixo MAA, Zapata LCC, Calil FA, Emery F da S, Nonato MC. Structural basis for the function and inhibition of dihydroorotate dehydrogenase from Schistosoma mansoni [Internet]. The FEBS Journal. 2021 ; 288( 3): 930-944.[citado 2024 maio 07 ] Available from: https://doi.org/10.1111/febs.15367
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WINANT, Pieterjan et al. A review of the synthetic strategies toward Dihydropyrrolo [1,2-a] Pyrazinones. Organics, v. 2, n. 2, p. 118-141, 2021Tradução . . Disponível em: https://doi.org/10.3390/org2020011. Acesso em: 07 maio 2024.
APA
Winant, P., Horsten, T., Melo, S. M. G. de, Emery, F. da S., & Dehaen, W. (2021). A review of the synthetic strategies toward Dihydropyrrolo [1,2-a] Pyrazinones. Organics, 2( 2), 118-141. doi:10.3390/org2020011
NLM
Winant P, Horsten T, Melo SMG de, Emery F da S, Dehaen W. A review of the synthetic strategies toward Dihydropyrrolo [1,2-a] Pyrazinones [Internet]. Organics. 2021 ; 2( 2): 118-141.[citado 2024 maio 07 ] Available from: https://doi.org/10.3390/org2020011
Vancouver
Winant P, Horsten T, Melo SMG de, Emery F da S, Dehaen W. A review of the synthetic strategies toward Dihydropyrrolo [1,2-a] Pyrazinones [Internet]. Organics. 2021 ; 2( 2): 118-141.[citado 2024 maio 07 ] Available from: https://doi.org/10.3390/org2020011
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RIBEIRO, L. M. B. C. et al. Structure-activity relationships and mechanism of action of tetragomycin derivatives as inhibitors of Staphylococcus aureus staphyloxanthin biosynthesis. Microbial Pathogenesis, v. 144, p. 1-8, 2020Tradução . . Disponível em: https://doi.org/10.1016/j.micpath.2020.104127. Acesso em: 07 maio 2024.
APA
Ribeiro, L. M. B. C., Fumagalli, F., Mello, R. B. de, Froes, T. Q., Silva, M. V. S. da, Villamizar Gómez, S. M., et al. (2020). Structure-activity relationships and mechanism of action of tetragomycin derivatives as inhibitors of Staphylococcus aureus staphyloxanthin biosynthesis. Microbial Pathogenesis, 144, 1-8. doi:10.1016/j.micpath.2020.104127
NLM
Ribeiro LMBC, Fumagalli F, Mello RB de, Froes TQ, Silva MVS da, Villamizar Gómez SM, Barros TF, Emery F da S, Castilho MS. Structure-activity relationships and mechanism of action of tetragomycin derivatives as inhibitors of Staphylococcus aureus staphyloxanthin biosynthesis [Internet]. Microbial Pathogenesis. 2020 ; 144 1-8.[citado 2024 maio 07 ] Available from: https://doi.org/10.1016/j.micpath.2020.104127
Vancouver
Ribeiro LMBC, Fumagalli F, Mello RB de, Froes TQ, Silva MVS da, Villamizar Gómez SM, Barros TF, Emery F da S, Castilho MS. Structure-activity relationships and mechanism of action of tetragomycin derivatives as inhibitors of Staphylococcus aureus staphyloxanthin biosynthesis [Internet]. Microbial Pathogenesis. 2020 ; 144 1-8.[citado 2024 maio 07 ] Available from: https://doi.org/10.1016/j.micpath.2020.104127
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MELO, Shaiani Maria Gil de et al. Nitrosation of BODIPY dyes and their applications in the development of thiol sensors. Dyes and Pigments, v. 173, p. 1-7, 2020Tradução . . Disponível em: https://doi.org/10.1016/j.dyepig.2019.107885. Acesso em: 07 maio 2024.
APA
Melo, S. M. G. de, Rezende, L. C. D. de, Petrilli, R., Lopez, R. F. V., Goulart, M. O. F., & Emery, F. da S. (2020). Nitrosation of BODIPY dyes and their applications in the development of thiol sensors. Dyes and Pigments, 173, 1-7. doi:10.1016/j.dyepig.2019.107885
NLM
Melo SMG de, Rezende LCD de, Petrilli R, Lopez RFV, Goulart MOF, Emery F da S. Nitrosation of BODIPY dyes and their applications in the development of thiol sensors [Internet]. Dyes and Pigments. 2020 ; 173 1-7.[citado 2024 maio 07 ] Available from: https://doi.org/10.1016/j.dyepig.2019.107885
Vancouver
Melo SMG de, Rezende LCD de, Petrilli R, Lopez RFV, Goulart MOF, Emery F da S. Nitrosation of BODIPY dyes and their applications in the development of thiol sensors [Internet]. Dyes and Pigments. 2020 ; 173 1-7.[citado 2024 maio 07 ] Available from: https://doi.org/10.1016/j.dyepig.2019.107885
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FERREIRA, Glaucio Monteiro et al. QSAR studies on the human sirtuin 2 inhibition by non-covalent 7,5,2-anilinobenzamide derivatives. Journal of Biomolecular Structure and Dynamics, v. 38, n. 2, p. 354-363, 2020Tradução . . Disponível em: https://doi.org/10.1080/07391102.2019.1574603. Acesso em: 07 maio 2024.
APA
Ferreira, G. M., Magalhães, J. G. de, Maltarollo, V. G., Kronenberger, T., Ganesan, A., Emery, F. da S., & Trossini, G. H. G. (2020). QSAR studies on the human sirtuin 2 inhibition by non-covalent 7,5,2-anilinobenzamide derivatives. Journal of Biomolecular Structure and Dynamics, 38( 2), 354-363. doi:10.1080/07391102.2019.1574603
NLM
Ferreira GM, Magalhães JG de, Maltarollo VG, Kronenberger T, Ganesan A, Emery F da S, Trossini GHG. QSAR studies on the human sirtuin 2 inhibition by non-covalent 7,5,2-anilinobenzamide derivatives [Internet]. Journal of Biomolecular Structure and Dynamics. 2020 ; 38( 2): 354-363.[citado 2024 maio 07 ] Available from: https://doi.org/10.1080/07391102.2019.1574603
Vancouver
Ferreira GM, Magalhães JG de, Maltarollo VG, Kronenberger T, Ganesan A, Emery F da S, Trossini GHG. QSAR studies on the human sirtuin 2 inhibition by non-covalent 7,5,2-anilinobenzamide derivatives [Internet]. Journal of Biomolecular Structure and Dynamics. 2020 ; 38( 2): 354-363.[citado 2024 maio 07 ] Available from: https://doi.org/10.1080/07391102.2019.1574603
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AMORIM, Vanessa G. et al. Synthesis and characterization of two novel red-shifted isothiocyanate BODIPYs and their application in protein conjugation. Dyes and Pigments, v. 182, p. 1-7, 2020Tradução . . Disponível em: https://doi.org/10.1016/j.dyepig.2020.108646. Acesso em: 07 maio 2024.
APA
Amorim, V. G., Melo, S. M. G. de, Leite, R. F., Coutinho, P. A., Silva, S. M. P. da, Silva, A. R., et al. (2020). Synthesis and characterization of two novel red-shifted isothiocyanate BODIPYs and their application in protein conjugation. Dyes and Pigments, 182, 1-7. doi:10.1016/j.dyepig.2020.108646
NLM
Amorim VG, Melo SMG de, Leite RF, Coutinho PA, Silva SMP da, Silva AR, Amorim FG, Pires RGW, Coitinho JB, Emery F da S, Rezende LCD. Synthesis and characterization of two novel red-shifted isothiocyanate BODIPYs and their application in protein conjugation [Internet]. Dyes and Pigments. 2020 ; 182 1-7.[citado 2024 maio 07 ] Available from: https://doi.org/10.1016/j.dyepig.2020.108646
Vancouver
Amorim VG, Melo SMG de, Leite RF, Coutinho PA, Silva SMP da, Silva AR, Amorim FG, Pires RGW, Coitinho JB, Emery F da S, Rezende LCD. Synthesis and characterization of two novel red-shifted isothiocyanate BODIPYs and their application in protein conjugation [Internet]. Dyes and Pigments. 2020 ; 182 1-7.[citado 2024 maio 07 ] Available from: https://doi.org/10.1016/j.dyepig.2020.108646
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MIRANDA, Mariza Abreu et al. Targeted uptake of folic acid-functionalized polymeric nanoparticles loading glycoalkaloidic extract in vitro and in vivo assays. Colloids and Surfaces B: Biointerfaces, v. 192, p. 1-8, 2020Tradução . . Disponível em: https://doi.org/10.1016/j.colsurfb.2020.111106. Acesso em: 07 maio 2024.
APA
Miranda, M. A., Silva, L. B., Carvalho, I., Amaral, R. L. F. do, Paula, M. H., Swiech, K., et al. (2020). Targeted uptake of folic acid-functionalized polymeric nanoparticles loading glycoalkaloidic extract in vitro and in vivo assays. Colloids and Surfaces B: Biointerfaces, 192, 1-8. doi:10.1016/j.colsurfb.2020.111106
NLM
Miranda MA, Silva LB, Carvalho I, Amaral RLF do, Paula MH, Swiech K, Bastos JK, Paschoal JAR, Emery F da S, Reis RB dos, Bentley MVLB, Gaspari PDM. Targeted uptake of folic acid-functionalized polymeric nanoparticles loading glycoalkaloidic extract in vitro and in vivo assays [Internet]. Colloids and Surfaces B: Biointerfaces. 2020 ; 192 1-8.[citado 2024 maio 07 ] Available from: https://doi.org/10.1016/j.colsurfb.2020.111106
Vancouver
Miranda MA, Silva LB, Carvalho I, Amaral RLF do, Paula MH, Swiech K, Bastos JK, Paschoal JAR, Emery F da S, Reis RB dos, Bentley MVLB, Gaspari PDM. Targeted uptake of folic acid-functionalized polymeric nanoparticles loading glycoalkaloidic extract in vitro and in vivo assays [Internet]. Colloids and Surfaces B: Biointerfaces. 2020 ; 192 1-8.[citado 2024 maio 07 ] Available from: https://doi.org/10.1016/j.colsurfb.2020.111106
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LIMA, Elys Juliane Cardoso et al. Synthesis and docking study for compounds analogs of LSD1 inhibitor. 2019, Anais.. Campinas: Galoá, 2019. Disponível em: https://proceedings.science/brazmed-chem-2019/trabajos. Acesso em: 07 maio 2024.
APA
Lima, E. J. C., Maltarollo, V. G., Ganesan, A., Emery, F. da S., Wünsch, B., & Trossini, G. H. G. (2019). Synthesis and docking study for compounds analogs of LSD1 inhibitor. In Abstracts. Campinas: Galoá. Recuperado de https://proceedings.science/brazmed-chem-2019/trabajos
NLM
Lima EJC, Maltarollo VG, Ganesan A, Emery F da S, Wünsch B, Trossini GHG. Synthesis and docking study for compounds analogs of LSD1 inhibitor [Internet]. Abstracts. 2019 ;[citado 2024 maio 07 ] Available from: https://proceedings.science/brazmed-chem-2019/trabajos
Vancouver
Lima EJC, Maltarollo VG, Ganesan A, Emery F da S, Wünsch B, Trossini GHG. Synthesis and docking study for compounds analogs of LSD1 inhibitor [Internet]. Abstracts. 2019 ;[citado 2024 maio 07 ] Available from: https://proceedings.science/brazmed-chem-2019/trabajos
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COITINHO, Luciana Barbosa et al. Lapachol biotransformation by filamentous fungi yields bioactive quinone derivatives and lapachol-stimulated secondary metabolites. Preparative Biochemistry and Biotechnology, v. 49, n. 5, p. 459-463, 2019Tradução . . Disponível em: https://doi.org/10.1080/10826068.2019.1591991. Acesso em: 07 maio 2024.
APA
Coitinho, L. B., Fumagalli, F., Rosa-Garzon, N. G. da, Emery, F. da S., & Cabral, H. (2019). Lapachol biotransformation by filamentous fungi yields bioactive quinone derivatives and lapachol-stimulated secondary metabolites. Preparative Biochemistry and Biotechnology, 49( 5), 459-463. doi:10.1080/10826068.2019.1591991
NLM
Coitinho LB, Fumagalli F, Rosa-Garzon NG da, Emery F da S, Cabral H. Lapachol biotransformation by filamentous fungi yields bioactive quinone derivatives and lapachol-stimulated secondary metabolites [Internet]. Preparative Biochemistry and Biotechnology. 2019 ; 49( 5): 459-463.[citado 2024 maio 07 ] Available from: https://doi.org/10.1080/10826068.2019.1591991
Vancouver
Coitinho LB, Fumagalli F, Rosa-Garzon NG da, Emery F da S, Cabral H. Lapachol biotransformation by filamentous fungi yields bioactive quinone derivatives and lapachol-stimulated secondary metabolites [Internet]. Preparative Biochemistry and Biotechnology. 2019 ; 49( 5): 459-463.[citado 2024 maio 07 ] Available from: https://doi.org/10.1080/10826068.2019.1591991
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SANTOS, Joicy Santamalvina dos et al. Cytotoxicity, cellular uptake, and subcellular localization of a nitrogen oxide and aminopropyl-β-lactose derivative ruthenium complex used as nitric oxide delivery agent. Nitric Oxide, v. 86, p. 38-47, 2019Tradução . . Disponível em: https://doi.org/10.1016/j.niox.2019.02.005. Acesso em: 07 maio 2024.
APA
Santos, J. S. dos, Ramos, L. C. B., Ferreira, L. P., Campo, V. L., Rezende, L. C. D. de, Emery, F. da S., & Silva, R. S. da. (2019). Cytotoxicity, cellular uptake, and subcellular localization of a nitrogen oxide and aminopropyl-β-lactose derivative ruthenium complex used as nitric oxide delivery agent. Nitric Oxide, 86, 38-47. doi:10.1016/j.niox.2019.02.005
NLM
Santos JS dos, Ramos LCB, Ferreira LP, Campo VL, Rezende LCD de, Emery F da S, Silva RS da. Cytotoxicity, cellular uptake, and subcellular localization of a nitrogen oxide and aminopropyl-β-lactose derivative ruthenium complex used as nitric oxide delivery agent [Internet]. Nitric Oxide. 2019 ; 86 38-47.[citado 2024 maio 07 ] Available from: https://doi.org/10.1016/j.niox.2019.02.005
Vancouver
Santos JS dos, Ramos LCB, Ferreira LP, Campo VL, Rezende LCD de, Emery F da S, Silva RS da. Cytotoxicity, cellular uptake, and subcellular localization of a nitrogen oxide and aminopropyl-β-lactose derivative ruthenium complex used as nitric oxide delivery agent [Internet]. Nitric Oxide. 2019 ; 86 38-47.[citado 2024 maio 07 ] Available from: https://doi.org/10.1016/j.niox.2019.02.005
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ALBIERO, Lucinéia Reuse et al. Immunomodulating action of the 3-phenylcoumarin derivative 6,7-dihydroxy-3-[3',4'-methylenedioxyphenyl]-coumarin in neutrophils from patients with rheumatoid arthritis and in rats with acute joint inflammation. Inflammation Research, v. 69, n. 1, p. 115-130, 2019Tradução . . Disponível em: https://doi.org/10.1007/s00011-019-01298-w. Acesso em: 07 maio 2024.
APA
Albiero, L. R., Andrade, M. F. de, Marchi, L. F., Landi-Librandi, A. P., Figueiredo-Rinhel, A. S. G. de, Carvalho, C. A., et al. (2019). Immunomodulating action of the 3-phenylcoumarin derivative 6,7-dihydroxy-3-[3',4'-methylenedioxyphenyl]-coumarin in neutrophils from patients with rheumatoid arthritis and in rats with acute joint inflammation. Inflammation Research, 69( 1), 115-130. doi:10.1007/s00011-019-01298-w
NLM
Albiero LR, Andrade MF de, Marchi LF, Landi-Librandi AP, Figueiredo-Rinhel ASG de, Carvalho CA, Kabeya LM, Oliveira RDR de, Azzolini AECS, Pupo MT, Emery F da S, Lucisano-Valim YM. Immunomodulating action of the 3-phenylcoumarin derivative 6,7-dihydroxy-3-[3',4'-methylenedioxyphenyl]-coumarin in neutrophils from patients with rheumatoid arthritis and in rats with acute joint inflammation [Internet]. Inflammation Research. 2019 ; 69( 1): 115-130.[citado 2024 maio 07 ] Available from: https://doi.org/10.1007/s00011-019-01298-w
Vancouver
Albiero LR, Andrade MF de, Marchi LF, Landi-Librandi AP, Figueiredo-Rinhel ASG de, Carvalho CA, Kabeya LM, Oliveira RDR de, Azzolini AECS, Pupo MT, Emery F da S, Lucisano-Valim YM. Immunomodulating action of the 3-phenylcoumarin derivative 6,7-dihydroxy-3-[3',4'-methylenedioxyphenyl]-coumarin in neutrophils from patients with rheumatoid arthritis and in rats with acute joint inflammation [Internet]. Inflammation Research. 2019 ; 69( 1): 115-130.[citado 2024 maio 07 ] Available from: https://doi.org/10.1007/s00011-019-01298-w