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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: 18 set. 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 set. 18 ] 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 set. 18 ] 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: 18 set. 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 set. 18 ] 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 set. 18 ] 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: 18 set. 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 set. 18 ] 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 set. 18 ] Available from: https://doi.org/10.1016/j.niox.2019.02.005
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MACHADO, Luana A. et al. On the synthesis, optical and computational studies of novel BODIPY-based phosphoramidate fluorescent dyes. Journal of Fluorine Chemistry, v. 220, p. 9-15, 2019Tradução . . Disponível em: https://doi.org/10.1016/j.jfluchem.2019.01.008. Acesso em: 18 set. 2024.
APA
Machado, L. A., Souza, M. C. de, Silva, C. M. da, Yoneda, J., Rezende, L. C. D. de, Emery, F. da S., et al. (2019). On the synthesis, optical and computational studies of novel BODIPY-based phosphoramidate fluorescent dyes. Journal of Fluorine Chemistry, 220, 9-15. doi:10.1016/j.jfluchem.2019.01.008
NLM
Machado LA, Souza MC de, Silva CM da, Yoneda J, Rezende LCD de, Emery F da S, Simone CA de, Silva Júnior EN da, Pedrosa LF. On the synthesis, optical and computational studies of novel BODIPY-based phosphoramidate fluorescent dyes [Internet]. Journal of Fluorine Chemistry. 2019 ; 220 9-15.[citado 2024 set. 18 ] Available from: https://doi.org/10.1016/j.jfluchem.2019.01.008
Vancouver
Machado LA, Souza MC de, Silva CM da, Yoneda J, Rezende LCD de, Emery F da S, Simone CA de, Silva Júnior EN da, Pedrosa LF. On the synthesis, optical and computational studies of novel BODIPY-based phosphoramidate fluorescent dyes [Internet]. Journal of Fluorine Chemistry. 2019 ; 220 9-15.[citado 2024 set. 18 ] Available from: https://doi.org/10.1016/j.jfluchem.2019.01.008
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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: 18 set. 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 set. 18 ] 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 set. 18 ] Available from: https://doi.org/10.1007/s00011-019-01298-w
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CALIL, Felipe Antunes et al. Ligand-based design, synthesis and biochemical evaluation of potent and selective inhibitors of Schistosoma mansoni dihydroorotate dehydrogenase. European Journal of Medicinal Chemistry, v. 167, p. 357-366, 2019Tradução . . Disponível em: https://doi.org/10.1016/j.ejmech.2019.02.018. Acesso em: 18 set. 2024.
APA
Calil, F. A., Costacurta, J. S. D., Chiappetta, E. R. C., Fumagalli, F., Mello, R. B. de, Leite, F. H. A., et al. (2019). Ligand-based design, synthesis and biochemical evaluation of potent and selective inhibitors of Schistosoma mansoni dihydroorotate dehydrogenase. European Journal of Medicinal Chemistry, 167, 357-366. doi:10.1016/j.ejmech.2019.02.018
NLM
Calil FA, Costacurta JSD, Chiappetta ERC, Fumagalli F, Mello RB de, Leite FHA, Castilho MS, Emery F da S, Nonato MC. Ligand-based design, synthesis and biochemical evaluation of potent and selective inhibitors of Schistosoma mansoni dihydroorotate dehydrogenase [Internet]. European Journal of Medicinal Chemistry. 2019 ; 167 357-366.[citado 2024 set. 18 ] Available from: https://doi.org/10.1016/j.ejmech.2019.02.018
Vancouver
Calil FA, Costacurta JSD, Chiappetta ERC, Fumagalli F, Mello RB de, Leite FHA, Castilho MS, Emery F da S, Nonato MC. Ligand-based design, synthesis and biochemical evaluation of potent and selective inhibitors of Schistosoma mansoni dihydroorotate dehydrogenase [Internet]. European Journal of Medicinal Chemistry. 2019 ; 167 357-366.[citado 2024 set. 18 ] Available from: https://doi.org/10.1016/j.ejmech.2019.02.018
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LUIZ, Marcela Tavares et al. In vitro evaluation of folate-modified PLGA nanoparticles containing paclitaxel for ovarian cancer therapy. Materials Science & Engineering C, v. 105, p. e110038, 2019Tradução . . Disponível em: https://doi.org/10.1016/j.msec.2019.110038. Acesso em: 18 set. 2024.
APA
Luiz, M. T., Abriata, J. P., Raspantini, G. L., Tofani, L. B., Fumagalli, F., Melo, S. M. G. de, et al. (2019). In vitro evaluation of folate-modified PLGA nanoparticles containing paclitaxel for ovarian cancer therapy. Materials Science & Engineering C, 105, e110038. doi:10.1016/j.msec.2019.110038
NLM
Luiz MT, Abriata JP, Raspantini GL, Tofani LB, Fumagalli F, Melo SMG de, Emery F da S, Swiech K, Marcato PD, Lee R, Marchetti JM. In vitro evaluation of folate-modified PLGA nanoparticles containing paclitaxel for ovarian cancer therapy [Internet]. Materials Science & Engineering C. 2019 ; 105 e110038.[citado 2024 set. 18 ] Available from: https://doi.org/10.1016/j.msec.2019.110038
Vancouver
Luiz MT, Abriata JP, Raspantini GL, Tofani LB, Fumagalli F, Melo SMG de, Emery F da S, Swiech K, Marcato PD, Lee R, Marchetti JM. In vitro evaluation of folate-modified PLGA nanoparticles containing paclitaxel for ovarian cancer therapy [Internet]. Materials Science & Engineering C. 2019 ; 105 e110038.[citado 2024 set. 18 ] Available from: https://doi.org/10.1016/j.msec.2019.110038
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FUMAGALLI, Fernando et al. Exploiting the furo[2,3-b]pyridine core against multidrug-resistant Mycobacterium tuberculosis. Bioorganic & Medicinal Chemistry Letters, v. 29, n. 8, p. 974-977, 2019Tradução . . Disponível em: https://doi.org/10.1016/j.bmcl.2019.02.019. Acesso em: 18 set. 2024.
APA
Fumagalli, F., Melo, S. M. G. de, Ribeiro, C. M., Solcia, M. C., Pavan, F. R., & Emery, F. da S. (2019). Exploiting the furo[2,3-b]pyridine core against multidrug-resistant Mycobacterium tuberculosis. Bioorganic & Medicinal Chemistry Letters, 29( 8), 974-977. doi:10.1016/j.bmcl.2019.02.019
NLM
Fumagalli F, Melo SMG de, Ribeiro CM, Solcia MC, Pavan FR, Emery F da S. Exploiting the furo[2,3-b]pyridine core against multidrug-resistant Mycobacterium tuberculosis [Internet]. Bioorganic & Medicinal Chemistry Letters. 2019 ; 29( 8): 974-977.[citado 2024 set. 18 ] Available from: https://doi.org/10.1016/j.bmcl.2019.02.019
Vancouver
Fumagalli F, Melo SMG de, Ribeiro CM, Solcia MC, Pavan FR, Emery F da S. Exploiting the furo[2,3-b]pyridine core against multidrug-resistant Mycobacterium tuberculosis [Internet]. Bioorganic & Medicinal Chemistry Letters. 2019 ; 29( 8): 974-977.[citado 2024 set. 18 ] Available from: https://doi.org/10.1016/j.bmcl.2019.02.019
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OLIVEIRA, Letícia Bueno de et al. Desenvolvimento de inibidores da enzima HDAC como candidatos terapêuticos contra a metástase de células cancerígenas. 2019, Anais.. Ribeirão Preto: FCFRP-USP, 2019. Disponível em: https://uspdigital.usp.br/siicusp/siicPublicacao.jsp?codmnu=7210. Acesso em: 18 set. 2024.
APA
Oliveira, L. B. de, Lee, A., Ganesan, A., & Emery, F. da S. (2019). Desenvolvimento de inibidores da enzima HDAC como candidatos terapêuticos contra a metástase de células cancerígenas. In Resumos. Ribeirão Preto: FCFRP-USP. Recuperado de https://uspdigital.usp.br/siicusp/siicPublicacao.jsp?codmnu=7210
NLM
Oliveira LB de, Lee A, Ganesan A, Emery F da S. Desenvolvimento de inibidores da enzima HDAC como candidatos terapêuticos contra a metástase de células cancerígenas [Internet]. Resumos. 2019 ;[citado 2024 set. 18 ] Available from: https://uspdigital.usp.br/siicusp/siicPublicacao.jsp?codmnu=7210
Vancouver
Oliveira LB de, Lee A, Ganesan A, Emery F da S. Desenvolvimento de inibidores da enzima HDAC como candidatos terapêuticos contra a metástase de células cancerígenas [Internet]. Resumos. 2019 ;[citado 2024 set. 18 ] Available from: https://uspdigital.usp.br/siicusp/siicPublicacao.jsp?codmnu=7210
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GRILO, Larissa Ribeiro et al. Síntese e estudo de relação estrutura-atividade de novos compostos heterociclos como potenciais agentes anti-infecciosos. 2019, Anais.. Ribeirão Preto: FCFRP-USP, 2019. Disponível em: https://uspdigital.usp.br/siicusp/siicPublicacao.jsp?codmnu=7210. Acesso em: 18 set. 2024.
APA
Grilo, L. R., Vaidergorn, M. de M., Silva, D. G., & Emery, F. da S. (2019). Síntese e estudo de relação estrutura-atividade de novos compostos heterociclos como potenciais agentes anti-infecciosos. In Resumos. Ribeirão Preto: FCFRP-USP. Recuperado de https://uspdigital.usp.br/siicusp/siicPublicacao.jsp?codmnu=7210
NLM
Grilo LR, Vaidergorn M de M, Silva DG, Emery F da S. Síntese e estudo de relação estrutura-atividade de novos compostos heterociclos como potenciais agentes anti-infecciosos [Internet]. Resumos. 2019 ;[citado 2024 set. 18 ] Available from: https://uspdigital.usp.br/siicusp/siicPublicacao.jsp?codmnu=7210
Vancouver
Grilo LR, Vaidergorn M de M, Silva DG, Emery F da S. Síntese e estudo de relação estrutura-atividade de novos compostos heterociclos como potenciais agentes anti-infecciosos [Internet]. Resumos. 2019 ;[citado 2024 set. 18 ] Available from: https://uspdigital.usp.br/siicusp/siicPublicacao.jsp?codmnu=7210
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SANTOS, Ana Clara Rolim dos e EMERY, Flavio da Silva. Síntese de análogos ao 1-(pirazolil)tetrazol para avaliação de inibição da enzima demetilase específica de lisina LSD1. 2019, Anais.. Ribeirão Preto: FCFRP-USP, 2019. Disponível em: https://uspdigital.usp.br/siicusp/siicPublicacao.jsp?codmnu=7210. Acesso em: 18 set. 2024.
APA
Santos, A. C. R. dos, & Emery, F. da S. (2019). Síntese de análogos ao 1-(pirazolil)tetrazol para avaliação de inibição da enzima demetilase específica de lisina LSD1. In Resumos. Ribeirão Preto: FCFRP-USP. Recuperado de https://uspdigital.usp.br/siicusp/siicPublicacao.jsp?codmnu=7210
NLM
Santos ACR dos, Emery F da S. Síntese de análogos ao 1-(pirazolil)tetrazol para avaliação de inibição da enzima demetilase específica de lisina LSD1 [Internet]. Resumos. 2019 ;[citado 2024 set. 18 ] Available from: https://uspdigital.usp.br/siicusp/siicPublicacao.jsp?codmnu=7210
Vancouver
Santos ACR dos, Emery F da S. Síntese de análogos ao 1-(pirazolil)tetrazol para avaliação de inibição da enzima demetilase específica de lisina LSD1 [Internet]. Resumos. 2019 ;[citado 2024 set. 18 ] Available from: https://uspdigital.usp.br/siicusp/siicPublicacao.jsp?codmnu=7210
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GONZÁLEZ, María Teresa Páez e MELLO, Shaiani Maria Gil de e EMERY, Flavio da Silva. Influence of 1,3,5-triazine core and electron donor group in photophysical properties of BODIPY dyes. Journal of Fluorescence, v. 29, n. 4, p. 845-852, 2019Tradução . . Disponível em: https://doi.org/10.1007/s10895-019-02389-x. Acesso em: 18 set. 2024.
APA
González, M. T. P., Mello, S. M. G. de, & Emery, F. da S. (2019). Influence of 1,3,5-triazine core and electron donor group in photophysical properties of BODIPY dyes. Journal of Fluorescence, 29( 4), 845-852. doi:10.1007/s10895-019-02389-x
NLM
González MTP, Mello SMG de, Emery F da S. Influence of 1,3,5-triazine core and electron donor group in photophysical properties of BODIPY dyes [Internet]. Journal of Fluorescence. 2019 ; 29( 4): 845-852.[citado 2024 set. 18 ] Available from: https://doi.org/10.1007/s10895-019-02389-x
Vancouver
González MTP, Mello SMG de, Emery F da S. Influence of 1,3,5-triazine core and electron donor group in photophysical properties of BODIPY dyes [Internet]. Journal of Fluorescence. 2019 ; 29( 4): 845-852.[citado 2024 set. 18 ] Available from: https://doi.org/10.1007/s10895-019-02389-x
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SILVA\2005JÚNIOR, Paulo Eliandro da et al. Flow photochemistry of azosulfones: application of “Sunflow” reactors. ChemPhotoChem, v. 2, n. 10, p. 878-883, 2018Tradução . . Disponível em: https://doi.org/10.1002/cptc.201800125. Acesso em: 18 set. 2024.
APA
Silva\2005Júnior, P. E. da, Amin, H. I. M., Nauth, A. M., Emery, F. da S., Protti, S., & Opatz, T. (2018). Flow photochemistry of azosulfones: application of “Sunflow” reactors. ChemPhotoChem, 2( 10), 878-883. doi:10.1002/cptc.201800125
NLM
Silva\2005Júnior PE da, Amin HIM, Nauth AM, Emery F da S, Protti S, Opatz T. Flow photochemistry of azosulfones: application of “Sunflow” reactors [Internet]. ChemPhotoChem. 2018 ; 2( 10): 878-883.[citado 2024 set. 18 ] Available from: https://doi.org/10.1002/cptc.201800125
Vancouver
Silva\2005Júnior PE da, Amin HIM, Nauth AM, Emery F da S, Protti S, Opatz T. Flow photochemistry of azosulfones: application of “Sunflow” reactors [Internet]. ChemPhotoChem. 2018 ; 2( 10): 878-883.[citado 2024 set. 18 ] Available from: https://doi.org/10.1002/cptc.201800125
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FRANCO, Márcia Silvana Freire et al. Palladium-catalyzed C–H alkenylation of quinoxaline N-oxide enabled by a mono-N-protected amino acid. Tetrahedron Letters, v. 59, n. 26, p. 2562-2566, 2018Tradução . . Disponível em: https://doi.org/10.1016/j.tetlet.2018.05.054. Acesso em: 18 set. 2024.
APA
Franco, M. S. F., Paula, M. H. de, Glowacka, P. C., Fumagalli, F., Clososki, G. C., & Emery, F. da S. (2018). Palladium-catalyzed C–H alkenylation of quinoxaline N-oxide enabled by a mono-N-protected amino acid. Tetrahedron Letters, 59( 26), 2562-2566. doi:10.1016/j.tetlet.2018.05.054
NLM
Franco MSF, Paula MH de, Glowacka PC, Fumagalli F, Clososki GC, Emery F da S. Palladium-catalyzed C–H alkenylation of quinoxaline N-oxide enabled by a mono-N-protected amino acid [Internet]. Tetrahedron Letters. 2018 ; 59( 26): 2562-2566.[citado 2024 set. 18 ] Available from: https://doi.org/10.1016/j.tetlet.2018.05.054
Vancouver
Franco MSF, Paula MH de, Glowacka PC, Fumagalli F, Clososki GC, Emery F da S. Palladium-catalyzed C–H alkenylation of quinoxaline N-oxide enabled by a mono-N-protected amino acid [Internet]. Tetrahedron Letters. 2018 ; 59( 26): 2562-2566.[citado 2024 set. 18 ] Available from: https://doi.org/10.1016/j.tetlet.2018.05.054
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ANDRADE, Micássio F. et al. The 3-phenylcoumarin derivative 6,7-dihydroxy-3-[3′,4′-methylenedioxyphenyl]-coumarin downmodulates the FcγR- and CR-mediated oxidative metabolism and elastase release in human neutrophils: possible mechanisms underlying inhibition of the formation and release of neutrophil extracellular traps. Free Radical Biology and Medicine, v. 115, p. 421-435, 2018Tradução . . Disponível em: https://doi.org/10.1016/j.freeradbiomed.2017.12.012. Acesso em: 18 set. 2024.
APA
Andrade, M. F., Kabeya, L. M., Bortot, L. O., Santos, G. B. dos, Santos, E. O. L., Albiero, L. R., et al. (2018). The 3-phenylcoumarin derivative 6,7-dihydroxy-3-[3′,4′-methylenedioxyphenyl]-coumarin downmodulates the FcγR- and CR-mediated oxidative metabolism and elastase release in human neutrophils: possible mechanisms underlying inhibition of the formation and release of neutrophil extracellular traps. Free Radical Biology and Medicine, 115, 421-435. doi:10.1016/j.freeradbiomed.2017.12.012
NLM
Andrade MF, Kabeya LM, Bortot LO, Santos GB dos, Santos EOL, Albiero LR, Figueiredo-Rinhel ASG, Carvalho CA, Azzolini AECS, Caliri A, Pupo MT, Emery F da S, Lucisano-Valim YM. The 3-phenylcoumarin derivative 6,7-dihydroxy-3-[3′,4′-methylenedioxyphenyl]-coumarin downmodulates the FcγR- and CR-mediated oxidative metabolism and elastase release in human neutrophils: possible mechanisms underlying inhibition of the formation and release of neutrophil extracellular traps [Internet]. Free Radical Biology and Medicine. 2018 ; 115 421-435.[citado 2024 set. 18 ] Available from: https://doi.org/10.1016/j.freeradbiomed.2017.12.012
Vancouver
Andrade MF, Kabeya LM, Bortot LO, Santos GB dos, Santos EOL, Albiero LR, Figueiredo-Rinhel ASG, Carvalho CA, Azzolini AECS, Caliri A, Pupo MT, Emery F da S, Lucisano-Valim YM. The 3-phenylcoumarin derivative 6,7-dihydroxy-3-[3′,4′-methylenedioxyphenyl]-coumarin downmodulates the FcγR- and CR-mediated oxidative metabolism and elastase release in human neutrophils: possible mechanisms underlying inhibition of the formation and release of neutrophil extracellular traps [Internet]. Free Radical Biology and Medicine. 2018 ; 115 421-435.[citado 2024 set. 18 ] Available from: https://doi.org/10.1016/j.freeradbiomed.2017.12.012
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VAIDERGORN, Miguel M et al. β-amino alcohols and their respective 2-phenyl-N-alkyl aziridines as potential DNA minor groove binders. European Journal of Medicinal Chemistry, v. 157, p. 657-664, 2018Tradução . . Disponível em: https://doi.org/10.1016/j.ejmech.2018.07.055. Acesso em: 18 set. 2024.
APA
Vaidergorn, M. M., Carneiro, Z. A., Lopes, C. D., Albuquerque, S. de, Reis, F. C. C., Nikolaou, S., et al. (2018). β-amino alcohols and their respective 2-phenyl-N-alkyl aziridines as potential DNA minor groove binders. European Journal of Medicinal Chemistry, 157, 657-664. doi:10.1016/j.ejmech.2018.07.055
NLM
Vaidergorn MM, Carneiro ZA, Lopes CD, Albuquerque S de, Reis FCC, Nikolaou S, Mello JFR, Genesi GL, Trossini GHG, Ganesan A, Emery F da S. β-amino alcohols and their respective 2-phenyl-N-alkyl aziridines as potential DNA minor groove binders [Internet]. European Journal of Medicinal Chemistry. 2018 ; 157 657-664.[citado 2024 set. 18 ] Available from: https://doi.org/10.1016/j.ejmech.2018.07.055
Vancouver
Vaidergorn MM, Carneiro ZA, Lopes CD, Albuquerque S de, Reis FCC, Nikolaou S, Mello JFR, Genesi GL, Trossini GHG, Ganesan A, Emery F da S. β-amino alcohols and their respective 2-phenyl-N-alkyl aziridines as potential DNA minor groove binders [Internet]. European Journal of Medicinal Chemistry. 2018 ; 157 657-664.[citado 2024 set. 18 ] Available from: https://doi.org/10.1016/j.ejmech.2018.07.055
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ABNT
REZENDE, Lucas C. D. et al. Thiocyanation of 3-substituted and 3,5-disubstituted BODIPYs and its application for the synthesis of new fluorescent sensors. Dyes and Pigments, v. 154, p. 155-163, 2018Tradução . . Disponível em: https://doi.org/10.1016/j.dyepig.2018.01.043. Acesso em: 18 set. 2024.
APA
Rezende, L. C. D., Melo, S. M. G., Boodts, S., Verbelen, B., Emery, F. da S., & Dehaen, W. (2018). Thiocyanation of 3-substituted and 3,5-disubstituted BODIPYs and its application for the synthesis of new fluorescent sensors. Dyes and Pigments, 154, 155-163. doi:10.1016/j.dyepig.2018.01.043
NLM
Rezende LCD, Melo SMG, Boodts S, Verbelen B, Emery F da S, Dehaen W. Thiocyanation of 3-substituted and 3,5-disubstituted BODIPYs and its application for the synthesis of new fluorescent sensors [Internet]. Dyes and Pigments. 2018 ; 154 155-163.[citado 2024 set. 18 ] Available from: https://doi.org/10.1016/j.dyepig.2018.01.043
Vancouver
Rezende LCD, Melo SMG, Boodts S, Verbelen B, Emery F da S, Dehaen W. Thiocyanation of 3-substituted and 3,5-disubstituted BODIPYs and its application for the synthesis of new fluorescent sensors [Internet]. Dyes and Pigments. 2018 ; 154 155-163.[citado 2024 set. 18 ] Available from: https://doi.org/10.1016/j.dyepig.2018.01.043
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
PEREIRA, Valeska S. Sena et al. In vitro antiplasmodial activity, pharmacokinetic profiles and interference in isoprenoid pathway of 2-aniline-3-hydroxy-1.4-naphthoquinone derivatives. Malaria Journal, v. 17, n. 1, 2018Tradução . . Disponível em: https://doi.org/10.1186/s12936-018-2615-8. Acesso em: 18 set. 2024.
APA
Pereira, V. S. S., Emery, F. da S., Lobo, L., Nogueira, F. , Oliveira, J. I. N. , Fulco, U. L., et al. (2018). In vitro antiplasmodial activity, pharmacokinetic profiles and interference in isoprenoid pathway of 2-aniline-3-hydroxy-1.4-naphthoquinone derivatives. Malaria Journal, 17( 1). doi:10.1186/s12936-018-2615-8
NLM
Pereira VSS, Emery F da S, Lobo L, Nogueira F , Oliveira J I N , Fulco U L, Albuquerque E L , Katzin AM, Andrade-Neto V F de . In vitro antiplasmodial activity, pharmacokinetic profiles and interference in isoprenoid pathway of 2-aniline-3-hydroxy-1.4-naphthoquinone derivatives [Internet]. Malaria Journal. 2018 ; 17( 1):[citado 2024 set. 18 ] Available from: https://doi.org/10.1186/s12936-018-2615-8
Vancouver
Pereira VSS, Emery F da S, Lobo L, Nogueira F , Oliveira J I N , Fulco U L, Albuquerque E L , Katzin AM, Andrade-Neto V F de . In vitro antiplasmodial activity, pharmacokinetic profiles and interference in isoprenoid pathway of 2-aniline-3-hydroxy-1.4-naphthoquinone derivatives [Internet]. Malaria Journal. 2018 ; 17( 1):[citado 2024 set. 18 ] Available from: https://doi.org/10.1186/s12936-018-2615-8
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
OGUNJIMI, Abayomi T. et al. Hydrophilic polymeric nanoparticles prepared from Delonix galactomannan with low cytotoxicity for ocular drug delivery. Carbohydrate Polymers, v. 157, p. 1065-1075, 2017Tradução . . Disponível em: https://doi.org/10.1016/j.carbpol.2016.10.076. Acesso em: 18 set. 2024.
APA
Ogunjimi, A. T., Melo, S. M. G., Vargas-Rechia, C. G., Emery, F. da S., & Lopez, R. F. V. (2017). Hydrophilic polymeric nanoparticles prepared from Delonix galactomannan with low cytotoxicity for ocular drug delivery. Carbohydrate Polymers, 157, 1065-1075. doi:10.1016/j.carbpol.2016.10.076
NLM
Ogunjimi AT, Melo SMG, Vargas-Rechia CG, Emery F da S, Lopez RFV. Hydrophilic polymeric nanoparticles prepared from Delonix galactomannan with low cytotoxicity for ocular drug delivery [Internet]. Carbohydrate Polymers. 2017 ; 157 1065-1075.[citado 2024 set. 18 ] Available from: https://doi.org/10.1016/j.carbpol.2016.10.076
Vancouver
Ogunjimi AT, Melo SMG, Vargas-Rechia CG, Emery F da S, Lopez RFV. Hydrophilic polymeric nanoparticles prepared from Delonix galactomannan with low cytotoxicity for ocular drug delivery [Internet]. Carbohydrate Polymers. 2017 ; 157 1065-1075.[citado 2024 set. 18 ] Available from: https://doi.org/10.1016/j.carbpol.2016.10.076