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Artigo de periodico
Palladium-catalyzed C–H alkenylation of quinoxaline N-oxide enabled by a mono-N-protected amino acid (2018)
Franco, Márcia Silvana Freire; Paula, Murilo Helder de; Glowacka, Paulina Cecylia; Fumagalli, Fernando; Clososki, Giuliano Cesar; Emery, Flavio da Silva
Source: Tetrahedron Letters. Unidade: FCFRP
Subjects: COMPOSTOS HETEROCÍCLICOS, PALÁDIO, FÁRMACOS
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ABNT
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: 14 nov. 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 nov. 14 ] 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 nov. 14 ] Available from: https://doi.org/10.1016/j.tetlet.2018.05.054
Artigo de periodico
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 (2018)
Andrade, Micássio F.; Kabeya, Luciana M.; Bortot, Leandro O.; Santos, Gabriela B. dos; Santos, Everton O. L.; Albiero, Lucinéia R.; Figueiredo-Rinhel, Andréa S. G.; Carvalho, Camila A.; Azzolini, Ana Elisa Caleiro Seixas; Caliri, Antônio; Pupo, Mônica Tallarico; Emery, Flavio da Silva; Lucisano-Valim, Yara Maria
Source: Free Radical Biology and Medicine. Unidade: FCFRP
Subjects: ANTI-INFLAMATÓRIOS, CÉLULAS CULTIVADAS, NEUTRÓFILOS, ESTRESSE OXIDATIVO, PEROXIDASE, FAGOCITOSE, ESPÉCIES REATIVAS DE OXIGÊNIO
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ABNT
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: 14 nov. 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 nov. 14 ] 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 nov. 14 ] Available from: https://doi.org/10.1016/j.freeradbiomed.2017.12.012
Artigo de periodico
Thiocyanation of 3-substituted and 3,5-disubstituted BODIPYs and its application for the synthesis of new fluorescent sensors (2018)
Rezende, Lucas C. D.; Melo, Shaiani M. G.; Boodts, Stijn; Verbelen, Bram; Emery, Flavio da Silva; Dehaen, Wim
Source: Dyes and Pigments. Unidade: FCFRP
Subjects: CORANTES FLUORESCENTES, RESSONÂNCIA MAGNÉTICA NUCLEAR, SENSORES QUÍMICOS
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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: 14 nov. 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 nov. 14 ] 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 nov. 14 ] Available from: https://doi.org/10.1016/j.dyepig.2018.01.043
Artigo de periodico
Hydrophilic polymeric nanoparticles prepared from Delonix galactomannan with low cytotoxicity for ocular drug delivery (2017)
Ogunjimi, Abayomi T.; Melo, Shaiani M.G.; Vargas-Rechia, Carem Gledes; Emery, Flavio da Silva; Lopez, Renata Fonseca Vianna
Source: Carbohydrate Polymers. Unidade: FCFRP
Subjects: NANOPARTÍCULAS, CITOTOXICIDADE IMUNOLÓGICA, FLUORESCÊNCIA
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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: 14 nov. 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 nov. 14 ] 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 nov. 14 ] Available from: https://doi.org/10.1016/j.carbpol.2016.10.076
Artigo de periodico
Inactivation of β-lapachone cytotoxicity by filamentous fungi that mimic the human blood metabolism (2017)
Paludo, Camila Raquel; Silva-Junior, Eduardo Afonso da; Silva, Eliane de Oliveira; Vessecchi, Ricardo; Lopes, Norberto Peporine; Pupo, Mônica Tallarico; Emery, Flavio da Silva; Gonçalves, Natália dos Santos; Santos, Raquel Alves dos; Furtado, Niege Araçari Jacometti Cardoso
Source: European Journal of Drug Metabolism and Pharmacokinetics. Unidade: FCFRP
Subjects: CITOTOXINAS, METABOLISMO, SANGUE
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ABNT
PALUDO, Camila Raquel et al. Inactivation of β-lapachone cytotoxicity by filamentous fungi that mimic the human blood metabolism. European Journal of Drug Metabolism and Pharmacokinetics, v. 42, n. 2, p. 213-220, 2017Tradução . . Disponível em: https://doi.org/10.1007/s13318-016-0337-2. Acesso em: 14 nov. 2024.
APA
Paludo, C. R., Silva-Junior, E. A. da, Silva, E. de O., Vessecchi, R., Lopes, N. P., Pupo, M. T., et al. (2017). Inactivation of β-lapachone cytotoxicity by filamentous fungi that mimic the human blood metabolism. European Journal of Drug Metabolism and Pharmacokinetics, 42( 2), 213-220. doi:10.1007/s13318-016-0337-2
NLM
Paludo CR, Silva-Junior EA da, Silva E de O, Vessecchi R, Lopes NP, Pupo MT, Emery F da S, Gonçalves N dos S, Santos RA dos, Furtado NAJC. Inactivation of β-lapachone cytotoxicity by filamentous fungi that mimic the human blood metabolism [Internet]. European Journal of Drug Metabolism and Pharmacokinetics. 2017 ; 42( 2): 213-220.[citado 2024 nov. 14 ] Available from: https://doi.org/10.1007/s13318-016-0337-2
Vancouver
Paludo CR, Silva-Junior EA da, Silva E de O, Vessecchi R, Lopes NP, Pupo MT, Emery F da S, Gonçalves N dos S, Santos RA dos, Furtado NAJC. Inactivation of β-lapachone cytotoxicity by filamentous fungi that mimic the human blood metabolism [Internet]. European Journal of Drug Metabolism and Pharmacokinetics. 2017 ; 42( 2): 213-220.[citado 2024 nov. 14 ] Available from: https://doi.org/10.1007/s13318-016-0337-2
Artigo de periodico
Lapachol, a compound targeting pyrimidine metabolism, ameliorates experimental autoimmune arthritis (2017)
Peres, Raphael S.; Santos, Gabriela B.; Cecilio, Nerry T.; Jabor, Valquíria Aparecida Polisel; Niehues, Michael; Torres, Bruna G. S.; Buqui, Gabriela; Silva, Carlos Henrique Tomich de Paula da; Costa, Teresa Dalla; Lopes, Norberto Peporine; Nonato, Maria Cristina; Ramalho, Fernando Silva; Louzada Júnior, Paulo; Cunha, Thiago Mattar; Cunha, Fernando de Queiroz; Emery, Flavio da Silva; Alves Filho, José Carlos Farias
Source: Arthritis Research & Therapy. Unidades: FCFRP, FMRP
Subjects: ARTRITE REUMATOIDE, LINFÓCITOS T, FÁRMACOS IMUNOSSUPRESSORES
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ABNT
PERES, Raphael S. et al. Lapachol, a compound targeting pyrimidine metabolism, ameliorates experimental autoimmune arthritis. Arthritis Research & Therapy, v. 19, n. 1, 2017Tradução . . Disponível em: https://doi.org/10.1186/s13075-017-1236-x. Acesso em: 14 nov. 2024.
APA
Peres, R. S., Santos, G. B., Cecilio, N. T., Jabor, V. A. P., Niehues, M., Torres, B. G. S., et al. (2017). Lapachol, a compound targeting pyrimidine metabolism, ameliorates experimental autoimmune arthritis. Arthritis Research & Therapy, 19( 1). doi:10.1186/s13075-017-1236-x
NLM
Peres RS, Santos GB, Cecilio NT, Jabor VAP, Niehues M, Torres BGS, Buqui G, Silva CHT de P da, Costa TD, Lopes NP, Nonato MC, Ramalho FS, Louzada Júnior P, Cunha TM, Cunha F de Q, Emery F da S, Alves Filho JCF. Lapachol, a compound targeting pyrimidine metabolism, ameliorates experimental autoimmune arthritis [Internet]. Arthritis Research & Therapy. 2017 ; 19( 1):[citado 2024 nov. 14 ] Available from: https://doi.org/10.1186/s13075-017-1236-x
Vancouver
Peres RS, Santos GB, Cecilio NT, Jabor VAP, Niehues M, Torres BGS, Buqui G, Silva CHT de P da, Costa TD, Lopes NP, Nonato MC, Ramalho FS, Louzada Júnior P, Cunha TM, Cunha F de Q, Emery F da S, Alves Filho JCF. Lapachol, a compound targeting pyrimidine metabolism, ameliorates experimental autoimmune arthritis [Internet]. Arthritis Research & Therapy. 2017 ; 19( 1):[citado 2024 nov. 14 ] Available from: https://doi.org/10.1186/s13075-017-1236-x
Artigo de periodico
Charting the chemical reactivity space of 2,3-substituted furo[2,3-b]pyridines synthesized via the heterocyclization of pyridine-N-oxide derivatives (2016)
Fumagalli, Fernando; Emery, Flavio da Silva
Source: The Journal of Organic Chemistry. Unidade: FCFRP
Subjects: QUÍMICA ORGÂNICA, REAÇÕES ORGÂNICAS
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ABNT
FUMAGALLI, Fernando e EMERY, Flavio da Silva. Charting the chemical reactivity space of 2,3-substituted furo[2,3-b]pyridines synthesized via the heterocyclization of pyridine-N-oxide derivatives. The Journal of Organic Chemistry, v. 81, n. 21, p. 10339-10347, 2016Tradução . . Disponível em: https://doi.org/10.1021/acs.joc.6b01329. Acesso em: 14 nov. 2024.
APA
Fumagalli, F., & Emery, F. da S. (2016). Charting the chemical reactivity space of 2,3-substituted furo[2,3-b]pyridines synthesized via the heterocyclization of pyridine-N-oxide derivatives. The Journal of Organic Chemistry, 81( 21), 10339-10347. doi:10.1021/acs.joc.6b01329
NLM
Fumagalli F, Emery F da S. Charting the chemical reactivity space of 2,3-substituted furo[2,3-b]pyridines synthesized via the heterocyclization of pyridine-N-oxide derivatives [Internet]. The Journal of Organic Chemistry. 2016 ; 81( 21): 10339-10347.[citado 2024 nov. 14 ] Available from: https://doi.org/10.1021/acs.joc.6b01329
Vancouver
Fumagalli F, Emery F da S. Charting the chemical reactivity space of 2,3-substituted furo[2,3-b]pyridines synthesized via the heterocyclization of pyridine-N-oxide derivatives [Internet]. The Journal of Organic Chemistry. 2016 ; 81( 21): 10339-10347.[citado 2024 nov. 14 ] Available from: https://doi.org/10.1021/acs.joc.6b01329
Artigo de periodico
Synthesis and photophysical properties of iron-carbonyl complex–coumarin conjugates as potential bimodal IR–fluorescent probes (2016)
Glowacka, Paulina C.; Maindron, Nicolas; Stephenson, G. Richard; Romieu, Anthony; Renard, Pierre-Yves; Emery, Flavio da Silva
Source: Tetrahedron Letters. Unidade: FCFRP
Subjects: FLUORESCÊNCIA, COMPOSTOS ORGÂNICOS
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ABNT
GLOWACKA, Paulina C. et al. Synthesis and photophysical properties of iron-carbonyl complex–coumarin conjugates as potential bimodal IR–fluorescent probes. Tetrahedron Letters, v. 57, n. 45, p. 4991-4996, 2016Tradução . . Disponível em: https://doi.org/10.1016/j.tetlet.2016.09.091. Acesso em: 14 nov. 2024.
APA
Glowacka, P. C., Maindron, N., Stephenson, G. R., Romieu, A., Renard, P. -Y., & Emery, F. da S. (2016). Synthesis and photophysical properties of iron-carbonyl complex–coumarin conjugates as potential bimodal IR–fluorescent probes. Tetrahedron Letters, 57( 45), 4991-4996. doi:10.1016/j.tetlet.2016.09.091
NLM
Glowacka PC, Maindron N, Stephenson GR, Romieu A, Renard P-Y, Emery F da S. Synthesis and photophysical properties of iron-carbonyl complex–coumarin conjugates as potential bimodal IR–fluorescent probes [Internet]. Tetrahedron Letters. 2016 ; 57( 45): 4991-4996.[citado 2024 nov. 14 ] Available from: https://doi.org/10.1016/j.tetlet.2016.09.091
Vancouver
Glowacka PC, Maindron N, Stephenson GR, Romieu A, Renard P-Y, Emery F da S. Synthesis and photophysical properties of iron-carbonyl complex–coumarin conjugates as potential bimodal IR–fluorescent probes [Internet]. Tetrahedron Letters. 2016 ; 57( 45): 4991-4996.[citado 2024 nov. 14 ] Available from: https://doi.org/10.1016/j.tetlet.2016.09.091
Artigo de periodico
Thiocyanation of BODIPY dyes and their conversion to thioalkylated derivatives (2015)
Rezende, Lucas Cunha Dias de; Melo, Shaiani Maria Gil de; Boodts, Stijn; Verbelen, Bram; Dehaen, Wim; Emery, Flavio da Silva
Source: Organic and Biomolecular Chemistry. Unidade: FCFRP
Subjects: SÍNTESE ORGÂNICA, COMPOSTOS ORGÂNICOS, CORANTES FLUORESCENTES
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ABNT
REZENDE, Lucas Cunha Dias de et al. Thiocyanation of BODIPY dyes and their conversion to thioalkylated derivatives. Organic and Biomolecular Chemistry, v. 13, n. 21, p. 6031-6038, 2015Tradução . . Disponível em: https://doi.org/10.1039/c5ob00499c. Acesso em: 14 nov. 2024.
APA
Rezende, L. C. D. de, Melo, S. M. G. de, Boodts, S., Verbelen, B., Dehaen, W., & Emery, F. da S. (2015). Thiocyanation of BODIPY dyes and their conversion to thioalkylated derivatives. Organic and Biomolecular Chemistry, 13( 21), 6031-6038. doi:10.1039/c5ob00499c
NLM
Rezende LCD de, Melo SMG de, Boodts S, Verbelen B, Dehaen W, Emery F da S. Thiocyanation of BODIPY dyes and their conversion to thioalkylated derivatives [Internet]. Organic and Biomolecular Chemistry. 2015 ; 13( 21): 6031-6038.[citado 2024 nov. 14 ] Available from: https://doi.org/10.1039/c5ob00499c
Vancouver
Rezende LCD de, Melo SMG de, Boodts S, Verbelen B, Dehaen W, Emery F da S. Thiocyanation of BODIPY dyes and their conversion to thioalkylated derivatives [Internet]. Organic and Biomolecular Chemistry. 2015 ; 13( 21): 6031-6038.[citado 2024 nov. 14 ] Available from: https://doi.org/10.1039/c5ob00499c
Artigo de periodico
Drug likeness and selective functionalization of quinoxalines (2015)
Ferreira, Samuel R. A; Franco, Marcia S. F; Diniz, Evelyn M. L. P; Emery, Flavio da Silva; Clososki, Giuliano Cesar
Source: Current Organic Synthesis. Unidade: FCFRP
Subjects: FARMACOLOGIA CLÍNICA, FÁRMACOS, PLANEJAMENTO DE FÁRMACOS
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ABNT
FERREIRA, Samuel R. A et al. Drug likeness and selective functionalization of quinoxalines. Current Organic Synthesis, v. 12, n. 6, p. 714-729, 2015Tradução . . Disponível em: https://doi.org/10.2174/157017941206150828110053. Acesso em: 14 nov. 2024.
APA
Ferreira, S. R. A., Franco, M. S. F., Diniz, E. M. L. P., Emery, F. da S., & Clososki, G. C. (2015). Drug likeness and selective functionalization of quinoxalines. Current Organic Synthesis, 12( 6), 714-729. doi:10.2174/157017941206150828110053
NLM
Ferreira SRA, Franco MSF, Diniz EMLP, Emery F da S, Clososki GC. Drug likeness and selective functionalization of quinoxalines [Internet]. Current Organic Synthesis. 2015 ; 12( 6): 714-729.[citado 2024 nov. 14 ] Available from: https://doi.org/10.2174/157017941206150828110053
Vancouver
Ferreira SRA, Franco MSF, Diniz EMLP, Emery F da S, Clososki GC. Drug likeness and selective functionalization of quinoxalines [Internet]. Current Organic Synthesis. 2015 ; 12( 6): 714-729.[citado 2024 nov. 14 ] Available from: https://doi.org/10.2174/157017941206150828110053
Artigo de periodico
Synthesis of some functionalized peptomers via UGI four-component reaction (2015)
Silva, Eduardo H. B; Emery, Flavio da Silva; Del Ponte, Gino; Donate, Paulo Marcos
Source: Synthetic Communications. Unidades: FCFRP, FFCLRP
Subjects: PEPTÍDEOS, SÍNTESE ORGÂNICA, QUÍMICA ORGÂNICA
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ABNT
SILVA, Eduardo H. B et al. Synthesis of some functionalized peptomers via UGI four-component reaction. Synthetic Communications, v. 45, n. 15, p. 1761-1767, 2015Tradução . . Disponível em: https://doi.org/10.1080/00397911.2015.1042591. Acesso em: 14 nov. 2024.
APA
Silva, E. H. B., Emery, F. da S., Del Ponte, G., & Donate, P. M. (2015). Synthesis of some functionalized peptomers via UGI four-component reaction. Synthetic Communications, 45( 15), 1761-1767. doi:10.1080/00397911.2015.1042591
NLM
Silva EHB, Emery F da S, Del Ponte G, Donate PM. Synthesis of some functionalized peptomers via UGI four-component reaction [Internet]. Synthetic Communications. 2015 ; 45( 15): 1761-1767.[citado 2024 nov. 14 ] Available from: https://doi.org/10.1080/00397911.2015.1042591
Vancouver
Silva EHB, Emery F da S, Del Ponte G, Donate PM. Synthesis of some functionalized peptomers via UGI four-component reaction [Internet]. Synthetic Communications. 2015 ; 45( 15): 1761-1767.[citado 2024 nov. 14 ] Available from: https://doi.org/10.1080/00397911.2015.1042591
Artigo de periodico
In vivo antimalarial activity of novel 2-hydroxy-3-anilino-1,4-naphthoquinones obtained by epoxide ring-opening reaction (2013)
Rezende, Lucas Cunha Dias de; Fumagalli, Fernando; Bortolin, Marraiana Schiavon; Oliveira, Marianne Garcia de; Paula, Murilo Helder de; Andrade-Neto, Valter Ferreira de; Emery, Flavio da Silva
Source: Bioorganic and Medicinal Chemistry Letters. Unidade: FCFRP
Subjects: ANTIPARASITÁRIOS, PLASMODIUM, PRODUTOS NATURAIS (FARMACOLOGIA)
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ABNT
REZENDE, Lucas Cunha Dias de et al. In vivo antimalarial activity of novel 2-hydroxy-3-anilino-1,4-naphthoquinones obtained by epoxide ring-opening reaction. Bioorganic and Medicinal Chemistry Letters, v. 23, n. 16, p. 4583-4586, 2013Tradução . . Disponível em: https://doi.org/10.1016/j.bmcl.2013.06.033. Acesso em: 14 nov. 2024.
APA
Rezende, L. C. D. de, Fumagalli, F., Bortolin, M. S., Oliveira, M. G. de, Paula, M. H. de, Andrade-Neto, V. F. de, & Emery, F. da S. (2013). In vivo antimalarial activity of novel 2-hydroxy-3-anilino-1,4-naphthoquinones obtained by epoxide ring-opening reaction. Bioorganic and Medicinal Chemistry Letters, 23( 16), 4583-4586. doi:10.1016/j.bmcl.2013.06.033
NLM
Rezende LCD de, Fumagalli F, Bortolin MS, Oliveira MG de, Paula MH de, Andrade-Neto VF de, Emery F da S. In vivo antimalarial activity of novel 2-hydroxy-3-anilino-1,4-naphthoquinones obtained by epoxide ring-opening reaction [Internet]. Bioorganic and Medicinal Chemistry Letters. 2013 ; 23( 16): 4583-4586.[citado 2024 nov. 14 ] Available from: https://doi.org/10.1016/j.bmcl.2013.06.033
Vancouver
Rezende LCD de, Fumagalli F, Bortolin MS, Oliveira MG de, Paula MH de, Andrade-Neto VF de, Emery F da S. In vivo antimalarial activity of novel 2-hydroxy-3-anilino-1,4-naphthoquinones obtained by epoxide ring-opening reaction [Internet]. Bioorganic and Medicinal Chemistry Letters. 2013 ; 23( 16): 4583-4586.[citado 2024 nov. 14 ] Available from: https://doi.org/10.1016/j.bmcl.2013.06.033
Artigo de periodico
Synthesis of quinoidal molecules: strategies towards bioactive compounds with an emphasis on lapachones (2013)
Castro, Solange L. de; Emery, Flavio da Silva; Silva Júnior, Eufrânio N. da
Source: European Journal of Medicinal Chemistry. Unidade: FCFRP
Subjects: DOENÇA DE CHAGAS, LEISHMANIA
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ABNT
CASTRO, Solange L. de e EMERY, Flavio da Silva e SILVA JÚNIOR, Eufrânio N. da. Synthesis of quinoidal molecules: strategies towards bioactive compounds with an emphasis on lapachones. European Journal of Medicinal Chemistry, v. 69, p. 678-700, 2013Tradução . . Disponível em: https://doi.org/10.1016/j.ejmech.2013.07.057. Acesso em: 14 nov. 2024.
APA
Castro, S. L. de, Emery, F. da S., & Silva Júnior, E. N. da. (2013). Synthesis of quinoidal molecules: strategies towards bioactive compounds with an emphasis on lapachones. European Journal of Medicinal Chemistry, 69, 678-700. doi:10.1016/j.ejmech.2013.07.057
NLM
Castro SL de, Emery F da S, Silva Júnior EN da. Synthesis of quinoidal molecules: strategies towards bioactive compounds with an emphasis on lapachones [Internet]. European Journal of Medicinal Chemistry. 2013 ; 69 678-700.[citado 2024 nov. 14 ] Available from: https://doi.org/10.1016/j.ejmech.2013.07.057
Vancouver
Castro SL de, Emery F da S, Silva Júnior EN da. Synthesis of quinoidal molecules: strategies towards bioactive compounds with an emphasis on lapachones [Internet]. European Journal of Medicinal Chemistry. 2013 ; 69 678-700.[citado 2024 nov. 14 ] Available from: https://doi.org/10.1016/j.ejmech.2013.07.057

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