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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: 10 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. 10 ] 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. 10 ] Available from: https://doi.org/10.1016/j.tetlet.2018.05.054
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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: 10 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. 10 ] 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. 10 ] Available from: https://doi.org/10.1016/j.freeradbiomed.2017.12.012
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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: 10 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. 10 ] 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. 10 ] Available from: https://doi.org/10.1016/j.carbpol.2016.10.076
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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: 10 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. 10 ] 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. 10 ] Available from: https://doi.org/10.1007/s13318-016-0337-2
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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: 10 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. 10 ] 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. 10 ] Available from: https://doi.org/10.1016/j.tetlet.2016.09.091
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ABNT
SOUZA, Joel G et al. Transcorneal iontophoresis of dendrimers: PAMAM corneal penetration and dexamethasone delivery. Journal of Controlled Release, v. 200, p. 115-124, 2015Tradução . . Disponível em: https://doi.org/10.1016/j.jconrel.2014.12.037. Acesso em: 10 nov. 2024.
APA
Souza, J. G., Dias, K., Silva, S. A. M., Rezende, L. C. D. de, Rocha, E. M., Emery, F. da S., & Lopez, R. F. V. (2015). Transcorneal iontophoresis of dendrimers: PAMAM corneal penetration and dexamethasone delivery. Journal of Controlled Release, 200, 115-124. doi:10.1016/j.jconrel.2014.12.037
NLM
Souza JG, Dias K, Silva SAM, Rezende LCD de, Rocha EM, Emery F da S, Lopez RFV. Transcorneal iontophoresis of dendrimers: PAMAM corneal penetration and dexamethasone delivery [Internet]. Journal of Controlled Release. 2015 ; 200 115-124.[citado 2024 nov. 10 ] Available from: https://doi.org/10.1016/j.jconrel.2014.12.037
Vancouver
Souza JG, Dias K, Silva SAM, Rezende LCD de, Rocha EM, Emery F da S, Lopez RFV. Transcorneal iontophoresis of dendrimers: PAMAM corneal penetration and dexamethasone delivery [Internet]. Journal of Controlled Release. 2015 ; 200 115-124.[citado 2024 nov. 10 ] Available from: https://doi.org/10.1016/j.jconrel.2014.12.037
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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: 10 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. 10 ] 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. 10 ] Available from: https://doi.org/10.1039/c5ob00499c
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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: 10 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. 10 ] 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. 10 ] Available from: https://doi.org/10.1016/j.bmcl.2013.06.033
