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SILVA, João Vitor da et al. Neglected tropical diseases and infectious illnesses: potential targeted peptides employed as hits compounds in drug design. Journal of Drug Targeting, v. 29, n. 3, p. 269–283, 2021Tradução . . Disponível em: https://doi.org/10.1080/1061186X.2020.1837843. Acesso em: 02 set. 2024.
APA
Silva, J. V. da, Santos, S. da S., Machini, M. T., & Giarolla, J. (2021). Neglected tropical diseases and infectious illnesses: potential targeted peptides employed as hits compounds in drug design. Journal of Drug Targeting, 29( 3), 269–283. doi:10.1080/1061186X.2020.1837843
NLM
Silva JV da, Santos S da S, Machini MT, Giarolla J. Neglected tropical diseases and infectious illnesses: potential targeted peptides employed as hits compounds in drug design [Internet]. Journal of Drug Targeting. 2021 ; 29( 3): 269–283.[citado 2024 set. 02 ] Available from: https://doi.org/10.1080/1061186X.2020.1837843
Vancouver
Silva JV da, Santos S da S, Machini MT, Giarolla J. Neglected tropical diseases and infectious illnesses: potential targeted peptides employed as hits compounds in drug design [Internet]. Journal of Drug Targeting. 2021 ; 29( 3): 269–283.[citado 2024 set. 02 ] Available from: https://doi.org/10.1080/1061186X.2020.1837843
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OBI, Lígia Passos Maia et al. Non-inclusion complexation of peracetylated β-Cyclodextrin with ibuprofen in supercritical carbon dioxide. Journal of Supercritical Fluids, v. 169, p. 1-9 art. 105098, 2021Tradução . . Disponível em: https://doi.org/10.1016/j.supflu.2020.105098. Acesso em: 02 set. 2024.
APA
Obi, L. P. M., Vidinha, P., Ferraz, H. G., & Bazito, R. C. (2021). Non-inclusion complexation of peracetylated β-Cyclodextrin with ibuprofen in supercritical carbon dioxide. Journal of Supercritical Fluids, 169, 1-9 art. 105098. doi:10.1016/j.supflu.2020.105098
NLM
Obi LPM, Vidinha P, Ferraz HG, Bazito RC. Non-inclusion complexation of peracetylated β-Cyclodextrin with ibuprofen in supercritical carbon dioxide [Internet]. Journal of Supercritical Fluids. 2021 ; 169 1-9 art. 105098.[citado 2024 set. 02 ] Available from: https://doi.org/10.1016/j.supflu.2020.105098
Vancouver
Obi LPM, Vidinha P, Ferraz HG, Bazito RC. Non-inclusion complexation of peracetylated β-Cyclodextrin with ibuprofen in supercritical carbon dioxide [Internet]. Journal of Supercritical Fluids. 2021 ; 169 1-9 art. 105098.[citado 2024 set. 02 ] Available from: https://doi.org/10.1016/j.supflu.2020.105098
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SILVEIRA, Gabriela de Oliveira et al. Essential oil-based dispersive liquid-liquid microextraction for the determination of N,N-dimethyltryptamine and β-carbolines in human plasma: a novel solvent-free alternative. Talanta, v. 225, p. 1-11 art. 121976, 2021Tradução . . Disponível em: https://doi.org/10.1016/j.talanta.2020.121976. Acesso em: 02 set. 2024.
APA
Silveira, G. de O., Lourenço, F. R., Pego, A. M. F., Santos, R. G. dos, Rossi, G. N., Hallak, J. E. C., & Yonamine, M. (2021). Essential oil-based dispersive liquid-liquid microextraction for the determination of N,N-dimethyltryptamine and β-carbolines in human plasma: a novel solvent-free alternative. Talanta, 225, 1-11 art. 121976. doi:10.1016/j.talanta.2020.121976
NLM
Silveira G de O, Lourenço FR, Pego AMF, Santos RG dos, Rossi GN, Hallak JEC, Yonamine M. Essential oil-based dispersive liquid-liquid microextraction for the determination of N,N-dimethyltryptamine and β-carbolines in human plasma: a novel solvent-free alternative [Internet]. Talanta. 2021 ; 225 1-11 art. 121976.[citado 2024 set. 02 ] Available from: https://doi.org/10.1016/j.talanta.2020.121976
Vancouver
Silveira G de O, Lourenço FR, Pego AMF, Santos RG dos, Rossi GN, Hallak JEC, Yonamine M. Essential oil-based dispersive liquid-liquid microextraction for the determination of N,N-dimethyltryptamine and β-carbolines in human plasma: a novel solvent-free alternative [Internet]. Talanta. 2021 ; 225 1-11 art. 121976.[citado 2024 set. 02 ] Available from: https://doi.org/10.1016/j.talanta.2020.121976
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SANZ, Caroline Gomes et al. Electrochemical characterization of para- and meta-nitro substituents in aqueous media of new antichagasic pharmaceutical leaders. Electrochimica Acta, v. 368, p. 1-12 art. 137582, 2021Tradução . . Disponível em: https://doi.org/10.1016/j.electacta.2020.137582. Acesso em: 02 set. 2024.
APA
Sanz, C. G., Dias, K. de A., Bacil, R. P., Serafim, R. A. M., Andrade, L. H., Ferreira, E. I., & Serrano, S. H. P. (2021). Electrochemical characterization of para- and meta-nitro substituents in aqueous media of new antichagasic pharmaceutical leaders. Electrochimica Acta, 368, 1-12 art. 137582. doi:10.1016/j.electacta.2020.137582
NLM
Sanz CG, Dias K de A, Bacil RP, Serafim RAM, Andrade LH, Ferreira EI, Serrano SHP. Electrochemical characterization of para- and meta-nitro substituents in aqueous media of new antichagasic pharmaceutical leaders [Internet]. Electrochimica Acta. 2021 ; 368 1-12 art. 137582.[citado 2024 set. 02 ] Available from: https://doi.org/10.1016/j.electacta.2020.137582
Vancouver
Sanz CG, Dias K de A, Bacil RP, Serafim RAM, Andrade LH, Ferreira EI, Serrano SHP. Electrochemical characterization of para- and meta-nitro substituents in aqueous media of new antichagasic pharmaceutical leaders [Internet]. Electrochimica Acta. 2021 ; 368 1-12 art. 137582.[citado 2024 set. 02 ] Available from: https://doi.org/10.1016/j.electacta.2020.137582
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MARTINEZA, Renata Miliani et al. Vitamin E-loaded bigels and emulsions: physicochemical characterization and potential biological application. Colloids and Surfaces B, v. 201 , p. 1-10 art. 111651, 2021Tradução . . Disponível em: https://doi.org/10.1016/j.colsurfb.2021.111651. Acesso em: 02 set. 2024.
APA
Martineza, R. M., Magalhães, W. V., Sufi, B. da S., Padovani, G., Nazato, L. I. S., Velasco, M. V. R., et al. (2021). Vitamin E-loaded bigels and emulsions: physicochemical characterization and potential biological application. Colloids and Surfaces B, 201 , 1-10 art. 111651. doi:10.1016/j.colsurfb.2021.111651
NLM
Martineza RM, Magalhães WV, Sufi B da S, Padovani G, Nazato LIS, Velasco MVR, Lannes SC da S, Baby AR. Vitamin E-loaded bigels and emulsions: physicochemical characterization and potential biological application [Internet]. Colloids and Surfaces B. 2021 ; 201 1-10 art. 111651.[citado 2024 set. 02 ] Available from: https://doi.org/10.1016/j.colsurfb.2021.111651
Vancouver
Martineza RM, Magalhães WV, Sufi B da S, Padovani G, Nazato LIS, Velasco MVR, Lannes SC da S, Baby AR. Vitamin E-loaded bigels and emulsions: physicochemical characterization and potential biological application [Internet]. Colloids and Surfaces B. 2021 ; 201 1-10 art. 111651.[citado 2024 set. 02 ] Available from: https://doi.org/10.1016/j.colsurfb.2021.111651
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ROSALES, Thiecla Katiane Osvaldt et al. Nanoencapsulation of anthocyanins from blackberry (Rubus spp.) through pectin and lysozyme self-assembling. Food Hydrocolloids, v. 114, p. 1-50 art. 106563, 2021Tradução . . Disponível em: https://doi.org/10.1016/j.foodhyd.2020.106563. Acesso em: 02 set. 2024.
APA
Rosales, T. K. O., Silva, M. P. da, Lourenço, F. R., Hassimotto, N. M. A., & Fabi, J. P. (2021). Nanoencapsulation of anthocyanins from blackberry (Rubus spp.) through pectin and lysozyme self-assembling. Food Hydrocolloids, 114, 1-50 art. 106563. doi:10.1016/j.foodhyd.2020.106563
NLM
Rosales TKO, Silva MP da, Lourenço FR, Hassimotto NMA, Fabi JP. Nanoencapsulation of anthocyanins from blackberry (Rubus spp.) through pectin and lysozyme self-assembling [Internet]. Food Hydrocolloids. 2021 ; 114 1-50 art. 106563.[citado 2024 set. 02 ] Available from: https://doi.org/10.1016/j.foodhyd.2020.106563
Vancouver
Rosales TKO, Silva MP da, Lourenço FR, Hassimotto NMA, Fabi JP. Nanoencapsulation of anthocyanins from blackberry (Rubus spp.) through pectin and lysozyme self-assembling [Internet]. Food Hydrocolloids. 2021 ; 114 1-50 art. 106563.[citado 2024 set. 02 ] Available from: https://doi.org/10.1016/j.foodhyd.2020.106563
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PAULINO, Antonio Augusto Soares et al. Nanomolar detection of palladium (II) through a novel seleno-rhodamine-based fluorescent and colorimetric chemosensor. Dyes and Pigments, v. 179, p. 1-10 art. 108355, 2020Tradução . . Disponível em: https://doi.org/10.1016/j.dyepig.2020.108355. Acesso em: 02 set. 2024.
APA
Paulino, A. A. S., Giroldo, L., Pradie, N. A., Reis, J. S. dos, Back, D. F., Braga, A. A. C., et al. (2020). Nanomolar detection of palladium (II) through a novel seleno-rhodamine-based fluorescent and colorimetric chemosensor. Dyes and Pigments, 179, 1-10 art. 108355. doi:10.1016/j.dyepig.2020.108355
NLM
Paulino AAS, Giroldo L, Pradie NA, Reis JS dos, Back DF, Braga AAC, Stefani HA, Lodeiro C, Santos AA dos. Nanomolar detection of palladium (II) through a novel seleno-rhodamine-based fluorescent and colorimetric chemosensor [Internet]. Dyes and Pigments. 2020 ; 179 1-10 art. 108355.[citado 2024 set. 02 ] Available from: https://doi.org/10.1016/j.dyepig.2020.108355
Vancouver
Paulino AAS, Giroldo L, Pradie NA, Reis JS dos, Back DF, Braga AAC, Stefani HA, Lodeiro C, Santos AA dos. Nanomolar detection of palladium (II) through a novel seleno-rhodamine-based fluorescent and colorimetric chemosensor [Internet]. Dyes and Pigments. 2020 ; 179 1-10 art. 108355.[citado 2024 set. 02 ] Available from: https://doi.org/10.1016/j.dyepig.2020.108355
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OLIVEIRA, Isadora Maria de et al. Stereo- and regioselective Cu-catalyzed hydroboration of alkynyl chalcogenoethers. ChemCatChem, v. 12, p. 3545–3552, 2020Tradução . . Disponível em: https://doi.org/10.1002/cctc.202000395. Acesso em: 02 set. 2024.
APA
Oliveira, I. M. de, Esteves, H. A., Darbem, M. P., Sartorelli, A., Correra, T. C., Oliveira, A. F. R., et al. (2020). Stereo- and regioselective Cu-catalyzed hydroboration of alkynyl chalcogenoethers. ChemCatChem, 12, 3545–3552. doi:10.1002/cctc.202000395
NLM
Oliveira IM de, Esteves HA, Darbem MP, Sartorelli A, Correra TC, Oliveira AFR, Pimenta DC, Zukerman-Schpector J, Stefani HA. Stereo- and regioselective Cu-catalyzed hydroboration of alkynyl chalcogenoethers [Internet]. ChemCatChem. 2020 ; 12 3545–3552.[citado 2024 set. 02 ] Available from: https://doi.org/10.1002/cctc.202000395
Vancouver
Oliveira IM de, Esteves HA, Darbem MP, Sartorelli A, Correra TC, Oliveira AFR, Pimenta DC, Zukerman-Schpector J, Stefani HA. Stereo- and regioselective Cu-catalyzed hydroboration of alkynyl chalcogenoethers [Internet]. ChemCatChem. 2020 ; 12 3545–3552.[citado 2024 set. 02 ] Available from: https://doi.org/10.1002/cctc.202000395
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SILVEIRA, Gabriela de Oliveira et al. Stability evaluation of DMT and harmala alkaloids in ayahuasca tea samples. Molecules, v. 25, n. 9, p. 1-11 art. 2.072, 2020Tradução . . Disponível em: https://doi.org/10.3390/molecules25092072. Acesso em: 02 set. 2024.
APA
Silveira, G. de O., Santos, R. G. dos, Lourenço, F. R., Rossi, G. N., Hallak, J. E. C., & Yonamine, M. (2020). Stability evaluation of DMT and harmala alkaloids in ayahuasca tea samples. Molecules, 25( 9), 1-11 art. 2.072. doi:10.3390/molecules25092072
NLM
Silveira G de O, Santos RG dos, Lourenço FR, Rossi GN, Hallak JEC, Yonamine M. Stability evaluation of DMT and harmala alkaloids in ayahuasca tea samples [Internet]. Molecules. 2020 ; 25( 9): 1-11 art. 2.072.[citado 2024 set. 02 ] Available from: https://doi.org/10.3390/molecules25092072
Vancouver
Silveira G de O, Santos RG dos, Lourenço FR, Rossi GN, Hallak JEC, Yonamine M. Stability evaluation of DMT and harmala alkaloids in ayahuasca tea samples [Internet]. Molecules. 2020 ; 25( 9): 1-11 art. 2.072.[citado 2024 set. 02 ] Available from: https://doi.org/10.3390/molecules25092072
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FERREIRA, Glaucio Monteiro et al. Inhibition of Porcine Aminopeptidase M (pAMP) by the Pentapeptide Microginins. Molecules, v. 24, p. 1-14 art. 4369, 2019Tradução . . Disponível em: https://doi.org/10.3390/molecules24234369. Acesso em: 02 set. 2024.
APA
Ferreira, G. M., Kronenberger, T., Almeida, É. C. de, Sampaio, J., Ferreira, C., Pinto, E., & Trossini, G. H. G. (2019). Inhibition of Porcine Aminopeptidase M (pAMP) by the Pentapeptide Microginins. Molecules, 24, 1-14 art. 4369. doi:10.3390/molecules24234369
NLM
Ferreira GM, Kronenberger T, Almeida ÉC de, Sampaio J, Ferreira C, Pinto E, Trossini GHG. Inhibition of Porcine Aminopeptidase M (pAMP) by the Pentapeptide Microginins [Internet]. Molecules. 2019 ; 24 1-14 art. 4369.[citado 2024 set. 02 ] Available from: https://doi.org/10.3390/molecules24234369
Vancouver
Ferreira GM, Kronenberger T, Almeida ÉC de, Sampaio J, Ferreira C, Pinto E, Trossini GHG. Inhibition of Porcine Aminopeptidase M (pAMP) by the Pentapeptide Microginins [Internet]. Molecules. 2019 ; 24 1-14 art. 4369.[citado 2024 set. 02 ] Available from: https://doi.org/10.3390/molecules24234369
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COMPRI, Jéssica de Cássia Zaghi et al. Highly water-soluble orotic acid nanocrystals produced by high-energy milling. Journal of Pharmaceutical Sciences, v. 108, n. 5, p. 1848-1856, 2019Tradução . . Disponível em: https://doi.org/10.1016/j.xphs.2018.12.015. Acesso em: 02 set. 2024.
APA
Compri, J. de C. Z., Felli, V. M. A., Lourenço, F. R., Takatsuka, T., Fotaki, N., Löbenberg, R., et al. (2019). Highly water-soluble orotic acid nanocrystals produced by high-energy milling. Journal of Pharmaceutical Sciences, 108( 5), 1848-1856. doi:10.1016/j.xphs.2018.12.015
NLM
Compri J de CZ, Felli VMA, Lourenço FR, Takatsuka T, Fotaki N, Löbenberg R, Bou-Chacra NA, Araujo GLB de. Highly water-soluble orotic acid nanocrystals produced by high-energy milling [Internet]. Journal of Pharmaceutical Sciences. 2019 ; 108( 5): 1848-1856.[citado 2024 set. 02 ] Available from: https://doi.org/10.1016/j.xphs.2018.12.015
Vancouver
Compri J de CZ, Felli VMA, Lourenço FR, Takatsuka T, Fotaki N, Löbenberg R, Bou-Chacra NA, Araujo GLB de. Highly water-soluble orotic acid nanocrystals produced by high-energy milling [Internet]. Journal of Pharmaceutical Sciences. 2019 ; 108( 5): 1848-1856.[citado 2024 set. 02 ] Available from: https://doi.org/10.1016/j.xphs.2018.12.015
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OLIVEIRA, Isadora M. de et al. Iron (III)-Promoted synthesis of substituted 4H-Chalcogenochromenes and chemoselective functionalization. Advanced Synthesis and Catalysis, v. 361, n. 13, p. 3163-3172, 2019Tradução . . Disponível em: https://doi.org/10.1002/adsc.201900142. Acesso em: 02 set. 2024.
APA
Oliveira, I. M. de, Esteves, C. H. A., Darbem, M. P., Pimenta, D. C., Schpector, J. Z., Ferreira, A. G., et al. (2019). Iron (III)-Promoted synthesis of substituted 4H-Chalcogenochromenes and chemoselective functionalization. Advanced Synthesis and Catalysis, 361( 13), 3163-3172. doi:10.1002/adsc.201900142
NLM
Oliveira IM de, Esteves CHA, Darbem MP, Pimenta DC, Schpector JZ, Ferreira AG, Stefani HA, Manarin F. Iron (III)-Promoted synthesis of substituted 4H-Chalcogenochromenes and chemoselective functionalization [Internet]. Advanced Synthesis and Catalysis. 2019 ; 361( 13): 3163-3172.[citado 2024 set. 02 ] Available from: https://doi.org/10.1002/adsc.201900142
Vancouver
Oliveira IM de, Esteves CHA, Darbem MP, Pimenta DC, Schpector JZ, Ferreira AG, Stefani HA, Manarin F. Iron (III)-Promoted synthesis of substituted 4H-Chalcogenochromenes and chemoselective functionalization [Internet]. Advanced Synthesis and Catalysis. 2019 ; 361( 13): 3163-3172.[citado 2024 set. 02 ] Available from: https://doi.org/10.1002/adsc.201900142
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AHMED, Faiz et al. A Facile single pot synthesis of highly functionalized tricyclic heterocycle compounds via sequential Knoevenagel-Michael addition and their α-glucosidase inhibition, antioxidants and antibacterial studies. Journal of the Chemical Society of Pakistan, v. 40, n. 4, p. 761-772, 2018Tradução . . Disponível em: https://www.jcsp.org.pk/PublishedVersion/94e37a96-6278-4cec-bb45-0d63c32f069eManuscript%20no%2014,%20Final%20Gally%20Proof%20of%2011601%20(Ashfaq%20Mahmood%20Qureshi).pdf. Acesso em: 02 set. 2024.
APA
Ahmed, F., Rauf, A., Sharif, A., Ahmad, E., Arshad, M., Espósito, B. P., et al. (2018). A Facile single pot synthesis of highly functionalized tricyclic heterocycle compounds via sequential Knoevenagel-Michael addition and their α-glucosidase inhibition, antioxidants and antibacterial studies. Journal of the Chemical Society of Pakistan, 40( 4), 761-772. Recuperado de https://www.jcsp.org.pk/PublishedVersion/94e37a96-6278-4cec-bb45-0d63c32f069eManuscript%20no%2014,%20Final%20Gally%20Proof%20of%2011601%20(Ashfaq%20Mahmood%20Qureshi).pdf
NLM
Ahmed F, Rauf A, Sharif A, Ahmad E, Arshad M, Espósito BP, Kaneko TM, Qureshi AM. A Facile single pot synthesis of highly functionalized tricyclic heterocycle compounds via sequential Knoevenagel-Michael addition and their α-glucosidase inhibition, antioxidants and antibacterial studies [Internet]. Journal of the Chemical Society of Pakistan. 2018 ; 40( 4): 761-772.[citado 2024 set. 02 ] Available from: https://www.jcsp.org.pk/PublishedVersion/94e37a96-6278-4cec-bb45-0d63c32f069eManuscript%20no%2014,%20Final%20Gally%20Proof%20of%2011601%20(Ashfaq%20Mahmood%20Qureshi).pdf
Vancouver
Ahmed F, Rauf A, Sharif A, Ahmad E, Arshad M, Espósito BP, Kaneko TM, Qureshi AM. A Facile single pot synthesis of highly functionalized tricyclic heterocycle compounds via sequential Knoevenagel-Michael addition and their α-glucosidase inhibition, antioxidants and antibacterial studies [Internet]. Journal of the Chemical Society of Pakistan. 2018 ; 40( 4): 761-772.[citado 2024 set. 02 ] Available from: https://www.jcsp.org.pk/PublishedVersion/94e37a96-6278-4cec-bb45-0d63c32f069eManuscript%20no%2014,%20Final%20Gally%20Proof%20of%2011601%20(Ashfaq%20Mahmood%20Qureshi).pdf
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ABNT
REIS, Joel S et al. Oxazoline as acceptor moiety for excited-state intramolecular proton transfer. Tetrahedron, v. 74, p. 6866-6872, 2018Tradução . . Disponível em: https://doi.org/10.1016/j.tet.2018.10.019. Acesso em: 02 set. 2024.
APA
Reis, J. S., Fernandes, A. B., Dörr, B. C. de F., Bastos, E. L., & Stefani, H. A. (2018). Oxazoline as acceptor moiety for excited-state intramolecular proton transfer. Tetrahedron, 74, 6866-6872. doi:10.1016/j.tet.2018.10.019
NLM
Reis JS, Fernandes AB, Dörr BC de F, Bastos EL, Stefani HA. Oxazoline as acceptor moiety for excited-state intramolecular proton transfer [Internet]. Tetrahedron. 2018 ; 74 6866-6872.[citado 2024 set. 02 ] Available from: https://doi.org/10.1016/j.tet.2018.10.019
Vancouver
Reis JS, Fernandes AB, Dörr BC de F, Bastos EL, Stefani HA. Oxazoline as acceptor moiety for excited-state intramolecular proton transfer [Internet]. Tetrahedron. 2018 ; 74 6866-6872.[citado 2024 set. 02 ] Available from: https://doi.org/10.1016/j.tet.2018.10.019