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Trabalho de evento-resumo
Free radical formation evidence from nimorazole electrochemical reduction in aqueous media (2022)
Brito, Charles de Lima; Lins, Renato Soares de Oliveira ; Bertotti, Mauro ; Ferreira, Elizabeth Igne ; La Scalea, Mauro Aquiles
Fonte: Anais. Nome do evento: Reunião Anual da Sociedade Brasileira de Química. Unidades: FCF, RUSP, IQ
Assuntos: RADICAIS LIVRES, ELETROQUÍMICA
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ABNT
BRITO, Charles de Lima et al. Free radical formation evidence from nimorazole electrochemical reduction in aqueous media. 2022, Anais.. São Paulo: Sociedade Brasileira de Química/SBQ, 2022. Disponível em: http://www.sbq.org.br/45ra/anexos/45RASBQ_resumos.pdf. Acesso em: 26 maio 2024.
APA
Brito, C. de L., Lins, R. S. de O., Bertotti, M., Ferreira, E. I., & La Scalea, M. A. (2022). Free radical formation evidence from nimorazole electrochemical reduction in aqueous media. In Anais. São Paulo: Sociedade Brasileira de Química/SBQ. Recuperado de http://www.sbq.org.br/45ra/anexos/45RASBQ_resumos.pdf
NLM
Brito C de L, Lins RS de O, Bertotti M, Ferreira EI, La Scalea MA. Free radical formation evidence from nimorazole electrochemical reduction in aqueous media [Internet]. Anais. 2022 ;[citado 2024 maio 26 ] Available from: http://www.sbq.org.br/45ra/anexos/45RASBQ_resumos.pdf
Vancouver
Brito C de L, Lins RS de O, Bertotti M, Ferreira EI, La Scalea MA. Free radical formation evidence from nimorazole electrochemical reduction in aqueous media [Internet]. Anais. 2022 ;[citado 2024 maio 26 ] Available from: http://www.sbq.org.br/45ra/anexos/45RASBQ_resumos.pdf
Artigo de periodico
Hot-melt extrudability of amorphous solid dispersions of flubendazole-copovidone: an exploratory study of the effect of drug loading and the balance of adjuvants on extrudability and dissolution (2022)
Assis, João Marcos Cabral de; Barbosa, Eduardo José ; Bezzon, Vinícius Danilo Nonato ; Lourenço, Felipe Rebello ; Carvalho, Flavio Machado de Souza ; Matos, Jivaldo do Rosário ; Bou-Chacra, Nadia Araci ; Benmore, Chris J ; Byrn, Stephen R; Costa, Fanny N; Araujo, Gabriel Lima Barros de
Fonte: International Journal of Pharmaceutics. Unidades: FCF, IGC, IQ
Assuntos: ANTI-HELMÍNTICOS, EXTRUSÃO
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ABNT
ASSIS, João Marcos Cabral de et al. Hot-melt extrudability of amorphous solid dispersions of flubendazole-copovidone: an exploratory study of the effect of drug loading and the balance of adjuvants on extrudability and dissolution. International Journal of Pharmaceutics, v. 614, p. 1-10 art. 121456, 2022Tradução . . Disponível em: https://doi.org/10.1016/j.ijpharm.2022.121456. Acesso em: 26 maio 2024.
APA
Assis, J. M. C. de, Barbosa, E. J., Bezzon, V. D. N., Lourenço, F. R., Carvalho, F. M. de S., Matos, J. do R., et al. (2022). Hot-melt extrudability of amorphous solid dispersions of flubendazole-copovidone: an exploratory study of the effect of drug loading and the balance of adjuvants on extrudability and dissolution. International Journal of Pharmaceutics, 614, 1-10 art. 121456. doi:10.1016/j.ijpharm.2022.121456
NLM
Assis JMC de, Barbosa EJ, Bezzon VDN, Lourenço FR, Carvalho FM de S, Matos J do R, Bou-Chacra NA, Benmore CJ, Byrn SR, Costa FN, Araujo GLB de. Hot-melt extrudability of amorphous solid dispersions of flubendazole-copovidone: an exploratory study of the effect of drug loading and the balance of adjuvants on extrudability and dissolution [Internet]. International Journal of Pharmaceutics. 2022 ; 614 1-10 art. 121456.[citado 2024 maio 26 ] Available from: https://doi.org/10.1016/j.ijpharm.2022.121456
Vancouver
Assis JMC de, Barbosa EJ, Bezzon VDN, Lourenço FR, Carvalho FM de S, Matos J do R, Bou-Chacra NA, Benmore CJ, Byrn SR, Costa FN, Araujo GLB de. Hot-melt extrudability of amorphous solid dispersions of flubendazole-copovidone: an exploratory study of the effect of drug loading and the balance of adjuvants on extrudability and dissolution [Internet]. International Journal of Pharmaceutics. 2022 ; 614 1-10 art. 121456.[citado 2024 maio 26 ] Available from: https://doi.org/10.1016/j.ijpharm.2022.121456
Artigo de periodico
Free radical formation evidence from Nimorazole electrochemical reduction in aqueous media (2022)
Brito, Charles de Lima; Lins, Renato Soares de Oliveira ; Bertotti, Mauro ; Ferreira, Elizabeth Igne ; Scalea, Mauro A. La
Fonte: Electrochimica Acta. Unidades: FCF, IQ
Assuntos: RADICAIS LIVRES, ELETROQUÍMICA, VOLTAMETRIA
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ABNT
BRITO, Charles de Lima et al. Free radical formation evidence from Nimorazole electrochemical reduction in aqueous media. Electrochimica Acta, v. 403, p. 1-8 art. 139709, 2022Tradução . . Disponível em: https://doi.org/10.1016/j.electacta.2021.139709. Acesso em: 26 maio 2024.
APA
Brito, C. de L., Lins, R. S. de O., Bertotti, M., Ferreira, E. I., & Scalea, M. A. L. (2022). Free radical formation evidence from Nimorazole electrochemical reduction in aqueous media. Electrochimica Acta, 403, 1-8 art. 139709. doi:10.1016/j.electacta.2021.139709
NLM
Brito C de L, Lins RS de O, Bertotti M, Ferreira EI, Scalea MAL. Free radical formation evidence from Nimorazole electrochemical reduction in aqueous media [Internet]. Electrochimica Acta. 2022 ; 403 1-8 art. 139709.[citado 2024 maio 26 ] Available from: https://doi.org/10.1016/j.electacta.2021.139709
Vancouver
Brito C de L, Lins RS de O, Bertotti M, Ferreira EI, Scalea MAL. Free radical formation evidence from Nimorazole electrochemical reduction in aqueous media [Internet]. Electrochimica Acta. 2022 ; 403 1-8 art. 139709.[citado 2024 maio 26 ] Available from: https://doi.org/10.1016/j.electacta.2021.139709
Artigo de periodico
Succinylated isoniazid potential prodrug: design of Experiments (DoE) for synthesis optimization and computational study of the reaction mechanism by DFT calculations (2022)
Prieto, Diego Campos ; Araujo, Renan Vinicius de ; Lima, Sara de Souza; Assad, Felipe Zauith; Grayson, Scott M; Braga, Ataualpa Albert Carmo ; Lourenço, Felipe Rebello ; Giarolla, Jeanine
Fonte: Journal of Molecular Structure. Unidades: IQ, FCF
Assuntos: TUBERCULOSE, FÁRMACOS
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ABNT
PRIETO, Diego Campos et al. Succinylated isoniazid potential prodrug: design of Experiments (DoE) for synthesis optimization and computational study of the reaction mechanism by DFT calculations. Journal of Molecular Structure, v. 1254, p. 1-7 art. 132323, 2022Tradução . . Disponível em: https://doi.org/10.1016/j.molstruc.2021.132323. Acesso em: 26 maio 2024.
APA
Prieto, D. C., Araujo, R. V. de, Lima, S. de S., Assad, F. Z., Grayson, S. M., Braga, A. A. C., et al. (2022). Succinylated isoniazid potential prodrug: design of Experiments (DoE) for synthesis optimization and computational study of the reaction mechanism by DFT calculations. Journal of Molecular Structure, 1254, 1-7 art. 132323. doi:10.1016/j.molstruc.2021.132323
NLM
Prieto DC, Araujo RV de, Lima S de S, Assad FZ, Grayson SM, Braga AAC, Lourenço FR, Giarolla J. Succinylated isoniazid potential prodrug: design of Experiments (DoE) for synthesis optimization and computational study of the reaction mechanism by DFT calculations [Internet]. Journal of Molecular Structure. 2022 ; 1254 1-7 art. 132323.[citado 2024 maio 26 ] Available from: https://doi.org/10.1016/j.molstruc.2021.132323
Vancouver
Prieto DC, Araujo RV de, Lima S de S, Assad FZ, Grayson SM, Braga AAC, Lourenço FR, Giarolla J. Succinylated isoniazid potential prodrug: design of Experiments (DoE) for synthesis optimization and computational study of the reaction mechanism by DFT calculations [Internet]. Journal of Molecular Structure. 2022 ; 1254 1-7 art. 132323.[citado 2024 maio 26 ] Available from: https://doi.org/10.1016/j.molstruc.2021.132323
Artigo de periodico
Non-inclusion complexation of peracetylated β-Cyclodextrin with ibuprofen in supercritical carbon dioxide (2021)
Obi, Lígia Passos Maia; Vidinha, Pedro ; Ferraz, Humberto Gomes ; Bazito, Reinaldo Camino
Fonte: Journal of Supercritical Fluids. Unidades: FCF, IQ
Assuntos: ANTI-INFLAMATÓRIOS, DIÓXIDO DE CARBONO
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ABNT
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: 26 maio 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 maio 26 ] 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 maio 26 ] Available from: https://doi.org/10.1016/j.supflu.2020.105098
Artigo de periodico
Electrochemical characterization of para- and meta-nitro substituents in aqueous media of new antichagasic pharmaceutical leaders (2021)
Sanz, Caroline Gomes ; Dias, Kevin de Aquino ; Bacil, Raphael Prata ; Serafim, Ricardo Augusto Massarico; Andrade, Leandro Helgueira ; Ferreira, Elizabeth Igne ; Serrano, Silvia Helena Pires
Fonte: Electrochimica Acta. Unidades: IQ, FCF
Assuntos: DOENÇA DE CHAGAS, VOLTAMETRIA, ELETROQUÍMICA, DOENÇAS NEGLIGENCIADAS
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ABNT
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: 26 maio 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 maio 26 ] 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 maio 26 ] Available from: https://doi.org/10.1016/j.electacta.2020.137582
Artigo de periodico
Nanomolar detection of palladium (II) through a novel seleno-rhodamine-based fluorescent and colorimetric chemosensor (2020)
Paulino, Antonio Augusto Soares; Giroldo, Lilian; Pradie, Noriberto Araújo; Reis, Joel Savi dos; Back, Davi F; Braga, Ataualpa Albert Carmo ; Stefani, Hélio Alexandre ; Lodeiro, Carlos; Santos, Alcindo Aparecido dos
Fonte: Dyes and Pigments. Unidades: IQ, FCF
Assuntos: SELÊNIO, PALÁDIO, FLUORESCÊNCIA
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ABNT
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: 26 maio 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 maio 26 ] 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 maio 26 ] Available from: https://doi.org/10.1016/j.dyepig.2020.108355
Artigo de periodico
Stereo- and regioselective Cu-catalyzed hydroboration of alkynyl chalcogenoethers (2020)
Oliveira, Isadora Maria de ; Esteves, Henrique A; Darbem, Mariana P; Sartorelli, Arthur; Correra, Thiago Carita ; Oliveira, Andre F. Rodrigues ; Pimenta, Daniel C; Zukerman-Schpector, Júlio ; Stefani, Hélio Alexandre
Fonte: ChemCatChem. Unidades: FCF, IQ
Assuntos: LIGANTES, CATALISADORES
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ABNT
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: 26 maio 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 maio 26 ] 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 maio 26 ] Available from: https://doi.org/10.1002/cctc.202000395
Trabalho de evento-resumo periodico
Determination of co-encapsulation efficiency of tuberculostatic drugs in PLGA nanospheres by capillary electrophoresis (2018)
Yataco Lazaro, Lourdes Marcela; Prado, Fernando Kaneko; Santamaria, Jesus; Fernandez, Javier; Arruebo, Manuel; Sebastian, Victor; Tavares, Marina Franco Maggi ; Aurora-Prado, Maria Segunda
Fonte: Brazilian Journal of Pharmaceutical Sciences. Nome do evento: Pharmaceutical Science and Technology Meeting of the Faculty of Pharmaceutical Sciences, University of São Paulo. Unidades: IQ, FCF
Assuntos: TUBERCULOSE, FÁRMACOS, TÉCNICAS DE DIAGNÓSTICO E PROCEDIMENTOS
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ABNT
YATACO LAZARO, Lourdes Marcela et al. Determination of co-encapsulation efficiency of tuberculostatic drugs in PLGA nanospheres by capillary electrophoresis. Brazilian Journal of Pharmaceutical Sciences. São Paulo: Instituto de Química, Universidade de São Paulo. . Acesso em: 26 maio 2024. , 2018
APA
Yataco Lazaro, L. M., Prado, F. K., Santamaria, J., Fernandez, J., Arruebo, M., Sebastian, V., et al. (2018). Determination of co-encapsulation efficiency of tuberculostatic drugs in PLGA nanospheres by capillary electrophoresis. Brazilian Journal of Pharmaceutical Sciences. São Paulo: Instituto de Química, Universidade de São Paulo.
NLM
Yataco Lazaro LM, Prado FK, Santamaria J, Fernandez J, Arruebo M, Sebastian V, Tavares MFM, Aurora-Prado MS. Determination of co-encapsulation efficiency of tuberculostatic drugs in PLGA nanospheres by capillary electrophoresis. Brazilian Journal of Pharmaceutical Sciences. 2018 ; 54 17 res. FCF030.[citado 2024 maio 26 ]
Vancouver
Yataco Lazaro LM, Prado FK, Santamaria J, Fernandez J, Arruebo M, Sebastian V, Tavares MFM, Aurora-Prado MS. Determination of co-encapsulation efficiency of tuberculostatic drugs in PLGA nanospheres by capillary electrophoresis. Brazilian Journal of Pharmaceutical Sciences. 2018 ; 54 17 res. FCF030.[citado 2024 maio 26 ]
Trabalho de evento-resumo periodico
Development of a free solution capillary electrophoresis method to assay aminophylline in pharmaceuticals (2018)
Nascimento, Larissa Cesar Fernandes do; Fajardo, Frank Alonso Gavilano; Picossi, Carolina Raíssa Costa; Tavares, Marina Franco Maggi ; Santoro, Maria Inês Rocha Miritello; Kedor-Hackmann, Erika Rosa Maria; Aurora-Prado, Maria Segunda
Fonte: Brazilian Journal of Pharmaceutical Sciences. Nome do evento: Pharmaceutical Science and Technology Meeting of the Faculty of Pharmaceutical Sciences, University of São Paulo. Unidades: IQ, FCF
Assuntos: ELETROFORESE, COMPRIMIDOS
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ABNT
NASCIMENTO, Larissa Cesar Fernandes do et al. Development of a free solution capillary electrophoresis method to assay aminophylline in pharmaceuticals. Brazilian Journal of Pharmaceutical Sciences. São Paulo: Instituto de Química, Universidade de São Paulo. . Acesso em: 26 maio 2024. , 2018
APA
Nascimento, L. C. F. do, Fajardo, F. A. G., Picossi, C. R. C., Tavares, M. F. M., Santoro, M. I. R. M., Kedor-Hackmann, E. R. M., & Aurora-Prado, M. S. (2018). Development of a free solution capillary electrophoresis method to assay aminophylline in pharmaceuticals. Brazilian Journal of Pharmaceutical Sciences. São Paulo: Instituto de Química, Universidade de São Paulo.
NLM
Nascimento LCF do, Fajardo FAG, Picossi CRC, Tavares MFM, Santoro MIRM, Kedor-Hackmann ERM, Aurora-Prado MS. Development of a free solution capillary electrophoresis method to assay aminophylline in pharmaceuticals. Brazilian Journal of Pharmaceutical Sciences. 2018 ; 54 20 res. FCF035.[citado 2024 maio 26 ]
Vancouver
Nascimento LCF do, Fajardo FAG, Picossi CRC, Tavares MFM, Santoro MIRM, Kedor-Hackmann ERM, Aurora-Prado MS. Development of a free solution capillary electrophoresis method to assay aminophylline in pharmaceuticals. Brazilian Journal of Pharmaceutical Sciences. 2018 ; 54 20 res. FCF035.[citado 2024 maio 26 ]
Artigo de periodico
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 (2018)
Ahmed, Faiz; Rauf, Abdul; Sharif, Ahsan; Ahmad, Ejaz; Arshad, Muhammad; Espósito, Breno Pannia ; Kaneko, Telma Mary ; Qureshi, Ashfaq Mahmood
Fonte: Journal of the Chemical Society of Pakistan. Unidades: IQ, FCF
Assuntos: COMPOSTOS HETEROCÍCLICOS, ANTIOXIDANTES
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ABNT
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: 26 maio 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 maio 26 ] 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 maio 26 ] 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
Artigo de periodico
Oxazoline as acceptor moiety for excited-state intramolecular proton transfer (2018)
Reis, Joel S; Fernandes, Arthur Bonfá; Dörr, Barbara Coelho de Freitas; Bastos, Erick Leite ; Stefani, Hélio Alexandre
Fonte: Tetrahedron. Unidades: IQ, FCF
Assuntos: FLUORESCÊNCIA, COMPOSTOS ORGÂNICOS
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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: 26 maio 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 maio 26 ] 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 maio 26 ] Available from: https://doi.org/10.1016/j.tet.2018.10.019
Artigo de periodico
Validation cytotoxicity assay for lipophilic substances (2018)
Pedro, Natália Mencacci Esteves; Sugibayashi, Kenji; Ostrosky, Elissa Arantes; Ferrari, Márcio; Sufi, Bianca da Silva; Mathor, Monica Beatriz; Moreno, Paulo Roberto Hrihorowitsch ; Lourenço, Felipe Rebello ; Consiglieri, Vladi Olga ; Baby, André Rolim ; Kaneko, Telma Mary
Fonte: Current Topics in Medicinal Chemistry. Unidades: IQ, FCF
Assuntos: PIMENTA, ÓLEOS ESSENCIAIS
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ABNT
PEDRO, Natália Mencacci Esteves et al. Validation cytotoxicity assay for lipophilic substances. Current Topics in Medicinal Chemistry, v. 18, n. 4, p. 275-286, 2018Tradução . . Disponível em: https://doi.org/10.2174/1568026618666180410142829. Acesso em: 26 maio 2024.
APA
Pedro, N. M. E., Sugibayashi, K., Ostrosky, E. A., Ferrari, M., Sufi, B. da S., Mathor, M. B., et al. (2018). Validation cytotoxicity assay for lipophilic substances. Current Topics in Medicinal Chemistry, 18( 4), 275-286. doi:10.2174/1568026618666180410142829
NLM
Pedro NME, Sugibayashi K, Ostrosky EA, Ferrari M, Sufi B da S, Mathor MB, Moreno PRH, Lourenço FR, Consiglieri VO, Baby AR, Kaneko TM. Validation cytotoxicity assay for lipophilic substances [Internet]. Current Topics in Medicinal Chemistry. 2018 ; 18( 4): 275-286.[citado 2024 maio 26 ] Available from: https://doi.org/10.2174/1568026618666180410142829
Vancouver
Pedro NME, Sugibayashi K, Ostrosky EA, Ferrari M, Sufi B da S, Mathor MB, Moreno PRH, Lourenço FR, Consiglieri VO, Baby AR, Kaneko TM. Validation cytotoxicity assay for lipophilic substances [Internet]. Current Topics in Medicinal Chemistry. 2018 ; 18( 4): 275-286.[citado 2024 maio 26 ] Available from: https://doi.org/10.2174/1568026618666180410142829
Artigo de periodico
Chemical composition, antimicrobial and antioxidant activities of eugenia dysenterica DC essential oil (2018)
Oliveira, Danielle C. S. de; Kaneko, Telma Mary ; Young, Maria Cláudia M; Murakami, Cynthia; Cordeiro, Inês; Moreno, Paulo Roberto Hrihorowitsch
Fonte: Emerging Science Journal. Unidades: FCF, IQ
Assuntos: ÓLEOS ESSENCIAIS, MYRTALES
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
OLIVEIRA, Danielle C. S. de et al. Chemical composition, antimicrobial and antioxidant activities of eugenia dysenterica DC essential oil. Emerging Science Journal, v. 2, n. 6, p. 410-416, 2018Tradução . . Disponível em: https://doi.org/10.28991/esj-2018-01160. Acesso em: 26 maio 2024.
APA
Oliveira, D. C. S. de, Kaneko, T. M., Young, M. C. M., Murakami, C., Cordeiro, I., & Moreno, P. R. H. (2018). Chemical composition, antimicrobial and antioxidant activities of eugenia dysenterica DC essential oil. Emerging Science Journal, 2( 6), 410-416. doi:10.28991/esj-2018-01160
NLM
Oliveira DCS de, Kaneko TM, Young MCM, Murakami C, Cordeiro I, Moreno PRH. Chemical composition, antimicrobial and antioxidant activities of eugenia dysenterica DC essential oil [Internet]. Emerging Science Journal. 2018 ; 2( 6): 410-416.[citado 2024 maio 26 ] Available from: https://doi.org/10.28991/esj-2018-01160
Vancouver
Oliveira DCS de, Kaneko TM, Young MCM, Murakami C, Cordeiro I, Moreno PRH. Chemical composition, antimicrobial and antioxidant activities of eugenia dysenterica DC essential oil [Internet]. Emerging Science Journal. 2018 ; 2( 6): 410-416.[citado 2024 maio 26 ] Available from: https://doi.org/10.28991/esj-2018-01160
Trabalho de evento-resumo
3-Alkenyltyrosines accessed by suzukim Miyaura coupling: a key Intermediate in the synthesis and mechanistic study of povarov multicomponent reactions (2017)
Vasconcelos, Stanley Nunes Siqueira; Silva, Vitor Hugo Menezes da; Braga, Ataualpa Albert Carmo ; Pimenta, Daniel Carvalho; Stefani, Hélio Alexandre
Fonte: Abstracts. Nome do evento: Tetrahedron Symposium - New Development in Organic Chemistry. Unidades: IQ, FCF
Assuntos: SÍNTESE ORGÂNICA, COMPOSTOS ORGÂNICOS
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
VASCONCELOS, Stanley Nunes Siqueira et al. 3-Alkenyltyrosines accessed by suzukim Miyaura coupling: a key Intermediate in the synthesis and mechanistic study of povarov multicomponent reactions. 2017, Anais.. Budapest: Elsevier, 2017. . Acesso em: 26 maio 2024.
APA
Vasconcelos, S. N. S., Silva, V. H. M. da, Braga, A. A. C., Pimenta, D. C., & Stefani, H. A. (2017). 3-Alkenyltyrosines accessed by suzukim Miyaura coupling: a key Intermediate in the synthesis and mechanistic study of povarov multicomponent reactions. In Abstracts. Budapest: Elsevier.
NLM
Vasconcelos SNS, Silva VHM da, Braga AAC, Pimenta DC, Stefani HA. 3-Alkenyltyrosines accessed by suzukim Miyaura coupling: a key Intermediate in the synthesis and mechanistic study of povarov multicomponent reactions. Abstracts. 2017 ;[citado 2024 maio 26 ]
Vancouver
Vasconcelos SNS, Silva VHM da, Braga AAC, Pimenta DC, Stefani HA. 3-Alkenyltyrosines accessed by suzukim Miyaura coupling: a key Intermediate in the synthesis and mechanistic study of povarov multicomponent reactions. Abstracts. 2017 ;[citado 2024 maio 26 ]
Artigo de periodico
Synthesis of a tyr-tyr peptide library and fluorescence of the stilbenyl derivatives (2016)
Vasconcelos, Stanley Nunes Siqueira; Rodrigues, Ana Clara Beltran; Bastos, Erick Leite ; Stefani, Hélio Alexandre
Fonte: Chemistry Select. Unidades: IQ, FCF
Assuntos: FLUORESCÊNCIA, PEPTÍDEOS
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
VASCONCELOS, Stanley Nunes Siqueira et al. Synthesis of a tyr-tyr peptide library and fluorescence of the stilbenyl derivatives. Chemistry Select, v. 1, n. 6, p. 1287-1291, 2016Tradução . . Disponível em: https://doi.org/10.1002/slct.201600319. Acesso em: 26 maio 2024.
APA
Vasconcelos, S. N. S., Rodrigues, A. C. B., Bastos, E. L., & Stefani, H. A. (2016). Synthesis of a tyr-tyr peptide library and fluorescence of the stilbenyl derivatives. Chemistry Select, 1( 6), 1287-1291. doi:10.1002/slct.201600319
NLM
Vasconcelos SNS, Rodrigues ACB, Bastos EL, Stefani HA. Synthesis of a tyr-tyr peptide library and fluorescence of the stilbenyl derivatives [Internet]. Chemistry Select. 2016 ; 1( 6): 1287-1291.[citado 2024 maio 26 ] Available from: https://doi.org/10.1002/slct.201600319
Vancouver
Vasconcelos SNS, Rodrigues ACB, Bastos EL, Stefani HA. Synthesis of a tyr-tyr peptide library and fluorescence of the stilbenyl derivatives [Internet]. Chemistry Select. 2016 ; 1( 6): 1287-1291.[citado 2024 maio 26 ] Available from: https://doi.org/10.1002/slct.201600319
Artigo de periodico
Thermoanalytical characterization study of hair from different ethnicities (2016)
Lima, Cibele Rosana Ribeiro de Castro; Almeida, Mariana Mandelli de; Velasco, Maria Valéria Robles ; Matos, Jivaldo do Rosário
Fonte: Journal of Thermal Analysis and Calorimetry. Unidades: FCF, IQ
Assuntos: CABELO, ANÁLISE TÉRMICA, IDENTIDADE ÉTNICA
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
LIMA, Cibele Rosana Ribeiro de Castro et al. Thermoanalytical characterization study of hair from different ethnicities. Journal of Thermal Analysis and Calorimetry, v. 123, n. 3, p. 2321-2328, 2016Tradução . . Disponível em: https://doi.org/10.1007/s10973-015-5070-6. Acesso em: 26 maio 2024.
APA
Lima, C. R. R. de C., Almeida, M. M. de, Velasco, M. V. R., & Matos, J. do R. (2016). Thermoanalytical characterization study of hair from different ethnicities. Journal of Thermal Analysis and Calorimetry, 123( 3), 2321-2328. doi:10.1007/s10973-015-5070-6
NLM
Lima CRR de C, Almeida MM de, Velasco MVR, Matos J do R. Thermoanalytical characterization study of hair from different ethnicities [Internet]. Journal of Thermal Analysis and Calorimetry. 2016 ; 123( 3): 2321-2328.[citado 2024 maio 26 ] Available from: https://doi.org/10.1007/s10973-015-5070-6
Vancouver
Lima CRR de C, Almeida MM de, Velasco MVR, Matos J do R. Thermoanalytical characterization study of hair from different ethnicities [Internet]. Journal of Thermal Analysis and Calorimetry. 2016 ; 123( 3): 2321-2328.[citado 2024 maio 26 ] Available from: https://doi.org/10.1007/s10973-015-5070-6

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