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Artigo de periodico
Effect of cis-9, trans-11 conjugated linoleic acid (CLA) on the metabolism profile of breast cancer cells determined by 1H HR-MAS NMR spectroscopy (2019)
Maria, Roberta M.; Altei, Wanessa F.; Valadares, Napoleão F.; Garratt, Richard Charles; Andricopulo, Adriano Defini; Venâncio, Tiago; Colnago, Luiz A.
Source: Journal of the Brazilian Chemical Society. Unidade: IFSC
Subjects: NEOPLASIAS MAMÁRIAS, CRISTALOGRAFIA FÍSICA, RESSONÂNCIA MAGNÉTICA NUCLEAR
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ABNT
MARIA, Roberta M. et al. Effect of cis-9, trans-11 conjugated linoleic acid (CLA) on the metabolism profile of breast cancer cells determined by 1H HR-MAS NMR spectroscopy. Journal of the Brazilian Chemical Society, v. 30, n. 1, p. 3-7, 2019Tradução . . Disponível em: https://doi.org/10.21577/0103-5053.20180200. Acesso em: 13 set. 2024.
APA
Maria, R. M., Altei, W. F., Valadares, N. F., Garratt, R. C., Andricopulo, A. D., Venâncio, T., & Colnago, L. A. (2019). Effect of cis-9, trans-11 conjugated linoleic acid (CLA) on the metabolism profile of breast cancer cells determined by 1H HR-MAS NMR spectroscopy. Journal of the Brazilian Chemical Society, 30( 1), 3-7. doi:10.21577/0103-5053.20180200
NLM
Maria RM, Altei WF, Valadares NF, Garratt RC, Andricopulo AD, Venâncio T, Colnago LA. Effect of cis-9, trans-11 conjugated linoleic acid (CLA) on the metabolism profile of breast cancer cells determined by 1H HR-MAS NMR spectroscopy [Internet]. Journal of the Brazilian Chemical Society. 2019 ; 30( 1): 3-7.[citado 2024 set. 13 ] Available from: https://doi.org/10.21577/0103-5053.20180200
Vancouver
Maria RM, Altei WF, Valadares NF, Garratt RC, Andricopulo AD, Venâncio T, Colnago LA. Effect of cis-9, trans-11 conjugated linoleic acid (CLA) on the metabolism profile of breast cancer cells determined by 1H HR-MAS NMR spectroscopy [Internet]. Journal of the Brazilian Chemical Society. 2019 ; 30( 1): 3-7.[citado 2024 set. 13 ] Available from: https://doi.org/10.21577/0103-5053.20180200
Artigo de periodico
Linear peptide analogues from Jatropha's orbitides promote migration of human neonatal foreskin fibroblasts in vitro and collagen deposition (2019)
Ramalho, Suelem D.; Pinto, Meri Emili F.; Andricopulo, Renata Krogh; Sanches, Paulo R. S.; Silveira, Edilberto R.; Cilli, Eduardo M.; Andricopulo, Adriano Defini ; Bolzani, Vanderlan S.
Source: Journal of the Brazilian Chemical Society. Unidade: IFSC
Subjects: FIBROBLASTOS, PEPTÍDEOS, PLANEJAMENTO DE FÁRMACOS
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ABNT
RAMALHO, Suelem D. et al. Linear peptide analogues from Jatropha's orbitides promote migration of human neonatal foreskin fibroblasts in vitro and collagen deposition. Journal of the Brazilian Chemical Society, v. 30, n. 10, p. 2153-2161, 2019Tradução . . Disponível em: https://doi.org/10.21577/0103-5053.20190102. Acesso em: 13 set. 2024.
APA
Ramalho, S. D., Pinto, M. E. F., Andricopulo, R. K., Sanches, P. R. S., Silveira, E. R., Cilli, E. M., et al. (2019). Linear peptide analogues from Jatropha's orbitides promote migration of human neonatal foreskin fibroblasts in vitro and collagen deposition. Journal of the Brazilian Chemical Society, 30( 10), 2153-2161. doi:10.21577/0103-5053.20190102
NLM
Ramalho SD, Pinto MEF, Andricopulo RK, Sanches PRS, Silveira ER, Cilli EM, Andricopulo AD, Bolzani VS. Linear peptide analogues from Jatropha's orbitides promote migration of human neonatal foreskin fibroblasts in vitro and collagen deposition [Internet]. Journal of the Brazilian Chemical Society. 2019 ; 30( 10): 2153-2161.[citado 2024 set. 13 ] Available from: https://doi.org/10.21577/0103-5053.20190102
Vancouver
Ramalho SD, Pinto MEF, Andricopulo RK, Sanches PRS, Silveira ER, Cilli EM, Andricopulo AD, Bolzani VS. Linear peptide analogues from Jatropha's orbitides promote migration of human neonatal foreskin fibroblasts in vitro and collagen deposition [Internet]. Journal of the Brazilian Chemical Society. 2019 ; 30( 10): 2153-2161.[citado 2024 set. 13 ] Available from: https://doi.org/10.21577/0103-5053.20190102
Artigo de periodico-carta/editorial
Sustainability and diversity through chemistry: together, we made that happen. [Editorial] (2018)
Andricopulo, Adriano Defini; Zarbin, Aldo J. G.
Source: Journal of the Brazilian Chemical Society. Unidade: IFSC
Subjects: QUÍMICA, EVENTOS, SUSTENTABILIDADE
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ABNT
ANDRICOPULO, Adriano Defini e ZARBIN, Aldo J. G. Sustainability and diversity through chemistry: together, we made that happen. [Editorial]. Journal of the Brazilian Chemical Society. São Paulo: Instituto de Física de São Carlos, Universidade de São Paulo. Disponível em: https://doi.org/10.21577/0103-5053.20180050. Acesso em: 13 set. 2024. , 2018
APA
Andricopulo, A. D., & Zarbin, A. J. G. (2018). Sustainability and diversity through chemistry: together, we made that happen. [Editorial]. Journal of the Brazilian Chemical Society. São Paulo: Instituto de Física de São Carlos, Universidade de São Paulo. doi:10.21577/0103-5053.20180050
NLM
Andricopulo AD, Zarbin AJG. Sustainability and diversity through chemistry: together, we made that happen. [Editorial] [Internet]. Journal of the Brazilian Chemical Society. 2018 ; 29( 5): 895.[citado 2024 set. 13 ] Available from: https://doi.org/10.21577/0103-5053.20180050
Vancouver
Andricopulo AD, Zarbin AJG. Sustainability and diversity through chemistry: together, we made that happen. [Editorial] [Internet]. Journal of the Brazilian Chemical Society. 2018 ; 29( 5): 895.[citado 2024 set. 13 ] Available from: https://doi.org/10.21577/0103-5053.20180050
Artigo de periodico
Synthetic analogue of the natural product piperlongumine as a potent inhibitor of breast cancer cell line migration (2017)
Valli, Marilia; Altei, Wanessa; Santos, Ricardo N.; Lucca Junior, Emilio C.; Dessoy, Marco A.; Pioli, Renan M.; Cotinguiba, Fernando; Cachet, Xavier; Michel, Sylvie; Furlan, Maysa; Dias, Luiz C.; Andricopulo, Adriano Defini; Bolzani, Vanderlan S.
Source: Journal of the Brazilian Chemical Society. Unidade: IFSC
Subjects: NEOPLASIAS MAMÁRIAS, CITOTOXINAS, METÁSTASE NEOPLÁSICA
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ABNT
VALLI, Marilia et al. Synthetic analogue of the natural product piperlongumine as a potent inhibitor of breast cancer cell line migration. Journal of the Brazilian Chemical Society, v. 28, n. 3, p. 475-484, 2017Tradução . . Disponível em: https://doi.org/10.21577/0103-5053.20160303. Acesso em: 13 set. 2024.
APA
Valli, M., Altei, W., Santos, R. N., Lucca Junior, E. C., Dessoy, M. A., Pioli, R. M., et al. (2017). Synthetic analogue of the natural product piperlongumine as a potent inhibitor of breast cancer cell line migration. Journal of the Brazilian Chemical Society, 28( 3), 475-484. doi:10.21577/0103-5053.20160303
NLM
Valli M, Altei W, Santos RN, Lucca Junior EC, Dessoy MA, Pioli RM, Cotinguiba F, Cachet X, Michel S, Furlan M, Dias LC, Andricopulo AD, Bolzani VS. Synthetic analogue of the natural product piperlongumine as a potent inhibitor of breast cancer cell line migration [Internet]. Journal of the Brazilian Chemical Society. 2017 ; 28( 3): 475-484.[citado 2024 set. 13 ] Available from: https://doi.org/10.21577/0103-5053.20160303
Vancouver
Valli M, Altei W, Santos RN, Lucca Junior EC, Dessoy MA, Pioli RM, Cotinguiba F, Cachet X, Michel S, Furlan M, Dias LC, Andricopulo AD, Bolzani VS. Synthetic analogue of the natural product piperlongumine as a potent inhibitor of breast cancer cell line migration [Internet]. Journal of the Brazilian Chemical Society. 2017 ; 28( 3): 475-484.[citado 2024 set. 13 ] Available from: https://doi.org/10.21577/0103-5053.20160303
Artigo de periodico-carta/editorial
Sustainability and diversity through chemistry. [Editorial] (2016)
Andricopulo, Adriano Defini; Catalani, Luiz Henrique
Source: Journal of the Brazilian Chemical Society. Unidades: IFSC, IQ
Subjects: QUÍMICA, EVENTOS, SUSTENTABILIDADE
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ABNT
ANDRICOPULO, Adriano Defini e CATALANI, Luiz Henrique. Sustainability and diversity through chemistry. [Editorial]. Journal of the Brazilian Chemical Society. São Paulo: Instituto de Física de São Carlos, Universidade de São Paulo. Disponível em: https://doi.org/10.5935/0103-5053.20160127. Acesso em: 13 set. 2024. , 2016
APA
Andricopulo, A. D., & Catalani, L. H. (2016). Sustainability and diversity through chemistry. [Editorial]. Journal of the Brazilian Chemical Society. São Paulo: Instituto de Física de São Carlos, Universidade de São Paulo. doi:10.5935/0103-5053.20160127
NLM
Andricopulo AD, Catalani LH. Sustainability and diversity through chemistry. [Editorial] [Internet]. Journal of the Brazilian Chemical Society. 2016 ; 27( 5): 807-808.[citado 2024 set. 13 ] Available from: https://doi.org/10.5935/0103-5053.20160127
Vancouver
Andricopulo AD, Catalani LH. Sustainability and diversity through chemistry. [Editorial] [Internet]. Journal of the Brazilian Chemical Society. 2016 ; 27( 5): 807-808.[citado 2024 set. 13 ] Available from: https://doi.org/10.5935/0103-5053.20160127
Artigo de periodico
Structure-based drug design studies on a series of aldolase inhibitors (2013)
Ferreira, Leonardo Luiz Gomes ; Santos, Ricardo N.; Andricopulo, Adriano Defini
Source: Journal of the Brazilian Chemical Society. Unidade: IFSC
Subjects: TRYPANOSOMA, ENZIMAS, PLANEJAMENTO DE FÁRMACOS
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ABNT
FERREIRA, Leonardo Luiz Gomes e SANTOS, Ricardo N. e ANDRICOPULO, Adriano Defini. Structure-based drug design studies on a series of aldolase inhibitors. Journal of the Brazilian Chemical Society, v. 24, n. 2, p. 201-211, 2013Tradução . . Disponível em: https://doi.org/10.5935/0103-5053.20130026. Acesso em: 13 set. 2024.
APA
Ferreira, L. L. G., Santos, R. N., & Andricopulo, A. D. (2013). Structure-based drug design studies on a series of aldolase inhibitors. Journal of the Brazilian Chemical Society, 24( 2), 201-211. doi:10.5935/0103-5053.20130026
NLM
Ferreira LLG, Santos RN, Andricopulo AD. Structure-based drug design studies on a series of aldolase inhibitors [Internet]. Journal of the Brazilian Chemical Society. 2013 ; 24( 2): 201-211.[citado 2024 set. 13 ] Available from: https://doi.org/10.5935/0103-5053.20130026
Vancouver
Ferreira LLG, Santos RN, Andricopulo AD. Structure-based drug design studies on a series of aldolase inhibitors [Internet]. Journal of the Brazilian Chemical Society. 2013 ; 24( 2): 201-211.[citado 2024 set. 13 ] Available from: https://doi.org/10.5935/0103-5053.20130026
Artigo de periodico
A fragment-based approach for the in silico prediction of blood-brain barrier permeation (2012)
Moda, Tiago L.; Carrara, Alexandre E.; Andricopulo, Adriano Defini
Source: Journal of the Brazilian Chemical Society. Unidade: IFSC
Subjects: PLANEJAMENTO DE FÁRMACOS, SISTEMA NERVOSO CENTRAL, FARMACOCINÉTICA
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ABNT
MODA, Tiago L. e CARRARA, Alexandre E. e ANDRICOPULO, Adriano Defini. A fragment-based approach for the in silico prediction of blood-brain barrier permeation. Journal of the Brazilian Chemical Society, v. 23, n. 12, p. 2191-2196, 2012Tradução . . Disponível em: https://doi.org/10.1590/S0103-50532013005000001. Acesso em: 13 set. 2024.
APA
Moda, T. L., Carrara, A. E., & Andricopulo, A. D. (2012). A fragment-based approach for the in silico prediction of blood-brain barrier permeation. Journal of the Brazilian Chemical Society, 23( 12), 2191-2196. doi:10.1590/S0103-50532013005000001
NLM
Moda TL, Carrara AE, Andricopulo AD. A fragment-based approach for the in silico prediction of blood-brain barrier permeation [Internet]. Journal of the Brazilian Chemical Society. 2012 ; 23( 12): 2191-2196.[citado 2024 set. 13 ] Available from: https://doi.org/10.1590/S0103-50532013005000001
Vancouver
Moda TL, Carrara AE, Andricopulo AD. A fragment-based approach for the in silico prediction of blood-brain barrier permeation [Internet]. Journal of the Brazilian Chemical Society. 2012 ; 23( 12): 2191-2196.[citado 2024 set. 13 ] Available from: https://doi.org/10.1590/S0103-50532013005000001
Artigo de periodico-carta/editorial
G-Protein-Coupled Receptors: the 2012 Nobel Prize in Chemistry. [Editorial] (2012)
Andricopulo, Adriano Defini; Oliva, Glaucius
Source: Journal of the Brazilian Chemical Society. Unidade: IFSC
Subjects: RECEPTORES, PROTEÍNAS, QUÍMICA (PESQUISA)
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ABNT
ANDRICOPULO, Adriano Defini e OLIVA, Glaucius. G-Protein-Coupled Receptors: the 2012 Nobel Prize in Chemistry. [Editorial]. Journal of the Brazilian Chemical Society. São Paulo: Instituto de Física de São Carlos, Universidade de São Paulo. Disponível em: https://doi.org/10.1590/S0103-50532012001000001. Acesso em: 13 set. 2024. , 2012
APA
Andricopulo, A. D., & Oliva, G. (2012). G-Protein-Coupled Receptors: the 2012 Nobel Prize in Chemistry. [Editorial]. Journal of the Brazilian Chemical Society. São Paulo: Instituto de Física de São Carlos, Universidade de São Paulo. doi:10.1590/S0103-50532012001000001
NLM
Andricopulo AD, Oliva G. G-Protein-Coupled Receptors: the 2012 Nobel Prize in Chemistry. [Editorial] [Internet]. Journal of the Brazilian Chemical Society. 2012 ; 23( 10): 1769-1770.[citado 2024 set. 13 ] Available from: https://doi.org/10.1590/S0103-50532012001000001
Vancouver
Andricopulo AD, Oliva G. G-Protein-Coupled Receptors: the 2012 Nobel Prize in Chemistry. [Editorial] [Internet]. Journal of the Brazilian Chemical Society. 2012 ; 23( 10): 1769-1770.[citado 2024 set. 13 ] Available from: https://doi.org/10.1590/S0103-50532012001000001
Artigo de periodico
Descriptor and fragment-based QSAR models for a series of Schistosoma mansoni purine nucleoside inhibitors (2011)
Freitas, Humberto F.; Postigo, Matheus P.; Andricopulo, Adriano Defini; Castilho, Marcelo S.
Source: Journal of the Brazilian Chemical Society. Unidade: IFSC
Subjects: ENZIMAS (ESTUDO), FÁRMACOS (PESQUISA), INIBIDORES DE ENZIMAS
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ABNT
FREITAS, Humberto F. et al. Descriptor and fragment-based QSAR models for a series of Schistosoma mansoni purine nucleoside inhibitors. Journal of the Brazilian Chemical Society, v. 22, n. 9, p. 1718-1726, 2011Tradução . . Disponível em: https://doi.org/10.1590/S0103-50532011000900014. Acesso em: 13 set. 2024.
APA
Freitas, H. F., Postigo, M. P., Andricopulo, A. D., & Castilho, M. S. (2011). Descriptor and fragment-based QSAR models for a series of Schistosoma mansoni purine nucleoside inhibitors. Journal of the Brazilian Chemical Society, 22( 9), 1718-1726. doi:10.1590/S0103-50532011000900014
NLM
Freitas HF, Postigo MP, Andricopulo AD, Castilho MS. Descriptor and fragment-based QSAR models for a series of Schistosoma mansoni purine nucleoside inhibitors [Internet]. Journal of the Brazilian Chemical Society. 2011 ; 22( 9): 1718-1726.[citado 2024 set. 13 ] Available from: https://doi.org/10.1590/S0103-50532011000900014
Vancouver
Freitas HF, Postigo MP, Andricopulo AD, Castilho MS. Descriptor and fragment-based QSAR models for a series of Schistosoma mansoni purine nucleoside inhibitors [Internet]. Journal of the Brazilian Chemical Society. 2011 ; 22( 9): 1718-1726.[citado 2024 set. 13 ] Available from: https://doi.org/10.1590/S0103-50532011000900014
Artigo de periodico
Enzyme kinetics, structural analysis and molecular modeling studies on a series of schistosoma mansoni PNP inhibitors (2011)
Postigo, Matheus P.; Krogh, Renata; Terni, Marcela F.; Pereira, Humberto D'Muniz; Oliva, Glaucius; Castilho, Marcelo S.; Andricopulo, Adriano Defini
Source: Journal of the Brazilian Chemical Society. Unidade: IFSC
Subjects: INIBIDORES DE ENZIMAS, PLANEJAMENTO DE FÁRMACOS, SCHISTOSOMA MANSONI, NUCLEOSÍDEOS, ESQUISTOSSOMOSE (TRATAMENTO)
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ABNT
POSTIGO, Matheus P. et al. Enzyme kinetics, structural analysis and molecular modeling studies on a series of schistosoma mansoni PNP inhibitors. Journal of the Brazilian Chemical Society, v. 22, n. 3, p. 583-591, 2011Tradução . . Disponível em: https://doi.org/10.1590/S0103-50532011000300024. Acesso em: 13 set. 2024.
APA
Postigo, M. P., Krogh, R., Terni, M. F., Pereira, H. D. 'M., Oliva, G., Castilho, M. S., & Andricopulo, A. D. (2011). Enzyme kinetics, structural analysis and molecular modeling studies on a series of schistosoma mansoni PNP inhibitors. Journal of the Brazilian Chemical Society, 22( 3), 583-591. doi:10.1590/S0103-50532011000300024
NLM
Postigo MP, Krogh R, Terni MF, Pereira HD'M, Oliva G, Castilho MS, Andricopulo AD. Enzyme kinetics, structural analysis and molecular modeling studies on a series of schistosoma mansoni PNP inhibitors [Internet]. Journal of the Brazilian Chemical Society. 2011 ; 22( 3): 583-591.[citado 2024 set. 13 ] Available from: https://doi.org/10.1590/S0103-50532011000300024
Vancouver
Postigo MP, Krogh R, Terni MF, Pereira HD'M, Oliva G, Castilho MS, Andricopulo AD. Enzyme kinetics, structural analysis and molecular modeling studies on a series of schistosoma mansoni PNP inhibitors [Internet]. Journal of the Brazilian Chemical Society. 2011 ; 22( 3): 583-591.[citado 2024 set. 13 ] Available from: https://doi.org/10.1590/S0103-50532011000300024
Artigo de periodico
Biochemical evaluation of a series of synthetic chalcone and hydrazide derivatives as novel inhibitors of cruzain from Trypanosoma cruzi (2010)
Borchhardt, Deise M.; Mascarello, Alessandra; Chiaradia, Louise Domeneghini; Nunes, Ricardo J.; Oliva, Glaucius; Yunes, Rosendo A.; Andricopulo, Adriano Defini
Source: Journal of the Brazilian Chemical Society. Unidade: IFSC
Subjects: INIBIDORES DE ENZIMAS, TRYPANOSOMA CRUZI (ESTUDO), COMPOSTOS DE OXIGÊNIO, DOENÇA DE CHAGAS (CONTROLE;TRATAMENTO)
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ABNT
BORCHHARDT, Deise M. et al. Biochemical evaluation of a series of synthetic chalcone and hydrazide derivatives as novel inhibitors of cruzain from Trypanosoma cruzi. Journal of the Brazilian Chemical Society, v. 21, n. 1, p. 142-150, 2010Tradução . . Disponível em: https://doi.org/10.1590/S0103-50532010000100021. Acesso em: 13 set. 2024.
APA
Borchhardt, D. M., Mascarello, A., Chiaradia, L. D., Nunes, R. J., Oliva, G., Yunes, R. A., & Andricopulo, A. D. (2010). Biochemical evaluation of a series of synthetic chalcone and hydrazide derivatives as novel inhibitors of cruzain from Trypanosoma cruzi. Journal of the Brazilian Chemical Society, 21( 1), 142-150. doi:10.1590/S0103-50532010000100021
NLM
Borchhardt DM, Mascarello A, Chiaradia LD, Nunes RJ, Oliva G, Yunes RA, Andricopulo AD. Biochemical evaluation of a series of synthetic chalcone and hydrazide derivatives as novel inhibitors of cruzain from Trypanosoma cruzi [Internet]. Journal of the Brazilian Chemical Society. 2010 ; 21( 1): 142-150.[citado 2024 set. 13 ] Available from: https://doi.org/10.1590/S0103-50532010000100021
Vancouver
Borchhardt DM, Mascarello A, Chiaradia LD, Nunes RJ, Oliva G, Yunes RA, Andricopulo AD. Biochemical evaluation of a series of synthetic chalcone and hydrazide derivatives as novel inhibitors of cruzain from Trypanosoma cruzi [Internet]. Journal of the Brazilian Chemical Society. 2010 ; 21( 1): 142-150.[citado 2024 set. 13 ] Available from: https://doi.org/10.1590/S0103-50532010000100021
Artigo de periodico
Structural insights into the molecular basis responsible for the effects of immobilization on the kinetic parameters of glyceraldehyde-3-phosphate dehydrogenase from Trypanosoma cruzi and human (2010)
Guido, Rafael Victorio Carvalho ; Cardoso, Cármen Lúcia; Moraes, Marcela C. de; Andricopulo, Adriano Defini; Cass, Quezia B.; Oliva, Glaucius
Source: Journal of the Brazilian Chemical Society. Unidades: IFSC, FFCLRP
Subjects: FÁRMACOS (DESENVOLVIMENTO), TRYPANOSOMA CRUZI, ENZIMAS, PLANEJAMENTO DE FÁRMACOS, IMOBILIZAÇÃO, CINÉTICA (PARÂMETROS)
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ABNT
GUIDO, Rafael Victorio Carvalho et al. Structural insights into the molecular basis responsible for the effects of immobilization on the kinetic parameters of glyceraldehyde-3-phosphate dehydrogenase from Trypanosoma cruzi and human. Journal of the Brazilian Chemical Society, v. 21, n. 10, p. 1845-1853, 2010Tradução . . Disponível em: https://doi.org/10.1590/s0103-50532010001000008. Acesso em: 13 set. 2024.
APA
Guido, R. V. C., Cardoso, C. L., Moraes, M. C. de, Andricopulo, A. D., Cass, Q. B., & Oliva, G. (2010). Structural insights into the molecular basis responsible for the effects of immobilization on the kinetic parameters of glyceraldehyde-3-phosphate dehydrogenase from Trypanosoma cruzi and human. Journal of the Brazilian Chemical Society, 21( 10), 1845-1853. doi:10.1590/s0103-50532010001000008
NLM
Guido RVC, Cardoso CL, Moraes MC de, Andricopulo AD, Cass QB, Oliva G. Structural insights into the molecular basis responsible for the effects of immobilization on the kinetic parameters of glyceraldehyde-3-phosphate dehydrogenase from Trypanosoma cruzi and human [Internet]. Journal of the Brazilian Chemical Society. 2010 ; 21( 10): 1845-1853.[citado 2024 set. 13 ] Available from: https://doi.org/10.1590/s0103-50532010001000008
Vancouver
Guido RVC, Cardoso CL, Moraes MC de, Andricopulo AD, Cass QB, Oliva G. Structural insights into the molecular basis responsible for the effects of immobilization on the kinetic parameters of glyceraldehyde-3-phosphate dehydrogenase from Trypanosoma cruzi and human [Internet]. Journal of the Brazilian Chemical Society. 2010 ; 21( 10): 1845-1853.[citado 2024 set. 13 ] Available from: https://doi.org/10.1590/s0103-50532010001000008
Artigo de periodico
A new bianthron glycoside as inhibitor of Trypanosoma cruzi glyceraldehyde 3-phosphate dehydrogenase activity (2009)
Macedo, Edângelo M. S.; Wiggers, Helton J.; Silva, Maria G. V.; Braz Filho, Raimundo; Andricopulo, Adriano Defini; Montanari, Carlos Alberto
Source: Journal of the Brazilian Chemical Society. Unidades: IFSC, IQSC
Subjects: ENZIMAS (ESTUDO), ESPECTROSCOPIA, TRYPANOSOMA CRUZI, PLANEJAMENTO DE FÁRMACOS, DOENÇA DE CHAGAS, CRISTALOGRAFIA
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ABNT
MACEDO, Edângelo M. S. et al. A new bianthron glycoside as inhibitor of Trypanosoma cruzi glyceraldehyde 3-phosphate dehydrogenase activity. Journal of the Brazilian Chemical Society, v. 20, n. 5, p. 947-953, 2009Tradução . . Disponível em: https://doi.org/10.1590/s0103-50532009000500021. Acesso em: 13 set. 2024.
APA
Macedo, E. M. S., Wiggers, H. J., Silva, M. G. V., Braz Filho, R., Andricopulo, A. D., & Montanari, C. A. (2009). A new bianthron glycoside as inhibitor of Trypanosoma cruzi glyceraldehyde 3-phosphate dehydrogenase activity. Journal of the Brazilian Chemical Society, 20( 5), 947-953. doi:10.1590/s0103-50532009000500021
NLM
Macedo EMS, Wiggers HJ, Silva MGV, Braz Filho R, Andricopulo AD, Montanari CA. A new bianthron glycoside as inhibitor of Trypanosoma cruzi glyceraldehyde 3-phosphate dehydrogenase activity [Internet]. Journal of the Brazilian Chemical Society. 2009 ; 20( 5): 947-953.[citado 2024 set. 13 ] Available from: https://doi.org/10.1590/s0103-50532009000500021
Vancouver
Macedo EMS, Wiggers HJ, Silva MGV, Braz Filho R, Andricopulo AD, Montanari CA. A new bianthron glycoside as inhibitor of Trypanosoma cruzi glyceraldehyde 3-phosphate dehydrogenase activity [Internet]. Journal of the Brazilian Chemical Society. 2009 ; 20( 5): 947-953.[citado 2024 set. 13 ] Available from: https://doi.org/10.1590/s0103-50532009000500021
Artigo de periodico
Structural and chemical basis for anticancer activity of a series of beta-tubulin ligands: molecular modeling and 3D QSAR studies (2009)
Salum, Lívia B.; Dias, Luiz C.; Andricopulo, Adriano Defini
Source: Journal of the Brazilian Chemical Society. Unidade: IFSC
Subjects: ESTRUTURA MOLECULAR, PLANEJAMENTO DE FÁRMACOS, PROTEÍNAS, MICROTÚBULOS, NEOPLASIAS (TRATAMENTO), MODELOS, RELAÇÕES QUANTITATIVAS ENTRE ESTRUTURA QUÍMICA E ATIVIDADE BIOLÓGICA
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ABNT
SALUM, Lívia B. e DIAS, Luiz C. e ANDRICOPULO, Adriano Defini. Structural and chemical basis for anticancer activity of a series of beta-tubulin ligands: molecular modeling and 3D QSAR studies. Journal of the Brazilian Chemical Society, v. 20, n. 4, p. 693-703, 2009Tradução . . Disponível em: https://doi.org/10.1590/S0103-50532009000400013. Acesso em: 13 set. 2024.
APA
Salum, L. B., Dias, L. C., & Andricopulo, A. D. (2009). Structural and chemical basis for anticancer activity of a series of beta-tubulin ligands: molecular modeling and 3D QSAR studies. Journal of the Brazilian Chemical Society, 20( 4), 693-703. doi:10.1590/S0103-50532009000400013
NLM
Salum LB, Dias LC, Andricopulo AD. Structural and chemical basis for anticancer activity of a series of beta-tubulin ligands: molecular modeling and 3D QSAR studies [Internet]. Journal of the Brazilian Chemical Society. 2009 ; 20( 4): 693-703.[citado 2024 set. 13 ] Available from: https://doi.org/10.1590/S0103-50532009000400013
Vancouver
Salum LB, Dias LC, Andricopulo AD. Structural and chemical basis for anticancer activity of a series of beta-tubulin ligands: molecular modeling and 3D QSAR studies [Internet]. Journal of the Brazilian Chemical Society. 2009 ; 20( 4): 693-703.[citado 2024 set. 13 ] Available from: https://doi.org/10.1590/S0103-50532009000400013
Artigo de periodico
Synthesis, screening for antiacetylcholinesterase activity and binding mode prediction of a new series of [3-(disubstituted-phosphate)-4,4,4-trifluoro-butyl] -carbamic acid ethyl esters (2008)
Zanatta, Nilo; Borchhardt, Deise M.; Carpes, Adriana D.; Marchi, Tiago, M.; Andricopulo, Adriano Defini; Salum, Lívia; Schetinger, Maria R. C.; Bonacorso, Helio G.; Martins, Marcos A. P.; Flores, Alex F. C.
Source: Journal of the Brazilian Chemical Society. Unidade: IFSC
Subjects: FOSFATOS, PLANEJAMENTO DE FÁRMACOS
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
ZANATTA, Nilo et al. Synthesis, screening for antiacetylcholinesterase activity and binding mode prediction of a new series of [3-(disubstituted-phosphate)-4,4,4-trifluoro-butyl] -carbamic acid ethyl esters. Journal of the Brazilian Chemical Society, v. 19, n. 6, p. 1118-1124, 2008Tradução . . Disponível em: https://doi.org/10.1590/s0103-50532008000600010. Acesso em: 13 set. 2024.
APA
Zanatta, N., Borchhardt, D. M., Carpes, A. D., Marchi, T., Andricopulo, A. D., Salum, L., et al. (2008). Synthesis, screening for antiacetylcholinesterase activity and binding mode prediction of a new series of [3-(disubstituted-phosphate)-4,4,4-trifluoro-butyl] -carbamic acid ethyl esters. Journal of the Brazilian Chemical Society, 19( 6), 1118-1124. doi:10.1590/s0103-50532008000600010
NLM
Zanatta N, Borchhardt DM, Carpes AD, Marchi T, Andricopulo AD, Salum L, Schetinger MRC, Bonacorso HG, Martins MAP, Flores AFC. Synthesis, screening for antiacetylcholinesterase activity and binding mode prediction of a new series of [3-(disubstituted-phosphate)-4,4,4-trifluoro-butyl] -carbamic acid ethyl esters [Internet]. Journal of the Brazilian Chemical Society. 2008 ; 19( 6): 1118-1124.[citado 2024 set. 13 ] Available from: https://doi.org/10.1590/s0103-50532008000600010
Vancouver
Zanatta N, Borchhardt DM, Carpes AD, Marchi T, Andricopulo AD, Salum L, Schetinger MRC, Bonacorso HG, Martins MAP, Flores AFC. Synthesis, screening for antiacetylcholinesterase activity and binding mode prediction of a new series of [3-(disubstituted-phosphate)-4,4,4-trifluoro-butyl] -carbamic acid ethyl esters [Internet]. Journal of the Brazilian Chemical Society. 2008 ; 19( 6): 1118-1124.[citado 2024 set. 13 ] Available from: https://doi.org/10.1590/s0103-50532008000600010

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