ReP USP - Resultado da busca

Artigo de periodico
Coordination of nitro-thiosemicarbazones to ruthenium(II) as a strategy for anti-trypanosomal activity improvement (2010)
Rodrigues, Claudia; Batista, Alzir A.; Ellena, Javier; Castellano, Eduardo Ernesto; Benítez, Diego; Cerecetto, Hugo; González, Mercedes; Teixeira, Letícia R.; Beraldo, Heloisa
Fonte: European Journal of Medicinal Chemistry. Unidade: IFSC
Assuntos: TRYPANOSOMA CRUZI (CONTROLE), PLANEJAMENTO DE FÁRMACOS, RUTÊNIO, LIGANTES, DOENÇAS PARASITÁRIAS
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
RODRIGUES, Claudia et al. Coordination of nitro-thiosemicarbazones to ruthenium(II) as a strategy for anti-trypanosomal activity improvement. European Journal of Medicinal Chemistry, v. 45, n. 7, p. 2847-2853, 2010Tradução . . Disponível em: https://doi.org/10.1016/j.ejmech.2010.03.005. Acesso em: 25 jun. 2024.
APA
Rodrigues, C., Batista, A. A., Ellena, J., Castellano, E. E., Benítez, D., Cerecetto, H., et al. (2010). Coordination of nitro-thiosemicarbazones to ruthenium(II) as a strategy for anti-trypanosomal activity improvement. European Journal of Medicinal Chemistry, 45( 7), 2847-2853. doi:10.1016/j.ejmech.2010.03.005
NLM
Rodrigues C, Batista AA, Ellena J, Castellano EE, Benítez D, Cerecetto H, González M, Teixeira LR, Beraldo H. Coordination of nitro-thiosemicarbazones to ruthenium(II) as a strategy for anti-trypanosomal activity improvement [Internet]. European Journal of Medicinal Chemistry. 2010 ; 45( 7): 2847-2853.[citado 2024 jun. 25 ] Available from: https://doi.org/10.1016/j.ejmech.2010.03.005
Vancouver
Rodrigues C, Batista AA, Ellena J, Castellano EE, Benítez D, Cerecetto H, González M, Teixeira LR, Beraldo H. Coordination of nitro-thiosemicarbazones to ruthenium(II) as a strategy for anti-trypanosomal activity improvement [Internet]. European Journal of Medicinal Chemistry. 2010 ; 45( 7): 2847-2853.[citado 2024 jun. 25 ] Available from: https://doi.org/10.1016/j.ejmech.2010.03.005
Artigo de periodico
Synthetic chalcones, flavanones, and flavones as antitumoral agents: biological evaluation and structure-activity relationships (2007)
Cabrera, Mauricio; Simoens, Macarena; Falchi, Gabriela; Lavaggi, María Laura; Piro, Oscar E.; Castellano, Eduardo Ernesto; Vidal, Anabel; Azqueta, Amaia; Monge, Antonio; Caráin, Adela López de; Sagrera, Gabriel; Seoane, Gustavo; Cerecetto, Hugo; González, Mercedes
Fonte: Bioorganic and Medicinal Chemistry. Unidade: IFSC
Assuntos: CARCINOMA, ADENOCARCINOMA, CÉLULAS, PROTEÍNAS
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
CABRERA, Mauricio et al. Synthetic chalcones, flavanones, and flavones as antitumoral agents: biological evaluation and structure-activity relationships. Bioorganic and Medicinal Chemistry, v. 15, p. 3356-3367, 2007Tradução . . Disponível em: https://doi.org/10.1016/j.bmc.2007.03.031. Acesso em: 25 jun. 2024.
APA
Cabrera, M., Simoens, M., Falchi, G., Lavaggi, M. L., Piro, O. E., Castellano, E. E., et al. (2007). Synthetic chalcones, flavanones, and flavones as antitumoral agents: biological evaluation and structure-activity relationships. Bioorganic and Medicinal Chemistry, 15, 3356-3367. doi:10.1016/j.bmc.2007.03.031
NLM
Cabrera M, Simoens M, Falchi G, Lavaggi ML, Piro OE, Castellano EE, Vidal A, Azqueta A, Monge A, Caráin AL de, Sagrera G, Seoane G, Cerecetto H, González M. Synthetic chalcones, flavanones, and flavones as antitumoral agents: biological evaluation and structure-activity relationships [Internet]. Bioorganic and Medicinal Chemistry. 2007 ; 15 3356-3367.[citado 2024 jun. 25 ] Available from: https://doi.org/10.1016/j.bmc.2007.03.031
Vancouver
Cabrera M, Simoens M, Falchi G, Lavaggi ML, Piro OE, Castellano EE, Vidal A, Azqueta A, Monge A, Caráin AL de, Sagrera G, Seoane G, Cerecetto H, González M. Synthetic chalcones, flavanones, and flavones as antitumoral agents: biological evaluation and structure-activity relationships [Internet]. Bioorganic and Medicinal Chemistry. 2007 ; 15 3356-3367.[citado 2024 jun. 25 ] Available from: https://doi.org/10.1016/j.bmc.2007.03.031
Artigo de periodico
Novel antitrypanosomal agents based on palladium nitrofurylthiosemicarbazone complexes: DNA and redox metabolism as potential therapeutic targets (2006)
Otero, Lucía; Vieites, Marisol; Boiani, Lucía; Denicola, Ana; Rigol, Carolina; Opazo, Lucia; Azar, Claudio Olea; Maya, Juan Diego; Morello, Antonio; Siegel, R. Luise Krauth; Piro, Oscar E.; Castellano, Eduardo Ernesto; González, Mercedes; Gambino, Dinorah; Cerecetto, Hugo (Universidad de la República, Departamento de Química Orgánica, Montevideo, Uruguay)
Fonte: Journal of Medicinal Chemistry. Unidade: IFSC
Assuntos: DOENÇA DE CHAGAS, DOENÇAS INFECCIOSAS, DNA, REDUÇÃO, DIFRAÇÃO POR RAIOS X, TRYPANOSOMA CRUZI
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
OTERO, Lucía et al. Novel antitrypanosomal agents based on palladium nitrofurylthiosemicarbazone complexes: DNA and redox metabolism as potential therapeutic targets. Journal of Medicinal Chemistry, v. 49, n. Ju 2006, p. 3322-3331, 2006Tradução . . Acesso em: 25 jun. 2024.
APA
Otero, L., Vieites, M., Boiani, L., Denicola, A., Rigol, C., Opazo, L., et al. (2006). Novel antitrypanosomal agents based on palladium nitrofurylthiosemicarbazone complexes: DNA and redox metabolism as potential therapeutic targets. Journal of Medicinal Chemistry, 49( Ju 2006), 3322-3331.
NLM
Otero L, Vieites M, Boiani L, Denicola A, Rigol C, Opazo L, Azar CO, Maya JD, Morello A, Siegel RLK, Piro OE, Castellano EE, González M, Gambino D. Novel antitrypanosomal agents based on palladium nitrofurylthiosemicarbazone complexes: DNA and redox metabolism as potential therapeutic targets. Journal of Medicinal Chemistry. 2006 ;49( Ju 2006): 3322-3331.[citado 2024 jun. 25 ]
Vancouver
Otero L, Vieites M, Boiani L, Denicola A, Rigol C, Opazo L, Azar CO, Maya JD, Morello A, Siegel RLK, Piro OE, Castellano EE, González M, Gambino D. Novel antitrypanosomal agents based on palladium nitrofurylthiosemicarbazone complexes: DNA and redox metabolism as potential therapeutic targets. Journal of Medicinal Chemistry. 2006 ;49( Ju 2006): 3322-3331.[citado 2024 jun. 25 ]
Artigo de periodico
Synthesis and biological properties of new 5-nitroindazole derivatives (2005)
Arán, Vicente J.; Ochoa, Carmen; Boiani, Lucía; Buccino, Pablo; Cerecetto, Hugo; Gerpe, Alejandra; González, Mercedes; Montero, David; Nogal, Juan José; Gómez-Barrio, Alicia; Azqueta, Amaya; Ceráin, Adela López de; Piro, Oscar E.; Castellano, Eduardo Ernesto
Fonte: Bioorganic and Medicinal Chemistry. Unidade: IFSC
Assuntos: TRYPANOSOMA CRUZI, CRISTALOGRAFIA
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
ARÁN, Vicente J. et al. Synthesis and biological properties of new 5-nitroindazole derivatives. Bioorganic and Medicinal Chemistry, v. 13, n. 9, p. 3197-3207, 2005Tradução . . Disponível em: https://doi.org/10.1016/j.bmc.2005.02.043. Acesso em: 25 jun. 2024.
APA
Arán, V. J., Ochoa, C., Boiani, L., Buccino, P., Cerecetto, H., Gerpe, A., et al. (2005). Synthesis and biological properties of new 5-nitroindazole derivatives. Bioorganic and Medicinal Chemistry, 13( 9), 3197-3207. doi:10.1016/j.bmc.2005.02.043
NLM
Arán VJ, Ochoa C, Boiani L, Buccino P, Cerecetto H, Gerpe A, González M, Montero D, Nogal JJ, Gómez-Barrio A, Azqueta A, Ceráin AL de, Piro OE, Castellano EE. Synthesis and biological properties of new 5-nitroindazole derivatives [Internet]. Bioorganic and Medicinal Chemistry. 2005 ; 13( 9): 3197-3207.[citado 2024 jun. 25 ] Available from: https://doi.org/10.1016/j.bmc.2005.02.043
Vancouver
Arán VJ, Ochoa C, Boiani L, Buccino P, Cerecetto H, Gerpe A, González M, Montero D, Nogal JJ, Gómez-Barrio A, Azqueta A, Ceráin AL de, Piro OE, Castellano EE. Synthesis and biological properties of new 5-nitroindazole derivatives [Internet]. Bioorganic and Medicinal Chemistry. 2005 ; 13( 9): 3197-3207.[citado 2024 jun. 25 ] Available from: https://doi.org/10.1016/j.bmc.2005.02.043
Artigo de periodico
New potent 5-substituted benzofuroxans as inhibitors of Trypanosoma cruzi growth: quantitative structure-activity relationship studies (2005)
Aguirre, Gabriela; Boiani, Lucía; Boiani, Mariana; Cerecetto, Hugo; Maio, Rossanna Di; González, Mercedes; Porcal, Williams; Denicola, Ana; Piro, Oscar E.; Castellano, Eduardo Ernesto; Sant'Ana, Carlos Mauricio R.; Barreiro, Eliezer J.
Fonte: Bioorganic and Medicinal Chemistry. Unidade: IFSC
Assuntos: TRYPANOSOMA CRUZI, CRISTALOGRAFIA, DOENÇA DE CHAGAS
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
AGUIRRE, Gabriela et al. New potent 5-substituted benzofuroxans as inhibitors of Trypanosoma cruzi growth: quantitative structure-activity relationship studies. Bioorganic and Medicinal Chemistry, v. 13, n. 23, p. 6336-6346, 2005Tradução . . Disponível em: https://doi.org/10.1016/j.bmc.2005.07.072. Acesso em: 25 jun. 2024.
APA
Aguirre, G., Boiani, L., Boiani, M., Cerecetto, H., Maio, R. D., González, M., et al. (2005). New potent 5-substituted benzofuroxans as inhibitors of Trypanosoma cruzi growth: quantitative structure-activity relationship studies. Bioorganic and Medicinal Chemistry, 13( 23), 6336-6346. doi:10.1016/j.bmc.2005.07.072
NLM
Aguirre G, Boiani L, Boiani M, Cerecetto H, Maio RD, González M, Porcal W, Denicola A, Piro OE, Castellano EE, Sant'Ana CMR, Barreiro EJ. New potent 5-substituted benzofuroxans as inhibitors of Trypanosoma cruzi growth: quantitative structure-activity relationship studies [Internet]. Bioorganic and Medicinal Chemistry. 2005 ; 13( 23): 6336-6346.[citado 2024 jun. 25 ] Available from: https://doi.org/10.1016/j.bmc.2005.07.072
Vancouver
Aguirre G, Boiani L, Boiani M, Cerecetto H, Maio RD, González M, Porcal W, Denicola A, Piro OE, Castellano EE, Sant'Ana CMR, Barreiro EJ. New potent 5-substituted benzofuroxans as inhibitors of Trypanosoma cruzi growth: quantitative structure-activity relationship studies [Internet]. Bioorganic and Medicinal Chemistry. 2005 ; 13( 23): 6336-6346.[citado 2024 jun. 25 ] Available from: https://doi.org/10.1016/j.bmc.2005.07.072
Artigo de periodico
New vanadium(v) complexes with salicylaldehyde semicarbazone derivatives: synthesis, characterization, and in vitro insulin-mimetic activity - crystal structure of ['V POT.v''O IND.2'(salicylaldehyde semicarbazone)] (2004)
Noblia, Pabla; Baran, Enrique J.; Otero, Lucía; Draper, Patricia; Cerecetto, Hugo; González, Mercedes; Piro, Oscar E.; Castellano, Eduardo Ernesto; Inohara, Toshifumi; Adachi, Yusuke; Sakurai, Hiromu; Gambino, Dinorah
Fonte: European Journal of Inorganic Chemistry. Unidade: IFSC
Assuntos: CRISTALOGRAFIA, VANÁDIO
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
NOBLIA, Pabla et al. New vanadium(v) complexes with salicylaldehyde semicarbazone derivatives: synthesis, characterization, and in vitro insulin-mimetic activity - crystal structure of ['V POT.v''O IND.2'(salicylaldehyde semicarbazone)]. European Journal of Inorganic Chemistry, v. 2004, n. Ja 2004, p. 322-328, 2004Tradução . . Acesso em: 25 jun. 2024.
APA
Noblia, P., Baran, E. J., Otero, L., Draper, P., Cerecetto, H., González, M., et al. (2004). New vanadium(v) complexes with salicylaldehyde semicarbazone derivatives: synthesis, characterization, and in vitro insulin-mimetic activity - crystal structure of ['V POT.v''O IND.2'(salicylaldehyde semicarbazone)]. European Journal of Inorganic Chemistry, 2004( Ja 2004), 322-328.
NLM
Noblia P, Baran EJ, Otero L, Draper P, Cerecetto H, González M, Piro OE, Castellano EE, Inohara T, Adachi Y, Sakurai H, Gambino D. New vanadium(v) complexes with salicylaldehyde semicarbazone derivatives: synthesis, characterization, and in vitro insulin-mimetic activity - crystal structure of ['V POT.v''O IND.2'(salicylaldehyde semicarbazone)]. European Journal of Inorganic Chemistry. 2004 ; 2004( Ja 2004): 322-328.[citado 2024 jun. 25 ]
Vancouver
Noblia P, Baran EJ, Otero L, Draper P, Cerecetto H, González M, Piro OE, Castellano EE, Inohara T, Adachi Y, Sakurai H, Gambino D. New vanadium(v) complexes with salicylaldehyde semicarbazone derivatives: synthesis, characterization, and in vitro insulin-mimetic activity - crystal structure of ['V POT.v''O IND.2'(salicylaldehyde semicarbazone)]. European Journal of Inorganic Chemistry. 2004 ; 2004( Ja 2004): 322-328.[citado 2024 jun. 25 ]
Artigo de periodico
Mass spectrometry of 1,2,5-Oxadiazole N-Oxide derivates. Use of deuterated analogues in fragmentation pattern studies (2004)
Cerecetto, Hugo; González, Mercedes; Seoane, Gustavo; Stanko, Carola; Piro, Oscar E.; Castellano, Eduardo Ernesto
Fonte: Journal of the Brazilian Chemical Society. Unidade: IFSC
Assuntos: CRISTALOGRAFIA, ESPECTROSCOPIA DE MASSA
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
CERECETTO, Hugo et al. Mass spectrometry of 1,2,5-Oxadiazole N-Oxide derivates. Use of deuterated analogues in fragmentation pattern studies. Journal of the Brazilian Chemical Society, v. 15, n. 2, p. 232-240, 2004Tradução . . Disponível em: https://doi.org/10.1590/s0103-50532004000200012. Acesso em: 25 jun. 2024.
APA
Cerecetto, H., González, M., Seoane, G., Stanko, C., Piro, O. E., & Castellano, E. E. (2004). Mass spectrometry of 1,2,5-Oxadiazole N-Oxide derivates. Use of deuterated analogues in fragmentation pattern studies. Journal of the Brazilian Chemical Society, 15( 2), 232-240. doi:10.1590/s0103-50532004000200012
NLM
Cerecetto H, González M, Seoane G, Stanko C, Piro OE, Castellano EE. Mass spectrometry of 1,2,5-Oxadiazole N-Oxide derivates. Use of deuterated analogues in fragmentation pattern studies [Internet]. Journal of the Brazilian Chemical Society. 2004 ; 15( 2): 232-240.[citado 2024 jun. 25 ] Available from: https://doi.org/10.1590/s0103-50532004000200012
Vancouver
Cerecetto H, González M, Seoane G, Stanko C, Piro OE, Castellano EE. Mass spectrometry of 1,2,5-Oxadiazole N-Oxide derivates. Use of deuterated analogues in fragmentation pattern studies [Internet]. Journal of the Brazilian Chemical Society. 2004 ; 15( 2): 232-240.[citado 2024 jun. 25 ] Available from: https://doi.org/10.1590/s0103-50532004000200012
Artigo de periodico
Tautomerism and reactivity in heterocyclic N-oxides. A spectroscopic and theoretical study of benzimidazole N-oxide derivatives (N-hydroxybenzimidazoles) (2004)
Boiani, Mariana; Cerecetto, Hugo; González, Mercedes; Piro, Oscar E.; Castellano, Eduardo Ernesto
Fonte: Journal of Physical Chemistry A. Unidade: IFSC
Assuntos: CRISTALOGRAFIA, EQUILÍBRIO
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
BOIANI, Mariana et al. Tautomerism and reactivity in heterocyclic N-oxides. A spectroscopic and theoretical study of benzimidazole N-oxide derivatives (N-hydroxybenzimidazoles). Journal of Physical Chemistry A, v. 108, n. 51, p. 11241-11248, 2004Tradução . . Acesso em: 25 jun. 2024.
APA
Boiani, M., Cerecetto, H., González, M., Piro, O. E., & Castellano, E. E. (2004). Tautomerism and reactivity in heterocyclic N-oxides. A spectroscopic and theoretical study of benzimidazole N-oxide derivatives (N-hydroxybenzimidazoles). Journal of Physical Chemistry A, 108( 51), 11241-11248.
NLM
Boiani M, Cerecetto H, González M, Piro OE, Castellano EE. Tautomerism and reactivity in heterocyclic N-oxides. A spectroscopic and theoretical study of benzimidazole N-oxide derivatives (N-hydroxybenzimidazoles). Journal of Physical Chemistry A. 2004 ; 108( 51): 11241-11248.[citado 2024 jun. 25 ]
Vancouver
Boiani M, Cerecetto H, González M, Piro OE, Castellano EE. Tautomerism and reactivity in heterocyclic N-oxides. A spectroscopic and theoretical study of benzimidazole N-oxide derivatives (N-hydroxybenzimidazoles). Journal of Physical Chemistry A. 2004 ; 108( 51): 11241-11248.[citado 2024 jun. 25 ]

Unidades USP

ReP

Filtros

Autores

Assuntos

Título da fonte

Afiliação dos autores externos não normalizada