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
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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: 17 maio 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 maio 17 ] 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 maio 17 ] 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
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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: 17 maio 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 maio 17 ] 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 maio 17 ] 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
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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: 17 maio 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 maio 17 ]
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 maio 17 ]
Artigo de periodico
Vanadium(V) complexes with salicylaldehyde semicarbazone derivatives bearing in vitro anti-tumor activity toward kidney tumor cells (TK-10): crystal structure of ['V POT.v''O IND.2'(5-bromosalicylaldehyde semicarbazone)] (2005)
Noblia, Pabla; Vieites, Marisol (Universidad de la Republica, Facultad de Química, Cátedra de Química, Montevideo, Uruguay); Parajon-Costa, Beatriz S.; Baran, Enrique J.; Cerecetto, Hugo; Draper, Patricia; Gonzalez, Mercedes; Piro, Oscar E.; Castellano, Eduardo Ernesto; Azqueta, Amaia; Ceráin, Adela Lopez de; Monge-Vega, Antonio; Gambino, Dinorah
Fonte: Journal of Inorganic Biochemistry. Unidade: IFSC
Assuntos: CRISTALOGRAFIA, VANÁDIO
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ABNT
NOBLIA, Pabla et al. Vanadium(V) complexes with salicylaldehyde semicarbazone derivatives bearing in vitro anti-tumor activity toward kidney tumor cells (TK-10): crystal structure of ['V POT.v''O IND.2'(5-bromosalicylaldehyde semicarbazone)]. Journal of Inorganic Biochemistry, v. 99, n. 2, p. 443-451, 2005Tradução . . Disponível em: https://doi.org/10.1016/j.jinorgbio.2004.10.019. Acesso em: 17 maio 2024.
APA
Noblia, P., Parajon-Costa, B. S., Baran, E. J., Cerecetto, H., Draper, P., Gonzalez, M., et al. (2005). Vanadium(V) complexes with salicylaldehyde semicarbazone derivatives bearing in vitro anti-tumor activity toward kidney tumor cells (TK-10): crystal structure of ['V POT.v''O IND.2'(5-bromosalicylaldehyde semicarbazone)]. Journal of Inorganic Biochemistry, 99( 2), 443-451. doi:10.1016/j.jinorgbio.2004.10.019
NLM
Noblia P, Parajon-Costa BS, Baran EJ, Cerecetto H, Draper P, Gonzalez M, Piro OE, Castellano EE, Azqueta A, Ceráin AL de, Monge-Vega A, Gambino D. Vanadium(V) complexes with salicylaldehyde semicarbazone derivatives bearing in vitro anti-tumor activity toward kidney tumor cells (TK-10): crystal structure of ['V POT.v''O IND.2'(5-bromosalicylaldehyde semicarbazone)] [Internet]. Journal of Inorganic Biochemistry. 2005 ; 99( 2): 443-451.[citado 2024 maio 17 ] Available from: https://doi.org/10.1016/j.jinorgbio.2004.10.019
Vancouver
Noblia P, Parajon-Costa BS, Baran EJ, Cerecetto H, Draper P, Gonzalez M, Piro OE, Castellano EE, Azqueta A, Ceráin AL de, Monge-Vega A, Gambino D. Vanadium(V) complexes with salicylaldehyde semicarbazone derivatives bearing in vitro anti-tumor activity toward kidney tumor cells (TK-10): crystal structure of ['V POT.v''O IND.2'(5-bromosalicylaldehyde semicarbazone)] [Internet]. Journal of Inorganic Biochemistry. 2005 ; 99( 2): 443-451.[citado 2024 maio 17 ] Available from: https://doi.org/10.1016/j.jinorgbio.2004.10.019
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
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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: 17 maio 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 maio 17 ] 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 maio 17 ] 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
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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: 17 maio 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 maio 17 ] 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 maio 17 ] Available from: https://doi.org/10.1016/j.bmc.2005.07.072
Artigo de periodico
2-imidazolone derivatives obtained as unexpected products throughout imidazole N-3-oxide rearrangement (2005)
Cerecetto, Hugo; Gerpe, A.; González, M.; Piro, Oscar E.; Castellano, Eduardo Ernesto
Fonte: Letters in Organic Chemistry. Unidade: IFSC
Assuntos: DENSIDADE, OXIGÊNIO, QUÍMICA ORGÂNICA
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ABNT
CERECETTO, Hugo et al. 2-imidazolone derivatives obtained as unexpected products throughout imidazole N-3-oxide rearrangement. Letters in Organic Chemistry, v. 2, n. 6, p. 501-506, 2005Tradução . . Acesso em: 17 maio 2024.
APA
Cerecetto, H., Gerpe, A., González, M., Piro, O. E., & Castellano, E. E. (2005). 2-imidazolone derivatives obtained as unexpected products throughout imidazole N-3-oxide rearrangement. Letters in Organic Chemistry, 2( 6), 501-506.
NLM
Cerecetto H, Gerpe A, González M, Piro OE, Castellano EE. 2-imidazolone derivatives obtained as unexpected products throughout imidazole N-3-oxide rearrangement. Letters in Organic Chemistry. 2005 ; 2( 6): 501-506.[citado 2024 maio 17 ]
Vancouver
Cerecetto H, Gerpe A, González M, Piro OE, Castellano EE. 2-imidazolone derivatives obtained as unexpected products throughout imidazole N-3-oxide rearrangement. Letters in Organic Chemistry. 2005 ; 2( 6): 501-506.[citado 2024 maio 17 ]
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
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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: 17 maio 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 maio 17 ]
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 maio 17 ]
Artigo de periodico
New synthetic approach for the preparation of imidazole 'N IND.3'-oxide (2004)
Cerecetto, Hugo; Gerpe, Alejandra; Gonzalez, Mercedes; Sainz, Yolanda Fernández; Piro, Oscar E.; Castellano, Eduardo Ernesto
Fonte: Synthesis. Unidade: IFSC
Assuntos: CRISTALOGRAFIA, OXIDAÇÃO
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ABNT
CERECETTO, Hugo et al. New synthetic approach for the preparation of imidazole 'N IND.3'-oxide. Synthesis, v. No 2004, n. 16, p. 2678-2684, 2004Tradução . . Acesso em: 17 maio 2024.
APA
Cerecetto, H., Gerpe, A., Gonzalez, M., Sainz, Y. F., Piro, O. E., & Castellano, E. E. (2004). New synthetic approach for the preparation of imidazole 'N IND.3'-oxide. Synthesis, No 2004( 16), 2678-2684.
NLM
Cerecetto H, Gerpe A, Gonzalez M, Sainz YF, Piro OE, Castellano EE. New synthetic approach for the preparation of imidazole 'N IND.3'-oxide. Synthesis. 2004 ; No 2004( 16): 2678-2684.[citado 2024 maio 17 ]
Vancouver
Cerecetto H, Gerpe A, Gonzalez M, Sainz YF, Piro OE, Castellano EE. New synthetic approach for the preparation of imidazole 'N IND.3'-oxide. Synthesis. 2004 ; No 2004( 16): 2678-2684.[citado 2024 maio 17 ]
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
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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: 17 maio 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 maio 17 ] 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 maio 17 ] 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
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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: 17 maio 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 maio 17 ]
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 maio 17 ]
Artigo de periodico
1,2,5-oxadiazole N-oxide derivatives as potential anti-cancer agents: synthesis and biological evaluation. Part IV (2001)
Boiani, Mariana; Cerecetto, Hugo; Gonzalez, Mercedes; Risso, Mariela; Olea-Azar, Claudio; Piro, Oscar E.; Castellano, Eduardo Ernesto; Ceráin, Adela Lopez de; Ezpeleta, Olga; Monge Vega, Antonio
Fonte: European Journal of Medicinal Chemistry. Unidade: IFSC
Assuntos: ANTINEOPLÁSICOS, FARMACOLOGIA
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ABNT
BOIANI, Mariana et al. 1,2,5-oxadiazole N-oxide derivatives as potential anti-cancer agents: synthesis and biological evaluation. Part IV. European Journal of Medicinal Chemistry, v. 36, n. 10, p. 771-782, 2001Tradução . . Disponível em: https://doi.org/10.1016/S0223-5234(01)01265-X. Acesso em: 17 maio 2024.
APA
Boiani, M., Cerecetto, H., Gonzalez, M., Risso, M., Olea-Azar, C., Piro, O. E., et al. (2001). 1,2,5-oxadiazole N-oxide derivatives as potential anti-cancer agents: synthesis and biological evaluation. Part IV. European Journal of Medicinal Chemistry, 36( 10), 771-782. doi:10.1016/S0223-5234(01)01265-X
NLM
Boiani M, Cerecetto H, Gonzalez M, Risso M, Olea-Azar C, Piro OE, Castellano EE, Ceráin AL de, Ezpeleta O, Monge Vega A. 1,2,5-oxadiazole N-oxide derivatives as potential anti-cancer agents: synthesis and biological evaluation. Part IV [Internet]. European Journal of Medicinal Chemistry. 2001 ;36( 10): 771-782.[citado 2024 maio 17 ] Available from: https://doi.org/10.1016/S0223-5234(01)01265-X
Vancouver
Boiani M, Cerecetto H, Gonzalez M, Risso M, Olea-Azar C, Piro OE, Castellano EE, Ceráin AL de, Ezpeleta O, Monge Vega A. 1,2,5-oxadiazole N-oxide derivatives as potential anti-cancer agents: synthesis and biological evaluation. Part IV [Internet]. European Journal of Medicinal Chemistry. 2001 ;36( 10): 771-782.[citado 2024 maio 17 ] Available from: https://doi.org/10.1016/S0223-5234(01)01265-X

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