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Trabalho de evento-resumo
99mtechnetium-Tocilizumab Fragments As Molecular Imaging Agent for Multiple Myeloma (2015)
Camacho, Ximena; Machado, Camila; Garcia, Maria Fernanda; Fernandez, Marcelo; Alonso, Omar; Cerecetto, Hugo; Chammas, Roger; Gambini, Juan Pablo; Cabral, Pablo; Riva, Eloisa
Source: Abstracts. Conference titles: Annual Meeting & Exposition. Unidade: FM
Subjects: TÉCNICAS DE DIAGNÓSTICO MOLECULAR, RATOS, MIELOMA MULTIPLO, PROLIFERAÇÃO CELULAR
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ABNT
CAMACHO, Ximena et al. 99mtechnetium-Tocilizumab Fragments As Molecular Imaging Agent for Multiple Myeloma. 2015, Anais.. Orlando, FL: AOAC International, 2015. Disponível em: https://ash.confex.com/ash/2015/webprogramscheduler/Session6836.html. Acesso em: 05 nov. 2024.
APA
Camacho, X., Machado, C., Garcia, M. F., Fernandez, M., Alonso, O., Cerecetto, H., et al. (2015). 99mtechnetium-Tocilizumab Fragments As Molecular Imaging Agent for Multiple Myeloma. In Abstracts. Orlando, FL: AOAC International. Recuperado de https://ash.confex.com/ash/2015/webprogramscheduler/Session6836.html
NLM
Camacho X, Machado C, Garcia MF, Fernandez M, Alonso O, Cerecetto H, Chammas R, Gambini JP, Cabral P, Riva E. 99mtechnetium-Tocilizumab Fragments As Molecular Imaging Agent for Multiple Myeloma [Internet]. Abstracts. 2015 ;[citado 2024 nov. 05 ] Available from: https://ash.confex.com/ash/2015/webprogramscheduler/Session6836.html
Vancouver
Camacho X, Machado C, Garcia MF, Fernandez M, Alonso O, Cerecetto H, Chammas R, Gambini JP, Cabral P, Riva E. 99mtechnetium-Tocilizumab Fragments As Molecular Imaging Agent for Multiple Myeloma [Internet]. Abstracts. 2015 ;[citado 2024 nov. 05 ] Available from: https://ash.confex.com/ash/2015/webprogramscheduler/Session6836.html
Artigo de periodico
Understanding the solid forms of 5E-phenylethenylbenzofuroxan with different in vivo anti-T. cruzi activity (2013)
Honorato, Sara B.; Porcal, Williams; Merlino, Alicia; Ellena, Javier ; Cerecetto, Hugo; Ayala, Alejandro P.; González, Mercedes
Source: Revista Virtual de Química. Unidade: IFSC
Subjects: TRYPANOSOMA CRUZI (PREVENÇÃO E CONTROLE), FÁRMACOS, CRISTALOGRAFIA
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ABNT
HONORATO, Sara B. et al. Understanding the solid forms of 5E-phenylethenylbenzofuroxan with different in vivo anti-T. cruzi activity. Revista Virtual de Química, v. No 2013, n. 6, p. 1179-1190, 2013Tradução . . Disponível em: https://doi.org/10.5935/1984-6835.20130085. Acesso em: 05 nov. 2024.
APA
Honorato, S. B., Porcal, W., Merlino, A., Ellena, J., Cerecetto, H., Ayala, A. P., & González, M. (2013). Understanding the solid forms of 5E-phenylethenylbenzofuroxan with different in vivo anti-T. cruzi activity. Revista Virtual de Química, No 2013( 6), 1179-1190. doi:10.5935/1984-6835.20130085
NLM
Honorato SB, Porcal W, Merlino A, Ellena J, Cerecetto H, Ayala AP, González M. Understanding the solid forms of 5E-phenylethenylbenzofuroxan with different in vivo anti-T. cruzi activity [Internet]. Revista Virtual de Química. 2013 ; No 2013( 6): 1179-1190.[citado 2024 nov. 05 ] Available from: https://doi.org/10.5935/1984-6835.20130085
Vancouver
Honorato SB, Porcal W, Merlino A, Ellena J, Cerecetto H, Ayala AP, González M. Understanding the solid forms of 5E-phenylethenylbenzofuroxan with different in vivo anti-T. cruzi activity [Internet]. Revista Virtual de Química. 2013 ; No 2013( 6): 1179-1190.[citado 2024 nov. 05 ] Available from: https://doi.org/10.5935/1984-6835.20130085
Artigo de periodico
Synthesis and in vitro activity of limonene derivatives against Leishmania and Trypanosoma (2010)
Graebin, Cedric S.; Madeira, Maria de F.; Yasunaka, Jenicer Kazumi Umada Yokoyama; Miguel, Danilo Ciccone; Uliana, Sílvia Reni Bortolin; Benitez, Diego; Cerecetto, Hugo; González, Mercedes; Rosa, Ricardo Gomes da; Eifler-Lima, Vera Lucia
Source: European Journal of Medicinal Chemistry. Unidade: ICB
Assunto: PARASITOLOGIA
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ABNT
GRAEBIN, Cedric S. et al. Synthesis and in vitro activity of limonene derivatives against Leishmania and Trypanosoma. European Journal of Medicinal Chemistry, v. 45, n. 4, p. 1524-1528, 2010Tradução . . Disponível em: https://doi.org/10.1016/j.ejmech.2009.12.061. Acesso em: 05 nov. 2024.
APA
Graebin, C. S., Madeira, M. de F., Yasunaka, J. K. U. Y., Miguel, D. C., Uliana, S. R. B., Benitez, D., et al. (2010). Synthesis and in vitro activity of limonene derivatives against Leishmania and Trypanosoma. European Journal of Medicinal Chemistry, 45( 4), 1524-1528. doi:10.1016/j.ejmech.2009.12.061
NLM
Graebin CS, Madeira M de F, Yasunaka JKUY, Miguel DC, Uliana SRB, Benitez D, Cerecetto H, González M, Rosa RG da, Eifler-Lima VL. Synthesis and in vitro activity of limonene derivatives against Leishmania and Trypanosoma [Internet]. European Journal of Medicinal Chemistry. 2010 ; 45( 4): 1524-1528.[citado 2024 nov. 05 ] Available from: https://doi.org/10.1016/j.ejmech.2009.12.061
Vancouver
Graebin CS, Madeira M de F, Yasunaka JKUY, Miguel DC, Uliana SRB, Benitez D, Cerecetto H, González M, Rosa RG da, Eifler-Lima VL. Synthesis and in vitro activity of limonene derivatives against Leishmania and Trypanosoma [Internet]. European Journal of Medicinal Chemistry. 2010 ; 45( 4): 1524-1528.[citado 2024 nov. 05 ] Available from: https://doi.org/10.1016/j.ejmech.2009.12.061
Artigo de periodico
Structural relationships in the solid state of the anti-chagas agent (E)-phenylethenylbenzofuroxam (2010)
Martins, Felipe Terra ; Ayala, Alejandro Pedro ; Porcal, Williams; Cerecetto, Hugo; González, Mercedes; Ellena, Javier
Source: Molecular Diversity. Unidade: IFSC
Subjects: PLANEJAMENTO DE FÁRMACOS, DOENÇA DE CHAGAS (TRATAMENTO), ESPECTROSCOPIA RAMAN, CRISTALOGRAFIA
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ABNT
MARTINS, Felipe Terra et al. Structural relationships in the solid state of the anti-chagas agent (E)-phenylethenylbenzofuroxam. Molecular Diversity, v. No 2010, n. 4, p. 643-652, 2010Tradução . . Disponível em: https://doi.org/10.1007/s11030-009-9202-4. Acesso em: 05 nov. 2024.
APA
Martins, F. T., Ayala, A. P., Porcal, W., Cerecetto, H., González, M., & Ellena, J. (2010). Structural relationships in the solid state of the anti-chagas agent (E)-phenylethenylbenzofuroxam. Molecular Diversity, No 2010( 4), 643-652. doi:10.1007/s11030-009-9202-4
NLM
Martins FT, Ayala AP, Porcal W, Cerecetto H, González M, Ellena J. Structural relationships in the solid state of the anti-chagas agent (E)-phenylethenylbenzofuroxam [Internet]. Molecular Diversity. 2010 ; No 2010( 4): 643-652.[citado 2024 nov. 05 ] Available from: https://doi.org/10.1007/s11030-009-9202-4
Vancouver
Martins FT, Ayala AP, Porcal W, Cerecetto H, González M, Ellena J. Structural relationships in the solid state of the anti-chagas agent (E)-phenylethenylbenzofuroxam [Internet]. Molecular Diversity. 2010 ; No 2010( 4): 643-652.[citado 2024 nov. 05 ] Available from: https://doi.org/10.1007/s11030-009-9202-4
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
Source: European Journal of Medicinal Chemistry. Unidade: IFSC
Subjects: 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: 05 nov. 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 nov. 05 ] 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 nov. 05 ] Available from: https://doi.org/10.1016/j.ejmech.2010.03.005
Trabalho de evento-resumo
Study of the solid-state properties of two non-bioequivalent forms of 5e-phenylethenylbenzofuroxan (2010)
Gonzalez, Mercedes; Cerecetto, Hugo; Honorato, Sara B.; Ellena, Javier ; Ayala, Alejandro P.
Source: Abstracts. Conference titles: Reunión Anual de la Asociación Argentina de Cristalografia - AACr. Unidade: IFSC
Subjects: DOENÇA DE CHAGAS, TRYPANOSOMA CRUZI, PLANEJAMENTO DE FÁRMACOS, DIFRAÇÃO POR RAIOS X
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ABNT
GONZALEZ, Mercedes et al. Study of the solid-state properties of two non-bioequivalent forms of 5e-phenylethenylbenzofuroxan. 2010, Anais.. Chester: International Union of Crystallography - IUCr, 2010. . Acesso em: 05 nov. 2024.
APA
Gonzalez, M., Cerecetto, H., Honorato, S. B., Ellena, J., & Ayala, A. P. (2010). Study of the solid-state properties of two non-bioequivalent forms of 5e-phenylethenylbenzofuroxan. In Abstracts. Chester: International Union of Crystallography - IUCr.
NLM
Gonzalez M, Cerecetto H, Honorato SB, Ellena J, Ayala AP. Study of the solid-state properties of two non-bioequivalent forms of 5e-phenylethenylbenzofuroxan. Abstracts. 2010 ;[citado 2024 nov. 05 ]
Vancouver
Gonzalez M, Cerecetto H, Honorato SB, Ellena J, Ayala AP. Study of the solid-state properties of two non-bioequivalent forms of 5e-phenylethenylbenzofuroxan. Abstracts. 2010 ;[citado 2024 nov. 05 ]
Trabalho de evento-resumo
Conformação e interações intermoleculares no estado sólido de compostos com atividade antichagásica: E-feniletenilbenzofuroxano (2009)
Ellena, Javier ; Martins, Felipe Terra ; Porcal, Williams; Cerecetto, Hugo; González, Mercedes; Ayala, Alejandro Pedro
Conference titles: Reunião Anual Sociedade Brasileira de Química - SBQ. Unidade: IFSC
Subjects: CRISTALOGRAFIA, DOENÇA DE CHAGAS (TRATAMENTO), PLANEJAMENTO DE FÁRMACOS, ESPECTROSCOPIA
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ABNT
ELLENA, Javier et al. Conformação e interações intermoleculares no estado sólido de compostos com atividade antichagásica: E-feniletenilbenzofuroxano. 2009, Anais.. São Paulo: Sociedade Brasileira de Química - SBQ, 2009. Disponível em: http://sec.sbq.org.br/cdrom/32ra/resumos/T2114-1.pdf. Acesso em: 05 nov. 2024.
APA
Ellena, J., Martins, F. T., Porcal, W., Cerecetto, H., González, M., & Ayala, A. P. (2009). Conformação e interações intermoleculares no estado sólido de compostos com atividade antichagásica: E-feniletenilbenzofuroxano. In . São Paulo: Sociedade Brasileira de Química - SBQ. Recuperado de http://sec.sbq.org.br/cdrom/32ra/resumos/T2114-1.pdf
NLM
Ellena J, Martins FT, Porcal W, Cerecetto H, González M, Ayala AP. Conformação e interações intermoleculares no estado sólido de compostos com atividade antichagásica: E-feniletenilbenzofuroxano [Internet]. 2009 ;[citado 2024 nov. 05 ] Available from: http://sec.sbq.org.br/cdrom/32ra/resumos/T2114-1.pdf
Vancouver
Ellena J, Martins FT, Porcal W, Cerecetto H, González M, Ayala AP. Conformação e interações intermoleculares no estado sólido de compostos com atividade antichagásica: E-feniletenilbenzofuroxano [Internet]. 2009 ;[citado 2024 nov. 05 ] Available from: http://sec.sbq.org.br/cdrom/32ra/resumos/T2114-1.pdf
Artigo de periodico
New copper-based complexes with quinoxaline 'N POT.1', 'N POT.4'-dioxide derivatives, potential antitumoral agents (2008)
Urquiola, Carolina; Gambino, Dinorah; Cabrera, Mauricio; Lavaggi, María Laura; Cerecetto, Hugo; González, Mercedes; Cerain, Adela López de; Monge, Antonio; Costa Filho, Antonio José da; Torre, María H.
Source: Journal of Inorganic Biochemistry. Unidade: IFSC
Subjects: CITOTOXINAS, CÉLULAS, ANTINEOPLÁSICOS
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ABNT
URQUIOLA, Carolina et al. New copper-based complexes with quinoxaline 'N POT.1', 'N POT.4'-dioxide derivatives, potential antitumoral agents. Journal of Inorganic Biochemistry, v. 102, n. 1, p. 119-126, 2008Tradução . . Acesso em: 05 nov. 2024.
APA
Urquiola, C., Gambino, D., Cabrera, M., Lavaggi, M. L., Cerecetto, H., González, M., et al. (2008). New copper-based complexes with quinoxaline 'N POT.1', 'N POT.4'-dioxide derivatives, potential antitumoral agents. Journal of Inorganic Biochemistry, 102( 1), 119-126.
NLM
Urquiola C, Gambino D, Cabrera M, Lavaggi ML, Cerecetto H, González M, Cerain AL de, Monge A, Costa Filho AJ da, Torre MH. New copper-based complexes with quinoxaline 'N POT.1', 'N POT.4'-dioxide derivatives, potential antitumoral agents. Journal of Inorganic Biochemistry. 2008 ; 102( 1): 119-126.[citado 2024 nov. 05 ]
Vancouver
Urquiola C, Gambino D, Cabrera M, Lavaggi ML, Cerecetto H, González M, Cerain AL de, Monge A, Costa Filho AJ da, Torre MH. New copper-based complexes with quinoxaline 'N POT.1', 'N POT.4'-dioxide derivatives, potential antitumoral agents. Journal of Inorganic Biochemistry. 2008 ; 102( 1): 119-126.[citado 2024 nov. 05 ]
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
Source: Bioorganic and Medicinal Chemistry. Unidade: IFSC
Subjects: 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: 05 nov. 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 nov. 05 ] 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 nov. 05 ] Available from: https://doi.org/10.1016/j.bmc.2007.03.031
Trabalho de evento-resumo
5-Phenylethenylbenzofuroxans with distinct in vivo anti-chagasic activities (2007)
Boiani, Lucía; Davies, Carolina; Porcal, Williams; Merlino, Alicia; Gerpe, Alejandra; Boiani, Mariana; Basombrío, Miguel Ángel; Cerecetto, Hugo; González, Mercedes; Ayala, Alejandro Pedro ; Honorato, Sara B.; Ellena, Javier
Source: Resumos. Conference titles: Simpósio Latino Americano de Polimorfismo e Cristalização em Fármacos e Medicamentos - LAPOLC. Unidade: IFSC
Subjects: POLIMORFISMO, FÁRMACOS, DOENÇAS PARASITÁRIAS, TRYPANOSOMA CRUZI, DIFRAÇÃO POR RAIOS X
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ABNT
BOIANI, Lucía et al. 5-Phenylethenylbenzofuroxans with distinct in vivo anti-chagasic activities. 2007, Anais.. Fortaleza: Universidade Federal do Ceará, 2007. . Acesso em: 05 nov. 2024.
APA
Boiani, L., Davies, C., Porcal, W., Merlino, A., Gerpe, A., Boiani, M., et al. (2007). 5-Phenylethenylbenzofuroxans with distinct in vivo anti-chagasic activities. In Resumos. Fortaleza: Universidade Federal do Ceará.
NLM
Boiani L, Davies C, Porcal W, Merlino A, Gerpe A, Boiani M, Basombrío MÁ, Cerecetto H, González M, Ayala AP, Honorato SB, Ellena J. 5-Phenylethenylbenzofuroxans with distinct in vivo anti-chagasic activities. Resumos. 2007 ;[citado 2024 nov. 05 ]
Vancouver
Boiani L, Davies C, Porcal W, Merlino A, Gerpe A, Boiani M, Basombrío MÁ, Cerecetto H, González M, Ayala AP, Honorato SB, Ellena J. 5-Phenylethenylbenzofuroxans with distinct in vivo anti-chagasic activities. Resumos. 2007 ;[citado 2024 nov. 05 ]
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)
Source: Journal of Medicinal Chemistry. Unidade: IFSC
Subjects: 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: 05 nov. 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 nov. 05 ]
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 nov. 05 ]
Artigo de periodico
Novel vanadyl complexes quinoxaline 'N POT. 1', 'N POT. 4'-dioxide derivatives as potent in vitro insulin-mimetic compounds (2006)
Noblia, Pabla; Vieites, Marisol; Torre, María H.; Costa Filho, Antonio José da; Cerecetto, Hugo; González, Mercedes; Lavaggi, María Laura; Adachi, Yusuke; Sakurai, Hiromu; Gambino, Dinorah
Source: Journal of Inorganic Biochemistry. Unidade: IFSC
Subjects: BIOQUÍMICA, VANÁDIO, DIABETES MELLITUS, RESSONÂNCIA PARAMAGNÉTICA ELETRÔNICA
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ABNT
NOBLIA, Pabla et al. Novel vanadyl complexes quinoxaline 'N POT. 1', 'N POT. 4'-dioxide derivatives as potent in vitro insulin-mimetic compounds. Journal of Inorganic Biochemistry, v. 100, n. 2, p. 281-287, 2006Tradução . . Acesso em: 05 nov. 2024.
APA
Noblia, P., Vieites, M., Torre, M. H., Costa Filho, A. J. da, Cerecetto, H., González, M., et al. (2006). Novel vanadyl complexes quinoxaline 'N POT. 1', 'N POT. 4'-dioxide derivatives as potent in vitro insulin-mimetic compounds. Journal of Inorganic Biochemistry, 100( 2), 281-287.
NLM
Noblia P, Vieites M, Torre MH, Costa Filho AJ da, Cerecetto H, González M, Lavaggi ML, Adachi Y, Sakurai H, Gambino D. Novel vanadyl complexes quinoxaline 'N POT. 1', 'N POT. 4'-dioxide derivatives as potent in vitro insulin-mimetic compounds. Journal of Inorganic Biochemistry. 2006 ;100( 2): 281-287.[citado 2024 nov. 05 ]
Vancouver
Noblia P, Vieites M, Torre MH, Costa Filho AJ da, Cerecetto H, González M, Lavaggi ML, Adachi Y, Sakurai H, Gambino D. Novel vanadyl complexes quinoxaline 'N POT. 1', 'N POT. 4'-dioxide derivatives as potent in vitro insulin-mimetic compounds. Journal of Inorganic Biochemistry. 2006 ;100( 2): 281-287.[citado 2024 nov. 05 ]
Artigo de periodico
Selective hypoxia-cytotoxins based on vanadyl complexes with 3-aminoquinoxaline-2-carbonitrile-'N POT.1','N POT.4'-dioxide derivatives (2006)
Vieites, Marisol; Noblía, Pabla; Torre, María H.; Cerecetto, Hugo; Lavaggi, María Laura; Costa Filho, Antonio José da; Azqueta, Amaia; Cerain, Adela López de; Monge, Antonio; Parajón-Costa, Beatriz S.; González, Mercedes; Gambino, Dinorah
Source: Journal of Inorganic Biochemistry. Unidade: IFSC
Subjects: VANÁDIO, CITOTOXINAS, RESSONÂNCIA MAGNÉTICA NUCLEAR, RESSONÂNCIA PARAMAGNÉTICA ELETRÔNICA, ESPECTROSCOPIA RAMAN
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ABNT
VIEITES, Marisol et al. Selective hypoxia-cytotoxins based on vanadyl complexes with 3-aminoquinoxaline-2-carbonitrile-'N POT.1','N POT.4'-dioxide derivatives. Journal of Inorganic Biochemistry, v. 100, n. 8, p. 1358-1367, 2006Tradução . . Acesso em: 05 nov. 2024.
APA
Vieites, M., Noblía, P., Torre, M. H., Cerecetto, H., Lavaggi, M. L., Costa Filho, A. J. da, et al. (2006). Selective hypoxia-cytotoxins based on vanadyl complexes with 3-aminoquinoxaline-2-carbonitrile-'N POT.1','N POT.4'-dioxide derivatives. Journal of Inorganic Biochemistry, 100( 8), 1358-1367.
NLM
Vieites M, Noblía P, Torre MH, Cerecetto H, Lavaggi ML, Costa Filho AJ da, Azqueta A, Cerain AL de, Monge A, Parajón-Costa BS, González M, Gambino D. Selective hypoxia-cytotoxins based on vanadyl complexes with 3-aminoquinoxaline-2-carbonitrile-'N POT.1','N POT.4'-dioxide derivatives. Journal of Inorganic Biochemistry. 2006 ;100( 8): 1358-1367.[citado 2024 nov. 05 ]
Vancouver
Vieites M, Noblía P, Torre MH, Cerecetto H, Lavaggi ML, Costa Filho AJ da, Azqueta A, Cerain AL de, Monge A, Parajón-Costa BS, González M, Gambino D. Selective hypoxia-cytotoxins based on vanadyl complexes with 3-aminoquinoxaline-2-carbonitrile-'N POT.1','N POT.4'-dioxide derivatives. Journal of Inorganic Biochemistry. 2006 ;100( 8): 1358-1367.[citado 2024 nov. 05 ]
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
Source: Journal of Inorganic Biochemistry. Unidade: IFSC
Subjects: CRISTALOGRAFIA, VANÁDIO
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
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: 05 nov. 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 nov. 05 ] 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 nov. 05 ] 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
Source: Bioorganic and Medicinal Chemistry. Unidade: IFSC
Subjects: 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: 05 nov. 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 nov. 05 ] 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 nov. 05 ] Available from: https://doi.org/10.1016/j.bmc.2005.02.043
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
Source: Letters in Organic Chemistry. Unidade: IFSC
Subjects: DENSIDADE, OXIGÊNIO, QUÍMICA ORGÂNICA
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
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: 05 nov. 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 nov. 05 ]
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 nov. 05 ]
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.
Source: Bioorganic and Medicinal Chemistry. Unidade: IFSC
Subjects: 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: 05 nov. 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 nov. 05 ] 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 nov. 05 ] Available from: https://doi.org/10.1016/j.bmc.2005.07.072
Artigo de periodico
Novel Cu(II) quinoxaline 'N POT.1', 'N POT.4'-dioxide complexes as selective hypoxic cytotoxins (2005)
Torre, María H.; Gambino, Dinorah; Araujo, Jeannette; Cerecetto, Hugo; González, Mercedes; Lavaggi, María Laura; Azqueta, Amaya; Lopez de Ceráin, Adela; Monge Vega, Antonio; Abram, Ulrich; Costa Filho, Antônio José da
Source: European Journal of Medicinal Chemistry. Unidade: IFSC
Subjects: BIOFÍSICA, CITOTOXINAS
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
TORRE, María H. et al. Novel Cu(II) quinoxaline 'N POT.1', 'N POT.4'-dioxide complexes as selective hypoxic cytotoxins. European Journal of Medicinal Chemistry, v. 40, n. 5, p. 473-480, 2005Tradução . . Acesso em: 05 nov. 2024.
APA
Torre, M. H., Gambino, D., Araujo, J., Cerecetto, H., González, M., Lavaggi, M. L., et al. (2005). Novel Cu(II) quinoxaline 'N POT.1', 'N POT.4'-dioxide complexes as selective hypoxic cytotoxins. European Journal of Medicinal Chemistry, 40( 5), 473-480.
NLM
Torre MH, Gambino D, Araujo J, Cerecetto H, González M, Lavaggi ML, Azqueta A, Lopez de Ceráin A, Monge Vega A, Abram U, Costa Filho AJ da. Novel Cu(II) quinoxaline 'N POT.1', 'N POT.4'-dioxide complexes as selective hypoxic cytotoxins. European Journal of Medicinal Chemistry. 2005 ; 40( 5): 473-480.[citado 2024 nov. 05 ]
Vancouver
Torre MH, Gambino D, Araujo J, Cerecetto H, González M, Lavaggi ML, Azqueta A, Lopez de Ceráin A, Monge Vega A, Abram U, Costa Filho AJ da. Novel Cu(II) quinoxaline 'N POT.1', 'N POT.4'-dioxide complexes as selective hypoxic cytotoxins. European Journal of Medicinal Chemistry. 2005 ; 40( 5): 473-480.[citado 2024 nov. 05 ]
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
Source: European Journal of Inorganic Chemistry. Unidade: IFSC
Subjects: 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: 05 nov. 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 nov. 05 ]
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 nov. 05 ]
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
Source: Synthesis. Unidade: IFSC
Subjects: CRISTALOGRAFIA, OXIDAÇÃO
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
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: 05 nov. 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 nov. 05 ]
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 nov. 05 ]

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