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Artigo de periodico
Synthesis and anti-trypanosoma cruzi activity of 3-cyanopyridine derivatives (2024)
Slafer, Brian Wayne ; Dessoy, Marco Aurélio ; Oliveira, Ramon Guerra de ; Mollo, María Cruz ; Lee, Eun ; Matheeussen, An ; Maes, Louis ; Caljon, Guy ; Ferreira, Leonardo Luiz Gomes ; Krogh, Renata ; Andricopulo, Adriano Defini ; Cruz, Luiza dos Reis ; Mowbray, Charles E. ; Kratz, Jadel M. ; Dias, Luiz Carlos
Source: ACS Omega. Unidade: IFSC
Subjects: TRYPANOSOMA CRUZI, COMPOSTOS AROMÁTICOS, CRISTALOGRAFIA
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ABNT
SLAFER, Brian Wayne et al. Synthesis and anti-trypanosoma cruzi activity of 3-cyanopyridine derivatives. ACS Omega, v. 9, n. 20, p. 22360-22370 + supporting information, 2024Tradução . . Disponível em: https://doi.org/10.1021/acsomega.4c01919. Acesso em: 30 dez. 2024.
APA
Slafer, B. W., Dessoy, M. A., Oliveira, R. G. de, Mollo, M. C., Lee, E., Matheeussen, A., et al. (2024). Synthesis and anti-trypanosoma cruzi activity of 3-cyanopyridine derivatives. ACS Omega, 9( 20), 22360-22370 + supporting information. doi:10.1021/acsomega.4c01919
NLM
Slafer BW, Dessoy MA, Oliveira RG de, Mollo MC, Lee E, Matheeussen A, Maes L, Caljon G, Ferreira LLG, Krogh R, Andricopulo AD, Cruz L dos R, Mowbray CE, Kratz JM, Dias LC. Synthesis and anti-trypanosoma cruzi activity of 3-cyanopyridine derivatives [Internet]. ACS Omega. 2024 ; 9( 20): 22360-22370 + supporting information.[citado 2024 dez. 30 ] Available from: https://doi.org/10.1021/acsomega.4c01919
Vancouver
Slafer BW, Dessoy MA, Oliveira RG de, Mollo MC, Lee E, Matheeussen A, Maes L, Caljon G, Ferreira LLG, Krogh R, Andricopulo AD, Cruz L dos R, Mowbray CE, Kratz JM, Dias LC. Synthesis and anti-trypanosoma cruzi activity of 3-cyanopyridine derivatives [Internet]. ACS Omega. 2024 ; 9( 20): 22360-22370 + supporting information.[citado 2024 dez. 30 ] Available from: https://doi.org/10.1021/acsomega.4c01919
Artigo de periodico
Discovery of potent, reversible, and competitive cruzain inhibitors with trypanocidal activity: a structure-based drug design approach (2020)
Souza, Mariana Laureano de; Rezende Junior, Celso de Oliveira; Ferreira, Rafaela S. ; Chávez, Rocio Marisol Espinoza; Ferreira, Leonardo Luiz Gomes ; Slafer, Brian W.; Magalhães, Luma Godoy; Andricopulo, Renata Krogh; Oliva, Glaucius ; Cruz, Fabio Cardoso; Dias, Luiz Carlos; Andricopulo, Adriano Defini
Source: Journal of Chemical Information and Modeling. Unidade: IFSC
Subjects: TRIPANOSSOMICIDAS, PLANEJAMENTO DE FÁRMACOS, INIBIDORES QUÍMICOS
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ABNT
SOUZA, Mariana Laureano de et al. Discovery of potent, reversible, and competitive cruzain inhibitors with trypanocidal activity: a structure-based drug design approach. Journal of Chemical Information and Modeling, v. 60, n. 2, p. 1028-1041, 2020Tradução . . Disponível em: https://doi.org/10.1021/acs.jcim.9b00802. Acesso em: 30 dez. 2024.
APA
Souza, M. L. de, Rezende Junior, C. de O., Ferreira, R. S., Chávez, R. M. E., Ferreira, L. L. G., Slafer, B. W., et al. (2020). Discovery of potent, reversible, and competitive cruzain inhibitors with trypanocidal activity: a structure-based drug design approach. Journal of Chemical Information and Modeling, 60( 2), 1028-1041. doi:10.1021/acs.jcim.9b00802
NLM
Souza ML de, Rezende Junior C de O, Ferreira RS, Chávez RME, Ferreira LLG, Slafer BW, Magalhães LG, Andricopulo RK, Oliva G, Cruz FC, Dias LC, Andricopulo AD. Discovery of potent, reversible, and competitive cruzain inhibitors with trypanocidal activity: a structure-based drug design approach [Internet]. Journal of Chemical Information and Modeling. 2020 ; 60( 2): 1028-1041.[citado 2024 dez. 30 ] Available from: https://doi.org/10.1021/acs.jcim.9b00802
Vancouver
Souza ML de, Rezende Junior C de O, Ferreira RS, Chávez RME, Ferreira LLG, Slafer BW, Magalhães LG, Andricopulo RK, Oliva G, Cruz FC, Dias LC, Andricopulo AD. Discovery of potent, reversible, and competitive cruzain inhibitors with trypanocidal activity: a structure-based drug design approach [Internet]. Journal of Chemical Information and Modeling. 2020 ; 60( 2): 1028-1041.[citado 2024 dez. 30 ] Available from: https://doi.org/10.1021/acs.jcim.9b00802
Trabalho de evento-resumo
Orbitides: a quite unusual class of biologically active small peptides in some plant species from brazilian biodiversity (2017)
Pinto, Meri Emili F.; Ramalho, Suelem D.; Nascimento, Marlon de O.; Sanches, Paulo R. S.; Silveira, Edilberto R.; Krogh, Renata; Cilli, Eduardo M.; Andricopulo, Adriano Defini ; Lopes, Norberto Peporine; Bolzani, Vanderlan S.
Source: Proceedings. Conference titles: IUPAC World Chemistry Congress. Unidade: IFSC
Subjects: QUÍMICA MÉDICA, BIODIVERSIDADE
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ABNT
PINTO, Meri Emili F. et al. Orbitides: a quite unusual class of biologically active small peptides in some plant species from brazilian biodiversity. 2017, Anais.. Durham: International Union of Pure and Applied Chemistry - IUPAC, 2017. Disponível em: http://www.neopixdmi.com.br/@mci/iupac2017/. Acesso em: 30 dez. 2024.
APA
Pinto, M. E. F., Ramalho, S. D., Nascimento, M. de O., Sanches, P. R. S., Silveira, E. R., Krogh, R., et al. (2017). Orbitides: a quite unusual class of biologically active small peptides in some plant species from brazilian biodiversity. In Proceedings. Durham: International Union of Pure and Applied Chemistry - IUPAC. Recuperado de http://www.neopixdmi.com.br/@mci/iupac2017/
NLM
Pinto MEF, Ramalho SD, Nascimento M de O, Sanches PRS, Silveira ER, Krogh R, Cilli EM, Andricopulo AD, Lopes NP, Bolzani VS. Orbitides: a quite unusual class of biologically active small peptides in some plant species from brazilian biodiversity [Internet]. Proceedings. 2017 ;[citado 2024 dez. 30 ] Available from: http://www.neopixdmi.com.br/@mci/iupac2017/
Vancouver
Pinto MEF, Ramalho SD, Nascimento M de O, Sanches PRS, Silveira ER, Krogh R, Cilli EM, Andricopulo AD, Lopes NP, Bolzani VS. Orbitides: a quite unusual class of biologically active small peptides in some plant species from brazilian biodiversity [Internet]. Proceedings. 2017 ;[citado 2024 dez. 30 ] Available from: http://www.neopixdmi.com.br/@mci/iupac2017/
Trabalho de evento-resumo
Multi parametric optimization of a series of potent cruzain inhibitors as drug candidates for chagas disease (2017)
Pauli, Ivani; R. Junior, Celso; Slafer, Brian; Dessoy, Marco A.; Souza, Mariana L.; Ferreira, Rafaela S.; Magalhães, Luma G.; Krogh, Renata; Dias, Luiz C.; Andricopulo, Adriano Defini
Source: Proceedings. Conference titles: IUPAC World Chemistry Congress. Unidade: IFSC
Subjects: DOENÇA DE CHAGAS, TRYPANOSOMA CRUZI, MODELAGEM MOLECULAR
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ABNT
PAULI, Ivani et al. Multi parametric optimization of a series of potent cruzain inhibitors as drug candidates for chagas disease. 2017, Anais.. Durham: International Union of Pure and Applied Chemistry - IUPAC, 2017. Disponível em: http://www.neopixdmi.com.br/@mci/iupac2017/. Acesso em: 30 dez. 2024.
APA
Pauli, I., R. Junior, C., Slafer, B., Dessoy, M. A., Souza, M. L., Ferreira, R. S., et al. (2017). Multi parametric optimization of a series of potent cruzain inhibitors as drug candidates for chagas disease. In Proceedings. Durham: International Union of Pure and Applied Chemistry - IUPAC. Recuperado de http://www.neopixdmi.com.br/@mci/iupac2017/
NLM
Pauli I, R. Junior C, Slafer B, Dessoy MA, Souza ML, Ferreira RS, Magalhães LG, Krogh R, Dias LC, Andricopulo AD. Multi parametric optimization of a series of potent cruzain inhibitors as drug candidates for chagas disease [Internet]. Proceedings. 2017 ;[citado 2024 dez. 30 ] Available from: http://www.neopixdmi.com.br/@mci/iupac2017/
Vancouver
Pauli I, R. Junior C, Slafer B, Dessoy MA, Souza ML, Ferreira RS, Magalhães LG, Krogh R, Dias LC, Andricopulo AD. Multi parametric optimization of a series of potent cruzain inhibitors as drug candidates for chagas disease [Internet]. Proceedings. 2017 ;[citado 2024 dez. 30 ] Available from: http://www.neopixdmi.com.br/@mci/iupac2017/
Trabalho de evento-resumo
Identification of carbamoylimidazoles as novel cruzain inhibitors with in vitro and in vivo trypanocidal activity (2017)
Souza, Mariana L.; Ferreira, Rafaela S.; Magalhães, Luma Godoy; Rezende Jr, Celso; Slafer, Brian; Chavez, Rocio; Krogh, Renata; Cruz, Fábio C.; Oliva, Glaucius ; Dias, Luiz C.; Andricopulo, Adriano Defini
Source: Proceedings. Conference titles: IUPAC World Chemistry Congress. Unidade: IFSC
Subjects: DOENÇA DE CHAGAS, TRYPANOSOMA CRUZI, MODELAGEM MOLECULAR
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ABNT
SOUZA, Mariana L. et al. Identification of carbamoylimidazoles as novel cruzain inhibitors with in vitro and in vivo trypanocidal activity. 2017, Anais.. Durham: International Union of Pure and Applied Chemistry - IUPAC, 2017. Disponível em: http://www.neopixdmi.com.br/@mci/iupac2017/. Acesso em: 30 dez. 2024.
APA
Souza, M. L., Ferreira, R. S., Magalhães, L. G., Rezende Jr, C., Slafer, B., Chavez, R., et al. (2017). Identification of carbamoylimidazoles as novel cruzain inhibitors with in vitro and in vivo trypanocidal activity. In Proceedings. Durham: International Union of Pure and Applied Chemistry - IUPAC. Recuperado de http://www.neopixdmi.com.br/@mci/iupac2017/
NLM
Souza ML, Ferreira RS, Magalhães LG, Rezende Jr C, Slafer B, Chavez R, Krogh R, Cruz FC, Oliva G, Dias LC, Andricopulo AD. Identification of carbamoylimidazoles as novel cruzain inhibitors with in vitro and in vivo trypanocidal activity [Internet]. Proceedings. 2017 ;[citado 2024 dez. 30 ] Available from: http://www.neopixdmi.com.br/@mci/iupac2017/
Vancouver
Souza ML, Ferreira RS, Magalhães LG, Rezende Jr C, Slafer B, Chavez R, Krogh R, Cruz FC, Oliva G, Dias LC, Andricopulo AD. Identification of carbamoylimidazoles as novel cruzain inhibitors with in vitro and in vivo trypanocidal activity [Internet]. Proceedings. 2017 ;[citado 2024 dez. 30 ] Available from: http://www.neopixdmi.com.br/@mci/iupac2017/
Trabalho de evento-resumo
Virtual screening strategies for the discovery of new inhibitors of cruzain from Trypanosoma cruzi (2014)
Souza, Mariana Laureano de; Ferreira, Rafaela S.; Krogh, Renata; Oliva, Glaucius ; Dias, Luiz C.; Andricopulo, Adriano Defini
Source: Abstracts. Conference titles: ACS National Meeting and Exposition. Unidade: IFSC
Subjects: TRYPANOSOMA CRUZI, DOENÇA DE CHAGAS, PLANEJAMENTO DE FÁRMACOS
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ABNT
SOUZA, Mariana Laureano de et al. Virtual screening strategies for the discovery of new inhibitors of cruzain from Trypanosoma cruzi. 2014, Anais.. Washington, DC: American Chemical Society - ACS, 2014. . Acesso em: 30 dez. 2024.
APA
Souza, M. L. de, Ferreira, R. S., Krogh, R., Oliva, G., Dias, L. C., & Andricopulo, A. D. (2014). Virtual screening strategies for the discovery of new inhibitors of cruzain from Trypanosoma cruzi. In Abstracts. Washington, DC: American Chemical Society - ACS.
NLM
Souza ML de, Ferreira RS, Krogh R, Oliva G, Dias LC, Andricopulo AD. Virtual screening strategies for the discovery of new inhibitors of cruzain from Trypanosoma cruzi. Abstracts. 2014 ;[citado 2024 dez. 30 ]
Vancouver
Souza ML de, Ferreira RS, Krogh R, Oliva G, Dias LC, Andricopulo AD. Virtual screening strategies for the discovery of new inhibitors of cruzain from Trypanosoma cruzi. Abstracts. 2014 ;[citado 2024 dez. 30 ]
Artigo de periodico
Synthesis, biological evaluation, and structure-activity relationships of potent noncovalent and nonpeptidic cruzain inhibitors as anti-Trypanosoma cruzi agents (2014)
Ferreira, Rafaela S.; Dessoy, Marco A.; Pauli, Ivani; Souza, Mariana L.; Krogh, Renata; Sales, Ana I. L.; Oliva, Glaucius ; Dias, Luiz C.; Andricopulo, Adriano Defini
Source: Journal of Medicinal Chemistry. Unidade: IFSC
Subjects: PLANEJAMENTO DE FÁRMACOS, TRYPANOSOMA CRUZI, DOENÇA DE CHAGAS (TRATAMENTO)
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ABNT
FERREIRA, Rafaela S. et al. Synthesis, biological evaluation, and structure-activity relationships of potent noncovalent and nonpeptidic cruzain inhibitors as anti-Trypanosoma cruzi agents. Journal of Medicinal Chemistry, v. 57, n. 6, p. 2380-2392, 2014Tradução . . Disponível em: https://doi.org/10.1021/jm401709b. Acesso em: 30 dez. 2024.
APA
Ferreira, R. S., Dessoy, M. A., Pauli, I., Souza, M. L., Krogh, R., Sales, A. I. L., et al. (2014). Synthesis, biological evaluation, and structure-activity relationships of potent noncovalent and nonpeptidic cruzain inhibitors as anti-Trypanosoma cruzi agents. Journal of Medicinal Chemistry, 57( 6), 2380-2392. doi:10.1021/jm401709b
NLM
Ferreira RS, Dessoy MA, Pauli I, Souza ML, Krogh R, Sales AIL, Oliva G, Dias LC, Andricopulo AD. Synthesis, biological evaluation, and structure-activity relationships of potent noncovalent and nonpeptidic cruzain inhibitors as anti-Trypanosoma cruzi agents [Internet]. Journal of Medicinal Chemistry. 2014 ; 57( 6): 2380-2392.[citado 2024 dez. 30 ] Available from: https://doi.org/10.1021/jm401709b
Vancouver
Ferreira RS, Dessoy MA, Pauli I, Souza ML, Krogh R, Sales AIL, Oliva G, Dias LC, Andricopulo AD. Synthesis, biological evaluation, and structure-activity relationships of potent noncovalent and nonpeptidic cruzain inhibitors as anti-Trypanosoma cruzi agents [Internet]. Journal of Medicinal Chemistry. 2014 ; 57( 6): 2380-2392.[citado 2024 dez. 30 ] Available from: https://doi.org/10.1021/jm401709b
Trabalho de evento-resumo
Application of bioisosterism approach in the design, synthesis, and biological evaluation of nitrofurazone derivatives as antichagasic candidates (2013)
Trossini, Gustavo Henrique Goulart ; Arribas, Marco; Nishikawa, Michele; Gonçalves, José Eduardo; Oliveira, Tiago Franco de; Loureiro, Ana Paula de Melo ; Storpirtis, Silvia ; Krogh, Renata; Andricopulo, Adriano Defini ; Ferreira, Elizabeth Igne
Source: Abstracts. Conference titles: Spring National Meeting and Exposition. Unidades: FCF, IFSC
Subjects: PLANEJAMENTO DE FÁRMACOS, TRYPANOSOMA CRUZI, DOENÇA DE CHAGAS (ESTUDO;TRATAMENTO)
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ABNT
TROSSINI, Gustavo Henrique Goulart et al. Application of bioisosterism approach in the design, synthesis, and biological evaluation of nitrofurazone derivatives as antichagasic candidates. 2013, Anais.. Washington, DC: American Chemical Society - ACS, 2013. . Acesso em: 30 dez. 2024.
APA
Trossini, G. H. G., Arribas, M., Nishikawa, M., Gonçalves, J. E., Oliveira, T. F. de, Loureiro, A. P. de M., et al. (2013). Application of bioisosterism approach in the design, synthesis, and biological evaluation of nitrofurazone derivatives as antichagasic candidates. In Abstracts. Washington, DC: American Chemical Society - ACS.
NLM
Trossini GHG, Arribas M, Nishikawa M, Gonçalves JE, Oliveira TF de, Loureiro AP de M, Storpirtis S, Krogh R, Andricopulo AD, Ferreira EI. Application of bioisosterism approach in the design, synthesis, and biological evaluation of nitrofurazone derivatives as antichagasic candidates. Abstracts. 2013 ;[citado 2024 dez. 30 ]
Vancouver
Trossini GHG, Arribas M, Nishikawa M, Gonçalves JE, Oliveira TF de, Loureiro AP de M, Storpirtis S, Krogh R, Andricopulo AD, Ferreira EI. Application of bioisosterism approach in the design, synthesis, and biological evaluation of nitrofurazone derivatives as antichagasic candidates. Abstracts. 2013 ;[citado 2024 dez. 30 ]
Trabalho de evento-resumo
SAR studies on a series of reversible competitive inhibitors of cruzain from Trypanosoma cruzi (2013)
Pauli, Ivani; Souza, Mariana L. de Souza; Ferreira, Rafaela S.; Krogh, Renata; Duarte, Simone Michelan; Dessoy, Marco Aurélio; Dias, Luiz Carlos; Andricopulo, Adriano Defini
Source: Abstracts. Conference titles: Spring National Meeting and Exposition. Unidade: IFSC
Subjects: PLANEJAMENTO DE FÁRMACOS, TRYPANOSOMA CRUZI, DOENÇA DE CHAGAS (ESTUDO;TRATAMENTO), ENZIMAS
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
PAULI, Ivani et al. SAR studies on a series of reversible competitive inhibitors of cruzain from Trypanosoma cruzi. 2013, Anais.. Washington, DC: American Chemical Society - ACS, 2013. . Acesso em: 30 dez. 2024.
APA
Pauli, I., Souza, M. L. de S., Ferreira, R. S., Krogh, R., Duarte, S. M., Dessoy, M. A., et al. (2013). SAR studies on a series of reversible competitive inhibitors of cruzain from Trypanosoma cruzi. In Abstracts. Washington, DC: American Chemical Society - ACS.
NLM
Pauli I, Souza ML de S, Ferreira RS, Krogh R, Duarte SM, Dessoy MA, Dias LC, Andricopulo AD. SAR studies on a series of reversible competitive inhibitors of cruzain from Trypanosoma cruzi. Abstracts. 2013 ;[citado 2024 dez. 30 ]
Vancouver
Pauli I, Souza ML de S, Ferreira RS, Krogh R, Duarte SM, Dessoy MA, Dias LC, Andricopulo AD. SAR studies on a series of reversible competitive inhibitors of cruzain from Trypanosoma cruzi. Abstracts. 2013 ;[citado 2024 dez. 30 ]

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