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Artigo de periodico
Structure-activity relationships of novel N-imidazoylpiperazines with potent anti-trypanosoma cruzi activity (2024)
Chávez, Rocio Marisol Espinoza ; Rezende Junior, Celso de Oliveira ; Souza, Mariana Laureano de ; Pauli, Ivani; Valli, Marilia ; Ferreira, Leonardo Luiz Gomes ; Chelucci, Rafael Consolin; Duarte, Simone Michelan ; Krogh, Renata; Silva, Fernando Bezerra Romualdo da; Cruz, Fábio Cardoso; Oliveira, Aldo Sena de ; Andricopulo, Adriano Defini ; Dias, Luiz Carlos
Fonte: Future Medicinal Chemistry. Unidade: IFSC
Assuntos: FÁRMACOS, PLANEJAMENTO DE FÁRMACOS, DOENÇAS PARASITÁRIAS, DOENÇA DE CHAGAS, TRYPANOSOMA CRUZI
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ABNT
CHÁVEZ, Rocio Marisol Espinoza et al. Structure-activity relationships of novel N-imidazoylpiperazines with potent anti-trypanosoma cruzi activity. Future Medicinal Chemistry, v. 16, n. Ja 2024, p. 253-269, 2024Tradução . . Disponível em: https://doi.org/10.4155/fmc-2023-0185. Acesso em: 20 jul. 2024.
APA
Chávez, R. M. E., Rezende Junior, C. de O., Souza, M. L. de, Pauli, I., Valli, M., Ferreira, L. L. G., et al. (2024). Structure-activity relationships of novel N-imidazoylpiperazines with potent anti-trypanosoma cruzi activity. Future Medicinal Chemistry, 16( Ja 2024), 253-269. doi:10.4155/fmc-2023-0185
NLM
Chávez RME, Rezende Junior C de O, Souza ML de, Pauli I, Valli M, Ferreira LLG, Chelucci RC, Duarte SM, Krogh R, Silva FBR da, Cruz FC, Oliveira AS de, Andricopulo AD, Dias LC. Structure-activity relationships of novel N-imidazoylpiperazines with potent anti-trypanosoma cruzi activity [Internet]. Future Medicinal Chemistry. 2024 ; 16( Ja 2024): 253-269.[citado 2024 jul. 20 ] Available from: https://doi.org/10.4155/fmc-2023-0185
Vancouver
Chávez RME, Rezende Junior C de O, Souza ML de, Pauli I, Valli M, Ferreira LLG, Chelucci RC, Duarte SM, Krogh R, Silva FBR da, Cruz FC, Oliveira AS de, Andricopulo AD, Dias LC. Structure-activity relationships of novel N-imidazoylpiperazines with potent anti-trypanosoma cruzi activity [Internet]. Future Medicinal Chemistry. 2024 ; 16( Ja 2024): 253-269.[citado 2024 jul. 20 ] Available from: https://doi.org/10.4155/fmc-2023-0185
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
Fonte: ACS Omega. Unidade: IFSC
Assuntos: 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: 20 jul. 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 jul. 20 ] 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 jul. 20 ] Available from: https://doi.org/10.1021/acsomega.4c01919
Artigo de periodico
Hit-to-lead optimization of a 2-aminobenzimidazole series as new candidates for chagas disease (2023)
Rezende Junior, Celso de Oliveira ; Martinez, Pablo David Grigol; Ferreira, Rafael Augusto Alves; Koovits, Paul John ; Soares, Bruna Miranda ; Ferreira, Leonardo Luiz Gomes ; Duarte, Simone Michelan ; Chelucci, Rafael Consolin; Andricopulo, Adriano Defini ; Matheeussen, An ; Van Pelt, Natascha; Caljon, Guy ; Maes, Louis ; Campbell, Simon; Kratz, Jadel Muller ; Mowbray, Charles E. ; Dias, Luiz Carlos
Fonte: European Journal of Medicinal Chemistry. Unidade: IFSC
Assuntos: DOENÇA DE CHAGAS, PLANEJAMENTO DE FÁRMACOS, TRYPANOSOMA CRUZI
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ABNT
REZENDE JUNIOR, Celso de Oliveira et al. Hit-to-lead optimization of a 2-aminobenzimidazole series as new candidates for chagas disease. European Journal of Medicinal Chemistry, v. 246, n. Ja 2023, p. 114925-1-114925-10 + supplementary data, 2023Tradução . . Disponível em: https://doi.org/10.1016/j.ejmech.2022.114925. Acesso em: 20 jul. 2024.
APA
Rezende Junior, C. de O., Martinez, P. D. G., Ferreira, R. A. A., Koovits, P. J., Soares, B. M., Ferreira, L. L. G., et al. (2023). Hit-to-lead optimization of a 2-aminobenzimidazole series as new candidates for chagas disease. European Journal of Medicinal Chemistry, 246( Ja 2023), 114925-1-114925-10 + supplementary data. doi:10.1016/j.ejmech.2022.114925
NLM
Rezende Junior C de O, Martinez PDG, Ferreira RAA, Koovits PJ, Soares BM, Ferreira LLG, Duarte SM, Chelucci RC, Andricopulo AD, Matheeussen A, Van Pelt N, Caljon G, Maes L, Campbell S, Kratz JM, Mowbray CE, Dias LC. Hit-to-lead optimization of a 2-aminobenzimidazole series as new candidates for chagas disease [Internet]. European Journal of Medicinal Chemistry. 2023 ; 246( Ja 2023): 114925-1-114925-10 + supplementary data.[citado 2024 jul. 20 ] Available from: https://doi.org/10.1016/j.ejmech.2022.114925
Vancouver
Rezende Junior C de O, Martinez PDG, Ferreira RAA, Koovits PJ, Soares BM, Ferreira LLG, Duarte SM, Chelucci RC, Andricopulo AD, Matheeussen A, Van Pelt N, Caljon G, Maes L, Campbell S, Kratz JM, Mowbray CE, Dias LC. Hit-to-lead optimization of a 2-aminobenzimidazole series as new candidates for chagas disease [Internet]. European Journal of Medicinal Chemistry. 2023 ; 246( Ja 2023): 114925-1-114925-10 + supplementary data.[citado 2024 jul. 20 ] Available from: https://doi.org/10.1016/j.ejmech.2022.114925
Artigo de periodico
Multiparameter optimization of Trypanocidal cruzain inhibitors with in vivo activity and favorable pharmacokinetics (2022)
Pauli, Ivani; Rezende Junior, Celso de Oliveira ; Slafer, Brian W.; Dessoy, Marco A.; Souza, Mariana Laureano de ; Ferreira, Leonardo Luiz Gomes ; Adjanohun, Abraham L. M.; Ferreira, Rafaela S.; Magalhães, Luma Godoy; Andricopulo, Renata Krogh; Duarte, Simone Michelan ; Del Pintor, Ricardo Vaz; Silva, Fernando B. R. da; Cruz, Fabio C.; Dias, Luiz C.; Andricopulo, Adriano Defini
Fonte: Frontiers in Pharmacology. Unidade: IFSC
Assuntos: DOENÇA DE CHAGAS, TRYPANOSOMA CRUZI, QUÍMICA MÉDICA, MODELAGEM MOLECULAR, PLANEJAMENTO DE FÁRMACOS
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ABNT
PAULI, Ivani et al. Multiparameter optimization of Trypanocidal cruzain inhibitors with in vivo activity and favorable pharmacokinetics. Frontiers in Pharmacology, v. 12, n. Ja 2022, p. 774069-1-774069-21 + supplementary material, 2022Tradução . . Disponível em: https://doi.org/10.3389/fphar.2021.774069. Acesso em: 20 jul. 2024.
APA
Pauli, I., Rezende Junior, C. de O., Slafer, B. W., Dessoy, M. A., Souza, M. L. de, Ferreira, L. L. G., et al. (2022). Multiparameter optimization of Trypanocidal cruzain inhibitors with in vivo activity and favorable pharmacokinetics. Frontiers in Pharmacology, 12( Ja 2022), 774069-1-774069-21 + supplementary material. doi:10.3389/fphar.2021.774069
NLM
Pauli I, Rezende Junior C de O, Slafer BW, Dessoy MA, Souza ML de, Ferreira LLG, Adjanohun ALM, Ferreira RS, Magalhães LG, Andricopulo RK, Duarte SM, Del Pintor RV, Silva FBR da, Cruz FC, Dias LC, Andricopulo AD. Multiparameter optimization of Trypanocidal cruzain inhibitors with in vivo activity and favorable pharmacokinetics [Internet]. Frontiers in Pharmacology. 2022 ; 12( Ja 2022): 774069-1-774069-21 + supplementary material.[citado 2024 jul. 20 ] Available from: https://doi.org/10.3389/fphar.2021.774069
Vancouver
Pauli I, Rezende Junior C de O, Slafer BW, Dessoy MA, Souza ML de, Ferreira LLG, Adjanohun ALM, Ferreira RS, Magalhães LG, Andricopulo RK, Duarte SM, Del Pintor RV, Silva FBR da, Cruz FC, Dias LC, Andricopulo AD. Multiparameter optimization of Trypanocidal cruzain inhibitors with in vivo activity and favorable pharmacokinetics [Internet]. Frontiers in Pharmacology. 2022 ; 12( Ja 2022): 774069-1-774069-21 + supplementary material.[citado 2024 jul. 20 ] Available from: https://doi.org/10.3389/fphar.2021.774069
Trabalho de evento-resumo
Antitrypanosomal Benzoxazinone series: hit-to-lead campaign and multiparametric optimization (2022)
Mollo, María Cruz; Cruz, Luiza; Dessoy, Marco Aurélio; Lee, Eun; Oliveira, Ramon Guerra de; Dutra, Francielle; Duarte, Simone Michelan ; Andricopulo, Renata Krogh; Ferreira, Leonardo Luiz Gomes ; Chelucci, Rafael Consolin; Feltrin, Clarissa; Moraes, Carolina Borsoi; Andricopulo, Adriano Defini ; Kratz, Jadel; Sjö, Peter; Mowbray, Charles; Dias, Luiz Carlos
Fonte: Anais eletrônicos. Nome do evento: Brazilian Symposium on Medicinal Chemistry - BrazMedChem. Unidades: IFSC, ICB
Assuntos: TRYPANOSOMA CRUZI, PLANEJAMENTO DE FÁRMACOS
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ABNT
MOLLO, María Cruz et al. Antitrypanosomal Benzoxazinone series: hit-to-lead campaign and multiparametric optimization. 2022, Anais.. Campinas: Galoá, 2022. Disponível em: https://proceedings.science/brazmedchem-2022/papers/antitrypanosomal-benzoxazinone-series--hit-to-lead-campaign-and-multiparametric-optimization-. Acesso em: 20 jul. 2024.
APA
Mollo, M. C., Cruz, L., Dessoy, M. A., Lee, E., Oliveira, R. G. de, Dutra, F., et al. (2022). Antitrypanosomal Benzoxazinone series: hit-to-lead campaign and multiparametric optimization. In Anais eletrônicos. Campinas: Galoá. Recuperado de https://proceedings.science/brazmedchem-2022/papers/antitrypanosomal-benzoxazinone-series--hit-to-lead-campaign-and-multiparametric-optimization-.
NLM
Mollo MC, Cruz L, Dessoy MA, Lee E, Oliveira RG de, Dutra F, Duarte SM, Andricopulo RK, Ferreira LLG, Chelucci RC, Feltrin C, Moraes CB, Andricopulo AD, Kratz J, Sjö P, Mowbray C, Dias LC. Antitrypanosomal Benzoxazinone series: hit-to-lead campaign and multiparametric optimization [Internet]. Anais eletrônicos. 2022 ;[citado 2024 jul. 20 ] Available from: https://proceedings.science/brazmedchem-2022/papers/antitrypanosomal-benzoxazinone-series--hit-to-lead-campaign-and-multiparametric-optimization-.
Vancouver
Mollo MC, Cruz L, Dessoy MA, Lee E, Oliveira RG de, Dutra F, Duarte SM, Andricopulo RK, Ferreira LLG, Chelucci RC, Feltrin C, Moraes CB, Andricopulo AD, Kratz J, Sjö P, Mowbray C, Dias LC. Antitrypanosomal Benzoxazinone series: hit-to-lead campaign and multiparametric optimization [Internet]. Anais eletrônicos. 2022 ;[citado 2024 jul. 20 ] Available from: https://proceedings.science/brazmedchem-2022/papers/antitrypanosomal-benzoxazinone-series--hit-to-lead-campaign-and-multiparametric-optimization-.
Artigo de periodico
Hit-to-lead optimization of a benzene sulfonamide series for potential antileishmanial agents (2020)
Koovits, Paul J.; Dessoy, Marcos A.; Matheeussen, An; Maes, Louis; Caljon, Guy; Ferreira, Leonardo Luiz Gomes ; Chelucci, Rafael Consolin; Duarte, Simone Michelan; Andricopulo, Adriano Defini ; Campbell, Simon; Kratz, Jadel M. ; Mowbray, Charles E. ; Dias, Luiz C.
Fonte: RSC Medicinal Chemistry. Unidade: IFSC
Assuntos: TRYPANOSOMA CRUZI, LEISHMANIA INFANTUM, PLANEJAMENTO DE FÁRMACOS
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ABNT
KOOVITS, Paul J. et al. Hit-to-lead optimization of a benzene sulfonamide series for potential antileishmanial agents. RSC Medicinal Chemistry, v. No 2020, n. 11, p. 1267-1274, 2020Tradução . . Disponível em: https://doi.org/10.1039/d0md00165a. Acesso em: 20 jul. 2024.
APA
Koovits, P. J., Dessoy, M. A., Matheeussen, A., Maes, L., Caljon, G., Ferreira, L. L. G., et al. (2020). Hit-to-lead optimization of a benzene sulfonamide series for potential antileishmanial agents. RSC Medicinal Chemistry, No 2020( 11), 1267-1274. doi:10.1039/d0md00165a
NLM
Koovits PJ, Dessoy MA, Matheeussen A, Maes L, Caljon G, Ferreira LLG, Chelucci RC, Duarte SM, Andricopulo AD, Campbell S, Kratz JM, Mowbray CE, Dias LC. Hit-to-lead optimization of a benzene sulfonamide series for potential antileishmanial agents [Internet]. RSC Medicinal Chemistry. 2020 ; No 2020( 11): 1267-1274.[citado 2024 jul. 20 ] Available from: https://doi.org/10.1039/d0md00165a
Vancouver
Koovits PJ, Dessoy MA, Matheeussen A, Maes L, Caljon G, Ferreira LLG, Chelucci RC, Duarte SM, Andricopulo AD, Campbell S, Kratz JM, Mowbray CE, Dias LC. Hit-to-lead optimization of a benzene sulfonamide series for potential antileishmanial agents [Internet]. RSC Medicinal Chemistry. 2020 ; No 2020( 11): 1267-1274.[citado 2024 jul. 20 ] Available from: https://doi.org/10.1039/d0md00165a
Artigo de periodico
Crystal structure, anti-Trypanosoma cruzi and cytotoxic activities of Cu(II) complexes bearing β-diketone and α-diimine ligands (2020)
Paixão, Drielly A.; Oliveira, Barbara C. A.; Almeida, Janaina do Couto; Sousa, Luana M.; Lopes, Carla Duque ; Carneiro, Zumira Aparecida ; Tezuka, Daiane Yukie; Clavijo, Juan Carlos T.; Ellena, Javier ; Polloni, Lorena; Machado, Pedro H. A.; Albuquerque, Sérgio de ; Oliveira Junior, Robson J.; Guilardi, Silvana; Guerra, Wendell
Fonte: Inorganica Chimica Acta. Unidades: IFSC, FCFRP, EESC, BIOENGENHARIA
Assuntos: TRYPANOSOMA CRUZI, PLANEJAMENTO DE FÁRMACOS, CRISTALOGRAFIA
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ABNT
PAIXÃO, Drielly A. et al. Crystal structure, anti-Trypanosoma cruzi and cytotoxic activities of Cu(II) complexes bearing β-diketone and α-diimine ligands. Inorganica Chimica Acta, v. 499, n. Ja 2020, p. 119164-1- 119164-8, 2020Tradução . . Disponível em: https://doi.org/10.1016/j.ica.2019.119164. Acesso em: 20 jul. 2024.
APA
Paixão, D. A., Oliveira, B. C. A., Almeida, J. do C., Sousa, L. M., Lopes, C. D., Carneiro, Z. A., et al. (2020). Crystal structure, anti-Trypanosoma cruzi and cytotoxic activities of Cu(II) complexes bearing β-diketone and α-diimine ligands. Inorganica Chimica Acta, 499( Ja 2020), 119164-1- 119164-8. doi:10.1016/j.ica.2019.119164
NLM
Paixão DA, Oliveira BCA, Almeida J do C, Sousa LM, Lopes CD, Carneiro ZA, Tezuka DY, Clavijo JCT, Ellena J, Polloni L, Machado PHA, Albuquerque S de, Oliveira Junior RJ, Guilardi S, Guerra W. Crystal structure, anti-Trypanosoma cruzi and cytotoxic activities of Cu(II) complexes bearing β-diketone and α-diimine ligands [Internet]. Inorganica Chimica Acta. 2020 ; 499( Ja 2020): 119164-1- 119164-8.[citado 2024 jul. 20 ] Available from: https://doi.org/10.1016/j.ica.2019.119164
Vancouver
Paixão DA, Oliveira BCA, Almeida J do C, Sousa LM, Lopes CD, Carneiro ZA, Tezuka DY, Clavijo JCT, Ellena J, Polloni L, Machado PHA, Albuquerque S de, Oliveira Junior RJ, Guilardi S, Guerra W. Crystal structure, anti-Trypanosoma cruzi and cytotoxic activities of Cu(II) complexes bearing β-diketone and α-diimine ligands [Internet]. Inorganica Chimica Acta. 2020 ; 499( Ja 2020): 119164-1- 119164-8.[citado 2024 jul. 20 ] Available from: https://doi.org/10.1016/j.ica.2019.119164
Artigo de periodico
Discovery of highly potent and selective antiparasitic new oxadiazole and hydroxy-oxindole small molecule hybrids (2020)
Fernandes, Fábio S.; Santos, Hugo; Conti, Caroline; Rodrigues Junior, Manoel T.; Zeoly, Lucas A.; Ferreira, Leonardo Luiz Gomes; Andricopulo, Renata Krogh; Andricopulo, Adriano Defini ; Coelho, Fernando
Fonte: European Journal of Medicinal Chemistry. Unidade: IFSC
Assuntos: ANTIPARASITÁRIOS, TRYPANOSOMA CRUZI, LEISHMANIA INFANTUM, DOENÇA DE CHAGAS
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ABNT
FERNANDES, Fábio S. et al. Discovery of highly potent and selective antiparasitic new oxadiazole and hydroxy-oxindole small molecule hybrids. European Journal of Medicinal Chemistry, v. 201, p. 112418-1-112418-14, 2020Tradução . . Disponível em: https://doi.org/10.1016/j.ejmech.2020.112418. Acesso em: 20 jul. 2024.
APA
Fernandes, F. S., Santos, H., Conti, C., Rodrigues Junior, M. T., Zeoly, L. A., Ferreira, L. L. G., et al. (2020). Discovery of highly potent and selective antiparasitic new oxadiazole and hydroxy-oxindole small molecule hybrids. European Journal of Medicinal Chemistry, 201, 112418-1-112418-14. doi:10.1016/j.ejmech.2020.112418
NLM
Fernandes FS, Santos H, Conti C, Rodrigues Junior MT, Zeoly LA, Ferreira LLG, Andricopulo RK, Andricopulo AD, Coelho F. Discovery of highly potent and selective antiparasitic new oxadiazole and hydroxy-oxindole small molecule hybrids [Internet]. European Journal of Medicinal Chemistry. 2020 ; 201 112418-1-112418-14.[citado 2024 jul. 20 ] Available from: https://doi.org/10.1016/j.ejmech.2020.112418
Vancouver
Fernandes FS, Santos H, Conti C, Rodrigues Junior MT, Zeoly LA, Ferreira LLG, Andricopulo RK, Andricopulo AD, Coelho F. Discovery of highly potent and selective antiparasitic new oxadiazole and hydroxy-oxindole small molecule hybrids [Internet]. European Journal of Medicinal Chemistry. 2020 ; 201 112418-1-112418-14.[citado 2024 jul. 20 ] Available from: https://doi.org/10.1016/j.ejmech.2020.112418
Trabalho de evento-resumo
Antitrypanosomal aminobenzimidazoles: hit to lead expansion of new chemical entities against Trypanosoma cruzi and Leishmania infantum (2019)
Ferreira, R. A. A.; Oliveira Junior, C. R.; Martinez, P. G.; Soares, B. M.; Koovits, P.; Duarte, Simone Michelan; Andricopulo, Renata Krogh; Ferreira, Leonardo Luiz Gomes; Chelucci, Rafael Consolin; Magalhães, Luma Godoy; Andricopulo, Adriano Defini ; Mowbray, C. E.; Kratz, J. M.; Dias, L. C.
Fonte: Anais eletrônicos. Nome do evento: Brazilian Symposium on Medicinal Chemistry - BrazMedChem. Unidade: IFSC
Assuntos: TRYPANOSOMA CRUZI, LEISHMANIA INFANTUM, PLANEJAMENTO DE FÁRMACOS
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
FERREIRA, R. A. A. et al. Antitrypanosomal aminobenzimidazoles: hit to lead expansion of new chemical entities against Trypanosoma cruzi and Leishmania infantum. 2019, Anais.. Campinas: Galoá, 2019. Disponível em: https://proceedings.science/p/107147. Acesso em: 20 jul. 2024.
APA
Ferreira, R. A. A., Oliveira Junior, C. R., Martinez, P. G., Soares, B. M., Koovits, P., Duarte, S. M., et al. (2019). Antitrypanosomal aminobenzimidazoles: hit to lead expansion of new chemical entities against Trypanosoma cruzi and Leishmania infantum. In Anais eletrônicos. Campinas: Galoá. Recuperado de https://proceedings.science/p/107147
NLM
Ferreira RAA, Oliveira Junior CR, Martinez PG, Soares BM, Koovits P, Duarte SM, Andricopulo RK, Ferreira LLG, Chelucci RC, Magalhães LG, Andricopulo AD, Mowbray CE, Kratz JM, Dias LC. Antitrypanosomal aminobenzimidazoles: hit to lead expansion of new chemical entities against Trypanosoma cruzi and Leishmania infantum [Internet]. Anais eletrônicos. 2019 ;[citado 2024 jul. 20 ] Available from: https://proceedings.science/p/107147
Vancouver
Ferreira RAA, Oliveira Junior CR, Martinez PG, Soares BM, Koovits P, Duarte SM, Andricopulo RK, Ferreira LLG, Chelucci RC, Magalhães LG, Andricopulo AD, Mowbray CE, Kratz JM, Dias LC. Antitrypanosomal aminobenzimidazoles: hit to lead expansion of new chemical entities against Trypanosoma cruzi and Leishmania infantum [Internet]. Anais eletrônicos. 2019 ;[citado 2024 jul. 20 ] Available from: https://proceedings.science/p/107147
Artigo de periodico
Structure-based and molecular modeling studies for the discovery of cyclic imides as reversible cruzain inhibitors with potent anti-Trypanosoma cruzi activity (2019)
Ferreira, Rafael A. A.; Pauli, Ivani; Sampaio, Thiago S.; Souza, Mariana Laureano de; Ferreira, Leonardo Luiz Gomes; Magalhães, Luma Godoy; Rezende Junior, Celso O.; Ferreira, Rafaela S.; Andricopulo, Renata Krogh; Dias, Luiz C.; Andricopulo, Adriano Defini
Fonte: Frontiers in Chemistry. Unidade: IFSC
Assuntos: DOENÇA DE CHAGAS, TRYPANOSOMA CRUZI, PLANEJAMENTO DE FÁRMACOS
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
FERREIRA, Rafael A. A. et al. Structure-based and molecular modeling studies for the discovery of cyclic imides as reversible cruzain inhibitors with potent anti-Trypanosoma cruzi activity. Frontiers in Chemistry, v. No 2019, p. 798-1-798-21, 2019Tradução . . Disponível em: https://doi.org/10.3389/fchem.2019.00798. Acesso em: 20 jul. 2024.
APA
Ferreira, R. A. A., Pauli, I., Sampaio, T. S., Souza, M. L. de, Ferreira, L. L. G., Magalhães, L. G., et al. (2019). Structure-based and molecular modeling studies for the discovery of cyclic imides as reversible cruzain inhibitors with potent anti-Trypanosoma cruzi activity. Frontiers in Chemistry, No 2019, 798-1-798-21. doi:10.3389/fchem.2019.00798
NLM
Ferreira RAA, Pauli I, Sampaio TS, Souza ML de, Ferreira LLG, Magalhães LG, Rezende Junior CO, Ferreira RS, Andricopulo RK, Dias LC, Andricopulo AD. Structure-based and molecular modeling studies for the discovery of cyclic imides as reversible cruzain inhibitors with potent anti-Trypanosoma cruzi activity [Internet]. Frontiers in Chemistry. 2019 ; No 2019 798-1-798-21.[citado 2024 jul. 20 ] Available from: https://doi.org/10.3389/fchem.2019.00798
Vancouver
Ferreira RAA, Pauli I, Sampaio TS, Souza ML de, Ferreira LLG, Magalhães LG, Rezende Junior CO, Ferreira RS, Andricopulo RK, Dias LC, Andricopulo AD. Structure-based and molecular modeling studies for the discovery of cyclic imides as reversible cruzain inhibitors with potent anti-Trypanosoma cruzi activity [Internet]. Frontiers in Chemistry. 2019 ; No 2019 798-1-798-21.[citado 2024 jul. 20 ] Available from: https://doi.org/10.3389/fchem.2019.00798
Trabalho de evento-resumo
Carbamoylimidazoles as potent cruzain inhibitors with in vitro and in vivo trypanocidal activity: a structure-based drug design approach (2019)
Rezende Junior, Celso; Souza, Mariana L.; Chavez, Rocio; Ferreira, Rafaela S.; Slafer, Brian W.; Cruz, Fábio C.; Ferreira, Leonardo Luiz Gomes; Magalhães, Luma Godoy; Andricopulo, Renata Krogh; Oliva, Glaucius ; Andricopulo, Adriano Defini ; Dias, Luiz C.
Fonte: Anais eletrônicos. Nome do evento: Brazilian Symposium on Medicinal Chemistry - BrazMedChem. Unidade: IFSC
Assuntos: DOENÇA DE CHAGAS, TRYPANOSOMA CRUZI, PLANEJAMENTO DE FÁRMACOS
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ABNT
REZENDE JUNIOR, Celso et al. Carbamoylimidazoles as potent cruzain inhibitors with in vitro and in vivo trypanocidal activity: a structure-based drug design approach. 2019, Anais.. Campinas: Galoá, 2019. Disponível em: https://proceedings.science/p/107156. Acesso em: 20 jul. 2024.
APA
Rezende Junior, C., Souza, M. L., Chavez, R., Ferreira, R. S., Slafer, B. W., Cruz, F. C., et al. (2019). Carbamoylimidazoles as potent cruzain inhibitors with in vitro and in vivo trypanocidal activity: a structure-based drug design approach. In Anais eletrônicos. Campinas: Galoá. Recuperado de https://proceedings.science/p/107156
NLM
Rezende Junior C, Souza ML, Chavez R, Ferreira RS, Slafer BW, Cruz FC, Ferreira LLG, Magalhães LG, Andricopulo RK, Oliva G, Andricopulo AD, Dias LC. Carbamoylimidazoles as potent cruzain inhibitors with in vitro and in vivo trypanocidal activity: a structure-based drug design approach [Internet]. Anais eletrônicos. 2019 ;[citado 2024 jul. 20 ] Available from: https://proceedings.science/p/107156
Vancouver
Rezende Junior C, Souza ML, Chavez R, Ferreira RS, Slafer BW, Cruz FC, Ferreira LLG, Magalhães LG, Andricopulo RK, Oliva G, Andricopulo AD, Dias LC. Carbamoylimidazoles as potent cruzain inhibitors with in vitro and in vivo trypanocidal activity: a structure-based drug design approach [Internet]. Anais eletrônicos. 2019 ;[citado 2024 jul. 20 ] Available from: https://proceedings.science/p/107156
Artigo de periodico
Occurrences of triatomines (Hemiptera: Reduviidae) and first reports of Panstrongylus geniculatus in urban environments in the city of Sao Paulo, Brazil (2018)
Ceretti Junior, Walter; Alvarez, Julia Vono; Duarte, Agnaldo Nepomuceno; Marques, Sandro; Marrelli, Mauro Toledo ; Matos Júnior, Marco Otávio de; Ribeiro, Aline Rimoldi ; Rosa, Joao Aristeu da; Silva, Rubens Antonio da; Vendrami, Daniel Pagotto
Fonte: Revista do Instituto de Medicina Tropical de São Paulo. Unidade: FSP
Assuntos: HEMIPTERA, VIGILÂNCIA EPIDEMIOLÓGICA, TRIATOMINAE, ENTOMOLOGIA, DOENÇA DE CHAGAS, TRYPANOSOMA CRUZI
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ABNT
CERETTI JUNIOR, Walter et al. Occurrences of triatomines (Hemiptera: Reduviidae) and first reports of Panstrongylus geniculatus in urban environments in the city of Sao Paulo, Brazil. Revista do Instituto de Medicina Tropical de São Paulo, v. 60, p. [16], 2018Tradução . . Disponível em: https://doi.org/10.1590/s1678-9946201860033. Acesso em: 20 jul. 2024.
APA
Ceretti Junior, W., Alvarez, J. V., Duarte, A. N., Marques, S., Marrelli, M. T., Matos Júnior, M. O. de, et al. (2018). Occurrences of triatomines (Hemiptera: Reduviidae) and first reports of Panstrongylus geniculatus in urban environments in the city of Sao Paulo, Brazil. Revista do Instituto de Medicina Tropical de São Paulo, 60, [16]. doi:10.1590/s1678-9946201860033
NLM
Ceretti Junior W, Alvarez JV, Duarte AN, Marques S, Marrelli MT, Matos Júnior MO de, Ribeiro AR , Rosa JA da, Silva RA da, Vendrami DP. Occurrences of triatomines (Hemiptera: Reduviidae) and first reports of Panstrongylus geniculatus in urban environments in the city of Sao Paulo, Brazil [Internet]. Revista do Instituto de Medicina Tropical de São Paulo. 2018 ;60 [16].[citado 2024 jul. 20 ] Available from: https://doi.org/10.1590/s1678-9946201860033
Vancouver
Ceretti Junior W, Alvarez JV, Duarte AN, Marques S, Marrelli MT, Matos Júnior MO de, Ribeiro AR , Rosa JA da, Silva RA da, Vendrami DP. Occurrences of triatomines (Hemiptera: Reduviidae) and first reports of Panstrongylus geniculatus in urban environments in the city of Sao Paulo, Brazil [Internet]. Revista do Instituto de Medicina Tropical de São Paulo. 2018 ;60 [16].[citado 2024 jul. 20 ] Available from: https://doi.org/10.1590/s1678-9946201860033
Trabalho de evento-resumo
Structure-activity relationships for a series of benzimidazole derivatives as cruzain inhibitors (2018)
Ferreira, Leonardo Luiz Gomes; Pauli, Ivani; Souza, Mariana L.; Oliva, Glaucius; Ferreira, Rafaela S.; Dessoy, Marco A.; Slafer, Brian W.; Dias, Luiz C.; Andricopulo, Adriano Defini
Fonte: Livro de Resumos. Nome do evento: Reunião Anual da Sociedade Brasileira de Química - SBQ. Unidade: IFSC
Assuntos: DOENÇA DE CHAGAS, TRYPANOSOMA CRUZI, QUÍMICA MÉDICA, MODELAGEM MOLECULAR
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ABNT
FERREIRA, Leonardo Luiz Gomes et al. Structure-activity relationships for a series of benzimidazole derivatives as cruzain inhibitors. 2018, Anais.. São Paulo: Sociedade Brasileira de Química - SBQ, 2018. Disponível em: http://www.sbq.org.br/41ra/anexos/livro-resumos-41ra.pdf. Acesso em: 20 jul. 2024.
APA
Ferreira, L. L. G., Pauli, I., Souza, M. L., Oliva, G., Ferreira, R. S., Dessoy, M. A., et al. (2018). Structure-activity relationships for a series of benzimidazole derivatives as cruzain inhibitors. In Livro de Resumos. São Paulo: Sociedade Brasileira de Química - SBQ. Recuperado de http://www.sbq.org.br/41ra/anexos/livro-resumos-41ra.pdf
NLM
Ferreira LLG, Pauli I, Souza ML, Oliva G, Ferreira RS, Dessoy MA, Slafer BW, Dias LC, Andricopulo AD. Structure-activity relationships for a series of benzimidazole derivatives as cruzain inhibitors [Internet]. Livro de Resumos. 2018 ;[citado 2024 jul. 20 ] Available from: http://www.sbq.org.br/41ra/anexos/livro-resumos-41ra.pdf
Vancouver
Ferreira LLG, Pauli I, Souza ML, Oliva G, Ferreira RS, Dessoy MA, Slafer BW, Dias LC, Andricopulo AD. Structure-activity relationships for a series of benzimidazole derivatives as cruzain inhibitors [Internet]. Livro de Resumos. 2018 ;[citado 2024 jul. 20 ] Available from: http://www.sbq.org.br/41ra/anexos/livro-resumos-41ra.pdf
Artigo de periodico
Antiplasmodial and trypanocidal activity of violacein and deoxyviolacein produced from synthetic operons (2018)
Bilsland, Elizabeth; Tavella, Tatyana A.; Krogh, Renata; Stokes, Jamie E.; Roberts, Annabelle; Ajioka, James; Spring, David R.; Andricopulo, Adriano Defini; Costa, Fabio T. M.; Oliver, Stephen G.
Fonte: BMC Biotechnology. Unidade: IFSC
Assuntos: QUÍMICA MÉDICA, TRYPANOSOMA CRUZI, PLANEJAMENTO DE FÁRMACOS, MODELAGEM MOLECULAR
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ABNT
BILSLAND, Elizabeth et al. Antiplasmodial and trypanocidal activity of violacein and deoxyviolacein produced from synthetic operons. BMC Biotechnology, v. 18, p. 22-1-22-8, 2018Tradução . . Disponível em: https://doi.org/10.1186/s12896-018-0428-z. Acesso em: 20 jul. 2024.
APA
Bilsland, E., Tavella, T. A., Krogh, R., Stokes, J. E., Roberts, A., Ajioka, J., et al. (2018). Antiplasmodial and trypanocidal activity of violacein and deoxyviolacein produced from synthetic operons. BMC Biotechnology, 18, 22-1-22-8. doi:10.1186/s12896-018-0428-z
NLM
Bilsland E, Tavella TA, Krogh R, Stokes JE, Roberts A, Ajioka J, Spring DR, Andricopulo AD, Costa FTM, Oliver SG. Antiplasmodial and trypanocidal activity of violacein and deoxyviolacein produced from synthetic operons [Internet]. BMC Biotechnology. 2018 ; 18 22-1-22-8.[citado 2024 jul. 20 ] Available from: https://doi.org/10.1186/s12896-018-0428-z
Vancouver
Bilsland E, Tavella TA, Krogh R, Stokes JE, Roberts A, Ajioka J, Spring DR, Andricopulo AD, Costa FTM, Oliver SG. Antiplasmodial and trypanocidal activity of violacein and deoxyviolacein produced from synthetic operons [Internet]. BMC Biotechnology. 2018 ; 18 22-1-22-8.[citado 2024 jul. 20 ] Available from: https://doi.org/10.1186/s12896-018-0428-z
Artigo de periodico
Isolation, derivative synthesis, and structure-activity relationships of antiparasitic bromopyrrole alkaloids from the marine sponge tedania brasiliensis (2018)
Parra, Lizbeth Lorena López; Bertonha, Ariane Fernandes; Severo, Ivan Rodrigues Maranho; Aguiar, Anna Caroline Campos; Souza, Guilherme Eduardo de; Oliva, Glaucius; Guido, Rafael Victorio Carvalho; Grazzia, Nathalia; Costa, Tábata C.; Miguel, Danilo Ciccone; Gadelha, Fernanda Ramos; Ferreira, Antonio G.; Hadju, Eduardo; Romo, Daniel; Berlinck, Roberto Gomes de Souza
Fonte: Journal of Natural Products. Unidades: IFSC, IQSC
Assuntos: TRYPANOSOMA CRUZI, PRODUTOS NATURAIS
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
PARRA, Lizbeth Lorena López et al. Isolation, derivative synthesis, and structure-activity relationships of antiparasitic bromopyrrole alkaloids from the marine sponge tedania brasiliensis. Journal of Natural Products, v. 81, n. 1, p. 188-202, 2018Tradução . . Disponível em: https://doi.org/10.1021/acs.jnatprod.7b00876. Acesso em: 20 jul. 2024.
APA
Parra, L. L. L., Bertonha, A. F., Severo, I. R. M., Aguiar, A. C. C., Souza, G. E. de, Oliva, G., et al. (2018). Isolation, derivative synthesis, and structure-activity relationships of antiparasitic bromopyrrole alkaloids from the marine sponge tedania brasiliensis. Journal of Natural Products, 81( 1), 188-202. doi:10.1021/acs.jnatprod.7b00876
NLM
Parra LLL, Bertonha AF, Severo IRM, Aguiar ACC, Souza GE de, Oliva G, Guido RVC, Grazzia N, Costa TC, Miguel DC, Gadelha FR, Ferreira AG, Hadju E, Romo D, Berlinck RG de S. Isolation, derivative synthesis, and structure-activity relationships of antiparasitic bromopyrrole alkaloids from the marine sponge tedania brasiliensis [Internet]. Journal of Natural Products. 2018 ; 81( 1): 188-202.[citado 2024 jul. 20 ] Available from: https://doi.org/10.1021/acs.jnatprod.7b00876
Vancouver
Parra LLL, Bertonha AF, Severo IRM, Aguiar ACC, Souza GE de, Oliva G, Guido RVC, Grazzia N, Costa TC, Miguel DC, Gadelha FR, Ferreira AG, Hadju E, Romo D, Berlinck RG de S. Isolation, derivative synthesis, and structure-activity relationships of antiparasitic bromopyrrole alkaloids from the marine sponge tedania brasiliensis [Internet]. Journal of Natural Products. 2018 ; 81( 1): 188-202.[citado 2024 jul. 20 ] Available from: https://doi.org/10.1021/acs.jnatprod.7b00876
Artigo de periodico
Molecular modeling and structure-activity relationships for a series of benzimidazole derivatives as cruzain inhibitors (2017)
Pauli, Ivani; Ferreira, Leonardo Luiz Gomes; Souza, Mariana L.; Oliva, Glaucius; Ferreira, Rafaela S.; Dessoy, Marco A.; Slafer, Brian W.; Dias, Luiz C.; Andricopulo, Adriano Defini
Fonte: Future Medicinal Chemistry. Unidade: IFSC
Assuntos: DOENÇA DE CHAGAS, TRYPANOSOMA CRUZI, MODELAGEM MOLECULAR
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ABNT
PAULI, Ivani et al. Molecular modeling and structure-activity relationships for a series of benzimidazole derivatives as cruzain inhibitors. Future Medicinal Chemistry, v. 9, n. 7, p. 641-657, 2017Tradução . . Disponível em: https://doi.org/10.4155/fmc-2016-0236. Acesso em: 20 jul. 2024.
APA
Pauli, I., Ferreira, L. L. G., Souza, M. L., Oliva, G., Ferreira, R. S., Dessoy, M. A., et al. (2017). Molecular modeling and structure-activity relationships for a series of benzimidazole derivatives as cruzain inhibitors. Future Medicinal Chemistry, 9( 7), 641-657. doi:10.4155/fmc-2016-0236
NLM
Pauli I, Ferreira LLG, Souza ML, Oliva G, Ferreira RS, Dessoy MA, Slafer BW, Dias LC, Andricopulo AD. Molecular modeling and structure-activity relationships for a series of benzimidazole derivatives as cruzain inhibitors [Internet]. Future Medicinal Chemistry. 2017 ; 9( 7): 641-657.[citado 2024 jul. 20 ] Available from: https://doi.org/10.4155/fmc-2016-0236
Vancouver
Pauli I, Ferreira LLG, Souza ML, Oliva G, Ferreira RS, Dessoy MA, Slafer BW, Dias LC, Andricopulo AD. Molecular modeling and structure-activity relationships for a series of benzimidazole derivatives as cruzain inhibitors [Internet]. Future Medicinal Chemistry. 2017 ; 9( 7): 641-657.[citado 2024 jul. 20 ] Available from: https://doi.org/10.4155/fmc-2016-0236
Trabalho de evento-resumo
Molecular modeling studies for a series of benzimidazole derivatives as cruzain inhibitors with anti-Trypanosoma cruzi activity (2017)
Pauli, Ivani; Ferreira, Leonardo Luiz Gomes; Souza, Mariana de; Ferreira, Rafaela; Dessoy, Marco; Slafer, Brian; Oliva, Glaucius; Dias, Luiz; Andricopulo, Adriano Defini
Fonte: Abstracts. Nome do evento: ACS National Meeting and Exposition. Unidade: IFSC
Assuntos: TRYPANOSOMA CRUZI, DOENÇA DE CHAGAS, PLANEJAMENTO DE FÁRMACOS
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
PAULI, Ivani et al. Molecular modeling studies for a series of benzimidazole derivatives as cruzain inhibitors with anti-Trypanosoma cruzi activity. 2017, Anais.. Washington, DC: American Chemical Society - ACS, 2017. Disponível em: https://ep70.eventpilot.us/web/page.php?page=IntHtml&project=ACS17SPRING&id=2645407. Acesso em: 20 jul. 2024.
APA
Pauli, I., Ferreira, L. L. G., Souza, M. de, Ferreira, R., Dessoy, M., Slafer, B., et al. (2017). Molecular modeling studies for a series of benzimidazole derivatives as cruzain inhibitors with anti-Trypanosoma cruzi activity. In Abstracts. Washington, DC: American Chemical Society - ACS. Recuperado de https://ep70.eventpilot.us/web/page.php?page=IntHtml&project=ACS17SPRING&id=2645407
NLM
Pauli I, Ferreira LLG, Souza M de, Ferreira R, Dessoy M, Slafer B, Oliva G, Dias L, Andricopulo AD. Molecular modeling studies for a series of benzimidazole derivatives as cruzain inhibitors with anti-Trypanosoma cruzi activity [Internet]. Abstracts. 2017 ;[citado 2024 jul. 20 ] Available from: https://ep70.eventpilot.us/web/page.php?page=IntHtml&project=ACS17SPRING&id=2645407
Vancouver
Pauli I, Ferreira LLG, Souza M de, Ferreira R, Dessoy M, Slafer B, Oliva G, Dias L, Andricopulo AD. Molecular modeling studies for a series of benzimidazole derivatives as cruzain inhibitors with anti-Trypanosoma cruzi activity [Internet]. Abstracts. 2017 ;[citado 2024 jul. 20 ] Available from: https://ep70.eventpilot.us/web/page.php?page=IntHtml&project=ACS17SPRING&id=2645407
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
Fonte: Proceedings. Nome do evento: IUPAC World Chemistry Congress. Unidade: IFSC
Assuntos: 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: 20 jul. 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 jul. 20 ] 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 jul. 20 ] 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
Fonte: Proceedings. Nome do evento: IUPAC World Chemistry Congress. Unidade: IFSC
Assuntos: DOENÇA DE CHAGAS, TRYPANOSOMA CRUZI, MODELAGEM MOLECULAR
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
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: 20 jul. 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 jul. 20 ] 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 jul. 20 ] Available from: http://www.neopixdmi.com.br/@mci/iupac2017/
Trabalho de evento-resumo
Bioisoster hybrids of N-acylhydrazone and furoxan groups: is cruzain the target for those potential anti-T. cruzi compounds? (2016)
Serafim, Ricardo A. M.; Oliveira, Tiago F.; Loureiro, Ana Paula de Melo ; Krogh, Renata; Andricopulo, Adriano Defini; Dias, Luiz C.; Ferreira, Elizabeth Igne
Fonte: Full Abstracts. Nome do evento: Brazilian Symposium on Medicinal Chemistry - BrazMedChem. Unidades: FCF, IFSC
Assuntos: TRYPANOSOMA CRUZI, PLANEJAMENTO DE FÁRMACOS, ANTIPARASITÁRIOS
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
SERAFIM, Ricardo A. M. et al. Bioisoster hybrids of N-acylhydrazone and furoxan groups: is cruzain the target for those potential anti-T. cruzi compounds? 2016, Anais.. São Paulo: Sociedade Brasileira de Química - SBQ, 2016. Disponível em: http://brazmedchem2016.com.br/images/mcd_session.pdf. Acesso em: 20 jul. 2024.
APA
Serafim, R. A. M., Oliveira, T. F., Loureiro, A. P. de M., Krogh, R., Andricopulo, A. D., Dias, L. C., & Ferreira, E. I. (2016). Bioisoster hybrids of N-acylhydrazone and furoxan groups: is cruzain the target for those potential anti-T. cruzi compounds? In Full Abstracts. São Paulo: Sociedade Brasileira de Química - SBQ. Recuperado de http://brazmedchem2016.com.br/images/mcd_session.pdf
NLM
Serafim RAM, Oliveira TF, Loureiro AP de M, Krogh R, Andricopulo AD, Dias LC, Ferreira EI. Bioisoster hybrids of N-acylhydrazone and furoxan groups: is cruzain the target for those potential anti-T. cruzi compounds? [Internet]. Full Abstracts. 2016 ;[citado 2024 jul. 20 ] Available from: http://brazmedchem2016.com.br/images/mcd_session.pdf
Vancouver
Serafim RAM, Oliveira TF, Loureiro AP de M, Krogh R, Andricopulo AD, Dias LC, Ferreira EI. Bioisoster hybrids of N-acylhydrazone and furoxan groups: is cruzain the target for those potential anti-T. cruzi compounds? [Internet]. Full Abstracts. 2016 ;[citado 2024 jul. 20 ] Available from: http://brazmedchem2016.com.br/images/mcd_session.pdf

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