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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
Source: Future Medicinal Chemistry. Unidade: IFSC
Subjects: 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: 28 jun. 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 jun. 28 ] 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 jun. 28 ] 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
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: 28 jun. 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 jun. 28 ] 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 jun. 28 ] Available from: https://doi.org/10.1021/acsomega.4c01919
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
Source: Frontiers in Pharmacology. Unidade: IFSC
Subjects: 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: 28 jun. 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 jun. 28 ] 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 jun. 28 ] Available from: https://doi.org/10.3389/fphar.2021.774069
Artigo de periodico
Synthesis and investigation of the trypanocidal potential of novel 1,2,3-triazole-selenide hybrids (2022)
Chipoline, Ingrid C.; Brasil, Beatrice F. A; S. Neto, José S.; Valli, Marilia; Andricopulo, Renata Krogh; Cenci, Arthur R.; Teixeira, Kerolain F.; Zapp, Eduardo; Brondani, Daniela; Ferreira, Leonardo Luiz Gomes; Andricopulo, Adriano Defini ; Oliveira, Aldo S.; Nascimento, Vanessa
Source: European Journal of Medicinal Chemistry. Unidade: IFSC
Subjects: DOENÇA DE CHAGAS, TRIPANOSSOMICIDAS, TRYPANOSOMA CRUZI
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ABNT
CHIPOLINE, Ingrid C. et al. Synthesis and investigation of the trypanocidal potential of novel 1,2,3-triazole-selenide hybrids. European Journal of Medicinal Chemistry, v. 243, p. 114687-1-114687-9, 2022Tradução . . Disponível em: https://doi.org/10.1016/j.ejmech.2022.114687. Acesso em: 28 jun. 2024.
APA
Chipoline, I. C., Brasil, B. F. A., S. Neto, J. S., Valli, M., Andricopulo, R. K., Cenci, A. R., et al. (2022). Synthesis and investigation of the trypanocidal potential of novel 1,2,3-triazole-selenide hybrids. European Journal of Medicinal Chemistry, 243, 114687-1-114687-9. doi:10.1016/j.ejmech.2022.114687
NLM
Chipoline IC, Brasil BFA, S. Neto JS, Valli M, Andricopulo RK, Cenci AR, Teixeira KF, Zapp E, Brondani D, Ferreira LLG, Andricopulo AD, Oliveira AS, Nascimento V. Synthesis and investigation of the trypanocidal potential of novel 1,2,3-triazole-selenide hybrids [Internet]. European Journal of Medicinal Chemistry. 2022 ; 243 114687-1-114687-9.[citado 2024 jun. 28 ] Available from: https://doi.org/10.1016/j.ejmech.2022.114687
Vancouver
Chipoline IC, Brasil BFA, S. Neto JS, Valli M, Andricopulo RK, Cenci AR, Teixeira KF, Zapp E, Brondani D, Ferreira LLG, Andricopulo AD, Oliveira AS, Nascimento V. Synthesis and investigation of the trypanocidal potential of novel 1,2,3-triazole-selenide hybrids [Internet]. European Journal of Medicinal Chemistry. 2022 ; 243 114687-1-114687-9.[citado 2024 jun. 28 ] Available from: https://doi.org/10.1016/j.ejmech.2022.114687
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
Source: Anais eletrônicos. Conference titles: Brazilian Symposium on Medicinal Chemistry - BrazMedChem. Unidades: IFSC, ICB
Subjects: 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: 28 jun. 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 jun. 28 ] 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 jun. 28 ] Available from: https://proceedings.science/brazmedchem-2022/papers/antitrypanosomal-benzoxazinone-series--hit-to-lead-campaign-and-multiparametric-optimization-.
Artigo de periodico
Trypanosomatid selenophosphate synthetase structure, function and interaction with selenocysteine lyase (2020)
Silva, Marco Túlio Alves da ; Silva, Ivan Rosa e ; Faim, Lívia Maria ; Bellini, Natália Karla ; Pereira, Murilo Leão ; Lima, Ana Laura; Jesus, Teresa Cristina Leandro de; Costa, Fernanda Cristina ; Watanabe, Tatiana Faria; Pereira, Humberto d'Muniz ; Valentini, Sandro Roberto ; Zanelli, Cleslei Fernando ; Borges, Julio Cesar ; Dias, Marcio Vinicius Bertacine ; Cunha, Júlia Pinheiro Chagas da ; Mittra, Bidyottam ; Andrews, Norma W. ; Thiemann, Otávio Henrique
Source: PLOS Neglected Tropical Diseases. Unidades: IFSC, IQSC, ICB
Subjects: TRYPANOSOMA CRUZI, TRYPANOSOMA, SELÊNIO, PROTEÍNAS, MICROBIOLOGIA
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ABNT
SILVA, Marco Túlio Alves da et al. Trypanosomatid selenophosphate synthetase structure, function and interaction with selenocysteine lyase. PLOS Neglected Tropical Diseases, v. 14, n. 10, p. e0008091-1-e0008091-31, 2020Tradução . . Disponível em: https://doi.org/10.1371/journal.pntd.0008091. Acesso em: 28 jun. 2024.
APA
Silva, M. T. A. da, Silva, I. R. e, Faim, L. M., Bellini, N. K., Pereira, M. L., Lima, A. L., et al. (2020). Trypanosomatid selenophosphate synthetase structure, function and interaction with selenocysteine lyase. PLOS Neglected Tropical Diseases, 14( 10), e0008091-1-e0008091-31. doi:10.1371/journal.pntd.0008091
NLM
Silva MTA da, Silva IR e, Faim LM, Bellini NK, Pereira ML, Lima AL, Jesus TCL de, Costa FC, Watanabe TF, Pereira H d'M, Valentini SR, Zanelli CF, Borges JC, Dias MVB, Cunha JPC da, Mittra B, Andrews NW, Thiemann OH. Trypanosomatid selenophosphate synthetase structure, function and interaction with selenocysteine lyase [Internet]. PLOS Neglected Tropical Diseases. 2020 ; 14( 10): e0008091-1-e0008091-31.[citado 2024 jun. 28 ] Available from: https://doi.org/10.1371/journal.pntd.0008091
Vancouver
Silva MTA da, Silva IR e, Faim LM, Bellini NK, Pereira ML, Lima AL, Jesus TCL de, Costa FC, Watanabe TF, Pereira H d'M, Valentini SR, Zanelli CF, Borges JC, Dias MVB, Cunha JPC da, Mittra B, Andrews NW, Thiemann OH. Trypanosomatid selenophosphate synthetase structure, function and interaction with selenocysteine lyase [Internet]. PLOS Neglected Tropical Diseases. 2020 ; 14( 10): e0008091-1-e0008091-31.[citado 2024 jun. 28 ] Available from: https://doi.org/10.1371/journal.pntd.0008091
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
Source: European Journal of Medicinal Chemistry. Unidade: IFSC
Subjects: 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: 28 jun. 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 jun. 28 ] 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 jun. 28 ] Available from: https://doi.org/10.1016/j.ejmech.2020.112418
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.
Source: RSC Medicinal Chemistry. Unidade: IFSC
Subjects: 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: 28 jun. 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 jun. 28 ] 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 jun. 28 ] Available from: https://doi.org/10.1039/d0md00165a
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
Source: Frontiers in Chemistry. Unidade: IFSC
Subjects: DOENÇA DE CHAGAS, TRYPANOSOMA CRUZI, PLANEJAMENTO DE FÁRMACOS
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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: 28 jun. 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 jun. 28 ] 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 jun. 28 ] 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.
Source: Anais eletrônicos. Conference titles: Brazilian Symposium on Medicinal Chemistry - BrazMedChem. Unidade: IFSC
Subjects: DOENÇA DE CHAGAS, TRYPANOSOMA CRUZI, PLANEJAMENTO DE FÁRMACOS
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
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: 28 jun. 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 jun. 28 ] 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 jun. 28 ] Available from: https://proceedings.science/p/107156
Artigo de periodico
Investigating the structure-activity relationships of N’-[(5-nitrofuran-2-yl) methylene] substituted hydrazides against Trypanosoma cruzi to design novel active compounds (2018)
Palace-Berl, Fanny; Pasqualoto, Kerly Fernanda Mesquita; Zingales, Bianca ; Moraes, Carolina Borsoi; Bury, Mariana; Franco, Caio Haddad; Silva Neto, Adelson Lopes da; Murayama, João Sussumu; Nunes, Solange Lessa; Silva, Marcelo Nunes da; Tavares, Leoberto Costa
Source: European Journal of Medicinal Chemistry. Unidades: IQ, FCF
Subjects: TRYPANOSOMA CRUZI, DOENÇA DE CHAGAS
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ABNT
PALACE-BERL, Fanny et al. Investigating the structure-activity relationships of N’-[(5-nitrofuran-2-yl) methylene] substituted hydrazides against Trypanosoma cruzi to design novel active compounds. European Journal of Medicinal Chemistry, v. 144, p. 29-40, 2018Tradução . . Disponível em: https://doi.org/10.1016/j.ejmech.2017.12.011. Acesso em: 28 jun. 2024.
APA
Palace-Berl, F., Pasqualoto, K. F. M., Zingales, B., Moraes, C. B., Bury, M., Franco, C. H., et al. (2018). Investigating the structure-activity relationships of N’-[(5-nitrofuran-2-yl) methylene] substituted hydrazides against Trypanosoma cruzi to design novel active compounds. European Journal of Medicinal Chemistry, 144, 29-40. doi:10.1016/j.ejmech.2017.12.011
NLM
Palace-Berl F, Pasqualoto KFM, Zingales B, Moraes CB, Bury M, Franco CH, Silva Neto AL da, Murayama JS, Nunes SL, Silva MN da, Tavares LC. Investigating the structure-activity relationships of N’-[(5-nitrofuran-2-yl) methylene] substituted hydrazides against Trypanosoma cruzi to design novel active compounds [Internet]. European Journal of Medicinal Chemistry. 2018 ; 144 29-40.[citado 2024 jun. 28 ] Available from: https://doi.org/10.1016/j.ejmech.2017.12.011
Vancouver
Palace-Berl F, Pasqualoto KFM, Zingales B, Moraes CB, Bury M, Franco CH, Silva Neto AL da, Murayama JS, Nunes SL, Silva MN da, Tavares LC. Investigating the structure-activity relationships of N’-[(5-nitrofuran-2-yl) methylene] substituted hydrazides against Trypanosoma cruzi to design novel active compounds [Internet]. European Journal of Medicinal Chemistry. 2018 ; 144 29-40.[citado 2024 jun. 28 ] Available from: https://doi.org/10.1016/j.ejmech.2017.12.011
Artigo de periodico
Kinetics, subcellular localization, and contribution to parasite virulence of a Trypanosoma cruzi hybrid type A heme peroxidase (TcAPx-CcP) (2017)
Hugo, Martin; Martínez, Alejandra; Trujillo, Madia; Estrada, Damián; Mastrogiovanni, Mauricio; Linares, Edlaine ; Augusto, Ohara ; Issoglio, Federico; Zeida, Ari; Estrín, Darío A; Heijnen, Harry F. G; Piacenza, Lucía; Radi, Rafael
Source: Proceedings of the National Academy of Sciences. Unidade: IQ
Subjects: TRYPANOSOMA CRUZI, PEROXIDASE, VIRULÊNCIA
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ABNT
HUGO, Martin et al. Kinetics, subcellular localization, and contribution to parasite virulence of a Trypanosoma cruzi hybrid type A heme peroxidase (TcAPx-CcP). Proceedings of the National Academy of Sciences, v. 114, n. 8, p. E1326-E1335, 2017Tradução . . Disponível em: https://doi.org/10.1073/pnas.1618611114. Acesso em: 28 jun. 2024.
APA
Hugo, M., Martínez, A., Trujillo, M., Estrada, D., Mastrogiovanni, M., Linares, E., et al. (2017). Kinetics, subcellular localization, and contribution to parasite virulence of a Trypanosoma cruzi hybrid type A heme peroxidase (TcAPx-CcP). Proceedings of the National Academy of Sciences, 114( 8), E1326-E1335. doi:10.1073/pnas.1618611114
NLM
Hugo M, Martínez A, Trujillo M, Estrada D, Mastrogiovanni M, Linares E, Augusto O, Issoglio F, Zeida A, Estrín DA, Heijnen HFG, Piacenza L, Radi R. Kinetics, subcellular localization, and contribution to parasite virulence of a Trypanosoma cruzi hybrid type A heme peroxidase (TcAPx-CcP) [Internet]. Proceedings of the National Academy of Sciences. 2017 ; 114( 8): E1326-E1335.[citado 2024 jun. 28 ] Available from: https://doi.org/10.1073/pnas.1618611114
Vancouver
Hugo M, Martínez A, Trujillo M, Estrada D, Mastrogiovanni M, Linares E, Augusto O, Issoglio F, Zeida A, Estrín DA, Heijnen HFG, Piacenza L, Radi R. Kinetics, subcellular localization, and contribution to parasite virulence of a Trypanosoma cruzi hybrid type A heme peroxidase (TcAPx-CcP) [Internet]. Proceedings of the National Academy of Sciences. 2017 ; 114( 8): E1326-E1335.[citado 2024 jun. 28 ] Available from: https://doi.org/10.1073/pnas.1618611114
Artigo de periodico
A novel ABCG-like transporter of Trypanosoma cruzi is involved in natural resistance to benznidazole (2015)
Zingales, Bianca ; Araújo, Rafael Gomes Aquino de; Moreno, Margoth; Franco, Jaques; Aguiar, Pedro Henrique Nascimento; Nunes, Solange Lessa; Silva, Marcelo Nunes da; Ienne, Susan; Machado, Carlos Renato; Brandão, Adeilton
Source: Memórias do Instituto Oswaldo Cruz. Unidade: IQ
Subjects: TRYPANOSOMA CRUZI, DOENÇA DE CHAGAS
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
ZINGALES, Bianca et al. A novel ABCG-like transporter of Trypanosoma cruzi is involved in natural resistance to benznidazole. Memórias do Instituto Oswaldo Cruz, v. 110, n. 3, p. 433-444, 2015Tradução . . Disponível em: https://doi.org/10.1590/0074-02760140407. Acesso em: 28 jun. 2024.
APA
Zingales, B., Araújo, R. G. A. de, Moreno, M., Franco, J., Aguiar, P. H. N., Nunes, S. L., et al. (2015). A novel ABCG-like transporter of Trypanosoma cruzi is involved in natural resistance to benznidazole. Memórias do Instituto Oswaldo Cruz, 110( 3), 433-444. doi:10.1590/0074-02760140407
NLM
Zingales B, Araújo RGA de, Moreno M, Franco J, Aguiar PHN, Nunes SL, Silva MN da, Ienne S, Machado CR, Brandão A. A novel ABCG-like transporter of Trypanosoma cruzi is involved in natural resistance to benznidazole [Internet]. Memórias do Instituto Oswaldo Cruz. 2015 ; 110( 3): 433-444.[citado 2024 jun. 28 ] Available from: https://doi.org/10.1590/0074-02760140407
Vancouver
Zingales B, Araújo RGA de, Moreno M, Franco J, Aguiar PHN, Nunes SL, Silva MN da, Ienne S, Machado CR, Brandão A. A novel ABCG-like transporter of Trypanosoma cruzi is involved in natural resistance to benznidazole [Internet]. Memórias do Instituto Oswaldo Cruz. 2015 ; 110( 3): 433-444.[citado 2024 jun. 28 ] Available from: https://doi.org/10.1590/0074-02760140407
Trabalho de evento-resumo
Identificação in silico de potenciais inibidores da lipoamida desidrogenase de Trypanosoma cruzi (2014)
Amaral, Antonia Tavares do ; Viviani, Lucas Gasparello; Piccirillo, Erika; Rezende, Leandro de
Source: Resumos. Conference titles: Simpósio Internacional de Iniciação Científica da Universidade de São Paulo (SIICUSP). Unidade: IQ
Subjects: DOENÇA DE CHAGAS, TRYPANOSOMA CRUZI
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
AMARAL, Antonia Tavares do et al. Identificação in silico de potenciais inibidores da lipoamida desidrogenase de Trypanosoma cruzi. 2014, Anais.. São Paulo: USP/Pró-Reitoria de Pesquisa, 2014. . Acesso em: 28 jun. 2024.
APA
Amaral, A. T. do, Viviani, L. G., Piccirillo, E., & Rezende, L. de. (2014). Identificação in silico de potenciais inibidores da lipoamida desidrogenase de Trypanosoma cruzi. In Resumos. São Paulo: USP/Pró-Reitoria de Pesquisa.
NLM
Amaral AT do, Viviani LG, Piccirillo E, Rezende L de. Identificação in silico de potenciais inibidores da lipoamida desidrogenase de Trypanosoma cruzi. Resumos. 2014 ;[citado 2024 jun. 28 ]
Vancouver
Amaral AT do, Viviani LG, Piccirillo E, Rezende L de. Identificação in silico de potenciais inibidores da lipoamida desidrogenase de Trypanosoma cruzi. Resumos. 2014 ;[citado 2024 jun. 28 ]
Trabalho de evento-resumo
Síntese total das marinoquinolinas A, B, C e E e análogos não-naturais (2013)
Schwalm, Cristiane Storck; Causs, Flávia Cristiane; Andricopulo, Adriano Defini; Krogh, Renata; Correia, Carlos Roque Duarte
Source: Programa e Resumos. Conference titles: Reunião Anual da Sociedade Brasileira de Química - SBQ. Unidade: IFSC
Subjects: TRYPANOSOMA CRUZI, PLANEJAMENTO DE FÁRMACOS, PRODUTOS NATURAIS
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ABNT
SCHWALM, Cristiane Storck et al. Síntese total das marinoquinolinas A, B, C e E e análogos não-naturais. 2013, Anais.. São Paulo: Sociedade Brasileira de Química - SBQ, 2013. Disponível em: http://sec.sbq.org.br/eventos/36ra/resumos/T1168-1.pdf. Acesso em: 28 jun. 2024.
APA
Schwalm, C. S., Causs, F. C., Andricopulo, A. D., Krogh, R., & Correia, C. R. D. (2013). Síntese total das marinoquinolinas A, B, C e E e análogos não-naturais. In Programa e Resumos. São Paulo: Sociedade Brasileira de Química - SBQ. Recuperado de http://sec.sbq.org.br/eventos/36ra/resumos/T1168-1.pdf
NLM
Schwalm CS, Causs FC, Andricopulo AD, Krogh R, Correia CRD. Síntese total das marinoquinolinas A, B, C e E e análogos não-naturais [Internet]. Programa e Resumos. 2013 ;[citado 2024 jun. 28 ] Available from: http://sec.sbq.org.br/eventos/36ra/resumos/T1168-1.pdf
Vancouver
Schwalm CS, Causs FC, Andricopulo AD, Krogh R, Correia CRD. Síntese total das marinoquinolinas A, B, C e E e análogos não-naturais [Internet]. Programa e Resumos. 2013 ;[citado 2024 jun. 28 ] Available from: http://sec.sbq.org.br/eventos/36ra/resumos/T1168-1.pdf
Trabalho de evento-resumo periodico
Structural biology and medicinal chemistry in neglected diseases of poverty (2011)
Oliva, Glaucius; Ferreira, Rafaela S.; Guido, Rafael Victorio Carvalho; Pereira, Humberto D'Muniz.; Garratt, Richard Charles; Andricopulo, Adriano Defini
Source: Acta Crystallographica A. Conference titles: Congress and General Assembly of the International Union of Crystallography - IUCr. Unidade: IFSC
Subjects: PLANEJAMENTO DE FÁRMACOS, TRYPANOSOMA CRUZI, DOENÇAS PARASITÁRIAS (TRATAMENTO)
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ABNT
OLIVA, Glaucius et al. Structural biology and medicinal chemistry in neglected diseases of poverty. Acta Crystallographica A. Chester: International Union of Crystallography - IUCr. . Acesso em: 28 jun. 2024. , 2011
APA
Oliva, G., Ferreira, R. S., Guido, R. V. C., Pereira, H. D. 'M., Garratt, R. C., & Andricopulo, A. D. (2011). Structural biology and medicinal chemistry in neglected diseases of poverty. Acta Crystallographica A. Chester: International Union of Crystallography - IUCr.
NLM
Oliva G, Ferreira RS, Guido RVC, Pereira HD'M, Garratt RC, Andricopulo AD. Structural biology and medicinal chemistry in neglected diseases of poverty. Acta Crystallographica A. 2011 ; 67 C51-C52.[citado 2024 jun. 28 ]
Vancouver
Oliva G, Ferreira RS, Guido RVC, Pereira HD'M, Garratt RC, Andricopulo AD. Structural biology and medicinal chemistry in neglected diseases of poverty. Acta Crystallographica A. 2011 ; 67 C51-C52.[citado 2024 jun. 28 ]
Artigo de periodico
Synthesis, molecular modeling and preliminary biological evaluation of a set of 3-acetyl-2,5-disubstituted-2,3-dihydro-1,3,4-oxadiazole as potential antibacterial, anti-Trypanosoma cruzi and antifungal agents (2011)
Ishii, Marina ; Jorge, Salomão Dória; Oliveira, Alex Alfredo de; Palace-Berl, Fanny; Sonehara, Ieda Yuriko; Pasqualoto, Kerly Fernanda Mesquita; Tavares, Leoberto Costa
Source: Bioorganic & Medicinal Chemistry. Unidade: FCF
Subjects: TRYPANOSOMA CRUZI, CANDIDA ALBICANS, ANTIFÚNGICOS
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
ISHII, Marina et al. Synthesis, molecular modeling and preliminary biological evaluation of a set of 3-acetyl-2,5-disubstituted-2,3-dihydro-1,3,4-oxadiazole as potential antibacterial, anti-Trypanosoma cruzi and antifungal agents. Bioorganic & Medicinal Chemistry, v. 19, n. 21, p. 6292-6301, 2011Tradução . . Disponível em: https://doi.org/10.1016/j.bmc.2011.09.009. Acesso em: 28 jun. 2024.
APA
Ishii, M., Jorge, S. D., Oliveira, A. A. de, Palace-Berl, F., Sonehara, I. Y., Pasqualoto, K. F. M., & Tavares, L. C. (2011). Synthesis, molecular modeling and preliminary biological evaluation of a set of 3-acetyl-2,5-disubstituted-2,3-dihydro-1,3,4-oxadiazole as potential antibacterial, anti-Trypanosoma cruzi and antifungal agents. Bioorganic & Medicinal Chemistry, 19( 21), 6292-6301. doi:10.1016/j.bmc.2011.09.009
NLM
Ishii M, Jorge SD, Oliveira AA de, Palace-Berl F, Sonehara IY, Pasqualoto KFM, Tavares LC. Synthesis, molecular modeling and preliminary biological evaluation of a set of 3-acetyl-2,5-disubstituted-2,3-dihydro-1,3,4-oxadiazole as potential antibacterial, anti-Trypanosoma cruzi and antifungal agents [Internet]. Bioorganic & Medicinal Chemistry. 2011 ; 19( 21): 6292-6301.[citado 2024 jun. 28 ] Available from: https://doi.org/10.1016/j.bmc.2011.09.009
Vancouver
Ishii M, Jorge SD, Oliveira AA de, Palace-Berl F, Sonehara IY, Pasqualoto KFM, Tavares LC. Synthesis, molecular modeling and preliminary biological evaluation of a set of 3-acetyl-2,5-disubstituted-2,3-dihydro-1,3,4-oxadiazole as potential antibacterial, anti-Trypanosoma cruzi and antifungal agents [Internet]. Bioorganic & Medicinal Chemistry. 2011 ; 19( 21): 6292-6301.[citado 2024 jun. 28 ] Available from: https://doi.org/10.1016/j.bmc.2011.09.009

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