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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: 30 dez. 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 dez. 30 ] 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 dez. 30 ] 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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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
Structure-metabolism relationships of benzimidazole derivatives with anti-Trypanosoma cruzi activity for Chagas disease (2024)
Espinoza-Chávez, Rocío Marisol ; Rezende Junior, Celso de Oliveira ; Souza, Mariana Laureano de ; Chelucci, Rafael Consolin; Duarte, Simone Michelan ; Krogh, Renata ; Ferreira, Leonardo Luiz Gomes ; Valli, Marilia ; Oliveira, Aldo Sena de ; Andricopulo, Adriano Defini ; Dias, Luiz Carlos
Source: ChemMedChem. Unidade: IFSC
Subjects: TRYPANOSOMA CRUZI, PLANEJAMENTO DE FÁRMACOS, DOENÇAS PARASITÁRIAS, FÁRMACOS
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ABNT
ESPINOZA-CHÁVEZ, Rocío Marisol et al. Structure-metabolism relationships of benzimidazole derivatives with anti-Trypanosoma cruzi activity for Chagas disease. ChemMedChem, v. 19, n. 20, p. e202400293, 2024Tradução . . Disponível em: https://doi.org/10.1002/cmdc.202400293. Acesso em: 30 dez. 2024.
APA
Espinoza-Chávez, R. M., Rezende Junior, C. de O., Souza, M. L. de, Chelucci, R. C., Duarte, S. M., Krogh, R., et al. (2024). Structure-metabolism relationships of benzimidazole derivatives with anti-Trypanosoma cruzi activity for Chagas disease. ChemMedChem, 19( 20), e202400293. doi:10.1002/cmdc.202400293
NLM
Espinoza-Chávez RM, Rezende Junior C de O, Souza ML de, Chelucci RC, Duarte SM, Krogh R, Ferreira LLG, Valli M, Oliveira AS de, Andricopulo AD, Dias LC. Structure-metabolism relationships of benzimidazole derivatives with anti-Trypanosoma cruzi activity for Chagas disease [Internet]. ChemMedChem. 2024 ; 19( 20): e202400293.[citado 2024 dez. 30 ] Available from: https://doi.org/10.1002/cmdc.202400293
Vancouver
Espinoza-Chávez RM, Rezende Junior C de O, Souza ML de, Chelucci RC, Duarte SM, Krogh R, Ferreira LLG, Valli M, Oliveira AS de, Andricopulo AD, Dias LC. Structure-metabolism relationships of benzimidazole derivatives with anti-Trypanosoma cruzi activity for Chagas disease [Internet]. ChemMedChem. 2024 ; 19( 20): e202400293.[citado 2024 dez. 30 ] Available from: https://doi.org/10.1002/cmdc.202400293
Trabalho de evento-resumo
Convergent synthesis of proline-functionalized pyrazolopyrimidines as anti-T. cruzi bioactive compounds (2024)
Bonesconto, João Pedro Nogueira; Jardim, Guilherme Augusto de Melo ; Chelucci, Rafael Consolin; Ferreira, Leonardo Luiz Gomes ; Duarte, Simone Michelan ; Krogh, Renata; Andricopulo, Adriano Defini ; Cruz, Luiza dos Reis ; Kratz, Jadel M. ; Dias, Luiz Carlos
Source: Book of Abstracts. Conference titles: Brazilian Meeting on Organic Synthesis - BMOS. Unidade: IFSC
Subjects: DOENÇA DE CHAGAS, TRYPANOSOMA CRUZI, FÁRMACOS
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ABNT
BONESCONTO, João Pedro Nogueira et al. Convergent synthesis of proline-functionalized pyrazolopyrimidines as anti-T. cruzi bioactive compounds. 2024, Anais.. Porto Alegre: Universidade Federal do Rio Grande do Sul - UFRGS, 2024. Disponível em: https://schenautomacao.com.br/bmos/envio/files/trabalho1_5.pdf. Acesso em: 30 dez. 2024.
APA
Bonesconto, J. P. N., Jardim, G. A. de M., Chelucci, R. C., Ferreira, L. L. G., Duarte, S. M., Krogh, R., et al. (2024). Convergent synthesis of proline-functionalized pyrazolopyrimidines as anti-T. cruzi bioactive compounds. In Book of Abstracts. Porto Alegre: Universidade Federal do Rio Grande do Sul - UFRGS. Recuperado de https://schenautomacao.com.br/bmos/envio/files/trabalho1_5.pdf
NLM
Bonesconto JPN, Jardim GA de M, Chelucci RC, Ferreira LLG, Duarte SM, Krogh R, Andricopulo AD, Cruz L dos R, Kratz JM, Dias LC. Convergent synthesis of proline-functionalized pyrazolopyrimidines as anti-T. cruzi bioactive compounds [Internet]. Book of Abstracts. 2024 ;[citado 2024 dez. 30 ] Available from: https://schenautomacao.com.br/bmos/envio/files/trabalho1_5.pdf
Vancouver
Bonesconto JPN, Jardim GA de M, Chelucci RC, Ferreira LLG, Duarte SM, Krogh R, Andricopulo AD, Cruz L dos R, Kratz JM, Dias LC. Convergent synthesis of proline-functionalized pyrazolopyrimidines as anti-T. cruzi bioactive compounds [Internet]. Book of Abstracts. 2024 ;[citado 2024 dez. 30 ] Available from: https://schenautomacao.com.br/bmos/envio/files/trabalho1_5.pdf
Artigo de periodico
Novel trypanocidal thiophen-chalcone cruzain inhibitors: structure- and ligand-based studies (2022)
Oliveira, Aldo Sena de ; Valli, Marilia ; Ferreira, Leonardo Luiz Gomes ; Souza, Julia Medeiros ; Andricopulo, Renata Krogh; Meier, Lidiane; Abreu, Heitor R.; Voltolini, Bruna G.; Llanes, Luana C.; Nunes, Ricardo José; Braga, Antonio L.; Andricopulo, Adriano Defini
Source: Future Medicinal Chemistry. Unidade: IFSC
Subjects: FÁRMACOS, PLANEJAMENTO DE FÁRMACOS, DOENÇAS PARASITÁRIAS, DOENÇA DE CHAGAS
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ABNT
OLIVEIRA, Aldo Sena de et al. Novel trypanocidal thiophen-chalcone cruzain inhibitors: structure- and ligand-based studies. Future Medicinal Chemistry, v. 14, n. 11, p. 795-808, 2022Tradução . . Disponível em: https://doi.org/10.4155/fmc-2022-0013. Acesso em: 30 dez. 2024.
APA
Oliveira, A. S. de, Valli, M., Ferreira, L. L. G., Souza, J. M., Andricopulo, R. K., Meier, L., et al. (2022). Novel trypanocidal thiophen-chalcone cruzain inhibitors: structure- and ligand-based studies. Future Medicinal Chemistry, 14( 11), 795-808. doi:10.4155/fmc-2022-0013
NLM
Oliveira AS de, Valli M, Ferreira LLG, Souza JM, Andricopulo RK, Meier L, Abreu HR, Voltolini BG, Llanes LC, Nunes RJ, Braga AL, Andricopulo AD. Novel trypanocidal thiophen-chalcone cruzain inhibitors: structure- and ligand-based studies [Internet]. Future Medicinal Chemistry. 2022 ; 14( 11): 795-808.[citado 2024 dez. 30 ] Available from: https://doi.org/10.4155/fmc-2022-0013
Vancouver
Oliveira AS de, Valli M, Ferreira LLG, Souza JM, Andricopulo RK, Meier L, Abreu HR, Voltolini BG, Llanes LC, Nunes RJ, Braga AL, Andricopulo AD. Novel trypanocidal thiophen-chalcone cruzain inhibitors: structure- and ligand-based studies [Internet]. Future Medicinal Chemistry. 2022 ; 14( 11): 795-808.[citado 2024 dez. 30 ] Available from: https://doi.org/10.4155/fmc-2022-0013
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: 30 dez. 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 dez. 30 ] 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 dez. 30 ] 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: 30 dez. 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 dez. 30 ] 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 dez. 30 ] 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: 30 dez. 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 dez. 30 ] 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 dez. 30 ] Available from: https://proceedings.science/brazmedchem-2022/papers/antitrypanosomal-benzoxazinone-series--hit-to-lead-campaign-and-multiparametric-optimization-.
Trabalho de evento-resumo
Indoles hit-to-lead for chagas disease: lessons learned within the LOLA consortium (2022)
Cruz, Luiza; Silva, Adriana Corrêa da; Feltrin, Clarissa; Dichiara, Maria; Ferrins, Lori; Moraes, Carolina Borsoi; Sjo, Peter; Andricopulo, Adriano Defini ; Mowbray, Charles; Oliveira, Ramon Guerra de; Dessoy, Marco Aurélio; Santos, Deborah Araújo dos; Oliveira, Luiz Fernando Nascimento de; Mollo, María Cruz; Lee, Eun; Duarte, Simone Michelan ; Andricopulo, Renata Krogh; Chelucci, Rafael Consolin; Ferreira, Leonardo Luiz Gomes ; Kratz, Jadel Muller; Dias, Luiz Carlos
Source: Anais eletrônicos. Conference titles: Brazilian Symposium on Medicinal Chemistry - BrazMedChem. Unidade: IFSC
Subjects: DOENÇAS NEGLIGENCIADAS, DOENÇA DE CHAGAS
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ABNT
CRUZ, Luiza et al. Indoles hit-to-lead for chagas disease: lessons learned within the LOLA consortium. 2022, Anais.. Campinas: Galoá, 2022. Disponível em: https://proceedings.science/brazmedchem-2022/papers/indoles-hit-to-lead-for-chagas-disease---lessons-learned-within-the-lola-consortium. Acesso em: 30 dez. 2024.
APA
Cruz, L., Silva, A. C. da, Feltrin, C., Dichiara, M., Ferrins, L., Moraes, C. B., et al. (2022). Indoles hit-to-lead for chagas disease: lessons learned within the LOLA consortium. In Anais eletrônicos. Campinas: Galoá. Recuperado de https://proceedings.science/brazmedchem-2022/papers/indoles-hit-to-lead-for-chagas-disease---lessons-learned-within-the-lola-consortium.
NLM
Cruz L, Silva AC da, Feltrin C, Dichiara M, Ferrins L, Moraes CB, Sjo P, Andricopulo AD, Mowbray C, Oliveira RG de, Dessoy MA, Santos DA dos, Oliveira LFN de, Mollo MC, Lee E, Duarte SM, Andricopulo RK, Chelucci RC, Ferreira LLG, Kratz JM, Dias LC. Indoles hit-to-lead for chagas disease: lessons learned within the LOLA consortium [Internet]. Anais eletrônicos. 2022 ;[citado 2024 dez. 30 ] Available from: https://proceedings.science/brazmedchem-2022/papers/indoles-hit-to-lead-for-chagas-disease---lessons-learned-within-the-lola-consortium.
Vancouver
Cruz L, Silva AC da, Feltrin C, Dichiara M, Ferrins L, Moraes CB, Sjo P, Andricopulo AD, Mowbray C, Oliveira RG de, Dessoy MA, Santos DA dos, Oliveira LFN de, Mollo MC, Lee E, Duarte SM, Andricopulo RK, Chelucci RC, Ferreira LLG, Kratz JM, Dias LC. Indoles hit-to-lead for chagas disease: lessons learned within the LOLA consortium [Internet]. Anais eletrônicos. 2022 ;[citado 2024 dez. 30 ] Available from: https://proceedings.science/brazmedchem-2022/papers/indoles-hit-to-lead-for-chagas-disease---lessons-learned-within-the-lola-consortium.
Artigo de periodico
Liquid fungal cocultivation as a strategy to access bioactive metabolites (2021)
Silva, Airton Damasceno; Ambrozin, Alessandra Regina Pepe; Camargo, Ana Flávia Silveira de; Cruz, Felipe de Paula Nogueira; Ferreira, Leonardo Luiz Gomes ; Andricopulo, Renata Krogh; Silva, Taynara Lopes; Camargo, Ilana Lopes Baratella da Cunha ; Andricopulo, Adriano Defini ; Vieira, Paulo Cezar
Source: Planta Medica. Unidades: IFSC, FCFRP
Subjects: FARMACOLOGIA, FUNGOS, PLANEJAMENTO DE FÁRMACOS, CRISTALOGRAFIA
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ABNT
SILVA, Airton Damasceno et al. Liquid fungal cocultivation as a strategy to access bioactive metabolites. Planta Medica, v. 87, n. 1/2, p. 187-195, 2021Tradução . . Disponível em: https://doi.org/10.1055/a-1200-2046. Acesso em: 30 dez. 2024.
APA
Silva, A. D., Ambrozin, A. R. P., Camargo, A. F. S. de, Cruz, F. de P. N., Ferreira, L. L. G., Andricopulo, R. K., et al. (2021). Liquid fungal cocultivation as a strategy to access bioactive metabolites. Planta Medica, 87( 1/2), 187-195. doi:10.1055/a-1200-2046
NLM
Silva AD, Ambrozin ARP, Camargo AFS de, Cruz F de PN, Ferreira LLG, Andricopulo RK, Silva TL, Camargo ILB da C, Andricopulo AD, Vieira PC. Liquid fungal cocultivation as a strategy to access bioactive metabolites [Internet]. Planta Medica. 2021 ; 87( 1/2): 187-195.[citado 2024 dez. 30 ] Available from: https://doi.org/10.1055/a-1200-2046
Vancouver
Silva AD, Ambrozin ARP, Camargo AFS de, Cruz F de PN, Ferreira LLG, Andricopulo RK, Silva TL, Camargo ILB da C, Andricopulo AD, Vieira PC. Liquid fungal cocultivation as a strategy to access bioactive metabolites [Internet]. Planta Medica. 2021 ; 87( 1/2): 187-195.[citado 2024 dez. 30 ] Available from: https://doi.org/10.1055/a-1200-2046
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: 30 dez. 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 dez. 30 ] 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 dez. 30 ] Available from: https://doi.org/10.1016/j.ejmech.2020.112418
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
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.
Source: Anais eletrônicos. Conference titles: Brazilian Symposium on Medicinal Chemistry - BrazMedChem. Unidade: IFSC
Subjects: TRYPANOSOMA CRUZI, LEISHMANIA INFANTUM, PLANEJAMENTO DE FÁRMACOS
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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: 30 dez. 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 dez. 30 ] 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 dez. 30 ] 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
Source: Frontiers in Chemistry. 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
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: 30 dez. 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 dez. 30 ] 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 dez. 30 ] 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: 30 dez. 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 dez. 30 ] 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 dez. 30 ] Available from: https://proceedings.science/p/107156
Artigo de periodico
Linear peptide analogues from Jatropha's orbitides promote migration of human neonatal foreskin fibroblasts in vitro and collagen deposition (2019)
Ramalho, Suelem D.; Pinto, Meri Emili F.; Andricopulo, Renata Krogh; Sanches, Paulo R. S.; Silveira, Edilberto R.; Cilli, Eduardo M.; Andricopulo, Adriano Defini ; Bolzani, Vanderlan S.
Source: Journal of the Brazilian Chemical Society. Unidade: IFSC
Subjects: FIBROBLASTOS, PEPTÍDEOS, PLANEJAMENTO DE FÁRMACOS
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ABNT
RAMALHO, Suelem D. et al. Linear peptide analogues from Jatropha's orbitides promote migration of human neonatal foreskin fibroblasts in vitro and collagen deposition. Journal of the Brazilian Chemical Society, v. 30, n. 10, p. 2153-2161, 2019Tradução . . Disponível em: https://doi.org/10.21577/0103-5053.20190102. Acesso em: 30 dez. 2024.
APA
Ramalho, S. D., Pinto, M. E. F., Andricopulo, R. K., Sanches, P. R. S., Silveira, E. R., Cilli, E. M., et al. (2019). Linear peptide analogues from Jatropha's orbitides promote migration of human neonatal foreskin fibroblasts in vitro and collagen deposition. Journal of the Brazilian Chemical Society, 30( 10), 2153-2161. doi:10.21577/0103-5053.20190102
NLM
Ramalho SD, Pinto MEF, Andricopulo RK, Sanches PRS, Silveira ER, Cilli EM, Andricopulo AD, Bolzani VS. Linear peptide analogues from Jatropha's orbitides promote migration of human neonatal foreskin fibroblasts in vitro and collagen deposition [Internet]. Journal of the Brazilian Chemical Society. 2019 ; 30( 10): 2153-2161.[citado 2024 dez. 30 ] Available from: https://doi.org/10.21577/0103-5053.20190102
Vancouver
Ramalho SD, Pinto MEF, Andricopulo RK, Sanches PRS, Silveira ER, Cilli EM, Andricopulo AD, Bolzani VS. Linear peptide analogues from Jatropha's orbitides promote migration of human neonatal foreskin fibroblasts in vitro and collagen deposition [Internet]. Journal of the Brazilian Chemical Society. 2019 ; 30( 10): 2153-2161.[citado 2024 dez. 30 ] Available from: https://doi.org/10.21577/0103-5053.20190102
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.
Source: BMC Biotechnology. Unidade: IFSC
Subjects: 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: 30 dez. 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 dez. 30 ] 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 dez. 30 ] Available from: https://doi.org/10.1186/s12896-018-0428-z
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
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
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/
Artigo de periodico
Molecular modeling and structure-activity relationships studies of bioisoster hybrids of N-acylhydrazone and furoxan groups on cruzain (2017)
Serafim, Ricardo A. M.; Oliveira, Tiago F.; Loureiro, Ana Paula de Melo ; Krogh, Renata; Andricopulo, Adriano Defini ; Dias, Luiz C.; Ferreira, Elizabeth Igne
Source: Medicinal Chemistry Research. Unidades: IFSC, FCF
Subjects: QUÍMICA MÉDICA, PRODUTOS NATURAIS, PLANTAS MEDICINAIS
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ABNT
SERAFIM, Ricardo A. M. et al. Molecular modeling and structure-activity relationships studies of bioisoster hybrids of N-acylhydrazone and furoxan groups on cruzain. Medicinal Chemistry Research, v. 26, n. 4, p. 760-769, 2017Tradução . . Disponível em: https://doi.org/10.1007/s00044-016-1776-7. Acesso em: 30 dez. 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. (2017). Molecular modeling and structure-activity relationships studies of bioisoster hybrids of N-acylhydrazone and furoxan groups on cruzain. Medicinal Chemistry Research, 26( 4), 760-769. doi:10.1007/s00044-016-1776-7
NLM
Serafim RAM, Oliveira TF, Loureiro AP de M, Krogh R, Andricopulo AD, Dias LC, Ferreira EI. Molecular modeling and structure-activity relationships studies of bioisoster hybrids of N-acylhydrazone and furoxan groups on cruzain [Internet]. Medicinal Chemistry Research. 2017 ; 26( 4): 760-769.[citado 2024 dez. 30 ] Available from: https://doi.org/10.1007/s00044-016-1776-7
Vancouver
Serafim RAM, Oliveira TF, Loureiro AP de M, Krogh R, Andricopulo AD, Dias LC, Ferreira EI. Molecular modeling and structure-activity relationships studies of bioisoster hybrids of N-acylhydrazone and furoxan groups on cruzain [Internet]. Medicinal Chemistry Research. 2017 ; 26( 4): 760-769.[citado 2024 dez. 30 ] Available from: https://doi.org/10.1007/s00044-016-1776-7

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