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Artigo de periodico
In silico studies on the interaction between bioactive ligands and DPP-IV: insights on potential candidates for the treatment of type 2 diabetes mellitus (2021)
Martins, Michelle C.M.R.; Pantaleão, Simone Queiroz ; Almeida, Michell de Oliveira ; Weber, Karen C; Honório, Káthia Maria
Fonte: Medicinal Chemistry. Unidades: EACH, IQSC
Assuntos: PÂNCREAS, ENZIMAS, QUÍMICA MÉDICA
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ABNT
MARTINS, Michelle C.M.R. et al. In silico studies on the interaction between bioactive ligands and DPP-IV: insights on potential candidates for the treatment of type 2 diabetes mellitus. Medicinal Chemistry, v. 17, n. 3, p. 247-263, 2021Tradução . . Disponível em: https://doi.org/10.2174/1573406416666200129151256. Acesso em: 18 nov. 2024.
APA
Martins, M. C. M. R., Pantaleão, S. Q., Almeida, M. de O., Weber, K. C., & Honório, K. M. (2021). In silico studies on the interaction between bioactive ligands and DPP-IV: insights on potential candidates for the treatment of type 2 diabetes mellitus. Medicinal Chemistry, 17( 3), 247-263. doi:10.2174/1573406416666200129151256
NLM
Martins MCMR, Pantaleão SQ, Almeida M de O, Weber KC, Honório KM. In silico studies on the interaction between bioactive ligands and DPP-IV: insights on potential candidates for the treatment of type 2 diabetes mellitus [Internet]. Medicinal Chemistry. 2021 ; 17( 3): 247-263.[citado 2024 nov. 18 ] Available from: https://doi.org/10.2174/1573406416666200129151256
Vancouver
Martins MCMR, Pantaleão SQ, Almeida M de O, Weber KC, Honório KM. In silico studies on the interaction between bioactive ligands and DPP-IV: insights on potential candidates for the treatment of type 2 diabetes mellitus [Internet]. Medicinal Chemistry. 2021 ; 17( 3): 247-263.[citado 2024 nov. 18 ] Available from: https://doi.org/10.2174/1573406416666200129151256
Artigo de periodico
Design of arylsulfonylhydrazones as potential FabH inhibitors: synthesis, antimicrobial evaluation and molecular docking (2021)
Fernandes, Thais Batista; Segretti, Natanael Dante; Lourenço, Felipe Rebello ; Cândido, Thalita Marcílio ; Baby, André Rolim ; Barbosa, Euzébio Guimarães ; Parise Filho, Roberto
Fonte: Medicinal Chemistry. Unidade: FCF
Assuntos: AGENTES ANTIMICROBIANOS, ANTIOXIDANTES, RESISTÊNCIA MICROBIANA ÀS DROGAS
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ABNT
FERNANDES, Thais Batista et al. Design of arylsulfonylhydrazones as potential FabH inhibitors: synthesis, antimicrobial evaluation and molecular docking. Medicinal Chemistry, v. 17, p. 474-484, 2021Tradução . . Disponível em: https://doi.org/10.2174/1573406415666191122111228. Acesso em: 18 nov. 2024.
APA
Fernandes, T. B., Segretti, N. D., Lourenço, F. R., Cândido, T. M., Baby, A. R., Barbosa, E. G., & Parise Filho, R. (2021). Design of arylsulfonylhydrazones as potential FabH inhibitors: synthesis, antimicrobial evaluation and molecular docking. Medicinal Chemistry, 17, 474-484. doi:10.2174/1573406415666191122111228
NLM
Fernandes TB, Segretti ND, Lourenço FR, Cândido TM, Baby AR, Barbosa EG, Parise Filho R. Design of arylsulfonylhydrazones as potential FabH inhibitors: synthesis, antimicrobial evaluation and molecular docking [Internet]. Medicinal Chemistry. 2021 ; 17 474-484.[citado 2024 nov. 18 ] Available from: https://doi.org/10.2174/1573406415666191122111228
Vancouver
Fernandes TB, Segretti ND, Lourenço FR, Cândido TM, Baby AR, Barbosa EG, Parise Filho R. Design of arylsulfonylhydrazones as potential FabH inhibitors: synthesis, antimicrobial evaluation and molecular docking [Internet]. Medicinal Chemistry. 2021 ; 17 474-484.[citado 2024 nov. 18 ] Available from: https://doi.org/10.2174/1573406415666191122111228
Artigo de periodico
Design of Inhibitors for Glyceraldehyde-3-phosphate Dehydrogenase (GAPDH) Enzyme of Leishmania mexicana (2020)
Alves, Krisnna M.A. ; Cardoso, Fábio José Bonfim ; Honório, Káthia Maria ; Molfetta, Fábio A. de
Fonte: Medicinal Chemistry. Unidade: EACH
Assuntos: LEISHMANIA MEXICANA, ENZIMAS, QUÍMICA MÉDICA
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ABNT
ALVES, Krisnna M.A. et al. Design of Inhibitors for Glyceraldehyde-3-phosphate Dehydrogenase (GAPDH) Enzyme of Leishmania mexicana. Medicinal Chemistry, v. 16, n. 6, p. 784-795, 2020Tradução . . Disponível em: https://doi.org/10.2174/1573406415666190712111139. Acesso em: 18 nov. 2024.
APA
Alves, K. M. A., Cardoso, F. J. B., Honório, K. M., & Molfetta, F. A. de. (2020). Design of Inhibitors for Glyceraldehyde-3-phosphate Dehydrogenase (GAPDH) Enzyme of Leishmania mexicana. Medicinal Chemistry, 16( 6), 784-795. doi:10.2174/1573406415666190712111139
NLM
Alves KMA, Cardoso FJB, Honório KM, Molfetta FA de. Design of Inhibitors for Glyceraldehyde-3-phosphate Dehydrogenase (GAPDH) Enzyme of Leishmania mexicana [Internet]. Medicinal Chemistry. 2020 ; 16( 6): 784-795.[citado 2024 nov. 18 ] Available from: https://doi.org/10.2174/1573406415666190712111139
Vancouver
Alves KMA, Cardoso FJB, Honório KM, Molfetta FA de. Design of Inhibitors for Glyceraldehyde-3-phosphate Dehydrogenase (GAPDH) Enzyme of Leishmania mexicana [Internet]. Medicinal Chemistry. 2020 ; 16( 6): 784-795.[citado 2024 nov. 18 ] Available from: https://doi.org/10.2174/1573406415666190712111139
Artigo de periodico
Synthesis of a Tyr-Tyr dipeptide library and evaluation against tumor cells (2018)
Vasconcelos, Stanley Nunes Siqueira ; Sciani, Juliana Mozer ; Lisboa, Nicole Mambeli; Stefani, Hélio Alexandre
Fonte: Medicinal Chemistry. Unidade: FCF
Assuntos: MOLÉCULA, ANTINEOPLÁSICOS
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ABNT
VASCONCELOS, Stanley Nunes Siqueira et al. Synthesis of a Tyr-Tyr dipeptide library and evaluation against tumor cells. Medicinal Chemistry, v. 14, n. 7, p. 709-714, 2018Tradução . . Disponível em: https://doi.org/10.2174/1573406414666180309153142. Acesso em: 18 nov. 2024.
APA
Vasconcelos, S. N. S., Sciani, J. M., Lisboa, N. M., & Stefani, H. A. (2018). Synthesis of a Tyr-Tyr dipeptide library and evaluation against tumor cells. Medicinal Chemistry, 14( 7), 709-714. doi:10.2174/1573406414666180309153142
NLM
Vasconcelos SNS, Sciani JM, Lisboa NM, Stefani HA. Synthesis of a Tyr-Tyr dipeptide library and evaluation against tumor cells [Internet]. Medicinal Chemistry. 2018 ; 14( 7): 709-714.[citado 2024 nov. 18 ] Available from: https://doi.org/10.2174/1573406414666180309153142
Vancouver
Vasconcelos SNS, Sciani JM, Lisboa NM, Stefani HA. Synthesis of a Tyr-Tyr dipeptide library and evaluation against tumor cells [Internet]. Medicinal Chemistry. 2018 ; 14( 7): 709-714.[citado 2024 nov. 18 ] Available from: https://doi.org/10.2174/1573406414666180309153142
Artigo de periodico
The role of QSAR and virtual screening studies in type 2 diabetes drug discovery (2017)
Pantaleão, Simone Queiroz; Fujii, Drielli Gomes Vital; Maltarollo, Vinicius Gonçalves; Silva, Danielle da C; Trossini, Gustavo Henrique Goulart ; Weber, Karen C; Honório, Káthia Maria
Fonte: Medicinal Chemistry. Unidades: FCF, EACH
Assuntos: FÁRMACOS, RELAÇÕES QUANTITATIVAS ENTRE ESTRUTURA QUÍMICA E ATIVIDADE BIOLÓGICA
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ABNT
PANTALEÃO, Simone Queiroz et al. The role of QSAR and virtual screening studies in type 2 diabetes drug discovery. Medicinal Chemistry, v. 13, p. 706-720, 2017Tradução . . Disponível em: https://doi.org/10.2174/1573406413666170522152102. Acesso em: 18 nov. 2024.
APA
Pantaleão, S. Q., Fujii, D. G. V., Maltarollo, V. G., Silva, D. da C., Trossini, G. H. G., Weber, K. C., & Honório, K. M. (2017). The role of QSAR and virtual screening studies in type 2 diabetes drug discovery. Medicinal Chemistry, 13, 706-720. doi:10.2174/1573406413666170522152102
NLM
Pantaleão SQ, Fujii DGV, Maltarollo VG, Silva D da C, Trossini GHG, Weber KC, Honório KM. The role of QSAR and virtual screening studies in type 2 diabetes drug discovery [Internet]. Medicinal Chemistry. 2017 ; 13 706-720.[citado 2024 nov. 18 ] Available from: https://doi.org/10.2174/1573406413666170522152102
Vancouver
Pantaleão SQ, Fujii DGV, Maltarollo VG, Silva D da C, Trossini GHG, Weber KC, Honório KM. The role of QSAR and virtual screening studies in type 2 diabetes drug discovery [Internet]. Medicinal Chemistry. 2017 ; 13 706-720.[citado 2024 nov. 18 ] Available from: https://doi.org/10.2174/1573406413666170522152102
Artigo de periodico
Bergenin from peltophorum dubium: isolation, characterization, and antioxidant activities in non-biological systems and erythrocytes (2017)
Oliveira, Guilherme A. L.; Oliveira, George L. da Silva; Nicolau, Lucas A. D.; Mafud, Ana Carolina; Batista, Larissa F.; Mascarenhas, Yvonne Primerano ; Souza, Luan K. M.; David, Jorge M.; Pinto, Larissa S.; Alves, Clayton Q.; Medeiros, Jand V. R.
Fonte: Medicinal Chemistry. Unidade: IFSC
Assuntos: PROTEÍNAS, FÍSICA DA MATÉRIA CONDENSADA
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ABNT
OLIVEIRA, Guilherme A. L. et al. Bergenin from peltophorum dubium: isolation, characterization, and antioxidant activities in non-biological systems and erythrocytes. Medicinal Chemistry, v. 13, n. 6, p. 592-603, 2017Tradução . . Disponível em: https://doi.org/10.2174/1573406413666170306120152. Acesso em: 18 nov. 2024.
APA
Oliveira, G. A. L., Oliveira, G. L. da S., Nicolau, L. A. D., Mafud, A. C., Batista, L. F., Mascarenhas, Y. P., et al. (2017). Bergenin from peltophorum dubium: isolation, characterization, and antioxidant activities in non-biological systems and erythrocytes. Medicinal Chemistry, 13( 6), 592-603. doi:10.2174/1573406413666170306120152
NLM
Oliveira GAL, Oliveira GL da S, Nicolau LAD, Mafud AC, Batista LF, Mascarenhas YP, Souza LKM, David JM, Pinto LS, Alves CQ, Medeiros JVR. Bergenin from peltophorum dubium: isolation, characterization, and antioxidant activities in non-biological systems and erythrocytes [Internet]. Medicinal Chemistry. 2017 ; 13( 6): 592-603.[citado 2024 nov. 18 ] Available from: https://doi.org/10.2174/1573406413666170306120152
Vancouver
Oliveira GAL, Oliveira GL da S, Nicolau LAD, Mafud AC, Batista LF, Mascarenhas YP, Souza LKM, David JM, Pinto LS, Alves CQ, Medeiros JVR. Bergenin from peltophorum dubium: isolation, characterization, and antioxidant activities in non-biological systems and erythrocytes [Internet]. Medicinal Chemistry. 2017 ; 13( 6): 592-603.[citado 2024 nov. 18 ] Available from: https://doi.org/10.2174/1573406413666170306120152
Artigo de periodico
Molecular design, synthesis and evaluation of 2,3-diarylquinoxalines as estrogen receptor ligands (2015)
Sangi, Diego P.; Cominetti, Márcia Regina; Becceneri, Amanda B.; Resende, Flavia A.; Varanda, Eliana Aparecida; Montanari, Carlos Alberto ; Paixão, Márcio Weber; Corrêa, Arlene Gonçalves
Fonte: Medicinal Chemistry. Unidade: IQSC
Assuntos: QUÍMICA MÉDICA, ESTRÓGENOS
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ABNT
SANGI, Diego P. et al. Molecular design, synthesis and evaluation of 2,3-diarylquinoxalines as estrogen receptor ligands. Medicinal Chemistry, v. 11, n. 8, p. 736-746, 2015Tradução . . Disponível em: https://doi.org/10.2174/1573406411666150513093039. Acesso em: 18 nov. 2024.
APA
Sangi, D. P., Cominetti, M. R., Becceneri, A. B., Resende, F. A., Varanda, E. A., Montanari, C. A., et al. (2015). Molecular design, synthesis and evaluation of 2,3-diarylquinoxalines as estrogen receptor ligands. Medicinal Chemistry, 11( 8), 736-746. doi:10.2174/1573406411666150513093039
NLM
Sangi DP, Cominetti MR, Becceneri AB, Resende FA, Varanda EA, Montanari CA, Paixão MW, Corrêa AG. Molecular design, synthesis and evaluation of 2,3-diarylquinoxalines as estrogen receptor ligands [Internet]. Medicinal Chemistry. 2015 ; 11( 8): 736-746.[citado 2024 nov. 18 ] Available from: https://doi.org/10.2174/1573406411666150513093039
Vancouver
Sangi DP, Cominetti MR, Becceneri AB, Resende FA, Varanda EA, Montanari CA, Paixão MW, Corrêa AG. Molecular design, synthesis and evaluation of 2,3-diarylquinoxalines as estrogen receptor ligands [Internet]. Medicinal Chemistry. 2015 ; 11( 8): 736-746.[citado 2024 nov. 18 ] Available from: https://doi.org/10.2174/1573406411666150513093039

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