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Artigo de periodico
Trypanosoma cruzi Sirtuin 2 as a relevant druggable target: new inhibitors developed by computer-aided drug design (2023)
Ferreira, Glaucio Monteiro ; Kronenberger, Thales ; Maltarollo, Vinícius Gonçalves ; Poso, Antti ; Gatti, Fernando de Moura ; Almeida, Vitor Medeiros ; Marana, Sandro Roberto ; Lopes, Carla Duque ; Tezuka, Daiane Yukie; Albuquerque, Sérgio de ; Emery, Flavio da Silva ; Trossini, Gustavo Henrique Goulart
Fonte: Pharmaceuticals. Unidades: FCF, IQ, FCFRP
Assuntos: TRYPANOSOMA CRUZI, ENZIMAS
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ABNT
FERREIRA, Glaucio Monteiro et al. Trypanosoma cruzi Sirtuin 2 as a relevant druggable target: new inhibitors developed by computer-aided drug design. Pharmaceuticals, v. 16 , p. 1-14 art. 428, 2023Tradução . . Disponível em: https://doi.org/10.3390/ph16030428. Acesso em: 14 nov. 2024.
APA
Ferreira, G. M., Kronenberger, T., Maltarollo, V. G., Poso, A., Gatti, F. de M., Almeida, V. M., et al. (2023). Trypanosoma cruzi Sirtuin 2 as a relevant druggable target: new inhibitors developed by computer-aided drug design. Pharmaceuticals, 16 , 1-14 art. 428. doi:10.3390/ph16030428
NLM
Ferreira GM, Kronenberger T, Maltarollo VG, Poso A, Gatti F de M, Almeida VM, Marana SR, Lopes CD, Tezuka DY, Albuquerque S de, Emery F da S, Trossini GHG. Trypanosoma cruzi Sirtuin 2 as a relevant druggable target: new inhibitors developed by computer-aided drug design [Internet]. Pharmaceuticals. 2023 ; 16 1-14 art. 428.[citado 2024 nov. 14 ] Available from: https://doi.org/10.3390/ph16030428
Vancouver
Ferreira GM, Kronenberger T, Maltarollo VG, Poso A, Gatti F de M, Almeida VM, Marana SR, Lopes CD, Tezuka DY, Albuquerque S de, Emery F da S, Trossini GHG. Trypanosoma cruzi Sirtuin 2 as a relevant druggable target: new inhibitors developed by computer-aided drug design [Internet]. Pharmaceuticals. 2023 ; 16 1-14 art. 428.[citado 2024 nov. 14 ] Available from: https://doi.org/10.3390/ph16030428
Artigo de periodico
Structure-activity relationship and mechanistic studies for a series of cinnamyl hydroxamate histone deacetylase inhibitors (2021)
Tavares, Maurício Temotheo ; Almeida, Larissa Costa de ; Kronenberger, Thales ; Ferreira, Glaucio Monteiro ; Divitiis, Thainá Fujii de ; Toledo, Mônica Franco Zannini Junqueira ; Hassimotto, Neuza Mariko Aymoto ; Machado Neto, João Agostinho ; Costa-Lotufo, Letícia Veras ; Parise Filho, Roberto
Fonte: Bioorganic and Medicinal Chemistry. Unidades: FCF, ICB, PRÓ-G
Assuntos: CITOTOXICIDADE IMUNOLÓGICA, ENZIMAS, FARMACOLOGIA, CÉLULAS CULTIVADAS DE TUMOR, APOPTOSE, PROLIFERAÇÃO CELULAR
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
TAVARES, Maurício Temotheo et al. Structure-activity relationship and mechanistic studies for a series of cinnamyl hydroxamate histone deacetylase inhibitors. Bioorganic and Medicinal Chemistry, v. 35, p. 1-42 art. 116085, 2021Tradução . . Disponível em: https://doi.org/10.1016/j.bmc.2021.116085. Acesso em: 14 nov. 2024.
APA
Tavares, M. T., Almeida, L. C. de, Kronenberger, T., Ferreira, G. M., Divitiis, T. F. de, Toledo, M. F. Z. J., et al. (2021). Structure-activity relationship and mechanistic studies for a series of cinnamyl hydroxamate histone deacetylase inhibitors. Bioorganic and Medicinal Chemistry, 35, 1-42 art. 116085. doi:10.1016/j.bmc.2021.116085
NLM
Tavares MT, Almeida LC de, Kronenberger T, Ferreira GM, Divitiis TF de, Toledo MFZJ, Hassimotto NMA, Machado Neto JA, Costa-Lotufo LV, Parise Filho R. Structure-activity relationship and mechanistic studies for a series of cinnamyl hydroxamate histone deacetylase inhibitors [Internet]. Bioorganic and Medicinal Chemistry. 2021 ; 35 1-42 art. 116085.[citado 2024 nov. 14 ] Available from: https://doi.org/10.1016/j.bmc.2021.116085
Vancouver
Tavares MT, Almeida LC de, Kronenberger T, Ferreira GM, Divitiis TF de, Toledo MFZJ, Hassimotto NMA, Machado Neto JA, Costa-Lotufo LV, Parise Filho R. Structure-activity relationship and mechanistic studies for a series of cinnamyl hydroxamate histone deacetylase inhibitors [Internet]. Bioorganic and Medicinal Chemistry. 2021 ; 35 1-42 art. 116085.[citado 2024 nov. 14 ] Available from: https://doi.org/10.1016/j.bmc.2021.116085
Artigo de periodico
Targeting SUMOylation in plasmodium as a potential target for malaria therapy (2021)
Oliveira, Daffiny Sumam de ; Kronenberger, Thales ; Palmisano, Giuseppe ; Wrenger, Carsten ; Souza, Edmarcia Elisa de
Fonte: Frontiers in Cellular and Infection Microbiology. Unidade: ICB
Assuntos: PARASITOLOGIA, MALÁRIA, PLASMODIUM FALCIPARUM, ANTIMALÁRICOS, ANIMAIS PARASITOS, ENZIMAS
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
OLIVEIRA, Daffiny Sumam de et al. Targeting SUMOylation in plasmodium as a potential target for malaria therapy. Frontiers in Cellular and Infection Microbiology, v. 11, p. 1-7, 2021Tradução . . Disponível em: https://doi.org/10.3389/fcimb.2021.685866. Acesso em: 14 nov. 2024.
APA
Oliveira, D. S. de, Kronenberger, T., Palmisano, G., Wrenger, C., & Souza, E. E. de. (2021). Targeting SUMOylation in plasmodium as a potential target for malaria therapy. Frontiers in Cellular and Infection Microbiology, 11, 1-7. doi:10.3389/fcimb.2021.685866
NLM
Oliveira DS de, Kronenberger T, Palmisano G, Wrenger C, Souza EE de. Targeting SUMOylation in plasmodium as a potential target for malaria therapy [Internet]. Frontiers in Cellular and Infection Microbiology. 2021 ; 11 1-7.[citado 2024 nov. 14 ] Available from: https://doi.org/10.3389/fcimb.2021.685866
Vancouver
Oliveira DS de, Kronenberger T, Palmisano G, Wrenger C, Souza EE de. Targeting SUMOylation in plasmodium as a potential target for malaria therapy [Internet]. Frontiers in Cellular and Infection Microbiology. 2021 ; 11 1-7.[citado 2024 nov. 14 ] Available from: https://doi.org/10.3389/fcimb.2021.685866

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