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Trabalho de evento-resumo periodico
A novel HDAC inhibitor potentiates Venetoclax-induced apoptosis in acute myeloid leukemia cells (2022)
Jaeg, Carlos; Almeida, LC; Lima, K; Tavares, M. T; Waitman, K. B; Costa-Lotufo, Letícia Veras ; Parise Filho, Roberto ; Machado Neto, João Agostinho
Source: Hematology, Transfusion and Cell Therapy. Conference titles: Congresso Brasileiro de Hematologia, Hemoterapia e Terapia Celular (HEMO). Unidades: ICB, FCF
Subjects: INIBIDORES DE ENZIMAS, APOPTOSE, LEUCEMIA MIELOIDE AGUDA
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ABNT
JAEG, Carlos et al. A novel HDAC inhibitor potentiates Venetoclax-induced apoptosis in acute myeloid leukemia cells. Hematology, Transfusion and Cell Therapy. Amsterdam: Instituto de Ciências Biomédicas, Universidade de São Paulo. Disponível em: https://doi.org/10.1016/j.htct.2022.09.267. Acesso em: 09 nov. 2024. , 2022
APA
Jaeg, C., Almeida, L. C., Lima, K., Tavares, M. T., Waitman, K. B., Costa-Lotufo, L. V., et al. (2022). A novel HDAC inhibitor potentiates Venetoclax-induced apoptosis in acute myeloid leukemia cells. Hematology, Transfusion and Cell Therapy. Amsterdam: Instituto de Ciências Biomédicas, Universidade de São Paulo. doi:10.1016/j.htct.2022.09.267
NLM
Jaeg C, Almeida LC, Lima K, Tavares MT, Waitman KB, Costa-Lotufo LV, Parise Filho R, Machado Neto JA. A novel HDAC inhibitor potentiates Venetoclax-induced apoptosis in acute myeloid leukemia cells [Internet]. Hematology, Transfusion and Cell Therapy. 2022 ; 44 s158-s159.[citado 2024 nov. 09 ] Available from: https://doi.org/10.1016/j.htct.2022.09.267
Vancouver
Jaeg C, Almeida LC, Lima K, Tavares MT, Waitman KB, Costa-Lotufo LV, Parise Filho R, Machado Neto JA. A novel HDAC inhibitor potentiates Venetoclax-induced apoptosis in acute myeloid leukemia cells [Internet]. Hematology, Transfusion and Cell Therapy. 2022 ; 44 s158-s159.[citado 2024 nov. 09 ] Available from: https://doi.org/10.1016/j.htct.2022.09.267
Artigo de periodico
Peppers: a “hot” natural source for antitumor compounds (2021)
Cunha, Micael Rodrigues ; Tavares, Maurício Temotheo ; Fernandes, Thais Batista; Parise Filho, Roberto
Source: Molecules. Unidade: FCF
Subjects: PIMENTA, APOPTOSE, METABÓLITOS SECUNDÁRIOS
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ABNT
CUNHA, Micael Rodrigues et al. Peppers: a “hot” natural source for antitumor compounds. Molecules, v. 26, n. 6, p. 1-21 art. 1521, 2021Tradução . . Disponível em: https://doi.org/10.3390/molecules26061521. Acesso em: 09 nov. 2024.
APA
Cunha, M. R., Tavares, M. T., Fernandes, T. B., & Parise Filho, R. (2021). Peppers: a “hot” natural source for antitumor compounds. Molecules, 26( 6), 1-21 art. 1521. doi:10.3390/molecules26061521
NLM
Cunha MR, Tavares MT, Fernandes TB, Parise Filho R. Peppers: a “hot” natural source for antitumor compounds [Internet]. Molecules. 2021 ; 26( 6): 1-21 art. 1521.[citado 2024 nov. 09 ] Available from: https://doi.org/10.3390/molecules26061521
Vancouver
Cunha MR, Tavares MT, Fernandes TB, Parise Filho R. Peppers: a “hot” natural source for antitumor compounds [Internet]. Molecules. 2021 ; 26( 6): 1-21 art. 1521.[citado 2024 nov. 09 ] Available from: https://doi.org/10.3390/molecules26061521
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
Source: Bioorganic and Medicinal Chemistry. Unidades: FCF, ICB, PRÓ-G
Subjects: CITOTOXICIDADE IMUNOLÓGICA, ENZIMAS, FARMACOLOGIA, CÉLULAS CULTIVADAS DE TUMOR, APOPTOSE, PROLIFERAÇÃO CELULAR
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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: 09 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. 09 ] 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. 09 ] Available from: https://doi.org/10.1016/j.bmc.2021.116085
Artigo de periodico
Cytotoxicity of 4-substituted quinoline derivatives: Anticancer and antileishmanial potential (2020)
Costa, Claudia A; Lopes, Rayssa M; Ferraz, Letícia Silva; Esteves, Gabriela N. N; Di Iorio, Juliana F; Souza, Aline A; Oliveira, Isadora M. de; Manarin, Flávia ; Judice, Wagner Alves de Souza; Stefani, Hélio Alexandre ; Rodrigues, Tiago
Source: Bioorganic & Medicinal Chemistry. Unidade: FCF
Subjects: ANTINEOPLÁSICOS, ANTIPROTOZOÁRIOS, APOPTOSE
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ABNT
COSTA, Claudia A et al. Cytotoxicity of 4-substituted quinoline derivatives: Anticancer and antileishmanial potential. Bioorganic & Medicinal Chemistry, v. 28, p. 1-13 art. 115511, 2020Tradução . . Disponível em: https://doi.org/10.1016/j.bmc.2020.115511. Acesso em: 09 nov. 2024.
APA
Costa, C. A., Lopes, R. M., Ferraz, L. S., Esteves, G. N. N., Di Iorio, J. F., Souza, A. A., et al. (2020). Cytotoxicity of 4-substituted quinoline derivatives: Anticancer and antileishmanial potential. Bioorganic & Medicinal Chemistry, 28, 1-13 art. 115511. doi:10.1016/j.bmc.2020.115511
NLM
Costa CA, Lopes RM, Ferraz LS, Esteves GNN, Di Iorio JF, Souza AA, Oliveira IM de, Manarin F, Judice WA de S, Stefani HA, Rodrigues T. Cytotoxicity of 4-substituted quinoline derivatives: Anticancer and antileishmanial potential [Internet]. Bioorganic & Medicinal Chemistry. 2020 ; 28 1-13 art. 115511.[citado 2024 nov. 09 ] Available from: https://doi.org/10.1016/j.bmc.2020.115511
Vancouver
Costa CA, Lopes RM, Ferraz LS, Esteves GNN, Di Iorio JF, Souza AA, Oliveira IM de, Manarin F, Judice WA de S, Stefani HA, Rodrigues T. Cytotoxicity of 4-substituted quinoline derivatives: Anticancer and antileishmanial potential [Internet]. Bioorganic & Medicinal Chemistry. 2020 ; 28 1-13 art. 115511.[citado 2024 nov. 09 ] Available from: https://doi.org/10.1016/j.bmc.2020.115511
Artigo de periodico
Capsaicin-like analogue induced selective apoptosis in A2058 melanoma cells: design, synthesis and molecular modeling (2019)
Pereira, Gustavo José Vasco; Tavares, Maurício Temotheo ; Azevedo, Ricardo Alexandre de ; Martins, Barbara Behr; Cunha, Micael Rodrigues ; Bhardwaj, Rajesh ; Cury, Yara ; Zambelli, Vanessa Olzon ; Barbosa, Euzébio Guimarães ; Hediger, Matthias A ; Parise Filho, Roberto
Source: Bioorganic and Medicinal Chemistry. Unidade: FCF
Subjects: APOPTOSE, PRODUTOS NATURAIS, ANTINEOPLÁSICOS, UREIA
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ABNT
PEREIRA, Gustavo José Vasco et al. Capsaicin-like analogue induced selective apoptosis in A2058 melanoma cells: design, synthesis and molecular modeling. Bioorganic and Medicinal Chemistry, v. 27, n. 13, p. 2893-2904, 2019Tradução . . Disponível em: https://doi.org/10.1016/j.bmc.2019.05.020. Acesso em: 09 nov. 2024.
APA
Pereira, G. J. V., Tavares, M. T., Azevedo, R. A. de, Martins, B. B., Cunha, M. R., Bhardwaj, R., et al. (2019). Capsaicin-like analogue induced selective apoptosis in A2058 melanoma cells: design, synthesis and molecular modeling. Bioorganic and Medicinal Chemistry, 27( 13), 2893-2904. doi:10.1016/j.bmc.2019.05.020
NLM
Pereira GJV, Tavares MT, Azevedo RA de, Martins BB, Cunha MR, Bhardwaj R, Cury Y, Zambelli VO, Barbosa EG, Hediger MA, Parise Filho R. Capsaicin-like analogue induced selective apoptosis in A2058 melanoma cells: design, synthesis and molecular modeling [Internet]. Bioorganic and Medicinal Chemistry. 2019 ; 27( 13): 2893-2904.[citado 2024 nov. 09 ] Available from: https://doi.org/10.1016/j.bmc.2019.05.020
Vancouver
Pereira GJV, Tavares MT, Azevedo RA de, Martins BB, Cunha MR, Bhardwaj R, Cury Y, Zambelli VO, Barbosa EG, Hediger MA, Parise Filho R. Capsaicin-like analogue induced selective apoptosis in A2058 melanoma cells: design, synthesis and molecular modeling [Internet]. Bioorganic and Medicinal Chemistry. 2019 ; 27( 13): 2893-2904.[citado 2024 nov. 09 ] Available from: https://doi.org/10.1016/j.bmc.2019.05.020
Artigo de periodico
Arylsulfonylhydrazone induced apoptosis in MDA-MB-231 breast cancer cells (2018)
Fernandes, Thais Batista; Azevedo, Ricardo Alexandre de; Yang, Rosania; Teixeira, Sarah Fernandes; Trossini, Gustavo Henrique Goulart ; Barbuto, José Alexandre Marzagão ; Ferreira, Adilson Kleber; Parise Filho, Roberto
Source: Letters in Drug Design and Discovery. Unidades: FCF, ICB
Subjects: APOPTOSE, NEOPLASIAS MAMÁRIAS
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ABNT
FERNANDES, Thais Batista et al. Arylsulfonylhydrazone induced apoptosis in MDA-MB-231 breast cancer cells. Letters in Drug Design and Discovery, v. 15, n. 12, p. 1288-1298, 2018Tradução . . Disponível em: https://doi.org/10.2174/1570180815666180321161513. Acesso em: 09 nov. 2024.
APA
Fernandes, T. B., Azevedo, R. A. de, Yang, R., Teixeira, S. F., Trossini, G. H. G., Barbuto, J. A. M., et al. (2018). Arylsulfonylhydrazone induced apoptosis in MDA-MB-231 breast cancer cells. Letters in Drug Design and Discovery, 15( 12), 1288-1298. doi:10.2174/1570180815666180321161513
NLM
Fernandes TB, Azevedo RA de, Yang R, Teixeira SF, Trossini GHG, Barbuto JAM, Ferreira AK, Parise Filho R. Arylsulfonylhydrazone induced apoptosis in MDA-MB-231 breast cancer cells [Internet]. Letters in Drug Design and Discovery. 2018 ; 15( 12): 1288-1298.[citado 2024 nov. 09 ] Available from: https://doi.org/10.2174/1570180815666180321161513
Vancouver
Fernandes TB, Azevedo RA de, Yang R, Teixeira SF, Trossini GHG, Barbuto JAM, Ferreira AK, Parise Filho R. Arylsulfonylhydrazone induced apoptosis in MDA-MB-231 breast cancer cells [Internet]. Letters in Drug Design and Discovery. 2018 ; 15( 12): 1288-1298.[citado 2024 nov. 09 ] Available from: https://doi.org/10.2174/1570180815666180321161513
Artigo de periodico
Role of microRNAs (miRNAs) in pathophysiology of Diabetes mellitus (2018)
Tiwari, Juhi; Gupta, Gaurav; Pinto, Terezinha de Jesus Andreoli ; Sharma, Rahul; Pabreja, Kavita; Matta, Yogesh; Arora, Neha; Mishra, Anurag; Sharma, Rakesh; Dua, Kamal
Source: Panminerva Medica. Unidade: FCF
Subjects: DIABETES MELLITUS, APOPTOSE, SÍNDROME X METABÓLICA
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ABNT
TIWARI, Juhi et al. Role of microRNAs (miRNAs) in pathophysiology of Diabetes mellitus. Panminerva Medica, v. 60, n. 1, p. 25-28, 2018Tradução . . Disponível em: https://doi.org/10.23736/S0031-0808.17.03382-1. Acesso em: 09 nov. 2024.
APA
Tiwari, J., Gupta, G., Pinto, T. de J. A., Sharma, R., Pabreja, K., Matta, Y., et al. (2018). Role of microRNAs (miRNAs) in pathophysiology of Diabetes mellitus. Panminerva Medica, 60( 1), 25-28. doi:10.23736/S0031-0808.17.03382-1
NLM
Tiwari J, Gupta G, Pinto T de JA, Sharma R, Pabreja K, Matta Y, Arora N, Mishra A, Sharma R, Dua K. Role of microRNAs (miRNAs) in pathophysiology of Diabetes mellitus [Internet]. Panminerva Medica. 2018 ; 60( 1): 25-28.[citado 2024 nov. 09 ] Available from: https://doi.org/10.23736/S0031-0808.17.03382-1
Vancouver
Tiwari J, Gupta G, Pinto T de JA, Sharma R, Pabreja K, Matta Y, Arora N, Mishra A, Sharma R, Dua K. Role of microRNAs (miRNAs) in pathophysiology of Diabetes mellitus [Internet]. Panminerva Medica. 2018 ; 60( 1): 25-28.[citado 2024 nov. 09 ] Available from: https://doi.org/10.23736/S0031-0808.17.03382-1
Artigo de periodico
Cytotoxic effects of dillapiole on MDA-MB-231 cells involve the induction of apoptosis through the mitochondrial pathway by inducing an oxidative stress while altering the cytoskeleton network (2014)
Ferreira, Adilson Kleber; Sá Júnior, Paulo Luiz de; Pasqualoto, Kerly Fernanda Mesquita; Azevedo, Ricardo Alexandre de; Câmara, Diana Aparecida Dias; Costa, André Santos; Figueiredo, Carlos Rogério; Matsuo, Alisson Leonardo; Massaoka, Mariana Hiromi; Auada, Aline Vivian Vatti; Lebrun, Ivo; Damião, Mariana Celestina Frojuello Costa Bernstorff; Tavares, Maurício Temotheo; Magri, Fatima Maria Motter; Kerkis, Irina; Parise Filho, Roberto
Source: Biochimie. Unidade: FCF
Subjects: CITOESQUELETO, ESTRESSE OXIDATIVO, APOPTOSE
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ABNT
FERREIRA, Adilson Kleber et al. Cytotoxic effects of dillapiole on MDA-MB-231 cells involve the induction of apoptosis through the mitochondrial pathway by inducing an oxidative stress while altering the cytoskeleton network. Biochimie, v. 99, p. 195-207, 2014Tradução . . Disponível em: https://doi.org/10.1016/j.biochi.2013.12.008. Acesso em: 09 nov. 2024.
APA
Ferreira, A. K., Sá Júnior, P. L. de, Pasqualoto, K. F. M., Azevedo, R. A. de, Câmara, D. A. D., Costa, A. S., et al. (2014). Cytotoxic effects of dillapiole on MDA-MB-231 cells involve the induction of apoptosis through the mitochondrial pathway by inducing an oxidative stress while altering the cytoskeleton network. Biochimie, 99, 195-207. doi:10.1016/j.biochi.2013.12.008
NLM
Ferreira AK, Sá Júnior PL de, Pasqualoto KFM, Azevedo RA de, Câmara DAD, Costa AS, Figueiredo CR, Matsuo AL, Massaoka MH, Auada AVV, Lebrun I, Damião MCFCB, Tavares MT, Magri FMM, Kerkis I, Parise Filho R. Cytotoxic effects of dillapiole on MDA-MB-231 cells involve the induction of apoptosis through the mitochondrial pathway by inducing an oxidative stress while altering the cytoskeleton network [Internet]. Biochimie. 2014 ; 99 195-207.[citado 2024 nov. 09 ] Available from: https://doi.org/10.1016/j.biochi.2013.12.008
Vancouver
Ferreira AK, Sá Júnior PL de, Pasqualoto KFM, Azevedo RA de, Câmara DAD, Costa AS, Figueiredo CR, Matsuo AL, Massaoka MH, Auada AVV, Lebrun I, Damião MCFCB, Tavares MT, Magri FMM, Kerkis I, Parise Filho R. Cytotoxic effects of dillapiole on MDA-MB-231 cells involve the induction of apoptosis through the mitochondrial pathway by inducing an oxidative stress while altering the cytoskeleton network [Internet]. Biochimie. 2014 ; 99 195-207.[citado 2024 nov. 09 ] Available from: https://doi.org/10.1016/j.biochi.2013.12.008
Trabalho de evento-resumo periodico
Synthesis and purification of N-(benzodioxol-5-ylmethylene) aryl-sulfonylhydrazones (2013)
Fernandes, Thais Batista; Damião, Mariana Celestina Frojuello Bernstorff; Tavares, Maurício Temotheo; Parise Filho, Roberto
Source: Brazilian Journal of Pharmaceutical Sciences. Conference titles: Pharmaceutical Science and Technology Meeting of the Faculty of Pharmaceutical Sciences. Unidade: FCF
Subjects: APOPTOSE, PROLIFERAÇÃO CELULAR
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ABNT
FERNANDES, Thais Batista et al. Synthesis and purification of N-(benzodioxol-5-ylmethylene) aryl-sulfonylhydrazones. Brazilian Journal of Pharmaceutical Sciences. São Paulo: Faculdade de Ciências Farmacêuticas, Universidade de São Paulo. . Acesso em: 09 nov. 2024. , 2013
APA
Fernandes, T. B., Damião, M. C. F. B., Tavares, M. T., & Parise Filho, R. (2013). Synthesis and purification of N-(benzodioxol-5-ylmethylene) aryl-sulfonylhydrazones. Brazilian Journal of Pharmaceutical Sciences. São Paulo: Faculdade de Ciências Farmacêuticas, Universidade de São Paulo.
NLM
Fernandes TB, Damião MCFB, Tavares MT, Parise Filho R. Synthesis and purification of N-(benzodioxol-5-ylmethylene) aryl-sulfonylhydrazones. Brazilian Journal of Pharmaceutical Sciences. 2013 ; 49 63 res. FCF121.[citado 2024 nov. 09 ]
Vancouver
Fernandes TB, Damião MCFB, Tavares MT, Parise Filho R. Synthesis and purification of N-(benzodioxol-5-ylmethylene) aryl-sulfonylhydrazones. Brazilian Journal of Pharmaceutical Sciences. 2013 ; 49 63 res. FCF121.[citado 2024 nov. 09 ]
Artigo de periodico
RPF101, a new capsaicin-like analogue, disrupts the microtubule network accompanied by arrest in the G2/M phase, inducing apoptosis and mitotic catastrophe in the MCF-7 breast cancer cells (2013)
Sá Júnior, Paulo Luiz de; Pasqualoto, Kerly Fernanda Mesquita; Ferreira, Adilson Kleber; Tavares, Maurício Temotheo; Damião, Mariana Celestina Frojuello Bernstorff; Azevedo, Ricardo Alexandre de; Câmara, Diana Aparecida Dias; Pereira, Alexandre; Souza, Dener Madeiro de; Parise Filho, Roberto
Source: Toxicology and Applied Pharmacology. Unidade: FCF
Subjects: MODELAGEM MOLECULAR, CICLO CELULAR, APOPTOSE
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ABNT
SÁ JÚNIOR, Paulo Luiz de et al. RPF101, a new capsaicin-like analogue, disrupts the microtubule network accompanied by arrest in the G2/M phase, inducing apoptosis and mitotic catastrophe in the MCF-7 breast cancer cells. Toxicology and Applied Pharmacology, v. 266, n. 3, p. 385-398, 2013Tradução . . Disponível em: https://doi.org/10.1016/j.taap.2012.11.029. Acesso em: 09 nov. 2024.
APA
Sá Júnior, P. L. de, Pasqualoto, K. F. M., Ferreira, A. K., Tavares, M. T., Damião, M. C. F. B., Azevedo, R. A. de, et al. (2013). RPF101, a new capsaicin-like analogue, disrupts the microtubule network accompanied by arrest in the G2/M phase, inducing apoptosis and mitotic catastrophe in the MCF-7 breast cancer cells. Toxicology and Applied Pharmacology, 266( 3), 385-398. doi:10.1016/j.taap.2012.11.029
NLM
Sá Júnior PL de, Pasqualoto KFM, Ferreira AK, Tavares MT, Damião MCFB, Azevedo RA de, Câmara DAD, Pereira A, Souza DM de, Parise Filho R. RPF101, a new capsaicin-like analogue, disrupts the microtubule network accompanied by arrest in the G2/M phase, inducing apoptosis and mitotic catastrophe in the MCF-7 breast cancer cells [Internet]. Toxicology and Applied Pharmacology. 2013 ; 266( 3): 385-398.[citado 2024 nov. 09 ] Available from: https://doi.org/10.1016/j.taap.2012.11.029
Vancouver
Sá Júnior PL de, Pasqualoto KFM, Ferreira AK, Tavares MT, Damião MCFB, Azevedo RA de, Câmara DAD, Pereira A, Souza DM de, Parise Filho R. RPF101, a new capsaicin-like analogue, disrupts the microtubule network accompanied by arrest in the G2/M phase, inducing apoptosis and mitotic catastrophe in the MCF-7 breast cancer cells [Internet]. Toxicology and Applied Pharmacology. 2013 ; 266( 3): 385-398.[citado 2024 nov. 09 ] Available from: https://doi.org/10.1016/j.taap.2012.11.029

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