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Artigo de periodico
Structural and thermodynamic analyses of human TMED1 (p24γ1) Golgi dynamics (2022)
Mota, Danielly Christine Adriani Maia ; Cardoso, Iara Aimê ; Mori, Renan Minin de ; Batista, Mariana R. B.; Basso, Luis G. M.; Nonato, Maria Cristina ; Costa Filho, Antonio José da ; Mendes, Luís Felipe Santos
Source: Biochimie. Unidades: FCFRP, FFCLRP, ESALQ
Subjects: COMPLEXO DE GOLGI, FILOGENIA, TERMODINÂMICA, PROTEÍNAS DE TRANSPORTE
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MOTA, Danielly Christine Adriani Maia et al. Structural and thermodynamic analyses of human TMED1 (p24γ1) Golgi dynamics. Biochimie, v. 192, p. 72-82, 2022Tradução . . Disponível em: https://doi.org/10.1016/j.biochi.2021.10.002. Acesso em: 10 nov. 2024.
APA
Mota, D. C. A. M., Cardoso, I. A., Mori, R. M. de, Batista, M. R. B., Basso, L. G. M., Nonato, M. C., et al. (2022). Structural and thermodynamic analyses of human TMED1 (p24γ1) Golgi dynamics. Biochimie, 192, 72-82. doi:10.1016/j.biochi.2021.10.002
NLM
Mota DCAM, Cardoso IA, Mori RM de, Batista MRB, Basso LGM, Nonato MC, Costa Filho AJ da, Mendes LFS. Structural and thermodynamic analyses of human TMED1 (p24γ1) Golgi dynamics [Internet]. Biochimie. 2022 ; 192 72-82.[citado 2024 nov. 10 ] Available from: https://doi.org/10.1016/j.biochi.2021.10.002
Vancouver
Mota DCAM, Cardoso IA, Mori RM de, Batista MRB, Basso LGM, Nonato MC, Costa Filho AJ da, Mendes LFS. Structural and thermodynamic analyses of human TMED1 (p24γ1) Golgi dynamics [Internet]. Biochimie. 2022 ; 192 72-82.[citado 2024 nov. 10 ] Available from: https://doi.org/10.1016/j.biochi.2021.10.002
Artigo de periodico
Andrographis paniculata formulations: impact on diterpene lactone oral bioavailability (2021)
Damasceno, João Paulo Loureiro ; Rosa, Hemerson Silva da; Araújo, Luciana Silva de; Furtado, Niege Araçari Jacometti Cardoso
Source: European Journal of Drug Metabolism and Pharmacokinetics. Unidade: FCFRP
Subjects: PLANTAS MEDICINAIS, FITOTERAPIA, EXTRATOS (FORMAS FARMACÊUTICAS), FARMACOCINÉTICA
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DAMASCENO, João Paulo Loureiro et al. Andrographis paniculata formulations: impact on diterpene lactone oral bioavailability. European Journal of Drug Metabolism and Pharmacokinetics, v. 47, p. 19-30, 2021Tradução . . Disponível em: https://doi.org/10.1007/s13318-021-00736-7. Acesso em: 10 nov. 2024.
APA
Damasceno, J. P. L., Rosa, H. S. da, Araújo, L. S. de, & Furtado, N. A. J. C. (2021). Andrographis paniculata formulations: impact on diterpene lactone oral bioavailability. European Journal of Drug Metabolism and Pharmacokinetics, 47, 19-30. doi:10.1007/s13318-021-00736-7
NLM
Damasceno JPL, Rosa HS da, Araújo LS de, Furtado NAJC. Andrographis paniculata formulations: impact on diterpene lactone oral bioavailability [Internet]. European Journal of Drug Metabolism and Pharmacokinetics. 2021 ; 47 19-30.[citado 2024 nov. 10 ] Available from: https://doi.org/10.1007/s13318-021-00736-7
Vancouver
Damasceno JPL, Rosa HS da, Araújo LS de, Furtado NAJC. Andrographis paniculata formulations: impact on diterpene lactone oral bioavailability [Internet]. European Journal of Drug Metabolism and Pharmacokinetics. 2021 ; 47 19-30.[citado 2024 nov. 10 ] Available from: https://doi.org/10.1007/s13318-021-00736-7
Artigo de periodico
Comparative study between the anti-P. falciparum activity of triazolopyrimidine, pyrazolopyrimidine and quinoline derivatives and the identification of new PfDHODH inhibitors (2021)
Silveira, Flávia F.; Souza, Juliana Oliveira de; Hoelz, Lucas V. B.; Campos, Vinícius R.; Jabor, Valquíria Aparecida Polisel; Aguiar, Anna Caroline Campos; Nonato, Maria Cristina ; Albuquerque, Magaly G. ; Guido, Rafael Victorio Carvalho ; Boechat, Nubia; Pinheiro, Luiz C. S.
Source: European Journal of Medicinal Chemistry. Unidades: IFSC, FCFRP
Subjects: ANTIMALÁRICOS, ANTIPARASITÁRIOS, MALÁRIA
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SILVEIRA, Flávia F. et al. Comparative study between the anti-P. falciparum activity of triazolopyrimidine, pyrazolopyrimidine and quinoline derivatives and the identification of new PfDHODH inhibitors. European Journal of Medicinal Chemistry, v. 209, n. Ja 2021, p. 112941-1-112941-16, 2021Tradução . . Disponível em: https://doi.org/10.1016/j.ejmech.2020.112941. Acesso em: 10 nov. 2024.
APA
Silveira, F. F., Souza, J. O. de, Hoelz, L. V. B., Campos, V. R., Jabor, V. A. P., Aguiar, A. C. C., et al. (2021). Comparative study between the anti-P. falciparum activity of triazolopyrimidine, pyrazolopyrimidine and quinoline derivatives and the identification of new PfDHODH inhibitors. European Journal of Medicinal Chemistry, 209( Ja 2021), 112941-1-112941-16. doi:10.1016/j.ejmech.2020.112941
NLM
Silveira FF, Souza JO de, Hoelz LVB, Campos VR, Jabor VAP, Aguiar ACC, Nonato MC, Albuquerque MG, Guido RVC, Boechat N, Pinheiro LCS. Comparative study between the anti-P. falciparum activity of triazolopyrimidine, pyrazolopyrimidine and quinoline derivatives and the identification of new PfDHODH inhibitors [Internet]. European Journal of Medicinal Chemistry. 2021 ; 209( Ja 2021): 112941-1-112941-16.[citado 2024 nov. 10 ] Available from: https://doi.org/10.1016/j.ejmech.2020.112941
Vancouver
Silveira FF, Souza JO de, Hoelz LVB, Campos VR, Jabor VAP, Aguiar ACC, Nonato MC, Albuquerque MG, Guido RVC, Boechat N, Pinheiro LCS. Comparative study between the anti-P. falciparum activity of triazolopyrimidine, pyrazolopyrimidine and quinoline derivatives and the identification of new PfDHODH inhibitors [Internet]. European Journal of Medicinal Chemistry. 2021 ; 209( Ja 2021): 112941-1-112941-16.[citado 2024 nov. 10 ] Available from: https://doi.org/10.1016/j.ejmech.2020.112941
Artigo de periodico
Assessment of the antibacterial, antivirulence, and action mechanism of Copaifera pubiflora oleoresin and isolated compounds against oral bacteria (2020)
Moraes, Thaís da Silva; Leandro, Luis Fernando; Santiago, Mariana Brentini; Silva, Larissa de Oliveira; Bianchi, Thamires Chiquini; Veneziani, Rodrigo Cássio Sola; Ambrósio, Sérgio Ricardo; Ramos, Salvador Boccaletti; Bastos, Jairo Kenupp ; Martins, Carlos Henrique Gomes
Source: Biomedicine & Pharmacotherapy. Unidade: FCFRP
Subjects: CÁRIE DENTÁRIA, ENDODONTIA, PRODUTOS NATURAIS, AGENTES ANTIMICROBIANOS
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MORAES, Thaís da Silva et al. Assessment of the antibacterial, antivirulence, and action mechanism of Copaifera pubiflora oleoresin and isolated compounds against oral bacteria. Biomedicine & Pharmacotherapy, v. 129, p. 1-16, 2020Tradução . . Disponível em: https://doi.org/10.1016/j.biopha.2020.110467. Acesso em: 10 nov. 2024.
APA
Moraes, T. da S., Leandro, L. F., Santiago, M. B., Silva, L. de O., Bianchi, T. C., Veneziani, R. C. S., et al. (2020). Assessment of the antibacterial, antivirulence, and action mechanism of Copaifera pubiflora oleoresin and isolated compounds against oral bacteria. Biomedicine & Pharmacotherapy, 129, 1-16. doi:10.1016/j.biopha.2020.110467
NLM
Moraes T da S, Leandro LF, Santiago MB, Silva L de O, Bianchi TC, Veneziani RCS, Ambrósio SR, Ramos SB, Bastos JK, Martins CHG. Assessment of the antibacterial, antivirulence, and action mechanism of Copaifera pubiflora oleoresin and isolated compounds against oral bacteria [Internet]. Biomedicine & Pharmacotherapy. 2020 ; 129 1-16.[citado 2024 nov. 10 ] Available from: https://doi.org/10.1016/j.biopha.2020.110467
Vancouver
Moraes T da S, Leandro LF, Santiago MB, Silva L de O, Bianchi TC, Veneziani RCS, Ambrósio SR, Ramos SB, Bastos JK, Martins CHG. Assessment of the antibacterial, antivirulence, and action mechanism of Copaifera pubiflora oleoresin and isolated compounds against oral bacteria [Internet]. Biomedicine & Pharmacotherapy. 2020 ; 129 1-16.[citado 2024 nov. 10 ] Available from: https://doi.org/10.1016/j.biopha.2020.110467
Artigo de periodico
Baseline resistance associated substitutions in HCV genotype 1 infected cohort treated with Simeprevir, Daclatasvir and Sofosbuvir in Brazil (2020)
Aguiar, Bruna Forte; Campos, Guilherme Rodrigues Fernandes; Rodrigues, João Paulo Vilela ; Marques, Nayara Nathie; Molina, Bárbara Floriano; Bittar, Cíntia ; Souza, Fernanda Fernandes; Martinelli, Ana de Lourdes Candolo ; Rahal, Paula ; Pereira, Leonardo Régis Leira
Source: Clinics and Research in Hepatology and Gastroenterology. Unidades: FMRP, FCFRP
Subjects: GENÓTIPOS, MUTAÇÃO, ANTIVIRAIS
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ABNT
AGUIAR, Bruna Forte et al. Baseline resistance associated substitutions in HCV genotype 1 infected cohort treated with Simeprevir, Daclatasvir and Sofosbuvir in Brazil. Clinics and Research in Hepatology and Gastroenterology, v. 44, n. 3, p. 329-339, 2020Tradução . . Disponível em: https://doi.org/10.1016/j.clinre.2019.07.015. Acesso em: 10 nov. 2024.
APA
Aguiar, B. F., Campos, G. R. F., Rodrigues, J. P. V., Marques, N. N., Molina, B. F., Bittar, C., et al. (2020). Baseline resistance associated substitutions in HCV genotype 1 infected cohort treated with Simeprevir, Daclatasvir and Sofosbuvir in Brazil. Clinics and Research in Hepatology and Gastroenterology, 44( 3), 329-339. doi:10.1016/j.clinre.2019.07.015
NLM
Aguiar BF, Campos GRF, Rodrigues JPV, Marques NN, Molina BF, Bittar C, Souza FF, Martinelli A de LC, Rahal P, Pereira LRL. Baseline resistance associated substitutions in HCV genotype 1 infected cohort treated with Simeprevir, Daclatasvir and Sofosbuvir in Brazil [Internet]. Clinics and Research in Hepatology and Gastroenterology. 2020 ; 44( 3): 329-339.[citado 2024 nov. 10 ] Available from: https://doi.org/10.1016/j.clinre.2019.07.015
Vancouver
Aguiar BF, Campos GRF, Rodrigues JPV, Marques NN, Molina BF, Bittar C, Souza FF, Martinelli A de LC, Rahal P, Pereira LRL. Baseline resistance associated substitutions in HCV genotype 1 infected cohort treated with Simeprevir, Daclatasvir and Sofosbuvir in Brazil [Internet]. Clinics and Research in Hepatology and Gastroenterology. 2020 ; 44( 3): 329-339.[citado 2024 nov. 10 ] Available from: https://doi.org/10.1016/j.clinre.2019.07.015
Artigo de periodico
Aluminum directly inhibits alternative oxidase pathway and changes metabolic and redox parameters on Jatropha curcas cell culture (2019)
Vicentini, Tatiane Maira; Cavalheiro, Amanda Henriques; Dechandt, Carlos Roberto Porto ; Alberici, Luciane Carla ; Vargas-Rechia, Carem Gledes
Source: Plant Physiology and Biochemistry. Unidade: FCFRP
Subjects: COMPOSTOS FENÓLICOS, AÇUCARES, ENZIMAS
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ABNT
VICENTINI, Tatiane Maira et al. Aluminum directly inhibits alternative oxidase pathway and changes metabolic and redox parameters on Jatropha curcas cell culture. Plant Physiology and Biochemistry, v. 136, p. 92-97, 2019Tradução . . Disponível em: https://doi.org/10.1016/j.plaphy.2019.01.012. Acesso em: 10 nov. 2024.
APA
Vicentini, T. M., Cavalheiro, A. H., Dechandt, C. R. P., Alberici, L. C., & Vargas-Rechia, C. G. (2019). Aluminum directly inhibits alternative oxidase pathway and changes metabolic and redox parameters on Jatropha curcas cell culture. Plant Physiology and Biochemistry, 136, 92-97. doi:10.1016/j.plaphy.2019.01.012
NLM
Vicentini TM, Cavalheiro AH, Dechandt CRP, Alberici LC, Vargas-Rechia CG. Aluminum directly inhibits alternative oxidase pathway and changes metabolic and redox parameters on Jatropha curcas cell culture [Internet]. Plant Physiology and Biochemistry. 2019 ; 136 92-97.[citado 2024 nov. 10 ] Available from: https://doi.org/10.1016/j.plaphy.2019.01.012
Vancouver
Vicentini TM, Cavalheiro AH, Dechandt CRP, Alberici LC, Vargas-Rechia CG. Aluminum directly inhibits alternative oxidase pathway and changes metabolic and redox parameters on Jatropha curcas cell culture [Internet]. Plant Physiology and Biochemistry. 2019 ; 136 92-97.[citado 2024 nov. 10 ] Available from: https://doi.org/10.1016/j.plaphy.2019.01.012
Artigo de periodico
Insights into the structure, function and stability of bordonein-L, the first L-amino acid oxidase from Crotalus durissus terrificus snake venom (2019)
Wiezel, Gisele Adriano ; Rustiguel, Joane Kathelen ; Morgenstern, David; Zoccal, Karina Furlani ; Faccioli, Lucia Helena ; Nonato, Maria Cristina ; Ueberheide, Beatrix ; Arantes, Eliane Candiani
Source: Biochimie. Unidade: FCFRP
Subjects: CITOTOXICIDADE IMUNOLÓGICA, SEQUÊNCIA DE AMINOÁCIDOS, SERPENTES, VENENOS, ESPECTROMETRIA DE MASSAS
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WIEZEL, Gisele Adriano et al. Insights into the structure, function and stability of bordonein-L, the first L-amino acid oxidase from Crotalus durissus terrificus snake venom. Biochimie, v. 163, p. 33-49, 2019Tradução . . Disponível em: https://doi.org/10.1016/j.biochi.2019.05.009. Acesso em: 10 nov. 2024.
APA
Wiezel, G. A., Rustiguel, J. K., Morgenstern, D., Zoccal, K. F., Faccioli, L. H., Nonato, M. C., et al. (2019). Insights into the structure, function and stability of bordonein-L, the first L-amino acid oxidase from Crotalus durissus terrificus snake venom. Biochimie, 163, 33-49. doi:10.1016/j.biochi.2019.05.009
NLM
Wiezel GA, Rustiguel JK, Morgenstern D, Zoccal KF, Faccioli LH, Nonato MC, Ueberheide B, Arantes EC. Insights into the structure, function and stability of bordonein-L, the first L-amino acid oxidase from Crotalus durissus terrificus snake venom [Internet]. Biochimie. 2019 ; 163 33-49.[citado 2024 nov. 10 ] Available from: https://doi.org/10.1016/j.biochi.2019.05.009
Vancouver
Wiezel GA, Rustiguel JK, Morgenstern D, Zoccal KF, Faccioli LH, Nonato MC, Ueberheide B, Arantes EC. Insights into the structure, function and stability of bordonein-L, the first L-amino acid oxidase from Crotalus durissus terrificus snake venom [Internet]. Biochimie. 2019 ; 163 33-49.[citado 2024 nov. 10 ] Available from: https://doi.org/10.1016/j.biochi.2019.05.009
Artigo de periodico
Occurrence, chemical composition, biological activities and analytical methods on Copaifera genus: a review (2019)
Arruda, Caroline ; Mejía, Jennyfer Andrea Aldana; Ribeiro, Victor Pena ; Borges, Carly Henrique Gambeta; Martins, Carlos Henrique Gomes ; Veneziani, Rodrigo Cássio Sola ; Ambrosio, Sérgio Ricardo ; Bastos, Jairo Kenupp
Source: Biomedicine & Pharmacotherapy. Unidade: FCFRP
Subjects: PRODUTOS NATURAIS, QUALIDADE DOS MEDICAMENTOS, FABACEAE, MEDICINA TRADICIONAL, TERPENOS
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ABNT
ARRUDA, Caroline et al. Occurrence, chemical composition, biological activities and analytical methods on Copaifera genus: a review. Biomedicine & Pharmacotherapy, v. 109, p. 1-20, 2019Tradução . . Disponível em: https://doi.org/10.1016/j.biopha.2018.10.030. Acesso em: 10 nov. 2024.
APA
Arruda, C., Mejía, J. A. A., Ribeiro, V. P., Borges, C. H. G., Martins, C. H. G., Veneziani, R. C. S., et al. (2019). Occurrence, chemical composition, biological activities and analytical methods on Copaifera genus: a review. Biomedicine & Pharmacotherapy, 109, 1-20. doi:10.1016/j.biopha.2018.10.030
NLM
Arruda C, Mejía JAA, Ribeiro VP, Borges CHG, Martins CHG, Veneziani RCS, Ambrosio SR, Bastos JK. Occurrence, chemical composition, biological activities and analytical methods on Copaifera genus: a review [Internet]. Biomedicine & Pharmacotherapy. 2019 ; 109 1-20.[citado 2024 nov. 10 ] Available from: https://doi.org/10.1016/j.biopha.2018.10.030
Vancouver
Arruda C, Mejía JAA, Ribeiro VP, Borges CHG, Martins CHG, Veneziani RCS, Ambrosio SR, Bastos JK. Occurrence, chemical composition, biological activities and analytical methods on Copaifera genus: a review [Internet]. Biomedicine & Pharmacotherapy. 2019 ; 109 1-20.[citado 2024 nov. 10 ] Available from: https://doi.org/10.1016/j.biopha.2018.10.030
Artigo de periodico
Chemopreventive role of Copaifera reticulata Ducke oleoresin in colon carcinogenesis (2019)
Senedese, Juliana Marques; Rinaldi-Neto, Francisco; Furtado, Ricardo Andrade ; Nicollela, Heloiza Diniz ; Souza, Larissa Daniela Ribeiro de; Ribeiro, Arthur Barcelos; Ferreira, Lucas Souza ; Magalhães, Geórgia Modé ; Carlos, Iracilda Zeppone ; Silva, Jonas Joaquim Mangabeira da ; Tavares, Denise Crispim ; Bastos, Jairo Kenupp
Source: Biomedicine & Pharmacotherapy. Unidades: FCFRP, FMRP
Subjects: ANTI-INFLAMATÓRIOS, CARCINOGÊNESE, SOBREVIVÊNCIA CELULAR, FABACEAE
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SENEDESE, Juliana Marques et al. Chemopreventive role of Copaifera reticulata Ducke oleoresin in colon carcinogenesis. Biomedicine & Pharmacotherapy, v. 111, p. 331-337, 2019Tradução . . Disponível em: https://doi.org/10.1016/j.biopha.2018.12.091. Acesso em: 10 nov. 2024.
APA
Senedese, J. M., Rinaldi-Neto, F., Furtado, R. A., Nicollela, H. D., Souza, L. D. R. de, Ribeiro, A. B., et al. (2019). Chemopreventive role of Copaifera reticulata Ducke oleoresin in colon carcinogenesis. Biomedicine & Pharmacotherapy, 111, 331-337. doi:10.1016/j.biopha.2018.12.091
NLM
Senedese JM, Rinaldi-Neto F, Furtado RA, Nicollela HD, Souza LDR de, Ribeiro AB, Ferreira LS, Magalhães GM, Carlos IZ, Silva JJM da, Tavares DC, Bastos JK. Chemopreventive role of Copaifera reticulata Ducke oleoresin in colon carcinogenesis [Internet]. Biomedicine & Pharmacotherapy. 2019 ; 111 331-337.[citado 2024 nov. 10 ] Available from: https://doi.org/10.1016/j.biopha.2018.12.091
Vancouver
Senedese JM, Rinaldi-Neto F, Furtado RA, Nicollela HD, Souza LDR de, Ribeiro AB, Ferreira LS, Magalhães GM, Carlos IZ, Silva JJM da, Tavares DC, Bastos JK. Chemopreventive role of Copaifera reticulata Ducke oleoresin in colon carcinogenesis [Internet]. Biomedicine & Pharmacotherapy. 2019 ; 111 331-337.[citado 2024 nov. 10 ] Available from: https://doi.org/10.1016/j.biopha.2018.12.091
Artigo de periodico
Ligand-based design, synthesis and biochemical evaluation of potent and selective inhibitors of Schistosoma mansoni dihydroorotate dehydrogenase (2019)
Calil, Felipe Antunes ; Costacurta, Juliana Serafim David; Chiappetta, Estela Rodrigues Cardoso; Fumagalli, Fernando ; Mello, Rodrigo Brito de; Leite, Franco Henrique Andrade ; Castilho, Marcelo S. ; Emery, Flavio da Silva ; Nonato, Maria Cristina
Source: European Journal of Medicinal Chemistry. Unidade: FCFRP
Subjects: SCHISTOSOMA, INIBIDORES DE ENZIMAS
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ABNT
CALIL, Felipe Antunes et al. Ligand-based design, synthesis and biochemical evaluation of potent and selective inhibitors of Schistosoma mansoni dihydroorotate dehydrogenase. European Journal of Medicinal Chemistry, v. 167, p. 357-366, 2019Tradução . . Disponível em: https://doi.org/10.1016/j.ejmech.2019.02.018. Acesso em: 10 nov. 2024.
APA
Calil, F. A., Costacurta, J. S. D., Chiappetta, E. R. C., Fumagalli, F., Mello, R. B. de, Leite, F. H. A., et al. (2019). Ligand-based design, synthesis and biochemical evaluation of potent and selective inhibitors of Schistosoma mansoni dihydroorotate dehydrogenase. European Journal of Medicinal Chemistry, 167, 357-366. doi:10.1016/j.ejmech.2019.02.018
NLM
Calil FA, Costacurta JSD, Chiappetta ERC, Fumagalli F, Mello RB de, Leite FHA, Castilho MS, Emery F da S, Nonato MC. Ligand-based design, synthesis and biochemical evaluation of potent and selective inhibitors of Schistosoma mansoni dihydroorotate dehydrogenase [Internet]. European Journal of Medicinal Chemistry. 2019 ; 167 357-366.[citado 2024 nov. 10 ] Available from: https://doi.org/10.1016/j.ejmech.2019.02.018
Vancouver
Calil FA, Costacurta JSD, Chiappetta ERC, Fumagalli F, Mello RB de, Leite FHA, Castilho MS, Emery F da S, Nonato MC. Ligand-based design, synthesis and biochemical evaluation of potent and selective inhibitors of Schistosoma mansoni dihydroorotate dehydrogenase [Internet]. European Journal of Medicinal Chemistry. 2019 ; 167 357-366.[citado 2024 nov. 10 ] Available from: https://doi.org/10.1016/j.ejmech.2019.02.018
Artigo de periodico
Structural basis for the design of selective inhibitors for Schistosoma mansoni dihydroorotate dehydrogenase (2019)
Nonato, Maria Cristina; Pádua, Ricardo A. P.; David, Juliana S.; Reis, Renata A. G.; Tomaleri, Giovani P.; Pereira, Humberto D'Muniz; Calil, Felipe A.
Source: Biochimie. Unidades: FCFRP, IFSC
Subjects: SCHISTOSOMA MANSONI, INIBIDORES DE ENZIMAS
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ABNT
NONATO, Maria Cristina et al. Structural basis for the design of selective inhibitors for Schistosoma mansoni dihydroorotate dehydrogenase. Biochimie, v. 158, n. 1, p. 180-190, 2019Tradução . . Disponível em: https://doi.org/10.1016/j.biochi.2019.01.006. Acesso em: 10 nov. 2024.
APA
Nonato, M. C., Pádua, R. A. P., David, J. S., Reis, R. A. G., Tomaleri, G. P., Pereira, H. D. 'M., & Calil, F. A. (2019). Structural basis for the design of selective inhibitors for Schistosoma mansoni dihydroorotate dehydrogenase. Biochimie, 158( 1), 180-190. doi:10.1016/j.biochi.2019.01.006
NLM
Nonato MC, Pádua RAP, David JS, Reis RAG, Tomaleri GP, Pereira HD'M, Calil FA. Structural basis for the design of selective inhibitors for Schistosoma mansoni dihydroorotate dehydrogenase [Internet]. Biochimie. 2019 ; 158( 1): 180-190.[citado 2024 nov. 10 ] Available from: https://doi.org/10.1016/j.biochi.2019.01.006
Vancouver
Nonato MC, Pádua RAP, David JS, Reis RAG, Tomaleri GP, Pereira HD'M, Calil FA. Structural basis for the design of selective inhibitors for Schistosoma mansoni dihydroorotate dehydrogenase [Internet]. Biochimie. 2019 ; 158( 1): 180-190.[citado 2024 nov. 10 ] Available from: https://doi.org/10.1016/j.biochi.2019.01.006
Artigo de periodico
Heterobimetallic nickel(II) and palladium(II) complexes derived from S-benzyl-N- (ferrocenyl)methylenedithiocarbazate: Trypanocidal activity and interaction with Trypanosoma cruzi Old Yellow Enzyme (TcOYE) (2019)
Carneiro, Zumira A; Gaspari, Ana P S; Lima, Jackelinne C; Lopes, Carla D; Gaspari, Ana P S; Albuquerque, Sérgio de ; Dinelli, Luis R; Silva, Laudimir Leonardo Walbert Veloso da; Paganelli, Marcella Oliva; Libardi, Silvia Helena; Deflon, Victor Marcelo ; Oliveira, Carolina G; Oliveira, Ronaldo J; Borges, Julio Cesar ; Maia, Pedro I. S
Source: European Journal of Medicinal Chemistry. Unidades: IQSC, FCFRP, FMRP
Assunto: DOENÇA DE CHAGAS
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ABNT
CARNEIRO, Zumira A et al. Heterobimetallic nickel(II) and palladium(II) complexes derived from S-benzyl-N- (ferrocenyl)methylenedithiocarbazate: Trypanocidal activity and interaction with Trypanosoma cruzi Old Yellow Enzyme (TcOYE). European Journal of Medicinal Chemistry, v. 180, p. 213-223, 2019Tradução . . Disponível em: https://doi.org/10.1016/j.ejmech.2019.07.014. Acesso em: 10 nov. 2024.
APA
Carneiro, Z. A., Gaspari, A. P. S., Lima, J. C., Lopes, C. D., Gaspari, A. P. S., Albuquerque, S. de, et al. (2019). Heterobimetallic nickel(II) and palladium(II) complexes derived from S-benzyl-N- (ferrocenyl)methylenedithiocarbazate: Trypanocidal activity and interaction with Trypanosoma cruzi Old Yellow Enzyme (TcOYE). European Journal of Medicinal Chemistry, 180, 213-223. doi:10.1016/j.ejmech.2019.07.014
NLM
Carneiro ZA, Gaspari APS, Lima JC, Lopes CD, Gaspari APS, Albuquerque S de, Dinelli LR, Silva LLWV da, Paganelli MO, Libardi SH, Deflon VM, Oliveira CG, Oliveira RJ, Borges JC, Maia PIS. Heterobimetallic nickel(II) and palladium(II) complexes derived from S-benzyl-N- (ferrocenyl)methylenedithiocarbazate: Trypanocidal activity and interaction with Trypanosoma cruzi Old Yellow Enzyme (TcOYE) [Internet]. European Journal of Medicinal Chemistry. 2019 ; 180 213-223.[citado 2024 nov. 10 ] Available from: https://doi.org/10.1016/j.ejmech.2019.07.014
Vancouver
Carneiro ZA, Gaspari APS, Lima JC, Lopes CD, Gaspari APS, Albuquerque S de, Dinelli LR, Silva LLWV da, Paganelli MO, Libardi SH, Deflon VM, Oliveira CG, Oliveira RJ, Borges JC, Maia PIS. Heterobimetallic nickel(II) and palladium(II) complexes derived from S-benzyl-N- (ferrocenyl)methylenedithiocarbazate: Trypanocidal activity and interaction with Trypanosoma cruzi Old Yellow Enzyme (TcOYE) [Internet]. European Journal of Medicinal Chemistry. 2019 ; 180 213-223.[citado 2024 nov. 10 ] Available from: https://doi.org/10.1016/j.ejmech.2019.07.014
Artigo de periodico
Quercetin attenuates zymosan-induced arthritis in mice (2018)
Guazelli, Carla F. S.; Staurengo-Ferrari, Larissa; Zarpelon, Ana C.; Pinho-Ribeiro, Felipe A.; Ruiz-Miyazawa, Kenji W.; Vicentini, Fabiana Testa Moura-de-Carvalho ; Vignoli, Josiane A.; Camilios-Neto, Doumit; Georgetti, Sandra R.; Baracat, Marcela M.; Casagrande, Rubia; Verri Jr., Waldiceu A.
Source: Biomedicine & Pharmacotherapy. Unidade: FCFRP
Subjects: INFLAMAÇÃO, ESTRESSE OXIDATIVO, ARTRITE REUMATOIDE, PROTEÍNAS DA MEMBRANA, ANTIOXIDANTES
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
GUAZELLI, Carla F. S. et al. Quercetin attenuates zymosan-induced arthritis in mice. Biomedicine & Pharmacotherapy, v. 102, p. 175-184, 2018Tradução . . Disponível em: https://doi.org/10.1016/j.biopha.2018.03.057. Acesso em: 10 nov. 2024.
APA
Guazelli, C. F. S., Staurengo-Ferrari, L., Zarpelon, A. C., Pinho-Ribeiro, F. A., Ruiz-Miyazawa, K. W., Vicentini, F. T. M. -de-C., et al. (2018). Quercetin attenuates zymosan-induced arthritis in mice. Biomedicine & Pharmacotherapy, 102, 175-184. doi:10.1016/j.biopha.2018.03.057
NLM
Guazelli CFS, Staurengo-Ferrari L, Zarpelon AC, Pinho-Ribeiro FA, Ruiz-Miyazawa KW, Vicentini FTM-de-C, Vignoli JA, Camilios-Neto D, Georgetti SR, Baracat MM, Casagrande R, Verri Jr. WA. Quercetin attenuates zymosan-induced arthritis in mice [Internet]. Biomedicine & Pharmacotherapy. 2018 ; 102 175-184.[citado 2024 nov. 10 ] Available from: https://doi.org/10.1016/j.biopha.2018.03.057
Vancouver
Guazelli CFS, Staurengo-Ferrari L, Zarpelon AC, Pinho-Ribeiro FA, Ruiz-Miyazawa KW, Vicentini FTM-de-C, Vignoli JA, Camilios-Neto D, Georgetti SR, Baracat MM, Casagrande R, Verri Jr. WA. Quercetin attenuates zymosan-induced arthritis in mice [Internet]. Biomedicine & Pharmacotherapy. 2018 ; 102 175-184.[citado 2024 nov. 10 ] Available from: https://doi.org/10.1016/j.biopha.2018.03.057
Artigo de periodico
Natural products as inhibitors of Leishmania major dihydroorotate dehydrogenase (2018)
Chibli, Lucas Apolinário ; Schmidt, Thomas J.; Nonato, Maria Cristina; Calil, Felipe Antunes ; Costa, Fernando Batista da
Source: European Journal of Medicinal Chemistry. Unidade: FCFRP
Subjects: COMPOSITAE, LEISHMANIA, DOENÇAS NEGLIGENCIADAS, SESQUITERPENOS, INIBIDORES DE ENZIMAS, ENZIMAS OXIRREDUTORAS
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
CHIBLI, Lucas Apolinário et al. Natural products as inhibitors of Leishmania major dihydroorotate dehydrogenase. European Journal of Medicinal Chemistry, v. 157, p. 852-866, 2018Tradução . . Disponível em: https://doi.org/10.1016/j.ejmech.2018.08.033. Acesso em: 10 nov. 2024.
APA
Chibli, L. A., Schmidt, T. J., Nonato, M. C., Calil, F. A., & Costa, F. B. da. (2018). Natural products as inhibitors of Leishmania major dihydroorotate dehydrogenase. European Journal of Medicinal Chemistry, 157, 852-866. doi:10.1016/j.ejmech.2018.08.033
NLM
Chibli LA, Schmidt TJ, Nonato MC, Calil FA, Costa FB da. Natural products as inhibitors of Leishmania major dihydroorotate dehydrogenase [Internet]. European Journal of Medicinal Chemistry. 2018 ; 157 852-866.[citado 2024 nov. 10 ] Available from: https://doi.org/10.1016/j.ejmech.2018.08.033
Vancouver
Chibli LA, Schmidt TJ, Nonato MC, Calil FA, Costa FB da. Natural products as inhibitors of Leishmania major dihydroorotate dehydrogenase [Internet]. European Journal of Medicinal Chemistry. 2018 ; 157 852-866.[citado 2024 nov. 10 ] Available from: https://doi.org/10.1016/j.ejmech.2018.08.033
Artigo de periodico
Morphological diversity and function of the stigma in Ficus species (Moraceae) (2018)
Teixeira, Simone Pádua; Costa, Marina F. B.; Basso-Alves, João Paulo; Kjellberg, Finn; Pereira, Rodrigo Augusto Santinelo
Source: Acta Oecologica. Unidades: FCFRP, FFCLRP
Subjects: POLINIZAÇÃO, MORACEAE, GERMINAÇÃO, MORFOLOGIA VEGETAL
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
TEIXEIRA, Simone Pádua et al. Morphological diversity and function of the stigma in Ficus species (Moraceae). Acta Oecologica, v. 90, p. 117-131, 2018Tradução . . Disponível em: https://doi.org/10.1016/j.actao.2018.02.008. Acesso em: 10 nov. 2024.
APA
Teixeira, S. P., Costa, M. F. B., Basso-Alves, J. P., Kjellberg, F., & Pereira, R. A. S. (2018). Morphological diversity and function of the stigma in Ficus species (Moraceae). Acta Oecologica, 90, 117-131. doi:10.1016/j.actao.2018.02.008
NLM
Teixeira SP, Costa MFB, Basso-Alves JP, Kjellberg F, Pereira RAS. Morphological diversity and function of the stigma in Ficus species (Moraceae) [Internet]. Acta Oecologica. 2018 ; 90 117-131.[citado 2024 nov. 10 ] Available from: https://doi.org/10.1016/j.actao.2018.02.008
Vancouver
Teixeira SP, Costa MFB, Basso-Alves JP, Kjellberg F, Pereira RAS. Morphological diversity and function of the stigma in Ficus species (Moraceae) [Internet]. Acta Oecologica. 2018 ; 90 117-131.[citado 2024 nov. 10 ] Available from: https://doi.org/10.1016/j.actao.2018.02.008
Artigo de periodico
β-amino alcohols and their respective 2-phenyl-N-alkyl aziridines as potential DNA minor groove binders (2018)
Vaidergorn, Miguel M; Carneiro, Zumira A; Lopes, Carla D; Albuquerque, Sérgio de; Reis, Felipe C. C; Nikolaou, Sofia; Mello, Juliana F. R; Genesi, Giovani L; Trossini, Gustavo Henrique Goulart ; Ganesan, A; Emery, Flavio da Silva
Source: European Journal of Medicinal Chemistry. Unidades: FCFRP, FFCLRP, FCF
Subjects: DNA, COMPOSTOS ORGÂNICOS
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ABNT
VAIDERGORN, Miguel M et al. β-amino alcohols and their respective 2-phenyl-N-alkyl aziridines as potential DNA minor groove binders. European Journal of Medicinal Chemistry, v. 157, p. 657-664, 2018Tradução . . Disponível em: https://doi.org/10.1016/j.ejmech.2018.07.055. Acesso em: 10 nov. 2024.
APA
Vaidergorn, M. M., Carneiro, Z. A., Lopes, C. D., Albuquerque, S. de, Reis, F. C. C., Nikolaou, S., et al. (2018). β-amino alcohols and their respective 2-phenyl-N-alkyl aziridines as potential DNA minor groove binders. European Journal of Medicinal Chemistry, 157, 657-664. doi:10.1016/j.ejmech.2018.07.055
NLM
Vaidergorn MM, Carneiro ZA, Lopes CD, Albuquerque S de, Reis FCC, Nikolaou S, Mello JFR, Genesi GL, Trossini GHG, Ganesan A, Emery F da S. β-amino alcohols and their respective 2-phenyl-N-alkyl aziridines as potential DNA minor groove binders [Internet]. European Journal of Medicinal Chemistry. 2018 ; 157 657-664.[citado 2024 nov. 10 ] Available from: https://doi.org/10.1016/j.ejmech.2018.07.055
Vancouver
Vaidergorn MM, Carneiro ZA, Lopes CD, Albuquerque S de, Reis FCC, Nikolaou S, Mello JFR, Genesi GL, Trossini GHG, Ganesan A, Emery F da S. β-amino alcohols and their respective 2-phenyl-N-alkyl aziridines as potential DNA minor groove binders [Internet]. European Journal of Medicinal Chemistry. 2018 ; 157 657-664.[citado 2024 nov. 10 ] Available from: https://doi.org/10.1016/j.ejmech.2018.07.055
Artigo de periodico
Chameleon-like behavior of indolylpiperidines in complex with cholinesterases targets: potent butyrylcholinesterase inhibitors (2018)
Chierrito, Talita Perez Cantuaria; Pedersoli-Mantoani, Susimaire; Roca, Carlos; Sebastian-Pérez, Victor; Martínez-Gonzalez, Loreto; Pérez, Daniel I.; Perez, Concepción; Canales, Angeles; Cañada, F. Javier; Campillo, Nuria E.; Carvalho, Ivone; Martinez, Ana
Source: European Journal of Medicinal Chemistry. Unidade: FCFRP
Subjects: DOENÇA DE ALZHEIMER, FARMACOTÉCNICA
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ABNT
CHIERRITO, Talita Perez Cantuaria et al. Chameleon-like behavior of indolylpiperidines in complex with cholinesterases targets: potent butyrylcholinesterase inhibitors. European Journal of Medicinal Chemistry, v. 145, p. 431-444, 2018Tradução . . Disponível em: https://doi.org/10.1016/j.ejmech.2018.01.007. Acesso em: 10 nov. 2024.
APA
Chierrito, T. P. C., Pedersoli-Mantoani, S., Roca, C., Sebastian-Pérez, V., Martínez-Gonzalez, L., Pérez, D. I., et al. (2018). Chameleon-like behavior of indolylpiperidines in complex with cholinesterases targets: potent butyrylcholinesterase inhibitors. European Journal of Medicinal Chemistry, 145, 431-444. doi:10.1016/j.ejmech.2018.01.007
NLM
Chierrito TPC, Pedersoli-Mantoani S, Roca C, Sebastian-Pérez V, Martínez-Gonzalez L, Pérez DI, Perez C, Canales A, Cañada FJ, Campillo NE, Carvalho I, Martinez A. Chameleon-like behavior of indolylpiperidines in complex with cholinesterases targets: potent butyrylcholinesterase inhibitors [Internet]. European Journal of Medicinal Chemistry. 2018 ; 145 431-444.[citado 2024 nov. 10 ] Available from: https://doi.org/10.1016/j.ejmech.2018.01.007
Vancouver
Chierrito TPC, Pedersoli-Mantoani S, Roca C, Sebastian-Pérez V, Martínez-Gonzalez L, Pérez DI, Perez C, Canales A, Cañada FJ, Campillo NE, Carvalho I, Martinez A. Chameleon-like behavior of indolylpiperidines in complex with cholinesterases targets: potent butyrylcholinesterase inhibitors [Internet]. European Journal of Medicinal Chemistry. 2018 ; 145 431-444.[citado 2024 nov. 10 ] Available from: https://doi.org/10.1016/j.ejmech.2018.01.007
Artigo de periodico
Evaluation of 7-arylaminopyrazolo[1,5- a ]pyrimidines as anti- Plasmodium falciparum , antimalarial, and Pf- dihydroorotate dehydrogenase inhibitors (2017)
Azeredo, Luís Felipe S. P.; Coutinho, Julia P.; Jabor, Valquíria Aparecida Polisel; Feliciano, Patricia R.; Nonato, Maria Cristina; Kaiser, Carlos R.; Menezes, Carla Maria S.; Hammes, Amanda S. O.; Caffarena, Ernesto Raul; Hoelz, Lucas V. B.; Souza, Nicolli B. de; Pereira, Glaécia A. N.; Cerávolo, Isabela P.; Krettli, Antoniana U.; Boechat, Nubia
Source: European Journal of Medicinal Chemistry. Unidade: FCFRP
Subjects: ANTIMALÁRICOS, INIBIDORES DE ENZIMAS
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ABNT
AZEREDO, Luís Felipe S. P. et al. Evaluation of 7-arylaminopyrazolo[1,5- a ]pyrimidines as anti- Plasmodium falciparum , antimalarial, and Pf- dihydroorotate dehydrogenase inhibitors. European Journal of Medicinal Chemistry, v. 126, p. 72-83, 2017Tradução . . Disponível em: https://doi.org/10.1016/j.ejmech.2016.09.073. Acesso em: 10 nov. 2024.
APA
Azeredo, L. F. S. P., Coutinho, J. P., Jabor, V. A. P., Feliciano, P. R., Nonato, M. C., Kaiser, C. R., et al. (2017). Evaluation of 7-arylaminopyrazolo[1,5- a ]pyrimidines as anti- Plasmodium falciparum , antimalarial, and Pf- dihydroorotate dehydrogenase inhibitors. European Journal of Medicinal Chemistry, 126, 72-83. doi:10.1016/j.ejmech.2016.09.073
NLM
Azeredo LFSP, Coutinho JP, Jabor VAP, Feliciano PR, Nonato MC, Kaiser CR, Menezes CMS, Hammes ASO, Caffarena ER, Hoelz LVB, Souza NB de, Pereira GAN, Cerávolo IP, Krettli AU, Boechat N. Evaluation of 7-arylaminopyrazolo[1,5- a ]pyrimidines as anti- Plasmodium falciparum , antimalarial, and Pf- dihydroorotate dehydrogenase inhibitors [Internet]. European Journal of Medicinal Chemistry. 2017 ; 126 72-83.[citado 2024 nov. 10 ] Available from: https://doi.org/10.1016/j.ejmech.2016.09.073
Vancouver
Azeredo LFSP, Coutinho JP, Jabor VAP, Feliciano PR, Nonato MC, Kaiser CR, Menezes CMS, Hammes ASO, Caffarena ER, Hoelz LVB, Souza NB de, Pereira GAN, Cerávolo IP, Krettli AU, Boechat N. Evaluation of 7-arylaminopyrazolo[1,5- a ]pyrimidines as anti- Plasmodium falciparum , antimalarial, and Pf- dihydroorotate dehydrogenase inhibitors [Internet]. European Journal of Medicinal Chemistry. 2017 ; 126 72-83.[citado 2024 nov. 10 ] Available from: https://doi.org/10.1016/j.ejmech.2016.09.073
Artigo de periodico
Inactivation of β-lapachone cytotoxicity by filamentous fungi that mimic the human blood metabolism (2017)
Paludo, Camila Raquel; Silva-Junior, Eduardo Afonso da; Silva, Eliane de Oliveira; Vessecchi, Ricardo; Lopes, Norberto Peporine; Pupo, Mônica Tallarico; Emery, Flavio da Silva; Gonçalves, Natália dos Santos; Santos, Raquel Alves dos; Furtado, Niege Araçari Jacometti Cardoso
Source: European Journal of Drug Metabolism and Pharmacokinetics. Unidade: FCFRP
Subjects: CITOTOXINAS, METABOLISMO, SANGUE
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
PALUDO, Camila Raquel et al. Inactivation of β-lapachone cytotoxicity by filamentous fungi that mimic the human blood metabolism. European Journal of Drug Metabolism and Pharmacokinetics, v. 42, n. 2, p. 213-220, 2017Tradução . . Disponível em: https://doi.org/10.1007/s13318-016-0337-2. Acesso em: 10 nov. 2024.
APA
Paludo, C. R., Silva-Junior, E. A. da, Silva, E. de O., Vessecchi, R., Lopes, N. P., Pupo, M. T., et al. (2017). Inactivation of β-lapachone cytotoxicity by filamentous fungi that mimic the human blood metabolism. European Journal of Drug Metabolism and Pharmacokinetics, 42( 2), 213-220. doi:10.1007/s13318-016-0337-2
NLM
Paludo CR, Silva-Junior EA da, Silva E de O, Vessecchi R, Lopes NP, Pupo MT, Emery F da S, Gonçalves N dos S, Santos RA dos, Furtado NAJC. Inactivation of β-lapachone cytotoxicity by filamentous fungi that mimic the human blood metabolism [Internet]. European Journal of Drug Metabolism and Pharmacokinetics. 2017 ; 42( 2): 213-220.[citado 2024 nov. 10 ] Available from: https://doi.org/10.1007/s13318-016-0337-2
Vancouver
Paludo CR, Silva-Junior EA da, Silva E de O, Vessecchi R, Lopes NP, Pupo MT, Emery F da S, Gonçalves N dos S, Santos RA dos, Furtado NAJC. Inactivation of β-lapachone cytotoxicity by filamentous fungi that mimic the human blood metabolism [Internet]. European Journal of Drug Metabolism and Pharmacokinetics. 2017 ; 42( 2): 213-220.[citado 2024 nov. 10 ] Available from: https://doi.org/10.1007/s13318-016-0337-2
Artigo de periodico
From dual binding site acetylcholinesterase inhibitors to allosteric modulators: a new avenue for disease-modifying drugs in Alzheimer's disease (2017)
Chierrito, Talita P. C.; Mantoani, Susimaire Pedersoli; Roca, Carlos; Requena, Carlos; Perez, Victor Sebastian; Castillo, Willian O.; Moreira, Natalia C. S.; Pérez, Concepción; Sakamoto-Hojo, Elza Tiemi; Takahashi, Catarina Satie; Barbero, Jesús Jiménez; Cañada, F. Javier; Campillo, Nuria E.; Martinez, Ana; Carvalho, Ivone
Source: European Journal of Medicinal Chemistry. Unidades: FFCLRP, FCFRP
Subjects: DOENÇA DE ALZHEIMER, INIBIDORES DE ENZIMAS, PROLIFERAÇÃO CELULAR
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ABNT
CHIERRITO, Talita P. C. et al. From dual binding site acetylcholinesterase inhibitors to allosteric modulators: a new avenue for disease-modifying drugs in Alzheimer's disease. European Journal of Medicinal Chemistry, v. 139, p. 773-791, 2017Tradução . . Disponível em: https://doi.org/10.1016/j.ejmech.2017.08.051. Acesso em: 10 nov. 2024.
APA
Chierrito, T. P. C., Mantoani, S. P., Roca, C., Requena, C., Perez, V. S., Castillo, W. O., et al. (2017). From dual binding site acetylcholinesterase inhibitors to allosteric modulators: a new avenue for disease-modifying drugs in Alzheimer's disease. European Journal of Medicinal Chemistry, 139, 773-791. doi:10.1016/j.ejmech.2017.08.051
NLM
Chierrito TPC, Mantoani SP, Roca C, Requena C, Perez VS, Castillo WO, Moreira NCS, Pérez C, Sakamoto-Hojo ET, Takahashi CS, Barbero JJ, Cañada FJ, Campillo NE, Martinez A, Carvalho I. From dual binding site acetylcholinesterase inhibitors to allosteric modulators: a new avenue for disease-modifying drugs in Alzheimer's disease [Internet]. European Journal of Medicinal Chemistry. 2017 ; 139 773-791.[citado 2024 nov. 10 ] Available from: https://doi.org/10.1016/j.ejmech.2017.08.051
Vancouver
Chierrito TPC, Mantoani SP, Roca C, Requena C, Perez VS, Castillo WO, Moreira NCS, Pérez C, Sakamoto-Hojo ET, Takahashi CS, Barbero JJ, Cañada FJ, Campillo NE, Martinez A, Carvalho I. From dual binding site acetylcholinesterase inhibitors to allosteric modulators: a new avenue for disease-modifying drugs in Alzheimer's disease [Internet]. European Journal of Medicinal Chemistry. 2017 ; 139 773-791.[citado 2024 nov. 10 ] Available from: https://doi.org/10.1016/j.ejmech.2017.08.051

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