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Artigo de periodico
In situ interaction between the hormone 17α-ethynylestradiol and the liquid-ordered phase composed of the lipid rafts sphingomyelin and cholesterol (2024)
Ruiz, Gilia Cristine Marques; Morato, Luis Fernando do Carmo; Pazin, Wallance Moreira ; Oliveira Junior, Osvaldo Novais de ; Constantino, Carlos José Leopoldo
Source: Bioorganic Chemistry. Unidade: IFSC
Subjects: COLESTEROL, FILMES FINOS, MEMBRANAS CELULARES, POLÍMEROS (MATERIAIS)
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ABNT
RUIZ, Gilia Cristine Marques et al. In situ interaction between the hormone 17α-ethynylestradiol and the liquid-ordered phase composed of the lipid rafts sphingomyelin and cholesterol. Bioorganic Chemistry, v. 143, p. 107002-1-107002-8, 2024Tradução . . Disponível em: https://doi.org/10.1016/j.bioorg.2023.107002. Acesso em: 14 ago. 2024.
APA
Ruiz, G. C. M., Morato, L. F. do C., Pazin, W. M., Oliveira Junior, O. N. de, & Constantino, C. J. L. (2024). In situ interaction between the hormone 17α-ethynylestradiol and the liquid-ordered phase composed of the lipid rafts sphingomyelin and cholesterol. Bioorganic Chemistry, 143, 107002-1-107002-8. doi:10.1016/j.bioorg.2023.107002
NLM
Ruiz GCM, Morato LF do C, Pazin WM, Oliveira Junior ON de, Constantino CJL. In situ interaction between the hormone 17α-ethynylestradiol and the liquid-ordered phase composed of the lipid rafts sphingomyelin and cholesterol [Internet]. Bioorganic Chemistry. 2024 ; 143 107002-1-107002-8.[citado 2024 ago. 14 ] Available from: https://doi.org/10.1016/j.bioorg.2023.107002
Vancouver
Ruiz GCM, Morato LF do C, Pazin WM, Oliveira Junior ON de, Constantino CJL. In situ interaction between the hormone 17α-ethynylestradiol and the liquid-ordered phase composed of the lipid rafts sphingomyelin and cholesterol [Internet]. Bioorganic Chemistry. 2024 ; 143 107002-1-107002-8.[citado 2024 ago. 14 ] Available from: https://doi.org/10.1016/j.bioorg.2023.107002
Artigo de periodico
Integration of biophysical and biological approaches to validate fragment-like compounds targeting l,d-transpeptidases from Mycobacterium tuberculosis (2024)
Zúñiga, Gerardo Andrés Libreros ; Pavão, Danilo Pavão e ; Barroso, Vinícius de Morais ; Mesquita, Nathalya Cristina de Moraes Roso; Braga, Saulo Fehelberg Pinto; Oliva, Glaucius ; Ferreira, Rafaela Salgado ; Ishida, Kelly ; Dias, Marcio Vinicius Bertacine
Source: Bioorganic Chemistry. Unidades: IFSC, ICB
Subjects: QUÍMICA MÉDICA, TUBERCULOSE, PLANEJAMENTO DE FÁRMACOS, MYCOBACTERIUM TUBERCULOSIS
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ABNT
ZÚÑIGA, Gerardo Andrés Libreros et al. Integration of biophysical and biological approaches to validate fragment-like compounds targeting l,d-transpeptidases from Mycobacterium tuberculosis. Bioorganic Chemistry, v. 142, n. Ja 2024, p. 106960-1-106960-11, 2024Tradução . . Disponível em: https://doi.org/10.1016/j.bioorg.2023.106960. Acesso em: 14 ago. 2024.
APA
Zúñiga, G. A. L., Pavão, D. P. e, Barroso, V. de M., Mesquita, N. C. de M. R., Braga, S. F. P., Oliva, G., et al. (2024). Integration of biophysical and biological approaches to validate fragment-like compounds targeting l,d-transpeptidases from Mycobacterium tuberculosis. Bioorganic Chemistry, 142( Ja 2024), 106960-1-106960-11. doi:10.1016/j.bioorg.2023.106960
NLM
Zúñiga GAL, Pavão DP e, Barroso V de M, Mesquita NC de MR, Braga SFP, Oliva G, Ferreira RS, Ishida K, Dias MVB. Integration of biophysical and biological approaches to validate fragment-like compounds targeting l,d-transpeptidases from Mycobacterium tuberculosis [Internet]. Bioorganic Chemistry. 2024 ; 142( Ja 2024): 106960-1-106960-11.[citado 2024 ago. 14 ] Available from: https://doi.org/10.1016/j.bioorg.2023.106960
Vancouver
Zúñiga GAL, Pavão DP e, Barroso V de M, Mesquita NC de MR, Braga SFP, Oliva G, Ferreira RS, Ishida K, Dias MVB. Integration of biophysical and biological approaches to validate fragment-like compounds targeting l,d-transpeptidases from Mycobacterium tuberculosis [Internet]. Bioorganic Chemistry. 2024 ; 142( Ja 2024): 106960-1-106960-11.[citado 2024 ago. 14 ] Available from: https://doi.org/10.1016/j.bioorg.2023.106960
Artigo de periodico
Chalcones from Angelica keiskei (ashitaba) inhibit key Zika virus replication proteins (2022)
Mottin, Melina; Caesar, Lindsay K.; Brodsky, David; Mesquita, Nathalya Cristina de Moraes Roso; Oliveira, Ketllyn Irene Zagato de; Noske, Gabriela Dias; Sousa, Bruna K. P.; Ramos, Paulo R. P. S.; Jarmer, Hannah; Loh, Bonnie; Zorn, Kimberley M.; Foil, Daniel H.; Torres, Pedro M.; Guido, Rafael Victorio Carvalho ; Oliva, Glaucius ; Scholle, Frank; Ekins, Sean; Cech, Nadja B.; Andrade, Carolina Horta; Laster, Scott M.
Source: Bioorganic Chemistry. Unidade: IFSC
Subjects: ZIKA VÍRUS, PRODUTOS NATURAIS, FLAVIVIRIDAE, ENZIMAS, PROTEÍNAS, FARMACOLOGIA
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ABNT
MOTTIN, Melina et al. Chalcones from Angelica keiskei (ashitaba) inhibit key Zika virus replication proteins. Bioorganic Chemistry, v. 120, p. 105649-1-105649-12 + supplementary data: 1-13, 2022Tradução . . Disponível em: https://doi.org/10.1016/j.bioorg.2022.105649. Acesso em: 14 ago. 2024.
APA
Mottin, M., Caesar, L. K., Brodsky, D., Mesquita, N. C. de M. R., Oliveira, K. I. Z. de, Noske, G. D., et al. (2022). Chalcones from Angelica keiskei (ashitaba) inhibit key Zika virus replication proteins. Bioorganic Chemistry, 120, 105649-1-105649-12 + supplementary data: 1-13. doi:10.1016/j.bioorg.2022.105649
NLM
Mottin M, Caesar LK, Brodsky D, Mesquita NC de MR, Oliveira KIZ de, Noske GD, Sousa BKP, Ramos PRPS, Jarmer H, Loh B, Zorn KM, Foil DH, Torres PM, Guido RVC, Oliva G, Scholle F, Ekins S, Cech NB, Andrade CH, Laster SM. Chalcones from Angelica keiskei (ashitaba) inhibit key Zika virus replication proteins [Internet]. Bioorganic Chemistry. 2022 ; 120 105649-1-105649-12 + supplementary data: 1-13.[citado 2024 ago. 14 ] Available from: https://doi.org/10.1016/j.bioorg.2022.105649
Vancouver
Mottin M, Caesar LK, Brodsky D, Mesquita NC de MR, Oliveira KIZ de, Noske GD, Sousa BKP, Ramos PRPS, Jarmer H, Loh B, Zorn KM, Foil DH, Torres PM, Guido RVC, Oliva G, Scholle F, Ekins S, Cech NB, Andrade CH, Laster SM. Chalcones from Angelica keiskei (ashitaba) inhibit key Zika virus replication proteins [Internet]. Bioorganic Chemistry. 2022 ; 120 105649-1-105649-12 + supplementary data: 1-13.[citado 2024 ago. 14 ] Available from: https://doi.org/10.1016/j.bioorg.2022.105649
Artigo de periodico
Discovery of (E)-4-styrylphenoxy-propanamide: a dual PPARα/γ partial agonist that regulates high-density lipoprotein-cholesterol levels, modulates adipogenesis, and improves glucose tolerance in diet-induced obese mice (2022)
Dutra, Luiz A.; Lacerda, Mariella G.; Inácio, Maiara Destro; Martins, Johnny W. L.; Silva, Ana C. Lopes; Silva, Patricia Bento da; Chorilli, Marlus; Amato, Angélica A.; Baviera, Amanda M.; Passarelli, Marisa ; Guido, Rafael Victorio Carvalho ; Santos, Jean L. dos
Source: Bioorganic Chemistry. Unidades: FM, IFSC
Subjects: COLESTEROL, ADIPOSIDADE, PLANEJAMENTO DE FÁRMACOS
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ABNT
DUTRA, Luiz A. et al. Discovery of (E)-4-styrylphenoxy-propanamide: a dual PPARα/γ partial agonist that regulates high-density lipoprotein-cholesterol levels, modulates adipogenesis, and improves glucose tolerance in diet-induced obese mice. Bioorganic Chemistry, v. 120, p. 105600-1-105600-12 + supplementary material: S1-S44, 2022Tradução . . Disponível em: https://doi.org/10.1016/j.bioorg.2022.105600. Acesso em: 14 ago. 2024.
APA
Dutra, L. A., Lacerda, M. G., Inácio, M. D., Martins, J. W. L., Silva, A. C. L., Silva, P. B. da, et al. (2022). Discovery of (E)-4-styrylphenoxy-propanamide: a dual PPARα/γ partial agonist that regulates high-density lipoprotein-cholesterol levels, modulates adipogenesis, and improves glucose tolerance in diet-induced obese mice. Bioorganic Chemistry, 120, 105600-1-105600-12 + supplementary material: S1-S44. doi:10.1016/j.bioorg.2022.105600
NLM
Dutra LA, Lacerda MG, Inácio MD, Martins JWL, Silva ACL, Silva PB da, Chorilli M, Amato AA, Baviera AM, Passarelli M, Guido RVC, Santos JL dos. Discovery of (E)-4-styrylphenoxy-propanamide: a dual PPARα/γ partial agonist that regulates high-density lipoprotein-cholesterol levels, modulates adipogenesis, and improves glucose tolerance in diet-induced obese mice [Internet]. Bioorganic Chemistry. 2022 ; 120 105600-1-105600-12 + supplementary material: S1-S44.[citado 2024 ago. 14 ] Available from: https://doi.org/10.1016/j.bioorg.2022.105600
Vancouver
Dutra LA, Lacerda MG, Inácio MD, Martins JWL, Silva ACL, Silva PB da, Chorilli M, Amato AA, Baviera AM, Passarelli M, Guido RVC, Santos JL dos. Discovery of (E)-4-styrylphenoxy-propanamide: a dual PPARα/γ partial agonist that regulates high-density lipoprotein-cholesterol levels, modulates adipogenesis, and improves glucose tolerance in diet-induced obese mice [Internet]. Bioorganic Chemistry. 2022 ; 120 105600-1-105600-12 + supplementary material: S1-S44.[citado 2024 ago. 14 ] Available from: https://doi.org/10.1016/j.bioorg.2022.105600
Artigo de periodico
Synthesis, biological evaluation and molecular docking studies of novel 1,2,3-triazole-quinazolines as antiproliferative agents displaying ERK inhibitory activity (2021)
Nunes, Paulo Sergio Gonçalves; Silva, Gabriel da ; Nascimento, Sofia; Mantoani, Susimaire Pedersoli; Andrade, Peterson de; Bernardes, Emerson Soares; Kawano, Daniel Fábio; Leopoldino, Andréia Machado ; Carvalho, Ivone
Source: Bioorganic Chemistry. Unidades: IPEN, FCFRP
Subjects: ANTINEOPLÁSICOS, LINHAGEM CELULAR, PROLIFERAÇÃO CELULAR, PROTEÍNAS QUINASES, ESTRUTURA MOLECULAR (QUÍMICA TEÓRICA)
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ABNT
NUNES, Paulo Sergio Gonçalves et al. Synthesis, biological evaluation and molecular docking studies of novel 1,2,3-triazole-quinazolines as antiproliferative agents displaying ERK inhibitory activity. Bioorganic Chemistry, v. 113, 2021Tradução . . Disponível em: https://doi.org/10.1016/j.bioorg.2021.104982. Acesso em: 14 ago. 2024.
APA
Nunes, P. S. G., Silva, G. da, Nascimento, S., Mantoani, S. P., Andrade, P. de, Bernardes, E. S., et al. (2021). Synthesis, biological evaluation and molecular docking studies of novel 1,2,3-triazole-quinazolines as antiproliferative agents displaying ERK inhibitory activity. Bioorganic Chemistry, 113. doi:10.1016/j.bioorg.2021.104982
NLM
Nunes PSG, Silva G da, Nascimento S, Mantoani SP, Andrade P de, Bernardes ES, Kawano DF, Leopoldino AM, Carvalho I. Synthesis, biological evaluation and molecular docking studies of novel 1,2,3-triazole-quinazolines as antiproliferative agents displaying ERK inhibitory activity [Internet]. Bioorganic Chemistry. 2021 ; 113[citado 2024 ago. 14 ] Available from: https://doi.org/10.1016/j.bioorg.2021.104982
Vancouver
Nunes PSG, Silva G da, Nascimento S, Mantoani SP, Andrade P de, Bernardes ES, Kawano DF, Leopoldino AM, Carvalho I. Synthesis, biological evaluation and molecular docking studies of novel 1,2,3-triazole-quinazolines as antiproliferative agents displaying ERK inhibitory activity [Internet]. Bioorganic Chemistry. 2021 ; 113[citado 2024 ago. 14 ] Available from: https://doi.org/10.1016/j.bioorg.2021.104982
Artigo de periodico
Synthesis of chalcones derived from 1-naphthylacetophenone and evaluation of their cytotoxic and apoptotic effects in acute leukemia cell lines (2021)
Jacques, Amanda Virtuoso; Stefanes, Natália Marcéli; Walter, Laura Otto; Perondia, Daiane Mari; Efe, Fernanda da Luz; Souza, Luiz Felipe Schmitz de; Sens, Larissa; Syracuse, Stephanie Milis; Moraes, Ana Carolina Rabello de; Oliveira, Aldo Sena de ; Martins, Carolina Teixeira; Magalhães, Luma Godoy; Andricopulo, Adriano Defini ; Silva, Lisandra de Oliveira; Nunes, Ricardo José; Santos-Silva, Maria Cláudia
Source: Bioorganic Chemistry. Unidades: IFSC, IQSC
Subjects: CRISTALOGRAFIA, FARMACOLOGIA, LEUCEMIA MIELOIDE AGUDA, PROTEÍNAS, PROLIFERAÇÃO CELULAR
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ABNT
JACQUES, Amanda Virtuoso et al. Synthesis of chalcones derived from 1-naphthylacetophenone and evaluation of their cytotoxic and apoptotic effects in acute leukemia cell lines. Bioorganic Chemistry, v. No 2021, p. 105315-1-105315-11, 2021Tradução . . Disponível em: https://doi.org/10.1016/j.bioorg.2021.105315. Acesso em: 14 ago. 2024.
APA
Jacques, A. V., Stefanes, N. M., Walter, L. O., Perondia, D. M., Efe, F. da L., Souza, L. F. S. de, et al. (2021). Synthesis of chalcones derived from 1-naphthylacetophenone and evaluation of their cytotoxic and apoptotic effects in acute leukemia cell lines. Bioorganic Chemistry, No 2021, 105315-1-105315-11. doi:10.1016/j.bioorg.2021.105315
NLM
Jacques AV, Stefanes NM, Walter LO, Perondia DM, Efe F da L, Souza LFS de, Sens L, Syracuse SM, Moraes ACR de, Oliveira AS de, Martins CT, Magalhães LG, Andricopulo AD, Silva L de O, Nunes RJ, Santos-Silva MC. Synthesis of chalcones derived from 1-naphthylacetophenone and evaluation of their cytotoxic and apoptotic effects in acute leukemia cell lines [Internet]. Bioorganic Chemistry. 2021 ; No 2021 105315-1-105315-11.[citado 2024 ago. 14 ] Available from: https://doi.org/10.1016/j.bioorg.2021.105315
Vancouver
Jacques AV, Stefanes NM, Walter LO, Perondia DM, Efe F da L, Souza LFS de, Sens L, Syracuse SM, Moraes ACR de, Oliveira AS de, Martins CT, Magalhães LG, Andricopulo AD, Silva L de O, Nunes RJ, Santos-Silva MC. Synthesis of chalcones derived from 1-naphthylacetophenone and evaluation of their cytotoxic and apoptotic effects in acute leukemia cell lines [Internet]. Bioorganic Chemistry. 2021 ; No 2021 105315-1-105315-11.[citado 2024 ago. 14 ] Available from: https://doi.org/10.1016/j.bioorg.2021.105315

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