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Artigo de periodico
New copper(II)-L-dipeptide-bathophenanthroline complexes as potential anticancer agents: synthesis, characterization and cytotoxicity studies - and comparative DNA-binding study of related phen complexes (2023)
Fernández, Carlos Y.; Failache, Natalia Alvarez ; Costa, Analu Rocha; Ellena, Javier ; Costa Filho, Antonio José da ; Batista, Alzir Azevedo ; Facchin, Gianella
Source: Molecules. Unidades: IFSC, FFCLRP
Subjects: CRISTALOGRAFIA, PLANEJAMENTO DE FÁRMACOS, NEOPLASIAS (TRATAMENTO), CITOTOXINAS
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ABNT
FERNÁNDEZ, Carlos Y. et al. New copper(II)-L-dipeptide-bathophenanthroline complexes as potential anticancer agents: synthesis, characterization and cytotoxicity studies - and comparative DNA-binding study of related phen complexes. Molecules, v. 28, n. Ja 2023, p. 896-1-896-14 + supplementary material, 2023Tradução . . Disponível em: https://doi.org/10.3390/molecules28020896. Acesso em: 14 nov. 2024.
APA
Fernández, C. Y., Failache, N. A., Costa, A. R., Ellena, J., Costa Filho, A. J. da, Batista, A. A., & Facchin, G. (2023). New copper(II)-L-dipeptide-bathophenanthroline complexes as potential anticancer agents: synthesis, characterization and cytotoxicity studies - and comparative DNA-binding study of related phen complexes. Molecules, 28( Ja 2023), 896-1-896-14 + supplementary material. doi:10.3390/molecules28020896
NLM
Fernández CY, Failache NA, Costa AR, Ellena J, Costa Filho AJ da, Batista AA, Facchin G. New copper(II)-L-dipeptide-bathophenanthroline complexes as potential anticancer agents: synthesis, characterization and cytotoxicity studies - and comparative DNA-binding study of related phen complexes [Internet]. Molecules. 2023 ; 28( Ja 2023): 896-1-896-14 + supplementary material.[citado 2024 nov. 14 ] Available from: https://doi.org/10.3390/molecules28020896
Vancouver
Fernández CY, Failache NA, Costa AR, Ellena J, Costa Filho AJ da, Batista AA, Facchin G. New copper(II)-L-dipeptide-bathophenanthroline complexes as potential anticancer agents: synthesis, characterization and cytotoxicity studies - and comparative DNA-binding study of related phen complexes [Internet]. Molecules. 2023 ; 28( Ja 2023): 896-1-896-14 + supplementary material.[citado 2024 nov. 14 ] Available from: https://doi.org/10.3390/molecules28020896
Artigo de periodico
It takes two to tango, part II: synthesis of A-ring functionalised quinones containing two redox-active centres with antitumour activities (2023)
Oliveira, Joyce Cristina de; Carvalho, Renato Lúcio de; Sampaio, Hugo Gustavo Silva; Honorato, João ; Ellena, Javier ; Martins, Felipe Terra ; Pereira, João Victor de Melo; Costa, Pedro Mikael da Silva; Pessoa, Claudia do Ó; Ferreira, Rafaela Salgado ; Araújo, Maria Helena de; Jacob, Claus ; Silva Júnior, Eufrânio Nunes da
Source: Molecules. Unidade: IFSC
Subjects: CRISTALOGRAFIA, PLANEJAMENTO DE FÁRMACOS, NEOPLASIAS (TRATAMENTO), ANTINEOPLÁSICOS
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OLIVEIRA, Joyce Cristina de et al. It takes two to tango, part II: synthesis of A-ring functionalised quinones containing two redox-active centres with antitumour activities. Molecules, v. 28, n. 5, p. 2222-1-2222-24 + supplementary material: 1-54, 2023Tradução . . Disponível em: https://doi.org/10.3390/molecules28052222. Acesso em: 14 nov. 2024.
APA
Oliveira, J. C. de, Carvalho, R. L. de, Sampaio, H. G. S., Honorato, J., Ellena, J., Martins, F. T., et al. (2023). It takes two to tango, part II: synthesis of A-ring functionalised quinones containing two redox-active centres with antitumour activities. Molecules, 28( 5), 2222-1-2222-24 + supplementary material: 1-54. doi:10.3390/molecules28052222
NLM
Oliveira JC de, Carvalho RL de, Sampaio HGS, Honorato J, Ellena J, Martins FT, Pereira JV de M, Costa PM da S, Pessoa C do Ó, Ferreira RS, Araújo MH de, Jacob C, Silva Júnior EN da. It takes two to tango, part II: synthesis of A-ring functionalised quinones containing two redox-active centres with antitumour activities [Internet]. Molecules. 2023 ; 28( 5): 2222-1-2222-24 + supplementary material: 1-54.[citado 2024 nov. 14 ] Available from: https://doi.org/10.3390/molecules28052222
Vancouver
Oliveira JC de, Carvalho RL de, Sampaio HGS, Honorato J, Ellena J, Martins FT, Pereira JV de M, Costa PM da S, Pessoa C do Ó, Ferreira RS, Araújo MH de, Jacob C, Silva Júnior EN da. It takes two to tango, part II: synthesis of A-ring functionalised quinones containing two redox-active centres with antitumour activities [Internet]. Molecules. 2023 ; 28( 5): 2222-1-2222-24 + supplementary material: 1-54.[citado 2024 nov. 14 ] Available from: https://doi.org/10.3390/molecules28052222
Artigo de periodico
Highlighting recent crystalline engineering aspects of luminescent coordination polymers based on F-elements and ditopic aliphatic ligands (2022)
D'Vries, Richard F.; Gomez, Germán E. ; Ellena, Javier
Source: Molecules. Unidade: IFSC
Subjects: PLANTAS MEDICINAIS, PIPERALES, METABÓLITOS
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D'VRIES, Richard F. e GOMEZ, Germán E. e ELLENA, Javier. Highlighting recent crystalline engineering aspects of luminescent coordination polymers based on F-elements and ditopic aliphatic ligands. Molecules, v. 27, n. 12, p. 3830-1-3830-14, 2022Tradução . . Disponível em: https://doi.org/10.3390/molecules27123830. Acesso em: 14 nov. 2024.
APA
D'Vries, R. F., Gomez, G. E., & Ellena, J. (2022). Highlighting recent crystalline engineering aspects of luminescent coordination polymers based on F-elements and ditopic aliphatic ligands. Molecules, 27( 12), 3830-1-3830-14. doi:10.3390/molecules27123830
NLM
D'Vries RF, Gomez GE, Ellena J. Highlighting recent crystalline engineering aspects of luminescent coordination polymers based on F-elements and ditopic aliphatic ligands [Internet]. Molecules. 2022 ; 27( 12): 3830-1-3830-14.[citado 2024 nov. 14 ] Available from: https://doi.org/10.3390/molecules27123830
Vancouver
D'Vries RF, Gomez GE, Ellena J. Highlighting recent crystalline engineering aspects of luminescent coordination polymers based on F-elements and ditopic aliphatic ligands [Internet]. Molecules. 2022 ; 27( 12): 3830-1-3830-14.[citado 2024 nov. 14 ] Available from: https://doi.org/10.3390/molecules27123830
Artigo de periodico
Comparative study of antioxidant and pro-oxidant properties of homoleptic and heteroleptic copper complexes with amino acids, dipeptides and 1,10-phenanthroline: the quest for antitumor compounds (2021)
Veiga, Nicolás ; Alvarez, Natalia ; Castellano, Eduardo Ernesto ; Ellena, Javier ; Facchin, Gianella; Torre, María H.
Source: Molecules. Unidade: IFSC
Subjects: CRISTALOGRAFIA, NEOPLASIAS, ANTIOXIDANTES (ATIVIDADE), ESTRUTURA MOLECULAR (QUÍMICA TEÓRICA)
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ABNT
VEIGA, Nicolás et al. Comparative study of antioxidant and pro-oxidant properties of homoleptic and heteroleptic copper complexes with amino acids, dipeptides and 1,10-phenanthroline: the quest for antitumor compounds. Molecules, v. 26, n. 21, p. 6520-1-6520-20, 2021Tradução . . Disponível em: https://doi.org/10.3390/molecules26216520. Acesso em: 14 nov. 2024.
APA
Veiga, N., Alvarez, N., Castellano, E. E., Ellena, J., Facchin, G., & Torre, M. H. (2021). Comparative study of antioxidant and pro-oxidant properties of homoleptic and heteroleptic copper complexes with amino acids, dipeptides and 1,10-phenanthroline: the quest for antitumor compounds. Molecules, 26( 21), 6520-1-6520-20. doi:10.3390/molecules26216520
NLM
Veiga N, Alvarez N, Castellano EE, Ellena J, Facchin G, Torre MH. Comparative study of antioxidant and pro-oxidant properties of homoleptic and heteroleptic copper complexes with amino acids, dipeptides and 1,10-phenanthroline: the quest for antitumor compounds [Internet]. Molecules. 2021 ; 26( 21): 6520-1-6520-20.[citado 2024 nov. 14 ] Available from: https://doi.org/10.3390/molecules26216520
Vancouver
Veiga N, Alvarez N, Castellano EE, Ellena J, Facchin G, Torre MH. Comparative study of antioxidant and pro-oxidant properties of homoleptic and heteroleptic copper complexes with amino acids, dipeptides and 1,10-phenanthroline: the quest for antitumor compounds [Internet]. Molecules. 2021 ; 26( 21): 6520-1-6520-20.[citado 2024 nov. 14 ] Available from: https://doi.org/10.3390/molecules26216520
Artigo de periodico
Antibacterial activity of the non-cytotoxic peptide (p-BthTX-I)2 and its serum degradation product against multidrug-resistant bacteria (2017)
Santos-Filho, Norival A.; Fernandes, Rafaela S.; Sgardioli, Bruna F.; Ramos, Matheus A. S.; Piccoli, Julia P.; Camargo, Ilana Lopes Baratella da Cunha ; Bauab, Tais M.; Cilli, Eduardo M.
Source: Molecules. Unidade: IFSC
Subjects: RESISTÊNCIA MICROBIANA ÀS DROGAS, BIOFILMES, PEPTÍDEOS
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ABNT
SANTOS-FILHO, Norival A. et al. Antibacterial activity of the non-cytotoxic peptide (p-BthTX-I)2 and its serum degradation product against multidrug-resistant bacteria. Molecules, v. No 2017, n. 11, p. 1898-1-1898-14, 2017Tradução . . Disponível em: https://doi.org/10.3390/molecules22111898. Acesso em: 14 nov. 2024.
APA
Santos-Filho, N. A., Fernandes, R. S., Sgardioli, B. F., Ramos, M. A. S., Piccoli, J. P., Camargo, I. L. B. da C., et al. (2017). Antibacterial activity of the non-cytotoxic peptide (p-BthTX-I)2 and its serum degradation product against multidrug-resistant bacteria. Molecules, No 2017( 11), 1898-1-1898-14. doi:10.3390/molecules22111898
NLM
Santos-Filho NA, Fernandes RS, Sgardioli BF, Ramos MAS, Piccoli JP, Camargo ILB da C, Bauab TM, Cilli EM. Antibacterial activity of the non-cytotoxic peptide (p-BthTX-I)2 and its serum degradation product against multidrug-resistant bacteria [Internet]. Molecules. 2017 ; No 2017( 11): 1898-1-1898-14.[citado 2024 nov. 14 ] Available from: https://doi.org/10.3390/molecules22111898
Vancouver
Santos-Filho NA, Fernandes RS, Sgardioli BF, Ramos MAS, Piccoli JP, Camargo ILB da C, Bauab TM, Cilli EM. Antibacterial activity of the non-cytotoxic peptide (p-BthTX-I)2 and its serum degradation product against multidrug-resistant bacteria [Internet]. Molecules. 2017 ; No 2017( 11): 1898-1-1898-14.[citado 2024 nov. 14 ] Available from: https://doi.org/10.3390/molecules22111898
Artigo de periodico
Molecular docking and structure-based drug design strategies (2015)
Ferreira, Leonardo Luiz Gomes ; Santos, Ricardo N.; Oliva, Glaucius ; Andricopulo, Adriano Defini
Source: Molecules. Unidade: IFSC
Subjects: PLANEJAMENTO DE FÁRMACOS, MODELAGEM MOLECULAR
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ABNT
FERREIRA, Leonardo Luiz Gomes et al. Molecular docking and structure-based drug design strategies. Molecules, v. 20, n. 7, p. 13384-13421, 2015Tradução . . Disponível em: https://doi.org/10.3390/molecules200713384. Acesso em: 14 nov. 2024.
APA
Ferreira, L. L. G., Santos, R. N., Oliva, G., & Andricopulo, A. D. (2015). Molecular docking and structure-based drug design strategies. Molecules, 20( 7), 13384-13421. doi:10.3390/molecules200713384
NLM
Ferreira LLG, Santos RN, Oliva G, Andricopulo AD. Molecular docking and structure-based drug design strategies [Internet]. Molecules. 2015 ; 20( 7): 13384-13421.[citado 2024 nov. 14 ] Available from: https://doi.org/10.3390/molecules200713384
Vancouver
Ferreira LLG, Santos RN, Oliva G, Andricopulo AD. Molecular docking and structure-based drug design strategies [Internet]. Molecules. 2015 ; 20( 7): 13384-13421.[citado 2024 nov. 14 ] Available from: https://doi.org/10.3390/molecules200713384
Artigo de periodico
Identification of electronic and structural descriptors of adenosine analogues related to inhibition of leishmanial glyceraldehyde-3-phosphate dehydrogenase (2013)
Lozano, Norka B. H.; Oliveira, Rafael F.; Weber, Karen C.; Honório, Kathia Maria; Guido, Rafael Victorio Carvalho ; Andricopulo, Adriano Defini ; Silva, Alberico Borges Ferreira da
Source: Molecules. Unidades: EACH, IFSC, IQSC
Subjects: ENZIMAS, LEISHMANIA (CONTROLE), MALÁRIA (TRATAMENTO)
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ABNT
LOZANO, Norka B. H. et al. Identification of electronic and structural descriptors of adenosine analogues related to inhibition of leishmanial glyceraldehyde-3-phosphate dehydrogenase. Molecules, v. 18, n. 5, p. 5032-5050, 2013Tradução . . Disponível em: https://doi.org/10.3390/molecules18055032. Acesso em: 14 nov. 2024.
APA
Lozano, N. B. H., Oliveira, R. F., Weber, K. C., Honório, K. M., Guido, R. V. C., Andricopulo, A. D., & Silva, A. B. F. da. (2013). Identification of electronic and structural descriptors of adenosine analogues related to inhibition of leishmanial glyceraldehyde-3-phosphate dehydrogenase. Molecules, 18( 5), 5032-5050. doi:10.3390/molecules18055032
NLM
Lozano NBH, Oliveira RF, Weber KC, Honório KM, Guido RVC, Andricopulo AD, Silva ABF da. Identification of electronic and structural descriptors of adenosine analogues related to inhibition of leishmanial glyceraldehyde-3-phosphate dehydrogenase [Internet]. Molecules. 2013 ; 18( 5): 5032-5050.[citado 2024 nov. 14 ] Available from: https://doi.org/10.3390/molecules18055032
Vancouver
Lozano NBH, Oliveira RF, Weber KC, Honório KM, Guido RVC, Andricopulo AD, Silva ABF da. Identification of electronic and structural descriptors of adenosine analogues related to inhibition of leishmanial glyceraldehyde-3-phosphate dehydrogenase [Internet]. Molecules. 2013 ; 18( 5): 5032-5050.[citado 2024 nov. 14 ] Available from: https://doi.org/10.3390/molecules18055032
Artigo de periodico
Analgesic and anti-inflammatory activities of salicylaldehyde 2-chlorobenzoyl hydrazone ('H IND. 2'LASSBio-466), salicylaldehyde 4-chlorobenzoyl hydrazone ('H IND. 2'LASSBio-1064) and their Zinc(II) complexes (2011)
Bispo Júnior, Walfrido; Moreira, Magna S. Alexandre; Alves, Marina A.; Pérez-Rebolledo, Anayive; Parrilha, Gabrieli L.; Castellano, Eduardo Ernesto ; Piro, Oscar E.; Barreiro, Eliezer J.; Lima, Lídia Moreira; Beraldo, Heloisa
Source: Molecules. Unidade: IFSC
Subjects: ANALGÉSICOS, ANTI-INFLAMATÓRIOS (ATIVIDADE), ZINCO, CRISTALOGRAFIA
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ABNT
BISPO JÚNIOR, Walfrido et al. Analgesic and anti-inflammatory activities of salicylaldehyde 2-chlorobenzoyl hydrazone ('H IND. 2'LASSBio-466), salicylaldehyde 4-chlorobenzoyl hydrazone ('H IND. 2'LASSBio-1064) and their Zinc(II) complexes. Molecules, v. 16, n. 8, p. 6902-6915, 2011Tradução . . Disponível em: https://doi.org/10.3390/molecules16086902. Acesso em: 14 nov. 2024.
APA
Bispo Júnior, W., Moreira, M. S. A., Alves, M. A., Pérez-Rebolledo, A., Parrilha, G. L., Castellano, E. E., et al. (2011). Analgesic and anti-inflammatory activities of salicylaldehyde 2-chlorobenzoyl hydrazone ('H IND. 2'LASSBio-466), salicylaldehyde 4-chlorobenzoyl hydrazone ('H IND. 2'LASSBio-1064) and their Zinc(II) complexes. Molecules, 16( 8), 6902-6915. doi:10.3390/molecules16086902
NLM
Bispo Júnior W, Moreira MSA, Alves MA, Pérez-Rebolledo A, Parrilha GL, Castellano EE, Piro OE, Barreiro EJ, Lima LM, Beraldo H. Analgesic and anti-inflammatory activities of salicylaldehyde 2-chlorobenzoyl hydrazone ('H IND. 2'LASSBio-466), salicylaldehyde 4-chlorobenzoyl hydrazone ('H IND. 2'LASSBio-1064) and their Zinc(II) complexes [Internet]. Molecules. 2011 ; 16( 8): 6902-6915.[citado 2024 nov. 14 ] Available from: https://doi.org/10.3390/molecules16086902
Vancouver
Bispo Júnior W, Moreira MSA, Alves MA, Pérez-Rebolledo A, Parrilha GL, Castellano EE, Piro OE, Barreiro EJ, Lima LM, Beraldo H. Analgesic and anti-inflammatory activities of salicylaldehyde 2-chlorobenzoyl hydrazone ('H IND. 2'LASSBio-466), salicylaldehyde 4-chlorobenzoyl hydrazone ('H IND. 2'LASSBio-1064) and their Zinc(II) complexes [Internet]. Molecules. 2011 ; 16( 8): 6902-6915.[citado 2024 nov. 14 ] Available from: https://doi.org/10.3390/molecules16086902

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