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Artigo de periodico
Synthetic cyclopenta[b]indoles exhibit antineoplastic activity by targeting microtubule dynamics in acute myeloid leukemia cells (2021)
Vicari, Hugo Passos ; Lima, Keli ; Gomes, Ralph da Costa ; Fernandes, Daniara Cristina ; Silva, Jean Carlos Lipreri da ; Rodrigues Junior, Manoel Trindade; Oliveira, Aline Silva Barroso de; Santos, Ricardo Nascimento dos ; Andricopulo, Adriano Defini ; Coelho, Fernando; Lotufo, Leticia Veras Costa ; Machado Neto, João Agostinho
Source: European Journal of Pharmacology. Unidades: IFSC, ICB
Subjects: FARMACOLOGIA, QUIMIOTERAPIA, LEUCEMIA MIELOIDE AGUDA, CÉLULAS SANGUÍNEAS, ANTINEOPLÁSICOS, ONCOGENES, CITOTOXICIDADE IMUNOLÓGICA, LEUCÓCITOS, PROLIFERAÇÃO CELULAR, APOPTOSE
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VICARI, Hugo Passos et al. Synthetic cyclopenta[b]indoles exhibit antineoplastic activity by targeting microtubule dynamics in acute myeloid leukemia cells. European Journal of Pharmacology, v. 894, p. 173853-1-173853-10, 2021Tradução . . Disponível em: https://doi.org/10.1016/j.ejphar.2021.173853. Acesso em: 06 jul. 2024.
APA
Vicari, H. P., Lima, K., Gomes, R. da C., Fernandes, D. C., Silva, J. C. L. da, Rodrigues Junior, M. T., et al. (2021). Synthetic cyclopenta[b]indoles exhibit antineoplastic activity by targeting microtubule dynamics in acute myeloid leukemia cells. European Journal of Pharmacology, 894, 173853-1-173853-10. doi:10.1016/j.ejphar.2021.173853
NLM
Vicari HP, Lima K, Gomes R da C, Fernandes DC, Silva JCL da, Rodrigues Junior MT, Oliveira ASB de, Santos RN dos, Andricopulo AD, Coelho F, Lotufo LVC, Machado Neto JA. Synthetic cyclopenta[b]indoles exhibit antineoplastic activity by targeting microtubule dynamics in acute myeloid leukemia cells [Internet]. European Journal of Pharmacology. 2021 ; 894 173853-1-173853-10.[citado 2024 jul. 06 ] Available from: https://doi.org/10.1016/j.ejphar.2021.173853
Vancouver
Vicari HP, Lima K, Gomes R da C, Fernandes DC, Silva JCL da, Rodrigues Junior MT, Oliveira ASB de, Santos RN dos, Andricopulo AD, Coelho F, Lotufo LVC, Machado Neto JA. Synthetic cyclopenta[b]indoles exhibit antineoplastic activity by targeting microtubule dynamics in acute myeloid leukemia cells [Internet]. European Journal of Pharmacology. 2021 ; 894 173853-1-173853-10.[citado 2024 jul. 06 ] Available from: https://doi.org/10.1016/j.ejphar.2021.173853
Artigo de periodico
In vitro and in silico assessment of antitumor properties and biomolecular binding studies for two new complexes based on NiII bearing k2N, S-donor ligands (2021)
Farias, R. L.; Polez, A. M. R.; Silva, D. E. S.; Zanetti, R. D.; Moreira, M. B.; Batista, V. S.; Reis, B. L.; Nascimento-Júnior, N. M.; Rocha, F. V.; Lima, M. A.; Oliveira, A. B.; Ellena, Javier ; Scarim, C. B.; Zambom, C. R.; Brito, L. D.; Garrido, S. S.; Melo, A. P. L.; Bresolin, L.; Tirloni, B.; Pereira, J. C. M.; Netto, A. V. G.
Source: Materials Science and Engineering C. Unidade: IFSC
Subjects: CRISTALOGRAFIA, ANTINEOPLÁSICOS, CITOTOXINAS
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FARIAS, R. L. et al. In vitro and in silico assessment of antitumor properties and biomolecular binding studies for two new complexes based on NiII bearing k2N, S-donor ligands. Materials Science and Engineering C, v. 121, p. 111815-1-111815-12, 2021Tradução . . Disponível em: https://doi.org/10.1016/j.msec.2020.111815. Acesso em: 06 jul. 2024.
APA
Farias, R. L., Polez, A. M. R., Silva, D. E. S., Zanetti, R. D., Moreira, M. B., Batista, V. S., et al. (2021). In vitro and in silico assessment of antitumor properties and biomolecular binding studies for two new complexes based on NiII bearing k2N, S-donor ligands. Materials Science and Engineering C, 121, 111815-1-111815-12. doi:10.1016/j.msec.2020.111815
NLM
Farias RL, Polez AMR, Silva DES, Zanetti RD, Moreira MB, Batista VS, Reis BL, Nascimento-Júnior NM, Rocha FV, Lima MA, Oliveira AB, Ellena J, Scarim CB, Zambom CR, Brito LD, Garrido SS, Melo APL, Bresolin L, Tirloni B, Pereira JCM, Netto AVG. In vitro and in silico assessment of antitumor properties and biomolecular binding studies for two new complexes based on NiII bearing k2N, S-donor ligands [Internet]. Materials Science and Engineering C. 2021 ; 121 111815-1-111815-12.[citado 2024 jul. 06 ] Available from: https://doi.org/10.1016/j.msec.2020.111815
Vancouver
Farias RL, Polez AMR, Silva DES, Zanetti RD, Moreira MB, Batista VS, Reis BL, Nascimento-Júnior NM, Rocha FV, Lima MA, Oliveira AB, Ellena J, Scarim CB, Zambom CR, Brito LD, Garrido SS, Melo APL, Bresolin L, Tirloni B, Pereira JCM, Netto AVG. In vitro and in silico assessment of antitumor properties and biomolecular binding studies for two new complexes based on NiII bearing k2N, S-donor ligands [Internet]. Materials Science and Engineering C. 2021 ; 121 111815-1-111815-12.[citado 2024 jul. 06 ] Available from: https://doi.org/10.1016/j.msec.2020.111815
Artigo de periodico
Discovery of a novel lineage Burkholderia cepacia ST 1870 endophytically isolated from medicinal Polygala paniculata which shows potent in vitro antileishmanial and antimicrobial effects (2021)
Cruz, Felipe de Paula Nogueira ; Paula, Ailton Ferreira de; Nogueira, Camila Tita ; Andrade, Paulo Henrique Marques de; Borges, Leonardo Maurici; Lacava, Paulo Teixeira; Camargo, Ilana Lopes Baratella da Cunha ; Aníbal, Fernanda de Freitas; Sousa, Cristina Paiva de
Source: International Journal of Microbiology. Unidade: IFSC
Subjects: FARMACOLOGIA, FUNGOS, PLANEJAMENTO DE FÁRMACOS, CRISTALOGRAFIA
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CRUZ, Felipe de Paula Nogueira et al. Discovery of a novel lineage Burkholderia cepacia ST 1870 endophytically isolated from medicinal Polygala paniculata which shows potent in vitro antileishmanial and antimicrobial effects. International Journal of Microbiology, v. 2021, p. 6618559-1-6618559-17, 2021Tradução . . Disponível em: https://doi.org/10.1155/2021/6618559. Acesso em: 06 jul. 2024.
APA
Cruz, F. de P. N., Paula, A. F. de, Nogueira, C. T., Andrade, P. H. M. de, Borges, L. M., Lacava, P. T., et al. (2021). Discovery of a novel lineage Burkholderia cepacia ST 1870 endophytically isolated from medicinal Polygala paniculata which shows potent in vitro antileishmanial and antimicrobial effects. International Journal of Microbiology, 2021, 6618559-1-6618559-17. doi:10.1155/2021/6618559
NLM
Cruz F de PN, Paula AF de, Nogueira CT, Andrade PHM de, Borges LM, Lacava PT, Camargo ILB da C, Aníbal F de F, Sousa CP de. Discovery of a novel lineage Burkholderia cepacia ST 1870 endophytically isolated from medicinal Polygala paniculata which shows potent in vitro antileishmanial and antimicrobial effects [Internet]. International Journal of Microbiology. 2021 ; 2021 6618559-1-6618559-17.[citado 2024 jul. 06 ] Available from: https://doi.org/10.1155/2021/6618559
Vancouver
Cruz F de PN, Paula AF de, Nogueira CT, Andrade PHM de, Borges LM, Lacava PT, Camargo ILB da C, Aníbal F de F, Sousa CP de. Discovery of a novel lineage Burkholderia cepacia ST 1870 endophytically isolated from medicinal Polygala paniculata which shows potent in vitro antileishmanial and antimicrobial effects [Internet]. International Journal of Microbiology. 2021 ; 2021 6618559-1-6618559-17.[citado 2024 jul. 06 ] Available from: https://doi.org/10.1155/2021/6618559
Artigo de periodico
Glycosylated narciclasine alkaloid in Hippeastrum puniceum (Lam.) Kuntze (2021)
Feu, Amanda Eiriz ; Andrade, Jean Paulo de ; Ayala, Alejandro Pedro ; Almeida, Larissa Costa de ; Lotufo, Leticia Veras Costa ; Bastida, Jaume ; Ellena, Javier ; Borges, Warley de Souza
Source: South African Journal of Botany. Unidades: ICB, IFSC
Subjects: FARMACOLOGIA, CROMATOGRAFIA, ALCALOIDES, AMARYLLIDACEAE, RESSONÂNCIA MAGNÉTICA NUCLEAR, CÉLULAS CULTIVADAS DE TUMOR, NEOPLASIAS DO COLON, NEOPLASIAS MAMÁRIAS, CROMATOGRAFIA
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FEU, Amanda Eiriz et al. Glycosylated narciclasine alkaloid in Hippeastrum puniceum (Lam.) Kuntze. South African Journal of Botany, v. 136, n. Ja 2021, p. 30-34, 2021Tradução . . Disponível em: https://doi.org/10.1016/j.sajb.2020.09.006. Acesso em: 06 jul. 2024.
APA
Feu, A. E., Andrade, J. P. de, Ayala, A. P., Almeida, L. C. de, Lotufo, L. V. C., Bastida, J., et al. (2021). Glycosylated narciclasine alkaloid in Hippeastrum puniceum (Lam.) Kuntze. South African Journal of Botany, 136( Ja 2021), 30-34. doi:10.1016/j.sajb.2020.09.006
NLM
Feu AE, Andrade JP de, Ayala AP, Almeida LC de, Lotufo LVC, Bastida J, Ellena J, Borges W de S. Glycosylated narciclasine alkaloid in Hippeastrum puniceum (Lam.) Kuntze [Internet]. South African Journal of Botany. 2021 ; 136( Ja 2021): 30-34.[citado 2024 jul. 06 ] Available from: https://doi.org/10.1016/j.sajb.2020.09.006
Vancouver
Feu AE, Andrade JP de, Ayala AP, Almeida LC de, Lotufo LVC, Bastida J, Ellena J, Borges W de S. Glycosylated narciclasine alkaloid in Hippeastrum puniceum (Lam.) Kuntze [Internet]. South African Journal of Botany. 2021 ; 136( Ja 2021): 30-34.[citado 2024 jul. 06 ] Available from: https://doi.org/10.1016/j.sajb.2020.09.006
Artigo de periodico
Synthesis and X-ray crystal structures of polyfunctionalized 4 H -chromene derivatives via tricomponent reaction with Knoevenagel adducts as intermediates in aqueous medium (2021)
Zanin, Lucas Lima; Jimenez, David Esteban Quintero; Jesus, Matheus Pereira de ; Diniz, Luan Farinelli ; Ellena, Javier ; Porto, Andre Luiz Meleiro
Source: Journal of Molecular Structure. Unidades: IFSC, IQSC
Subjects: CRISTALOGRAFIA, DIFRAÇÃO POR RAIOS X, ESTRUTURA MOLECULAR (QUÍMICA TEÓRICA)
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ABNT
ZANIN, Lucas Lima et al. Synthesis and X-ray crystal structures of polyfunctionalized 4 H -chromene derivatives via tricomponent reaction with Knoevenagel adducts as intermediates in aqueous medium. Journal of Molecular Structure, v. 1223, n. Ja 2021, p. 129226-1-129226-10, 2021Tradução . . Disponível em: https://doi.org/10.1016/j.molstruc.2020.129226. Acesso em: 06 jul. 2024.
APA
Zanin, L. L., Jimenez, D. E. Q., Jesus, M. P. de, Diniz, L. F., Ellena, J., & Porto, A. L. M. (2021). Synthesis and X-ray crystal structures of polyfunctionalized 4 H -chromene derivatives via tricomponent reaction with Knoevenagel adducts as intermediates in aqueous medium. Journal of Molecular Structure, 1223( Ja 2021), 129226-1-129226-10. doi:10.1016/j.molstruc.2020.129226
NLM
Zanin LL, Jimenez DEQ, Jesus MP de, Diniz LF, Ellena J, Porto ALM. Synthesis and X-ray crystal structures of polyfunctionalized 4 H -chromene derivatives via tricomponent reaction with Knoevenagel adducts as intermediates in aqueous medium [Internet]. Journal of Molecular Structure. 2021 ; 1223( Ja 2021): 129226-1-129226-10.[citado 2024 jul. 06 ] Available from: https://doi.org/10.1016/j.molstruc.2020.129226
Vancouver
Zanin LL, Jimenez DEQ, Jesus MP de, Diniz LF, Ellena J, Porto ALM. Synthesis and X-ray crystal structures of polyfunctionalized 4 H -chromene derivatives via tricomponent reaction with Knoevenagel adducts as intermediates in aqueous medium [Internet]. Journal of Molecular Structure. 2021 ; 1223( Ja 2021): 129226-1-129226-10.[citado 2024 jul. 06 ] Available from: https://doi.org/10.1016/j.molstruc.2020.129226
Artigo de periodico
Amino-imino tautomerism in the salt formation of albendazole: hydrobromide and nitrate salts (2021)
Carvalho Junior, Paulo de S. ; Diniz, Luan F. ; Silva, Gelson T. S. T. da; Coutinho, Nayara Dantas; Santos, Priscila Gomes dos; Carvalho-Silva, Valter Henrique ; Ribeiro, Caue ; Ellena, Javier
Source: Crystal Growth and Design. Unidade: IFSC
Subjects: CRISTALOGRAFIA, ESTRUTURA MOLECULAR (QUÍMICA TEÓRICA), SAIS, TAUTOMERIA, PLANEJAMENTO DE FÁRMACOS
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CARVALHO JUNIOR, Paulo de S. et al. Amino-imino tautomerism in the salt formation of albendazole: hydrobromide and nitrate salts. Crystal Growth and Design, v. 21, n. 2, p. 1122-1135, 2021Tradução . . Disponível em: https://doi.org/10.1021/acs.cgd.0c01444. Acesso em: 06 jul. 2024.
APA
Carvalho Junior, P. de S., Diniz, L. F., Silva, G. T. S. T. da, Coutinho, N. D., Santos, P. G. dos, Carvalho-Silva, V. H., et al. (2021). Amino-imino tautomerism in the salt formation of albendazole: hydrobromide and nitrate salts. Crystal Growth and Design, 21( 2), 1122-1135. doi:10.1021/acs.cgd.0c01444
NLM
Carvalho Junior P de S, Diniz LF, Silva GTST da, Coutinho ND, Santos PG dos, Carvalho-Silva VH, Ribeiro C, Ellena J. Amino-imino tautomerism in the salt formation of albendazole: hydrobromide and nitrate salts [Internet]. Crystal Growth and Design. 2021 ; 21( 2): 1122-1135.[citado 2024 jul. 06 ] Available from: https://doi.org/10.1021/acs.cgd.0c01444
Vancouver
Carvalho Junior P de S, Diniz LF, Silva GTST da, Coutinho ND, Santos PG dos, Carvalho-Silva VH, Ribeiro C, Ellena J. Amino-imino tautomerism in the salt formation of albendazole: hydrobromide and nitrate salts [Internet]. Crystal Growth and Design. 2021 ; 21( 2): 1122-1135.[citado 2024 jul. 06 ] Available from: https://doi.org/10.1021/acs.cgd.0c01444
Artigo de periodico
Silver(I) complexes of 3-methoxy-4- hydroxybenzaldehyde thiosemicarbazones and triphenylphosphine: structural, cytotoxicity, and apoptotic studies (2020)
Silva, Débora E. S. ; Becceneri, Amanda B.; Santiago, João V. B. ; Gomes Neto, José A.; Ellena, Javier ; Cominetti, Márcia R. ; Pereira, José C. M.; Hannon, Michael J. ; Godoy Netto, Adelino Vieira de
Source: Dalton Transactions. Unidade: IFSC
Subjects: PLANEJAMENTO DE FÁRMACOS, QUÍMICA INORGÂNICA, CRISTALOGRAFIA ESTRUTURAL, CRISTALOGRAFIA FÍSICA (ESTRUTURA)
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ABNT
SILVA, Débora E. S. et al. Silver(I) complexes of 3-methoxy-4- hydroxybenzaldehyde thiosemicarbazones and triphenylphosphine: structural, cytotoxicity, and apoptotic studies. Dalton Transactions, v. 49, n. 45, p. 16474-16487, 2020Tradução . . Disponível em: https://doi.org/10.1039/D0DT01134G. Acesso em: 06 jul. 2024.
APA
Silva, D. E. S., Becceneri, A. B., Santiago, J. V. B., Gomes Neto, J. A., Ellena, J., Cominetti, M. R., et al. (2020). Silver(I) complexes of 3-methoxy-4- hydroxybenzaldehyde thiosemicarbazones and triphenylphosphine: structural, cytotoxicity, and apoptotic studies. Dalton Transactions, 49( 45), 16474-16487. doi:10.1039/D0DT01134G
NLM
Silva DES, Becceneri AB, Santiago JVB, Gomes Neto JA, Ellena J, Cominetti MR, Pereira JCM, Hannon MJ, Godoy Netto AV de. Silver(I) complexes of 3-methoxy-4- hydroxybenzaldehyde thiosemicarbazones and triphenylphosphine: structural, cytotoxicity, and apoptotic studies [Internet]. Dalton Transactions. 2020 ; 49( 45): 16474-16487.[citado 2024 jul. 06 ] Available from: https://doi.org/10.1039/D0DT01134G
Vancouver
Silva DES, Becceneri AB, Santiago JVB, Gomes Neto JA, Ellena J, Cominetti MR, Pereira JCM, Hannon MJ, Godoy Netto AV de. Silver(I) complexes of 3-methoxy-4- hydroxybenzaldehyde thiosemicarbazones and triphenylphosphine: structural, cytotoxicity, and apoptotic studies [Internet]. Dalton Transactions. 2020 ; 49( 45): 16474-16487.[citado 2024 jul. 06 ] Available from: https://doi.org/10.1039/D0DT01134G
Artigo de periodico
"Half-sandwich"/RuII anticancer complexes containing triphenylphosphine and p-substituted benzoic acids (2020)
Honorato, João ; Oliveira, Katia M. ; Leite, Celisnolia M. ; Colina‑Vegas, Legna ; Nóbrega, Joaquim A. ; Castellano, Eduardo Ernesto ; Ellena, Javier ; Correa, Rodrigo S. ; Batista, Alzir A.
Source: Journal of the Brazilian Chemical Society. Unidade: IFSC
Subjects: PLANEJAMENTO DE FÁRMACOS, ANTIFÚNGICOS, CRISTALOGRAFIA ESTRUTURAL
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ABNT
HONORATO, João et al. "Half-sandwich"/RuII anticancer complexes containing triphenylphosphine and p-substituted benzoic acids. Journal of the Brazilian Chemical Society, v. No 2020, n. 11, p. 2237-2249, 2020Tradução . . Disponível em: https://doi.org/10.21577/0103-5053.20200076. Acesso em: 06 jul. 2024.
APA
Honorato, J., Oliveira, K. M., Leite, C. M., Colina‑Vegas, L., Nóbrega, J. A., Castellano, E. E., et al. (2020). "Half-sandwich"/RuII anticancer complexes containing triphenylphosphine and p-substituted benzoic acids. Journal of the Brazilian Chemical Society, No 2020( 11), 2237-2249. doi:10.21577/0103-5053.20200076
NLM
Honorato J, Oliveira KM, Leite CM, Colina‑Vegas L, Nóbrega JA, Castellano EE, Ellena J, Correa RS, Batista AA. "Half-sandwich"/RuII anticancer complexes containing triphenylphosphine and p-substituted benzoic acids [Internet]. Journal of the Brazilian Chemical Society. 2020 ; No 2020( 11): 2237-2249.[citado 2024 jul. 06 ] Available from: https://doi.org/10.21577/0103-5053.20200076
Vancouver
Honorato J, Oliveira KM, Leite CM, Colina‑Vegas L, Nóbrega JA, Castellano EE, Ellena J, Correa RS, Batista AA. "Half-sandwich"/RuII anticancer complexes containing triphenylphosphine and p-substituted benzoic acids [Internet]. Journal of the Brazilian Chemical Society. 2020 ; No 2020( 11): 2237-2249.[citado 2024 jul. 06 ] Available from: https://doi.org/10.21577/0103-5053.20200076
Artigo de periodico
Structures of substrate- and product-bound forms of a multi-domain copper nitrite reductase shed light on the role of domain tethering in protein complexes (2020)
Sasaki, Daisuke ; Watanabe, Tatiana F.; Eady, Robert R.; Garratt, Richard Charles ; Antonyuk, Svetlana V. ; Hasnain, S. Samar
Source: IUCrJ. Unidade: IFSC
Subjects: NITROGÊNIO, DESNITRIFICAÇÃO, CATÁLISE
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ABNT
SASAKI, Daisuke et al. Structures of substrate- and product-bound forms of a multi-domain copper nitrite reductase shed light on the role of domain tethering in protein complexes. IUCrJ, v. 7, p. 557-565 + sup1-sup6, 2020Tradução . . Disponível em: https://doi.org/10.1107/S2052252520005230. Acesso em: 06 jul. 2024.
APA
Sasaki, D., Watanabe, T. F., Eady, R. R., Garratt, R. C., Antonyuk, S. V., & Hasnain, S. S. (2020). Structures of substrate- and product-bound forms of a multi-domain copper nitrite reductase shed light on the role of domain tethering in protein complexes. IUCrJ, 7, 557-565 + sup1-sup6. doi:10.1107/S2052252520005230
NLM
Sasaki D, Watanabe TF, Eady RR, Garratt RC, Antonyuk SV, Hasnain SS. Structures of substrate- and product-bound forms of a multi-domain copper nitrite reductase shed light on the role of domain tethering in protein complexes [Internet]. IUCrJ. 2020 ; 7 557-565 + sup1-sup6.[citado 2024 jul. 06 ] Available from: https://doi.org/10.1107/S2052252520005230
Vancouver
Sasaki D, Watanabe TF, Eady RR, Garratt RC, Antonyuk SV, Hasnain SS. Structures of substrate- and product-bound forms of a multi-domain copper nitrite reductase shed light on the role of domain tethering in protein complexes [Internet]. IUCrJ. 2020 ; 7 557-565 + sup1-sup6.[citado 2024 jul. 06 ] Available from: https://doi.org/10.1107/S2052252520005230
Artigo de periodico
A novel scaffold to fight Pseudomonas aeruginosa pyocyanin production: early steps to novel antivirulence drugs (2020)
Froes, Thamires Quadros ; Guido, Rafael Victorio Carvalho ; Metwally, Kamel; Castilho, Marcelo Santos
Source: Future Medicinal Chemistry. Unidade: IFSC
Subjects: PSEUDOMONAS, BIOQUÍMICA, PLANEJAMENTO DE FÁRMACOS
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ABNT
FROES, Thamires Quadros et al. A novel scaffold to fight Pseudomonas aeruginosa pyocyanin production: early steps to novel antivirulence drugs. Future Medicinal Chemistry, v. 12, n. 16, p. 1489-1503, 2020Tradução . . Disponível em: https://doi.org/10.4155/fmc-2019-0351. Acesso em: 06 jul. 2024.
APA
Froes, T. Q., Guido, R. V. C., Metwally, K., & Castilho, M. S. (2020). A novel scaffold to fight Pseudomonas aeruginosa pyocyanin production: early steps to novel antivirulence drugs. Future Medicinal Chemistry, 12( 16), 1489-1503. doi:10.4155/fmc-2019-0351
NLM
Froes TQ, Guido RVC, Metwally K, Castilho MS. A novel scaffold to fight Pseudomonas aeruginosa pyocyanin production: early steps to novel antivirulence drugs [Internet]. Future Medicinal Chemistry. 2020 ; 12( 16): 1489-1503.[citado 2024 jul. 06 ] Available from: https://doi.org/10.4155/fmc-2019-0351
Vancouver
Froes TQ, Guido RVC, Metwally K, Castilho MS. A novel scaffold to fight Pseudomonas aeruginosa pyocyanin production: early steps to novel antivirulence drugs [Internet]. Future Medicinal Chemistry. 2020 ; 12( 16): 1489-1503.[citado 2024 jul. 06 ] Available from: https://doi.org/10.4155/fmc-2019-0351
Artigo de periodico
New allyldithiocarbimate salts: synthesis, structure and antifungal activity (2020)
Albuini-Oliveira, Nathália M.; Rubinger, Mayura M. M.; Guilardi, Silvana; Souza, Rafael A. C.; Ellena, Javier ; Alvarez, Natalia; Tavares, Eder C.; Zacchi, Carlos H. C.; Vidigal, Antonio E. C.; Lima, Marcelo S.; Zambolim, Laercio
Source: Journal of Molecular Structure. Unidade: IFSC
Subjects: CRISTALOGRAFIA, PLANEJAMENTO DE FÁRMACOS, ANTIFÚNGICOS
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ABNT
ALBUINI-OLIVEIRA, Nathália M. et al. New allyldithiocarbimate salts: synthesis, structure and antifungal activity. Journal of Molecular Structure, v. 1214, p. 128149-1-128149-16, 2020Tradução . . Disponível em: https://doi.org/10.1016/j.molstruc.2020.128149. Acesso em: 06 jul. 2024.
APA
Albuini-Oliveira, N. M., Rubinger, M. M. M., Guilardi, S., Souza, R. A. C., Ellena, J., Alvarez, N., et al. (2020). New allyldithiocarbimate salts: synthesis, structure and antifungal activity. Journal of Molecular Structure, 1214, 128149-1-128149-16. doi:10.1016/j.molstruc.2020.128149
NLM
Albuini-Oliveira NM, Rubinger MMM, Guilardi S, Souza RAC, Ellena J, Alvarez N, Tavares EC, Zacchi CHC, Vidigal AEC, Lima MS, Zambolim L. New allyldithiocarbimate salts: synthesis, structure and antifungal activity [Internet]. Journal of Molecular Structure. 2020 ; 1214 128149-1-128149-16.[citado 2024 jul. 06 ] Available from: https://doi.org/10.1016/j.molstruc.2020.128149
Vancouver
Albuini-Oliveira NM, Rubinger MMM, Guilardi S, Souza RAC, Ellena J, Alvarez N, Tavares EC, Zacchi CHC, Vidigal AEC, Lima MS, Zambolim L. New allyldithiocarbimate salts: synthesis, structure and antifungal activity [Internet]. Journal of Molecular Structure. 2020 ; 1214 128149-1-128149-16.[citado 2024 jul. 06 ] Available from: https://doi.org/10.1016/j.molstruc.2020.128149
Artigo de periodico
New allyldithiocarbimates: synthesis, structure and antifungal activity against Phakopsora pachyrhizi and Hemileia vastatrix (2020)
Vidigal, Antonio E. C.; Rubinger, Mayura M. M.; Silva, Lucas F.; Zambolim, Laércio; Pereira, Arthur B. D.; Guilardi, Silvana; Souza, Rafael A. C.; Ellena, Javier
Source: Journal of the Brazilian Chemical Society. Unidade: IFSC
Subjects: PLANEJAMENTO DE FÁRMACOS, ANTIFÚNGICOS, CRISTALOGRAFIA ESTRUTURAL
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ABNT
VIDIGAL, Antonio E. C. et al. New allyldithiocarbimates: synthesis, structure and antifungal activity against Phakopsora pachyrhizi and Hemileia vastatrix. Journal of the Brazilian Chemical Society, v. 31, n. 4, p. 703-715, 2020Tradução . . Disponível em: https://doi.org/10.21577/0103-5053.20190234. Acesso em: 06 jul. 2024.
APA
Vidigal, A. E. C., Rubinger, M. M. M., Silva, L. F., Zambolim, L., Pereira, A. B. D., Guilardi, S., et al. (2020). New allyldithiocarbimates: synthesis, structure and antifungal activity against Phakopsora pachyrhizi and Hemileia vastatrix. Journal of the Brazilian Chemical Society, 31( 4), 703-715. doi:10.21577/0103-5053.20190234
NLM
Vidigal AEC, Rubinger MMM, Silva LF, Zambolim L, Pereira ABD, Guilardi S, Souza RAC, Ellena J. New allyldithiocarbimates: synthesis, structure and antifungal activity against Phakopsora pachyrhizi and Hemileia vastatrix [Internet]. Journal of the Brazilian Chemical Society. 2020 ; 31( 4): 703-715.[citado 2024 jul. 06 ] Available from: https://doi.org/10.21577/0103-5053.20190234
Vancouver
Vidigal AEC, Rubinger MMM, Silva LF, Zambolim L, Pereira ABD, Guilardi S, Souza RAC, Ellena J. New allyldithiocarbimates: synthesis, structure and antifungal activity against Phakopsora pachyrhizi and Hemileia vastatrix [Internet]. Journal of the Brazilian Chemical Society. 2020 ; 31( 4): 703-715.[citado 2024 jul. 06 ] Available from: https://doi.org/10.21577/0103-5053.20190234
Artigo de periodico
Advanced glycation end product inhibition by Alkaloids from Ocotea paranapiacabensis for the prevention of skin aging (2020)
Freitas, Larissa de; Valli, Marilia; Dametto, Alessandra C.; Pennacchi, Paula Comune; Andricopulo, Adriano Defini ; Maria-Engler, Silvya Stuchi ; Bolzani, Vanderlan S.
Source: Journal of Natural Products. Unidades: IFSC, FCF
Subjects: BIOMARCADORES, ALCALOIDES, ENVELHECIMENTO CELULAR
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ABNT
FREITAS, Larissa de et al. Advanced glycation end product inhibition by Alkaloids from Ocotea paranapiacabensis for the prevention of skin aging. Journal of Natural Products, v. 83, n. 3, p. 649-656, 2020Tradução . . Disponível em: https://doi.org/10.1021/acs.jnatprod.9b01083. Acesso em: 06 jul. 2024.
APA
Freitas, L. de, Valli, M., Dametto, A. C., Pennacchi, P. C., Andricopulo, A. D., Maria-Engler, S. S., & Bolzani, V. S. (2020). Advanced glycation end product inhibition by Alkaloids from Ocotea paranapiacabensis for the prevention of skin aging. Journal of Natural Products, 83( 3), 649-656. doi:10.1021/acs.jnatprod.9b01083
NLM
Freitas L de, Valli M, Dametto AC, Pennacchi PC, Andricopulo AD, Maria-Engler SS, Bolzani VS. Advanced glycation end product inhibition by Alkaloids from Ocotea paranapiacabensis for the prevention of skin aging [Internet]. Journal of Natural Products. 2020 ; 83( 3): 649-656.[citado 2024 jul. 06 ] Available from: https://doi.org/10.1021/acs.jnatprod.9b01083
Vancouver
Freitas L de, Valli M, Dametto AC, Pennacchi PC, Andricopulo AD, Maria-Engler SS, Bolzani VS. Advanced glycation end product inhibition by Alkaloids from Ocotea paranapiacabensis for the prevention of skin aging [Internet]. Journal of Natural Products. 2020 ; 83( 3): 649-656.[citado 2024 jul. 06 ] Available from: https://doi.org/10.1021/acs.jnatprod.9b01083
Artigo de periodico
Chain-like uranyl-coordination polymer as a bright green light emitter for sensing and sunlight driven photocatalysis (2020)
Gomez, G. E. ; Onna, D.; D'Vries, R. F. ; Barja, B. C.; Ellena, Javier ; Narda, G. E.; Soler-Illia, G. J. A. A.
Source: Journal of Materials Chemistry C. Unidade: IFSC
Subjects: POLÍMEROS (MATERIAIS), FOTOCATÁLISE
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ABNT
GOMEZ, G. E. et al. Chain-like uranyl-coordination polymer as a bright green light emitter for sensing and sunlight driven photocatalysis. Journal of Materials Chemistry C, v. 8, n. 32, p. 11102-11109 + supplementary files, 2020Tradução . . Disponível em: https://doi.org/10.1039/d0tc02623a. Acesso em: 06 jul. 2024.
APA
Gomez, G. E., Onna, D., D'Vries, R. F., Barja, B. C., Ellena, J., Narda, G. E., & Soler-Illia, G. J. A. A. (2020). Chain-like uranyl-coordination polymer as a bright green light emitter for sensing and sunlight driven photocatalysis. Journal of Materials Chemistry C, 8( 32), 11102-11109 + supplementary files. doi:10.1039/d0tc02623a
NLM
Gomez GE, Onna D, D'Vries RF, Barja BC, Ellena J, Narda GE, Soler-Illia GJAA. Chain-like uranyl-coordination polymer as a bright green light emitter for sensing and sunlight driven photocatalysis [Internet]. Journal of Materials Chemistry C. 2020 ; 8( 32): 11102-11109 + supplementary files.[citado 2024 jul. 06 ] Available from: https://doi.org/10.1039/d0tc02623a
Vancouver
Gomez GE, Onna D, D'Vries RF, Barja BC, Ellena J, Narda GE, Soler-Illia GJAA. Chain-like uranyl-coordination polymer as a bright green light emitter for sensing and sunlight driven photocatalysis [Internet]. Journal of Materials Chemistry C. 2020 ; 8( 32): 11102-11109 + supplementary files.[citado 2024 jul. 06 ] Available from: https://doi.org/10.1039/d0tc02623a
Artigo de periodico
Study of the antibacterial property of tea tree oil and its incorporation into poly(Lactic Acid)-montmorillonite clay bionanocomposites (2020)
Proença, Larissa Braga; Pena, Carlos Alberto Pinheiro; Silva, Geovana Vieira da; Camargo, Ilana Lopes Baratella da Cunha ; Branciforti, Márcia Cristina
Source: Macromolecular Symposia. Unidades: IFSC, EESC
Subjects: RESISTÊNCIA MICROBIANA ÀS DROGAS, FARMACOLOGIA, CRISTALOGRAFIA
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ABNT
PROENÇA, Larissa Braga et al. Study of the antibacterial property of tea tree oil and its incorporation into poly(Lactic Acid)-montmorillonite clay bionanocomposites. Macromolecular Symposia, v. 394, n. 1, p. 2000073-1-2000073-6, 2020Tradução . . Disponível em: https://doi.org/10.1002/masy.202000073. Acesso em: 06 jul. 2024.
APA
Proença, L. B., Pena, C. A. P., Silva, G. V. da, Camargo, I. L. B. da C., & Branciforti, M. C. (2020). Study of the antibacterial property of tea tree oil and its incorporation into poly(Lactic Acid)-montmorillonite clay bionanocomposites. Macromolecular Symposia, 394( 1), 2000073-1-2000073-6. doi:10.1002/masy.202000073
NLM
Proença LB, Pena CAP, Silva GV da, Camargo ILB da C, Branciforti MC. Study of the antibacterial property of tea tree oil and its incorporation into poly(Lactic Acid)-montmorillonite clay bionanocomposites [Internet]. Macromolecular Symposia. 2020 ; 394( 1): 2000073-1-2000073-6.[citado 2024 jul. 06 ] Available from: https://doi.org/10.1002/masy.202000073
Vancouver
Proença LB, Pena CAP, Silva GV da, Camargo ILB da C, Branciforti MC. Study of the antibacterial property of tea tree oil and its incorporation into poly(Lactic Acid)-montmorillonite clay bionanocomposites [Internet]. Macromolecular Symposia. 2020 ; 394( 1): 2000073-1-2000073-6.[citado 2024 jul. 06 ] Available from: https://doi.org/10.1002/masy.202000073
Artigo de periodico
High-resolution structure of a modular hyperthermostable endo-β-1,4-mannanase from Thermotoga petrophila: the ancillary immunoglobulin-like module is a thermostabilizing domain (2020)
Silva, Viviam M.; Cabral, Aline D.; Sperança, Marcia A.; Squina, Fabio M.; Muniz, João Renato Carvalho ; Martin, Lydie; Nicolet, Yvain; Garcia, Wanius
Source: Biochimica et Biophysica Acta: Proteins and Proteomics. Unidade: IFSC
Subjects: IMUNOGLOBULINAS, BIOMASSA, MONOSSACARÍDEOS
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
SILVA, Viviam M. et al. High-resolution structure of a modular hyperthermostable endo-β-1,4-mannanase from Thermotoga petrophila: the ancillary immunoglobulin-like module is a thermostabilizing domain. Biochimica et Biophysica Acta: Proteins and Proteomics, v. 1868, n. 8, p. 140437-1-140437-8, 2020Tradução . . Disponível em: https://doi.org/10.1016/j.bbapap.2020.140437. Acesso em: 06 jul. 2024.
APA
Silva, V. M., Cabral, A. D., Sperança, M. A., Squina, F. M., Muniz, J. R. C., Martin, L., et al. (2020). High-resolution structure of a modular hyperthermostable endo-β-1,4-mannanase from Thermotoga petrophila: the ancillary immunoglobulin-like module is a thermostabilizing domain. Biochimica et Biophysica Acta: Proteins and Proteomics, 1868( 8), 140437-1-140437-8. doi:10.1016/j.bbapap.2020.140437
NLM
Silva VM, Cabral AD, Sperança MA, Squina FM, Muniz JRC, Martin L, Nicolet Y, Garcia W. High-resolution structure of a modular hyperthermostable endo-β-1,4-mannanase from Thermotoga petrophila: the ancillary immunoglobulin-like module is a thermostabilizing domain [Internet]. Biochimica et Biophysica Acta: Proteins and Proteomics. 2020 ; 1868( 8): 140437-1-140437-8.[citado 2024 jul. 06 ] Available from: https://doi.org/10.1016/j.bbapap.2020.140437
Vancouver
Silva VM, Cabral AD, Sperança MA, Squina FM, Muniz JRC, Martin L, Nicolet Y, Garcia W. High-resolution structure of a modular hyperthermostable endo-β-1,4-mannanase from Thermotoga petrophila: the ancillary immunoglobulin-like module is a thermostabilizing domain [Internet]. Biochimica et Biophysica Acta: Proteins and Proteomics. 2020 ; 1868( 8): 140437-1-140437-8.[citado 2024 jul. 06 ] Available from: https://doi.org/10.1016/j.bbapap.2020.140437
Artigo de periodico
Study of secondary porosity by SAXS and N2 adsorption in composite materials obtained from a Cuban natural clinoptilolite (2020)
Andrade-Ferreira, André; Costa-Marrero, Yailen; Autié-Castro, Giselle ; Farias, Tania ; Duque-Rodríguez, Julio ; Costa, Maria José Fonseca; Ellena, Javier ; Mascarenhas, Yvonne Primerano
Source: Surface and Interface Analysis. Unidades: IFSC, EESC
Subjects: MATERIAIS COMPÓSITOS, MATERIAIS POROSOS, NANOPARTÍCULAS
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ABNT
ANDRADE-FERREIRA, André et al. Study of secondary porosity by SAXS and N2 adsorption in composite materials obtained from a Cuban natural clinoptilolite. Surface and Interface Analysis, v. No 2020, n. 11, p. 735-741, 2020Tradução . . Disponível em: https://doi.org/10.1002/sia.6863. Acesso em: 06 jul. 2024.
APA
Andrade-Ferreira, A., Costa-Marrero, Y., Autié-Castro, G., Farias, T., Duque-Rodríguez, J., Costa, M. J. F., et al. (2020). Study of secondary porosity by SAXS and N2 adsorption in composite materials obtained from a Cuban natural clinoptilolite. Surface and Interface Analysis, No 2020( 11), 735-741. doi:10.1002/sia.6863
NLM
Andrade-Ferreira A, Costa-Marrero Y, Autié-Castro G, Farias T, Duque-Rodríguez J, Costa MJF, Ellena J, Mascarenhas YP. Study of secondary porosity by SAXS and N2 adsorption in composite materials obtained from a Cuban natural clinoptilolite [Internet]. Surface and Interface Analysis. 2020 ; No 2020( 11): 735-741.[citado 2024 jul. 06 ] Available from: https://doi.org/10.1002/sia.6863
Vancouver
Andrade-Ferreira A, Costa-Marrero Y, Autié-Castro G, Farias T, Duque-Rodríguez J, Costa MJF, Ellena J, Mascarenhas YP. Study of secondary porosity by SAXS and N2 adsorption in composite materials obtained from a Cuban natural clinoptilolite [Internet]. Surface and Interface Analysis. 2020 ; No 2020( 11): 735-741.[citado 2024 jul. 06 ] Available from: https://doi.org/10.1002/sia.6863
Artigo de periodico
Biguanide-transition metals complexes as potential drug for hyperglycemia treatment (2020)
Villamizar-Delgado, Stephanny; Porras-Osorio, Laura M.; Piñeros, Octavio; Ellena, Javier ; Balcazar, Norman; Varela-Miranda, Ruben E.; D'Vries, Richard F.
Source: RSC Advances. Unidades: IFSC, IQSC
Subjects: CRISTALOGRAFIA, HIPERGLICEMIA, PLANEJAMENTO DE FÁRMACOS
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ABNT
VILLAMIZAR-DELGADO, Stephanny et al. Biguanide-transition metals complexes as potential drug for hyperglycemia treatment. RSC Advances, v. 10, n. 38, p. 22856-22863, 2020Tradução . . Disponível em: https://doi.org/10.1039/d0ra04059b. Acesso em: 06 jul. 2024.
APA
Villamizar-Delgado, S., Porras-Osorio, L. M., Piñeros, O., Ellena, J., Balcazar, N., Varela-Miranda, R. E., & D'Vries, R. F. (2020). Biguanide-transition metals complexes as potential drug for hyperglycemia treatment. RSC Advances, 10( 38), 22856-22863. doi:10.1039/d0ra04059b
NLM
Villamizar-Delgado S, Porras-Osorio LM, Piñeros O, Ellena J, Balcazar N, Varela-Miranda RE, D'Vries RF. Biguanide-transition metals complexes as potential drug for hyperglycemia treatment [Internet]. RSC Advances. 2020 ; 10( 38): 22856-22863.[citado 2024 jul. 06 ] Available from: https://doi.org/10.1039/d0ra04059b
Vancouver
Villamizar-Delgado S, Porras-Osorio LM, Piñeros O, Ellena J, Balcazar N, Varela-Miranda RE, D'Vries RF. Biguanide-transition metals complexes as potential drug for hyperglycemia treatment [Internet]. RSC Advances. 2020 ; 10( 38): 22856-22863.[citado 2024 jul. 06 ] Available from: https://doi.org/10.1039/d0ra04059b
Artigo de periodico
Biotransformation of Ethinylestradiol by Whole Cells of Brazilian Marine-Derived Fungus Penicillium oxalicum CBMAI 1996 (2020)
Queiroz, Thayane Melo de; Ellena, Javier ; Porto, Andre Luiz Meleiro
Source: Marine Biotechnology. Unidades: IQSC, IFSC
Subjects: MEIO AMBIENTE, BIOTRANSFORMAÇÃO, FUNGOS, ESTEROIDES
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ABNT
QUEIROZ, Thayane Melo de e ELLENA, Javier e PORTO, Andre Luiz Meleiro. Biotransformation of Ethinylestradiol by Whole Cells of Brazilian Marine-Derived Fungus Penicillium oxalicum CBMAI 1996. Marine Biotechnology, v. 22, n. 5, p. 673-682, 2020Tradução . . Disponível em: https://doi.org/10.1007/s10126-020-09989-w. Acesso em: 06 jul. 2024.
APA
Queiroz, T. M. de, Ellena, J., & Porto, A. L. M. (2020). Biotransformation of Ethinylestradiol by Whole Cells of Brazilian Marine-Derived Fungus Penicillium oxalicum CBMAI 1996. Marine Biotechnology, 22( 5), 673-682. doi:10.1007/s10126-020-09989-w
NLM
Queiroz TM de, Ellena J, Porto ALM. Biotransformation of Ethinylestradiol by Whole Cells of Brazilian Marine-Derived Fungus Penicillium oxalicum CBMAI 1996 [Internet]. Marine Biotechnology. 2020 ; 22( 5): 673-682.[citado 2024 jul. 06 ] Available from: https://doi.org/10.1007/s10126-020-09989-w
Vancouver
Queiroz TM de, Ellena J, Porto ALM. Biotransformation of Ethinylestradiol by Whole Cells of Brazilian Marine-Derived Fungus Penicillium oxalicum CBMAI 1996 [Internet]. Marine Biotechnology. 2020 ; 22( 5): 673-682.[citado 2024 jul. 06 ] Available from: https://doi.org/10.1007/s10126-020-09989-w
Artigo de periodico
Discovery of potent, reversible, and competitive cruzain inhibitors with trypanocidal activity: a structure-based drug design approach (2020)
Souza, Mariana Laureano de; Rezende Junior, Celso de Oliveira; Ferreira, Rafaela S. ; Chávez, Rocio Marisol Espinoza; Ferreira, Leonardo Luiz Gomes; Slafer, Brian W.; Magalhães, Luma Godoy; Andricopulo, Renata Krogh; Oliva, Glaucius ; Cruz, Fabio Cardoso; Dias, Luiz Carlos; Andricopulo, Adriano Defini
Source: Journal of Chemical Information and Modeling. Unidade: IFSC
Subjects: TRIPANOSSOMICIDAS, PLANEJAMENTO DE FÁRMACOS, INIBIDORES QUÍMICOS
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ABNT
SOUZA, Mariana Laureano de et al. Discovery of potent, reversible, and competitive cruzain inhibitors with trypanocidal activity: a structure-based drug design approach. Journal of Chemical Information and Modeling, v. 60, n. 2, p. 1028-1041, 2020Tradução . . Disponível em: https://doi.org/10.1021/acs.jcim.9b00802. Acesso em: 06 jul. 2024.
APA
Souza, M. L. de, Rezende Junior, C. de O., Ferreira, R. S., Chávez, R. M. E., Ferreira, L. L. G., Slafer, B. W., et al. (2020). Discovery of potent, reversible, and competitive cruzain inhibitors with trypanocidal activity: a structure-based drug design approach. Journal of Chemical Information and Modeling, 60( 2), 1028-1041. doi:10.1021/acs.jcim.9b00802
NLM
Souza ML de, Rezende Junior C de O, Ferreira RS, Chávez RME, Ferreira LLG, Slafer BW, Magalhães LG, Andricopulo RK, Oliva G, Cruz FC, Dias LC, Andricopulo AD. Discovery of potent, reversible, and competitive cruzain inhibitors with trypanocidal activity: a structure-based drug design approach [Internet]. Journal of Chemical Information and Modeling. 2020 ; 60( 2): 1028-1041.[citado 2024 jul. 06 ] Available from: https://doi.org/10.1021/acs.jcim.9b00802
Vancouver
Souza ML de, Rezende Junior C de O, Ferreira RS, Chávez RME, Ferreira LLG, Slafer BW, Magalhães LG, Andricopulo RK, Oliva G, Cruz FC, Dias LC, Andricopulo AD. Discovery of potent, reversible, and competitive cruzain inhibitors with trypanocidal activity: a structure-based drug design approach [Internet]. Journal of Chemical Information and Modeling. 2020 ; 60( 2): 1028-1041.[citado 2024 jul. 06 ] Available from: https://doi.org/10.1021/acs.jcim.9b00802

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