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Artigo de periodico
Structure and dynamics of the staphylococcal pyridoxal 5-phosphate synthase complex reveal transient interactions at the enzyme interface (2024)
Barra, Angélica Luana Carrilho ; Ullah, Najeeb; Brognaro, Hévila; Gutierrez, Raissa Ferreira ; Wrenger, Carsten ; Betzel, Christian ; Nascimento, Alessandro Silva
Source: Journal of Biological Chemistry. Unidades: ICB, IFSC
Subjects: CRISTALOGRAFIA, STAPHYLOCOCCUS, ENZIMAS, VITAMINA B6, FOSFATOS, PROTEÍNAS, FÁRMACOS, CRISTALOGRAFIA DE RAIOS X
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BARRA, Angélica Luana Carrilho et al. Structure and dynamics of the staphylococcal pyridoxal 5-phosphate synthase complex reveal transient interactions at the enzyme interface. Journal of Biological Chemistry, v. 300, n. 6, p. 107404-1-107404-12 + supporting information, 2024Tradução . . Disponível em: https://doi.org/10.1016/j.jbc.2024.107404. Acesso em: 19 set. 2024.
APA
Barra, A. L. C., Ullah, N., Brognaro, H., Gutierrez, R. F., Wrenger, C., Betzel, C., & Nascimento, A. S. (2024). Structure and dynamics of the staphylococcal pyridoxal 5-phosphate synthase complex reveal transient interactions at the enzyme interface. Journal of Biological Chemistry, 300( 6), 107404-1-107404-12 + supporting information. doi:10.1016/j.jbc.2024.107404
NLM
Barra ALC, Ullah N, Brognaro H, Gutierrez RF, Wrenger C, Betzel C, Nascimento AS. Structure and dynamics of the staphylococcal pyridoxal 5-phosphate synthase complex reveal transient interactions at the enzyme interface [Internet]. Journal of Biological Chemistry. 2024 ; 300( 6): 107404-1-107404-12 + supporting information.[citado 2024 set. 19 ] Available from: https://doi.org/10.1016/j.jbc.2024.107404
Vancouver
Barra ALC, Ullah N, Brognaro H, Gutierrez RF, Wrenger C, Betzel C, Nascimento AS. Structure and dynamics of the staphylococcal pyridoxal 5-phosphate synthase complex reveal transient interactions at the enzyme interface [Internet]. Journal of Biological Chemistry. 2024 ; 300( 6): 107404-1-107404-12 + supporting information.[citado 2024 set. 19 ] Available from: https://doi.org/10.1016/j.jbc.2024.107404
Trabalho de evento-resumo
Discovery of Plasmodium falciparum inhibitors as lead candidates for malaria (2023)
Guido, Rafael Victorio Carvalho ; Oliveira, Juliana Roberta Torini de Souza; Souza, Guilherme Eduardo de ; Zanini, Camila Lima; Paim, Juliana Calit ; Bargieri, Daniel Youssef ; Oliva, Glaucius ; Aguiar, Anna Caroline Campos ; Barbosa, Camila de Souza ; Ahmad, Anees ; Burtoloso, Antonio Carlos Bender ; Maluf, Sarah El Chamy; Moura, Igor Mota Rodrigues de
Source: Anais eletrônicos. Conference titles: Annual Meeting of the Brazilian Biophysical Society - SBBf. Unidades: IFSC, ICB, IQSC
Subjects: COVID-19, ANTIMALÁRICOS, MALÁRIA, PLANEJAMENTO DE FÁRMACOS, PLASMODIUM FALCIPARUM
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GUIDO, Rafael Victorio Carvalho et al. Discovery of Plasmodium falciparum inhibitors as lead candidates for malaria. 2023, Anais.. Campinas: Galoá, 2023. Disponível em: https://proceedings.science/sbbf-2023/papers/discovery-of-plasmodium-falciparum-inhibitors-as-lead-candidates-for-malaria?lang=en. Acesso em: 19 set. 2024.
APA
Guido, R. V. C., Oliveira, J. R. T. de S., Souza, G. E. de, Zanini, C. L., Paim, J. C., Bargieri, D. Y., et al. (2023). Discovery of Plasmodium falciparum inhibitors as lead candidates for malaria. In Anais eletrônicos. Campinas: Galoá. Recuperado de https://proceedings.science/sbbf-2023/papers/discovery-of-plasmodium-falciparum-inhibitors-as-lead-candidates-for-malaria?lang=en
NLM
Guido RVC, Oliveira JRT de S, Souza GE de, Zanini CL, Paim JC, Bargieri DY, Oliva G, Aguiar ACC, Barbosa C de S, Ahmad A, Burtoloso ACB, Maluf SEC, Moura IMR de. Discovery of Plasmodium falciparum inhibitors as lead candidates for malaria [Internet]. Anais eletrônicos. 2023 ;[citado 2024 set. 19 ] Available from: https://proceedings.science/sbbf-2023/papers/discovery-of-plasmodium-falciparum-inhibitors-as-lead-candidates-for-malaria?lang=en
Vancouver
Guido RVC, Oliveira JRT de S, Souza GE de, Zanini CL, Paim JC, Bargieri DY, Oliva G, Aguiar ACC, Barbosa C de S, Ahmad A, Burtoloso ACB, Maluf SEC, Moura IMR de. Discovery of Plasmodium falciparum inhibitors as lead candidates for malaria [Internet]. Anais eletrônicos. 2023 ;[citado 2024 set. 19 ] Available from: https://proceedings.science/sbbf-2023/papers/discovery-of-plasmodium-falciparum-inhibitors-as-lead-candidates-for-malaria?lang=en
Trabalho de evento-resumo
Antitrypanosomal Benzoxazinone series: hit-to-lead campaign and multiparametric optimization (2022)
Mollo, María Cruz; Cruz, Luiza; Dessoy, Marco Aurélio; Lee, Eun; Oliveira, Ramon Guerra de; Dutra, Francielle; Duarte, Simone Michelan ; Andricopulo, Renata Krogh; Ferreira, Leonardo Luiz Gomes ; Chelucci, Rafael Consolin; Feltrin, Clarissa; Moraes, Carolina Borsoi; Andricopulo, Adriano Defini ; Kratz, Jadel; Sjö, Peter; Mowbray, Charles; Dias, Luiz Carlos
Source: Anais eletrônicos. Conference titles: Brazilian Symposium on Medicinal Chemistry - BrazMedChem. Unidades: IFSC, ICB
Subjects: TRYPANOSOMA CRUZI, PLANEJAMENTO DE FÁRMACOS
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MOLLO, María Cruz et al. Antitrypanosomal Benzoxazinone series: hit-to-lead campaign and multiparametric optimization. 2022, Anais.. Campinas: Galoá, 2022. Disponível em: https://proceedings.science/brazmedchem-2022/papers/antitrypanosomal-benzoxazinone-series--hit-to-lead-campaign-and-multiparametric-optimization-. Acesso em: 19 set. 2024.
APA
Mollo, M. C., Cruz, L., Dessoy, M. A., Lee, E., Oliveira, R. G. de, Dutra, F., et al. (2022). Antitrypanosomal Benzoxazinone series: hit-to-lead campaign and multiparametric optimization. In Anais eletrônicos. Campinas: Galoá. Recuperado de https://proceedings.science/brazmedchem-2022/papers/antitrypanosomal-benzoxazinone-series--hit-to-lead-campaign-and-multiparametric-optimization-.
NLM
Mollo MC, Cruz L, Dessoy MA, Lee E, Oliveira RG de, Dutra F, Duarte SM, Andricopulo RK, Ferreira LLG, Chelucci RC, Feltrin C, Moraes CB, Andricopulo AD, Kratz J, Sjö P, Mowbray C, Dias LC. Antitrypanosomal Benzoxazinone series: hit-to-lead campaign and multiparametric optimization [Internet]. Anais eletrônicos. 2022 ;[citado 2024 set. 19 ] Available from: https://proceedings.science/brazmedchem-2022/papers/antitrypanosomal-benzoxazinone-series--hit-to-lead-campaign-and-multiparametric-optimization-.
Vancouver
Mollo MC, Cruz L, Dessoy MA, Lee E, Oliveira RG de, Dutra F, Duarte SM, Andricopulo RK, Ferreira LLG, Chelucci RC, Feltrin C, Moraes CB, Andricopulo AD, Kratz J, Sjö P, Mowbray C, Dias LC. Antitrypanosomal Benzoxazinone series: hit-to-lead campaign and multiparametric optimization [Internet]. Anais eletrônicos. 2022 ;[citado 2024 set. 19 ] Available from: https://proceedings.science/brazmedchem-2022/papers/antitrypanosomal-benzoxazinone-series--hit-to-lead-campaign-and-multiparametric-optimization-.
Artigo de periodico
Non-Toxic dimeric peptides derived from the bothropstoxin-I are potent SARS-CoV-2 and papain-like protease inhibitors (2021)
Freire, Marjorie Caroline Liberato Cavalcanti ; Noske, Gabriela Dias; Bitencourt, Natália V.; Sanches, Paulo R. S.; Santos-Filho, Norival A.; Oliveira, Victor Gawriljuk Ferraro; Souza, Eduardo Pereira de ; Nogueira, Victor Henrique Rabesquine ; Godoy, Mariana Ortiz de; Nakamura, Aline Minali; Fernandes, Rafaela Sachetto ; Godoy, Andre Schutzer de ; Juliano, Maria A.; Peres, Bianca de Miranda ; Barbosa, Cecília G.; Moraes, Carolina B.; Freitas Junior, Lucio Holanda Gondim de ; Cilli, Eduardo Maffud ; Guido, Rafael Victorio Carvalho ; Oliva, Glaucius
Source: Molecules. Unidades: IFSC, ICB
Subjects: COVID-19, CORONAVIRUS, PLANEJAMENTO DE FÁRMACOS, PROTEÍNAS
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FREIRE, Marjorie Caroline Liberato Cavalcanti et al. Non-Toxic dimeric peptides derived from the bothropstoxin-I are potent SARS-CoV-2 and papain-like protease inhibitors. Molecules, v. 26, n. 16, p. 4896-1-4896-17, 2021Tradução . . Disponível em: https://doi.org/10.3390/molecules26164896. Acesso em: 19 set. 2024.
APA
Freire, M. C. L. C., Noske, G. D., Bitencourt, N. V., Sanches, P. R. S., Santos-Filho, N. A., Oliveira, V. G. F., et al. (2021). Non-Toxic dimeric peptides derived from the bothropstoxin-I are potent SARS-CoV-2 and papain-like protease inhibitors. Molecules, 26( 16), 4896-1-4896-17. doi:10.3390/molecules26164896
NLM
Freire MCLC, Noske GD, Bitencourt NV, Sanches PRS, Santos-Filho NA, Oliveira VGF, Souza EP de, Nogueira VHR, Godoy MO de, Nakamura AM, Fernandes RS, Godoy AS de, Juliano MA, Peres B de M, Barbosa CG, Moraes CB, Freitas Junior LHG de, Cilli EM, Guido RVC, Oliva G. Non-Toxic dimeric peptides derived from the bothropstoxin-I are potent SARS-CoV-2 and papain-like protease inhibitors [Internet]. Molecules. 2021 ; 26( 16): 4896-1-4896-17.[citado 2024 set. 19 ] Available from: https://doi.org/10.3390/molecules26164896
Vancouver
Freire MCLC, Noske GD, Bitencourt NV, Sanches PRS, Santos-Filho NA, Oliveira VGF, Souza EP de, Nogueira VHR, Godoy MO de, Nakamura AM, Fernandes RS, Godoy AS de, Juliano MA, Peres B de M, Barbosa CG, Moraes CB, Freitas Junior LHG de, Cilli EM, Guido RVC, Oliva G. Non-Toxic dimeric peptides derived from the bothropstoxin-I are potent SARS-CoV-2 and papain-like protease inhibitors [Internet]. Molecules. 2021 ; 26( 16): 4896-1-4896-17.[citado 2024 set. 19 ] Available from: https://doi.org/10.3390/molecules26164896
Artigo de periodico
Polymyxin resistance among XDR ST1 carbapenem-resistant Acinetobacter baumannii clone expanding in a teaching hospital (2021)
Carrasco, Letícia Dias de Melo ; Dabul, Andrei Nicoli Gebieluca ; Boralli, Camila Maria dos Santos ; Righetto, Gabriela Marinho; Carvalho, Iago Silva e; Dornelas, Janaína Valerini; Mata, Camila Pacheco Silveira Martins da ; Araújo, César Augusto de ; Leite, Edna Mariléa Meireles ; Lincopan, Nilton ; Camargo, Ilana Lopes Baratella da Cunha
Source: Frontiers in Microbiology. Unidades: ICB, IFSC
Subjects: RESISTÊNCIA MICROBIANA ÀS DROGAS, BACTÉRIAS PATOGÊNICAS, INFECÇÃO HOSPITALAR, MICROBIOLOGIA, POLIMIXINAS, MEDICAMENTO
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CARRASCO, Letícia Dias de Melo et al. Polymyxin resistance among XDR ST1 carbapenem-resistant Acinetobacter baumannii clone expanding in a teaching hospital. Frontiers in Microbiology, v. 12, p. 622704-1-622704-11 + supplementary material, 2021Tradução . . Disponível em: https://doi.org/10.3389/fmicb.2021.622704. Acesso em: 19 set. 2024.
APA
Carrasco, L. D. de M., Dabul, A. N. G., Boralli, C. M. dos S., Righetto, G. M., Carvalho, I. S. e, Dornelas, J. V., et al. (2021). Polymyxin resistance among XDR ST1 carbapenem-resistant Acinetobacter baumannii clone expanding in a teaching hospital. Frontiers in Microbiology, 12, 622704-1-622704-11 + supplementary material. doi:10.3389/fmicb.2021.622704
NLM
Carrasco LD de M, Dabul ANG, Boralli CM dos S, Righetto GM, Carvalho IS e, Dornelas JV, Mata CPSM da, Araújo CA de, Leite EMM, Lincopan N, Camargo ILB da C. Polymyxin resistance among XDR ST1 carbapenem-resistant Acinetobacter baumannii clone expanding in a teaching hospital [Internet]. Frontiers in Microbiology. 2021 ; 12 622704-1-622704-11 + supplementary material.[citado 2024 set. 19 ] Available from: https://doi.org/10.3389/fmicb.2021.622704
Vancouver
Carrasco LD de M, Dabul ANG, Boralli CM dos S, Righetto GM, Carvalho IS e, Dornelas JV, Mata CPSM da, Araújo CA de, Leite EMM, Lincopan N, Camargo ILB da C. Polymyxin resistance among XDR ST1 carbapenem-resistant Acinetobacter baumannii clone expanding in a teaching hospital [Internet]. Frontiers in Microbiology. 2021 ; 12 622704-1-622704-11 + supplementary material.[citado 2024 set. 19 ] Available from: https://doi.org/10.3389/fmicb.2021.622704
Artigo de periodico
2-aminobenzimidazoles for leishmaniasis: from initial hit discovery to in vivo profiling (2021)
Ferreira, Rafael Augusto Alves; Rezende Junior, Celso de ; Martinez, Pablo David Grigol ; Koovits, Paul John ; Soares, Bruna Miranda ; Ferreira, Leonardo Luiz Gomes ; Duarte, Simone Michelan ; Chelucci, Rafael Consolin; Andricopulo, Adriano Defini ; Galuppo, Mariana Kolos ; Uliana, Silvia Reni Bortolin ; Matheeussen, An ; Caljon, Guy ; Maes, Louis ; Campbell, Simon; Kratz, Jadel M. ; Mowbray, Charles E. ; Dias, Luiz Carlos
Source: PLOS Neglected Tropical Diseases. Unidades: IFSC, ICB
Subjects: ANTIPARASITÁRIOS, LEISHMANIA INFANTUM, PLANEJAMENTO DE FÁRMACOS, PARASITOLOGIA, MODELOS ANIMAIS DE DOENÇAS, CAMUNDONGOS, TOXICIDADE EM ANIMAL
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FERREIRA, Rafael Augusto Alves et al. 2-aminobenzimidazoles for leishmaniasis: from initial hit discovery to in vivo profiling. PLOS Neglected Tropical Diseases, v. 15, n. 2, p. e0009196-1-e0009196-20, 2021Tradução . . Disponível em: https://doi.org/10.1371/journal.pntd.0009196. Acesso em: 19 set. 2024.
APA
Ferreira, R. A. A., Rezende Junior, C. de, Martinez, P. D. G., Koovits, P. J., Soares, B. M., Ferreira, L. L. G., et al. (2021). 2-aminobenzimidazoles for leishmaniasis: from initial hit discovery to in vivo profiling. PLOS Neglected Tropical Diseases, 15( 2), e0009196-1-e0009196-20. doi:10.1371/journal.pntd.0009196
NLM
Ferreira RAA, Rezende Junior C de, Martinez PDG, Koovits PJ, Soares BM, Ferreira LLG, Duarte SM, Chelucci RC, Andricopulo AD, Galuppo MK, Uliana SRB, Matheeussen A, Caljon G, Maes L, Campbell S, Kratz JM, Mowbray CE, Dias LC. 2-aminobenzimidazoles for leishmaniasis: from initial hit discovery to in vivo profiling [Internet]. PLOS Neglected Tropical Diseases. 2021 ; 15( 2): e0009196-1-e0009196-20.[citado 2024 set. 19 ] Available from: https://doi.org/10.1371/journal.pntd.0009196
Vancouver
Ferreira RAA, Rezende Junior C de, Martinez PDG, Koovits PJ, Soares BM, Ferreira LLG, Duarte SM, Chelucci RC, Andricopulo AD, Galuppo MK, Uliana SRB, Matheeussen A, Caljon G, Maes L, Campbell S, Kratz JM, Mowbray CE, Dias LC. 2-aminobenzimidazoles for leishmaniasis: from initial hit discovery to in vivo profiling [Internet]. PLOS Neglected Tropical Diseases. 2021 ; 15( 2): e0009196-1-e0009196-20.[citado 2024 set. 19 ] Available from: https://doi.org/10.1371/journal.pntd.0009196
Artigo de periodico
Parasitological profiling shows 4(1H)-quinolone derivatives as new lead candidates for malaria (2021)
Souza, Juliana Oliveira de; Almeida, Suzete M.; Souza, Guilherme Eduardo de ; Zanini, Camila Lima; Silva, Everton Machado da; Paim, Juliana Calit ; Bargieri, Daniel Youssef ; Amporndanai, Kangsa; Antonyuk, Svetlana V. ; Hasnain, S. Samar ; Cruz, Fabio C.; Pereira, Dhelio Batista ; Oliva, Glaucius ; Corrêa, Arlene G. ; Aguiar, Anna Caroline Campos ; Guido, Rafael Victorio Carvalho
Source: European Journal of Medicinal Chemistry Reports. Unidades: ICB, IFSC
Subjects: ANTIMALÁRICOS, ANTIPARASITÁRIOS, MALÁRIA, PLASMODIUM FALCIPARUM
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SOUZA, Juliana Oliveira de et al. Parasitological profiling shows 4(1H)-quinolone derivatives as new lead candidates for malaria. European Journal of Medicinal Chemistry Reports, v. 3, p. 100012-1-100012-16 + supplementary data, 2021Tradução . . Disponível em: https://doi.org/10.1016/j.ejmcr.2021.100012. Acesso em: 19 set. 2024.
APA
Souza, J. O. de, Almeida, S. M., Souza, G. E. de, Zanini, C. L., Silva, E. M. da, Paim, J. C., et al. (2021). Parasitological profiling shows 4(1H)-quinolone derivatives as new lead candidates for malaria. European Journal of Medicinal Chemistry Reports, 3, 100012-1-100012-16 + supplementary data. doi:10.1016/j.ejmcr.2021.100012
NLM
Souza JO de, Almeida SM, Souza GE de, Zanini CL, Silva EM da, Paim JC, Bargieri DY, Amporndanai K, Antonyuk SV, Hasnain SS, Cruz FC, Pereira DB, Oliva G, Corrêa AG, Aguiar ACC, Guido RVC. Parasitological profiling shows 4(1H)-quinolone derivatives as new lead candidates for malaria [Internet]. European Journal of Medicinal Chemistry Reports. 2021 ; 3 100012-1-100012-16 + supplementary data.[citado 2024 set. 19 ] Available from: https://doi.org/10.1016/j.ejmcr.2021.100012
Vancouver
Souza JO de, Almeida SM, Souza GE de, Zanini CL, Silva EM da, Paim JC, Bargieri DY, Amporndanai K, Antonyuk SV, Hasnain SS, Cruz FC, Pereira DB, Oliva G, Corrêa AG, Aguiar ACC, Guido RVC. Parasitological profiling shows 4(1H)-quinolone derivatives as new lead candidates for malaria [Internet]. European Journal of Medicinal Chemistry Reports. 2021 ; 3 100012-1-100012-16 + supplementary data.[citado 2024 set. 19 ] Available from: https://doi.org/10.1016/j.ejmcr.2021.100012
Artigo de periodico
Trypanosomatid selenophosphate synthetase structure, function and interaction with selenocysteine lyase (2020)
Silva, Marco Túlio Alves da ; Silva, Ivan Rosa e ; Faim, Lívia Maria ; Bellini, Natália Karla ; Pereira, Murilo Leão ; Lima, Ana Laura; Jesus, Teresa Cristina Leandro de; Costa, Fernanda Cristina ; Watanabe, Tatiana Faria; Pereira, Humberto d'Muniz ; Valentini, Sandro Roberto ; Zanelli, Cleslei Fernando ; Borges, Julio Cesar ; Dias, Marcio Vinicius Bertacine ; Cunha, Júlia Pinheiro Chagas da ; Mittra, Bidyottam ; Andrews, Norma W. ; Thiemann, Otávio Henrique
Source: PLOS Neglected Tropical Diseases. Unidades: IFSC, IQSC, ICB
Subjects: TRYPANOSOMA CRUZI, TRYPANOSOMA, SELÊNIO, PROTEÍNAS, MICROBIOLOGIA
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SILVA, Marco Túlio Alves da et al. Trypanosomatid selenophosphate synthetase structure, function and interaction with selenocysteine lyase. PLOS Neglected Tropical Diseases, v. 14, n. 10, p. e0008091-1-e0008091-31, 2020Tradução . . Disponível em: https://doi.org/10.1371/journal.pntd.0008091. Acesso em: 19 set. 2024.
APA
Silva, M. T. A. da, Silva, I. R. e, Faim, L. M., Bellini, N. K., Pereira, M. L., Lima, A. L., et al. (2020). Trypanosomatid selenophosphate synthetase structure, function and interaction with selenocysteine lyase. PLOS Neglected Tropical Diseases, 14( 10), e0008091-1-e0008091-31. doi:10.1371/journal.pntd.0008091
NLM
Silva MTA da, Silva IR e, Faim LM, Bellini NK, Pereira ML, Lima AL, Jesus TCL de, Costa FC, Watanabe TF, Pereira H d'M, Valentini SR, Zanelli CF, Borges JC, Dias MVB, Cunha JPC da, Mittra B, Andrews NW, Thiemann OH. Trypanosomatid selenophosphate synthetase structure, function and interaction with selenocysteine lyase [Internet]. PLOS Neglected Tropical Diseases. 2020 ; 14( 10): e0008091-1-e0008091-31.[citado 2024 set. 19 ] Available from: https://doi.org/10.1371/journal.pntd.0008091
Vancouver
Silva MTA da, Silva IR e, Faim LM, Bellini NK, Pereira ML, Lima AL, Jesus TCL de, Costa FC, Watanabe TF, Pereira H d'M, Valentini SR, Zanelli CF, Borges JC, Dias MVB, Cunha JPC da, Mittra B, Andrews NW, Thiemann OH. Trypanosomatid selenophosphate synthetase structure, function and interaction with selenocysteine lyase [Internet]. PLOS Neglected Tropical Diseases. 2020 ; 14( 10): e0008091-1-e0008091-31.[citado 2024 set. 19 ] Available from: https://doi.org/10.1371/journal.pntd.0008091
Trabalho de evento-resumo
Structure-activity relationships of sulfonamides derived from carvacrol as new agents for the treatment of Alzheimer's disease (2019)
Oliveira, Aldo Sena de; Souza, Márcia Maria de; Andreolla, Marina Corrêa; Ribeiro, Thaís Cecília; Gonçalves, Ana Elisa; Medeiros, Alex Rogério; Souza, Anacleto Silva de; Ferreira, Leonardo Luiz Gomes ; Brighente, Inês Maria Costa; Nunes, Ricardo José; Yunes, Rosendo Augusto; Andricopulo, Adriano Defini
Source: Anais eletrônicos. Conference titles: Brazilian Symposium on Medicinal Chemistry - BrazMedChem. Unidades: IFSC, ICB
Subjects: DOENÇA DE ALZHEIMER, MANIFESTAÇÕES NEUROLÓGICAS, PLANEJAMENTO DE FÁRMACOS
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OLIVEIRA, Aldo Sena de et al. Structure-activity relationships of sulfonamides derived from carvacrol as new agents for the treatment of Alzheimer's disease. 2019, Anais.. Campinas: Galoá, 2019. Disponível em: https://proceedings.science/p/107173. Acesso em: 19 set. 2024.
APA
Oliveira, A. S. de, Souza, M. M. de, Andreolla, M. C., Ribeiro, T. C., Gonçalves, A. E., Medeiros, A. R., et al. (2019). Structure-activity relationships of sulfonamides derived from carvacrol as new agents for the treatment of Alzheimer's disease. In Anais eletrônicos. Campinas: Galoá. Recuperado de https://proceedings.science/p/107173
NLM
Oliveira AS de, Souza MM de, Andreolla MC, Ribeiro TC, Gonçalves AE, Medeiros AR, Souza AS de, Ferreira LLG, Brighente IMC, Nunes RJ, Yunes RA, Andricopulo AD. Structure-activity relationships of sulfonamides derived from carvacrol as new agents for the treatment of Alzheimer's disease [Internet]. Anais eletrônicos. 2019 ;[citado 2024 set. 19 ] Available from: https://proceedings.science/p/107173
Vancouver
Oliveira AS de, Souza MM de, Andreolla MC, Ribeiro TC, Gonçalves AE, Medeiros AR, Souza AS de, Ferreira LLG, Brighente IMC, Nunes RJ, Yunes RA, Andricopulo AD. Structure-activity relationships of sulfonamides derived from carvacrol as new agents for the treatment of Alzheimer's disease [Internet]. Anais eletrônicos. 2019 ;[citado 2024 set. 19 ] Available from: https://proceedings.science/p/107173
Artigo de periodico
Endophytic actinobacteria from the brazilian medicinal plant lychnophora ericoides MART. and the biological potential of their secondary metabolites (2016)
Conti, Raphael; Chagas, Fernanda Oliveira; Caraballo-Rodriguez, Andrés Mauricio; Paixão Melo, Weilan Gomes da; Nascimento, Andréa Mendes do; Cavalcanti, Bruno Coêlho; Moraes, Manoel Odorico de; Pessoa, Cláudia; Costa-Lotufo, Letícia Veras ; Krogh, Renata; Andricopulo, Adriano Defini; Lopes, Norberto Peporine; Pupo, Mônica Tallarico
Source: Chemistry and Biodiversity. Unidades: ICB, IFSC, FCFRP
Subjects: QUÍMICA MÉDICA, PRODUTOS NATURAIS, PLANTAS MEDICINAIS
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ABNT
CONTI, Raphael et al. Endophytic actinobacteria from the brazilian medicinal plant lychnophora ericoides MART. and the biological potential of their secondary metabolites. Chemistry and Biodiversity, v. 13, n. 6, p. 727-736, 2016Tradução . . Disponível em: https://doi.org/10.1002/cbdv.201500225. Acesso em: 19 set. 2024.
APA
Conti, R., Chagas, F. O., Caraballo-Rodriguez, A. M., Paixão Melo, W. G. da, Nascimento, A. M. do, Cavalcanti, B. C., et al. (2016). Endophytic actinobacteria from the brazilian medicinal plant lychnophora ericoides MART. and the biological potential of their secondary metabolites. Chemistry and Biodiversity, 13( 6), 727-736. doi:10.1002/cbdv.201500225
NLM
Conti R, Chagas FO, Caraballo-Rodriguez AM, Paixão Melo WG da, Nascimento AM do, Cavalcanti BC, Moraes MO de, Pessoa C, Costa-Lotufo LV, Krogh R, Andricopulo AD, Lopes NP, Pupo MT. Endophytic actinobacteria from the brazilian medicinal plant lychnophora ericoides MART. and the biological potential of their secondary metabolites [Internet]. Chemistry and Biodiversity. 2016 ; 13( 6): 727-736.[citado 2024 set. 19 ] Available from: https://doi.org/10.1002/cbdv.201500225
Vancouver
Conti R, Chagas FO, Caraballo-Rodriguez AM, Paixão Melo WG da, Nascimento AM do, Cavalcanti BC, Moraes MO de, Pessoa C, Costa-Lotufo LV, Krogh R, Andricopulo AD, Lopes NP, Pupo MT. Endophytic actinobacteria from the brazilian medicinal plant lychnophora ericoides MART. and the biological potential of their secondary metabolites [Internet]. Chemistry and Biodiversity. 2016 ; 13( 6): 727-736.[citado 2024 set. 19 ] Available from: https://doi.org/10.1002/cbdv.201500225

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