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Trabalho de evento-resumo
Synthesis and antimalarial activity of 4-(m-piperazin-1-yl)phenyl marinoquinolines and thieno[2,3-c]quinolines: a structure-activity relationship study (2022)
Trajano, Bruna Inacio; Souza, Guilherme Eduardo de; Guido, Rafael Victorio Carvalho ; Correia, Carlos Roque
Source: Anais eletrônicos. Conference titles: Brazilian Symposium on Medicinal Chemistry - BrazMedChem. Unidade: IFSC
Subjects: MALÁRIA, ANTIMALÁRICOS, ANTIPARASITÁRIOS
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ABNT
TRAJANO, Bruna Inacio et al. Synthesis and antimalarial activity of 4-(m-piperazin-1-yl)phenyl marinoquinolines and thieno[2,3-c]quinolines: a structure-activity relationship study. 2022, Anais.. Campinas: Galoá, 2022. Disponível em: https://proceedings.science/brazmedchem-2022/papers/synthesis-and-antimalarial-activity-of-4--m-piperazin-1-yl-phenyl-marinoquinolines-and-thieno-2-3-c-quinolines--a-struct. Acesso em: 04 nov. 2024.
APA
Trajano, B. I., Souza, G. E. de, Guido, R. V. C., & Correia, C. R. (2022). Synthesis and antimalarial activity of 4-(m-piperazin-1-yl)phenyl marinoquinolines and thieno[2,3-c]quinolines: a structure-activity relationship study. In Anais eletrônicos. Campinas: Galoá. Recuperado de https://proceedings.science/brazmedchem-2022/papers/synthesis-and-antimalarial-activity-of-4--m-piperazin-1-yl-phenyl-marinoquinolines-and-thieno-2-3-c-quinolines--a-struct.
NLM
Trajano BI, Souza GE de, Guido RVC, Correia CR. Synthesis and antimalarial activity of 4-(m-piperazin-1-yl)phenyl marinoquinolines and thieno[2,3-c]quinolines: a structure-activity relationship study [Internet]. Anais eletrônicos. 2022 ;[citado 2024 nov. 04 ] Available from: https://proceedings.science/brazmedchem-2022/papers/synthesis-and-antimalarial-activity-of-4--m-piperazin-1-yl-phenyl-marinoquinolines-and-thieno-2-3-c-quinolines--a-struct.
Vancouver
Trajano BI, Souza GE de, Guido RVC, Correia CR. Synthesis and antimalarial activity of 4-(m-piperazin-1-yl)phenyl marinoquinolines and thieno[2,3-c]quinolines: a structure-activity relationship study [Internet]. Anais eletrônicos. 2022 ;[citado 2024 nov. 04 ] Available from: https://proceedings.science/brazmedchem-2022/papers/synthesis-and-antimalarial-activity-of-4--m-piperazin-1-yl-phenyl-marinoquinolines-and-thieno-2-3-c-quinolines--a-struct.
Artigo de periodico
Approaches to advance drug discovery for neglected tropical diseases (2022)
Ferreira, Leonardo Luiz Gomes ; Moraes, Josué de; Andricopulo, Adriano Defini
Source: Drug Discovery Today. Unidade: IFSC
Subjects: QUÍMICA MÉDICA, SCHISTOSOMA, PLANEJAMENTO DE FÁRMACOS, DOENÇAS NEGLIGENCIADAS, ANTIPARASITÁRIOS, DOENÇA DE CHAGAS, LEISHMANIA INFANTUM, MODELAGEM MOLECULAR
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ABNT
FERREIRA, Leonardo Luiz Gomes e MORAES, Josué de e ANDRICOPULO, Adriano Defini. Approaches to advance drug discovery for neglected tropical diseases. Drug Discovery Today, v. 27, n. 8, p. 2278-2287, 2022Tradução . . Disponível em: https://doi.org/10.1016/j.drudis.2022.04.004. Acesso em: 04 nov. 2024.
APA
Ferreira, L. L. G., Moraes, J. de, & Andricopulo, A. D. (2022). Approaches to advance drug discovery for neglected tropical diseases. Drug Discovery Today, 27( 8), 2278-2287. doi:10.1016/j.drudis.2022.04.004
NLM
Ferreira LLG, Moraes J de, Andricopulo AD. Approaches to advance drug discovery for neglected tropical diseases [Internet]. Drug Discovery Today. 2022 ; 27( 8): 2278-2287.[citado 2024 nov. 04 ] Available from: https://doi.org/10.1016/j.drudis.2022.04.004
Vancouver
Ferreira LLG, Moraes J de, Andricopulo AD. Approaches to advance drug discovery for neglected tropical diseases [Internet]. Drug Discovery Today. 2022 ; 27( 8): 2278-2287.[citado 2024 nov. 04 ] Available from: https://doi.org/10.1016/j.drudis.2022.04.004
Trabalho de evento-resumo
Ligand-based drug design studies for a series of oxazole and oxadiazole derivatives with antileishmanial activity (2022)
Teles, Henrique Rodrigues; Ferreira, Leonardo Luiz Gomes ; Valli, Marilia ; Andricopulo, Adriano Defini
Source: Anais. Conference titles: Reunião Anual da Sociedade Brasileira de Química - RASBQ. Unidade: IFSC
Subjects: ANTIPARASITÁRIOS, LEISHMANIA INFANTUM
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ABNT
TELES, Henrique Rodrigues et al. Ligand-based drug design studies for a series of oxazole and oxadiazole derivatives with antileishmanial activity. 2022, Anais.. São Paulo: Sociedade Brasileira de Química - SBQ, 2022. Disponível em: https://www.eventweb.com.br/45rasbq/specific-files/manuscripts/45rasbq/732_1650850269.pdf. Acesso em: 04 nov. 2024.
APA
Teles, H. R., Ferreira, L. L. G., Valli, M., & Andricopulo, A. D. (2022). Ligand-based drug design studies for a series of oxazole and oxadiazole derivatives with antileishmanial activity. In Anais. São Paulo: Sociedade Brasileira de Química - SBQ. Recuperado de https://www.eventweb.com.br/45rasbq/specific-files/manuscripts/45rasbq/732_1650850269.pdf
NLM
Teles HR, Ferreira LLG, Valli M, Andricopulo AD. Ligand-based drug design studies for a series of oxazole and oxadiazole derivatives with antileishmanial activity [Internet]. Anais. 2022 ;[citado 2024 nov. 04 ] Available from: https://www.eventweb.com.br/45rasbq/specific-files/manuscripts/45rasbq/732_1650850269.pdf
Vancouver
Teles HR, Ferreira LLG, Valli M, Andricopulo AD. Ligand-based drug design studies for a series of oxazole and oxadiazole derivatives with antileishmanial activity [Internet]. Anais. 2022 ;[citado 2024 nov. 04 ] Available from: https://www.eventweb.com.br/45rasbq/specific-files/manuscripts/45rasbq/732_1650850269.pdf
Artigo de periodico
Hierarchical clustering and target-independent QSAR for antileishmanial oxazole and oxadiazole derivatives (2022)
Teles, Henrique Rodrigues; Ferreira, Leonardo Luiz Gomes ; Valli, Marilia ; Coelho, Fernando; Andricopulo, Adriano Defini
Source: International Journal of Molecular Sciences. Unidade: IFSC
Subjects: ANTIPARASITÁRIOS, LEISHMANIA INFANTUM
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ABNT
TELES, Henrique Rodrigues et al. Hierarchical clustering and target-independent QSAR for antileishmanial oxazole and oxadiazole derivatives. International Journal of Molecular Sciences, v. 23, n. 16, p. 8898-1-8898-16, 2022Tradução . . Disponível em: https://doi.org/10.3390/ijms23168898. Acesso em: 04 nov. 2024.
APA
Teles, H. R., Ferreira, L. L. G., Valli, M., Coelho, F., & Andricopulo, A. D. (2022). Hierarchical clustering and target-independent QSAR for antileishmanial oxazole and oxadiazole derivatives. International Journal of Molecular Sciences, 23( 16), 8898-1-8898-16. doi:10.3390/ijms23168898
NLM
Teles HR, Ferreira LLG, Valli M, Coelho F, Andricopulo AD. Hierarchical clustering and target-independent QSAR for antileishmanial oxazole and oxadiazole derivatives [Internet]. International Journal of Molecular Sciences. 2022 ; 23( 16): 8898-1-8898-16.[citado 2024 nov. 04 ] Available from: https://doi.org/10.3390/ijms23168898
Vancouver
Teles HR, Ferreira LLG, Valli M, Coelho F, Andricopulo AD. Hierarchical clustering and target-independent QSAR for antileishmanial oxazole and oxadiazole derivatives [Internet]. International Journal of Molecular Sciences. 2022 ; 23( 16): 8898-1-8898-16.[citado 2024 nov. 04 ] Available from: https://doi.org/10.3390/ijms23168898
Artigo de periodico
Preclinical characterization and target validation of the antimalarial pantothenamide MMV693183 (2022)
Vries, Laura E. ; Aguiar, Anna Caroline Campos ; Guido, Rafael Victorio Carvalho
Source: Nature Communications. Unidade: IFSC
Subjects: PLASMODIUM FALCIPARUM, PLANEJAMENTO DE FÁRMACOS, ANTIPARASITÁRIOS, MALÁRIA
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ABNT
VRIES, Laura E. e AGUIAR, Anna Caroline Campos e GUIDO, Rafael Victorio Carvalho. Preclinical characterization and target validation of the antimalarial pantothenamide MMV693183. Nature Communications, v. 13, p. 2158-1-2158-16, 2022Tradução . . Disponível em: https://doi.org/10.1038/s41467-022-29688-5. Acesso em: 04 nov. 2024.
APA
Vries, L. E., Aguiar, A. C. C., & Guido, R. V. C. (2022). Preclinical characterization and target validation of the antimalarial pantothenamide MMV693183. Nature Communications, 13, 2158-1-2158-16. doi:10.1038/s41467-022-29688-5
NLM
Vries LE, Aguiar ACC, Guido RVC. Preclinical characterization and target validation of the antimalarial pantothenamide MMV693183 [Internet]. Nature Communications. 2022 ; 13 2158-1-2158-16.[citado 2024 nov. 04 ] Available from: https://doi.org/10.1038/s41467-022-29688-5
Vancouver
Vries LE, Aguiar ACC, Guido RVC. Preclinical characterization and target validation of the antimalarial pantothenamide MMV693183 [Internet]. Nature Communications. 2022 ; 13 2158-1-2158-16.[citado 2024 nov. 04 ] Available from: https://doi.org/10.1038/s41467-022-29688-5
Artigo de periodico
Potent antimalarials with development potential identified by structure-guided computational optimization of a pyrrole-based dihydroorotate dehydrogenase inhibitor series (2021)
Palmer, Michael J.; Aguiar, Anna Caroline Campos; Guido, Rafael Victorio Carvalho
Source: Journal of Medicinal Chemistry. Unidade: IFSC
Subjects: ANTIMALÁRICOS, PLASMODIUM FALCIPARUM, PLANEJAMENTO DE FÁRMACOS, ANTIPARASITÁRIOS, MALÁRIA, BIOQUÍMICA, QUÍMICA MÉDICA
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ABNT
PALMER, Michael J. e AGUIAR, Anna Caroline Campos e GUIDO, Rafael Victorio Carvalho. Potent antimalarials with development potential identified by structure-guided computational optimization of a pyrrole-based dihydroorotate dehydrogenase inhibitor series. Journal of Medicinal Chemistry, v. 64, n. 9, p. 6085-6136, 2021Tradução . . Disponível em: https://doi.org/10.1021/acs.jmedchem.1c00173. Acesso em: 04 nov. 2024.
APA
Palmer, M. J., Aguiar, A. C. C., & Guido, R. V. C. (2021). Potent antimalarials with development potential identified by structure-guided computational optimization of a pyrrole-based dihydroorotate dehydrogenase inhibitor series. Journal of Medicinal Chemistry, 64( 9), 6085-6136. doi:10.1021/acs.jmedchem.1c00173
NLM
Palmer MJ, Aguiar ACC, Guido RVC. Potent antimalarials with development potential identified by structure-guided computational optimization of a pyrrole-based dihydroorotate dehydrogenase inhibitor series [Internet]. Journal of Medicinal Chemistry. 2021 ; 64( 9): 6085-6136.[citado 2024 nov. 04 ] Available from: https://doi.org/10.1021/acs.jmedchem.1c00173
Vancouver
Palmer MJ, Aguiar ACC, Guido RVC. Potent antimalarials with development potential identified by structure-guided computational optimization of a pyrrole-based dihydroorotate dehydrogenase inhibitor series [Internet]. Journal of Medicinal Chemistry. 2021 ; 64( 9): 6085-6136.[citado 2024 nov. 04 ] Available from: https://doi.org/10.1021/acs.jmedchem.1c00173
Artigo de periodico
Repositioning and characterization of 1‑(Pyridin-4-yl)pyrrolidin-2- one derivatives as plasmodium cytoplasmic prolyl-tRNA synthetase inhibitors (2021)
Okaniwa, Masanori; Aguiar, Anna Caroline Campos; Guido, Rafael Victorio Carvalho
Source: ACS Infectious Diseases. Unidade: IFSC
Subjects: PLASMODIUM, MALÁRIA, ANTIMALÁRICOS, ANTIPARASITÁRIOS
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ABNT
OKANIWA, Masanori e AGUIAR, Anna Caroline Campos e GUIDO, Rafael Victorio Carvalho. Repositioning and characterization of 1‑(Pyridin-4-yl)pyrrolidin-2- one derivatives as plasmodium cytoplasmic prolyl-tRNA synthetase inhibitors. ACS Infectious Diseases, v. 7, n. 6, p. 1680-1689, 2021Tradução . . Disponível em: https://doi.org/10.1021/acsinfecdis.1c00020. Acesso em: 04 nov. 2024.
APA
Okaniwa, M., Aguiar, A. C. C., & Guido, R. V. C. (2021). Repositioning and characterization of 1‑(Pyridin-4-yl)pyrrolidin-2- one derivatives as plasmodium cytoplasmic prolyl-tRNA synthetase inhibitors. ACS Infectious Diseases, 7( 6), 1680-1689. doi:10.1021/acsinfecdis.1c00020
NLM
Okaniwa M, Aguiar ACC, Guido RVC. Repositioning and characterization of 1‑(Pyridin-4-yl)pyrrolidin-2- one derivatives as plasmodium cytoplasmic prolyl-tRNA synthetase inhibitors [Internet]. ACS Infectious Diseases. 2021 ; 7( 6): 1680-1689.[citado 2024 nov. 04 ] Available from: https://doi.org/10.1021/acsinfecdis.1c00020
Vancouver
Okaniwa M, Aguiar ACC, Guido RVC. Repositioning and characterization of 1‑(Pyridin-4-yl)pyrrolidin-2- one derivatives as plasmodium cytoplasmic prolyl-tRNA synthetase inhibitors [Internet]. ACS Infectious Diseases. 2021 ; 7( 6): 1680-1689.[citado 2024 nov. 04 ] Available from: https://doi.org/10.1021/acsinfecdis.1c00020
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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ABNT
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: 04 nov. 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 nov. 04 ] 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 nov. 04 ] 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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ABNT
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: 04 nov. 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 nov. 04 ] 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 nov. 04 ] Available from: https://doi.org/10.1016/j.ejmcr.2021.100012
Artigo de periodico
Comparative study between the anti-P. falciparum activity of triazolopyrimidine, pyrazolopyrimidine and quinoline derivatives and the identification of new PfDHODH inhibitors (2021)
Silveira, Flávia F.; Souza, Juliana Oliveira de; Hoelz, Lucas V. B.; Campos, Vinícius R.; Jabor, Valquíria Aparecida Polisel; Aguiar, Anna Caroline Campos; Nonato, Maria Cristina ; Albuquerque, Magaly G. ; Guido, Rafael Victorio Carvalho ; Boechat, Nubia; Pinheiro, Luiz C. S.
Source: European Journal of Medicinal Chemistry. Unidades: IFSC, FCFRP
Subjects: ANTIMALÁRICOS, ANTIPARASITÁRIOS, MALÁRIA
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ABNT
SILVEIRA, Flávia F. et al. Comparative study between the anti-P. falciparum activity of triazolopyrimidine, pyrazolopyrimidine and quinoline derivatives and the identification of new PfDHODH inhibitors. European Journal of Medicinal Chemistry, v. 209, n. Ja 2021, p. 112941-1-112941-16, 2021Tradução . . Disponível em: https://doi.org/10.1016/j.ejmech.2020.112941. Acesso em: 04 nov. 2024.
APA
Silveira, F. F., Souza, J. O. de, Hoelz, L. V. B., Campos, V. R., Jabor, V. A. P., Aguiar, A. C. C., et al. (2021). Comparative study between the anti-P. falciparum activity of triazolopyrimidine, pyrazolopyrimidine and quinoline derivatives and the identification of new PfDHODH inhibitors. European Journal of Medicinal Chemistry, 209( Ja 2021), 112941-1-112941-16. doi:10.1016/j.ejmech.2020.112941
NLM
Silveira FF, Souza JO de, Hoelz LVB, Campos VR, Jabor VAP, Aguiar ACC, Nonato MC, Albuquerque MG, Guido RVC, Boechat N, Pinheiro LCS. Comparative study between the anti-P. falciparum activity of triazolopyrimidine, pyrazolopyrimidine and quinoline derivatives and the identification of new PfDHODH inhibitors [Internet]. European Journal of Medicinal Chemistry. 2021 ; 209( Ja 2021): 112941-1-112941-16.[citado 2024 nov. 04 ] Available from: https://doi.org/10.1016/j.ejmech.2020.112941
Vancouver
Silveira FF, Souza JO de, Hoelz LVB, Campos VR, Jabor VAP, Aguiar ACC, Nonato MC, Albuquerque MG, Guido RVC, Boechat N, Pinheiro LCS. Comparative study between the anti-P. falciparum activity of triazolopyrimidine, pyrazolopyrimidine and quinoline derivatives and the identification of new PfDHODH inhibitors [Internet]. European Journal of Medicinal Chemistry. 2021 ; 209( Ja 2021): 112941-1-112941-16.[citado 2024 nov. 04 ] Available from: https://doi.org/10.1016/j.ejmech.2020.112941
Trabalho de evento-resumo
Syntesis [i. e. synthesis] of new hydrazones triazololopyrimidines derivatives as antiplasmodium agents (2020)
Gandi, Marilia O.; Carvalho, Alcione S.; Souza, Juliana Oliveira de; Aguiar, Anna Caroline Campos; Guido, Rafael Victorio Carvalho ; Boechat, Núbia
Source: Anais. Conference titles: Reunião Anual Virtual da Sociedade Brasileira de Química - RASBQ. Unidade: IFSC
Subjects: ANTIMALÁRICOS, ANTIPARASITÁRIOS, MALÁRIA
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ABNT
GANDI, Marilia O. et al. Syntesis [i. e. synthesis] of new hydrazones triazololopyrimidines derivatives as antiplasmodium agents. 2020, Anais.. Campinas: Galoá, 2020. Disponível em: https://proceedings.science/rasbq-2020/papers/syntesis-of-new-hydrazones-triazolopyrimidines-derivatives-as-anti-plasmodium-agents. Acesso em: 04 nov. 2024.
APA
Gandi, M. O., Carvalho, A. S., Souza, J. O. de, Aguiar, A. C. C., Guido, R. V. C., & Boechat, N. (2020). Syntesis [i. e. synthesis] of new hydrazones triazololopyrimidines derivatives as antiplasmodium agents. In Anais. Campinas: Galoá. Recuperado de https://proceedings.science/rasbq-2020/papers/syntesis-of-new-hydrazones-triazolopyrimidines-derivatives-as-anti-plasmodium-agents
NLM
Gandi MO, Carvalho AS, Souza JO de, Aguiar ACC, Guido RVC, Boechat N. Syntesis [i. e. synthesis] of new hydrazones triazololopyrimidines derivatives as antiplasmodium agents [Internet]. Anais. 2020 ;[citado 2024 nov. 04 ] Available from: https://proceedings.science/rasbq-2020/papers/syntesis-of-new-hydrazones-triazolopyrimidines-derivatives-as-anti-plasmodium-agents
Vancouver
Gandi MO, Carvalho AS, Souza JO de, Aguiar ACC, Guido RVC, Boechat N. Syntesis [i. e. synthesis] of new hydrazones triazololopyrimidines derivatives as antiplasmodium agents [Internet]. Anais. 2020 ;[citado 2024 nov. 04 ] Available from: https://proceedings.science/rasbq-2020/papers/syntesis-of-new-hydrazones-triazolopyrimidines-derivatives-as-anti-plasmodium-agents
Trabalho de evento-resumo
New pyrazolopyrimidine and triazolopyrimidine derivatives with potential activity anti-P. falciparum (2020)
Feitosa, Lívia M.; Machado, Gustavo P.; Araujo, Gabriel M. S.; Ferreira, Maria de Lourdes G.; Oliveira, Larissa G.; Pinheiro, Luiz C. S.; Souza, Juliana Oliveira de; Aguiar, Anna Caroline Campos; Guido, Rafael Victorio Carvalho ; Boechat, Núbia
Source: Anais. Conference titles: Reunião Anual Virtual da Sociedade Brasileira de Química - RASBQ. Unidade: IFSC
Subjects: ANTIMALÁRICOS, ANTIPARASITÁRIOS, MALÁRIA
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ABNT
FEITOSA, Lívia M. et al. New pyrazolopyrimidine and triazolopyrimidine derivatives with potential activity anti-P. falciparum. 2020, Anais.. Campinas: Galoá, 2020. Disponível em: https://proceedings.science/rasbq-2020/papers/new-pyrazolopyrimidine-and-triazolopyrimidine-derivatives-with-potential-activity-anti-p--falciparum. Acesso em: 04 nov. 2024.
APA
Feitosa, L. M., Machado, G. P., Araujo, G. M. S., Ferreira, M. de L. G., Oliveira, L. G., Pinheiro, L. C. S., et al. (2020). New pyrazolopyrimidine and triazolopyrimidine derivatives with potential activity anti-P. falciparum. In Anais. Campinas: Galoá. Recuperado de https://proceedings.science/rasbq-2020/papers/new-pyrazolopyrimidine-and-triazolopyrimidine-derivatives-with-potential-activity-anti-p--falciparum
NLM
Feitosa LM, Machado GP, Araujo GMS, Ferreira M de LG, Oliveira LG, Pinheiro LCS, Souza JO de, Aguiar ACC, Guido RVC, Boechat N. New pyrazolopyrimidine and triazolopyrimidine derivatives with potential activity anti-P. falciparum [Internet]. Anais. 2020 ;[citado 2024 nov. 04 ] Available from: https://proceedings.science/rasbq-2020/papers/new-pyrazolopyrimidine-and-triazolopyrimidine-derivatives-with-potential-activity-anti-p--falciparum
Vancouver
Feitosa LM, Machado GP, Araujo GMS, Ferreira M de LG, Oliveira LG, Pinheiro LCS, Souza JO de, Aguiar ACC, Guido RVC, Boechat N. New pyrazolopyrimidine and triazolopyrimidine derivatives with potential activity anti-P. falciparum [Internet]. Anais. 2020 ;[citado 2024 nov. 04 ] Available from: https://proceedings.science/rasbq-2020/papers/new-pyrazolopyrimidine-and-triazolopyrimidine-derivatives-with-potential-activity-anti-p--falciparum
Trabalho de evento-resumo
Synthesis and evaluation of new pyridine-marinoquinolines as antimalarials (2020)
Capitão, Rebeca Monique; Espírito Santo, Rafael Dias do; Souza, Guilherme Eduardo de; Guido, Rafael Victorio Carvalho ; Correia, Carlos Roque Duarte
Source: Anais. Conference titles: Reunião Anual Virtual da Sociedade Brasileira de Química - RASBQ. Unidade: IFSC
Subjects: ANTIMALÁRICOS, ANTIPARASITÁRIOS, MALÁRIA
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
CAPITÃO, Rebeca Monique et al. Synthesis and evaluation of new pyridine-marinoquinolines as antimalarials. 2020, Anais.. Campinas: Galoá, 2020. Disponível em: https://proceedings.science/rasbq-2020/papers/synthesis-and-evaluation-of-new-pyridine-marinoquinolines-as-antimalarials. Acesso em: 04 nov. 2024.
APA
Capitão, R. M., Espírito Santo, R. D. do, Souza, G. E. de, Guido, R. V. C., & Correia, C. R. D. (2020). Synthesis and evaluation of new pyridine-marinoquinolines as antimalarials. In Anais. Campinas: Galoá. Recuperado de https://proceedings.science/rasbq-2020/papers/synthesis-and-evaluation-of-new-pyridine-marinoquinolines-as-antimalarials
NLM
Capitão RM, Espírito Santo RD do, Souza GE de, Guido RVC, Correia CRD. Synthesis and evaluation of new pyridine-marinoquinolines as antimalarials [Internet]. Anais. 2020 ;[citado 2024 nov. 04 ] Available from: https://proceedings.science/rasbq-2020/papers/synthesis-and-evaluation-of-new-pyridine-marinoquinolines-as-antimalarials
Vancouver
Capitão RM, Espírito Santo RD do, Souza GE de, Guido RVC, Correia CRD. Synthesis and evaluation of new pyridine-marinoquinolines as antimalarials [Internet]. Anais. 2020 ;[citado 2024 nov. 04 ] Available from: https://proceedings.science/rasbq-2020/papers/synthesis-and-evaluation-of-new-pyridine-marinoquinolines-as-antimalarials
Artigo de periodico
Discovery of highly potent and selective antiparasitic new oxadiazole and hydroxy-oxindole small molecule hybrids (2020)
Fernandes, Fábio S.; Santos, Hugo; Conti, Caroline; Rodrigues Junior, Manoel T.; Zeoly, Lucas A.; Ferreira, Leonardo Luiz Gomes ; Andricopulo, Renata Krogh; Andricopulo, Adriano Defini ; Coelho, Fernando
Source: European Journal of Medicinal Chemistry. Unidade: IFSC
Subjects: ANTIPARASITÁRIOS, TRYPANOSOMA CRUZI, LEISHMANIA INFANTUM, DOENÇA DE CHAGAS
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
FERNANDES, Fábio S. et al. Discovery of highly potent and selective antiparasitic new oxadiazole and hydroxy-oxindole small molecule hybrids. European Journal of Medicinal Chemistry, v. 201, p. 112418-1-112418-14, 2020Tradução . . Disponível em: https://doi.org/10.1016/j.ejmech.2020.112418. Acesso em: 04 nov. 2024.
APA
Fernandes, F. S., Santos, H., Conti, C., Rodrigues Junior, M. T., Zeoly, L. A., Ferreira, L. L. G., et al. (2020). Discovery of highly potent and selective antiparasitic new oxadiazole and hydroxy-oxindole small molecule hybrids. European Journal of Medicinal Chemistry, 201, 112418-1-112418-14. doi:10.1016/j.ejmech.2020.112418
NLM
Fernandes FS, Santos H, Conti C, Rodrigues Junior MT, Zeoly LA, Ferreira LLG, Andricopulo RK, Andricopulo AD, Coelho F. Discovery of highly potent and selective antiparasitic new oxadiazole and hydroxy-oxindole small molecule hybrids [Internet]. European Journal of Medicinal Chemistry. 2020 ; 201 112418-1-112418-14.[citado 2024 nov. 04 ] Available from: https://doi.org/10.1016/j.ejmech.2020.112418
Vancouver
Fernandes FS, Santos H, Conti C, Rodrigues Junior MT, Zeoly LA, Ferreira LLG, Andricopulo RK, Andricopulo AD, Coelho F. Discovery of highly potent and selective antiparasitic new oxadiazole and hydroxy-oxindole small molecule hybrids [Internet]. European Journal of Medicinal Chemistry. 2020 ; 201 112418-1-112418-14.[citado 2024 nov. 04 ] Available from: https://doi.org/10.1016/j.ejmech.2020.112418
Trabalho de evento-resumo
Bioisoster hybrids of N-acylhydrazone and furoxan groups: is cruzain the target for those potential anti-T. cruzi compounds? (2016)
Serafim, Ricardo A. M.; Oliveira, Tiago F.; Loureiro, Ana Paula de Melo ; Krogh, Renata; Andricopulo, Adriano Defini ; Dias, Luiz C.; Ferreira, Elizabeth Igne
Source: Full Abstracts. Conference titles: Brazilian Symposium on Medicinal Chemistry - BrazMedChem. Unidades: FCF, IFSC
Subjects: TRYPANOSOMA CRUZI, PLANEJAMENTO DE FÁRMACOS, ANTIPARASITÁRIOS
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
SERAFIM, Ricardo A. M. et al. Bioisoster hybrids of N-acylhydrazone and furoxan groups: is cruzain the target for those potential anti-T. cruzi compounds? 2016, Anais.. São Paulo: Sociedade Brasileira de Química - SBQ, 2016. Disponível em: http://brazmedchem2016.com.br/images/mcd_session.pdf. Acesso em: 04 nov. 2024.
APA
Serafim, R. A. M., Oliveira, T. F., Loureiro, A. P. de M., Krogh, R., Andricopulo, A. D., Dias, L. C., & Ferreira, E. I. (2016). Bioisoster hybrids of N-acylhydrazone and furoxan groups: is cruzain the target for those potential anti-T. cruzi compounds? In Full Abstracts. São Paulo: Sociedade Brasileira de Química - SBQ. Recuperado de http://brazmedchem2016.com.br/images/mcd_session.pdf
NLM
Serafim RAM, Oliveira TF, Loureiro AP de M, Krogh R, Andricopulo AD, Dias LC, Ferreira EI. Bioisoster hybrids of N-acylhydrazone and furoxan groups: is cruzain the target for those potential anti-T. cruzi compounds? [Internet]. Full Abstracts. 2016 ;[citado 2024 nov. 04 ] Available from: http://brazmedchem2016.com.br/images/mcd_session.pdf
Vancouver
Serafim RAM, Oliveira TF, Loureiro AP de M, Krogh R, Andricopulo AD, Dias LC, Ferreira EI. Bioisoster hybrids of N-acylhydrazone and furoxan groups: is cruzain the target for those potential anti-T. cruzi compounds? [Internet]. Full Abstracts. 2016 ;[citado 2024 nov. 04 ] Available from: http://brazmedchem2016.com.br/images/mcd_session.pdf

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