ReP USP - Resultado da busca

Trabalho de evento-resumo
Synthesis and docking study for compounds analogs of LSD1 inhibitor (2019)
Lima, Elys Juliane Cardoso; Maltarollo, Vinícius Gonçalves ; Ganesan, Arasu; Emery, Flavio da Silva ; Wünsch, B; Trossini, Gustavo Henrique Goulart
Source: Abstracts. Conference titles: Brazilian Symposium on Medicinal Chemistry - BrazMedChem. Unidades: FCFRP, FCF
Subjects: NEOPLASIAS, COMPOSTOS HETEROCÍCLICOS
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ABNT
LIMA, Elys Juliane Cardoso et al. Synthesis and docking study for compounds analogs of LSD1 inhibitor. 2019, Anais.. Campinas: Galoá, 2019. Disponível em: https://proceedings.science/brazmed-chem-2019/trabajos. Acesso em: 30 maio 2024.
APA
Lima, E. J. C., Maltarollo, V. G., Ganesan, A., Emery, F. da S., Wünsch, B., & Trossini, G. H. G. (2019). Synthesis and docking study for compounds analogs of LSD1 inhibitor. In Abstracts. Campinas: Galoá. Recuperado de https://proceedings.science/brazmed-chem-2019/trabajos
NLM
Lima EJC, Maltarollo VG, Ganesan A, Emery F da S, Wünsch B, Trossini GHG. Synthesis and docking study for compounds analogs of LSD1 inhibitor [Internet]. Abstracts. 2019 ;[citado 2024 maio 30 ] Available from: https://proceedings.science/brazmed-chem-2019/trabajos
Vancouver
Lima EJC, Maltarollo VG, Ganesan A, Emery F da S, Wünsch B, Trossini GHG. Synthesis and docking study for compounds analogs of LSD1 inhibitor [Internet]. Abstracts. 2019 ;[citado 2024 maio 30 ] Available from: https://proceedings.science/brazmed-chem-2019/trabajos
Trabalho de evento-resumo
Evaluation of nitroheterocyclics compounds against intracellular amastigotes of Leishmania infantum (2019)
Braz, Carolina Arruda; Tavares, Leoberto Costa ; Ozaki, Christiane Yumi; Lindoso, José Angelo Lauletta
Source: Abstracts. Conference titles: Brazilian Symposium on Medicinal Chemistry - BrazMedChem. Unidades: FCF, IMT, FM
Subjects: COMPOSTOS HETEROCÍCLICOS, LEISHMANIA INFANTUM
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ABNT
BRAZ, Carolina Arruda et al. Evaluation of nitroheterocyclics compounds against intracellular amastigotes of Leishmania infantum. 2019, Anais.. Campinas: Galoá, 2019. Disponível em: https://proceedings.science/brazmed-chem-2019/trabajos. Acesso em: 30 maio 2024.
APA
Braz, C. A., Tavares, L. C., Ozaki, C. Y., & Lindoso, J. A. L. (2019). Evaluation of nitroheterocyclics compounds against intracellular amastigotes of Leishmania infantum. In Abstracts. Campinas: Galoá. Recuperado de https://proceedings.science/brazmed-chem-2019/trabajos
NLM
Braz CA, Tavares LC, Ozaki CY, Lindoso JAL. Evaluation of nitroheterocyclics compounds against intracellular amastigotes of Leishmania infantum [Internet]. Abstracts. 2019 ;[citado 2024 maio 30 ] Available from: https://proceedings.science/brazmed-chem-2019/trabajos
Vancouver
Braz CA, Tavares LC, Ozaki CY, Lindoso JAL. Evaluation of nitroheterocyclics compounds against intracellular amastigotes of Leishmania infantum [Internet]. Abstracts. 2019 ;[citado 2024 maio 30 ] Available from: https://proceedings.science/brazmed-chem-2019/trabajos
Trabalho de evento-resumo
Antitrypanosomal aminobenzimidazoles: hit to lead expansion of new chemical entities against Trypanosoma cruzi and Leishmania infantum (2019)
Ferreira, R. A. A.; Oliveira Junior, C. R.; Martinez, P. G.; Soares, B. M.; Koovits, P.; Duarte, Simone Michelan; Andricopulo, Renata Krogh; Ferreira, Leonardo Luiz Gomes; Chelucci, Rafael Consolin; Magalhães, Luma Godoy; Andricopulo, Adriano Defini ; Mowbray, C. E.; Kratz, J. M.; Dias, L. C.
Source: Anais eletrônicos. Conference titles: Brazilian Symposium on Medicinal Chemistry - BrazMedChem. Unidade: IFSC
Subjects: TRYPANOSOMA CRUZI, LEISHMANIA INFANTUM, PLANEJAMENTO DE FÁRMACOS
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ABNT
FERREIRA, R. A. A. et al. Antitrypanosomal aminobenzimidazoles: hit to lead expansion of new chemical entities against Trypanosoma cruzi and Leishmania infantum. 2019, Anais.. Campinas: Galoá, 2019. Disponível em: https://proceedings.science/p/107147. Acesso em: 30 maio 2024.
APA
Ferreira, R. A. A., Oliveira Junior, C. R., Martinez, P. G., Soares, B. M., Koovits, P., Duarte, S. M., et al. (2019). Antitrypanosomal aminobenzimidazoles: hit to lead expansion of new chemical entities against Trypanosoma cruzi and Leishmania infantum. In Anais eletrônicos. Campinas: Galoá. Recuperado de https://proceedings.science/p/107147
NLM
Ferreira RAA, Oliveira Junior CR, Martinez PG, Soares BM, Koovits P, Duarte SM, Andricopulo RK, Ferreira LLG, Chelucci RC, Magalhães LG, Andricopulo AD, Mowbray CE, Kratz JM, Dias LC. Antitrypanosomal aminobenzimidazoles: hit to lead expansion of new chemical entities against Trypanosoma cruzi and Leishmania infantum [Internet]. Anais eletrônicos. 2019 ;[citado 2024 maio 30 ] Available from: https://proceedings.science/p/107147
Vancouver
Ferreira RAA, Oliveira Junior CR, Martinez PG, Soares BM, Koovits P, Duarte SM, Andricopulo RK, Ferreira LLG, Chelucci RC, Magalhães LG, Andricopulo AD, Mowbray CE, Kratz JM, Dias LC. Antitrypanosomal aminobenzimidazoles: hit to lead expansion of new chemical entities against Trypanosoma cruzi and Leishmania infantum [Internet]. Anais eletrônicos. 2019 ;[citado 2024 maio 30 ] Available from: https://proceedings.science/p/107147
Trabalho de evento-resumo
Discovery of 1,2,4-oxadiazole derivatives as a novel class of inhibitors of 3-hydroxykynurenine transaminase (HKT) from Aedes aegypti (2019)
Maciel, Larissa G.; Oliveira, Andrew Albert de; Romão, Tatiany P.; Leal, Laylla L. L.; Guido, Rafael Victorio Carvalho ; Silva Filha, Maria Helena N. L.; Anjos, Janaína V.; Soares, Thereza A.
Source: Anais eletrônicos. Conference titles: Brazilian Symposium on Medicinal Chemistry - BrazMedChem. Unidade: IFSC
Subjects: AEDES, EXPRESSÃO GÊNICA, LARVICIDAS
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ABNT
MACIEL, Larissa G. et al. Discovery of 1,2,4-oxadiazole derivatives as a novel class of inhibitors of 3-hydroxykynurenine transaminase (HKT) from Aedes aegypti. 2019, Anais.. Campinas: Galoá, 2019. Disponível em: https://proceedings.science/p/107216. Acesso em: 30 maio 2024.
APA
Maciel, L. G., Oliveira, A. A. de, Romão, T. P., Leal, L. L. L., Guido, R. V. C., Silva Filha, M. H. N. L., et al. (2019). Discovery of 1,2,4-oxadiazole derivatives as a novel class of inhibitors of 3-hydroxykynurenine transaminase (HKT) from Aedes aegypti. In Anais eletrônicos. Campinas: Galoá. Recuperado de https://proceedings.science/p/107216
NLM
Maciel LG, Oliveira AA de, Romão TP, Leal LLL, Guido RVC, Silva Filha MHNL, Anjos JV, Soares TA. Discovery of 1,2,4-oxadiazole derivatives as a novel class of inhibitors of 3-hydroxykynurenine transaminase (HKT) from Aedes aegypti [Internet]. Anais eletrônicos. 2019 ;[citado 2024 maio 30 ] Available from: https://proceedings.science/p/107216
Vancouver
Maciel LG, Oliveira AA de, Romão TP, Leal LLL, Guido RVC, Silva Filha MHNL, Anjos JV, Soares TA. Discovery of 1,2,4-oxadiazole derivatives as a novel class of inhibitors of 3-hydroxykynurenine transaminase (HKT) from Aedes aegypti [Internet]. Anais eletrônicos. 2019 ;[citado 2024 maio 30 ] Available from: https://proceedings.science/p/107216
Trabalho de evento-resumo
Hybridization approach for drug design in anti-leishmanial cinnamoylhydrazones (2019)
Gatti, Fernando de Moura; Heleno, R. A.; Ferreira, Leonardo Luiz Gomes; Andricopulo, Adriano Defini ; Trossini, Gustavo Henrique Goulart
Source: Anais eletrônicos. Conference titles: Brazilian Symposium on Medicinal Chemistry - BrazMedChem. Unidades: IFSC, FCF
Subjects: LEISHMANIA, HIBRIDIZAÇÃO, PLANEJAMENTO DE FÁRMACOS
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ABNT
GATTI, Fernando de Moura et al. Hybridization approach for drug design in anti-leishmanial cinnamoylhydrazones. 2019, Anais.. Campinas: Galoá, 2019. Disponível em: https://proceedings.science/p/107204. Acesso em: 30 maio 2024.
APA
Gatti, F. de M., Heleno, R. A., Ferreira, L. L. G., Andricopulo, A. D., & Trossini, G. H. G. (2019). Hybridization approach for drug design in anti-leishmanial cinnamoylhydrazones. In Anais eletrônicos. Campinas: Galoá. Recuperado de https://proceedings.science/p/107204
NLM
Gatti F de M, Heleno RA, Ferreira LLG, Andricopulo AD, Trossini GHG. Hybridization approach for drug design in anti-leishmanial cinnamoylhydrazones [Internet]. Anais eletrônicos. 2019 ;[citado 2024 maio 30 ] Available from: https://proceedings.science/p/107204
Vancouver
Gatti F de M, Heleno RA, Ferreira LLG, Andricopulo AD, Trossini GHG. Hybridization approach for drug design in anti-leishmanial cinnamoylhydrazones [Internet]. Anais eletrônicos. 2019 ;[citado 2024 maio 30 ] Available from: https://proceedings.science/p/107204
Trabalho de evento-resumo
Carbamoylimidazoles as potent cruzain inhibitors with in vitro and in vivo trypanocidal activity: a structure-based drug design approach (2019)
Rezende Junior, Celso; Souza, Mariana L.; Chavez, Rocio; Ferreira, Rafaela S.; Slafer, Brian W.; Cruz, Fábio C.; Ferreira, Leonardo Luiz Gomes; Magalhães, Luma Godoy; Andricopulo, Renata Krogh; Oliva, Glaucius ; Andricopulo, Adriano Defini ; Dias, Luiz C.
Source: Anais eletrônicos. Conference titles: Brazilian Symposium on Medicinal Chemistry - BrazMedChem. Unidade: IFSC
Subjects: DOENÇA DE CHAGAS, TRYPANOSOMA CRUZI, PLANEJAMENTO DE FÁRMACOS
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ABNT
REZENDE JUNIOR, Celso et al. Carbamoylimidazoles as potent cruzain inhibitors with in vitro and in vivo trypanocidal activity: a structure-based drug design approach. 2019, Anais.. Campinas: Galoá, 2019. Disponível em: https://proceedings.science/p/107156. Acesso em: 30 maio 2024.
APA
Rezende Junior, C., Souza, M. L., Chavez, R., Ferreira, R. S., Slafer, B. W., Cruz, F. C., et al. (2019). Carbamoylimidazoles as potent cruzain inhibitors with in vitro and in vivo trypanocidal activity: a structure-based drug design approach. In Anais eletrônicos. Campinas: Galoá. Recuperado de https://proceedings.science/p/107156
NLM
Rezende Junior C, Souza ML, Chavez R, Ferreira RS, Slafer BW, Cruz FC, Ferreira LLG, Magalhães LG, Andricopulo RK, Oliva G, Andricopulo AD, Dias LC. Carbamoylimidazoles as potent cruzain inhibitors with in vitro and in vivo trypanocidal activity: a structure-based drug design approach [Internet]. Anais eletrônicos. 2019 ;[citado 2024 maio 30 ] Available from: https://proceedings.science/p/107156
Vancouver
Rezende Junior C, Souza ML, Chavez R, Ferreira RS, Slafer BW, Cruz FC, Ferreira LLG, Magalhães LG, Andricopulo RK, Oliva G, Andricopulo AD, Dias LC. Carbamoylimidazoles as potent cruzain inhibitors with in vitro and in vivo trypanocidal activity: a structure-based drug design approach [Internet]. Anais eletrônicos. 2019 ;[citado 2024 maio 30 ] Available from: https://proceedings.science/p/107156
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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ABNT
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: 30 maio 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 maio 30 ] 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 maio 30 ] Available from: https://proceedings.science/p/107173
Trabalho de evento-resumo
Discovery of new Zika virus candidates: natural products from Angelica keiskei with activity against NS2B-NS3 protease (2019)
Sousa, Bruna K. P.; Mottin, Melina; Brodsky, David; Caesar, Lindsay; Mesquita, Nathalya Cristina de Moraes Roso; Zorn, Kimberley M.; Cech, Nadja; Oliva, Glaucius ; Ekins, Sean; Laster, Scott; Andrade, Carolina Horta
Source: Anais eletrônicos. Conference titles: Brazilian Symposium on Medicinal Chemistry - BrazMedChem. Unidade: IFSC
Subjects: ZIKA VÍRUS, PRODUTOS NATURAIS, ENZIMAS
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ABNT
SOUSA, Bruna K. P. et al. Discovery of new Zika virus candidates: natural products from Angelica keiskei with activity against NS2B-NS3 protease. 2019, Anais.. Campinas: Galoá, 2019. Disponível em: https://proceedings.science/p/107235. Acesso em: 30 maio 2024.
APA
Sousa, B. K. P., Mottin, M., Brodsky, D., Caesar, L., Mesquita, N. C. de M. R., Zorn, K. M., et al. (2019). Discovery of new Zika virus candidates: natural products from Angelica keiskei with activity against NS2B-NS3 protease. In Anais eletrônicos. Campinas: Galoá. Recuperado de https://proceedings.science/p/107235
NLM
Sousa BKP, Mottin M, Brodsky D, Caesar L, Mesquita NC de MR, Zorn KM, Cech N, Oliva G, Ekins S, Laster S, Andrade CH. Discovery of new Zika virus candidates: natural products from Angelica keiskei with activity against NS2B-NS3 protease [Internet]. Anais eletrônicos. 2019 ;[citado 2024 maio 30 ] Available from: https://proceedings.science/p/107235
Vancouver
Sousa BKP, Mottin M, Brodsky D, Caesar L, Mesquita NC de MR, Zorn KM, Cech N, Oliva G, Ekins S, Laster S, Andrade CH. Discovery of new Zika virus candidates: natural products from Angelica keiskei with activity against NS2B-NS3 protease [Internet]. Anais eletrônicos. 2019 ;[citado 2024 maio 30 ] Available from: https://proceedings.science/p/107235
Trabalho de evento-resumo
Structure-activity relationships of new Schiff bases derived from diaminomaleonitrile as new agents for the treatment of Chagas disease (2019)
Salcedo, David Leandro Palomino; Oliveira, Aldo Sena de; Mello, Lucas dos Santos; Cruz Junior, José Wilmo da; Dockal, Edward Ralph; Andricopulo, Adriano Defini
Source: Anais eletrônicos. Conference titles: Brazilian Symposium on Medicinal Chemistry - BrazMedChem. Unidade: IFSC
Subjects: TRYPANOSOMA CRUZI, DOENÇA DE CHAGAS, PLANEJAMENTO DE FÁRMACOS
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ABNT
SALCEDO, David Leandro Palomino et al. Structure-activity relationships of new Schiff bases derived from diaminomaleonitrile as new agents for the treatment of Chagas disease. 2019, Anais.. Campinas: Galoá, 2019. Disponível em: https://proceedings.science/p/107073. Acesso em: 30 maio 2024.
APA
Salcedo, D. L. P., Oliveira, A. S. de, Mello, L. dos S., Cruz Junior, J. W. da, Dockal, E. R., & Andricopulo, A. D. (2019). Structure-activity relationships of new Schiff bases derived from diaminomaleonitrile as new agents for the treatment of Chagas disease. In Anais eletrônicos. Campinas: Galoá. Recuperado de https://proceedings.science/p/107073
NLM
Salcedo DLP, Oliveira AS de, Mello L dos S, Cruz Junior JW da, Dockal ER, Andricopulo AD. Structure-activity relationships of new Schiff bases derived from diaminomaleonitrile as new agents for the treatment of Chagas disease [Internet]. Anais eletrônicos. 2019 ;[citado 2024 maio 30 ] Available from: https://proceedings.science/p/107073
Vancouver
Salcedo DLP, Oliveira AS de, Mello L dos S, Cruz Junior JW da, Dockal ER, Andricopulo AD. Structure-activity relationships of new Schiff bases derived from diaminomaleonitrile as new agents for the treatment of Chagas disease [Internet]. Anais eletrônicos. 2019 ;[citado 2024 maio 30 ] Available from: https://proceedings.science/p/107073

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