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Artigo de periodico
Interaction between diterpene icetexanes and old yellow enzymes of Leishmania braziliensis and Trypanosoma cruzi (2024)
Libardi, Silvia H ; Ahmad, Anees ; Ferreira, Francis B.; Oliveira, Ronaldo J.; Caruso, Ícaro P.; Melo, Fernando A.; Albuquerque, Sérgio de ; Cardoso, Daniel Rodrigues ; Burtoloso, Antonio Carlos Bender ; Borges, Julio Cesar
Fonte: International Journal of Biological Macromolecules. Unidades: FCFRP, IQSC
Assuntos: TRYPANOSOMA CRUZI, LEISHMANIA BRASILIENSIS, PROTOZOA, DOENÇAS NEGLIGENCIADAS
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LIBARDI, Silvia H et al. Interaction between diterpene icetexanes and old yellow enzymes of Leishmania braziliensis and Trypanosoma cruzi. International Journal of Biological Macromolecules, v. 259, p. 129192, 2024Tradução . . Disponível em: https://doi.org/10.1016/j.ijbiomac.2023.129192. Acesso em: 22 ago. 2024.
APA
Libardi, S. H., Ahmad, A., Ferreira, F. B., Oliveira, R. J., Caruso, Í. P., Melo, F. A., et al. (2024). Interaction between diterpene icetexanes and old yellow enzymes of Leishmania braziliensis and Trypanosoma cruzi. International Journal of Biological Macromolecules, 259, 129192. doi:10.1016/j.ijbiomac.2023.129192
NLM
Libardi SH, Ahmad A, Ferreira FB, Oliveira RJ, Caruso ÍP, Melo FA, Albuquerque S de, Cardoso DR, Burtoloso ACB, Borges JC. Interaction between diterpene icetexanes and old yellow enzymes of Leishmania braziliensis and Trypanosoma cruzi [Internet]. International Journal of Biological Macromolecules. 2024 ;259 129192.[citado 2024 ago. 22 ] Available from: https://doi.org/10.1016/j.ijbiomac.2023.129192
Vancouver
Libardi SH, Ahmad A, Ferreira FB, Oliveira RJ, Caruso ÍP, Melo FA, Albuquerque S de, Cardoso DR, Burtoloso ACB, Borges JC. Interaction between diterpene icetexanes and old yellow enzymes of Leishmania braziliensis and Trypanosoma cruzi [Internet]. International Journal of Biological Macromolecules. 2024 ;259 129192.[citado 2024 ago. 22 ] Available from: https://doi.org/10.1016/j.ijbiomac.2023.129192
Artigo de periodico
Ligand-based virtual screening, molecular dynamics, and biological evaluation of repurposed drugs as inhibitors of Trypanosoma cruzi proteasome (2023)
Gomes, Suzane Quintana ; Federico, Leonardo Bruno ; Silva, Guilherme Martins da ; Lopes, Carla Duque ; Albuquerque, Sérgio de ; Silva, Carlos Henrique Tomich de Paula da
Fonte: Journal of Biomolecular Structure and Dynamics. Unidades: FCFRP, FFCLRP
Assuntos: DOENÇA DE CHAGAS, TRIAGEM TOXICOLÓGICA, METODOLOGIA E TÉCNICAS DE COMPUTAÇÃO, MEDICAMENTO TÓPICO
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GOMES, Suzane Quintana et al. Ligand-based virtual screening, molecular dynamics, and biological evaluation of repurposed drugs as inhibitors of Trypanosoma cruzi proteasome. Journal of Biomolecular Structure and Dynamics, 2023Tradução . . Disponível em: https://doi.org/10.1080/07391102.2023.2182129. Acesso em: 22 ago. 2024.
APA
Gomes, S. Q., Federico, L. B., Silva, G. M. da, Lopes, C. D., Albuquerque, S. de, & Silva, C. H. T. de P. da. (2023). Ligand-based virtual screening, molecular dynamics, and biological evaluation of repurposed drugs as inhibitors of Trypanosoma cruzi proteasome. Journal of Biomolecular Structure and Dynamics. doi:10.1080/07391102.2023.2182129
NLM
Gomes SQ, Federico LB, Silva GM da, Lopes CD, Albuquerque S de, Silva CHT de P da. Ligand-based virtual screening, molecular dynamics, and biological evaluation of repurposed drugs as inhibitors of Trypanosoma cruzi proteasome [Internet]. Journal of Biomolecular Structure and Dynamics. 2023 ;[citado 2024 ago. 22 ] Available from: https://doi.org/10.1080/07391102.2023.2182129
Vancouver
Gomes SQ, Federico LB, Silva GM da, Lopes CD, Albuquerque S de, Silva CHT de P da. Ligand-based virtual screening, molecular dynamics, and biological evaluation of repurposed drugs as inhibitors of Trypanosoma cruzi proteasome [Internet]. Journal of Biomolecular Structure and Dynamics. 2023 ;[citado 2024 ago. 22 ] Available from: https://doi.org/10.1080/07391102.2023.2182129
Artigo de periodico
Repurposing of 5-nitrofuran-3,5-disubstituted isoxazoles: a thriving scaffold to antitrypanosomal agents (2023)
Carvalho, Diego B.; Neves, Amarith R. das; Portapilla, Gisele Bulhões ; Soares, Ozildeia; Santos, Larissa B. B.; Oliveira, Jefferson R. S.; Vianna, Luan S.; Judice, Wagner A. S.; Cardoso, Iara Aimê ; Luccas, Pedro Henrique; Nonato, Maria Cristina ; Lopes, Norberto Peporine ; Albuquerque, Sérgio de ; Baroni, Adriano C. M.
Fonte: Archiv der Pharmazie. Unidade: FCFRP
Assunto: DOENÇA DE CHAGAS
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CARVALHO, Diego B. et al. Repurposing of 5-nitrofuran-3,5-disubstituted isoxazoles: a thriving scaffold to antitrypanosomal agents. Archiv der Pharmazie, v. 356, n. 4, p. 1-9, 2023Tradução . . Disponível em: https://doi.org/10.1002/ardp.202200472. Acesso em: 22 ago. 2024.
APA
Carvalho, D. B., Neves, A. R. das, Portapilla, G. B., Soares, O., Santos, L. B. B., Oliveira, J. R. S., et al. (2023). Repurposing of 5-nitrofuran-3,5-disubstituted isoxazoles: a thriving scaffold to antitrypanosomal agents. Archiv der Pharmazie, 356( 4), 1-9. doi:10.1002/ardp.202200472
NLM
Carvalho DB, Neves AR das, Portapilla GB, Soares O, Santos LBB, Oliveira JRS, Vianna LS, Judice WAS, Cardoso IA, Luccas PH, Nonato MC, Lopes NP, Albuquerque S de, Baroni ACM. Repurposing of 5-nitrofuran-3,5-disubstituted isoxazoles: a thriving scaffold to antitrypanosomal agents [Internet]. Archiv der Pharmazie. 2023 ; 356( 4): 1-9.[citado 2024 ago. 22 ] Available from: https://doi.org/10.1002/ardp.202200472
Vancouver
Carvalho DB, Neves AR das, Portapilla GB, Soares O, Santos LBB, Oliveira JRS, Vianna LS, Judice WAS, Cardoso IA, Luccas PH, Nonato MC, Lopes NP, Albuquerque S de, Baroni ACM. Repurposing of 5-nitrofuran-3,5-disubstituted isoxazoles: a thriving scaffold to antitrypanosomal agents [Internet]. Archiv der Pharmazie. 2023 ; 356( 4): 1-9.[citado 2024 ago. 22 ] Available from: https://doi.org/10.1002/ardp.202200472
Artigo de periodico
Trypanosoma cruzi Sirtuin 2 as a relevant druggable target: new inhibitors developed by computer-aided drug design (2023)
Ferreira, Glaucio Monteiro ; Kronenberger, Thales ; Maltarollo, Vinícius Gonçalves ; Poso, Antti ; Gatti, Fernando de Moura ; Almeida, Vitor Medeiros ; Marana, Sandro Roberto ; Lopes, Carla Duque ; Tezuka, Daiane Yukie; Albuquerque, Sérgio de ; Emery, Flavio da Silva ; Trossini, Gustavo Henrique Goulart
Fonte: Pharmaceuticals. Unidades: FCF, IQ, FCFRP
Assuntos: TRYPANOSOMA CRUZI, ENZIMAS
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FERREIRA, Glaucio Monteiro et al. Trypanosoma cruzi Sirtuin 2 as a relevant druggable target: new inhibitors developed by computer-aided drug design. Pharmaceuticals, v. 16 , p. 1-14 art. 428, 2023Tradução . . Disponível em: https://doi.org/10.3390/ph16030428. Acesso em: 22 ago. 2024.
APA
Ferreira, G. M., Kronenberger, T., Maltarollo, V. G., Poso, A., Gatti, F. de M., Almeida, V. M., et al. (2023). Trypanosoma cruzi Sirtuin 2 as a relevant druggable target: new inhibitors developed by computer-aided drug design. Pharmaceuticals, 16 , 1-14 art. 428. doi:10.3390/ph16030428
NLM
Ferreira GM, Kronenberger T, Maltarollo VG, Poso A, Gatti F de M, Almeida VM, Marana SR, Lopes CD, Tezuka DY, Albuquerque S de, Emery F da S, Trossini GHG. Trypanosoma cruzi Sirtuin 2 as a relevant druggable target: new inhibitors developed by computer-aided drug design [Internet]. Pharmaceuticals. 2023 ; 16 1-14 art. 428.[citado 2024 ago. 22 ] Available from: https://doi.org/10.3390/ph16030428
Vancouver
Ferreira GM, Kronenberger T, Maltarollo VG, Poso A, Gatti F de M, Almeida VM, Marana SR, Lopes CD, Tezuka DY, Albuquerque S de, Emery F da S, Trossini GHG. Trypanosoma cruzi Sirtuin 2 as a relevant druggable target: new inhibitors developed by computer-aided drug design [Internet]. Pharmaceuticals. 2023 ; 16 1-14 art. 428.[citado 2024 ago. 22 ] Available from: https://doi.org/10.3390/ph16030428
Artigo de periodico
Mast cell-T cell axis alters development of colitis-dependent and colitis-independent colorectal tumours: potential for therapeutically targeting via mast cell inhibition (2022)
Ozawa, Juliana Yumi Sakita; Elias-Oliveira, Jefferson; Sartori, Daniela Carlos; Santos, Emerson de Souza ; Almeida, Luciana Yamamoto de; Malta, Tathiane Maistro; Brunaldi, Mariângela Ottoboni; Albuquerque, Sérgio de ; Silva, Cleide Lúcia Araújo; Andrade, Marcus V.; Bonato, Vânia Luiza Deperon; Garcia, Sérgio Britto; Cunha, Fernando de Queiroz ; Cebinelli, Guilherme Cesar Martelossi; Martins Júnior, Ronaldo Bragança; Matthews, Jason; Colli, Leandro Machado ; Martin, Francis L.; Uyemura, Sergio Akira ; Kannen, Vinicius
Fonte: Journal for ImmunoTherapy of Cancer. Unidades: FMRP, FCFRP, PUSP-RP
Assuntos: COLITE, NEOPLASIAS COLORRETAIS, ANTINEOPLÁSICOS, MASTÓCITOS
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ABNT
OZAWA, Juliana Yumi Sakita et al. Mast cell-T cell axis alters development of colitis-dependent and colitis-independent colorectal tumours: potential for therapeutically targeting via mast cell inhibition. Journal for ImmunoTherapy of Cancer, v. 10, n. 10, p. 1-15, 2022Tradução . . Disponível em: https://doi.org/10.1136/jitc-2022-004653. Acesso em: 22 ago. 2024.
APA
Ozawa, J. Y. S., Elias-Oliveira, J., Sartori, D. C., Santos, E. de S., Almeida, L. Y. de, Malta, T. M., et al. (2022). Mast cell-T cell axis alters development of colitis-dependent and colitis-independent colorectal tumours: potential for therapeutically targeting via mast cell inhibition. Journal for ImmunoTherapy of Cancer, 10( 10), 1-15. doi:10.1136/jitc-2022-004653
NLM
Ozawa JYS, Elias-Oliveira J, Sartori DC, Santos E de S, Almeida LY de, Malta TM, Brunaldi MO, Albuquerque S de, Silva CLA, Andrade MV, Bonato VLD, Garcia SB, Cunha F de Q, Cebinelli GCM, Martins Júnior RB, Matthews J, Colli LM, Martin FL, Uyemura SA, Kannen V. Mast cell-T cell axis alters development of colitis-dependent and colitis-independent colorectal tumours: potential for therapeutically targeting via mast cell inhibition [Internet]. Journal for ImmunoTherapy of Cancer. 2022 ; 10( 10): 1-15.[citado 2024 ago. 22 ] Available from: https://doi.org/10.1136/jitc-2022-004653
Vancouver
Ozawa JYS, Elias-Oliveira J, Sartori DC, Santos E de S, Almeida LY de, Malta TM, Brunaldi MO, Albuquerque S de, Silva CLA, Andrade MV, Bonato VLD, Garcia SB, Cunha F de Q, Cebinelli GCM, Martins Júnior RB, Matthews J, Colli LM, Martin FL, Uyemura SA, Kannen V. Mast cell-T cell axis alters development of colitis-dependent and colitis-independent colorectal tumours: potential for therapeutically targeting via mast cell inhibition [Internet]. Journal for ImmunoTherapy of Cancer. 2022 ; 10( 10): 1-15.[citado 2024 ago. 22 ] Available from: https://doi.org/10.1136/jitc-2022-004653
Artigo de periodico
Preparation, cytotoxic activity and DNA interaction studies of new platinum(II) complexes with 1,10-phenanthroline and 5-alkyl-1,3,4-oxadiazol-2(3H)-thione derivatives (2022)
Souza, Wesley A.; Ramos, Luana M. S.; Almeida, Angelina M. de; Tezuka, Daiane Y.; Lopes, Carla D.; Moreira, Mariete B.; Zanetti, Renan D.; Netto, Adelino V. G.; Ferreira, Francis B.; Oliveira, Ronaldo Junio de; Guedes, Guilherme P.; Albuquerque, Sérgio de ; Silva, Júlia R. L.; Pereira Maia, Elene C.; Resende, Jackson A. L. C.; Almeida, Mauro V. de; Guerra, Wendell
Fonte: Journal of Inorganic Biochemistry. Unidade: FCFRP
Assuntos: BACTÉRIAS, MEDICAMENTO, GENÔMICA, PLASMÍDEOS
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ABNT
SOUZA, Wesley A. et al. Preparation, cytotoxic activity and DNA interaction studies of new platinum(II) complexes with 1,10-phenanthroline and 5-alkyl-1,3,4-oxadiazol-2(3H)-thione derivatives. Journal of Inorganic Biochemistry, v. 237, p. 1-9, 2022Tradução . . Disponível em: https://doi.org/10.1016/j.jinorgbio.2022.111993. Acesso em: 22 ago. 2024.
APA
Souza, W. A., Ramos, L. M. S., Almeida, A. M. de, Tezuka, D. Y., Lopes, C. D., Moreira, M. B., et al. (2022). Preparation, cytotoxic activity and DNA interaction studies of new platinum(II) complexes with 1,10-phenanthroline and 5-alkyl-1,3,4-oxadiazol-2(3H)-thione derivatives. Journal of Inorganic Biochemistry, 237, 1-9. doi:10.1016/j.jinorgbio.2022.111993
NLM
Souza WA, Ramos LMS, Almeida AM de, Tezuka DY, Lopes CD, Moreira MB, Zanetti RD, Netto AVG, Ferreira FB, Oliveira RJ de, Guedes GP, Albuquerque S de, Silva JRL, Pereira Maia EC, Resende JALC, Almeida MV de, Guerra W. Preparation, cytotoxic activity and DNA interaction studies of new platinum(II) complexes with 1,10-phenanthroline and 5-alkyl-1,3,4-oxadiazol-2(3H)-thione derivatives [Internet]. Journal of Inorganic Biochemistry. 2022 ; 237 1-9.[citado 2024 ago. 22 ] Available from: https://doi.org/10.1016/j.jinorgbio.2022.111993
Vancouver
Souza WA, Ramos LMS, Almeida AM de, Tezuka DY, Lopes CD, Moreira MB, Zanetti RD, Netto AVG, Ferreira FB, Oliveira RJ de, Guedes GP, Albuquerque S de, Silva JRL, Pereira Maia EC, Resende JALC, Almeida MV de, Guerra W. Preparation, cytotoxic activity and DNA interaction studies of new platinum(II) complexes with 1,10-phenanthroline and 5-alkyl-1,3,4-oxadiazol-2(3H)-thione derivatives [Internet]. Journal of Inorganic Biochemistry. 2022 ; 237 1-9.[citado 2024 ago. 22 ] Available from: https://doi.org/10.1016/j.jinorgbio.2022.111993
Artigo de periodico
Gold(III) complexes with thiosemicarbazonate ligands as potential anticancer agents: cytotoxicity and interactions with biomolecular targets (2021)
Possato, Bruna; Dalmolin, Luciana Facco; Pereira, Luiz Miguel; Alves, Jacqueline Querino; Silva, Raphael Tristão Cruvinel; Gelamo, Rogerio Valentim; Yatsuda, Ana Patrícia ; Lopez, Renata Fonseca Vianna ; Albuquerque, Sérgio de ; Leite, Natália Bueno; Maia, Pedro Ivo da Silva
Fonte: European Journal of Pharmaceutical Sciences. Unidades: FCFRP, PUSP-RP
Assuntos: ANTINEOPLÁSICOS, APOPTOSE, LINHAGEM CELULAR, LIGANTES, NEOPLASIAS OVARIANAS
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POSSATO, Bruna et al. Gold(III) complexes with thiosemicarbazonate ligands as potential anticancer agents: cytotoxicity and interactions with biomolecular targets. European Journal of Pharmaceutical Sciences, v. 162, 2021Tradução . . Disponível em: https://doi.org/10.1016/j.ejps.2021.105834. Acesso em: 22 ago. 2024.
APA
Possato, B., Dalmolin, L. F., Pereira, L. M., Alves, J. Q., Silva, R. T. C., Gelamo, R. V., et al. (2021). Gold(III) complexes with thiosemicarbazonate ligands as potential anticancer agents: cytotoxicity and interactions with biomolecular targets. European Journal of Pharmaceutical Sciences, 162. doi:10.1016/j.ejps.2021.105834
NLM
Possato B, Dalmolin LF, Pereira LM, Alves JQ, Silva RTC, Gelamo RV, Yatsuda AP, Lopez RFV, Albuquerque S de, Leite NB, Maia PI da S. Gold(III) complexes with thiosemicarbazonate ligands as potential anticancer agents: cytotoxicity and interactions with biomolecular targets [Internet]. European Journal of Pharmaceutical Sciences. 2021 ; 162[citado 2024 ago. 22 ] Available from: https://doi.org/10.1016/j.ejps.2021.105834
Vancouver
Possato B, Dalmolin LF, Pereira LM, Alves JQ, Silva RTC, Gelamo RV, Yatsuda AP, Lopez RFV, Albuquerque S de, Leite NB, Maia PI da S. Gold(III) complexes with thiosemicarbazonate ligands as potential anticancer agents: cytotoxicity and interactions with biomolecular targets [Internet]. European Journal of Pharmaceutical Sciences. 2021 ; 162[citado 2024 ago. 22 ] Available from: https://doi.org/10.1016/j.ejps.2021.105834
Artigo de periodico
Synthesis, antitumor activity and in silico analyses of amino acid derivatives of artepillin C, drupanin and baccharin from green propolis (2021)
Rodrigues, Débora Munhoz; Portapilla, Gisele Bulhões; Silva, Guilherme Martins da ; Duarte, Andressa; Rotta, Cristiana Gonçalez; Silva, Carlos Henrique Tomich de Paula da; Albuquerque, Sérgio de ; Bastos, Jairo Kenupp ; Campo, Vanessa Leiria
Fonte: Bioorganic and Medicinal Chemistry. Unidades: FCFRP, FFCLRP, FMRP
Assuntos: PRODUTOS NATURAIS, NEOPLASIAS MAMÁRIAS, NEOPLASIAS PROSTÁTICAS, ALECRIM, PRÓPOLIS, SÍNTESE QUÍMICA
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RODRIGUES, Débora Munhoz et al. Synthesis, antitumor activity and in silico analyses of amino acid derivatives of artepillin C, drupanin and baccharin from green propolis. Bioorganic and Medicinal Chemistry, v. 47, 2021Tradução . . Disponível em: https://doi.org/10.1016/j.bmc.2021.116372. Acesso em: 22 ago. 2024.
APA
Rodrigues, D. M., Portapilla, G. B., Silva, G. M. da, Duarte, A., Rotta, C. G., Silva, C. H. T. de P. da, et al. (2021). Synthesis, antitumor activity and in silico analyses of amino acid derivatives of artepillin C, drupanin and baccharin from green propolis. Bioorganic and Medicinal Chemistry, 47. doi:10.1016/j.bmc.2021.116372
NLM
Rodrigues DM, Portapilla GB, Silva GM da, Duarte A, Rotta CG, Silva CHT de P da, Albuquerque S de, Bastos JK, Campo VL. Synthesis, antitumor activity and in silico analyses of amino acid derivatives of artepillin C, drupanin and baccharin from green propolis [Internet]. Bioorganic and Medicinal Chemistry. 2021 ; 47[citado 2024 ago. 22 ] Available from: https://doi.org/10.1016/j.bmc.2021.116372
Vancouver
Rodrigues DM, Portapilla GB, Silva GM da, Duarte A, Rotta CG, Silva CHT de P da, Albuquerque S de, Bastos JK, Campo VL. Synthesis, antitumor activity and in silico analyses of amino acid derivatives of artepillin C, drupanin and baccharin from green propolis [Internet]. Bioorganic and Medicinal Chemistry. 2021 ; 47[citado 2024 ago. 22 ] Available from: https://doi.org/10.1016/j.bmc.2021.116372
Artigo de periodico
In vitro anti-Trypanosoma cruzi activity enhancement of curcumin by its monoketone tetramethoxy analog diveratralacetone (2021)
Souza, Julia M.; Vieira, Tatiana Manzini ; Candido, Ana Carolina B. B.; Tezuka, Daiane Y.; Rao, G. Subba; Albuquerque, Sérgio de ; Crotti, Antonio Eduardo Miller ; Siqueira-Neto, Jair L.; Magalhães, Lizandra G.
Fonte: Current Research in Parasitology and Vector-Borne Diseases. Unidades: FCFRP, FFCLRP
Assuntos: TOXICIDADE EM ANIMAL, TRYPANOSOMA CRUZI, ANTIPARASITÁRIOS, AÇAFRÃO, DOENÇA DE CHAGAS
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ABNT
SOUZA, Julia M. et al. In vitro anti-Trypanosoma cruzi activity enhancement of curcumin by its monoketone tetramethoxy analog diveratralacetone. Current Research in Parasitology and Vector-Borne Diseases, v. 1, 2021Tradução . . Disponível em: https://doi.org/10.1016/j.crpvbd.2021.100031. Acesso em: 22 ago. 2024.
APA
Souza, J. M., Vieira, T. M., Candido, A. C. B. B., Tezuka, D. Y., Rao, G. S., Albuquerque, S. de, et al. (2021). In vitro anti-Trypanosoma cruzi activity enhancement of curcumin by its monoketone tetramethoxy analog diveratralacetone. Current Research in Parasitology and Vector-Borne Diseases, 1. doi:10.1016/j.crpvbd.2021.100031
NLM
Souza JM, Vieira TM, Candido ACBB, Tezuka DY, Rao GS, Albuquerque S de, Crotti AEM, Siqueira-Neto JL, Magalhães LG. In vitro anti-Trypanosoma cruzi activity enhancement of curcumin by its monoketone tetramethoxy analog diveratralacetone [Internet]. Current Research in Parasitology and Vector-Borne Diseases. 2021 ; 1[citado 2024 ago. 22 ] Available from: https://doi.org/10.1016/j.crpvbd.2021.100031
Vancouver
Souza JM, Vieira TM, Candido ACBB, Tezuka DY, Rao GS, Albuquerque S de, Crotti AEM, Siqueira-Neto JL, Magalhães LG. In vitro anti-Trypanosoma cruzi activity enhancement of curcumin by its monoketone tetramethoxy analog diveratralacetone [Internet]. Current Research in Parasitology and Vector-Borne Diseases. 2021 ; 1[citado 2024 ago. 22 ] Available from: https://doi.org/10.1016/j.crpvbd.2021.100031
Artigo de periodico
Trypanocidal activity of new 1,6-diphenyl-1H-pyrazolo[3,4-b]pyridine derivatives: synthesis, in vitro and in vivo studies (2021)
Ribeiro, Joana Lucius de Sousa; Soares, Júlio César de Araujo Vanelis; Portapilla, Gisele Bulhões; Providello, Maiara Voltarelli ; Lima, Camilo Henrique da Silva; Muri, Estela Maris Freitas; Albuquerque, Sérgio de ; Dias, Luiza Rosaria Sousa
Fonte: Bioorganic & Medicinal Chemistry. Unidade: FCFRP
Assuntos: DOENÇA DE CHAGAS, ANIMAIS PARASITOS, CIRCULAÇÃO SANGUÍNEA, COMPOSTOS HETEROCÍCLICOS
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ABNT
RIBEIRO, Joana Lucius de Sousa et al. Trypanocidal activity of new 1,6-diphenyl-1H-pyrazolo[3,4-b]pyridine derivatives: synthesis, in vitro and in vivo studies. Bioorganic & Medicinal Chemistry, v. 29, 2021Tradução . . Disponível em: https://doi.org/10.1016/j.bmc.2020.115855. Acesso em: 22 ago. 2024.
APA
Ribeiro, J. L. de S., Soares, J. C. de A. V., Portapilla, G. B., Providello, M. V., Lima, C. H. da S., Muri, E. M. F., et al. (2021). Trypanocidal activity of new 1,6-diphenyl-1H-pyrazolo[3,4-b]pyridine derivatives: synthesis, in vitro and in vivo studies. Bioorganic & Medicinal Chemistry, 29. doi:10.1016/j.bmc.2020.115855
NLM
Ribeiro JL de S, Soares JC de AV, Portapilla GB, Providello MV, Lima CH da S, Muri EMF, Albuquerque S de, Dias LRS. Trypanocidal activity of new 1,6-diphenyl-1H-pyrazolo[3,4-b]pyridine derivatives: synthesis, in vitro and in vivo studies [Internet]. Bioorganic & Medicinal Chemistry. 2021 ; 29[citado 2024 ago. 22 ] Available from: https://doi.org/10.1016/j.bmc.2020.115855
Vancouver
Ribeiro JL de S, Soares JC de AV, Portapilla GB, Providello MV, Lima CH da S, Muri EMF, Albuquerque S de, Dias LRS. Trypanocidal activity of new 1,6-diphenyl-1H-pyrazolo[3,4-b]pyridine derivatives: synthesis, in vitro and in vivo studies [Internet]. Bioorganic & Medicinal Chemistry. 2021 ; 29[citado 2024 ago. 22 ] Available from: https://doi.org/10.1016/j.bmc.2020.115855
Artigo de periodico
Synthesis of cardanol-based 1,2,3-triazoles as potential green agents against neoplastic cells (2021)
Braga, Felipe C.; Ojeda, Mariah; Perdomo, Renata T.; Albuquerque, Sérgio de ; Rafique, Jamal; Lima, Dênis P. de; Beatriz, Adilson
Fonte: Sustainable Chemistry and Pharmacy. Unidade: FCFRP
Assuntos: CARCINOMA, COMPOSTOS HETEROCÍCLICOS, LIPÍDEOS
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ABNT
BRAGA, Felipe C. et al. Synthesis of cardanol-based 1,2,3-triazoles as potential green agents against neoplastic cells. Sustainable Chemistry and Pharmacy, v. 20, 2021Tradução . . Disponível em: https://doi.org/10.1016/j.scp.2021.100408. Acesso em: 22 ago. 2024.
APA
Braga, F. C., Ojeda, M., Perdomo, R. T., Albuquerque, S. de, Rafique, J., Lima, D. P. de, & Beatriz, A. (2021). Synthesis of cardanol-based 1,2,3-triazoles as potential green agents against neoplastic cells. Sustainable Chemistry and Pharmacy, 20. doi:10.1016/j.scp.2021.100408
NLM
Braga FC, Ojeda M, Perdomo RT, Albuquerque S de, Rafique J, Lima DP de, Beatriz A. Synthesis of cardanol-based 1,2,3-triazoles as potential green agents against neoplastic cells [Internet]. Sustainable Chemistry and Pharmacy. 2021 ; 20[citado 2024 ago. 22 ] Available from: https://doi.org/10.1016/j.scp.2021.100408
Vancouver
Braga FC, Ojeda M, Perdomo RT, Albuquerque S de, Rafique J, Lima DP de, Beatriz A. Synthesis of cardanol-based 1,2,3-triazoles as potential green agents against neoplastic cells [Internet]. Sustainable Chemistry and Pharmacy. 2021 ; 20[citado 2024 ago. 22 ] Available from: https://doi.org/10.1016/j.scp.2021.100408
Artigo de periodico
Melatonin decreases circulating Trypanosoma cruzi load with no effect on tissue parasite replication (2021)
Providello, Maiara Voltarelli ; Portapilla, Gisele Bulhões ; Oliveira, Pedro Alexandre Sampaio ; Silva, Carla Brigagão Pacheco da ; Anchieta, Naira Ferreira ; Tirapelli, Carlos Renato ; Albuquerque, Sérgio de
Fonte: Canadian Journal of Physiology and Pharmacology. Unidades: EERP, FCFRP, FMRP
Assuntos: ANIMAIS, DOENÇA DE CHAGAS, CORAÇÃO, MELATONINA, TRYPANOSOMA CRUZI
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
PROVIDELLO, Maiara Voltarelli et al. Melatonin decreases circulating Trypanosoma cruzi load with no effect on tissue parasite replication. Canadian Journal of Physiology and Pharmacology, v. 99, n. 8, p. 795-802, 2021Tradução . . Disponível em: https://doi.org/10.1139/cjpp-2020-0473. Acesso em: 22 ago. 2024.
APA
Providello, M. V., Portapilla, G. B., Oliveira, P. A. S., Silva, C. B. P. da, Anchieta, N. F., Tirapelli, C. R., & Albuquerque, S. de. (2021). Melatonin decreases circulating Trypanosoma cruzi load with no effect on tissue parasite replication. Canadian Journal of Physiology and Pharmacology, 99( 8), 795-802. doi:10.1139/cjpp-2020-0473
NLM
Providello MV, Portapilla GB, Oliveira PAS, Silva CBP da, Anchieta NF, Tirapelli CR, Albuquerque S de. Melatonin decreases circulating Trypanosoma cruzi load with no effect on tissue parasite replication [Internet]. Canadian Journal of Physiology and Pharmacology. 2021 ; 99( 8): 795-802.[citado 2024 ago. 22 ] Available from: https://doi.org/10.1139/cjpp-2020-0473
Vancouver
Providello MV, Portapilla GB, Oliveira PAS, Silva CBP da, Anchieta NF, Tirapelli CR, Albuquerque S de. Melatonin decreases circulating Trypanosoma cruzi load with no effect on tissue parasite replication [Internet]. Canadian Journal of Physiology and Pharmacology. 2021 ; 99( 8): 795-802.[citado 2024 ago. 22 ] Available from: https://doi.org/10.1139/cjpp-2020-0473
Artigo de jornal-dep/entr
Substâncias estudadas pela USP de São Carlos se mostram 100% eficazes contra a Covid-19 (2021)
Albuquerque, Sérgio de ; Martins, Felipe Cardoso Prado ; Montanari, Carlos Alberto ; Silva, João Santana da
Fonte: Jornal da EPTV 2a. Edição. Unidades: FCFRP, IQSC, FMRP
Assuntos: DOENÇA DE CHAGAS, MOLÉCULA, CORONAVIRUS
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
ALBUQUERQUE, Sérgio de et al. Substâncias estudadas pela USP de São Carlos se mostram 100% eficazes contra a Covid-19. Jornal da EPTV 2a. Edição. São Carlos: Faculdade de Ciências Farmacêuticas de Ribeirão Preto, Universidade de São Paulo. Disponível em: https://g1.globo.com/sp/sao-carlos-regiao/noticia/2021/11/10/substancias-estudadas-pela-usp-de-sao-carlos-se-mostram-100percent-eficazes-contra-a-covid-19.ghtml. Acesso em: 22 ago. 2024. , 2021
APA
Albuquerque, S. de, Martins, F. C. P., Montanari, C. A., & Silva, J. S. da. (2021). Substâncias estudadas pela USP de São Carlos se mostram 100% eficazes contra a Covid-19. Jornal da EPTV 2a. Edição. São Carlos: Faculdade de Ciências Farmacêuticas de Ribeirão Preto, Universidade de São Paulo. Recuperado de https://g1.globo.com/sp/sao-carlos-regiao/noticia/2021/11/10/substancias-estudadas-pela-usp-de-sao-carlos-se-mostram-100percent-eficazes-contra-a-covid-19.ghtml
NLM
Albuquerque S de, Martins FCP, Montanari CA, Silva JS da. Substâncias estudadas pela USP de São Carlos se mostram 100% eficazes contra a Covid-19 [Internet]. Jornal da EPTV 2a. Edição. 2021 ;[citado 2024 ago. 22 ] Available from: https://g1.globo.com/sp/sao-carlos-regiao/noticia/2021/11/10/substancias-estudadas-pela-usp-de-sao-carlos-se-mostram-100percent-eficazes-contra-a-covid-19.ghtml
Vancouver
Albuquerque S de, Martins FCP, Montanari CA, Silva JS da. Substâncias estudadas pela USP de São Carlos se mostram 100% eficazes contra a Covid-19 [Internet]. Jornal da EPTV 2a. Edição. 2021 ;[citado 2024 ago. 22 ] Available from: https://g1.globo.com/sp/sao-carlos-regiao/noticia/2021/11/10/substancias-estudadas-pela-usp-de-sao-carlos-se-mostram-100percent-eficazes-contra-a-covid-19.ghtml
Artigo de periodico
Synthesis, characterization and antichagasic evaluation of thiosemicarbazones prepared from chalcones and dibenzalacetones (2021)
Silva, Aline Alves da; Maia, Pedro Ivo da Silva; Lopes, Carla Duque; Albuquerque, Sérgio de ; Valle, Marcelo Siqueira
Fonte: Journal of Molecular Structure. Unidade: FCFRP
Assuntos: DOENÇA DE CHAGAS, TRYPANOSOMA CRUZI, SÍNTESE QUÍMICA, CITOTOXINAS
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
SILVA, Aline Alves da et al. Synthesis, characterization and antichagasic evaluation of thiosemicarbazones prepared from chalcones and dibenzalacetones. Journal of Molecular Structure, v. 1232, 2021Tradução . . Disponível em: https://doi.org/10.1016/j.molstruc.2021.130014. Acesso em: 22 ago. 2024.
APA
Silva, A. A. da, Maia, P. I. da S., Lopes, C. D., Albuquerque, S. de, & Valle, M. S. (2021). Synthesis, characterization and antichagasic evaluation of thiosemicarbazones prepared from chalcones and dibenzalacetones. Journal of Molecular Structure, 1232. doi:10.1016/j.molstruc.2021.130014
NLM
Silva AA da, Maia PI da S, Lopes CD, Albuquerque S de, Valle MS. Synthesis, characterization and antichagasic evaluation of thiosemicarbazones prepared from chalcones and dibenzalacetones [Internet]. Journal of Molecular Structure. 2021 ; 1232[citado 2024 ago. 22 ] Available from: https://doi.org/10.1016/j.molstruc.2021.130014
Vancouver
Silva AA da, Maia PI da S, Lopes CD, Albuquerque S de, Valle MS. Synthesis, characterization and antichagasic evaluation of thiosemicarbazones prepared from chalcones and dibenzalacetones [Internet]. Journal of Molecular Structure. 2021 ; 1232[citado 2024 ago. 22 ] Available from: https://doi.org/10.1016/j.molstruc.2021.130014
Artigo de periodico
Activity of β-caryophyllene oxide derivatives against Trypanosoma cruzi, Mammalian Cells, and horseradish peroxidase (2020)
Portapilla, Gisele Bulhões; Pereira, Luiz Miguel; Soldi, Rafael Augusto; Abreu Filho, Péricles Gama; Gallo, Inara Fernanda Lage; Clososki, Giuliano Cesar ; Albuquerque, Sérgio de
Fonte: Revista Brasileira de Farmacognosia. Unidade: FCFRP
Assuntos: TERPENOS, CITOTOXICIDADE IMUNOLÓGICA, ANTIPARASITÁRIOS, TRYPANOSOMA CRUZI, PRODUTOS NATURAIS, COPAÍBA, DOENÇA DE CHAGAS
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
PORTAPILLA, Gisele Bulhões et al. Activity of β-caryophyllene oxide derivatives against Trypanosoma cruzi, Mammalian Cells, and horseradish peroxidase. Revista Brasileira de Farmacognosia, v. 30, n. 6, p. 824-831, 2020Tradução . . Disponível em: https://doi.org/10.1007/s43450-020-00118-1. Acesso em: 22 ago. 2024.
APA
Portapilla, G. B., Pereira, L. M., Soldi, R. A., Abreu Filho, P. G., Gallo, I. F. L., Clososki, G. C., & Albuquerque, S. de. (2020). Activity of β-caryophyllene oxide derivatives against Trypanosoma cruzi, Mammalian Cells, and horseradish peroxidase. Revista Brasileira de Farmacognosia, 30( 6), 824-831. doi:10.1007/s43450-020-00118-1
NLM
Portapilla GB, Pereira LM, Soldi RA, Abreu Filho PG, Gallo IFL, Clososki GC, Albuquerque S de. Activity of β-caryophyllene oxide derivatives against Trypanosoma cruzi, Mammalian Cells, and horseradish peroxidase [Internet]. Revista Brasileira de Farmacognosia. 2020 ; 30( 6): 824-831.[citado 2024 ago. 22 ] Available from: https://doi.org/10.1007/s43450-020-00118-1
Vancouver
Portapilla GB, Pereira LM, Soldi RA, Abreu Filho PG, Gallo IFL, Clososki GC, Albuquerque S de. Activity of β-caryophyllene oxide derivatives against Trypanosoma cruzi, Mammalian Cells, and horseradish peroxidase [Internet]. Revista Brasileira de Farmacognosia. 2020 ; 30( 6): 824-831.[citado 2024 ago. 22 ] Available from: https://doi.org/10.1007/s43450-020-00118-1
Artigo de periodico
On the intrinsic reactivity of highly potent trypanocidal cruzain inhibitors (2020)
Bonatt, Vinicius; Batista, Pedro Henrique Jatai ; Cianni, Lorenzo ; Vita, Daniela de ; Silva, Daniel G da; Cedron, Rodrigo; Tezuka, Daiane Yukie; Albuquerque, Sérgio de ; Moraes, Carolina Borsoi ; Franco, Caio Haddad ; Lameira, Jerônimo ; Leitão, Andrei ; Montanari, Carlos Alberto
Fonte: RSC Medicinal Chemistry. Unidades: PUSP-RP, IQSC, BIOENGENHARIA
Assunto: DOENÇA DE CHAGAS
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
BONATT, Vinicius et al. On the intrinsic reactivity of highly potent trypanocidal cruzain inhibitors. RSC Medicinal Chemistry, v. 11, n. 11, p. 1275-1284, 2020Tradução . . Disponível em: https://doi.org/10.1039/D0MD00097C. Acesso em: 22 ago. 2024.
APA
Bonatt, V., Batista, P. H. J., Cianni, L., Vita, D. de, Silva, D. G. da, Cedron, R., et al. (2020). On the intrinsic reactivity of highly potent trypanocidal cruzain inhibitors. RSC Medicinal Chemistry, 11( 11), 1275-1284. doi:10.1039/D0MD00097C
NLM
Bonatt V, Batista PHJ, Cianni L, Vita D de, Silva DG da, Cedron R, Tezuka DY, Albuquerque S de, Moraes CB, Franco CH, Lameira J, Leitão A, Montanari CA. On the intrinsic reactivity of highly potent trypanocidal cruzain inhibitors [Internet]. RSC Medicinal Chemistry. 2020 ; 11( 11): 1275-1284.[citado 2024 ago. 22 ] Available from: https://doi.org/10.1039/D0MD00097C
Vancouver
Bonatt V, Batista PHJ, Cianni L, Vita D de, Silva DG da, Cedron R, Tezuka DY, Albuquerque S de, Moraes CB, Franco CH, Lameira J, Leitão A, Montanari CA. On the intrinsic reactivity of highly potent trypanocidal cruzain inhibitors [Internet]. RSC Medicinal Chemistry. 2020 ; 11( 11): 1275-1284.[citado 2024 ago. 22 ] Available from: https://doi.org/10.1039/D0MD00097C
Artigo de periodico
Anti-Trypanosoma cruzi activity and molecular docking studies of 1Hpyrazolo[ 3, 4-b]pyridine derivatives (2020)
Lima, Camilo Henrique da Silva; Soares, Júlio César de Araujo Vanelis; Ribeiro, Joana Lucius de Sousa; Muri, Estela Maris Freitas; Albuquerque, Sérgio de ; Dias, Luiza Rosaria Sousa
Fonte: Letters in Drug Design & Discovery. Unidade: FCFRP
Assuntos: TRYPANOSOMA CRUZI, TRIPANOSSOMICIDAS, ENSAIO CLÍNICO, CITOTOXICIDADE IMUNOLÓGICA, ANTIPARASITÁRIOS
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
LIMA, Camilo Henrique da Silva et al. Anti-Trypanosoma cruzi activity and molecular docking studies of 1Hpyrazolo[ 3, 4-b]pyridine derivatives. Letters in Drug Design & Discovery, v. 17, n. 2, p. 184-191, 2020Tradução . . Disponível em: https://doi.org/10.2174/1570180816666190305141733. Acesso em: 22 ago. 2024.
APA
Lima, C. H. da S., Soares, J. C. de A. V., Ribeiro, J. L. de S., Muri, E. M. F., Albuquerque, S. de, & Dias, L. R. S. (2020). Anti-Trypanosoma cruzi activity and molecular docking studies of 1Hpyrazolo[ 3, 4-b]pyridine derivatives. Letters in Drug Design & Discovery, 17( 2), 184-191. doi:10.2174/1570180816666190305141733
NLM
Lima CH da S, Soares JC de AV, Ribeiro JL de S, Muri EMF, Albuquerque S de, Dias LRS. Anti-Trypanosoma cruzi activity and molecular docking studies of 1Hpyrazolo[ 3, 4-b]pyridine derivatives [Internet]. Letters in Drug Design & Discovery. 2020 ; 17( 2): 184-191.[citado 2024 ago. 22 ] Available from: https://doi.org/10.2174/1570180816666190305141733
Vancouver
Lima CH da S, Soares JC de AV, Ribeiro JL de S, Muri EMF, Albuquerque S de, Dias LRS. Anti-Trypanosoma cruzi activity and molecular docking studies of 1Hpyrazolo[ 3, 4-b]pyridine derivatives [Internet]. Letters in Drug Design & Discovery. 2020 ; 17( 2): 184-191.[citado 2024 ago. 22 ] Available from: https://doi.org/10.2174/1570180816666190305141733
Artigo de periodico
DNA binding, cleavage, apoptosis and cytotoxicity studies of three heteroleptic nickel complexes bearing β-diketones (2020)
Sousa, Luana M ; Souza, Wesley A; Paixão, Drielly A; Fazzi, Rodrigo Boni ; Tezuka, Daiane Yukie; Lopes, Carla Duque ; Carneiro, Zumira Aparecida ; Moreira, Mariete Barbosa; Pivatto, Marcos ; Netto, Adelino V. G; Albuquerque, Sérgio de ; Ferreira, Francis B; Oliveira, Ronaldo J. de; Resende, Jackson A. L. C; Lino, Ricardo C; Oliveira Junior, Robson J. de; Ferreira, Ana Maria da Costa ; Guerra, Wendell
Fonte: Inorganica Chimica Acta. Unidades: FCFRP, IQ
Assuntos: APOPTOSE, NÍQUEL
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
SOUSA, Luana M et al. DNA binding, cleavage, apoptosis and cytotoxicity studies of three heteroleptic nickel complexes bearing β-diketones. Inorganica Chimica Acta, v. 511, p. 1-10 art.119824, 2020Tradução . . Disponível em: https://doi.org/10.1016/j.ica.2020.119824. Acesso em: 22 ago. 2024.
APA
Sousa, L. M., Souza, W. A., Paixão, D. A., Fazzi, R. B., Tezuka, D. Y., Lopes, C. D., et al. (2020). DNA binding, cleavage, apoptosis and cytotoxicity studies of three heteroleptic nickel complexes bearing β-diketones. Inorganica Chimica Acta, 511, 1-10 art.119824. doi:10.1016/j.ica.2020.119824
NLM
Sousa LM, Souza WA, Paixão DA, Fazzi RB, Tezuka DY, Lopes CD, Carneiro ZA, Moreira MB, Pivatto M, Netto AVG, Albuquerque S de, Ferreira FB, Oliveira RJ de, Resende JALC, Lino RC, Oliveira Junior RJ de, Ferreira AM da C, Guerra W. DNA binding, cleavage, apoptosis and cytotoxicity studies of three heteroleptic nickel complexes bearing β-diketones [Internet]. Inorganica Chimica Acta. 2020 ; 511 1-10 art.119824.[citado 2024 ago. 22 ] Available from: https://doi.org/10.1016/j.ica.2020.119824
Vancouver
Sousa LM, Souza WA, Paixão DA, Fazzi RB, Tezuka DY, Lopes CD, Carneiro ZA, Moreira MB, Pivatto M, Netto AVG, Albuquerque S de, Ferreira FB, Oliveira RJ de, Resende JALC, Lino RC, Oliveira Junior RJ de, Ferreira AM da C, Guerra W. DNA binding, cleavage, apoptosis and cytotoxicity studies of three heteroleptic nickel complexes bearing β-diketones [Internet]. Inorganica Chimica Acta. 2020 ; 511 1-10 art.119824.[citado 2024 ago. 22 ] Available from: https://doi.org/10.1016/j.ica.2020.119824
Artigo de periodico
Mapping the S1 and S1’ subsites of cysteine proteases with new dipeptidyl nitrile inhibitors as trypanocidal agents (2020)
Cianni, Lorenzo ; Lemke, Carina; Gilberg, Erik; Feldmann, Christian; Rosini, Fabiana; Rocho, Fernanda dos Reis ; Ribeiro, Jean Francisco Rosa; Tezuka, Daiane Yukie; Lopes, Carla Duque ; Albuquerque, Sérgio de ; Bajorath, Jürgen; Laufer, Stefan; Leitão, Andrei ; Gütschow Michaell; Montanari, Carlos Alberto
Fonte: PLoS Neglected Tropical Diseases. Unidades: IQSC, FCFRP, FMRP
Assunto: QUÍMICA MÉDICA
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
CIANNI, Lorenzo et al. Mapping the S1 and S1’ subsites of cysteine proteases with new dipeptidyl nitrile inhibitors as trypanocidal agents. PLoS Neglected Tropical Diseases, v. 14, n. 3, p. 1-36, 2020Tradução . . Disponível em: https://doi.org/10.1371/journal.pntd.0007755. Acesso em: 22 ago. 2024.
APA
Cianni, L., Lemke, C., Gilberg, E., Feldmann, C., Rosini, F., Rocho, F. dos R., et al. (2020). Mapping the S1 and S1’ subsites of cysteine proteases with new dipeptidyl nitrile inhibitors as trypanocidal agents. PLoS Neglected Tropical Diseases, 14( 3), 1-36. doi:10.1371/journal.pntd.0007755
NLM
Cianni L, Lemke C, Gilberg E, Feldmann C, Rosini F, Rocho F dos R, Ribeiro JFR, Tezuka DY, Lopes CD, Albuquerque S de, Bajorath J, Laufer S, Leitão A, Gütschow Michaell, Montanari CA. Mapping the S1 and S1’ subsites of cysteine proteases with new dipeptidyl nitrile inhibitors as trypanocidal agents [Internet]. PLoS Neglected Tropical Diseases. 2020 ; 14( 3): 1-36.[citado 2024 ago. 22 ] Available from: https://doi.org/10.1371/journal.pntd.0007755
Vancouver
Cianni L, Lemke C, Gilberg E, Feldmann C, Rosini F, Rocho F dos R, Ribeiro JFR, Tezuka DY, Lopes CD, Albuquerque S de, Bajorath J, Laufer S, Leitão A, Gütschow Michaell, Montanari CA. Mapping the S1 and S1’ subsites of cysteine proteases with new dipeptidyl nitrile inhibitors as trypanocidal agents [Internet]. PLoS Neglected Tropical Diseases. 2020 ; 14( 3): 1-36.[citado 2024 ago. 22 ] Available from: https://doi.org/10.1371/journal.pntd.0007755
Artigo de periodico
Molecular design aided by random forests and synthesis of potent trypanocidal agents as cruzain inhibitors for Chagas disease treatment (2020)
Albuquerque, Sérgio de ; Cianni, Lorenzo ; Vita, Daniela de ; Lopes, Carla Duque ; Gomes, Ana S. M.; Gomes, Paula; Laughton, Charles; Leitão, Andrei ; Montanari, Carlos Alberto ; Montanari, Raphael ; Ribeiro, Jean Francisco Rosa ; Silva, João Santana da ; Teixeira, Cátia
Fonte: Chemical Biology & Drug Design. Unidades: FCFRP, IQSC, FMRP, EESC, ICMC
Assuntos: DOENÇA DE CHAGAS, TRYPANOSOMA CRUZI
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
ALBUQUERQUE, Sérgio de et al. Molecular design aided by random forests and synthesis of potent trypanocidal agents as cruzain inhibitors for Chagas disease treatment. Chemical Biology & Drug Design, v. 96, p. 948–960, 2020Tradução . . Disponível em: https://doi.org/10.1111/cbdd.13663. Acesso em: 22 ago. 2024.
APA
Albuquerque, S. de, Cianni, L., Vita, D. de, Lopes, C. D., Gomes, A. S. M., Gomes, P., et al. (2020). Molecular design aided by random forests and synthesis of potent trypanocidal agents as cruzain inhibitors for Chagas disease treatment. Chemical Biology & Drug Design, 96, 948–960. doi:10.1111/cbdd.13663
NLM
Albuquerque S de, Cianni L, Vita D de, Lopes CD, Gomes ASM, Gomes P, Laughton C, Leitão A, Montanari CA, Montanari R, Ribeiro JFR, Silva JS da, Teixeira C. Molecular design aided by random forests and synthesis of potent trypanocidal agents as cruzain inhibitors for Chagas disease treatment [Internet]. Chemical Biology & Drug Design. 2020 ; 96 948–960.[citado 2024 ago. 22 ] Available from: https://doi.org/10.1111/cbdd.13663
Vancouver
Albuquerque S de, Cianni L, Vita D de, Lopes CD, Gomes ASM, Gomes P, Laughton C, Leitão A, Montanari CA, Montanari R, Ribeiro JFR, Silva JS da, Teixeira C. Molecular design aided by random forests and synthesis of potent trypanocidal agents as cruzain inhibitors for Chagas disease treatment [Internet]. Chemical Biology & Drug Design. 2020 ; 96 948–960.[citado 2024 ago. 22 ] Available from: https://doi.org/10.1111/cbdd.13663

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