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Artigo de periodico
Synthesis, biological evaluation and molecular docking studies of novel 1,2,3-triazole-quinazolines as antiproliferative agents displaying ERK inhibitory activity (2021)
Nunes, Paulo Sergio Gonçalves; Silva, Gabriel da ; Nascimento, Sofia; Mantoani, Susimaire Pedersoli; Andrade, Peterson de; Bernardes, Emerson Soares; Kawano, Daniel Fábio; Leopoldino, Andréia Machado ; Carvalho, Ivone
Source: Bioorganic Chemistry. Unidades: IPEN, FCFRP
Subjects: ANTINEOPLÁSICOS, LINHAGEM CELULAR, PROLIFERAÇÃO CELULAR, PROTEÍNAS QUINASES, ESTRUTURA MOLECULAR (QUÍMICA TEÓRICA)
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NUNES, Paulo Sergio Gonçalves et al. Synthesis, biological evaluation and molecular docking studies of novel 1,2,3-triazole-quinazolines as antiproliferative agents displaying ERK inhibitory activity. Bioorganic Chemistry, v. 113, 2021Tradução . . Disponível em: https://doi.org/10.1016/j.bioorg.2021.104982. Acesso em: 15 nov. 2024.
APA
Nunes, P. S. G., Silva, G. da, Nascimento, S., Mantoani, S. P., Andrade, P. de, Bernardes, E. S., et al. (2021). Synthesis, biological evaluation and molecular docking studies of novel 1,2,3-triazole-quinazolines as antiproliferative agents displaying ERK inhibitory activity. Bioorganic Chemistry, 113. doi:10.1016/j.bioorg.2021.104982
NLM
Nunes PSG, Silva G da, Nascimento S, Mantoani SP, Andrade P de, Bernardes ES, Kawano DF, Leopoldino AM, Carvalho I. Synthesis, biological evaluation and molecular docking studies of novel 1,2,3-triazole-quinazolines as antiproliferative agents displaying ERK inhibitory activity [Internet]. Bioorganic Chemistry. 2021 ; 113[citado 2024 nov. 15 ] Available from: https://doi.org/10.1016/j.bioorg.2021.104982
Vancouver
Nunes PSG, Silva G da, Nascimento S, Mantoani SP, Andrade P de, Bernardes ES, Kawano DF, Leopoldino AM, Carvalho I. Synthesis, biological evaluation and molecular docking studies of novel 1,2,3-triazole-quinazolines as antiproliferative agents displaying ERK inhibitory activity [Internet]. Bioorganic Chemistry. 2021 ; 113[citado 2024 nov. 15 ] Available from: https://doi.org/10.1016/j.bioorg.2021.104982
Artigo de periodico
Synthesis and evaluation of [18F]FEtLos and [18F]AMBF3Los as novel 18F-Labelled Losartan derivatives for molecular imaging of Angiotensin II type 1 receptors (2020)
Ortega Pijeira, Martha Sahylí; Nunes, Paulo Sérgio Gonçalves ; Santos, Sofia Nascimento dos; Zhang, Zhengxing; Pérez Nario, Arian; Perini, Efrain Araujo; Turato, Walter Miguel; Rodríguez Riera, Zalua; Chammas, Roger ; Elsinga, Philip H.; Lin, Kuo-Shyan ; Carvalho, Ivone ; Bernardes, Emerson Soares
Source: Molecules. Unidades: FCF, FM, FCFRP
Subjects: ANGIOTENSINA II, RECEPTORES DE ANGIOTENSINA, DOENÇAS CARDIOVASCULARES, INFLAMAÇÃO, NEOPLASIAS
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ORTEGA PIJEIRA, Martha Sahylí et al. Synthesis and evaluation of [18F]FEtLos and [18F]AMBF3Los as novel 18F-Labelled Losartan derivatives for molecular imaging of Angiotensin II type 1 receptors. Molecules, v. 25, n. 8, p. 1-21, 2020Tradução . . Disponível em: https://doi.org/10.3390/molecules25081872. Acesso em: 15 nov. 2024.
APA
Ortega Pijeira, M. S., Nunes, P. S. G., Santos, S. N. dos, Zhang, Z., Pérez Nario, A., Perini, E. A., et al. (2020). Synthesis and evaluation of [18F]FEtLos and [18F]AMBF3Los as novel 18F-Labelled Losartan derivatives for molecular imaging of Angiotensin II type 1 receptors. Molecules, 25( 8), 1-21. doi:10.3390/molecules25081872
NLM
Ortega Pijeira MS, Nunes PSG, Santos SN dos, Zhang Z, Pérez Nario A, Perini EA, Turato WM, Rodríguez Riera Z, Chammas R, Elsinga PH, Lin K-S, Carvalho I, Bernardes ES. Synthesis and evaluation of [18F]FEtLos and [18F]AMBF3Los as novel 18F-Labelled Losartan derivatives for molecular imaging of Angiotensin II type 1 receptors [Internet]. Molecules. 2020 ; 25( 8): 1-21.[citado 2024 nov. 15 ] Available from: https://doi.org/10.3390/molecules25081872
Vancouver
Ortega Pijeira MS, Nunes PSG, Santos SN dos, Zhang Z, Pérez Nario A, Perini EA, Turato WM, Rodríguez Riera Z, Chammas R, Elsinga PH, Lin K-S, Carvalho I, Bernardes ES. Synthesis and evaluation of [18F]FEtLos and [18F]AMBF3Los as novel 18F-Labelled Losartan derivatives for molecular imaging of Angiotensin II type 1 receptors [Internet]. Molecules. 2020 ; 25( 8): 1-21.[citado 2024 nov. 15 ] Available from: https://doi.org/10.3390/molecules25081872
Artigo de periodico
Insights into anti-trypanosomal agents based on synthetic glycoconjugates (2018)
Campo, Vanessa Leiria; Marchiori, Marcelo Fiori; Carvalho, Ivone
Source: Current Topics in Medicinal Chemistry. Unidade: FCFRP
Subjects: TRIPANOSSOMICIDAS, DOENÇAS DE CHAGAS, GLICOCONJUGADOS, TRYPANOSOMA CRUZI, VACINAS
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CAMPO, Vanessa Leiria e MARCHIORI, Marcelo Fiori e CARVALHO, Ivone. Insights into anti-trypanosomal agents based on synthetic glycoconjugates. Current Topics in Medicinal Chemistry, v. 18, n. 5, p. 382-396, 2018Tradução . . Disponível em: https://doi.org/10.2174/1568026618666180509145305. Acesso em: 15 nov. 2024.
APA
Campo, V. L., Marchiori, M. F., & Carvalho, I. (2018). Insights into anti-trypanosomal agents based on synthetic glycoconjugates. Current Topics in Medicinal Chemistry, 18( 5), 382-396. doi:10.2174/1568026618666180509145305
NLM
Campo VL, Marchiori MF, Carvalho I. Insights into anti-trypanosomal agents based on synthetic glycoconjugates [Internet]. Current Topics in Medicinal Chemistry. 2018 ; 18( 5): 382-396.[citado 2024 nov. 15 ] Available from: https://doi.org/10.2174/1568026618666180509145305
Vancouver
Campo VL, Marchiori MF, Carvalho I. Insights into anti-trypanosomal agents based on synthetic glycoconjugates [Internet]. Current Topics in Medicinal Chemistry. 2018 ; 18( 5): 382-396.[citado 2024 nov. 15 ] Available from: https://doi.org/10.2174/1568026618666180509145305
Artigo de periodico
Chameleon-like behavior of indolylpiperidines in complex with cholinesterases targets: potent butyrylcholinesterase inhibitors (2018)
Chierrito, Talita Perez Cantuaria; Pedersoli-Mantoani, Susimaire; Roca, Carlos; Sebastian-Pérez, Victor; Martínez-Gonzalez, Loreto; Pérez, Daniel I.; Perez, Concepción; Canales, Angeles; Cañada, F. Javier; Campillo, Nuria E.; Carvalho, Ivone; Martinez, Ana
Source: European Journal of Medicinal Chemistry. Unidade: FCFRP
Subjects: DOENÇA DE ALZHEIMER, FARMACOTÉCNICA
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ABNT
CHIERRITO, Talita Perez Cantuaria et al. Chameleon-like behavior of indolylpiperidines in complex with cholinesterases targets: potent butyrylcholinesterase inhibitors. European Journal of Medicinal Chemistry, v. 145, p. 431-444, 2018Tradução . . Disponível em: https://doi.org/10.1016/j.ejmech.2018.01.007. Acesso em: 15 nov. 2024.
APA
Chierrito, T. P. C., Pedersoli-Mantoani, S., Roca, C., Sebastian-Pérez, V., Martínez-Gonzalez, L., Pérez, D. I., et al. (2018). Chameleon-like behavior of indolylpiperidines in complex with cholinesterases targets: potent butyrylcholinesterase inhibitors. European Journal of Medicinal Chemistry, 145, 431-444. doi:10.1016/j.ejmech.2018.01.007
NLM
Chierrito TPC, Pedersoli-Mantoani S, Roca C, Sebastian-Pérez V, Martínez-Gonzalez L, Pérez DI, Perez C, Canales A, Cañada FJ, Campillo NE, Carvalho I, Martinez A. Chameleon-like behavior of indolylpiperidines in complex with cholinesterases targets: potent butyrylcholinesterase inhibitors [Internet]. European Journal of Medicinal Chemistry. 2018 ; 145 431-444.[citado 2024 nov. 15 ] Available from: https://doi.org/10.1016/j.ejmech.2018.01.007
Vancouver
Chierrito TPC, Pedersoli-Mantoani S, Roca C, Sebastian-Pérez V, Martínez-Gonzalez L, Pérez DI, Perez C, Canales A, Cañada FJ, Campillo NE, Carvalho I, Martinez A. Chameleon-like behavior of indolylpiperidines in complex with cholinesterases targets: potent butyrylcholinesterase inhibitors [Internet]. European Journal of Medicinal Chemistry. 2018 ; 145 431-444.[citado 2024 nov. 15 ] Available from: https://doi.org/10.1016/j.ejmech.2018.01.007
Artigo de periodico
From dual binding site acetylcholinesterase inhibitors to allosteric modulators: a new avenue for disease-modifying drugs in Alzheimer's disease (2017)
Chierrito, Talita P. C.; Mantoani, Susimaire Pedersoli; Roca, Carlos; Requena, Carlos; Perez, Victor Sebastian; Castillo, Willian O.; Moreira, Natalia C. S.; Pérez, Concepción; Sakamoto-Hojo, Elza Tiemi; Takahashi, Catarina Satie; Barbero, Jesús Jiménez; Cañada, F. Javier; Campillo, Nuria E.; Martinez, Ana; Carvalho, Ivone
Source: European Journal of Medicinal Chemistry. Unidades: FFCLRP, FCFRP
Subjects: DOENÇA DE ALZHEIMER, INIBIDORES DE ENZIMAS, PROLIFERAÇÃO CELULAR
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ABNT
CHIERRITO, Talita P. C. et al. From dual binding site acetylcholinesterase inhibitors to allosteric modulators: a new avenue for disease-modifying drugs in Alzheimer's disease. European Journal of Medicinal Chemistry, v. 139, p. 773-791, 2017Tradução . . Disponível em: https://doi.org/10.1016/j.ejmech.2017.08.051. Acesso em: 15 nov. 2024.
APA
Chierrito, T. P. C., Mantoani, S. P., Roca, C., Requena, C., Perez, V. S., Castillo, W. O., et al. (2017). From dual binding site acetylcholinesterase inhibitors to allosteric modulators: a new avenue for disease-modifying drugs in Alzheimer's disease. European Journal of Medicinal Chemistry, 139, 773-791. doi:10.1016/j.ejmech.2017.08.051
NLM
Chierrito TPC, Mantoani SP, Roca C, Requena C, Perez VS, Castillo WO, Moreira NCS, Pérez C, Sakamoto-Hojo ET, Takahashi CS, Barbero JJ, Cañada FJ, Campillo NE, Martinez A, Carvalho I. From dual binding site acetylcholinesterase inhibitors to allosteric modulators: a new avenue for disease-modifying drugs in Alzheimer's disease [Internet]. European Journal of Medicinal Chemistry. 2017 ; 139 773-791.[citado 2024 nov. 15 ] Available from: https://doi.org/10.1016/j.ejmech.2017.08.051
Vancouver
Chierrito TPC, Mantoani SP, Roca C, Requena C, Perez VS, Castillo WO, Moreira NCS, Pérez C, Sakamoto-Hojo ET, Takahashi CS, Barbero JJ, Cañada FJ, Campillo NE, Martinez A, Carvalho I. From dual binding site acetylcholinesterase inhibitors to allosteric modulators: a new avenue for disease-modifying drugs in Alzheimer's disease [Internet]. European Journal of Medicinal Chemistry. 2017 ; 139 773-791.[citado 2024 nov. 15 ] Available from: https://doi.org/10.1016/j.ejmech.2017.08.051
Artigo de periodico
Synthesis and 2D-QSAR studies of neolignan-based diaryl-tetrahydrofuran and -furan analogues with remarkable activity against Trypanosoma cruzi and assessment of the trypanothione reductase activity (2017)
Hartmann, Ana Paula; Carvalho, Marcelo Rodrigues de; Bernardes, Lilian Sibelle Campos; Moraes, Milena Hoehr de; Melo, Eduardo Borges de; Lopes, Carla Duque; Steindel, Mario; Silva, João Santana da; Carvalho, Ivone
Source: European Journal of Medicinal Chemistry. Unidades: FCFRP, FMRP
Subjects: DOENÇA DE CHAGAS, TRYPANOSOMA CRUZI, INIBIDORES DE ENZIMAS
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HARTMANN, Ana Paula et al. Synthesis and 2D-QSAR studies of neolignan-based diaryl-tetrahydrofuran and -furan analogues with remarkable activity against Trypanosoma cruzi and assessment of the trypanothione reductase activity. European Journal of Medicinal Chemistry, v. 140, p. 187-199, 2017Tradução . . Disponível em: https://doi.org/10.1016/j.ejmech.2017.08.064. Acesso em: 15 nov. 2024.
APA
Hartmann, A. P., Carvalho, M. R. de, Bernardes, L. S. C., Moraes, M. H. de, Melo, E. B. de, Lopes, C. D., et al. (2017). Synthesis and 2D-QSAR studies of neolignan-based diaryl-tetrahydrofuran and -furan analogues with remarkable activity against Trypanosoma cruzi and assessment of the trypanothione reductase activity. European Journal of Medicinal Chemistry, 140, 187-199. doi:10.1016/j.ejmech.2017.08.064
NLM
Hartmann AP, Carvalho MR de, Bernardes LSC, Moraes MH de, Melo EB de, Lopes CD, Steindel M, Silva JS da, Carvalho I. Synthesis and 2D-QSAR studies of neolignan-based diaryl-tetrahydrofuran and -furan analogues with remarkable activity against Trypanosoma cruzi and assessment of the trypanothione reductase activity [Internet]. European Journal of Medicinal Chemistry. 2017 ; 140 187-199.[citado 2024 nov. 15 ] Available from: https://doi.org/10.1016/j.ejmech.2017.08.064
Vancouver
Hartmann AP, Carvalho MR de, Bernardes LSC, Moraes MH de, Melo EB de, Lopes CD, Steindel M, Silva JS da, Carvalho I. Synthesis and 2D-QSAR studies of neolignan-based diaryl-tetrahydrofuran and -furan analogues with remarkable activity against Trypanosoma cruzi and assessment of the trypanothione reductase activity [Internet]. European Journal of Medicinal Chemistry. 2017 ; 140 187-199.[citado 2024 nov. 15 ] Available from: https://doi.org/10.1016/j.ejmech.2017.08.064
Artigo de periodico
Benzoic acid derivatives with trypanocidal activity: enzymatic analysis and molecular docking studies toward trans-sialidase (2017)
Kashif, Muhammad; Herrera, Antonio Moreno; Rocha, Juan Villalobos; Torres, Benjamín Nogueda; Villanueva, Jaime Pérez; Villar, Karen Rodríguez; Franco, José Luis Medina; Andrade, Peterson de; Carvalho, Ivone; Rivera, Gildardo
Source: Molecules. Unidade: FCFRP
Subjects: DOENÇA DE CHAGAS, FÁRMACOS, INIBIDORES DE ENZIMAS, TRIPANOSSOMICIDAS
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ABNT
KASHIF, Muhammad et al. Benzoic acid derivatives with trypanocidal activity: enzymatic analysis and molecular docking studies toward trans-sialidase. Molecules, v. 22, n. 11, 2017Tradução . . Disponível em: https://doi.org/10.3390/molecules22111863. Acesso em: 15 nov. 2024.
APA
Kashif, M., Herrera, A. M., Rocha, J. V., Torres, B. N., Villanueva, J. P., Villar, K. R., et al. (2017). Benzoic acid derivatives with trypanocidal activity: enzymatic analysis and molecular docking studies toward trans-sialidase. Molecules, 22( 11). doi:10.3390/molecules22111863
NLM
Kashif M, Herrera AM, Rocha JV, Torres BN, Villanueva JP, Villar KR, Franco JLM, Andrade P de, Carvalho I, Rivera G. Benzoic acid derivatives with trypanocidal activity: enzymatic analysis and molecular docking studies toward trans-sialidase [Internet]. Molecules. 2017 ; 22( 11):[citado 2024 nov. 15 ] Available from: https://doi.org/10.3390/molecules22111863
Vancouver
Kashif M, Herrera AM, Rocha JV, Torres BN, Villanueva JP, Villar KR, Franco JLM, Andrade P de, Carvalho I, Rivera G. Benzoic acid derivatives with trypanocidal activity: enzymatic analysis and molecular docking studies toward trans-sialidase [Internet]. Molecules. 2017 ; 22( 11):[citado 2024 nov. 15 ] Available from: https://doi.org/10.3390/molecules22111863
Artigo de periodico
Binding of triazole-linked galactosyl arylsulfonamides to galectin-3 affects Trypanosoma cruzi cell invasion (2017)
Marchiori, Marcelo Fiori; Riula, Thalita B.; Bortot, Leandro Oliveira; Andrade, Peterson; Junqueira, Getúlio G.; Foca, Giuseppina; Doti, Nunzianna; Ruvo, Menotti; Dias-Baruffi, Marcelo; Carvalho, Ivone; Campo, Vanessa Leiria
Source: Bioorganic and Medicinal Chemistry. Unidade: FCFRP
Subjects: TRYPANOSOMA CRUZI, INIBIDORES DE ENZIMAS, TRIPANOSSOMICIDAS
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ABNT
MARCHIORI, Marcelo Fiori et al. Binding of triazole-linked galactosyl arylsulfonamides to galectin-3 affects Trypanosoma cruzi cell invasion. Bioorganic and Medicinal Chemistry, v. 25, p. 6049-6059, 2017Tradução . . Disponível em: https://doi.org/10.1016/j.bmc.2017.09.042. Acesso em: 15 nov. 2024.
APA
Marchiori, M. F., Riula, T. B., Bortot, L. O., Andrade, P., Junqueira, G. G., Foca, G., et al. (2017). Binding of triazole-linked galactosyl arylsulfonamides to galectin-3 affects Trypanosoma cruzi cell invasion. Bioorganic and Medicinal Chemistry, 25, 6049-6059. doi:10.1016/j.bmc.2017.09.042
NLM
Marchiori MF, Riula TB, Bortot LO, Andrade P, Junqueira GG, Foca G, Doti N, Ruvo M, Dias-Baruffi M, Carvalho I, Campo VL. Binding of triazole-linked galactosyl arylsulfonamides to galectin-3 affects Trypanosoma cruzi cell invasion [Internet]. Bioorganic and Medicinal Chemistry. 2017 ; 25 6049-6059.[citado 2024 nov. 15 ] Available from: https://doi.org/10.1016/j.bmc.2017.09.042
Vancouver
Marchiori MF, Riula TB, Bortot LO, Andrade P, Junqueira GG, Foca G, Doti N, Ruvo M, Dias-Baruffi M, Carvalho I, Campo VL. Binding of triazole-linked galactosyl arylsulfonamides to galectin-3 affects Trypanosoma cruzi cell invasion [Internet]. Bioorganic and Medicinal Chemistry. 2017 ; 25 6049-6059.[citado 2024 nov. 15 ] Available from: https://doi.org/10.1016/j.bmc.2017.09.042
Artigo de periodico
CuAAC click chemistry with N-propargyl 1,5-dideoxy-1,5-imino-D-gulitol and N-propargyl 1,6-dideoxy-1,6-imino-D-mannitol provides access to triazole-linked piperidine and azepane pseudo-disaccharide iminosugars displaying glycosidase inhibitory properties (2016)
Zamoner, Luis Otavio Bunhotto; Aragão-Leoneti, Valquíria; Mantoani, Susimaire P.; Rugen, Michael D.; Nepogodiev, Sergey A.; Field, Robert A.; Carvalho, Ivone
Source: Carbohydrate Research. Unidade: FCFRP
Subjects: MODELAGEM MOLECULAR, COMPOSTOS ORGÂNICOS, DIABETES MELLITUS, GLICOSÍDEOS, INIBIDORES DE ENZIMAS
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ABNT
ZAMONER, Luis Otavio Bunhotto et al. CuAAC click chemistry with N-propargyl 1,5-dideoxy-1,5-imino-D-gulitol and N-propargyl 1,6-dideoxy-1,6-imino-D-mannitol provides access to triazole-linked piperidine and azepane pseudo-disaccharide iminosugars displaying glycosidase inhibitory properties. Carbohydrate Research, v. 429, p. 29-37, 2016Tradução . . Disponível em: https://doi.org/10.1016/j.carres.2016.04.020. Acesso em: 15 nov. 2024.
APA
Zamoner, L. O. B., Aragão-Leoneti, V., Mantoani, S. P., Rugen, M. D., Nepogodiev, S. A., Field, R. A., & Carvalho, I. (2016). CuAAC click chemistry with N-propargyl 1,5-dideoxy-1,5-imino-D-gulitol and N-propargyl 1,6-dideoxy-1,6-imino-D-mannitol provides access to triazole-linked piperidine and azepane pseudo-disaccharide iminosugars displaying glycosidase inhibitory properties. Carbohydrate Research, 429, 29-37. doi:10.1016/j.carres.2016.04.020
NLM
Zamoner LOB, Aragão-Leoneti V, Mantoani SP, Rugen MD, Nepogodiev SA, Field RA, Carvalho I. CuAAC click chemistry with N-propargyl 1,5-dideoxy-1,5-imino-D-gulitol and N-propargyl 1,6-dideoxy-1,6-imino-D-mannitol provides access to triazole-linked piperidine and azepane pseudo-disaccharide iminosugars displaying glycosidase inhibitory properties [Internet]. Carbohydrate Research. 2016 ; 429 29-37.[citado 2024 nov. 15 ] Available from: https://doi.org/10.1016/j.carres.2016.04.020
Vancouver
Zamoner LOB, Aragão-Leoneti V, Mantoani SP, Rugen MD, Nepogodiev SA, Field RA, Carvalho I. CuAAC click chemistry with N-propargyl 1,5-dideoxy-1,5-imino-D-gulitol and N-propargyl 1,6-dideoxy-1,6-imino-D-mannitol provides access to triazole-linked piperidine and azepane pseudo-disaccharide iminosugars displaying glycosidase inhibitory properties [Internet]. Carbohydrate Research. 2016 ; 429 29-37.[citado 2024 nov. 15 ] Available from: https://doi.org/10.1016/j.carres.2016.04.020
Artigo de periodico
Trypanosoma cruzi invasion into host cells: a complex molecular targets interplay (2016)
Campo, Vanessa Leiria; Martins-Teixeira, Maristela Braga; Carvalho, Ivone
Source: Mini-Reviews in Medicinal Chemistry. Unidade: FCFRP
Subjects: TRYPANOSOMA CRUZI, DOENÇA DE CHAGAS, ESTRATÉGIAS TERAPÊUTICAS
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ABNT
CAMPO, Vanessa Leiria e MARTINS-TEIXEIRA, Maristela Braga e CARVALHO, Ivone. Trypanosoma cruzi invasion into host cells: a complex molecular targets interplay. Mini-Reviews in Medicinal Chemistry, v. 16, n. 13, p. 1084-1097, 2016Tradução . . Disponível em: https://doi.org/10.2174/1389557516666160607230238. Acesso em: 15 nov. 2024.
APA
Campo, V. L., Martins-Teixeira, M. B., & Carvalho, I. (2016). Trypanosoma cruzi invasion into host cells: a complex molecular targets interplay. Mini-Reviews in Medicinal Chemistry, 16( 13), 1084-1097. doi:10.2174/1389557516666160607230238
NLM
Campo VL, Martins-Teixeira MB, Carvalho I. Trypanosoma cruzi invasion into host cells: a complex molecular targets interplay [Internet]. Mini-Reviews in Medicinal Chemistry. 2016 ; 16( 13): 1084-1097.[citado 2024 nov. 15 ] Available from: https://doi.org/10.2174/1389557516666160607230238
Vancouver
Campo VL, Martins-Teixeira MB, Carvalho I. Trypanosoma cruzi invasion into host cells: a complex molecular targets interplay [Internet]. Mini-Reviews in Medicinal Chemistry. 2016 ; 16( 13): 1084-1097.[citado 2024 nov. 15 ] Available from: https://doi.org/10.2174/1389557516666160607230238
Artigo de periodico
Design, synthesis and enzymatic evaluation of 3-O-substituted aryl β-d-galactopyranosides as inhibitors of Trypanosoma cruzi trans-sialidase (2014)
Silva, Bruno L; S. Filho, José D; Andrade, Peterson; Carvalho, Ivone; Alves , Ricardo J
Source: Bioorganic & Medicinal Chemistry Letters. Unidade: FCFRP
Subjects: INIBIDORES DE ENZIMAS (FARMACOLOGIA), GLICOPROTEÍNAS (ANTAGONISTAS E INIBIDORES), TRYPANOSOMA CRUZI (ENZIMOLOGIA)
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ABNT
SILVA, Bruno L et al. Design, synthesis and enzymatic evaluation of 3-O-substituted aryl β-d-galactopyranosides as inhibitors of Trypanosoma cruzi trans-sialidase. Bioorganic & Medicinal Chemistry Letters, v. 24, n. 18, p. 4529-4532, 2014Tradução . . Disponível em: https://doi.org/10.1016/j.bmcl.2014.07.088. Acesso em: 15 nov. 2024.
APA
Silva, B. L., S. Filho, J. D., Andrade, P., Carvalho, I., & Alves , R. J. (2014). Design, synthesis and enzymatic evaluation of 3-O-substituted aryl β-d-galactopyranosides as inhibitors of Trypanosoma cruzi trans-sialidase. Bioorganic & Medicinal Chemistry Letters, 24( 18), 4529-4532. doi:10.1016/j.bmcl.2014.07.088
NLM
Silva BL, S. Filho JD, Andrade P, Carvalho I, Alves RJ. Design, synthesis and enzymatic evaluation of 3-O-substituted aryl β-d-galactopyranosides as inhibitors of Trypanosoma cruzi trans-sialidase [Internet]. Bioorganic & Medicinal Chemistry Letters. 2014 ; 24( 18): 4529-4532.[citado 2024 nov. 15 ] Available from: https://doi.org/10.1016/j.bmcl.2014.07.088
Vancouver
Silva BL, S. Filho JD, Andrade P, Carvalho I, Alves RJ. Design, synthesis and enzymatic evaluation of 3-O-substituted aryl β-d-galactopyranosides as inhibitors of Trypanosoma cruzi trans-sialidase [Internet]. Bioorganic & Medicinal Chemistry Letters. 2014 ; 24( 18): 4529-4532.[citado 2024 nov. 15 ] Available from: https://doi.org/10.1016/j.bmcl.2014.07.088
Artigo de periodico
'Click chemistry' synthesis of a library of 1,2,3-triazole-substituted galactose derivatives and their evaluation against Trypanosoma cruzi and its cell surface trans-sialidase (2010)
Carvalho, Ivone; Andrade, Peterson; Campo, Vanessa L.; Guedes, Paulo M. M.; Sesti-Costa, Renata; Silva, João Santana da; Schenkman, Sergio; Dedola, Simone; Hill, Lionel; Rejzek, Martin; Nepogodiev, Sergey A.; Field, Robert A.
Source: Bioorganic and Medicinal Chemistry. Unidades: FCFRP, FMRP
Subjects: TRYPANOSOMA CRUZI, QUÍMICA
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ABNT
CARVALHO, Ivone et al. 'Click chemistry' synthesis of a library of 1,2,3-triazole-substituted galactose derivatives and their evaluation against Trypanosoma cruzi and its cell surface trans-sialidase. Bioorganic and Medicinal Chemistry, v. 18, n. 7, p. 2412-2427, 2010Tradução . . Disponível em: https://doi.org/10.1016/j.bmc.2010.02.053. Acesso em: 15 nov. 2024.
APA
Carvalho, I., Andrade, P., Campo, V. L., Guedes, P. M. M., Sesti-Costa, R., Silva, J. S. da, et al. (2010). 'Click chemistry' synthesis of a library of 1,2,3-triazole-substituted galactose derivatives and their evaluation against Trypanosoma cruzi and its cell surface trans-sialidase. Bioorganic and Medicinal Chemistry, 18( 7), 2412-2427. doi:10.1016/j.bmc.2010.02.053
NLM
Carvalho I, Andrade P, Campo VL, Guedes PMM, Sesti-Costa R, Silva JS da, Schenkman S, Dedola S, Hill L, Rejzek M, Nepogodiev SA, Field RA. 'Click chemistry' synthesis of a library of 1,2,3-triazole-substituted galactose derivatives and their evaluation against Trypanosoma cruzi and its cell surface trans-sialidase [Internet]. Bioorganic and Medicinal Chemistry. 2010 ; 18( 7): 2412-2427.[citado 2024 nov. 15 ] Available from: https://doi.org/10.1016/j.bmc.2010.02.053
Vancouver
Carvalho I, Andrade P, Campo VL, Guedes PMM, Sesti-Costa R, Silva JS da, Schenkman S, Dedola S, Hill L, Rejzek M, Nepogodiev SA, Field RA. 'Click chemistry' synthesis of a library of 1,2,3-triazole-substituted galactose derivatives and their evaluation against Trypanosoma cruzi and its cell surface trans-sialidase [Internet]. Bioorganic and Medicinal Chemistry. 2010 ; 18( 7): 2412-2427.[citado 2024 nov. 15 ] Available from: https://doi.org/10.1016/j.bmc.2010.02.053
Artigo de periodico
Molecular dynamics, density functional, ADMET predictions, virtual screening, and molecular interaction field studies for identification and evaluation of novel potential CDK2 inhibitors in cancer therapy (2008)
Silva, Vinicius Barreto da; Kawano, Daniel Fábio; Gomes, Adriane da Silveira; Carvalho, Ivone; Taft, Carlton Anthony; Silva, Carlos Henrique Tomich de Paula da
Source: Journal of Physical Chemistry Part A. Unidade: FCFRP
Subjects: QUÍMICA FARMACÊUTICA, NEOPLASIAS (TERAPIA)
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
SILVA, Vinicius Barreto da et al. Molecular dynamics, density functional, ADMET predictions, virtual screening, and molecular interaction field studies for identification and evaluation of novel potential CDK2 inhibitors in cancer therapy. Journal of Physical Chemistry Part A, v. 112, n. 38, p. 8902-8910, 2008Tradução . . Acesso em: 15 nov. 2024.
APA
Silva, V. B. da, Kawano, D. F., Gomes, A. da S., Carvalho, I., Taft, C. A., & Silva, C. H. T. de P. da. (2008). Molecular dynamics, density functional, ADMET predictions, virtual screening, and molecular interaction field studies for identification and evaluation of novel potential CDK2 inhibitors in cancer therapy. Journal of Physical Chemistry Part A, 112( 38), 8902-8910.
NLM
Silva VB da, Kawano DF, Gomes A da S, Carvalho I, Taft CA, Silva CHT de P da. Molecular dynamics, density functional, ADMET predictions, virtual screening, and molecular interaction field studies for identification and evaluation of novel potential CDK2 inhibitors in cancer therapy. Journal of Physical Chemistry Part A. 2008 ; 112( 38): 8902-8910.[citado 2024 nov. 15 ]
Vancouver
Silva VB da, Kawano DF, Gomes A da S, Carvalho I, Taft CA, Silva CHT de P da. Molecular dynamics, density functional, ADMET predictions, virtual screening, and molecular interaction field studies for identification and evaluation of novel potential CDK2 inhibitors in cancer therapy. Journal of Physical Chemistry Part A. 2008 ; 112( 38): 8902-8910.[citado 2024 nov. 15 ]
Artigo de periodico
New insights into aminoglycoside antibiotics and derivatives (2007)
Silva, Julierme G. da; Carvalho, Ivone
Source: Current Medical Chemistry. Unidade: FCFRP
Subjects: ANTIBIÓTICOS, HIV
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
SILVA, Julierme G. da e CARVALHO, Ivone. New insights into aminoglycoside antibiotics and derivatives. Current Medical Chemistry, v. 14, p. 1101-1119, 2007Tradução . . Acesso em: 15 nov. 2024.
APA
Silva, J. G. da, & Carvalho, I. (2007). New insights into aminoglycoside antibiotics and derivatives. Current Medical Chemistry, 14, 1101-1119.
NLM
Silva JG da, Carvalho I. New insights into aminoglycoside antibiotics and derivatives. Current Medical Chemistry. 2007 ; 14 1101-1119.[citado 2024 nov. 15 ]
Vancouver
Silva JG da, Carvalho I. New insights into aminoglycoside antibiotics and derivatives. Current Medical Chemistry. 2007 ; 14 1101-1119.[citado 2024 nov. 15 ]
Artigo de periodico
Virtual screening, molecular interaction field, molecular dynamics, docking, density fuctional, and ADMET properties of novel AChE inhibitors in Alzheimer's disease (2007)
Silva, Carlos H. T. P. da; Carvalho, Ivone; Taft, C. A.
Source: Journal of Biomolecular Structure and Dynamics. Unidade: FCFRP
Subjects: QUÍMICA FARMACÊUTICA, DOENÇA DE ALZHEIMER
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
SILVA, Carlos H. T. P. da e CARVALHO, Ivone e TAFT, C. A. Virtual screening, molecular interaction field, molecular dynamics, docking, density fuctional, and ADMET properties of novel AChE inhibitors in Alzheimer's disease. Journal of Biomolecular Structure and Dynamics, v. 24, n. 6, p. 515-524, 2007Tradução . . Acesso em: 15 nov. 2024.
APA
Silva, C. H. T. P. da, Carvalho, I., & Taft, C. A. (2007). Virtual screening, molecular interaction field, molecular dynamics, docking, density fuctional, and ADMET properties of novel AChE inhibitors in Alzheimer's disease. Journal of Biomolecular Structure and Dynamics, 24( 6), 515-524.
NLM
Silva CHTP da, Carvalho I, Taft CA. Virtual screening, molecular interaction field, molecular dynamics, docking, density fuctional, and ADMET properties of novel AChE inhibitors in Alzheimer's disease. Journal of Biomolecular Structure and Dynamics. 2007 ; 24( 6): 515-524.[citado 2024 nov. 15 ]
Vancouver
Silva CHTP da, Carvalho I, Taft CA. Virtual screening, molecular interaction field, molecular dynamics, docking, density fuctional, and ADMET properties of novel AChE inhibitors in Alzheimer's disease. Journal of Biomolecular Structure and Dynamics. 2007 ; 24( 6): 515-524.[citado 2024 nov. 15 ]
Artigo de periodico
Dehydromonocrotaline inhibits mitochondrial complex I.: a potencial mechanism accounting for hepatotoxicity of monocrotaline (2007)
Mingatto, Fábio E.; Dorta, Daniel J.; Santos, Aline B. dos; Carvalho, Ivone; Silva, Carlos H. T. P. da; Silva, Vinícius B. da; Uyemura, Sérgio Akira; Santos, Antônio Cardozo dos; Curti, Carlos
Source: Toxicon. Unidade: FCFRP
Subjects: CROTALÁRIA, CITOTOXINAS
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
MINGATTO, Fábio E. et al. Dehydromonocrotaline inhibits mitochondrial complex I.: a potencial mechanism accounting for hepatotoxicity of monocrotaline. Toxicon, v. 50, n. 5, p. 724-730, 2007Tradução . . Disponível em: https://doi.org/10.1016/j.toxicon.2007.06.006. Acesso em: 15 nov. 2024.
APA
Mingatto, F. E., Dorta, D. J., Santos, A. B. dos, Carvalho, I., Silva, C. H. T. P. da, Silva, V. B. da, et al. (2007). Dehydromonocrotaline inhibits mitochondrial complex I.: a potencial mechanism accounting for hepatotoxicity of monocrotaline. Toxicon, 50( 5), 724-730. doi:10.1016/j.toxicon.2007.06.006
NLM
Mingatto FE, Dorta DJ, Santos AB dos, Carvalho I, Silva CHTP da, Silva VB da, Uyemura SA, Santos AC dos, Curti C. Dehydromonocrotaline inhibits mitochondrial complex I.: a potencial mechanism accounting for hepatotoxicity of monocrotaline [Internet]. Toxicon. 2007 ; 50( 5): 724-730.[citado 2024 nov. 15 ] Available from: https://doi.org/10.1016/j.toxicon.2007.06.006
Vancouver
Mingatto FE, Dorta DJ, Santos AB dos, Carvalho I, Silva CHTP da, Silva VB da, Uyemura SA, Santos AC dos, Curti C. Dehydromonocrotaline inhibits mitochondrial complex I.: a potencial mechanism accounting for hepatotoxicity of monocrotaline [Internet]. Toxicon. 2007 ; 50( 5): 724-730.[citado 2024 nov. 15 ] Available from: https://doi.org/10.1016/j.toxicon.2007.06.006

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