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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: 26 jun. 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 jun. 26 ] 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 jun. 26 ] Available from: https://doi.org/10.1016/j.bioorg.2021.104982
Artigo de periodico
Galactosyl and sialyl clusters: synthesis and evaluation against T. cruzi parasite (2019)
Figueredo, Andreza da Silva ; Andrade, Peterson de; Riul, Thalita Bachelli ; Marchiori, Marcelo Fiori ; Leo, Thais Canassa de ; Fleuri, Anna Karoline Aguiar; Schenkman, Sérgio; Baruffi, Marcelo Dias ; Carvalho, Ivone
Source: Pure and Applied Chemistry. Unidade: FCFRP
Subjects: DOENÇA DE CHAGAS, TRYPANOSOMA CRUZI
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FIGUEREDO, Andreza da Silva et al. Galactosyl and sialyl clusters: synthesis and evaluation against T. cruzi parasite. Pure and Applied Chemistry, v. 91, n. 7, p. 1191-1207, 2019Tradução . . Disponível em: https://doi.org/10.1515/pac-2019-0216. Acesso em: 26 jun. 2024.
APA
Figueredo, A. da S., Andrade, P. de, Riul, T. B., Marchiori, M. F., Leo, T. C. de, Fleuri, A. K. A., et al. (2019). Galactosyl and sialyl clusters: synthesis and evaluation against T. cruzi parasite. Pure and Applied Chemistry, 91( 7), 1191-1207. doi:10.1515/pac-2019-0216
NLM
Figueredo A da S, Andrade P de, Riul TB, Marchiori MF, Leo TC de, Fleuri AKA, Schenkman S, Baruffi MD, Carvalho I. Galactosyl and sialyl clusters: synthesis and evaluation against T. cruzi parasite [Internet]. Pure and Applied Chemistry. 2019 ; 91( 7): 1191-1207.[citado 2024 jun. 26 ] Available from: https://doi.org/10.1515/pac-2019-0216
Vancouver
Figueredo A da S, Andrade P de, Riul TB, Marchiori MF, Leo TC de, Fleuri AKA, Schenkman S, Baruffi MD, Carvalho I. Galactosyl and sialyl clusters: synthesis and evaluation against T. cruzi parasite [Internet]. Pure and Applied Chemistry. 2019 ; 91( 7): 1191-1207.[citado 2024 jun. 26 ] Available from: https://doi.org/10.1515/pac-2019-0216
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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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: 26 jun. 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 jun. 26 ] 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 jun. 26 ] Available from: https://doi.org/10.1016/j.carres.2016.04.020
Artigo de periodico
Combining the pharmacophore features of coumarins and 1,4-substituted 1,2,3-triazoles to design new acetylcholinesterase inhibitors: fast and easy generation of 4-methylcoumarins/1,2,3-triazoles conjugates via click chemistry (2016)
Torres, Fernando C.; Gonçalves, Guilherme A.; Vanzolini, Kenia L.; Merlo, Aloir A.; Gauer, Bruna; Holzschuh, Maribete; Andrade, Saulo; Piedade, Maristela; Garcia, Solange C.; Carvalho, Ivone; Poser, Gilsane L. von; Kawano, Daniel F.; Eifler-Lima, Vera L.; Cass, Quezia B.
Source: Journal of the Brazilian Chemical Society. Unidade: FCFRP
Subjects: DOENÇA DE ALZHEIMER, FARMACOLOGIA
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ABNT
TORRES, Fernando C. et al. Combining the pharmacophore features of coumarins and 1,4-substituted 1,2,3-triazoles to design new acetylcholinesterase inhibitors: fast and easy generation of 4-methylcoumarins/1,2,3-triazoles conjugates via click chemistry. Journal of the Brazilian Chemical Society, v. 27, n. 9, p. 1541-1550, 2016Tradução . . Disponível em: https://doi.org/10.5935/0103-5053.20160033. Acesso em: 26 jun. 2024.
APA
Torres, F. C., Gonçalves, G. A., Vanzolini, K. L., Merlo, A. A., Gauer, B., Holzschuh, M., et al. (2016). Combining the pharmacophore features of coumarins and 1,4-substituted 1,2,3-triazoles to design new acetylcholinesterase inhibitors: fast and easy generation of 4-methylcoumarins/1,2,3-triazoles conjugates via click chemistry. Journal of the Brazilian Chemical Society, 27( 9), 1541-1550. doi:10.5935/0103-5053.20160033
NLM
Torres FC, Gonçalves GA, Vanzolini KL, Merlo AA, Gauer B, Holzschuh M, Andrade S, Piedade M, Garcia SC, Carvalho I, Poser GL von, Kawano DF, Eifler-Lima VL, Cass QB. Combining the pharmacophore features of coumarins and 1,4-substituted 1,2,3-triazoles to design new acetylcholinesterase inhibitors: fast and easy generation of 4-methylcoumarins/1,2,3-triazoles conjugates via click chemistry [Internet]. Journal of the Brazilian Chemical Society. 2016 ; 27( 9): 1541-1550.[citado 2024 jun. 26 ] Available from: https://doi.org/10.5935/0103-5053.20160033
Vancouver
Torres FC, Gonçalves GA, Vanzolini KL, Merlo AA, Gauer B, Holzschuh M, Andrade S, Piedade M, Garcia SC, Carvalho I, Poser GL von, Kawano DF, Eifler-Lima VL, Cass QB. Combining the pharmacophore features of coumarins and 1,4-substituted 1,2,3-triazoles to design new acetylcholinesterase inhibitors: fast and easy generation of 4-methylcoumarins/1,2,3-triazoles conjugates via click chemistry [Internet]. Journal of the Brazilian Chemical Society. 2016 ; 27( 9): 1541-1550.[citado 2024 jun. 26 ] Available from: https://doi.org/10.5935/0103-5053.20160033
Artigo de periodico
Glycoclusters presenting lactose on calix[4]arene cores display trypanocidal activity (2011)
Galante, Eva; Geraci, Corrada; Sciuto, Sebastiano; Campo, Vanessa Leiria; Carvalho, Ivone; Sesti-Costa, Renata; Guedes, Paulo Marcos da Matta; Silva, João Santana da; Hill, Lionel; Nepogodiev, Sergey A; Field, Robert A.
Source: Tetrahedron. Unidades: FCFRP, FMRP
Subjects: TRIPANOSSOMICIDAS, TECNOLOGIA FARMACÊUTICA
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ABNT
GALANTE, Eva et al. Glycoclusters presenting lactose on calix[4]arene cores display trypanocidal activity. Tetrahedron, v. 67, n. 33, p. 5902-5912, 2011Tradução . . Disponível em: https://doi.org/10.1016/j.tet.2011.06.065. Acesso em: 26 jun. 2024.
APA
Galante, E., Geraci, C., Sciuto, S., Campo, V. L., Carvalho, I., Sesti-Costa, R., et al. (2011). Glycoclusters presenting lactose on calix[4]arene cores display trypanocidal activity. Tetrahedron, 67( 33), 5902-5912. doi:10.1016/j.tet.2011.06.065
NLM
Galante E, Geraci C, Sciuto S, Campo VL, Carvalho I, Sesti-Costa R, Guedes PM da M, Silva JS da, Hill L, Nepogodiev SA, Field RA. Glycoclusters presenting lactose on calix[4]arene cores display trypanocidal activity [Internet]. Tetrahedron. 2011 ; 67( 33): 5902-5912.[citado 2024 jun. 26 ] Available from: https://doi.org/10.1016/j.tet.2011.06.065
Vancouver
Galante E, Geraci C, Sciuto S, Campo VL, Carvalho I, Sesti-Costa R, Guedes PM da M, Silva JS da, Hill L, Nepogodiev SA, Field RA. Glycoclusters presenting lactose on calix[4]arene cores display trypanocidal activity [Internet]. Tetrahedron. 2011 ; 67( 33): 5902-5912.[citado 2024 jun. 26 ] Available from: https://doi.org/10.1016/j.tet.2011.06.065
Artigo de periodico
Application of copper(I)-catalysed azide/alkyne cycloaddition (CuAAC) 'click chemistry' in carbohydrate drug and neoglycopolymer synthesis (2010)
Leoneti, Valquiria Aragão; Campo, Vanessa Leiria; Gomes, Adriane da Silveira; Field, Robert A.; Carvalho, Ivone
Source: Tetrahedron. Unidade: FCFRP
Subjects: SÍNTESE QUÍMICA, FÁRMACOS
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LEONETI, Valquiria Aragão et al. Application of copper(I)-catalysed azide/alkyne cycloaddition (CuAAC) 'click chemistry' in carbohydrate drug and neoglycopolymer synthesis. Tetrahedron, v. 66, n. 49, p. 9475-9492, 2010Tradução . . Disponível em: https://doi.org/10.1016/j.tet.2010.10.001. Acesso em: 26 jun. 2024.
APA
Leoneti, V. A., Campo, V. L., Gomes, A. da S., Field, R. A., & Carvalho, I. (2010). Application of copper(I)-catalysed azide/alkyne cycloaddition (CuAAC) 'click chemistry' in carbohydrate drug and neoglycopolymer synthesis. Tetrahedron, 66( 49), 9475-9492. doi:10.1016/j.tet.2010.10.001
NLM
Leoneti VA, Campo VL, Gomes A da S, Field RA, Carvalho I. Application of copper(I)-catalysed azide/alkyne cycloaddition (CuAAC) 'click chemistry' in carbohydrate drug and neoglycopolymer synthesis [Internet]. Tetrahedron. 2010 ; 66( 49): 9475-9492.[citado 2024 jun. 26 ] Available from: https://doi.org/10.1016/j.tet.2010.10.001
Vancouver
Leoneti VA, Campo VL, Gomes A da S, Field RA, Carvalho I. Application of copper(I)-catalysed azide/alkyne cycloaddition (CuAAC) 'click chemistry' in carbohydrate drug and neoglycopolymer synthesis [Internet]. Tetrahedron. 2010 ; 66( 49): 9475-9492.[citado 2024 jun. 26 ] Available from: https://doi.org/10.1016/j.tet.2010.10.001
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: 26 jun. 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 jun. 26 ] 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 jun. 26 ] Available from: https://doi.org/10.1016/j.bmc.2010.02.053
Artigo de periodico
Carrageenans: biological properties, chemical modifications and structural analysis - a review (2009)
Campo, Vanessa Leiria; Kawano, Daniel Fábio; Silva Junior, Dilson Braz da; Carvalho, Ivone
Source: Carbohydrate Polymers. Unidade: FCFRP
Subjects: CARRAGENINA, FARMACOLOGIA
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ABNT
CAMPO, Vanessa Leiria et al. Carrageenans: biological properties, chemical modifications and structural analysis - a review. Carbohydrate Polymers, v. 77, n. 2, p. 167-180, 2009Tradução . . Disponível em: https://doi.org/10.1016/j.carbpol.2009.01.020. Acesso em: 26 jun. 2024.
APA
Campo, V. L., Kawano, D. F., Silva Junior, D. B. da, & Carvalho, I. (2009). Carrageenans: biological properties, chemical modifications and structural analysis - a review. Carbohydrate Polymers, 77( 2), 167-180. doi:10.1016/j.carbpol.2009.01.020
NLM
Campo VL, Kawano DF, Silva Junior DB da, Carvalho I. Carrageenans: biological properties, chemical modifications and structural analysis - a review [Internet]. Carbohydrate Polymers. 2009 ; 77( 2): 167-180.[citado 2024 jun. 26 ] Available from: https://doi.org/10.1016/j.carbpol.2009.01.020
Vancouver
Campo VL, Kawano DF, Silva Junior DB da, Carvalho I. Carrageenans: biological properties, chemical modifications and structural analysis - a review [Internet]. Carbohydrate Polymers. 2009 ; 77( 2): 167-180.[citado 2024 jun. 26 ] Available from: https://doi.org/10.1016/j.carbpol.2009.01.020
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)
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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: 26 jun. 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 jun. 26 ]
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 jun. 26 ]
Artigo de periodico
Diketopiperazines: biological activity and synthesis (2007)
Martins, Maristela B.; Carvalho, Ivone
Source: Tetrahedron. Unidade: FCFRP
Subjects: PEPTÍDEOS CÍCLICOS, QUÍMICA MÉDICA
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ABNT
MARTINS, Maristela B. e CARVALHO, Ivone. Diketopiperazines: biological activity and synthesis. Tetrahedron, v. 63, n. 40, p. 9923-9932, 2007Tradução . . Disponível em: https://doi.org/10.1016/j.tet.2007.04.105. Acesso em: 26 jun. 2024.
APA
Martins, M. B., & Carvalho, I. (2007). Diketopiperazines: biological activity and synthesis. Tetrahedron, 63( 40), 9923-9932. doi:10.1016/j.tet.2007.04.105
NLM
Martins MB, Carvalho I. Diketopiperazines: biological activity and synthesis [Internet]. Tetrahedron. 2007 ; 63( 40): 9923-9932.[citado 2024 jun. 26 ] Available from: https://doi.org/10.1016/j.tet.2007.04.105
Vancouver
Martins MB, Carvalho I. Diketopiperazines: biological activity and synthesis [Internet]. Tetrahedron. 2007 ; 63( 40): 9923-9932.[citado 2024 jun. 26 ] Available from: https://doi.org/10.1016/j.tet.2007.04.105
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
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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: 26 jun. 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 jun. 26 ]
Vancouver
Silva JG da, Carvalho I. New insights into aminoglycoside antibiotics and derivatives. Current Medical Chemistry. 2007 ; 14 1101-1119.[citado 2024 jun. 26 ]
Artigo de periodico
Chemical and chemoenzymatic synthesis of glycosyl-amino acids and glycopeptides related to Trypanosoma cruzi mucins (2007)
Campo, Vanessa Leiria; Carvalho, Ivone; Allman, Sarah; Davis, Benjamin G.; Field, Robert A.
Source: Organic and Biomolecular Chemistry. Unidade: FCFRP
Subjects: GLICOPEPTÍDEOS, TRYPANOSOMA CRUZI
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ABNT
CAMPO, Vanessa Leiria et al. Chemical and chemoenzymatic synthesis of glycosyl-amino acids and glycopeptides related to Trypanosoma cruzi mucins. Organic and Biomolecular Chemistry, v. 5, p. 2645-2657, 2007Tradução . . Disponível em: https://doi.org/10.1039/b707772f. Acesso em: 26 jun. 2024.
APA
Campo, V. L., Carvalho, I., Allman, S., Davis, B. G., & Field, R. A. (2007). Chemical and chemoenzymatic synthesis of glycosyl-amino acids and glycopeptides related to Trypanosoma cruzi mucins. Organic and Biomolecular Chemistry, 5, 2645-2657. doi:10.1039/b707772f
NLM
Campo VL, Carvalho I, Allman S, Davis BG, Field RA. Chemical and chemoenzymatic synthesis of glycosyl-amino acids and glycopeptides related to Trypanosoma cruzi mucins [Internet]. Organic and Biomolecular Chemistry. 2007 ; 5 2645-2657.[citado 2024 jun. 26 ] Available from: https://doi.org/10.1039/b707772f
Vancouver
Campo VL, Carvalho I, Allman S, Davis BG, Field RA. Chemical and chemoenzymatic synthesis of glycosyl-amino acids and glycopeptides related to Trypanosoma cruzi mucins [Internet]. Organic and Biomolecular Chemistry. 2007 ; 5 2645-2657.[citado 2024 jun. 26 ] Available from: https://doi.org/10.1039/b707772f
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
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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: 26 jun. 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 jun. 26 ] 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 jun. 26 ] Available from: https://doi.org/10.1016/j.toxicon.2007.06.006
Artigo de periodico
HPLC analysis of glycosylated amino acids (2006)
Campo, Vanessa Leiria; Borges, Áurea Donizete Lanchote; Carvalho, Ivone
Source: Journal of Brazilian Chemical Society. Unidade: FCFRP
Subjects: CROMATOGRAFIA LÍQUIDA DE ALTA EFICIÊNCIA, AMINOÁCIDOS, GLICOSÍDEOS
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
CAMPO, Vanessa Leiria e BORGES, Áurea Donizete Lanchote e CARVALHO, Ivone. HPLC analysis of glycosylated amino acids. Journal of Brazilian Chemical Society, v. 17, n. 4, p. 648-654, 2006Tradução . . Disponível em: https://doi.org/10.1590/s0103-50532006000400004. Acesso em: 26 jun. 2024.
APA
Campo, V. L., Borges, Á. D. L., & Carvalho, I. (2006). HPLC analysis of glycosylated amino acids. Journal of Brazilian Chemical Society, 17( 4), 648-654. doi:10.1590/s0103-50532006000400004
NLM
Campo VL, Borges ÁDL, Carvalho I. HPLC analysis of glycosylated amino acids [Internet]. Journal of Brazilian Chemical Society. 2006 ; 17( 4): 648-654.[citado 2024 jun. 26 ] Available from: https://doi.org/10.1590/s0103-50532006000400004
Vancouver
Campo VL, Borges ÁDL, Carvalho I. HPLC analysis of glycosylated amino acids [Internet]. Journal of Brazilian Chemical Society. 2006 ; 17( 4): 648-654.[citado 2024 jun. 26 ] Available from: https://doi.org/10.1590/s0103-50532006000400004
Artigo de periodico
'alfa' and 'beta' Glucosidase inhibitors: chemical structure and biological activity (2006)
Melo, Eduardo Borges de; Gomes, Adriane da Silveira; Carvalho, Ivone
Source: Tetrahedron. Unidade: FCFRP
Subjects: ENZIMAS GLICOLÍTICAS, INIBIDORES DE ENZIMAS
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
MELO, Eduardo Borges de e GOMES, Adriane da Silveira e CARVALHO, Ivone. 'alfa' and 'beta' Glucosidase inhibitors: chemical structure and biological activity. Tetrahedron, v. 62, n. 44, p. 10277-10302, 2006Tradução . . Acesso em: 26 jun. 2024.
APA
Melo, E. B. de, Gomes, A. da S., & Carvalho, I. (2006). 'alfa' and 'beta' Glucosidase inhibitors: chemical structure and biological activity. Tetrahedron, 62( 44), 10277-10302.
NLM
Melo EB de, Gomes A da S, Carvalho I. 'alfa' and 'beta' Glucosidase inhibitors: chemical structure and biological activity. Tetrahedron. 2006 ; 62( 44): 10277-10302.[citado 2024 jun. 26 ]
Vancouver
Melo EB de, Gomes A da S, Carvalho I. 'alfa' and 'beta' Glucosidase inhibitors: chemical structure and biological activity. Tetrahedron. 2006 ; 62( 44): 10277-10302.[citado 2024 jun. 26 ]
Artigo de periodico
Synthesis and trypanocidal activity of 1,4-bis(3,4,5-trimethoxy-phenyl)-1,4-butanediol and 1,4-bis-(3,4-dimethoxyphenyl)-1,4-butanediol (2006)
Bernardes, Lilian Sibelle Campos; Kato, Massuo Jorge ; Albuquerque, Sérgio de; Carvalho, Ivone
Source: Bioorganic and Medicinal Chemistry. Unidades: IQ, FCFRP
Subjects: ANTIPARASITÁRIOS, PRODUTOS NATURAIS, TRYPANOSOMA CRUZI
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
BERNARDES, Lilian Sibelle Campos et al. Synthesis and trypanocidal activity of 1,4-bis(3,4,5-trimethoxy-phenyl)-1,4-butanediol and 1,4-bis-(3,4-dimethoxyphenyl)-1,4-butanediol. Bioorganic and Medicinal Chemistry, v. 14, p. 7075-7082, 2006Tradução . . Disponível em: https://doi.org/10.1016/j.bmc.2006.07.006. Acesso em: 26 jun. 2024.
APA
Bernardes, L. S. C., Kato, M. J., Albuquerque, S. de, & Carvalho, I. (2006). Synthesis and trypanocidal activity of 1,4-bis(3,4,5-trimethoxy-phenyl)-1,4-butanediol and 1,4-bis-(3,4-dimethoxyphenyl)-1,4-butanediol. Bioorganic and Medicinal Chemistry, 14, 7075-7082. doi:10.1016/j.bmc.2006.07.006
NLM
Bernardes LSC, Kato MJ, Albuquerque S de, Carvalho I. Synthesis and trypanocidal activity of 1,4-bis(3,4,5-trimethoxy-phenyl)-1,4-butanediol and 1,4-bis-(3,4-dimethoxyphenyl)-1,4-butanediol [Internet]. Bioorganic and Medicinal Chemistry. 2006 ; 14 7075-7082.[citado 2024 jun. 26 ] Available from: https://doi.org/10.1016/j.bmc.2006.07.006
Vancouver
Bernardes LSC, Kato MJ, Albuquerque S de, Carvalho I. Synthesis and trypanocidal activity of 1,4-bis(3,4,5-trimethoxy-phenyl)-1,4-butanediol and 1,4-bis-(3,4-dimethoxyphenyl)-1,4-butanediol [Internet]. Bioorganic and Medicinal Chemistry. 2006 ; 14 7075-7082.[citado 2024 jun. 26 ] Available from: https://doi.org/10.1016/j.bmc.2006.07.006
Artigo de periodico
Molecular modeling, docking and ADMET studies applied to the design of a novel hybrid for treatment of Alzheimer's disease (2006)
Silva, Carlos H. T. P. da; Campo, Vanessa Leiria; Carvalho, Ivone; Taft, Carlton A.
Source: Journal of Molecular Graphics and Modelling. Unidade: FCFRP
Assunto: QUÍMICA FARMACÊUTICA
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
SILVA, Carlos H. T. P. da et al. Molecular modeling, docking and ADMET studies applied to the design of a novel hybrid for treatment of Alzheimer's disease. Journal of Molecular Graphics and Modelling, v. 25, p. 169-175, 2006Tradução . . Disponível em: https://doi.org/10.1016/j.jmgm.2005.12.002. Acesso em: 26 jun. 2024.
APA
Silva, C. H. T. P. da, Campo, V. L., Carvalho, I., & Taft, C. A. (2006). Molecular modeling, docking and ADMET studies applied to the design of a novel hybrid for treatment of Alzheimer's disease. Journal of Molecular Graphics and Modelling, 25, 169-175. doi:10.1016/j.jmgm.2005.12.002
NLM
Silva CHTP da, Campo VL, Carvalho I, Taft CA. Molecular modeling, docking and ADMET studies applied to the design of a novel hybrid for treatment of Alzheimer's disease [Internet]. Journal of Molecular Graphics and Modelling. 2006 ; 25 169-175.[citado 2024 jun. 26 ] Available from: https://doi.org/10.1016/j.jmgm.2005.12.002
Vancouver
Silva CHTP da, Campo VL, Carvalho I, Taft CA. Molecular modeling, docking and ADMET studies applied to the design of a novel hybrid for treatment of Alzheimer's disease [Internet]. Journal of Molecular Graphics and Modelling. 2006 ; 25 169-175.[citado 2024 jun. 26 ] Available from: https://doi.org/10.1016/j.jmgm.2005.12.002
Artigo de periodico
Diketopiperazines produced by an Aspergillus fumigatus Brazilian strain (2005)
Furtado, Niege Araçari Jacometti Cardoso; Pupo, Mônica Tallarico; Carvalho, Ivone; Campo, Vanessa L.; Duarte, Marta Cristina Teixeira; Bastos, Jairo Kenupp
Source: Journal of Brazilian Chemical Society. Unidade: FCFRP
Assunto: QUÍMICA FARMACÊUTICA
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
FURTADO, Niege Araçari Jacometti Cardoso et al. Diketopiperazines produced by an Aspergillus fumigatus Brazilian strain. Journal of Brazilian Chemical Society, v. 16, n. 6B, p. 1448-1453, 2005Tradução . . Disponível em: https://doi.org/10.1590/s0103-50532005000800026. Acesso em: 26 jun. 2024.
APA
Furtado, N. A. J. C., Pupo, M. T., Carvalho, I., Campo, V. L., Duarte, M. C. T., & Bastos, J. K. (2005). Diketopiperazines produced by an Aspergillus fumigatus Brazilian strain. Journal of Brazilian Chemical Society, 16( 6B), 1448-1453. doi:10.1590/s0103-50532005000800026
NLM
Furtado NAJC, Pupo MT, Carvalho I, Campo VL, Duarte MCT, Bastos JK. Diketopiperazines produced by an Aspergillus fumigatus Brazilian strain [Internet]. Journal of Brazilian Chemical Society. 2005 ; 16( 6B): 1448-1453.[citado 2024 jun. 26 ] Available from: https://doi.org/10.1590/s0103-50532005000800026
Vancouver
Furtado NAJC, Pupo MT, Carvalho I, Campo VL, Duarte MCT, Bastos JK. Diketopiperazines produced by an Aspergillus fumigatus Brazilian strain [Internet]. Journal of Brazilian Chemical Society. 2005 ; 16( 6B): 1448-1453.[citado 2024 jun. 26 ] Available from: https://doi.org/10.1590/s0103-50532005000800026
Artigo de periodico
Medicinal chemistry and molecular modeling:: An integration to teach drug structure-activity relationship and the molecular basis of drug action (2005)
Carvalho, Ivone; Borges, Áurea Donizete Lanchote; Bernardes, Lílian Sibelle Campos
Source: Journal of Chemical Education. Unidade: FCFRP
Assunto: QUÍMICA FARMACÊUTICA
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
CARVALHO, Ivone e BORGES, Áurea Donizete Lanchote e BERNARDES, Lílian Sibelle Campos. Medicinal chemistry and molecular modeling:: An integration to teach drug structure-activity relationship and the molecular basis of drug action. Journal of Chemical Education, v. 82, n. 4, p. 588-596, 2005Tradução . . Acesso em: 26 jun. 2024.
APA
Carvalho, I., Borges, Á. D. L., & Bernardes, L. S. C. (2005). Medicinal chemistry and molecular modeling:: An integration to teach drug structure-activity relationship and the molecular basis of drug action. Journal of Chemical Education, 82( 4), 588-596.
NLM
Carvalho I, Borges ÁDL, Bernardes LSC. Medicinal chemistry and molecular modeling:: An integration to teach drug structure-activity relationship and the molecular basis of drug action. Journal of Chemical Education. 2005 ; 82( 4): 588-596.[citado 2024 jun. 26 ]
Vancouver
Carvalho I, Borges ÁDL, Bernardes LSC. Medicinal chemistry and molecular modeling:: An integration to teach drug structure-activity relationship and the molecular basis of drug action. Journal of Chemical Education. 2005 ; 82( 4): 588-596.[citado 2024 jun. 26 ]
Artigo de periodico
Homology modeling and molecular interaction field studies of 'alfa'-glucosidases as a guide to structure-based design of novel proposed anti-HIV inhibitors (2005)
Tomich, C. H.; Silva, P. da; Carvalho, Ivone; Taft, C. A.
Source: Journal of Computer-Aided Molecular Design. Unidade: FCFRP
Assunto: SÍNDROME DE IMUNODEFICIÊNCIA ADQUIRIDA (TRATAMENTO)
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
TOMICH, C. H. et al. Homology modeling and molecular interaction field studies of 'alfa'-glucosidases as a guide to structure-based design of novel proposed anti-HIV inhibitors. Journal of Computer-Aided Molecular Design, v. 19, p. 83-92, 2005Tradução . . Disponível em: https://doi.org/10.1007/s10822-005-1486-6. Acesso em: 26 jun. 2024.
APA
Tomich, C. H., Silva, P. da, Carvalho, I., & Taft, C. A. (2005). Homology modeling and molecular interaction field studies of 'alfa'-glucosidases as a guide to structure-based design of novel proposed anti-HIV inhibitors. Journal of Computer-Aided Molecular Design, 19, 83-92. doi:10.1007/s10822-005-1486-6
NLM
Tomich CH, Silva P da, Carvalho I, Taft CA. Homology modeling and molecular interaction field studies of 'alfa'-glucosidases as a guide to structure-based design of novel proposed anti-HIV inhibitors [Internet]. Journal of Computer-Aided Molecular Design. 2005 ; 19 83-92.[citado 2024 jun. 26 ] Available from: https://doi.org/10.1007/s10822-005-1486-6
Vancouver
Tomich CH, Silva P da, Carvalho I, Taft CA. Homology modeling and molecular interaction field studies of 'alfa'-glucosidases as a guide to structure-based design of novel proposed anti-HIV inhibitors [Internet]. Journal of Computer-Aided Molecular Design. 2005 ; 19 83-92.[citado 2024 jun. 26 ] Available from: https://doi.org/10.1007/s10822-005-1486-6

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