ReP USP - Resultado da busca

Artigo de periodico
Crystal structure of 2-methoxy-2-[(4- methylphenyl)sulfanyl]-1-phenylethan-1- one (2015)
Zukerman-Schpector, Júlio; Olivato, Paulo Roberto ; Traesel, Henrique Joel; Valença, Jéssica; Rodrigues, Daniel Nopper Silva ; Edward R. T. Tiekink
Fonte: Acta Crystallographic Section E. Unidade: IQ
Assuntos: COMPOSTOS ALICÍCLICOS, QUÍMICA ORGÂNICA
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ZUKERMAN-SCHPECTOR, Júlio et al. Crystal structure of 2-methoxy-2-[(4- methylphenyl)sulfanyl]-1-phenylethan-1- one. Acta Crystallographic Section E, v. E71, p. 3-5 : + Supplementary materials ( S1-S7), 2015Tradução . . Disponível em: https://doi.org/10.1107/S205698901402550X. Acesso em: 12 jul. 2024.
APA
Zukerman-Schpector, J., Olivato, P. R., Traesel, H. J., Valença, J., Rodrigues, D. N. S., & Edward R. T. Tiekink,. (2015). Crystal structure of 2-methoxy-2-[(4- methylphenyl)sulfanyl]-1-phenylethan-1- one. Acta Crystallographic Section E, E71, 3-5 : + Supplementary materials ( S1-S7). doi:10.1107/S205698901402550X
NLM
Zukerman-Schpector J, Olivato PR, Traesel HJ, Valença J, Rodrigues DNS, Edward R. T. Tiekink. Crystal structure of 2-methoxy-2-[(4- methylphenyl)sulfanyl]-1-phenylethan-1- one [Internet]. Acta Crystallographic Section E. 2015 ; E71 3-5 : + Supplementary materials ( S1-S7).[citado 2024 jul. 12 ] Available from: https://doi.org/10.1107/S205698901402550X
Vancouver
Zukerman-Schpector J, Olivato PR, Traesel HJ, Valença J, Rodrigues DNS, Edward R. T. Tiekink. Crystal structure of 2-methoxy-2-[(4- methylphenyl)sulfanyl]-1-phenylethan-1- one [Internet]. Acta Crystallographic Section E. 2015 ; E71 3-5 : + Supplementary materials ( S1-S7).[citado 2024 jul. 12 ] Available from: https://doi.org/10.1107/S205698901402550X
Artigo de periodico
Cell Penetrating Peptide (CPP)-conjugated desferrioxamine for enhanced neuroprotection: synthesis and in vitro evaluation (2014)
Goswami, Dibakar; Machini, Maria Teresa ; Silvestre, Daniel Menezes; Nomura, Cassiana Seimi ; Espósito, Breno Pannia
Fonte: Bioconjugate Chemistry. Unidade: IQ
Assuntos: PEPTÍDEOS, FERRO
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GOSWAMI, Dibakar et al. Cell Penetrating Peptide (CPP)-conjugated desferrioxamine for enhanced neuroprotection: synthesis and in vitro evaluation. Bioconjugate Chemistry, v. 25, n. 11, p. 2067-2080, 2014Tradução . . Disponível em: https://doi.org/10.1021/bc5004197. Acesso em: 12 jul. 2024.
APA
Goswami, D., Machini, M. T., Silvestre, D. M., Nomura, C. S., & Espósito, B. P. (2014). Cell Penetrating Peptide (CPP)-conjugated desferrioxamine for enhanced neuroprotection: synthesis and in vitro evaluation. Bioconjugate Chemistry, 25( 11), 2067-2080. doi:10.1021/bc5004197
NLM
Goswami D, Machini MT, Silvestre DM, Nomura CS, Espósito BP. Cell Penetrating Peptide (CPP)-conjugated desferrioxamine for enhanced neuroprotection: synthesis and in vitro evaluation [Internet]. Bioconjugate Chemistry. 2014 ; 25( 11): 2067-2080.[citado 2024 jul. 12 ] Available from: https://doi.org/10.1021/bc5004197
Vancouver
Goswami D, Machini MT, Silvestre DM, Nomura CS, Espósito BP. Cell Penetrating Peptide (CPP)-conjugated desferrioxamine for enhanced neuroprotection: synthesis and in vitro evaluation [Internet]. Bioconjugate Chemistry. 2014 ; 25( 11): 2067-2080.[citado 2024 jul. 12 ] Available from: https://doi.org/10.1021/bc5004197
Trabalho de evento-resumo periodico
Theoretical study of oxalic peracid derivatives: insights on the high-energy intermadiate of the peroxyoxalate system (2014)
Augusto, Felipe Alberto; Pradie, Noriberto Araújo; Borin, Antonio Carlos ; Bastos, Erick Leite ; Baader, Wilhelm Josef
Fonte: Luminescence. Nome do evento: International Symposium on Bioluminescence and Chemiluminescence. Unidade: IQ
Assunto: REAÇÕES QUÍMICAS
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AUGUSTO, Felipe Alberto et al. Theoretical study of oxalic peracid derivatives: insights on the high-energy intermadiate of the peroxyoxalate system. Luminescence. Hoboken: Instituto de Química, Universidade de São Paulo. . Acesso em: 12 jul. 2024. , 2014
APA
Augusto, F. A., Pradie, N. A., Borin, A. C., Bastos, E. L., & Baader, W. J. (2014). Theoretical study of oxalic peracid derivatives: insights on the high-energy intermadiate of the peroxyoxalate system. Luminescence. Hoboken: Instituto de Química, Universidade de São Paulo.
NLM
Augusto FA, Pradie NA, Borin AC, Bastos EL, Baader WJ. Theoretical study of oxalic peracid derivatives: insights on the high-energy intermadiate of the peroxyoxalate system. Luminescence. 2014 ; 29 55 res. P0001.[citado 2024 jul. 12 ]
Vancouver
Augusto FA, Pradie NA, Borin AC, Bastos EL, Baader WJ. Theoretical study of oxalic peracid derivatives: insights on the high-energy intermadiate of the peroxyoxalate system. Luminescence. 2014 ; 29 55 res. P0001.[citado 2024 jul. 12 ]
Artigo de periodico
Effect of counterions on the shape, hydration, and degree of order at the interface of cationic micelles: the triflate case (2013)
Lima, Filipe da Silva ; Cuccovia, Iolanda Midea ; Horinek, Dominik; Amaral, Lia Queiroz do ; Riske, Karin do Amaral; Schreier, Shirley ; Salinas, Roberto Kopke ; Bastos, Erick Leite ; Pires, Paulo A R; Bozelli Junior, José Carlos ; Favaro, Denize C ; Rodrigues, Ana Clara B.; Dias, Luis Gustavo ; El Seoud, Omar A ; Chaimovich Guralnik, Hernan
Fonte: LANGMUIR. Unidades: IQ, IF, FFCLRP
Assuntos: RESSONÂNCIA MAGNÉTICA NUCLEAR, RAIOS X, FLUORESCÊNCIA
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LIMA, Filipe da Silva et al. Effect of counterions on the shape, hydration, and degree of order at the interface of cationic micelles: the triflate case. LANGMUIR, v. 29, n. 13, p. 4193-4203 , 2013Tradução . . Disponível em: https://doi.org/10.1021/la304658e. Acesso em: 12 jul. 2024.
APA
Lima, F. da S., Cuccovia, I. M., Horinek, D., Amaral, L. Q. do, Riske, K. do A., Schreier, S., et al. (2013). Effect of counterions on the shape, hydration, and degree of order at the interface of cationic micelles: the triflate case. LANGMUIR, 29( 13), 4193-4203 . doi:10.1021/la304658e
NLM
Lima F da S, Cuccovia IM, Horinek D, Amaral LQ do, Riske K do A, Schreier S, Salinas RK, Bastos EL, Pires PAR, Bozelli Junior JC, Favaro DC, Rodrigues ACB, Dias LG, El Seoud OA, Chaimovich Guralnik H. Effect of counterions on the shape, hydration, and degree of order at the interface of cationic micelles: the triflate case [Internet]. LANGMUIR. 2013 ; 29( 13): 4193-4203 .[citado 2024 jul. 12 ] Available from: https://doi.org/10.1021/la304658e
Vancouver
Lima F da S, Cuccovia IM, Horinek D, Amaral LQ do, Riske K do A, Schreier S, Salinas RK, Bastos EL, Pires PAR, Bozelli Junior JC, Favaro DC, Rodrigues ACB, Dias LG, El Seoud OA, Chaimovich Guralnik H. Effect of counterions on the shape, hydration, and degree of order at the interface of cationic micelles: the triflate case [Internet]. LANGMUIR. 2013 ; 29( 13): 4193-4203 .[citado 2024 jul. 12 ] Available from: https://doi.org/10.1021/la304658e
Artigo de periodico
Prediction of mono-, bi-, and trivalent metal cation relative toxicity to the seaweed Gracilaria domingensis (Gracilariales, Rhodophyta) in synthetic seawater (2013)
Mendes, Luiz Fernando; Villela, Leonardo Zambotti ; Yokoya, Nair Sumie; Bastos, Erick Leite ; Stevani, Cassius Vinicius ; Colepicolo, Pio
Fonte: Environmental Toxicology and Chemistry. Unidade: IQ
Assuntos: ÍONS, RHODOPHYTA
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ABNT
MENDES, Luiz Fernando et al. Prediction of mono-, bi-, and trivalent metal cation relative toxicity to the seaweed Gracilaria domingensis (Gracilariales, Rhodophyta) in synthetic seawater. Environmental Toxicology and Chemistry, v. 32, n. 11, p. 2571-2575, 2013Tradução . . Disponível em: https://doi.org/10.1002/etc.2340. Acesso em: 12 jul. 2024.
APA
Mendes, L. F., Villela, L. Z., Yokoya, N. S., Bastos, E. L., Stevani, C. V., & Colepicolo, P. (2013). Prediction of mono-, bi-, and trivalent metal cation relative toxicity to the seaweed Gracilaria domingensis (Gracilariales, Rhodophyta) in synthetic seawater. Environmental Toxicology and Chemistry, 32( 11), 2571-2575. doi:10.1002/etc.2340
NLM
Mendes LF, Villela LZ, Yokoya NS, Bastos EL, Stevani CV, Colepicolo P. Prediction of mono-, bi-, and trivalent metal cation relative toxicity to the seaweed Gracilaria domingensis (Gracilariales, Rhodophyta) in synthetic seawater [Internet]. Environmental Toxicology and Chemistry. 2013 ; 32( 11): 2571-2575.[citado 2024 jul. 12 ] Available from: https://doi.org/10.1002/etc.2340
Vancouver
Mendes LF, Villela LZ, Yokoya NS, Bastos EL, Stevani CV, Colepicolo P. Prediction of mono-, bi-, and trivalent metal cation relative toxicity to the seaweed Gracilaria domingensis (Gracilariales, Rhodophyta) in synthetic seawater [Internet]. Environmental Toxicology and Chemistry. 2013 ; 32( 11): 2571-2575.[citado 2024 jul. 12 ] Available from: https://doi.org/10.1002/etc.2340
Artigo de periodico
Functionalization of gold and silver nanoparticles with diphenyl dichalcogenides probed by surface enhanced Raman scattering (2012)
Takata, Leandro Mitsuo Shimura; Gonçalves, Augusto Cesar; Ando, Rômulo Augusto ; Santos, Alcindo Aparecido dos ; Camargo, Pedro Henrique Cury de
Fonte: Journal of Raman Spectroscopy. Unidade: IQ
Assuntos: NANOTECNOLOGIA, ESPECTROSCOPIA RAMAN
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ABNT
TAKATA, Leandro Mitsuo Shimura et al. Functionalization of gold and silver nanoparticles with diphenyl dichalcogenides probed by surface enhanced Raman scattering. Journal of Raman Spectroscopy, v. 43, n. 6, p. 712-717, 2012Tradução . . Disponível em: https://doi.org/10.1002/jrs.3081. Acesso em: 12 jul. 2024.
APA
Takata, L. M. S., Gonçalves, A. C., Ando, R. A., Santos, A. A. dos, & Camargo, P. H. C. de. (2012). Functionalization of gold and silver nanoparticles with diphenyl dichalcogenides probed by surface enhanced Raman scattering. Journal of Raman Spectroscopy, 43( 6), 712-717. doi:10.1002/jrs.3081
NLM
Takata LMS, Gonçalves AC, Ando RA, Santos AA dos, Camargo PHC de. Functionalization of gold and silver nanoparticles with diphenyl dichalcogenides probed by surface enhanced Raman scattering [Internet]. Journal of Raman Spectroscopy. 2012 ; 43( 6): 712-717.[citado 2024 jul. 12 ] Available from: https://doi.org/10.1002/jrs.3081
Vancouver
Takata LMS, Gonçalves AC, Ando RA, Santos AA dos, Camargo PHC de. Functionalization of gold and silver nanoparticles with diphenyl dichalcogenides probed by surface enhanced Raman scattering [Internet]. Journal of Raman Spectroscopy. 2012 ; 43( 6): 712-717.[citado 2024 jul. 12 ] Available from: https://doi.org/10.1002/jrs.3081
Artigo de periodico
Lipophilicity as a determinant of binding of procaine analogs to rat `α IND. 3´`β IND. 4´ nicotinic acetylcholine receptor (2012)
Cheffer, Arquimedes; Mustafa, Elba Vieira; Amaral, Antonia Tavares do ; Ulrich, Henning
Fonte: Journal of Neuroscience Research. Unidade: IQ
Assuntos: RECEPTORES, RELAÇÕES QUANTITATIVAS ENTRE ESTRUTURA QUÍMICA E ATIVIDADE BIOLÓGICA
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CHEFFER, Arquimedes et al. Lipophilicity as a determinant of binding of procaine analogs to rat `α IND. 3´`β IND. 4´ nicotinic acetylcholine receptor. Journal of Neuroscience Research, v. 90, n. 8, p. 1607-1614, 2012Tradução . . Disponível em: https://doi.org/10.1002/jnr.23047. Acesso em: 12 jul. 2024.
APA
Cheffer, A., Mustafa, E. V., Amaral, A. T. do, & Ulrich, H. (2012). Lipophilicity as a determinant of binding of procaine analogs to rat `α IND. 3´`β IND. 4´ nicotinic acetylcholine receptor. Journal of Neuroscience Research, 90( 8), 1607-1614. doi:10.1002/jnr.23047
NLM
Cheffer A, Mustafa EV, Amaral AT do, Ulrich H. Lipophilicity as a determinant of binding of procaine analogs to rat `α IND. 3´`β IND. 4´ nicotinic acetylcholine receptor [Internet]. Journal of Neuroscience Research. 2012 ; 90( 8): 1607-1614.[citado 2024 jul. 12 ] Available from: https://doi.org/10.1002/jnr.23047
Vancouver
Cheffer A, Mustafa EV, Amaral AT do, Ulrich H. Lipophilicity as a determinant of binding of procaine analogs to rat `α IND. 3´`β IND. 4´ nicotinic acetylcholine receptor [Internet]. Journal of Neuroscience Research. 2012 ; 90( 8): 1607-1614.[citado 2024 jul. 12 ] Available from: https://doi.org/10.1002/jnr.23047
Artigo de periodico
MPO inhibitors selected by virtual screening (2011)
Malvezzi, Alberto; Queiroz, Raphael Ferreira; Rezende, Leandro de; Augusto, Ohara ; Amaral, Antonia Tavares do
Fonte: Molecular Informatics. Unidade: IQ
Assuntos: PEROXIDASE, CINÉTICA, INIBIDORES DE ENZIMAS
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ABNT
MALVEZZI, Alberto et al. MPO inhibitors selected by virtual screening. Molecular Informatics, v. 30, n. 6-7, p. 605-613, 2011Tradução . . Disponível em: https://doi.org/10.1002/minf.201100016. Acesso em: 12 jul. 2024.
APA
Malvezzi, A., Queiroz, R. F., Rezende, L. de, Augusto, O., & Amaral, A. T. do. (2011). MPO inhibitors selected by virtual screening. Molecular Informatics, 30( 6-7), 605-613. doi:10.1002/minf.201100016
NLM
Malvezzi A, Queiroz RF, Rezende L de, Augusto O, Amaral AT do. MPO inhibitors selected by virtual screening [Internet]. Molecular Informatics. 2011 ; 30( 6-7): 605-613.[citado 2024 jul. 12 ] Available from: https://doi.org/10.1002/minf.201100016
Vancouver
Malvezzi A, Queiroz RF, Rezende L de, Augusto O, Amaral AT do. MPO inhibitors selected by virtual screening [Internet]. Molecular Informatics. 2011 ; 30( 6-7): 605-613.[citado 2024 jul. 12 ] Available from: https://doi.org/10.1002/minf.201100016
Artigo de periodico
Sulfanylation reactions of carbonyl compounds and carboxylic acid derivatives employing sulfur electrophiles: a review (2007)
Wladislaw, Blanka; Marzorati, Liliana ; Di Vitta, Cláudio
Fonte: Organic Preparations and Procedures International. Unidade: IQ
Assunto: SÍNTESE ORGÂNICA
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ABNT
WLADISLAW, Blanka e MARZORATI, Liliana e DI VITTA, Cláudio. Sulfanylation reactions of carbonyl compounds and carboxylic acid derivatives employing sulfur electrophiles: a review. Organic Preparations and Procedures International, v. 39, n. 5, p. 447-494, 2007Tradução . . Acesso em: 12 jul. 2024.
APA
Wladislaw, B., Marzorati, L., & Di Vitta, C. (2007). Sulfanylation reactions of carbonyl compounds and carboxylic acid derivatives employing sulfur electrophiles: a review. Organic Preparations and Procedures International, 39( 5), 447-494.
NLM
Wladislaw B, Marzorati L, Di Vitta C. Sulfanylation reactions of carbonyl compounds and carboxylic acid derivatives employing sulfur electrophiles: a review. Organic Preparations and Procedures International. 2007 ; 39( 5): 447-494.[citado 2024 jul. 12 ]
Vancouver
Wladislaw B, Marzorati L, Di Vitta C. Sulfanylation reactions of carbonyl compounds and carboxylic acid derivatives employing sulfur electrophiles: a review. Organic Preparations and Procedures International. 2007 ; 39( 5): 447-494.[citado 2024 jul. 12 ]

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