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Artigo de periodico
Copper(I)/succinic acid cooperatively catalyzed one-pot synthesis of organoseleniumpropargylamines via 'A POT. 3' -coupling (2018)
Oliveira, Isadora Maria de; Pimenta, Daniel Carvalho; Zukerman-Schpector, Júlio; Stefani, Hélio Alexandre ; Manarin, Flávia
Source: New Journal of Chemistry. Unidade: FCF
Subjects: SELÊNIO, ESTEREOQUÍMICA
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ABNT
OLIVEIRA, Isadora Maria de et al. Copper(I)/succinic acid cooperatively catalyzed one-pot synthesis of organoseleniumpropargylamines via 'A POT. 3' -coupling. New Journal of Chemistry, v. 42, n. 12, p. 10118-10123, 2018Tradução . . Disponível em: https://doi.org/10.1039/c8nj01543k. Acesso em: 14 nov. 2024.
APA
Oliveira, I. M. de, Pimenta, D. C., Zukerman-Schpector, J., Stefani, H. A., & Manarin, F. (2018). Copper(I)/succinic acid cooperatively catalyzed one-pot synthesis of organoseleniumpropargylamines via 'A POT. 3' -coupling. New Journal of Chemistry, 42( 12), 10118-10123. doi:10.1039/c8nj01543k
NLM
Oliveira IM de, Pimenta DC, Zukerman-Schpector J, Stefani HA, Manarin F. Copper(I)/succinic acid cooperatively catalyzed one-pot synthesis of organoseleniumpropargylamines via 'A POT. 3' -coupling [Internet]. New Journal of Chemistry. 2018 ; 42( 12): 10118-10123.[citado 2024 nov. 14 ] Available from: https://doi.org/10.1039/c8nj01543k
Vancouver
Oliveira IM de, Pimenta DC, Zukerman-Schpector J, Stefani HA, Manarin F. Copper(I)/succinic acid cooperatively catalyzed one-pot synthesis of organoseleniumpropargylamines via 'A POT. 3' -coupling [Internet]. New Journal of Chemistry. 2018 ; 42( 12): 10118-10123.[citado 2024 nov. 14 ] Available from: https://doi.org/10.1039/c8nj01543k
Artigo de periodico
Synthesis of a Tyr-Tyr dipeptide library and evaluation against tumor cells (2018)
Vasconcelos, Stanley Nunes Siqueira ; Sciani, Juliana Mozer ; Lisboa, Nicole Mambeli; Stefani, Hélio Alexandre
Source: Medicinal Chemistry. Unidade: FCF
Subjects: MOLÉCULA, ANTINEOPLÁSICOS
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ABNT
VASCONCELOS, Stanley Nunes Siqueira et al. Synthesis of a Tyr-Tyr dipeptide library and evaluation against tumor cells. Medicinal Chemistry, v. 14, n. 7, p. 709-714, 2018Tradução . . Disponível em: https://doi.org/10.2174/1573406414666180309153142. Acesso em: 14 nov. 2024.
APA
Vasconcelos, S. N. S., Sciani, J. M., Lisboa, N. M., & Stefani, H. A. (2018). Synthesis of a Tyr-Tyr dipeptide library and evaluation against tumor cells. Medicinal Chemistry, 14( 7), 709-714. doi:10.2174/1573406414666180309153142
NLM
Vasconcelos SNS, Sciani JM, Lisboa NM, Stefani HA. Synthesis of a Tyr-Tyr dipeptide library and evaluation against tumor cells [Internet]. Medicinal Chemistry. 2018 ; 14( 7): 709-714.[citado 2024 nov. 14 ] Available from: https://doi.org/10.2174/1573406414666180309153142
Vancouver
Vasconcelos SNS, Sciani JM, Lisboa NM, Stefani HA. Synthesis of a Tyr-Tyr dipeptide library and evaluation against tumor cells [Internet]. Medicinal Chemistry. 2018 ; 14( 7): 709-714.[citado 2024 nov. 14 ] Available from: https://doi.org/10.2174/1573406414666180309153142
Artigo de periodico
Synthesis of glycosyl azides and their applications using CuAAC click chemistry to generate bis- and tris(triazolyl)glycosyl derivatives (2017)
Shamim, Anwar; Vasconcelos, Stanley Nunes Siqueira; Oliveira, Isadora Maria de; Reis, Joel Savi dos; Pimenta, Daniel Carvalho; Zukerman-Schpector, Júlio; Stefani, Hélio Alexandre
Source: Synthesis. Unidade: FCF
Assunto: SÍNTESE ORGÂNICA
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ABNT
SHAMIM, Anwar et al. Synthesis of glycosyl azides and their applications using CuAAC click chemistry to generate bis- and tris(triazolyl)glycosyl derivatives. Synthesis, v. 49, n. 23, p. 5183-5196, 2017Tradução . . Disponível em: https://doi.org/10.1055/s-0036-1589090. Acesso em: 14 nov. 2024.
APA
Shamim, A., Vasconcelos, S. N. S., Oliveira, I. M. de, Reis, J. S. dos, Pimenta, D. C., Zukerman-Schpector, J., & Stefani, H. A. (2017). Synthesis of glycosyl azides and their applications using CuAAC click chemistry to generate bis- and tris(triazolyl)glycosyl derivatives. Synthesis, 49( 23), 5183-5196. doi:10.1055/s-0036-1589090
NLM
Shamim A, Vasconcelos SNS, Oliveira IM de, Reis JS dos, Pimenta DC, Zukerman-Schpector J, Stefani HA. Synthesis of glycosyl azides and their applications using CuAAC click chemistry to generate bis- and tris(triazolyl)glycosyl derivatives [Internet]. Synthesis. 2017 ; 49( 23): 5183-5196.[citado 2024 nov. 14 ] Available from: https://doi.org/10.1055/s-0036-1589090
Vancouver
Shamim A, Vasconcelos SNS, Oliveira IM de, Reis JS dos, Pimenta DC, Zukerman-Schpector J, Stefani HA. Synthesis of glycosyl azides and their applications using CuAAC click chemistry to generate bis- and tris(triazolyl)glycosyl derivatives [Internet]. Synthesis. 2017 ; 49( 23): 5183-5196.[citado 2024 nov. 14 ] Available from: https://doi.org/10.1055/s-0036-1589090
Artigo de periodico
3-Alkenyltyrosines accessed by suzukim Miyaura coupling: a key Intermediate in the synthesis and mechanistic study of povarov multicomponent reactions (2017)
Vasconcelos, Stanley N. S; Silva, Vitor Hugo Menezes da; Braga, Ataualpa Albert Carmo ; Shamim, Anwar; Souza, Frederico B; Pimenta, Daniel C; Stefani, Hélio Alexandre
Source: Asian Journal Organic of Chemistry. Unidades: IQ, FCF
Subjects: SÍNTESE ORGÂNICA, COMPOSTOS ORGÂNICOS
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ABNT
VASCONCELOS, Stanley N. S et al. 3-Alkenyltyrosines accessed by suzukim Miyaura coupling: a key Intermediate in the synthesis and mechanistic study of povarov multicomponent reactions. Asian Journal Organic of Chemistry, v. 6, n. 7, p. 913-920, 2017Tradução . . Disponível em: https://doi.org/10.1002/ajoc.201700154. Acesso em: 14 nov. 2024.
APA
Vasconcelos, S. N. S., Silva, V. H. M. da, Braga, A. A. C., Shamim, A., Souza, F. B., Pimenta, D. C., & Stefani, H. A. (2017). 3-Alkenyltyrosines accessed by suzukim Miyaura coupling: a key Intermediate in the synthesis and mechanistic study of povarov multicomponent reactions. Asian Journal Organic of Chemistry, 6( 7), 913-920. doi:10.1002/ajoc.201700154
NLM
Vasconcelos SNS, Silva VHM da, Braga AAC, Shamim A, Souza FB, Pimenta DC, Stefani HA. 3-Alkenyltyrosines accessed by suzukim Miyaura coupling: a key Intermediate in the synthesis and mechanistic study of povarov multicomponent reactions [Internet]. Asian Journal Organic of Chemistry. 2017 ; 6( 7): 913-920.[citado 2024 nov. 14 ] Available from: https://doi.org/10.1002/ajoc.201700154
Vancouver
Vasconcelos SNS, Silva VHM da, Braga AAC, Shamim A, Souza FB, Pimenta DC, Stefani HA. 3-Alkenyltyrosines accessed by suzukim Miyaura coupling: a key Intermediate in the synthesis and mechanistic study of povarov multicomponent reactions [Internet]. Asian Journal Organic of Chemistry. 2017 ; 6( 7): 913-920.[citado 2024 nov. 14 ] Available from: https://doi.org/10.1002/ajoc.201700154
Artigo de periodico
Synthesis and functionalization of N-sulfinyl imines: sonogashira reaction and copper-catalyzed azide-alkyne cycloaddition (2017)
Souza, Frederico Bernardes de; Vasconcelos, Stanley Nunes Siqueira; Reis, Joel Savi dos; Pimenta, Daniel Carvalho; Stefani, Hélio Alexandre
Source: Tetrahedron Letters. Unidade: FCF
Subjects: SÍNTESE ORGÂNICA, COBRE
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ABNT
SOUZA, Frederico Bernardes de et al. Synthesis and functionalization of N-sulfinyl imines: sonogashira reaction and copper-catalyzed azide-alkyne cycloaddition. Tetrahedron Letters, v. 58, n. 11, p. 1057-1060, 2017Tradução . . Disponível em: https://doi.org/10.1016/j.tetlet.2017.01.107. Acesso em: 14 nov. 2024.
APA
Souza, F. B. de, Vasconcelos, S. N. S., Reis, J. S. dos, Pimenta, D. C., & Stefani, H. A. (2017). Synthesis and functionalization of N-sulfinyl imines: sonogashira reaction and copper-catalyzed azide-alkyne cycloaddition. Tetrahedron Letters, 58( 11), 1057-1060. doi:10.1016/j.tetlet.2017.01.107
NLM
Souza FB de, Vasconcelos SNS, Reis JS dos, Pimenta DC, Stefani HA. Synthesis and functionalization of N-sulfinyl imines: sonogashira reaction and copper-catalyzed azide-alkyne cycloaddition [Internet]. Tetrahedron Letters. 2017 ; 58( 11): 1057-1060.[citado 2024 nov. 14 ] Available from: https://doi.org/10.1016/j.tetlet.2017.01.107
Vancouver
Souza FB de, Vasconcelos SNS, Reis JS dos, Pimenta DC, Stefani HA. Synthesis and functionalization of N-sulfinyl imines: sonogashira reaction and copper-catalyzed azide-alkyne cycloaddition [Internet]. Tetrahedron Letters. 2017 ; 58( 11): 1057-1060.[citado 2024 nov. 14 ] Available from: https://doi.org/10.1016/j.tetlet.2017.01.107
Artigo de periodico
Ytterbium(III)-catalyzed three-component reactions: synthesis of 4-organoselenium-quinolines (2017)
Oliveira, Isadora M. de; Vasconcelos, Stanley S. N; Barbeiro, Cristiane S; Correra, Thiago Carita ; Shamim, Anwar; Pimenta, Daniel Carvalho; Caracelli, Ignez; Schpector, Júlio Zukerman; Stefani, Hélio Alexandre ; Manarin, Flávia
Source: New Journal of Chemistry. Unidades: IQ, FCF
Subjects: SÍNTESE ORGÂNICA, REAÇÕES ORGÂNICAS
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ABNT
OLIVEIRA, Isadora M. de et al. Ytterbium(III)-catalyzed three-component reactions: synthesis of 4-organoselenium-quinolines. New Journal of Chemistry, v. 41, p. 9884-9888, 2017Tradução . . Disponível em: https://doi.org/10.1039/c7nj01803g. Acesso em: 14 nov. 2024.
APA
Oliveira, I. M. de, Vasconcelos, S. S. N., Barbeiro, C. S., Correra, T. C., Shamim, A., Pimenta, D. C., et al. (2017). Ytterbium(III)-catalyzed three-component reactions: synthesis of 4-organoselenium-quinolines. New Journal of Chemistry, 41, 9884-9888. doi:10.1039/c7nj01803g
NLM
Oliveira IM de, Vasconcelos SSN, Barbeiro CS, Correra TC, Shamim A, Pimenta DC, Caracelli I, Schpector JZ, Stefani HA, Manarin F. Ytterbium(III)-catalyzed three-component reactions: synthesis of 4-organoselenium-quinolines [Internet]. New Journal of Chemistry. 2017 ; 41 9884-9888.[citado 2024 nov. 14 ] Available from: https://doi.org/10.1039/c7nj01803g
Vancouver
Oliveira IM de, Vasconcelos SSN, Barbeiro CS, Correra TC, Shamim A, Pimenta DC, Caracelli I, Schpector JZ, Stefani HA, Manarin F. Ytterbium(III)-catalyzed three-component reactions: synthesis of 4-organoselenium-quinolines [Internet]. New Journal of Chemistry. 2017 ; 41 9884-9888.[citado 2024 nov. 14 ] Available from: https://doi.org/10.1039/c7nj01803g
Artigo de periodico
Chlorinated 2-hydroxynaphthalenoxazolines: synthesis, reaction mechanism and fluorescence properties (2016)
Barbeiro, Cristiane S; Vasconcelos, Stanley Nunes Siqueira; Schpector, Júlio Zukerman; Caracelli, Ignez; Pimenta, Daniel C; Rodrigues, Ana Clara Beltran; Fernandes, André S; Correra, Thiago Carita ; Bastos, Erick Leite ; Stefani, Hélio Alexandre
Source: ChemistrySelect. Unidades: IQ, FCF
Subjects: MECANISMOS, FLUORESCÊNCIA
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ABNT
BARBEIRO, Cristiane S et al. Chlorinated 2-hydroxynaphthalenoxazolines: synthesis, reaction mechanism and fluorescence properties. ChemistrySelect, v. 2, p. 5647–5652, 2016Tradução . . Disponível em: https://doi.org/10.1002/slct.201601526. Acesso em: 14 nov. 2024.
APA
Barbeiro, C. S., Vasconcelos, S. N. S., Schpector, J. Z., Caracelli, I., Pimenta, D. C., Rodrigues, A. C. B., et al. (2016). Chlorinated 2-hydroxynaphthalenoxazolines: synthesis, reaction mechanism and fluorescence properties. ChemistrySelect, 2, 5647–5652. doi:10.1002/slct.201601526
NLM
Barbeiro CS, Vasconcelos SNS, Schpector JZ, Caracelli I, Pimenta DC, Rodrigues ACB, Fernandes AS, Correra TC, Bastos EL, Stefani HA. Chlorinated 2-hydroxynaphthalenoxazolines: synthesis, reaction mechanism and fluorescence properties [Internet]. ChemistrySelect. 2016 ; 2 5647–5652.[citado 2024 nov. 14 ] Available from: https://doi.org/10.1002/slct.201601526
Vancouver
Barbeiro CS, Vasconcelos SNS, Schpector JZ, Caracelli I, Pimenta DC, Rodrigues ACB, Fernandes AS, Correra TC, Bastos EL, Stefani HA. Chlorinated 2-hydroxynaphthalenoxazolines: synthesis, reaction mechanism and fluorescence properties [Internet]. ChemistrySelect. 2016 ; 2 5647–5652.[citado 2024 nov. 14 ] Available from: https://doi.org/10.1002/slct.201601526
Artigo de periodico
Microwave-assisted one-pot three-component synthesis of imine 1,2,3-triazoles (2016)
Souza, Frederico B; Pimenta, Daniel Carvalho; Stefani, Hélio Alexandre
Source: Tetrahedron Letters. Unidade: FCF
Subjects: TECNOLOGIA DE MICRO-ONDAS, ALDEÍDOS
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ABNT
SOUZA, Frederico B e PIMENTA, Daniel Carvalho e STEFANI, Hélio Alexandre. Microwave-assisted one-pot three-component synthesis of imine 1,2,3-triazoles. Tetrahedron Letters, v. 57, n. 14, p. 1592-1596, 2016Tradução . . Disponível em: https://doi.org/10.1016/j.tetlet.2016.02.105. Acesso em: 14 nov. 2024.
APA
Souza, F. B., Pimenta, D. C., & Stefani, H. A. (2016). Microwave-assisted one-pot three-component synthesis of imine 1,2,3-triazoles. Tetrahedron Letters, 57( 14), 1592-1596. doi:10.1016/j.tetlet.2016.02.105
NLM
Souza FB, Pimenta DC, Stefani HA. Microwave-assisted one-pot three-component synthesis of imine 1,2,3-triazoles [Internet]. Tetrahedron Letters. 2016 ; 57( 14): 1592-1596.[citado 2024 nov. 14 ] Available from: https://doi.org/10.1016/j.tetlet.2016.02.105
Vancouver
Souza FB, Pimenta DC, Stefani HA. Microwave-assisted one-pot three-component synthesis of imine 1,2,3-triazoles [Internet]. Tetrahedron Letters. 2016 ; 57( 14): 1592-1596.[citado 2024 nov. 14 ] Available from: https://doi.org/10.1016/j.tetlet.2016.02.105
Artigo de periodico
In silico study to analyse the disassembly of quercetin-targeted dendrimers potentially leishmanicide (2015)
Santosa, Soraya da Silva; Giarolla, Jeanine ; Pasqualoto, Kerly F. M; Ferreira, Elizabeth Igne
Source: Molecular Simulation. Unidade: FCF
Subjects: MODELAGEM MOLECULAR, LEISHMANIA
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ABNT
SANTOSA, Soraya da Silva et al. In silico study to analyse the disassembly of quercetin-targeted dendrimers potentially leishmanicide. Molecular Simulation, v. 41, n. 18, p. 1495-1508, 2015Tradução . . Disponível em: https://doi.org/10.1080/08927022.2014.994622. Acesso em: 14 nov. 2024.
APA
Santosa, S. da S., Giarolla, J., Pasqualoto, K. F. M., & Ferreira, E. I. (2015). In silico study to analyse the disassembly of quercetin-targeted dendrimers potentially leishmanicide. Molecular Simulation, 41( 18), 1495-1508. doi:10.1080/08927022.2014.994622
NLM
Santosa S da S, Giarolla J, Pasqualoto KFM, Ferreira EI. In silico study to analyse the disassembly of quercetin-targeted dendrimers potentially leishmanicide [Internet]. Molecular Simulation. 2015 ; 41( 18): 1495-1508.[citado 2024 nov. 14 ] Available from: https://doi.org/10.1080/08927022.2014.994622
Vancouver
Santosa S da S, Giarolla J, Pasqualoto KFM, Ferreira EI. In silico study to analyse the disassembly of quercetin-targeted dendrimers potentially leishmanicide [Internet]. Molecular Simulation. 2015 ; 41( 18): 1495-1508.[citado 2024 nov. 14 ] Available from: https://doi.org/10.1080/08927022.2014.994622
Artigo de periodico
Lewis-acid catalyzed N-acyliminium ion cyclodimerization: synthesis of symmetrical 1,4-dioxanes (2015)
Ali, Bakhat; Schpector, Júlio Zukerman; Ferreira, Fernando P; Shamim, Anwar; Pimenta, Daniel Carvalho; Stefani, Hélio Alexandre
Source: Tetrahedron Letters. Unidade: FCF
Subjects: AMINAS, CATÁLISE
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ABNT
ALI, Bakhat et al. Lewis-acid catalyzed N-acyliminium ion cyclodimerization: synthesis of symmetrical 1,4-dioxanes. Tetrahedron Letters, v. 56, n. 9, p. 1153-1158, 2015Tradução . . Disponível em: https://doi.org/10.1016/j.tetlet.2015.01.059. Acesso em: 14 nov. 2024.
APA
Ali, B., Schpector, J. Z., Ferreira, F. P., Shamim, A., Pimenta, D. C., & Stefani, H. A. (2015). Lewis-acid catalyzed N-acyliminium ion cyclodimerization: synthesis of symmetrical 1,4-dioxanes. Tetrahedron Letters, 56( 9), 1153-1158. doi:10.1016/j.tetlet.2015.01.059
NLM
Ali B, Schpector JZ, Ferreira FP, Shamim A, Pimenta DC, Stefani HA. Lewis-acid catalyzed N-acyliminium ion cyclodimerization: synthesis of symmetrical 1,4-dioxanes [Internet]. Tetrahedron Letters. 2015 ; 56( 9): 1153-1158.[citado 2024 nov. 14 ] Available from: https://doi.org/10.1016/j.tetlet.2015.01.059
Vancouver
Ali B, Schpector JZ, Ferreira FP, Shamim A, Pimenta DC, Stefani HA. Lewis-acid catalyzed N-acyliminium ion cyclodimerization: synthesis of symmetrical 1,4-dioxanes [Internet]. Tetrahedron Letters. 2015 ; 56( 9): 1153-1158.[citado 2024 nov. 14 ] Available from: https://doi.org/10.1016/j.tetlet.2015.01.059
Artigo de periodico
Synthesis of enyne and aryl vinyl sulfoxides: functionalization via Pummerer rearrangement (2015)
Souza, Frederico B; Shamim, Anwar; Argomedo, Luiz M. Z; Pimenta, Daniel Carvalho; Stefani, Hélio Alexandre
Source: Molecular Diversity. Unidade: FCF
Subjects: SÍNTESE ORGÂNICA, REAGENTES ORGÂNICOS
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ABNT
SOUZA, Frederico B et al. Synthesis of enyne and aryl vinyl sulfoxides: functionalization via Pummerer rearrangement. Molecular Diversity, v. 19, n. 4, p. 773-785, 2015Tradução . . Disponível em: https://doi.org/10.1007/s11030-015-9619-x. Acesso em: 14 nov. 2024.
APA
Souza, F. B., Shamim, A., Argomedo, L. M. Z., Pimenta, D. C., & Stefani, H. A. (2015). Synthesis of enyne and aryl vinyl sulfoxides: functionalization via Pummerer rearrangement. Molecular Diversity, 19( 4), 773-785. doi:10.1007/s11030-015-9619-x
NLM
Souza FB, Shamim A, Argomedo LMZ, Pimenta DC, Stefani HA. Synthesis of enyne and aryl vinyl sulfoxides: functionalization via Pummerer rearrangement [Internet]. Molecular Diversity. 2015 ; 19( 4): 773-785.[citado 2024 nov. 14 ] Available from: https://doi.org/10.1007/s11030-015-9619-x
Vancouver
Souza FB, Shamim A, Argomedo LMZ, Pimenta DC, Stefani HA. Synthesis of enyne and aryl vinyl sulfoxides: functionalization via Pummerer rearrangement [Internet]. Molecular Diversity. 2015 ; 19( 4): 773-785.[citado 2024 nov. 14 ] Available from: https://doi.org/10.1007/s11030-015-9619-x
Artigo de periodico
The triterpenoid betulin protects against the neuromuscular effects of bothrops jararacussu snake venom in vivo (2015)
Ferraz, Miriéle Cristina; Oliveira, Jhones Luiz de; Oliveira Junior, Joel Reis de; Cogo, José Carlos; Santos, Márcio Garcia dos; Franco, Luiz Madaleno; Puebla, Pilar; Ferraz, Helena Onishi; Ferraz, Humberto Gomes ; Rocha, Marisa Maria Teixeira da; Hyslop, Stephen; Feliciano, Arturo San; Franco, Yoko Oshima
Source: Evidence Based Complementary and Alternative Medicine. Unidade: FCF
Subjects: VENENOS DE ORIGEM ANIMAL, SERPENTES, FARMACOLOGIA
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ABNT
FERRAZ, Miriéle Cristina et al. The triterpenoid betulin protects against the neuromuscular effects of bothrops jararacussu snake venom in vivo. Evidence Based Complementary and Alternative Medicine, p. 1-10, 2015Tradução . . Disponível em: https://doi.org/10.1155/2015/939523. Acesso em: 14 nov. 2024.
APA
Ferraz, M. C., Oliveira, J. L. de, Oliveira Junior, J. R. de, Cogo, J. C., Santos, M. G. dos, Franco, L. M., et al. (2015). The triterpenoid betulin protects against the neuromuscular effects of bothrops jararacussu snake venom in vivo. Evidence Based Complementary and Alternative Medicine, 1-10. doi:10.1155/2015/939523
NLM
Ferraz MC, Oliveira JL de, Oliveira Junior JR de, Cogo JC, Santos MG dos, Franco LM, Puebla P, Ferraz HO, Ferraz HG, Rocha MMT da, Hyslop S, Feliciano AS, Franco YO. The triterpenoid betulin protects against the neuromuscular effects of bothrops jararacussu snake venom in vivo [Internet]. Evidence Based Complementary and Alternative Medicine. 2015 ; 1-10.[citado 2024 nov. 14 ] Available from: https://doi.org/10.1155/2015/939523
Vancouver
Ferraz MC, Oliveira JL de, Oliveira Junior JR de, Cogo JC, Santos MG dos, Franco LM, Puebla P, Ferraz HO, Ferraz HG, Rocha MMT da, Hyslop S, Feliciano AS, Franco YO. The triterpenoid betulin protects against the neuromuscular effects of bothrops jararacussu snake venom in vivo [Internet]. Evidence Based Complementary and Alternative Medicine. 2015 ; 1-10.[citado 2024 nov. 14 ] Available from: https://doi.org/10.1155/2015/939523
Artigo de periodico
RPF151, a novel capsaicin-like analogue: in vitro studies and in vivo preclinical antitumor evaluation in a breast cancer model (2015)
Ferreira, Adilson Kleber; Tavares, Maurício Temotheo; Pasqualoto, Kerly Fernanda Mesquita; Azevedo, Ricardo Alexandre de; Teixeira, Sarah Fernandes; Ferreira Junior, Wilson Alves; Bertin, Ariane Matiello; Sá Júnior, Paulo Luiz de; Barbuto, José Alexandre Marzagão ; Figueiredo, Carlos Rogério; Cury, Yara; Damião, Mariana Celestina Frojuello Costa Bernstorff; Parise Filho, Roberto
Source: Tumor Biology. Unidades: ICB, FCF
Subjects: ANTINEOPLÁSICOS, NEOPLASIAS MAMÁRIAS, IMUNOLOGIA
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ABNT
FERREIRA, Adilson Kleber et al. RPF151, a novel capsaicin-like analogue: in vitro studies and in vivo preclinical antitumor evaluation in a breast cancer model. Tumor Biology, 2015Tradução . . Disponível em: https://doi.org/10.1007/s13277-015-3441-z. Acesso em: 14 nov. 2024.
APA
Ferreira, A. K., Tavares, M. T., Pasqualoto, K. F. M., Azevedo, R. A. de, Teixeira, S. F., Ferreira Junior, W. A., et al. (2015). RPF151, a novel capsaicin-like analogue: in vitro studies and in vivo preclinical antitumor evaluation in a breast cancer model. Tumor Biology. doi:10.1007/s13277-015-3441-z
NLM
Ferreira AK, Tavares MT, Pasqualoto KFM, Azevedo RA de, Teixeira SF, Ferreira Junior WA, Bertin AM, Sá Júnior PL de, Barbuto JAM, Figueiredo CR, Cury Y, Damião MCFCB, Parise Filho R. RPF151, a novel capsaicin-like analogue: in vitro studies and in vivo preclinical antitumor evaluation in a breast cancer model [Internet]. Tumor Biology. 2015 ;[citado 2024 nov. 14 ] Available from: https://doi.org/10.1007/s13277-015-3441-z
Vancouver
Ferreira AK, Tavares MT, Pasqualoto KFM, Azevedo RA de, Teixeira SF, Ferreira Junior WA, Bertin AM, Sá Júnior PL de, Barbuto JAM, Figueiredo CR, Cury Y, Damião MCFCB, Parise Filho R. RPF151, a novel capsaicin-like analogue: in vitro studies and in vivo preclinical antitumor evaluation in a breast cancer model [Internet]. Tumor Biology. 2015 ;[citado 2024 nov. 14 ] Available from: https://doi.org/10.1007/s13277-015-3441-z
Artigo de periodico
Alkylphosphocholines as promising antitumor agents: exploring the role of structural features on the hemolytic potential (2014)
Sá, Matheus Malta de; Pasqualoto, Kerly Fernanda Mesquita; Modestia, Silvestre Massimo; Rangel-Yagui, Carlota de Oliveira
Source: Molecular Informatics. Unidade: FCF
Subjects: ANTINEOPLÁSICOS, MODELAGEM MOLECULAR
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
SÁ, Matheus Malta de et al. Alkylphosphocholines as promising antitumor agents: exploring the role of structural features on the hemolytic potential. Molecular Informatics, v. 33, n. 1, p. 53-64, 2014Tradução . . Disponível em: https://doi.org/10.1002/minf.201300124. Acesso em: 14 nov. 2024.
APA
Sá, M. M. de, Pasqualoto, K. F. M., Modestia, S. M., & Rangel-Yagui, C. de O. (2014). Alkylphosphocholines as promising antitumor agents: exploring the role of structural features on the hemolytic potential. Molecular Informatics, 33( 1), 53-64. doi:10.1002/minf.201300124
NLM
Sá MM de, Pasqualoto KFM, Modestia SM, Rangel-Yagui C de O. Alkylphosphocholines as promising antitumor agents: exploring the role of structural features on the hemolytic potential [Internet]. Molecular Informatics. 2014 ; 33( 1): 53-64.[citado 2024 nov. 14 ] Available from: https://doi.org/10.1002/minf.201300124
Vancouver
Sá MM de, Pasqualoto KFM, Modestia SM, Rangel-Yagui C de O. Alkylphosphocholines as promising antitumor agents: exploring the role of structural features on the hemolytic potential [Internet]. Molecular Informatics. 2014 ; 33( 1): 53-64.[citado 2024 nov. 14 ] Available from: https://doi.org/10.1002/minf.201300124
Artigo de periodico
Synthesis of functionalized N-triazolyl maleimides (2014)
Stefani, Hélio Alexandre ; Ferreira, Fernando P; Ali, Bakhat; Pimenta, Daniel Carvalho
Source: Tetrahedron Letters. Unidade: FCF
Assunto: SÍNTESE ORGÂNICA
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
STEFANI, Hélio Alexandre et al. Synthesis of functionalized N-triazolyl maleimides. Tetrahedron Letters, v. 55, n. 31, p. 4355-4358, 2014Tradução . . Disponível em: https://doi.org/10.1016/j.tetlet.2014.05.095. Acesso em: 14 nov. 2024.
APA
Stefani, H. A., Ferreira, F. P., Ali, B., & Pimenta, D. C. (2014). Synthesis of functionalized N-triazolyl maleimides. Tetrahedron Letters, 55( 31), 4355-4358. doi:10.1016/j.tetlet.2014.05.095
NLM
Stefani HA, Ferreira FP, Ali B, Pimenta DC. Synthesis of functionalized N-triazolyl maleimides [Internet]. Tetrahedron Letters. 2014 ; 55( 31): 4355-4358.[citado 2024 nov. 14 ] Available from: https://doi.org/10.1016/j.tetlet.2014.05.095
Vancouver
Stefani HA, Ferreira FP, Ali B, Pimenta DC. Synthesis of functionalized N-triazolyl maleimides [Internet]. Tetrahedron Letters. 2014 ; 55( 31): 4355-4358.[citado 2024 nov. 14 ] Available from: https://doi.org/10.1016/j.tetlet.2014.05.095
Artigo de periodico
Cytotoxic effects of dillapiole on MDA-MB-231 cells involve the induction of apoptosis through the mitochondrial pathway by inducing an oxidative stress while altering the cytoskeleton network (2014)
Ferreira, Adilson Kleber; Sá Júnior, Paulo Luiz de; Pasqualoto, Kerly Fernanda Mesquita; Azevedo, Ricardo Alexandre de; Câmara, Diana Aparecida Dias; Costa, André Santos; Figueiredo, Carlos Rogério; Matsuo, Alisson Leonardo; Massaoka, Mariana Hiromi; Auada, Aline Vivian Vatti; Lebrun, Ivo; Damião, Mariana Celestina Frojuello Costa Bernstorff; Tavares, Maurício Temotheo; Magri, Fatima Maria Motter; Kerkis, Irina; Parise Filho, Roberto
Source: Biochimie. Unidade: FCF
Subjects: CITOESQUELETO, ESTRESSE OXIDATIVO, APOPTOSE
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
FERREIRA, Adilson Kleber et al. Cytotoxic effects of dillapiole on MDA-MB-231 cells involve the induction of apoptosis through the mitochondrial pathway by inducing an oxidative stress while altering the cytoskeleton network. Biochimie, v. 99, p. 195-207, 2014Tradução . . Disponível em: https://doi.org/10.1016/j.biochi.2013.12.008. Acesso em: 14 nov. 2024.
APA
Ferreira, A. K., Sá Júnior, P. L. de, Pasqualoto, K. F. M., Azevedo, R. A. de, Câmara, D. A. D., Costa, A. S., et al. (2014). Cytotoxic effects of dillapiole on MDA-MB-231 cells involve the induction of apoptosis through the mitochondrial pathway by inducing an oxidative stress while altering the cytoskeleton network. Biochimie, 99, 195-207. doi:10.1016/j.biochi.2013.12.008
NLM
Ferreira AK, Sá Júnior PL de, Pasqualoto KFM, Azevedo RA de, Câmara DAD, Costa AS, Figueiredo CR, Matsuo AL, Massaoka MH, Auada AVV, Lebrun I, Damião MCFCB, Tavares MT, Magri FMM, Kerkis I, Parise Filho R. Cytotoxic effects of dillapiole on MDA-MB-231 cells involve the induction of apoptosis through the mitochondrial pathway by inducing an oxidative stress while altering the cytoskeleton network [Internet]. Biochimie. 2014 ; 99 195-207.[citado 2024 nov. 14 ] Available from: https://doi.org/10.1016/j.biochi.2013.12.008
Vancouver
Ferreira AK, Sá Júnior PL de, Pasqualoto KFM, Azevedo RA de, Câmara DAD, Costa AS, Figueiredo CR, Matsuo AL, Massaoka MH, Auada AVV, Lebrun I, Damião MCFCB, Tavares MT, Magri FMM, Kerkis I, Parise Filho R. Cytotoxic effects of dillapiole on MDA-MB-231 cells involve the induction of apoptosis through the mitochondrial pathway by inducing an oxidative stress while altering the cytoskeleton network [Internet]. Biochimie. 2014 ; 99 195-207.[citado 2024 nov. 14 ] Available from: https://doi.org/10.1016/j.biochi.2013.12.008
Artigo de periodico
Novel capsaicin analogues as potential anticancer agents: synthesis, biological evaluation, and in silico approach (2014)
Damião, Mariana Celestina Frojuello Bernstorff; Pasqualoto, Kerly Fernanda Mesquita; Ferreira, Adilson Kleber; Teixeira, Sarah Fernandes; Azevedo, Ricardo Alexandre de; Barbuto, José Alexandre Marzagão ; Berl, Fanny Palace; Franchi Junior, Gilberto C; Nowill, Alexandre E; Tavares, Maurício Temotheo; Parise Filho, Roberto
Source: Archiv der Pharmazie Chemistry in Life Science. Unidades: ICB, FCF
Assunto: ANTINEOPLÁSICOS
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ABNT
DAMIÃO, Mariana Celestina Frojuello Bernstorff et al. Novel capsaicin analogues as potential anticancer agents: synthesis, biological evaluation, and in silico approach. Archiv der Pharmazie Chemistry in Life Science, v. 347, n. 12, p. 885-895, 2014Tradução . . Disponível em: https://doi.org/10.1002/ardp.201400233. Acesso em: 14 nov. 2024.
APA
Damião, M. C. F. B., Pasqualoto, K. F. M., Ferreira, A. K., Teixeira, S. F., Azevedo, R. A. de, Barbuto, J. A. M., et al. (2014). Novel capsaicin analogues as potential anticancer agents: synthesis, biological evaluation, and in silico approach. Archiv der Pharmazie Chemistry in Life Science, 347( 12), 885-895. doi:10.1002/ardp.201400233
NLM
Damião MCFB, Pasqualoto KFM, Ferreira AK, Teixeira SF, Azevedo RA de, Barbuto JAM, Berl FP, Franchi Junior GC, Nowill AE, Tavares MT, Parise Filho R. Novel capsaicin analogues as potential anticancer agents: synthesis, biological evaluation, and in silico approach [Internet]. Archiv der Pharmazie Chemistry in Life Science. 2014 ; 347( 12): 885-895.[citado 2024 nov. 14 ] Available from: https://doi.org/10.1002/ardp.201400233
Vancouver
Damião MCFB, Pasqualoto KFM, Ferreira AK, Teixeira SF, Azevedo RA de, Barbuto JAM, Berl FP, Franchi Junior GC, Nowill AE, Tavares MT, Parise Filho R. Novel capsaicin analogues as potential anticancer agents: synthesis, biological evaluation, and in silico approach [Internet]. Archiv der Pharmazie Chemistry in Life Science. 2014 ; 347( 12): 885-895.[citado 2024 nov. 14 ] Available from: https://doi.org/10.1002/ardp.201400233
Artigo de periodico
To be drug or prodrug: structure-property exploratory approach regarding oral bioavailability (2014)
Damião, Mariana Celestina Frojuello Costa Bernstorff; Pasqualoto, Kerly Fernanda Mesquita; Polli, Michelle Carneiro; Parise Filho, Roberto
Source: Journal of Pharmacy and Pharmaceutical Sciences. Unidade: FCF
Subjects: BIODISPONIBILIDADE, FÁRMACOS
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ABNT
DAMIÃO, Mariana Celestina Frojuello Costa Bernstorff et al. To be drug or prodrug: structure-property exploratory approach regarding oral bioavailability. Journal of Pharmacy and Pharmaceutical Sciences, v. 17, n. 4, p. 532-540, 2014Tradução . . Disponível em: http://ejournals.library.ualberta.ca/index.php/JPPS/article/view/23063. Acesso em: 14 nov. 2024.
APA
Damião, M. C. F. C. B., Pasqualoto, K. F. M., Polli, M. C., & Parise Filho, R. (2014). To be drug or prodrug: structure-property exploratory approach regarding oral bioavailability. Journal of Pharmacy and Pharmaceutical Sciences, 17( 4), 532-540. Recuperado de http://ejournals.library.ualberta.ca/index.php/JPPS/article/view/23063
NLM
Damião MCFCB, Pasqualoto KFM, Polli MC, Parise Filho R. To be drug or prodrug: structure-property exploratory approach regarding oral bioavailability [Internet]. Journal of Pharmacy and Pharmaceutical Sciences. 2014 ; 17( 4): 532-540.[citado 2024 nov. 14 ] Available from: http://ejournals.library.ualberta.ca/index.php/JPPS/article/view/23063
Vancouver
Damião MCFCB, Pasqualoto KFM, Polli MC, Parise Filho R. To be drug or prodrug: structure-property exploratory approach regarding oral bioavailability [Internet]. Journal of Pharmacy and Pharmaceutical Sciences. 2014 ; 17( 4): 532-540.[citado 2024 nov. 14 ] Available from: http://ejournals.library.ualberta.ca/index.php/JPPS/article/view/23063
Artigo de periodico
Design and exploratory data analysis of a second generation of dendrimer prodrugs potentially antichagasic and leishmanicide (2013)
Giarolla, Jeanine ; Pasqualoto, Kerly Fernanda Mesquita; Ferreira, Elizabeth Igne
Source: Molecular Diversity. Unidade: FCF
Subjects: MODELAGEM MOLECULAR, DOENÇA DE CHAGAS, LEISHMANIA
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
GIAROLLA, Jeanine e PASQUALOTO, Kerly Fernanda Mesquita e FERREIRA, Elizabeth Igne. Design and exploratory data analysis of a second generation of dendrimer prodrugs potentially antichagasic and leishmanicide. Molecular Diversity, v. 17, n. 4, p. 711-720, 2013Tradução . . Disponível em: https://doi.org/10.1007/s11030-013-9467-5. Acesso em: 14 nov. 2024.
APA
Giarolla, J., Pasqualoto, K. F. M., & Ferreira, E. I. (2013). Design and exploratory data analysis of a second generation of dendrimer prodrugs potentially antichagasic and leishmanicide. Molecular Diversity, 17( 4), 711-720. doi:10.1007/s11030-013-9467-5
NLM
Giarolla J, Pasqualoto KFM, Ferreira EI. Design and exploratory data analysis of a second generation of dendrimer prodrugs potentially antichagasic and leishmanicide [Internet]. Molecular Diversity. 2013 ; 17( 4): 711-720.[citado 2024 nov. 14 ] Available from: https://doi.org/10.1007/s11030-013-9467-5
Vancouver
Giarolla J, Pasqualoto KFM, Ferreira EI. Design and exploratory data analysis of a second generation of dendrimer prodrugs potentially antichagasic and leishmanicide [Internet]. Molecular Diversity. 2013 ; 17( 4): 711-720.[citado 2024 nov. 14 ] Available from: https://doi.org/10.1007/s11030-013-9467-5
Trabalho de evento-resumo periodico
Molecular properties evaluation of a second generation dendrimers pontentially antichagasic and leishmanicide (2013)
Giarolla, Jeanine ; Santos, Soraya; Pasqualoto, Kerly Fernanda Mesquita; Ferreira, Elizabeth Igne
Source: Brazilian Journal of Pharmaceutical Sciences. Conference titles: Pharmaceutical Science and Technology Meeting of the Faculty of Pharmaceutical Sciences. Unidade: FCF
Subjects: DOENÇA DE CHAGAS, PLANEJAMENTO DE FÁRMACOS
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
GIAROLLA, Jeanine et al. Molecular properties evaluation of a second generation dendrimers pontentially antichagasic and leishmanicide. Brazilian Journal of Pharmaceutical Sciences. São Paulo: Faculdade de Ciências Farmacêuticas, Universidade de São Paulo. . Acesso em: 14 nov. 2024. , 2013
APA
Giarolla, J., Santos, S., Pasqualoto, K. F. M., & Ferreira, E. I. (2013). Molecular properties evaluation of a second generation dendrimers pontentially antichagasic and leishmanicide. Brazilian Journal of Pharmaceutical Sciences. São Paulo: Faculdade de Ciências Farmacêuticas, Universidade de São Paulo.
NLM
Giarolla J, Santos S, Pasqualoto KFM, Ferreira EI. Molecular properties evaluation of a second generation dendrimers pontentially antichagasic and leishmanicide. Brazilian Journal of Pharmaceutical Sciences. 2013 ; 49 57 res. FCF110.[citado 2024 nov. 14 ]
Vancouver
Giarolla J, Santos S, Pasqualoto KFM, Ferreira EI. Molecular properties evaluation of a second generation dendrimers pontentially antichagasic and leishmanicide. Brazilian Journal of Pharmaceutical Sciences. 2013 ; 49 57 res. FCF110.[citado 2024 nov. 14 ]

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