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Artigo de periodico
Antibodies against mucin-based glycopeptides affect Trypanosoma cruzi cell invasion and tumor cell viability (2014)
Campo, Vanessa Leiria; Riul, Thalita Bachelli; Carvalho, Ivone; Dias-Baruffi, Marcelo
Source: ChemBioChem. Unidade: FCFRP
Subjects: GLICOPEPTÍDEOS (SÍNTESE), TRYPANOSOMA CRUZI, GLICOPROTEÍNAS
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ABNT
CAMPO, Vanessa Leiria et al. Antibodies against mucin-based glycopeptides affect Trypanosoma cruzi cell invasion and tumor cell viability. ChemBioChem, v. 15, n. 10, p. 1495–1507, 2014Tradução . . Disponível em: https://doi.org/10.1002/cbic.201400069. Acesso em: 27 ago. 2024.
APA
Campo, V. L., Riul, T. B., Carvalho, I., & Dias-Baruffi, M. (2014). Antibodies against mucin-based glycopeptides affect Trypanosoma cruzi cell invasion and tumor cell viability. ChemBioChem, 15( 10), 1495–1507. doi:10.1002/cbic.201400069
NLM
Campo VL, Riul TB, Carvalho I, Dias-Baruffi M. Antibodies against mucin-based glycopeptides affect Trypanosoma cruzi cell invasion and tumor cell viability [Internet]. ChemBioChem. 2014 ; 15( 10): 1495–1507.[citado 2024 ago. 27 ] Available from: https://doi.org/10.1002/cbic.201400069
Vancouver
Campo VL, Riul TB, Carvalho I, Dias-Baruffi M. Antibodies against mucin-based glycopeptides affect Trypanosoma cruzi cell invasion and tumor cell viability [Internet]. ChemBioChem. 2014 ; 15( 10): 1495–1507.[citado 2024 ago. 27 ] Available from: https://doi.org/10.1002/cbic.201400069
Parte de monografia/livro
Oligosaccharide-salicylaldehyde derivatives as precursors of water-soluble, biocompatible anion receptors (2014)
Bedini, Emiliano; Forte, Gianpiero; Carvalho, Ivone; Parrilli, Michelangelo; Dalla Cort, Antonella
Source: Carbohydrate chemistry : proven synthetic methods, v.2. Unidade: FCFRP
Subjects: CARBOIDRATOS, OLIGOSSACARÍDEOS
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
BEDINI, Emiliano et al. Oligosaccharide-salicylaldehyde derivatives as precursors of water-soluble, biocompatible anion receptors. Carbohydrate chemistry : proven synthetic methods, v.2. Tradução . Boca Raton: CRC Press, 2014. . . Acesso em: 27 ago. 2024.
APA
Bedini, E., Forte, G., Carvalho, I., Parrilli, M., & Dalla Cort, A. (2014). Oligosaccharide-salicylaldehyde derivatives as precursors of water-soluble, biocompatible anion receptors. In Carbohydrate chemistry : proven synthetic methods, v.2. Boca Raton: CRC Press.
NLM
Bedini E, Forte G, Carvalho I, Parrilli M, Dalla Cort A. Oligosaccharide-salicylaldehyde derivatives as precursors of water-soluble, biocompatible anion receptors. In: Carbohydrate chemistry : proven synthetic methods, v.2. Boca Raton: CRC Press; 2014. [citado 2024 ago. 27 ]
Vancouver
Bedini E, Forte G, Carvalho I, Parrilli M, Dalla Cort A. Oligosaccharide-salicylaldehyde derivatives as precursors of water-soluble, biocompatible anion receptors. In: Carbohydrate chemistry : proven synthetic methods, v.2. Boca Raton: CRC Press; 2014. [citado 2024 ago. 27 ]
Artigo de periodico
Synthesis and in vitro evaluation of novel galactosyl-triazolo-benzenesulfonamides against Trypanosoma cruzi (2014)
Junqueira, Getúlio Gomes; Carvalho, Marcelo Rodrigues de; Andrade, Peterson de; Lopes, Carla Duque; Carneiro, Zumira, A.; Sesti-Costa, Renata; Silva, João Santana da; Carvalho, Ivone
Source: Journal of the Brazilian Chemical Society. Unidades: FCFRP, FMRP
Subjects: TRIPANOSSOMICIDAS, DOENÇA DE CHAGAS (EFEITOS DE DROGAS), TECNOLOGIA FARMACÊUTICA
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
JUNQUEIRA, Getúlio Gomes et al. Synthesis and in vitro evaluation of novel galactosyl-triazolo-benzenesulfonamides against Trypanosoma cruzi. Journal of the Brazilian Chemical Society, v. 25, n. 10, p. 1872-1884, 2014Tradução . . Disponível em: https://doi.org/10.5935/0103-5053.20140158. Acesso em: 27 ago. 2024.
APA
Junqueira, G. G., Carvalho, M. R. de, Andrade, P. de, Lopes, C. D., Carneiro, Z., Sesti-Costa, R., et al. (2014). Synthesis and in vitro evaluation of novel galactosyl-triazolo-benzenesulfonamides against Trypanosoma cruzi. Journal of the Brazilian Chemical Society, 25( 10), 1872-1884. doi:10.5935/0103-5053.20140158
NLM
Junqueira GG, Carvalho MR de, Andrade P de, Lopes CD, Carneiro Z, Sesti-Costa R, Silva JS da, Carvalho I. Synthesis and in vitro evaluation of novel galactosyl-triazolo-benzenesulfonamides against Trypanosoma cruzi [Internet]. Journal of the Brazilian Chemical Society. 2014 ; 25( 10): 1872-1884.[citado 2024 ago. 27 ] Available from: https://doi.org/10.5935/0103-5053.20140158
Vancouver
Junqueira GG, Carvalho MR de, Andrade P de, Lopes CD, Carneiro Z, Sesti-Costa R, Silva JS da, Carvalho I. Synthesis and in vitro evaluation of novel galactosyl-triazolo-benzenesulfonamides against Trypanosoma cruzi [Internet]. Journal of the Brazilian Chemical Society. 2014 ; 25( 10): 1872-1884.[citado 2024 ago. 27 ] Available from: https://doi.org/10.5935/0103-5053.20140158
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)
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
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: 27 ago. 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 ago. 27 ] 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 ago. 27 ] Available from: https://doi.org/10.1016/j.bmcl.2014.07.088

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