Design, synthesis and the effect of 1,2,3-triazole sialylmimetic neoglycoconjugates on Trypanosoma cruzi and its cell surface trans-sialidase (2011)
- Authors:
- USP affiliated authors: SILVA, JOÃO SANTANA DA - FMRP ; CARVALHO, IVONE - FCFRP
- Unidades: FMRP; FCFRP
- DOI: 10.1016/j.bmc.2011.11.022
- Subjects: SÍNTESE ORGÂNICA; GLICOCONJUGADOS; TRIPANOSSOMICIDAS
- Language: Inglês
- Imprenta:
- Source:
- Título: Bioorganic and Medicinal Chemistry
- ISSN: 0968-0896
- Volume/Número/Paginação/Ano: v. 20, n. 1, p. 145-156, 2011
- Status:
- Artigo possui versão em acesso aberto em repositório (Green Open Access)
- Versão do Documento:
- Versão publicada (Published version)
- Acessar versão aberta:
-
ABNT
CAMPO, Vanessa L. et al. Design, synthesis and the effect of 1,2,3-triazole sialylmimetic neoglycoconjugates on Trypanosoma cruzi and its cell surface trans-sialidase. Bioorganic and Medicinal Chemistry, v. 20, n. 1, p. 145-156, 2011Tradução . . Disponível em: https://doi.org/10.1016/j.bmc.2011.11.022. Acesso em: 15 abr. 2026. -
APA
Campo, V. L., Sesti-Costa, R., Carneiro, Z. A., Silva, J. S. da, Schenkman, S., & Carvalho, I. (2011). Design, synthesis and the effect of 1,2,3-triazole sialylmimetic neoglycoconjugates on Trypanosoma cruzi and its cell surface trans-sialidase. Bioorganic and Medicinal Chemistry, 20( 1), 145-156. doi:10.1016/j.bmc.2011.11.022 -
NLM
Campo VL, Sesti-Costa R, Carneiro ZA, Silva JS da, Schenkman S, Carvalho I. Design, synthesis and the effect of 1,2,3-triazole sialylmimetic neoglycoconjugates on Trypanosoma cruzi and its cell surface trans-sialidase [Internet]. Bioorganic and Medicinal Chemistry. 2011 ; 20( 1): 145-156.[citado 2026 abr. 15 ] Available from: https://doi.org/10.1016/j.bmc.2011.11.022 -
Vancouver
Campo VL, Sesti-Costa R, Carneiro ZA, Silva JS da, Schenkman S, Carvalho I. Design, synthesis and the effect of 1,2,3-triazole sialylmimetic neoglycoconjugates on Trypanosoma cruzi and its cell surface trans-sialidase [Internet]. Bioorganic and Medicinal Chemistry. 2011 ; 20( 1): 145-156.[citado 2026 abr. 15 ] Available from: https://doi.org/10.1016/j.bmc.2011.11.022 - Glycoclusters presenting lactose on calix[4]arene cores display trypanocidal activity
- Click chemistry oligomerisation of azido-alkyne-functionalised galactose accesses triazole-linked linear oligomers and macrocycles that inhibit Trypanosoma cruzi macrophage invasion
- '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
- 'alfa'-Selective glycosylation affords mucin-related GalNAc amino acids and diketopiperazines active on Trypanosoma cruzi
- 1,2,3-Triazole-based analogue of benznidazole displays remarkable activity against Trypanosoma cruzi
- Synthesis and 2D-QSAR studies of neolignan-based diaryl-tetrahydrofuran and -furan analogues with remarkable activity against Trypanosoma cruzi and assessment of the trypanothione reductase activity
- Synthesis and in vitro evaluation of novel galactosyl-triazolo-benzenesulfonamides against Trypanosoma cruzi
- Estudo da reação de glicosilação de aminoácidos de Serina e Treonina
- Synthesis of N-linked pseudo-disaccharides for inhibition studies
- Synthesis of 1-3 disaccharide building bloks as substrates for Trypanosoma cruzi trans-sialidase
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