Source: Bioorganic & Medicinal Chemistry Letters. Unidade: FCFRP
Subjects: INIBIDORES DE ENZIMAS (FARMACOLOGIA), GLICOPROTEÍNAS (ANTAGONISTAS E INIBIDORES), TRYPANOSOMA CRUZI (ENZIMOLOGIA)
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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: 03 out. 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.2014.07.088NLM
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 out. 03 ] Available from: https://doi.org/10.1016/j.bmcl.2014.07.088Vancouver
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 out. 03 ] Available from: https://doi.org/10.1016/j.bmcl.2014.07.088