Source: Journal of Biomolecular Structure and Dynamics. Unidade: FCFRP
Subjects: DOENÇA DE CHAGAS (TRATAMENTO;QUIMIOTERAPIA), TRYPANOSOMA CRUZI
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SILVA, Carlos Henrique Tomich de Paula da et al. Novel aryl 'beta'-aminocarbonyl derivates as inhibitors of Trypanosoma cruzi trypanothione reductase: binding mode revised by docking and GRIND2-based 3D-QSAR procedures. Journal of Biomolecular Structure and Dynamics, v. 29, n. 6, p. 702-716, 2012Tradução . . Disponível em: https://doi.org/10.1080/07391102.2011.672633. Acesso em: 05 out. 2024.APA
Silva, C. H. T. de P. da, Bernardes, L. S. C., Silva, V. B., Zani, C. L., & Carvalho, I. (2012). Novel aryl 'beta'-aminocarbonyl derivates as inhibitors of Trypanosoma cruzi trypanothione reductase: binding mode revised by docking and GRIND2-based 3D-QSAR procedures. Journal of Biomolecular Structure and Dynamics, 29( 6), 702-716. doi:10.1080/07391102.2011.672633NLM
Silva CHT de P da, Bernardes LSC, Silva VB, Zani CL, Carvalho I. Novel aryl 'beta'-aminocarbonyl derivates as inhibitors of Trypanosoma cruzi trypanothione reductase: binding mode revised by docking and GRIND2-based 3D-QSAR procedures [Internet]. Journal of Biomolecular Structure and Dynamics. 2012 ; 29( 6): 702-716.[citado 2024 out. 05 ] Available from: https://doi.org/10.1080/07391102.2011.672633Vancouver
Silva CHT de P da, Bernardes LSC, Silva VB, Zani CL, Carvalho I. Novel aryl 'beta'-aminocarbonyl derivates as inhibitors of Trypanosoma cruzi trypanothione reductase: binding mode revised by docking and GRIND2-based 3D-QSAR procedures [Internet]. Journal of Biomolecular Structure and Dynamics. 2012 ; 29( 6): 702-716.[citado 2024 out. 05 ] Available from: https://doi.org/10.1080/07391102.2011.672633