Novel aryl 'beta'-aminocarbonyl derivates as inhibitors of Trypanosoma cruzi trypanothione reductase: binding mode revised by docking and GRIND2-based 3D-QSAR procedures (2012)
- Authors:
- USP affiliated authors: SILVA, CARLOS HENRIQUE TOMICH DE PAULA DA - FCFRP ; CARVALHO, IVONE - FCFRP
- Unidade: FCFRP
- DOI: 10.1080/07391102.2011.672633
- Subjects: DOENÇA DE CHAGAS (TRATAMENTO;QUIMIOTERAPIA); TRYPANOSOMA CRUZI
- Language: Inglês
- Imprenta:
- Publisher place: Schenectady
- Date published: 2012
- Source:
- Título do periódico: Journal of Biomolecular Structure and Dynamics
- ISSN: 0739-1102
- Volume/Número/Paginação/Ano: v. 29, n. 6, p. 702-716, 2012
- Este periódico é de assinatura
- Este artigo NÃO é de acesso aberto
- Cor do Acesso Aberto: closed
-
ABNT
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: 18 set. 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:10.1080/07391102.2011.672633 -
NLM
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 set. 18 ] Available from: https://doi.org/10.1080/07391102.2011.672633 -
Vancouver
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 set. 18 ] Available from: https://doi.org/10.1080/07391102.2011.672633 - In silico design and search for acetylcholinesterase inhibitors in Alzheimer's disease with a suitable pharmacokinetic profile and low toxicity
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Informações sobre o DOI: 10.1080/07391102.2011.672633 (Fonte: oaDOI API)
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