Please use this identifier to cite or link to this item: http://repositorio.ufla.br/jspui/handle/1/30797
metadata.artigo.dc.title: QSAR analysis of nicotinamidic compounds and design of potential Bruton’s tyrosine kinase (Btk) inhibitors
metadata.artigo.dc.creator: Santos-Garcia, Letícia
Assis, Letícia C.
Daniela R. Silva
Ramalho, Teodorico C.
Cunha, Elaine Fontes Ferreira da
metadata.artigo.dc.subject: Bruton’s tyrosine kinase
Quantitative structure-activity relationship (QSAR)
Nicotinamide
metadata.artigo.dc.publisher: Taylor and Francis Online
metadata.artigo.dc.date.issued: 2016
metadata.artigo.dc.identifier.citation: SANTOS-GARCIA, L. et al. QSAR analysis of nicotinamidic compounds and design of potential Bruton’s tyrosine kinase (Btk) inhibitors. Journal of Biomolecular Structure and Dynamics, [S.l.], v. 34, n. 7, 2016.
metadata.artigo.dc.description.abstract: Bruton’s tyrosine kinase (Btk) is an important enzyme in B-lymphocyte development and differentiation. Furthermore, Btk expression is considered essential for the proliferation and survival of these cells. Btk inhibition has become an attractive strategy for treating autoimmune diseases, B-cell leukemia, and lymphomas. With the objective of proposing new candidates for Btk inhibitors, we applied receptor-dependent four-dimensional quantitative structure–activity relationship (QSAR) methodology to a series of 96 nicotinamide analogs useful as Btk modulators. The QSAR models were developed using 71 compounds, the training set, and externally validated using 25 compounds, the test set. The conformations obtained by molecular dynamics simulation were overlapped in a virtual three-dimensional cubic box comprised of 2 and 5 Å cells, according to the six trial alignments. The models were generated by combining genetic function approximation and partial least squares regression technique. The analyses suggest that Model 1a yields the best results. The best equation shows , r2 = .743, RMSEC = .831, RMSECV = .879. Given the importance of the Tyr551, this residue could become a strategic target for the design of novel Btk inhibitors with improved potency. In addition, the good potency predicted for the proposed M2 compound indicates this compound as a potential Btk inhibitor candidate.
metadata.artigo.dc.identifier.uri: https://www.tandfonline.com/doi/abs/10.1080/07391102.2015.1070750?journalCode=tbsd20
http://repositorio.ufla.br/jspui/handle/1/30797
metadata.artigo.dc.language: en_US
Appears in Collections:DQI - Artigos publicados em periódicos

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