Use este identificador para citar ou linkar para este item: http://repositorio.ufla.br/jspui/handle/1/56083
Título: Modelagem MIA-QSAR e docking molecular na proposição de novas tricetonas como potenciais inibidoras da enzima
Título(s) alternativo(s): HPPD MIA-QSAR modeling and molecular docking to propose new triketones as potential HPPD enzyme inhibitors
Autores: Freitas, Matheus Puggina de
Antunes, João Eustáquio
Mancini, Daiana Teixeira
Palavras-chave: Tricetonas
HPPD
Herbicida
MIA-QSAR
Docking molecular
Triketones
Hydroxyphenylpyruvate deoxygenase (HPPD)
Herbicide
Multivariate image analysis applied to quantitative structure-activity relationship (MIA-QSAR)
Data do documento: 3-Mar-2023
Editor: Universidade Federal de Lavras
Citação: CAPUCHO, L. dos R. Modelagem MIA-QSAR e docking molecular na proposição de novas tricetonas como potenciais inibidoras da enzima HPPD. 2023. 96 p. Dissertação (Mestrado em Agroquímica)–Universidade Federal de Lavras, Lavras, 2023.
Resumo: The problem of weed resistance has caused significant concern and has guided studies regarding herbicidal compounds. To propose new candidates to overcome this recurring problem in the class of triketones, two sets of molecules were subjected to MIA-QSAR modeling. The descriptors initially obtained in pixel values of the RGB scale were translated to consider the effects of electronegativity (ε), van der Waals radius (rvdW) and the rvdW/ε ratio, and subsequently submitted to the PLS regression method, with validation carried out from a sample randomization procedure. The results obtained in both sets demonstrate that the three evaluated parameters contributed significantly to the observed activity of the compounds, with the set of activities at pIC50 showing better values for the parameter rvdW/ε, whose average for 15 cycles was R2 = 0.823 ± 0.022, Q2 = 0.685 ± 0.027, R2pred = 0.702 ± 0.099, all acceptable values being above 0.5. In the set of activities related to pKi, only one model proved to be predictive, generating statistical values of R2 = 0.7180, Q2 = 0.5090, R2pred = 0.7101. The MIA plot's b and VIP were used to evaluate the influence of substituents on the response variables and, subsequently, to propose new candidates; 8 and 14 structures with better activity than the standard commercial compound mesotrione were obtained for the sets containing in vitro activities in pIC50 and pKi respectively. Molecular docking analyzes were carried out in a complementary way, aiming at investigating the interactions of the proposed molecules with the active site of the enzyme hydroxyphenylpyruvate dioxygenase (HPPD), indicating that, for both sets, the proposals with better activity presented greater stability in the enzymatic complex of the than the highest activity structure of the total pool and the standard compound mesotrione. The chemical synthesis of compounds becomes, therefore, promising in validating the theoretical evidence presented in this work.
URI: http://repositorio.ufla.br/jspui/handle/1/56083
Aparece nas coleções:Agroquímica - Mestrado (Dissertações)



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