Journal
JOURNAL OF MOLECULAR GRAPHICS & MODELLING
Volume 116, Issue -, Pages -Publisher
ELSEVIER SCIENCE INC
DOI: 10.1016/j.jmgm.2022.108242
Keywords
Pyrimidine herbicides; AHAS; QSAR; Docking studies
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Funding
- Coordena?a?o de Aperfei?oamento de Pessoal de Nivel Superior (CAPES) [001]
- Conselho Nacio-nal de Desenvolvimento Cientifico e Tecnolo?gico (CNPq) [306830/2021-3]
- Funda?a?o de Amparo a` Pesquisa do Estado de Minas Gerais (FAPEMIG)
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This study proposes unprecedented pyrimidine compounds with herbicidal activity through QSAR modeling and analysis of MIA descriptors. By investigating the quantitative structure-activity relationship of derivatives, the study reveals the structural features responsible for herbicidal activity and analyzes the interaction with the target enzyme, leading to the identification of promising herbicidal candidates.
Pyrimidine compounds comprise a class of acetohydroxyacid synthase (AHAS) inhibitors, thus possessing herbicidal activity. Due to the ongoing development of resistance by weeds to current herbicides, the design of new agrochemical candidates is often required. This work reports the proposition of unprecedented pyrimidines as herbicides guided by quantitative structure-activity relationship (QSAR) modeling. Multivariate image analysis (MIA) descriptors for 66 pyrimidine derivatives obtained from different sources were regressed against inhibitory activity data, and the resulting QSAR models were found to be reliable and predictive (r2 = 0.88 +/- 0.07, q2 = 0.53 +/- 0.06, and r2pred = 0.51 +/- 0.10 in a bootstrapping experiment using electronegativity-based descriptors). The chemical features responsible for the herbicidal activities were analyzed through MIA contour maps that describe the substituent effects on the response variables, whereas the interaction between the proposed compounds and AHAS was analyzed through docking studies. From the proposed compounds, at least five pyrimidine derivatives exhibited promising performance as AHAS inhibitors compared to the known analogs.
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