Identification of Novel Arachidonic Acid 15-Lipoxygenase Inhibitors Based on the Bayesian Classifier Model and Computer-Aided High-Throughput Virtual Screening.

Yinglin Liao, Peng Cao, Lianxiang Luo
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引用次数: 3

Abstract

Ferroptosis is an iron-dependent lipid peroxidative form of cell death that is distinct from apoptosis and necrosis. ALOX15, also known as arachidonic acid 15-lipoxygenase, promotes ferroptosis by converting intracellular unsaturated lipids into oxidized lipid intermediates and is an important ferroptosis target. In this study, a naive Bayesian machine learning classifier with a structure-based, high-throughput screening approach and a molecular docking program were combined to screen for three compounds with excellent target-binding potential. In the absorption, distribution, metabolism, excretion, and toxicity characterization, three candidate molecules were predicted to exhibit drug-like properties. The subsequent molecular dynamics simulations confirmed their stable binding to the targets. The findings indicated that the compounds exhibited excellent potential ALOX15 inhibitor capacity, thereby providing novel candidates for the treatment of inflammatory ischemia-related diseases caused by ferroptosis.

Abstract Image

Abstract Image

Abstract Image

基于贝叶斯分类器模型和计算机辅助高通量虚拟筛选的新型花生四烯酸15-脂氧合酶抑制剂鉴定。
铁下垂是一种依赖铁的脂质过氧化形式的细胞死亡,不同于细胞凋亡和坏死。ALOX15,也被称为花生四烯酸15-脂氧合酶,通过将细胞内不饱和脂质转化为氧化脂质中间体来促进铁下垂,是铁下垂的重要靶点。本研究将朴素贝叶斯机器学习分类器与基于结构的高通量筛选方法和分子对接程序相结合,筛选出三种具有良好靶标结合潜力的化合物。在吸收、分布、代谢、排泄和毒性表征方面,预测了三个候选分子表现出药物样特性。随后的分子动力学模拟证实了它们与靶标的稳定结合。研究结果表明,这些化合物具有良好的潜在ALOX15抑制剂能力,从而为治疗由铁下垂引起的炎症性缺血相关疾病提供了新的候选药物。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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