在未来的农用化学品生产之前就对其进行风险排查:甲状腺过氧化物酶抑制的大规模体外筛选硅学模型。

IF 3.7 3区 医学 Q2 CHEMISTRY, MEDICINAL Chemical Research in Toxicology Pub Date : 2024-10-21 Epub Date: 2024-09-20 DOI:10.1021/acs.chemrestox.4c00248
Martin Adamczewski, Britta Nisius, Nina Kausch-Busies
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引用次数: 0

摘要

抑制甲状腺过氧化物酶(TPO)是导致甲状腺激素失调和甲状腺毒性的已知分子起始事件。因此,TPO 是设计更安全农用化学品的关键非靶标。迄今为止,已知的具有结构特征的 TPO 抑制剂不到 500 种,而在相同条件下产生的最全面的结果集包括来自 ToxCast 化合物集子集的约 1000 种化合物。在这里,我们介绍了湿法实验室和数据科学家之间的合作,他们将大型体外筛选与随后开发的用于预测 TPO 抑制的硅学模型相结合。这次筛选涵盖了 100,000 多种不同的类药物农用化学品化合物,产生了 6000 多种结构新颖的 TPO 抑制剂。在此基础上,我们应用了不同的机器学习技术,并比较了它们的性能。我们讨论了农用化学品研究中硅学 TPO 模型的用例,并解释了从大型虚拟化合物库中选择化合物时,模型的召回率尤为重要。此外,我们还表明,由于我们的训练数据具有更高的结构多样性,我们的最终模型比在 ToxCast 数据集上训练的模型具有更好的通用性。我们现在有了一种工具,可以预测 TPO 抑制作用,即使是虚拟筛选中的命中分子或考虑纳入我们筛选集合的化合物等只能虚拟获得的分子也不例外。提供了 34524 种化合物的结构和活性数据。该数据集包括几乎所有的抑制剂,其中有 3000 多种专有结构,以及很大一部分非活性物质。
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Derisking Future Agrochemicals before They Are Made: Large-Scale In Vitro Screening for In Silico Modeling of Thyroid Peroxidase Inhibition.

Inhibition of thyroid peroxidase (TPO) is a known molecular initiating event for thyroid hormone dysregulation and thyroid toxicity. Consequently, TPO is a critical off-target for the design of safer agrochemicals. To date, fewer than 500 structurally characterized TPO inhibitors are known, and the most comprehensive result set generated under identical conditions encompasses approximately 1000 compounds from a subset of the ToxCast compound collection. Here we describe a collaboration between wet lab and data scientists combining a large in vitro screen and the subsequent development of an in silico model for predicting TPO inhibition. The screen encompassed more than 100,000 diverse drug-like agrochemical compounds and yielded more than 6000 structurally novel TPO inhibitors. On this foundation, we applied different machine learning techniques and compared their performance. We discuss use cases for in silico TPO models in agrochemical research and explain that model recall is of particular importance when selecting compounds from large virtual compound collections. Furthermore, we show that due to the higher structural diversity of our training data, our final model allowed better generalization than models trained on the ToxCast data set. We now have a tool to predict TPO inhibition even for molecules that are only available virtually, such as hits from virtual screenings, or compounds under consideration for inclusion in our screening collection. Structures and activity data for 34,524 compounds are provided. This data set includes almost all inhibitors, including more than 3000 proprietary structures, and a large proportion of the inactives.

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来源期刊
CiteScore
7.90
自引率
7.30%
发文量
215
审稿时长
3.5 months
期刊介绍: Chemical Research in Toxicology publishes Articles, Rapid Reports, Chemical Profiles, Reviews, Perspectives, Letters to the Editor, and ToxWatch on a wide range of topics in Toxicology that inform a chemical and molecular understanding and capacity to predict biological outcomes on the basis of structures and processes. The overarching goal of activities reported in the Journal are to provide knowledge and innovative approaches needed to promote intelligent solutions for human safety and ecosystem preservation. The journal emphasizes insight concerning mechanisms of toxicity over phenomenological observations. It upholds rigorous chemical, physical and mathematical standards for characterization and application of modern techniques.
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