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基于朴素贝叶斯分类器建立化学诱导的尿路毒性的计算机预测模型。

Development of an in silico prediction model for chemical-induced urinary tract toxicity by using naïve Bayes classifier.

机构信息

College of Life Science, Northwest Normal University, Lanzhou, 730070, Gansu, People's Republic of China.

State Key Laboratory of Biotherapy and Cancer Center, West China Hospital, West China Medical School, Sichuan University, Chengdu, 610041, Sichuan, People's Republic of China.

出版信息

Mol Divers. 2019 May;23(2):381-392. doi: 10.1007/s11030-018-9882-8. Epub 2018 Oct 8.

Abstract

The urinary tract toxicity is one of the major reasons for investigational drugs not coming into the market and even marketed drugs being restricted or withdrawn. The objective of this investigation is to develop an easily interpretable and practically applicable in silico prediction model of chemical-induced urinary tract toxicity by using naïve Bayes classifier. The genetic algorithm was used to select important molecular descriptors related to urinary tract toxicity, and the ECFP-6 fingerprint descriptors were applied to the urinary tract toxic/non-toxic fragments production. The established naïve Bayes classifier (NB-2) produced 87.3% overall accuracy of fivefold cross-validation for the training set and 84.2% for the external test set, which can be employed for the chemical-induced urinary tract toxicity assessment. Furthermore, six important molecular descriptors (e.g., number of N atoms, AlogP, molecular weight, number of H acceptors, number of H donors and molecular fractional polar surface area) and toxic and non-toxic fragments were obtained, which would help medicinal chemists interpret the mechanisms of urinary tract toxicity, and even provide theoretical guidance for hit and lead optimization.

摘要

泌尿道毒性是导致研究药物无法进入市场,甚至已上市药物受到限制或撤回的主要原因之一。本研究旨在利用朴素贝叶斯分类器开发一种易于解释且具有实际应用价值的化学诱导泌尿道毒性的计算预测模型。该研究采用遗传算法选择与泌尿道毒性相关的重要分子描述符,并应用 ECFP-6 指纹描述符对泌尿道毒性/非毒性片段进行生成。所建立的朴素贝叶斯分类器(NB-2)对训练集进行五重交叉验证的整体准确率为 87.3%,对外部测试集的准确率为 84.2%,可用于化学诱导泌尿道毒性评估。此外,还获得了六个重要的分子描述符(例如,氮原子数、ALOGP、分子量、氢键受体数、氢键供体数和分子部分极性表面积)和毒性与非毒性片段,这有助于药物化学家解释泌尿道毒性的机制,甚至为命中和先导化合物优化提供理论指导。

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