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ADME Evaluation in Drug Discovery. 8. The Prediction of Human Intestinal Absorption by a Support Vector Machine

机译:药物发现中的ADME评估。 8.支持向量机对人体肠道吸收的预测

摘要

Human intestinal absorption (HIA) is an important roadblock in the formulation of new drug substances. In silico models for predicting the percentage of HIA based on calculated molecular descriptors are highly needed for the rapid estimation of this property. Here, we have studied the performance of a support vector machine (SVM) to classify compounds with high or low fractional absorption (%FA > 30% or %FA ≤ 30%). The analyzed data set consists of 578 structural diverse druglike molecules, which have been divided into a 480-molecule training set and a 98-molecule test set. Ten SVM classification models have been generated to investigate the impact of different individual molecular properties on %FA. Among these studied important molecule descriptors, topological polar surface area (TPSA) and predicted apparent octanol−water distribution coefficient at pH 6.5 (logD_(6.5)) show better classification performance than the others. To obtain the best SVM classifier, the influences of different kernel functions and different combinations of molecular descriptors were investigated using a rigorous training-validation procedure. The best SVM classifier can give satisfactory predictions for the training set (97.8% for the poor-absorption class and 94.5% for the good-absorption class). Moreover, 100% of the poor-absorption class and 97.8% of the good-absorption class in the external test set could be correctly classified. Finally, the influence of the size of the training set and the unbalanced nature of the data set have been studied. The analysis demonstrates that large data set is necessary for the stability of the classification models. Furthermore, the weights for the poor-absorption class and the good-absorption class should be properly balanced to generate unbiased classification models. Our work illustrates that SVMs used in combination with simple molecular descriptors can provide an extremely reliable assessment of intestinal absorption in an early in silico filtering process.
机译:人体肠道吸收(HIA)是新药配方中的重要障碍。在计算机模型中,基于此分子描述子预测HIA的百分比对于快速估算此特性非常必要。在这里,我们研究了支持向量机(SVM)对具有高吸收率或低吸收率(%FA> 30%或%FA≤30%)的化合物进行分类的性能。分析的数据集包含578个结构多样的类药物分子,这些分子已分为480分子训练集和98分子测试集。已经生成了十个SVM分类模型,以研究不同分子特性对%FA的影响。在这些研究的重要分子描述符中,拓扑极性表面积(TPSA)和在pH 6.5时预测的表观辛醇-水分布系数(logD_(6.5))显示出比其他更好的分类性能。为了获得最佳的SVM分类器,使用严格的训练验证程序研究了不同内核功能和分子描述符不同组合的影响。最佳的SVM分类器可以对训练集给出满意的预测(吸收不良的类别为97.8%,吸收良好的类别为94.5%)。此外,可以正确分类外部测试集中100%的不良吸收等级和97.8%的良好吸收等级。最后,研究了训练集大小和数据集不平衡性质的影响。分析表明,大数据集对于分类模型的稳定性是必需的。此外,应适当平衡不良吸收类别和良好吸收类别的权重,以生成无偏分类模型。我们的工作表明,与简单分子描述符结合使用的SVM可以在早期计算机过滤过程中提供非常可靠的肠道吸收评估。

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