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ADMET Evaluation in Drug Discovery.12.Development of Binary Classification Models for Prediction of hERG Potassium Channel Blockage

机译:药物发现中的ADMET评估12.预测hERG钾通道阻滞的二元分类模型的开发

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Inhibition of the human ether-a-go-go related gene (hERG) potassium channel may result in QT interval prolongation,which causes severe cardiac side effects and is a major problem in clinical studies of drug candidates.The development of in silico tools to filter out potential bERG potassium channel blockers in early stages of the drug discovery process is of considerable interest.Here,a diverse set of 806 compounds with bERG inhibition data was assembled,and the binary hERG dassification models using naive Bayesian classification and recursive partitioning (RP) techniques were established and evaluated.The naive Bayesian classifier based on molecular properties and the ECFP_8 fingerprints yielded 84.8% accuracy for the training set using the leave-one-out (LOO) cross-validation procedure and 85% accuracy for the test set of 120 molecules For the two additional test sets,the modal achieved 89.4% accuracy for the WOMBAT-PK test set,and 86.1% accuracy for the PubChem test set.The naive Bayesian classifiers gave better predictions than the RP classifiers.Moreover,the Bayesian classifier,employing molecular fingerprints,highlights the important structural fragments favorable or unfavorable for hERG potassium channel blockage,which offers extra valuable information for the design of compounds avoiding undesirable hERG activity.
机译:抑制人类以太相关基因(hERG)钾通道可能导致QT间期延长,这会导致严重的心脏副作用,这是候选药物临床研究中的主要问题。在药物开发过程的早期阶段就筛选出可能的bERG钾通道阻滞剂引起了人们的极大兴趣。在此,组装了806种具有bERG抑制数据的化合物,并使用朴素贝叶斯分类和递归分区(RP)进行了二元hERG简化模型。建立和评估技术。基于分子性质和ECFP_8指纹的朴素贝叶斯分类器使用留一法(LOO)交叉验证程序对训练集产生了84.8%的准确度,对测试集产生了85%的准确度。 120个分子对于另外两个测试集,该模态的WOMBAT-PK测试集准确度达到89.4%,PubChem测试集达到86.1%。此外,贝叶斯分类器利用分子指纹,突出显示了对hERG钾通道阻滞有利或不利的重要结构片段,这为避免hERG活性不佳的化合物设计提供了额外的有价值的信息。

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