Li Yang, Kong Yue, Zhang Mengdi, Yan Aixia, Liu Zhenming
State Key Laboratory of Chemical Resource Engineering, Department of Pharmaceutical Engineering, P. O. Box 53, Beijing University of Chemical Technology, 15 BeiSanHuan East Road, Beijing 100029, P. R. China.
Stake Key Laboratory of Natural and Biomimetic Drugs, Peking University.
Mol Inform. 2016 Apr;35(3-4):116-24. doi: 10.1002/minf.201500107. Epub 2016 Jan 15.
Inhibition of the neuraminidase is one of the most promising strategies for preventing influenza virus spreading. 479 neuraminidase inhibitors are collected for dataset 1 and 208 neuraminidase inhibitors for A/P/8/34 are collected for dataset 2. Using support vector machine (SVM), four computational models were built to predict whether a compound is an active or weakly active inhibitor of neuraminidase. Each compound is represented by MASSC fingerprints and ADRIANA.Code descriptors. The predication accuracies for the test sets of all the models are over 78 %. Model 2B, which is the best model, obtains a prediction accuracy and a Matthews Correlation Coefficient (MCC) of 89.71 % and 0.81 on test set, respectively. The molecular polarizability, molecular shape, molecular size and hydrogen bonding are related to the activities of neuraminidase inhibitors. The models can be obtained from the authors.
抑制神经氨酸酶是预防流感病毒传播最有前景的策略之一。数据集1收集了479种神经氨酸酶抑制剂,数据集2收集了208种针对A/P/8/34的神经氨酸酶抑制剂。使用支持向量机(SVM)构建了四个计算模型,以预测一种化合物是否为神经氨酸酶的活性或弱活性抑制剂。每种化合物由MASSC指纹和ADRIANA.Code描述符表示。所有模型测试集的预测准确率均超过78%。最佳模型2B在测试集上的预测准确率和马修斯相关系数(MCC)分别为89.71%和0.81。分子极化率、分子形状、分子大小和氢键与神经氨酸酶抑制剂的活性有关。模型可从作者处获得。