Li Jiazhong, Liu Huanxiang, Yao Xiaojun, Liu Mancang, Hu Zhide, Fan Botao
Department of Chemistry, Lanzhou University, Lanzhou 730000, China.
Anal Chim Acta. 2007 Jan 9;581(2):333-42. doi: 10.1016/j.aca.2006.08.031. Epub 2006 Aug 24.
The least-squares support vector machines (LS-SVMs), as an effective modified algorithm of support vector machine, was used to build structure-activity relationship (SAR) models to classify the oxindole-based inhibitors of cyclin-dependent kinases (CDKs) based on their activity. Each compound was depicted by the structural descriptors that encode constitutional, topological, geometrical, electrostatic and quantum-chemical features. The forward-step-wise linear discriminate analysis method was used to search the descriptor space and select the structural descriptors responsible for activity. The linear discriminant analysis (LDA) and nonlinear LS-SVMs method were employed to build classification models, and the best results were obtained by the LS-SVMs method with prediction accuracy of 100% on the test set and 90.91% for CDK1 and CDK2, respectively, as well as that of LDA models 95.45% and 86.36%. This paper provides an effective method to screen CDKs inhibitors.
最小二乘支持向量机(LS-SVMs)作为支持向量机的一种有效改进算法,被用于构建构效关系(SAR)模型,以根据其活性对基于氧化吲哚的细胞周期蛋白依赖性激酶(CDKs)抑制剂进行分类。每个化合物都由编码组成、拓扑、几何、静电和量子化学特征的结构描述符来描述。采用逐步线性判别分析方法搜索描述符空间,并选择负责活性的结构描述符。使用线性判别分析(LDA)和非线性LS-SVMs方法构建分类模型,通过LS-SVMs方法获得了最佳结果,在测试集上的预测准确率为100%,对CDK1和CDK2的预测准确率分别为90.91%,而LDA模型的预测准确率分别为95.45%和86.36%。本文提供了一种筛选CDKs抑制剂的有效方法。