TY - JOUR
T1 - Structure-activity relationship study of oxindole-based inhibitors of cyclin-dependent kinases based on least-squares support vector machines
AU - Li, Jiazhong
AU - Liu, Huanxiang
AU - Yao, Xiaojun
AU - Liu, Mancang
AU - Hu, Zhide
AU - Fan, Botao
PY - 2007/1/9
Y1 - 2007/1/9
N2 - 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.
AB - 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.
KW - Cyclin-dependent kinases (CDKs)
KW - Inhibitor
KW - Least-squares support vector machines (LS-SVMs)
KW - Linear discriminant analysis (LDA)
KW - Oxindole
KW - Structure-activity relationship (SAR)
UR - https://www.scopus.com/pages/publications/33751536091
U2 - 10.1016/j.aca.2006.08.031
DO - 10.1016/j.aca.2006.08.031
M3 - Article
C2 - 17386461
AN - SCOPUS:33751536091
SN - 0003-2670
VL - 581
SP - 333
EP - 342
JO - Analytica Chimica Acta
JF - Analytica Chimica Acta
IS - 2
ER -