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   Docking Analysis and Multidimensional Hybrid QSAR Model of 1,4-Benzodiazepine-2,5-Diones as HDM2 Antagonists  
   
نویسنده Yuji Dai ,Nan Chen ,Qiang Wang ,Heng Zhen ,Xiuli Zhang ,Shiru Jia ,Lilong Dong ,Dacheng Feng
منبع iranian journal of pharmaceutical research - 2012 - دوره : 11 - شماره : 3 - صفحه:807 -830
چکیده    The inhibitors of p53-hdm2 interaction are attractive molecules for the treatment of wild-type p53 tumors. in order to search more potent hdm2 inhibitors, docking operation with cdocker protocol in discovery studio 2.1 (ds2.1) and multidimensional hybrid quantitative structure-activity relationship (qsar) studies through the physiochemical properties obtained from ds2.1 and e-dragon 1.0 as descriptors, have been performed on 59 1,4-benzodiazepine-2,5-diones which have p53-hdm2 interaction inhibitory activities. the docking results indicate that π-π interaction between the imidazole group in his96 and the aryl ring at 4-n of 1,4-benzodiazepine-2,5-dione may be one of the key factors for the combination of ligands with hdm2. two qsar models were obtained using genetic function approximation (gfa) and genetic partial least squares (g/pls) based on the descriptors obtained from ds2.1 and e-dragon 1.0, respectively. the best model can explain 85.5% of the variance (2adjr) while it could predict 81.7% of the variance (2cvr). with this model, the bioactivities of some new compounds were predicted
کلیدواژه p53-HDM2 interaction; Docking; QSAR; 1 ,4-benzodiazepine-2 ,5-diones; CDOCKER
آدرس University of Science and Technology, Ministry of Education, College of Bioengineering, Key Laboratory of Industrial Fermentation Microbiology (Tianjin University of Science and Technology), China, Tianjin University of Science and Technology, Ministry of Education, College of Bioengineering, Key Laboratory of Industrial Fermentation Microbiology (Tianjin University of Science and Technology), China, Tianjin University of Science and Technology, Ministry of Education, College of Bioengineering, Key Laboratory of Industrial Fermentation Microbiology (Tianjin University of Science and Technology), China, China Pharmaceutical University, School of Life Science and Technology, China, University of Missouri-Columbia, Department of Biochemistry, USA, Tianjin University of Science and Technology, Ministry of Education, College of Bioengineering, Key Laboratory of Industrial Fermentation Microbiology (Tianjin University of Science and Technology), China, Hebei Medical University, School of Pharmaceutical Sciences, China, Shandong University, College of Chemistry and Chemical Engineering, China
پست الکترونیکی yjdai@126.com
 
     
   
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