ASIA unversity:Item 310904400/8774
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    题名: Dual-targeted drug design of HER2 and HSP90 by CoMFA model and pharmacophore analysis
    作者: Huang, Hung-Jin;Bau, Da-Tian;Tsai, Ming-Hsui;Hsu, Yuan-Man;Ho, Tin-Yun;Chen, Chien-Yu;Chang, Yea-Huey;Tsai, Fuu-Jen;Tsai, Chang-Hai;Chen, Calvin Yu-Chian
    贡献者: Department of Bioinformatics
    关键词: Biomedical engineering;Cell proliferation;Pharmacodynamics;Proteins;Targets;Cancer cells;Cancer therapy;CoMFA;Comparative molecular field analysis;Contour map;Cost differences;Cross validation;Drug Design;Heat shock protein;Human epidermal growth factor;Pharmacophore models;Pharmacophores;Predictive models;Signal pathways
    日期: 2009
    上传时间: 2010-04-08 20:05:57 (UTC+8)
    出版者: Asia University
    摘要: Heat shock protein 90 (HSP90) and human epidermal growth factor receptor 2 protein (HER2) are involved in several signal pathways for cancer cell proliferation. We focused on these two hallmarkers to design the dual-targeted inhibitors for cancer therapy. The comparative molecular field analysis (CoMFA) and pharmacophore analysis were employed for generating the predictive models. According the leave-one out (LOO) cross-validation, the CoMFA models obtained the significant r2 values of 0.978 and 0.974 for HSP90 and HER2, respectively. The contour maps of both targets indicated that there were amount of similar bulky favors area. Besides, the cost difference of pharmacophore models was 48.539 for 70% correlation with the experiment. The queries at 3-N and 6-N position of purine-based compound had the similar distributions. This study provided important information for design the HER2 and HSP90 dual-targeted inhibitors ©2009 IEEE.
    關聯: Proceedings of the 2009 2nd International Conference on Biomedical Engineering and Informatics, BMEI 2009
    显示于类别:[生物資訊與醫學工程學系 ] 會議論文

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