Quantitative structure-activity relationship study for quinolones(喹诺酮药物的定量结构-活性关系) 由 ZHAOWen-na(赵文娜), ZOUJian-wei(邹建卫), HURui-ding(胡瑞定), HUGui-xiang(胡桂香)

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QSAR studies on indazolyl urea TRPV1 channel antagonists(吲唑脲类辣椒素受体通道拮抗剂的定量构效关系) 由 SANGPeng(桑鹏), ZOUJian-wei(邹建卫), HUGui-xiang(胡桂香), JIANGYong-jun(蒋勇军), YUQing-sen(俞庆森)

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Molecular docking study of the cytochrome BC1 complexed with inhibitors(细胞色素BC1酶复合物抑制剂的对接研究) 由 GUOHui(郭辉), YUQing-sen(俞庆森), ZOUJian-wei(邹建卫), LIUHai-chun(刘海春), WANGHong-qing(王红青)

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Presuming the active conformation of tautomerized inhibitor by 3D-QSAR(利用三维构效关系确定互变异构抑制剂的活性构象) 由 XUHui-ying(许惠英), ZOUJian-wei(邹建卫), WANGYan-hua(王艳花), ZHANGNa(张娜), JINHai-xiao(金海晓)

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QSPR study and three-dimensional descriptor characterization of membrane-water partition coefficient of compounds(化合物膜水分配系数的QSPR研究和分子三维参数表征)... 由 HUGui-xiang(胡桂香), ZOUJian-wei(邹建卫), ZENGMin(曾敏), ZHANGBing(张兵), JINHai-xiao(金海晓), YUQing-sen(俞庆森)

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Quantitative structure-activity relationship of the inhibitors of acetylcholinesterase by comparative molecular field analysis(乙酰胆碱酯酶抑制剂定量构效关系的比较分子场分析)... 由 ZHAOWen-na(赵文娜), HUANGMei-lan(黄美兰), ZHANGBing(张兵), ZOUJian-wei(邹建卫), SHANGZhi-cai(商志才), YUQing-sen(俞庆森)

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