The 3D-QSAR model analysis of histamine H4 receptor ligands(组胺H4受体配体的3D-QSAR模型分析) по PANShan-fei(潘善飞), HUGui-xiang(胡桂香), LVYang(吕杨), YUQing-sen(俞庆森)

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

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QSPR Study on the permeability of drugs across Caco-2 monolayer(药物对Caco-2单细胞层穿透性的QSPR研究) по HUGui-xiang(胡桂香), ZHANGChang-hui(张长会), ZHAOWen-na(赵文娜), YUQing-sen(俞庆森)

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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) по 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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Study on the calculation method for molecular volume of chemical compounds(化合物分子体积计算方法的研究) по GUOMing(郭明), SHANGZhi-cai(商志才), YUQing-sen(俞庆森), LIUWen-jie(刘文杰), HUGui-xiang(胡桂香)

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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)... по 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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Theoretical chemistry study on metabolism influencing factors of two kinds of non-hormonal pregnancy-terminating drugs(两类非甾类终止妊娠药物代谢影响因素理论化学研究)... по HUGui-xiang(胡桂香), YUQing-sen(俞庆森), WANGYan-hua(王艳花), ZHANGBing(张兵), SHANGZhi-cai(商志才), WUTian-xing(吴天星)

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