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浏览/检索结果: 共7条，第1-7条 帮助 限定条件 发表日期：2019     已选(0)清除 条数/页：5101520253035404550556065707580859095100   排序方式：请选择作者升序作者降序题名升序题名降序发表日期升序发表日期降序提交时间升序提交时间降序 Cytochrome P450 3A Enzymes Are Key Contributors for Hepatic Metabolism of Bufotalin, a Natural Constitute in Chinese Medicine Chansu 期刊论文 FRONTIERS IN PHARMACOLOGY, 2019, 卷号: 10, 页码: 10 作者:  Ma, Hong-Ping;  Dai, Zi-Ru;  Ning, Jing;  Sun, Gui-Bo;  Wang, Ping 收藏  |  浏览/下载：67/0  |  提交时间：2019/06/20 bufotalin  cytochrome P450 3A (CYP3A)  hydroxylation  human liver microsomes (HLMs)  docking simulations   Cytochrome p450 3a enzymes are key contributors for hepatic metabolism of bufotalin, a natural constitute in chinese medicine chansu 期刊论文 Frontiers in pharmacology, 2019, 卷号: 10, 页码: 10 作者:  Dai, Zi-Ru;  Ning, Jing;  Sun, Gui-Bo;  Wang, Ping;  Zhang, Feng 收藏  |  浏览/下载：89/0  |  提交时间：2019/05/08 Bufotalin  Cytochrome p450 3a (cyp3a)  Hydroxylation  Human liver microsomes (hlms)  Docking simulations   Inhibition of human cytochrome P450 2A6 by 7-hydroxycoumarin analogues: Analysis of the structure-activity relationship and isoform selectivity 期刊论文 EUROPEAN JOURNAL OF PHARMACEUTICAL SCIENCES, 2019, 卷号: 136 作者:  Qi, Xiaoyi;  Dou, Tongyi;  Wang, Zhongqiong;  Wu, Jianming;  Yang, Ling 收藏  |  浏览/下载：17/0  |  提交时间：2019/12/05 CYP2A6  Inhibitor  7-Hydroxycoumarin  Structure-activity relationship  Isoform  Selectivity   Inhibition of human cytochrome P450 2A6 by 7-hydroxycoumarin analogues: Analysis of the structure-activity relationship and isoform selectivity 期刊论文 EUROPEAN JOURNAL OF PHARMACEUTICAL SCIENCES, 2019, 卷号: 136, 页码: 104944 作者:  Qi, Xiaoyi;  Dou, Tongyi;  Wang, Zhongqiong;  Wu, Jianming;  Yang, Ling 收藏  |  浏览/下载：12/0  |  提交时间：2019/12/02 CYP2A6  Inhibitor  7-Hydroxycoumarin  Structure-activity relationship  Isoform  Selectivity   Glucuronidation of d-Luciferin In Vitro: Isoform Selectivity and Kinetics Characterization 期刊论文 EUROPEAN JOURNAL OF DRUG METABOLISM AND PHARMACOKINETICS, 2019, 卷号: 44, 页码: 549-556 作者:  Xia, Yangliu;  Pang, Huilin 收藏  |  浏览/下载：10/0  |  提交时间：2019/12/02 Design, synthesis and biological evaluation of novel human monoamine oxidase B inhibitors based on a fragment in an X-ray crystal structure. 期刊论文 Bioorganic & medicinal chemistry letters, 2019 作者:  Kai Cheng;  Shiyu Li;  Xiao Lv;  Yongbin Tian;  Haiyan Kong 收藏  |  浏览/下载：71/0  |  提交时间：2019/12/13 Fragment-based drug design  Isatin  Isoform selectivity  Structure activity relationship  hMAO-B   Design, synthesis and biological evaluation of novel human monoamine oxidase B inhibitors based on a fragment in an X-ray crystal structure 期刊论文 Bioorganic & Medicinal Chemistry Letters, 2019 作者:  Kai Cheng;  Shiyu Li;  Xiao Lv;  Yongbin Tian;  Haiyan Kong 收藏  |  浏览/下载：21/0  |  提交时间：2019/12/17 hMAO-B  isatin  isoform  selectivity  fragment-based  drug  design  structure  activity  relationship