机构

• 昆明植物研究所 [4]
• 南海海洋研究所 [3]
• 化学研究所 [3]
• 上海药物研究所 [2]
• 西北高原生物研究所 [2]
• 海洋研究所 [1]
• 更多

采集方式

• OAI收割 [15]

内容类型

• 期刊论文 [14]
• 学位论文 [1]

发表日期

• 2023 [2]
• 2022 [2]
• 2021 [2]
• 2020 [1]
• 2018 [1]
• 2016 [3]
• 更多

学科主题

• Oceanograp... [2]

筛选

浏览/检索结果: 共15条，第1-10条 帮助 条数/页： 5101520253035404550556065707580859095100 排序方式： 请选择提交时间升序提交时间降序题名升序题名降序作者升序作者降序发表日期升序发表日期降序 Hypoglycemic effect of Nitraria tangutorum fruit by inhibiting glycosidase and regulating IRS1/PI3K/AKT signalling pathway and its active ingredient identification by UPLC-MS 期刊论文  OAI收割 FOOD & FUNCTION, 2023, 卷号: 14, 期号: 17, 页码: 7869 作者:  Jiang, Sirong;  Wang, Luya;  Jia, Wenjing;  Wu, Di;  Wu, Li   |  收藏  |  浏览/下载：8/0  |  提交时间：2023/12/01 New Hydrolyzable Tannin with Potent Antioxidant and α-Glucosidase Inhibitory Activity from Black Tea Produced from Camellia taliensis 期刊论文  OAI收割 FOODS, 2023, 卷号: 12, 期号: 13, 页码: 2512 作者:  Chen,Min;  Li,Na;  Zhu,Hong-Tao;  Zhang,Man;  Duan,Zhao-Hong   |  收藏  |  浏览/下载：0/0  |  提交时间：2024/05/09 Camellia taliensis  black tea  hydrolyzable tannins  antioxidant activity  alpha-glucosidase inhibitory activity  GREEN TEA  FLAVONOL GLYCOSIDES  CONSTITUENTS  IDENTIFICATION  POLYPHENOL  LEAVES  THEAFLAVINS  EXTRACT   Hypoglycemic activity of Codonopsis pilosula (Franch.) Nannf. in vitro and in vivo and its chemical composition identification by UPLC-Triple-TOF-MS/MS 期刊论文  OAI收割 FOOD & FUNCTION, 2022, 卷号: 13, 期号: 5, 页码: 2456 作者:  Jia, WJ;  Bi, QM;  Jiang, SR;  Tao, JH;  Liu, LY   |  收藏  |  浏览/下载：18/0  |  提交时间：2022/12/02 Pentacyclic Triterpenoids from Sabia discolor Dunn and Their alpha-Glycosidase Inhibitory Activities 期刊论文  OAI收割 MOLECULES, 2022, 卷号: 27, 期号: 7, 页码: 2161 作者:  Ma, Jin-Hong;  Hu, Dan;  Deng, Lu-Lu;  Li, Jiang;  Hao, Xiao-Jiang   |  收藏  |  浏览/下载：0/0  |  提交时间：2024/04/30 Sabia discolor Dunn  pentacyclic triterpenoids  isolation and purification  alpha-glycosidase inhibitory activities   Optimization of extractions of eumelanin from cuttlefish ink and the hypoglycemic effects: In vitro enzyme inhibitory activity and glucose consumption in HepG2 cells 期刊论文  OAI收割 JOURNAL OF FOOD PROCESSING AND PRESERVATION, 2021, 页码: 17 作者:  Song, Wen;  Xing, Rong-e;  Yang, Haoyue;  Liu, Song   |  收藏  |  浏览/下载：32/0  |  提交时间：2021/11/30 Discovery of New alpha-Glucosidase Inhibitors: Structure-Based Virtual Screening and Biological Evaluation 期刊论文  OAI收割 FRONTIERS IN CHEMISTRY, 2021, 卷号: 9, 页码: 9 作者:  Liu, Shan-Kui;  Hao, Haifang;  Bian, Yuan;  Ge, Yong-Xi;  Lu, Shengyuan   |  收藏  |  浏览/下载：33/0  |  提交时间：2021/05/24 α  -glycosidase  virtual screening  cytotoxicity  type 2 diabetes  molecular docking   Protein tyrosine phosphatase 1B (PTP1B) inhibitors from the deep-sea fungus Penicillium chrysogenum SCSIO 07007 期刊论文  OAI收割 BIOORGANIC CHEMISTRY, 2020, 卷号: 96, 页码: 103646 作者:  Han, Wenrong;  Cai, Jia;  Zhong, Weimao;  Xu, Guangming;  Wang, Fazuo   |  收藏  |  浏览/下载：43/0  |  提交时间：2020/09/22 Penicillium chrysogenum  alpha-pyrone  Indolyl diketopiperazine  Protein tyrosine phosphatase 1B inhibition   Polyoxygenated Cyclohexenoids with Promising alpha-Glycosidase Inhibitory Activity Produced by Phomopsis sp YE3250, an Endophytic Fungus Derived from Paeonia delavayi 期刊论文  OAI收割 JOURNAL OF AGRICULTURAL AND FOOD CHEMISTRY, 2018, 卷号: 66, 期号: 5, 页码: 1140-1146 作者:  Huang, Rong;  Jiang, Bo-Guang;  Li, Xiao-Nian;  Wang, Ya-Ting;  Liu, Si-Si   |  收藏  |  浏览/下载：29/0  |  提交时间：2018/05/08 Phomopsis  Paeonia Delavayi  Polyoxygenated Cyclohexenoids  Alpha-glucosidase Inhibitor   First total synthesis of (+)-broussonetine W: glycosidase inhibition of natural product & analogs 期刊论文  OAI收割 ORGANIC & BIOMOLECULAR CHEMISTRY, 2016, 卷号: 14, 期号: 22, 页码: 5157-5174 作者:  Song, Ying-Ying;  Kinami, Kyoko;  Kato, Atsushi;  Jia, Yue-Mei;  Li, Yi-Xian 收藏  |  浏览/下载：31/0  |  提交时间：2017/01/17 Fluorinated Radicamine A and B: Synthesis and Glycosidase Inhibition 期刊论文  OAI收割 EUROPEAN JOURNAL OF ORGANIC CHEMISTRY, 2016, 期号: 7, 页码: 1429-1438 作者:  Li, Yi-Xian;  Iwaki, Ren;  Kato, Atsushi;  Jia, Yue-Mei;  Fleet, George W. J. 收藏  |  浏览/下载：25/0  |  提交时间：2017/01/23 Azasugars  Iminosugar  Fluorine  Inhibitors  Structure-activity relationships  Drug design