机构

• 上海药物研究所 [8]
• 昆明植物研究所 [3]
• 过程工程研究所 [3]
• 昆明动物研究所 [2]
• 生态环境研究中心 [1]

采集方式

• OAI收割 [17]

内容类型

• 期刊论文 [17]

发表日期

• 2023 [1]
• 2019 [3]
• 2018 [1]
• 2015 [1]
• 2013 [1]
• 2012 [4]
• 更多

学科主题

• Biochemist... [2]
• Chemistry [1]
• Chemistry,... [1]
• Chemistry,... [1]

筛选

浏览/检索结果: 共17条，第1-10条 帮助 条数/页： 5101520253035404550556065707580859095100 排序方式： 请选择题名升序题名降序提交时间升序提交时间降序作者升序作者降序发表日期升序发表日期降序 Structurally modified Cyclovirobuxine-D Buxus alkaloids as effective analgesic agents through Cav3.2 T-Type calcium channel inhibition 期刊论文  OAI收割 BIOORGANIC CHEMISTRY, 2023, 卷号: 135, 页码: 106493 作者:  Munikishore,Rachakunta;  Liu,Rui;  Zhang,Shuqun;  Zhao,Qin-Shi;  Nian,Yin   |  收藏  |  浏览/下载：11/0  |  提交时间：2024/07/22 Buxus alkaloid  Structural modification  T -type calcium channel  Analgesic activity  Docking analysis  Structure -activity relationship study  BUXOZINE-C  SEMPERVIRENS  RING  CONSTITUTION   Chronic thiamethoxam exposure impairs the HPG and HPT axes in adult Chinese rare minnow (Gobiocypris rarus): Docking study, hormone levels, histology, and transcriptional responses 期刊论文  OAI收割 ECOTOXICOLOGY AND ENVIRONMENTAL SAFETY, 2019, 卷号: 185, 页码: - 作者:  Zhu Lifei;  Wei, Li;  Zha, Jinmiao;  Na, Li;  Wang, Zijian   |  收藏  |  浏览/下载：24/0  |  提交时间：2020/09/10 Docking study  Plasma hormones  Thiamethoxam  Chinese rare minnow (Gobiocypris rants)   Synthesis and PTP1B/TCPTP Inhibitory Activity Evaluation of Novel 2,5-Disubstituted-1,3,4-thiadiazolamide Derivatives Containing Carbazole/Benzimidazole Moity 期刊论文  OAI收割 CHINESE JOURNAL OF ORGANIC CHEMISTRY, 2019, 卷号: 39, 期号: 9, 页码: 2599-2608 作者:     |  收藏  |  浏览/下载：32/0  |  提交时间：2020/07/01 1,3,4-thiadiazolamide  carbazole  benzimidazole  synthesis  PTP1B inhibitor  molecular docking  density functional theory (DFT) study   Polybenzyls from Gastrodia elata, their agonistic effects on melatonin receptors and structure-activity relationships 期刊论文  OAI收割 BIOORGANIC & MEDICINAL CHEMISTRY, 2019, 卷号: 27, 期号: 15, 页码: 3299-3306 作者:  Chen, Si-Yue;  Geng, Chang-An;  Ma, Yun-Bao;  Huang, Xiao-Yan;  Yang, Xiao-Tong   |  收藏  |  浏览/下载：145/0  |  提交时间：2019/09/10 Gastrodia elata  Polybenzyls  Melatonin receptors  Structure-activity relationships  Docking study   A novel series of 4-methyl substituted pyrazole derivatives as potent glucagon receptor antagonists: Design, synthesis and evaluation of biological activities 期刊论文  OAI收割 BIOORGANIC & MEDICINAL CHEMISTRY, 2018, 卷号: 26, 期号: 8, 页码: 1896-1908 作者:  Shu, Shuangjie;  Dai, Antao;  Wang, Jiang;  Wang, Bin;  Feng, Yang   |  收藏  |  浏览/下载：23/0  |  提交时间：2019/01/08 Pyrazole derivatives  Glucagon receptor antagonist  Docking study  Binding pocket   Enhancing the cellular anti-proliferation activity of pyridazinones as c-met inhibitors using docking analysis 期刊论文  OAI收割 EUROPEAN JOURNAL OF MEDICINAL CHEMISTRY, 2015, 卷号: 95, 页码: 302-312 作者:  Xing, Weiqiang;  Ai, Jing;  Jin, Shiyu;  Shi, Zhangxing;  Peng, Xia   |  收藏  |  浏览/下载：20/0  |  提交时间：2019/01/08 Pyridazinone  c-Met inhibitor  Anticancer  Docking study   Discovery of novel 2,6-disubstituted pyridazinone derivatives as acetylcholinesterase inhibitors 期刊论文  OAI收割 EUROPEAN JOURNAL OF MEDICINAL CHEMISTRY, 2013, 卷号: 63, 页码: 95-103 作者:  Xing, Weiqiang;  Fu, Yan;  Shi, Zhangxing;  Lu, Dong;  Zhang, Haiyan   |  收藏  |  浏览/下载：28/0  |  提交时间：2019/01/08 Pyridazinone  Acetylcholinesterase  Alzheimer's disease  Docking study   Structural modifications of 5,6-dihydroxypyrimidines with anti-HIV activity 期刊论文  OAI收割 BIOORGANIC & MEDICINAL CHEMISTRY LETTERS, 2012, 卷号: 22, 期号: 23, 页码: 7114-7118 作者:  Guo, Di-Liang;  Zhang, Xing-Jie;  Wang, Rui-Rui;  Zhou, Yu;  Li, Zeng   |  收藏  |  浏览/下载：20/0  |  提交时间：2019/01/08 Dihydroxypyrimidine  Synthesis  HIV  Integrase inhibitor  Docking study   Synthesis and biological evaluation of novel amprenavir-based P1-substituted bi-aryl derivatives as ultra-potent HIV-1 protease inhibitors 期刊论文  OAI收割 BIOORGANIC & MEDICINAL CHEMISTRY LETTERS, 2012, 卷号: 22, 期号: 5, 页码: 1976-1979 作者:  Yan, Jianwei;  Huang, Ning;  Li, Shukun;  Yang, Liu-Meng;  Xing, Weiqiang   |  收藏  |  浏览/下载：26/0  |  提交时间：2019/01/08 HIV-1 protease inhibitors  Amprenavir  Darunavir biaryl compounds  Docking study   Synthesis and biological evaluation of novel amprenavir-based P1-substituted bi-aryl derivatives as ultra-potent HIV-1 protease inhibitors 期刊论文  OAI收割 BIOORGANIC & MEDICINAL CHEMISTRY LETTERS, 2012, 卷号: 22, 期号: 5, 页码: 1976-1979 作者:  Yan JW;  Huang N;  Li SK;  Yang LM;  Xing WQ 收藏  |  浏览/下载：18/0  |  提交时间：2012/03/19 HIV-1 protease inhibitors  Amprenavir  Darunavir biaryl compounds  Docking study