中国科学院机构知识库网格
Chinese Academy of Sciences Institutional Repositories Grid
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Buxus alkaloid compound destabilizes mutant p53 through inhibition of the HSF1 chaperone axis 期刊论文  OAI收割
PHYTOMEDICINE, 2020
作者:  
Wang Yu-Ling;  Wu Wei;  Su Yong-Nan;  Ai Zhi-Peng;  Mou Han-Chuan
  |  收藏  |  浏览/下载:14/0  |  提交时间:2021/01/05
Structurally Diverse Labdane Diterpenoids from Leonurus japonicus and Their Anti-inflammatory Properties in LPS-Induced RAW264.7 Cells 期刊论文  OAI收割
JOURNAL OF NATURAL PRODUCTS, 2020
作者:  
Zhang, Xing-Jie;  Zhong, Wei-Mao;  Liu, Rui-Xue;  Wang, Yong-Mei;  Luo, Ting
  |  收藏  |  浏览/下载:14/0  |  提交时间:2021/01/05
Phenolic derivatives from Blaps japanensis and their biological evaluation 期刊论文  OAI收割
FITOTERAPIA, 2017, 卷号: 120, 页码: 58-60
作者:  
Zheng, Tao;  Yan, Yong-Ming;  Tu, Zheng-Chao;  Luo, Qi;  Xu, Fu-Rong
  |  收藏  |  浏览/下载:31/0  |  提交时间:2017/10/23
Structure-Based Design of Tetrahydroisoquinoline-7-carboxamides as Selective Discoidin Domain Receptor 1 (DDR1) Inhibitors 期刊论文  OAI收割
JOURNAL OF MEDICINAL CHEMISTRY, 2016, 卷号: 59, 期号: 12, 页码: 5911-5916
Wang, Zhen; Bian, Huan; Bartual, Sergio G.; Du, Wenting; Luo, Jinfeng; Zhao, Hu; Zhang, Shasha; Mo, Cheng; Zhou, Yang; Xu, Yong; Tu, Zhengchao; Ren, Xiaomei; Lu, Xiaoyun; Brekken, Rolf A.; Yao, Libo; Bullock, Alex N.; Su, Jin; Ding, Ke
收藏  |  浏览/下载:50/0  |  提交时间:2016/12/16
Structure-Based Design of Tetrahydroisoquinoline-7-carboxamides as Selective Discoidin Domain Receptor 1 (DDR1) Inhibitors 期刊论文  OAI收割
JOURNAL OF MEDICINAL CHEMISTRY, 2016, 卷号: 59, 期号: 12, 页码: 5911-5916
作者:  
Yao, Libo;  Ding, Ke;  Su, Jin;  Bullock, Alex N.;  Brekken, Rolf A.
  |  收藏  |  浏览/下载:32/0  |  提交时间:2018/12/13
Design, Synthesis, and Biological Evaluation of Substituted Pyrimidines as Potential Phosphatidylinositol 3-Kinase (PI3K) Inhibitors 期刊论文  OAI收割
JOURNAL OF MEDICINAL CHEMISTRY, 2016, 卷号: 59, 期号: 15, 页码: 7268-7274
作者:  
Long, Zi-Jie;  Lai, Xiao-Ju;  Chen, Hui-Xuan;  Luo, Yu;  Weng, Jiang
  |  收藏  |  浏览/下载:19/0  |  提交时间:2018/12/13
Compounds from Polyphaga plancyi and their inhibitory activities against JAK3 and DDR1 kinases 期刊论文  OAI收割
FITOTERAPIA, 2016, 卷号: 114, 页码: 163-167
作者:  
Liang, Rui;  Tu, Zheng-Chao;  Yan, Yong-Ming;  Zhu, Hong-Jie;  Wang, Shu-Mei
  |  收藏  |  浏览/下载:12/0  |  提交时间:2018/12/13
Compounds from Polyphaga plancyi and their inhibitory activities against JAK3 and DDR1 kinases 期刊论文  OAI收割
FITOTERAPIA, 2016, 卷号: 114, 页码: 163-167
Zhu, Hong-Jie; Yan, Yong-Ming; Tu, Zheng-Chao; Luo, Jin-Feng; Liang, Rui; Yang, Tong-Hua; Cheng, Yong-Xian; Wang, Shu-Mei
收藏  |  浏览/下载:22/0  |  提交时间:2016/12/16
Design, Synthesis, and Biological Evaluation of Substituted Pyrimidines as Potential Phosphatidylinositol 3-Kinase (PI3K) Inhibitors 期刊论文  OAI收割
JOURNAL OF MEDICINAL CHEMISTRY, 2016, 卷号: 59, 期号: 15, 页码: 7268-7274
Zhang, Ji-Quan; Luo, Yong-Jie; Xiong, Yan-Shi; Yu, Yang; Tu, Zheng-Chao; Long, Zi-Jie; Lai, Xiao-Ju; Chen, Hui-Xuan; Luo, Yu; Weng, Jiang; Lu, Gui
收藏  |  浏览/下载:28/0  |  提交时间:2016/12/16
ROR nuclear receptors: structures, related diseases, and drug discovery 期刊论文  OAI收割
ACTA PHARMACOLOGICA SINICA, 2015, 卷号: 36, 期号: 1, 页码: 71-87
Zhang, Yan; Luo, Xiao-yu; Wu, Dong-hai; Xu, Yong
收藏  |  浏览/下载:10/0  |  提交时间:2016/12/16