中国科学院机构知识库网格
Chinese Academy of Sciences Institutional Repositories Grid
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浏览/检索结果: 共17条,第1-10条 帮助

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Identifying a non-conserved site for achieving allosteric covalent inhibition of CECR2 期刊论文  OAI收割
ACTA PHARMACOLOGICA SINICA, 2025, 页码: 16
作者:  
Tang, Cai-ling;  Li, Yuan-qing;  Du, Xi-kun;  Fang, Xiao-xia;  Guang, Yi-man
  |  收藏  |  浏览/下载:10/0  |  提交时间:2025/04/01
Design, synthesis and pharmacological evaluation of 1,2,3,4-tetrahydrobenzofuro[2,3-c] pyridine derivatives as p21-activated kinase 4 inhibitors for treatment of pancreatic cancer 期刊论文  OAI收割
ACTA PHARMACEUTICA SINICA B, 2025, 卷号: 15, 期号: 1, 页码: 438-466
作者:  
Li, Yang;  Fang, Yan;  Chen, Xiaoyu;  Tong, Linjiang;  Feng, Fang
  |  收藏  |  浏览/下载:12/0  |  提交时间:2025/04/01
Allosteric Regulation and Inhibition of Coronavirus 3CLpro Revealed by HDX-MS 期刊论文  OAI收割
CHEMBIOCHEM, 2024, 卷号: 25, 期号: 13, 页码: 9
作者:  
Song, Ning;  Zheng, Wen;  Song, Bin;  Zheng, Jie
  |  收藏  |  浏览/下载:11/0  |  提交时间:2024/08/20
From bench to bedside: current development and emerging trend of KRAS-targeted therapy 期刊论文  OAI收割
ACTA PHARMACOLOGICA SINICA, 2023, 页码: 18
作者:  
Chen, Yi;  Liu, Qiu-pei;  Xie, Hua
  |  收藏  |  浏览/下载:55/0  |  提交时间:2024/01/16
Drug design targeting active posttranslational modification protein isoforms 期刊论文  OAI收割
MEDICINAL RESEARCH REVIEWS, 2021, 卷号: 41, 期号: 3, 页码: 1701-1750
作者:  
Meng, Fanwang;  Liang, Zhongjie;  Zhao, Kehao;  Luo, Cheng
  |  收藏  |  浏览/下载:30/0  |  提交时间:2024/03/22
Allosteric Inhibitors of SHP2: An Updated Patent Review (2015-2020) 期刊论文  OAI收割
CURRENT MEDICINAL CHEMISTRY, 2021, 卷号: 28, 期号: 19, 页码: 3825-3842
作者:  
Wu, Jingwei;  Zhang, Huan;  Zhao, Guilong;  Wang, Runling
  |  收藏  |  浏览/下载:22/0  |  提交时间:2021/08/17
3-Deoxy-2 beta,16-dihydroxynagilactone E, a natural compound from Podocarpus nagi, preferentially inhibits JAK2/STAT3 signaling by allosterically interacting with the regulatory domain of JAK2 and induces apoptosis of cancer cells 期刊论文  OAI收割
ACTA PHARMACOLOGICA SINICA, 2019, 卷号: 40, 期号: 12, 页码: 1578-1586
作者:  
Shan, Hui;  Yao, Sheng;  Ye, Yang;  Yu, Qiang
  |  收藏  |  浏览/下载:19/0  |  提交时间:2020/07/01
3-Deoxy-2β,16-dihydroxynagilactone E, a natural compound from Podocarpus nagi, preferentially inhibits JAK2/ STAT3 signaling by allosterically interacting with the regulatory domain of JAK2 and induces apoptosis of cancer cells 期刊论文  OAI收割
中国药理学报:英文版, 2019, 卷号: 40.0, 期号: 012, 页码: 1578
作者:  
Hui Shan;  Sheng Yao;  Yang Ye;  Qiang Yu
  |  收藏  |  浏览/下载:12/0  |  提交时间:2020/12/24
Exploring molecular mechanism of allosteric inhibitor to relieve drug resistance of multiple mutations in HIV-1 protease by enhanced conformational sampling 期刊论文  OAI收割
PROTEINS-STRUCTURE FUNCTION AND BIOINFORMATICS, 2018, 卷号: 86, 期号: 12, 页码: 1294-1305
作者:  
Chen, Jianzhong;  Peng, Cheng;  Wang, Jinan;  Zhu, Weiliang
  |  收藏  |  浏览/下载:74/0  |  提交时间:2019/01/08
Discovery of novel 3-hydroxypicolinamides as selective inhibitors of HIV-1 integrase-LEDGF/p75 interaction 期刊论文  OAI收割
EUROPEAN JOURNAL OF MEDICINAL CHEMISTRY, 2017, 卷号: 125, 页码: 1051-1063
作者:  
Zhang, Feng-Hua;  Debnath, Bikash;  Xu, Zhong-Liang;  Yang, Liu-Meng;  Song, Li-Rui
  |  收藏  |  浏览/下载:22/0  |  提交时间:2019/01/08