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29条,第1-10条 帮助

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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
Functional characterization, structural basis, and protein engineering of a rare flavonoid 2'-O-glycosyltransferase from Scutellaria baicalensis 期刊论文  OAI收割
ACTA PHARMACEUTICA SINICA B, 2024, 卷号: 14, 期号: 8, 页码: 3746-3759
作者:  
Wang, Zilong;  Du, Xueqing;  Ye, Guo;  Wang, Haotian;  Liu, Yizhan
  |  收藏  |  浏览/下载:92/0  |  提交时间:2024/09/26
Reversal of subtype-selectivity and function by the introduction of a para-benzamidyl substituent to N-cyclopropylmethyl nornepenthone 期刊论文  OAI收割
EUROPEAN JOURNAL OF MEDICINAL CHEMISTRY, 2023, 卷号: 258, 页码: 15
作者:  
Kong, Linghui;  Ning, Kuan;  Liu, Xiao;  Lu, Jiashuo;  Chen, Baiyu
  |  收藏  |  浏览/下载:38/0  |  提交时间:2023/10/17
Discovery of seven-membered ring berberine analogues as highly potent and specific hCES2A inhibitors 期刊论文  OAI收割
CHEMICO-BIOLOGICAL INTERACTIONS, 2023, 卷号: 378, 页码: 11
作者:  
Yang, Yun;  Xiong, Yuan;  Zhu, Guanghao;  Sun, Mengru;  Zou, Kun
  |  收藏  |  浏览/下载:34/0  |  提交时间:2023/10/17
Optimization of potent, selective and orally bioavailable biphenyl scaffold as FABP4 inhibitors for anti-inflammation 期刊论文  OAI收割
EUROPEAN JOURNAL OF MEDICINAL CHEMISTRY, 2023, 卷号: 253, 页码: 16
作者:  
He, Yulong;  Li, Shunyi;  Zhu, Yueyue;  Wang, Yujie;  Chen, Yuqi
  |  收藏  |  浏览/下载:79/0  |  提交时间:2023/10/17
Discovery of pseudolaric acid A as a new Hsp90 inhibitor uncovers its potential anticancer mechanism 期刊论文  OAI收割
BIOORGANIC CHEMISTRY, 2021, 卷号: 112, 页码: 104963
作者:  
Liu,Jiangxin;  Wu,Xing-De;  Li,Wenyan;  Yuan,Zaifeng;  Yang,Kun
  |  收藏  |  浏览/下载:26/0  |  提交时间:2022/04/02
An oxygen vacancy-rich two-dimensional Au/TiO2 hybrid for synergistically enhanced electrochemical N2 activation and reduction 期刊论文  OAI收割
Journal of Materials Chemistry A, 2020, 卷号: 8, 期号: 14, 页码: 6586-6596
作者:  
Zhao, Sen;  Liu, Han-Xuan;  Qiu, Yu;  Liu, Shuang-Quan;  Diao, Jin-Xiang
  |  收藏  |  浏览/下载:68/0  |  提交时间:2021/09/06
Discovery of a series of dimethoxybenzene FGFR inhibitors with 5H-pyrrolo[2,3-b]pyrazine scaffold: structure-activity relationship, crystal structural characterization and and in vivo study 期刊论文  OAI收割
ACTA PHARMACEUTICA SINICA B, 2019, 卷号: 9, 期号: 2, 页码: 351-368
作者:  
Wei, Peng;  Liu, Bo;  Wang, Ruifeng;  Gao, Yinglei;  Li, Lanlan
  |  收藏  |  浏览/下载:52/0  |  提交时间:2020/07/01
Discovery and synthesis of 6,7,8,9-tetrahydro-5H-pyrido[4,3-c]azepin-5-one-based novel chemotype CCR2 antagonists via scaffold hopping strategy 期刊论文  OAI收割
BIOORGANIC & MEDICINAL CHEMISTRY, 2018, 卷号: 26, 期号: 12, 页码: 3559-3572
作者:  
Qin, Li-Huai;  Wang, Zhi-Long;  Xie, Xin;  Long, Ya-Qiu
  |  收藏  |  浏览/下载:42/0  |  提交时间:2019/01/08
Characterization and structure-activity relationship studies of flavonoids as inhibitors against human carboxylesterase 2 期刊论文  OAI收割
BIOORGANIC CHEMISTRY, 2018, 卷号: 77, 页码: 320-329
作者:  
Zou, Li-Wei;  Weng, Zi-Miao;  Ge, Guang-Bo;  Dou, Tong-Yi;  Wang, Ping
  |  收藏  |  浏览/下载:35/0  |  提交时间:2019/06/20