中国科学院机构知识库网格
Chinese Academy of Sciences Institutional Repositories Grid
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CAS IR Grid
机构
上海药物研究所 [12]
昆明植物研究所 [2]
合肥物质科学研究院 [1]
采集方式
OAI收割 [15]
内容类型
期刊论文 [15]
发表日期
2021 [2]
2019 [2]
2018 [3]
2017 [2]
2016 [1]
2013 [1]
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Chemistry,... [1]
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Discovery of a novel 53BP1 inhibitor through AlphaScreen-based high-throughput screening
期刊论文
OAI收割
BIOORGANIC & MEDICINAL CHEMISTRY, 2021, 卷号: 34, 页码: 116054
作者:
Sun, Yanli
;
Lu, Haibo
;
Fang, Xueyu
;
Xiao, Senhao
;
Yang, Feng
  |  
收藏
  |  
浏览/下载:10/0
  |  
提交时间:2024/03/21
53BP1-TTD
H4K2Ome2
AlphaScreen
HTS
Novel inhibitor
Targeting Protein Neddylation to Inactivate Cullin-RING Ligases by Gossypol: A Lucky Hit or a New Start?
期刊论文
OAI收割
DRUG DESIGN DEVELOPMENT AND THERAPY, 2021, 卷号: 15
作者:
Yu, Qing
;
Sun, Yi
  |  
收藏
  |  
浏览/下载:26/0
  |  
提交时间:2021/03/15
anti-cancer drug
cullin-RING E3 ligases
natural product
high-throughput screen
neddylation
small-molecule inhibitors
Orthogonal assays for the identification of inhibitors of the single-stranded nucleic acid binding protein YB-1
期刊论文
OAI收割
ACTA PHARMACEUTICA SINICA B, 2019, 卷号: 9, 期号: 5, 页码: 997-1007
作者:
Trevarton, Alexander J.
;
Zhou, Yan
;
Yang, Dehua
;
Rewcastle, Gordon W.
;
Flanagan, Jack U.
  |  
收藏
  |  
浏览/下载:18/0
  |  
提交时间:2020/07/01
Cancer
YB-1
Luciferase
AlphaScreen
Transcription factor
Single-stranded DNA
Discovery of trisubstituted nicotinonitrile derivatives as novel human GCN5 inhibitors through AlphaScreen-based high throughput screening
期刊论文
OAI收割
RSC ADVANCES, 2019, 卷号: 9, 期号: 9, 页码: 4917-4924
作者:
Tao, Hongru
;
Wang, Jun
;
Lu, Wenchao
;
Zhang, Rukang
;
Xie, Yiqian
  |  
收藏
  |  
浏览/下载:18/0
  |  
提交时间:2020/07/01
Identification of small molecule inhibitors targeting the SMARCA2 bromodomain from a high-throughput screening assay
期刊论文
OAI收割
ACTA PHARMACOLOGICA SINICA, 2018, 卷号: 39, 期号: 9, 页码: 1544-1552
作者:
Lu, Tian
;
Hu, Jun-chi
;
Lu, Wen-chao
;
Han, Jie
;
Ding, Hong
  |  
收藏
  |  
浏览/下载:33/0
  |  
提交时间:2019/01/08
AlphaScreen
high-throughput screening
SMARCA2
bromodomain
small molecule inhibitor
Design, synthesis and biological evaluation of benzo[cd]indo1-2(1H)-ones derivatives as BRD4 inhibitors
期刊论文
OAI收割
EUROPEAN JOURNAL OF MEDICINAL CHEMISTRY, 2018, 卷号: 152, 页码: 264-273
作者:
Feng, Yuxin
;
Xiao, Senhao
;
Chen, Yantao
;
Jiang, Hao
;
Liu, Na
  |  
收藏
  |  
浏览/下载:34/0
  |  
提交时间:2019/01/08
Benzo[cd]indol-2(1H)-one
Sulfonamide
BRD4 inhibitor
Bromodomain and extra-terminal domain
Acetyl-lysine binding pocket
A Highly Sensitive Non-Radioactive Activity Assay for AMP-Activated Protein Kinase (AMPK)
期刊论文
OAI收割
Methods and protocols, 2018, 卷号: 1, 期号: 1
作者:
Yan, Yan
;
Gu, Xin
;
Xu, H Eric
;
Melcher, Karsten
  |  
收藏
  |  
浏览/下载:12/0
  |  
提交时间:2019/01/08
Discovery of novel trimethoxy-ring BRD4 bromodomain inhibitors: AlphaScreen assay, crystallography and cell-based assay
期刊论文
OAI收割
MEDCHEMCOMM, 2017, 卷号: 8, 期号: 6, 页码: 1322-1331
作者:
Chen, Zhifeng
;
Zhang, Hao
;
Liu, Shien
;
Xie, Yiqian
;
Jiang, Hao
  |  
收藏
  |  
浏览/下载:90/0
  |  
提交时间:2019/01/08
Discovery of novel BRD4 inhibitors by high-throughput screening, crystallography, and cell-based assays
期刊论文
OAI收割
BIOORGANIC & MEDICINAL CHEMISTRY LETTERS, 2017, 卷号: 27, 期号: 9, 页码: 2003-2009
作者:
Sun, Zhongya
;
Zhang, Hao
;
Chen, Zhifeng
;
Xie, Yiqian
;
Jiang, Hao
  |  
收藏
  |  
浏览/下载:89/0
  |  
提交时间:2019/01/08
BRD4 inhibitor
High-throughput screening
Crystallography
Generation and characterization of a human nanobody against VEGFR-2
期刊论文
OAI收割
ACTA PHARMACOLOGICA SINICA, 2016, 卷号: 37, 期号: 6, 页码: 857-864
作者:
Ma, Lin
;
Gu, Kai
;
Zhang, Cheng-hai
;
Chen, Xue-tao
;
Jiang, Yi
  |  
收藏
  |  
浏览/下载:14/0
  |  
提交时间:2019/01/08
nanobody
VEGFR2
anticancer agent
anti-angiogenesis
phage display