中国科学院机构知识库网格
Chinese Academy of Sciences Institutional Repositories Grid
首页
机构
成果
学者
登录
注册
登陆
×
验证码:
换一张
忘记密码?
记住我
×
校外用户登录
CAS IR Grid
机构
上海药物研究所 [12]
上海应用物理研究所 [2]
天津工业生物技术研究... [2]
金属研究所 [1]
新疆理化技术研究所 [1]
青岛生物能源与过程研... [1]
更多
采集方式
OAI收割 [20]
iSwitch采集 [1]
内容类型
期刊论文 [20]
会议论文 [1]
发表日期
2024 [1]
2022 [1]
2020 [2]
2017 [4]
2016 [2]
2015 [4]
更多
学科主题
Biochemist... [1]
生物资源::代谢物组... [1]
筛选
浏览/检索结果:
共21条,第1-10条
帮助
条数/页:
5
10
15
20
25
30
35
40
45
50
55
60
65
70
75
80
85
90
95
100
排序方式:
请选择
提交时间升序
提交时间降序
题名升序
题名降序
作者升序
作者降序
发表日期升序
发表日期降序
Chemical Space Profiling of SARS-CoV-2 PL
pro
Using DNA-Encoded Focused Libraries
期刊论文
OAI收割
ACS MEDICINAL CHEMISTRY LETTERS, 2024, 页码: 10
作者:
Wang, Xudong
;
Zhu, Ying
;
Zhao, Qingyi
;
Lu, Weiwei
;
Xu, Yechun
  |  
收藏
  |  
浏览/下载:1/0
  |  
提交时间:2024/05/07
DNA-Encoded Focused Libraries (DEFLs)
SARS-CoV-2
Papain-like Protease
Library Design
ProteinInhibitors
Recent progress in fragment-based drug discovery facilitated by NMR spectroscopy
期刊论文
OAI收割
Magnetic Resonance Letters, 2022, 卷号: 2, 期号: 2, 页码: 107-118
作者:
Wang, Lei
;
Gao, Jia
;
Ma, Rongsheng
  |  
收藏
  |  
浏览/下载:7/0
  |  
提交时间:2024/03/14
Fragment-based lead/drug discovery
NMR spectroscopy
Protein-ligand interaction
Complex structure
Hit-to-lead evolution
Exploration of Fragment Binding Poses Leading to Efficient Discovery of Highly Potent and Orally Effective Inhibitors of FABP4 for Anti-inflammation
期刊论文
OAI收割
JOURNAL OF MEDICINAL CHEMISTRY, 2020, 卷号: 63, 期号: 8, 页码: 4090-4106
作者:
Su, Haixia
;
Zou, Yi
;
Chen, Guofeng
;
Dou, Huixia
;
Xie, Hang
  |  
收藏
  |  
浏览/下载:23/0
  |  
提交时间:2020/07/01
Lipoprotein-associated phospholipase A2: The story continues
期刊论文
OAI收割
MEDICINAL RESEARCH REVIEWS, 2020, 卷号: 40, 期号: 1, 页码: 79-134
作者:
Huang, Fubao
;
Wang, Kai
;
Shen, Jianhua
  |  
收藏
  |  
浏览/下载:11/0
  |  
提交时间:2020/07/01
fragment-based lead discovery
inflammation
inhibitors
lipoprotein-associated phospholipase A2
vascular diseases
Structure-Guided Discovery of Novel, Potent, and Orally Bioavailable Inhibitors of Lipoprotein-Associated Phospholipase A2
期刊论文
OAI收割
JOURNAL OF MEDICINAL CHEMISTRY, 2017, 卷号: 60, 期号: 24, 页码: 10231-10244
作者:
Liu, Qiufeng
;
Huang, Fubao
;
Yuan, Xiaojing
;
Wang, Kai
;
Zou, Yi
  |  
收藏
  |  
浏览/下载:32/0
  |  
提交时间:2019/01/08
Synthesis and in vitro biological evaluation of novel diaminothiophene scaffolds as antitumor and antiinfluenza virus agents. Part
期刊论文
OAI收割
RSC ADVANCES, 2017, 卷号: 7, 期号: 50, 页码: 31417-31427
作者:
Bozorov, K (Bozorov, Khurshed)
;
Zhao, JY (Zhao, Jiang Yu)
;
Nie, LF (Nie, Li Fei)
;
Ma, HR (Ma, Hai-Rong)
;
Bobakulov, K (Bobakulov, Khayrulla)
  |  
收藏
  |  
浏览/下载:32/0
  |  
提交时间:2018/01/09
Discovery of a novel small inhibitor RJ19 targeting to human Hsp90
期刊论文
OAI收割
NUCLEAR SCIENCE AND TECHNIQUES, 2017, 卷号: 28, 期号: 10, 页码: -
作者:
Cao, HL
;
Lyu, KK
;
Liu, B
;
Li, J
;
He, JH
  |  
收藏
  |  
浏览/下载:20/0
  |  
提交时间:2018/08/30
Shock-protein 90
Atp Hydrolysis
Chaperone
Identification
Binding
Design
Agent
Discovery of a novel small inhibitor RJ19 targeting to human Hsp90
期刊论文
OAI收割
NUCLEAR SCIENCE AND TECHNIQUES, 2017, 卷号: 28, 期号: 10
作者:
Cao HuiLing
;
Lyu KaiKai
;
Liu Bin
;
Li Jian
;
He JianHua
  |  
收藏
  |  
浏览/下载:8/0
  |  
提交时间:2021/02/26
ATP HYDROLYSIS
PROTEIN
CHAPERONE
IDENTIFICATION
BINDING
DESIGN
Heat shock protein 90
Drug target
Inhibitor
X-ray diffraction
Complex crystal structure
Nmr-based platform for fragment-based lead discovery used in screening brd4-targeted compounds
期刊论文
iSwitch采集
Acta pharmacologica sinica, 2016, 卷号: 37, 期号: 7, 页码: 984-993
作者:
Yu, Jun-lan
;
Chen, Tian-tian
;
Zhou, Chen
;
Lian, Fu-lin
;
Tang, Xu-long
收藏
  |  
浏览/下载:23/0
  |  
提交时间:2019/05/09
Fragment-based lead discovery
Nmr
Bromodomain
Brd4 inhibitors
NMR-based platform for fragment-based lead discovery used in screening BRD4-targeted compounds
期刊论文
OAI收割
ACTA PHARMACOLOGICA SINICA, 2016, 卷号: 37, 期号: 7, 页码: 984-993
作者:
Yu, Jun-lan
;
Chen, Tian-tian
;
Zhou, Chen
;
Lian, Fu-lin
;
Tang, Xu-long
  |  
收藏
  |  
浏览/下载:23/0
  |  
提交时间:2019/01/08
fragment-based lead discovery
NMR
bromodomain
BRD4 inhibitors