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科研机构
中南大学 [15]
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期刊论文 [15]
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2017 [3]
2016 [2]
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2014 [1]
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专题:中南大学
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Smart Self-Assembled Organic Nanoprobe for Protein-Specific Detection: Design, Synthesis, Application, and Mechanism Studies
期刊论文
Analytical Chemistry, 2017, 卷号: 89, 期号: 18, 页码: 10085-10093
作者:
Gao, Tang
;
Yang, Shuqi
;
Cao, Xiaozheng
;
Dong, Jie
;
Zhao, Ning
收藏
  |  
浏览/下载:7/0
  |  
提交时间:2019/12/03
Multipotent AChE and BACE-1 inhibitors for the treatment of Alzheimer's disease: Design, synthesis and bio-analysis of 7-amino-1,4-dihydro-2H-isoquilin-3-one derivates
期刊论文
European Journal of Medicinal Chemistry, 2017, 卷号: 138, 页码: 738-747
作者:
Zhao, Xiong-jie
;
Gong, Da-min
;
Jiang, Yu-ren*
;
Guo, Dong
;
Zhu, Yao
收藏
  |  
浏览/下载:56/0
  |  
提交时间:2019/12/03
Alzheimer's disease
Acetylcholinesterase
β-secretase
Metal chelators
Inhibitor
AChE
acetylcholinesterase
AChEIs
acetylcholinesterase inhibitors
Aβ
β-amyloid
AD
Alzheimer's disease
PAS
peripheral anionic sites
BACE-1
β-secretase
MTDLs
multi-target-directed ligands
PDB
Protein Data Bank
TLC
thin layer chromatography
Design, synthesis and biological evaluation of [1,2,4]triazolo[1,5-a]pyrimidines as potent lysine specific demethylase 1 (LSD1/KDM1A) inhibitors
期刊论文
EUROPEAN JOURNAL OF MEDICINAL CHEMISTRY, 2017, 卷号: 125, 页码: 940-951
作者:
Wang, Shuai
;
Zhao, Li-Jie
;
Zheng, Yi-Chao
;
Shen, Dan-Dan
;
Miao, Er-Fei
收藏
  |  
浏览/下载:10/0
  |  
提交时间:2019/12/03
[1,2,4]triazolo[1,5-a]pyrimidine
Cytotoxicity
LSD1 inactivation
Migration inhibition
Docking studies
Design, synthesis, and biological evaluation of crenatoside analogues as novel influenza neuraminidase inhibitors
期刊论文
European Journal of Medicinal Chemistry, 2016, 卷号: 109, 页码: 199-205
作者:
Chen, Bao-Long
;
Wang, Ya-Jing
;
Guo, Hong
;
Zeng, Guang-Yao*
收藏
  |  
浏览/下载:4/0
  |  
提交时间:2019/12/03
Design
Synthesis
Neuraminidases inhibitors
Crenatoside derivatives
Influenza virus
Shape controlled synthesis and optical properties of Cu2O micro-spheres and octahedrons
期刊论文
Materials and Design, 2016, 卷号: 92, 期号: Volume 92, 页码: 261-267
作者:
Ouyang, Jing*
;
Yang, Huaming*
;
Tang, Aidong
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  |  
浏览/下载:7/0
  |  
提交时间:2019/12/03
Cuprous oxides
Chemical synthesis
Lyophilizing
Optical properties
Characterization and application of porous Ti3SiC2 ceramic prepared through reactive synthesis
期刊论文
Materials and Design, 2015, 卷号: 79, 页码: 94-98
作者:
Liu, Xinli
;
Zhang, Huibin
;
Jiang, Yao*
;
He, Yuehui
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  |  
浏览/下载:1/0
  |  
提交时间:2019/12/03
Ti3SiC2
Porous
Reactive synthesis
Corrosion
Filter
Macrocyclic compounds as anti-cancer agents: Design and synthesis of multi-acting inhibitors against HDAC, FLT3 and JAK2
期刊论文
European Journal of Medicinal Chemistry, 2015, 卷号: 95, 页码: 104-115
作者:
Ning, Cheng-Qing
;
Lu, Cheng
;
Hu, Liang
;
Bi, Yan-Jing
;
Yao, Lei
收藏
  |  
浏览/下载:2/0
  |  
提交时间:2019/12/03
Histone deacetylase
FLT3
JAK2
Macrocyclic
Multi-target inhibitor
The stability of hydrogen evolution activity and corrosion behavior of porous Ni3Al-Mo electrode in alkaline solution during long-term electrolysis
期刊论文
Energy, 2014, 卷号: 67, 页码: 19-26
作者:
Wu, Liang
;
He, Yuehui*
;
Lei, Ting
;
Nan, Bo
;
Xu, Nanping
收藏
  |  
浏览/下载:4/0
  |  
提交时间:2019/12/03
Hydrogen evolution reaction
Porous Ni3Al-Mo electrodes
Reactive synthesis
Corrosion resistance
Stability
Design, synthesis and biological evaluation of indeno[1,2-d]thiazole derivatives as potent histone deacetylase inhibitors
期刊论文
Bioorganic and Medicinal Chemistry Letters, 2013, 卷号: 23, 期号: 11, 页码: 3200-3203
作者:
Zhou, Ming
;
Ning, Chengqing
;
Liu, Ruihuan
;
He, Yujun
;
Yu, Niefang*
收藏
  |  
浏览/下载:4/0
  |  
提交时间:2019/12/03
HDAC
Histone deacetylases
Hydroxamic acids
Indeno[1,2-d]thiazole
Tricyclic
Design, synthesis and biological evaluation of di-substituted cinnamic hydroxamic acids bearing urea/thiourea unit as potent histone deacetylase inhibitors
期刊论文
Bioorganic and Medicinal Chemistry Letters, 2013, 卷号: 23, 期号: 23, 页码: 6432-6435
作者:
Ning, Chengqing
;
Bi, Yanjing
;
He, Yujun
;
Huang, WenYuan
;
Liu, Lifei
收藏
  |  
浏览/下载:7/0
  |  
提交时间:2019/12/03
Histone deacetylase
HDAC
Urea
Thiourea
Cinnamic hydroxamaic acid
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