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 [9]
昆明动物研究所 [2]
大连化学物理研究所 [1]
海洋研究所 [1]
生态环境研究中心 [1]
天津工业生物技术研究... [1]
更多
采集方式
OAI收割 [15]
内容类型
期刊论文 [15]
发表日期
2024 [1]
2018 [1]
2017 [1]
2016 [2]
2014 [3]
2011 [1]
更多
学科主题
筛选
浏览/检索结果:
共15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
题名升序
题名降序
发表日期升序
发表日期降序
提交时间升序
提交时间降序
作者升序
作者降序
Discovery of the potent covalent inhibitor with an acrylate warhead for SARS-CoV-2 3CL protease
期刊论文
OAI收割
BIOORGANIC & MEDICINAL CHEMISTRY LETTERS, 2024, 卷号: 112, 页码: 5
作者:
Shen, Wen
;
Chen, Xinyao
;
Zhou, Liping
;
Cheng, Yan
;
Zhang, Yan
  |  
收藏
  |  
浏览/下载:30/0
  |  
提交时间:2024/10/21
COVID-19
SARS-CoV-2 3CL pro inhibitor
Drug design
Antiviral activities
Design and synthesis of selenazole-substituted ritonavir analogs
期刊论文
OAI收割
BIOORGANIC & MEDICINAL CHEMISTRY LETTERS, 2018, 卷号: 28, 期号: 14, 页码: 2379-2381
作者:
Liu, Jun
;
Zhao, Chuanfang
;
Qiao, Junfei
;
Du, Yuguo
  |  
收藏
  |  
浏览/下载:36/0
  |  
提交时间:2019/06/20
Selenazole
Ritonavir
Antiviral
Protease inhibitor
One-pot reaction
The Second-generation of Highly Potent Hepatitis C Virus (HCV) NS3/4A Protease Inhibitors: Evolutionary Design Based on Tailor-made Amino Acids, Synthesis and Major Features of Bio-activity
期刊论文
OAI收割
CURRENT PHARMACEUTICAL DESIGN, 2017, 卷号: 23, 期号: 30, 页码: 4493-4554
作者:
Wang, Shuni
;
Wang, Yibing
;
Wang, Jiang
;
Sato, Tatsunori
;
Izawa, Kunisuke
  |  
收藏
  |  
浏览/下载:55/0
  |  
提交时间:2019/01/08
Hepatitis C virus (HCV)
pandemic
direct-acting antiviral agents (DAAs)
NS3/4A protease inhibitor
tailor-made amino acids
structure-activity relationship (SAR)
asymmetric synthesis
ring-closing metathesis (RCM)
Multivalent S-sialoside protein conjugates block influenza hemagglutinin and neuraminidase
期刊论文
OAI收割
CARBOHYDRATE RESEARCH, 2016, 卷号: 435, 页码: 68-75
作者:
Yang, Yang
;
Liu, Hai-Peng
;
Yu, Qun
;
Yang, Mei-Bing
;
Wang, De-Min
收藏
  |  
浏览/下载:50/0
  |  
提交时间:2017/03/13
Multivalent effect
Glycoprotein
Click chemistry
Antiviral inhibitor
Structure-based optimization and derivatization of 2-substituted quinolone-based non-nucleoside HCV NS5B inhibitors with submicromolar cellular replicon potency
期刊论文
OAI收割
BIOORGANIC & MEDICINAL CHEMISTRY LETTERS, 2016, 卷号: 26, 期号: 12, 页码: 2900-2906
作者:
Cheng, Yu
;
Shen, Jian
;
Peng, Run-Ze
;
Wang, Gui-Feng
;
Zuo, Jian-Ping
  |  
收藏
  |  
浏览/下载:39/0
  |  
提交时间:2019/01/08
HCV NS5B polymerase
2-Alkyl quinolone
1,6-Naphthyridine-4,5-dione
Non-nucleoside inhibitor
Direct acting antiviral
Allosteric site
2-Aryl-3-carbonylquinolones: Design, Synthesis and Biological Evaluation of Novel HCV NS5B Polymerase Inhibitors
期刊论文
OAI收割
ACTA CHIMICA SINICA, 2014, 卷号: 72, 期号: 8, 页码: 906-913
作者:
Wang Shenfeng
;
Lin Jianping
;
He Peilan
;
Zuo Jianping
;
Long Yaqiu
  |  
收藏
  |  
浏览/下载:20/0
  |  
提交时间:2019/01/08
HCV NS5B polymerase
2-substituted quinolone-3-carboxylic acid
non-nucleoside inhibitor
direct acting antiviral
allosteric site
The Enterovirus Protease Inhibitor Rupintrivir Exerts Cross-Genotypic Anti-Norovirus Activity and Clears Cells from the Norovirus Replicon
期刊论文
OAI收割
ANTIMICROBIAL AGENTS AND CHEMOTHERAPY, 2014, 卷号: 58, 期号: 8, 页码: 4675-4681
Rocha-Pereira, J.
;
Nascimento, M. S. J.
;
Ma, Qingjun
;
Hilgenfeld, R.
;
Neyts, J.
;
Jochmans, D.
收藏
  |  
浏览/下载:38/0
  |  
提交时间:2014/09/08
RHINOVIRUS 3C PROTEASE
IN-VITRO
NORWALK VIRUS
SUBSTRATE-SPECIFICITY
ANTIVIRAL ACTIVITY
POTENT INHIBITOR
GASTROENTERITIS
MODEL
REPLICATION
2'-C-METHYLCYTIDINE
2芳基3羰基喹诺酮新型hcvns5b多聚酶抑制剂的设计合成和活性评估
期刊论文
OAI收割
化学学报, 2014, 卷号: 72, 期号: 8, 页码: 906
作者:
王沈丰
;
林建平
;
何佩岚
;
左建平
;
龙亚秋
  |  
收藏
  |  
浏览/下载:20/0
  |  
提交时间:2020/07/01
HEPATITIS-C VIRUS
HIV-1 INTEGRASE INHIBITORS
INFECTION
NUCLEOTIDE
SCAFFOLD
SOFOSBUVIR
DISCOVERY
LEDGF/P75
ACIDS
HCV NS5B polymerase
2-substituted quinolone-3-carboxylic acid
non-nucleoside inhibitor
direct acting antiviral
allosteric site
Peptide aldehyde inhibitors challenge the substrate specificity of the SARS-coronavirus main protease
期刊论文
OAI收割
ANTIVIRAL RESEARCH, 2011, 卷号: 92, 期号: 2, 页码: 204-212
作者:
Zhu, Lili
;
George, Shyla
;
Schmidt, Marco F.
;
Al-Gharabli, Samer I.
;
Rademann, Joerg
  |  
收藏
  |  
浏览/下载:33/0
  |  
提交时间:2019/01/08
Aldehyde inhibitor
Antiviral drug design
Cysteine protease
Methionine-aspartic acid interaction
X-ray crystallography
Efficient synthesis and utilization of phenyl-substituted heteroaromatic carboxylic acids as aryl diketo acid isosteres in the design of novel HIV-1 integrase inhibitors
期刊论文
OAI收割
BIOORGANIC & MEDICINAL CHEMISTRY LETTERS, 2008, 卷号: 18, 期号: 16, 页码: 4521-4524
作者:
Zeng, Li-Fan
;
Zhang, Hu-Shan
;
Wang, Yun-Hua
;
Sanchez, Tino
;
Zheng, Yong-Tang
  |  
收藏
  |  
浏览/下载:18/0
  |  
提交时间:2019/01/08
HIV-1 integrase inhibitor
bioisostere
heteroaromatic carboxylic acid
isoxazole
isothiazole
1H-pyrazole
bioavailability
antiviral effect