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 [7]
近代物理研究所 [1]
采集方式
OAI收割 [8]
内容类型
期刊论文 [8]
发表日期
2024 [1]
2023 [2]
2022 [1]
2021 [1]
2019 [1]
2016 [1]
更多
学科主题
筛选
浏览/检索结果:
共8条,第1-8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
提交时间升序
提交时间降序
作者升序
作者降序
发表日期升序
发表日期降序
Discovery of Preclinical Candidate AD1058 as a Highly Potent, Selective, and Brain-Penetrant ATR Inhibitor for the Treatment of Advanced Malignancies
期刊论文
OAI收割
JOURNAL OF MEDICINAL CHEMISTRY, 2024, 卷号: 67, 期号: 15, 页码: 12735-12759
作者:
Liu, Zhi
;
Jiang, Kailong
;
Liu, Yan
;
Li, Junfei
;
Huang, Siqi
  |  
收藏
  |  
浏览/下载:23/0
  |  
提交时间:2024/09/26
Discovery of JN122, a Spiroindoline-Containing Molecule that Inhibits MDM2/p53 Protein-Protein Interaction and Exerts Robust In Vivo Antitumor Efficacy
期刊论文
OAI收割
JOURNAL OF MEDICINAL CHEMISTRY, 2023, 卷号: 66, 期号: 24, 页码: 16991-17025
作者:
Cheng, Jing
;
Yan, Ziqin
;
Jiang, Kailong
;
Liu, Chen
;
Xu, Dehua
  |  
收藏
  |  
浏览/下载:23/0
  |  
提交时间:2024/02/19
Discovery of toxoflavin,a potent IRE1α inhibitor acting through structure-dependent oxidative inhibition
期刊论文
OAI收割
ACTA PHARMACOLOGICA SINICA, 2023, 卷号: 44, 期号: 1, 页码: 234
作者:
Liu Changmei
;
Nie Litong
;
Jiang Haini
;
Xu Lei
;
Zhang Kunzhi
  |  
收藏
  |  
浏览/下载:27/0
  |  
提交时间:2023/05/22
endoplasmic reticulum stress
toxoflavin
reactive oxygen species
IRE1α
XBP1
Dual inhibition of CHK1/FLT3 enhances cytotoxicity and overcomes adaptive and acquired resistance in FLT3-ITD acute myeloid leukemia
期刊论文
OAI收割
LEUKEMIA, 2022, 页码: 11
作者:
Jiang, Kailong
;
Li, Xuemei
;
Wang, Chang
;
Hu, Xiaobei
;
Wang, Peipei
  |  
收藏
  |  
浏览/下载:29/0
  |  
提交时间:2023/04/10
Design, Synthesis, and Biological Evaluation of Orally Bioavailable CHK1 Inhibitors Active against Acute Myeloid Leukemia
期刊论文
OAI收割
CHEMMEDCHEM, 2021, 页码: 12
作者:
Jin, Tingting
;
Wang, Peipei
;
Long, Xiubing
;
Jiang, Kailong
;
Song, Pinrao
  |  
收藏
  |  
浏览/下载:134/0
  |  
提交时间:2021/05/24
CHK1 inhibitor
diaminopyrimidine
DNA damage response
oral bioavailability
Discovery of (R)-5-((5-(1-methyl-1H-pyrazol-4-yl)-4-(methylamino) pyrimidin-2-yl)amino)-3-(piperidin-3-yloxy)picolinonitrile, a novel CHK1 inhibitor for hematologic malignancies
期刊论文
OAI收割
EUROPEAN JOURNAL OF MEDICINAL CHEMISTRY, 2019, 卷号: 173, 页码: 44-62
作者:
Tong, Lexian
;
Song, Pinrao
;
Jiang, Kailong
;
Xu, Lei
;
Jin, Tingting
  |  
收藏
  |  
浏览/下载:28/0
  |  
提交时间:2020/07/01
CHK1 kinase inhibitor
Selectivity
Monotherapy
Hematologic malignancies
Alpha Decay of the Neutron-deficient Isotopes 215,216U
期刊论文
OAI收割
原子核物理评论, 2016, 页码: 217-220
作者:
Zhang Zhiyuan
;
Gan Zaiguo
;
Ma Long
;
Yang Huabin
;
Wang Jianguo
  |  
收藏
  |  
浏览/下载:20/0
  |  
提交时间:2021/12/13
Disruption of the unfolded protein response (UPR) by lead compound selectively suppresses cancer cell growth
期刊论文
OAI收割
CANCER LETTERS, 2015, 卷号: 360, 期号: 2, 页码: 257-268
作者:
Huang, Hejing
;
Liu, Huanan
;
Liu, Changmei
;
Fan, Lixia
;
Zhang, Xinwen
  |  
收藏
  |  
浏览/下载:41/0
  |  
提交时间:2019/01/08
Selective cancer therapy
Unfolded protein response
2DG
UPR disrupter