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 [22]
近代物理研究所 [8]
昆明植物研究所 [6]
上海生物化学与细胞生... [2]
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OAI收割 [44]
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期刊论文 [39]
会议论文 [4]
学位论文 [1]
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2023 [3]
2022 [3]
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Oncology [5]
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Discovery of 5-trifluoromethyl-2-aminopyrimidine derivatives as potent dual inhibitors of FLT3 and CHK1
期刊论文
OAI收割
RSC MEDICINAL CHEMISTRY, 2023, 页码: 14
作者:
Deng, Minjie
;
Gao, Yue
;
Wang, Peipei
;
Du, Wenjing
;
Xu, Gaoya
  |  
收藏
  |  
浏览/下载:7/0
  |  
提交时间:2024/02/19
Discovery of 2-Aminopyrimidine Derivatives as Potent Dual FLT3/CHK1 Inhibitors with Significantly Reduced hERG Inhibitory Activities
期刊论文
OAI收割
JOURNAL OF MEDICINAL CHEMISTRY, 2023, 页码: 23
作者:
Li, Xuemei
;
Wang, Peipei
;
Wang, Chang
;
Jin, Tingting
;
Xu, Ran
  |  
收藏
  |  
浏览/下载:14/0
  |  
提交时间:2023/10/17
Design, Synthesis, and Biological Evaluation of 2-Aminothiazole Derivatives as Novel Checkpoint Kinase 1 (CHK1) Inhibitors
期刊论文
OAI收割
CHEMMEDCHEM, 2023, 页码: 19
作者:
Deng, Minjie
;
Wang, Peipei
;
Long, Xiubing
;
Xu, Gaoya
;
Wang, Chang
  |  
收藏
  |  
浏览/下载:13/0
  |  
提交时间:2023/04/10
2-aminothiazole
CHK1 inhibitors
antiproliferation
hematologic malignancies
biological activity
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:19/0
  |  
提交时间:2023/04/10
SOMCL-19-133, a novel, selective, and orally available inhibitor of NEDD8-activating enzyme (NAE) for cancer therapy
期刊论文
OAI收割
NEOPLASIA, 2022, 卷号: 32, 页码: 12
作者:
Zhou, Li-Na
;
Xiong, Chaodong
;
Cheng, Yong-Jun
;
Song, Shan-Shan
;
Bao, Xu-Bin
  |  
收藏
  |  
浏览/下载:14/0
  |  
提交时间:2023/04/10
SOMCL-19-133
NAE inhibitor
MLN4924
NEDD8
Oral administration
Repeated treatments of Capan-1 cells with PARP1 and Chk1 inhibitors promote drug resistance, migration and invasion
期刊论文
OAI收割
CANCER BIOLOGY & THERAPY, 2022, 页码: 14
作者:
Guo, Ne
;
Li, Meng-Zhu
;
Wang, Li-Min
;
Chen, Hua-Dong
;
Song, Shan-Shan
  |  
收藏
  |  
浏览/下载:27/0
  |  
提交时间:2022/06/15
Combination therapy
PARP1
resistance
CXCL3-ERK1/2 signaling
migration and invasion
Discovery and Development of a Potent, Selective, and Orally Bioavailable CHK1 Inhibitor Candidate: 5-((4-((3-Amino-3-methylbutyl)amino)-5-(trifluoromethyl)pyrimidin-2-yl)amino)picolinonitrile
期刊论文
OAI收割
JOURNAL OF MEDICINAL CHEMISTRY, 2021, 卷号: 64, 期号: 20, 页码: 15069-15090
作者:
Jin, Tingting
;
Xu, Lei
;
Wang, Peipei
;
Hu, Xiaobei
;
Zhang, Runyuan
  |  
收藏
  |  
浏览/下载:27/0
  |  
提交时间:2022/01/04
Comparable radiation sensitivity in p53 wild-type and p53 deficient tumor cells associated with different cell death modalities
期刊论文
OAI收割
CELL DEATH DISCOVERY, 2021, 卷号: 7, 期号: 1, 页码: 8
作者:
Li, Ping
;
Liu, Xiongxiong
;
Zhao, Ting
;
Li, Feifei
;
Wang, Qiqi
  |  
收藏
  |  
浏览/下载:40/0
  |  
提交时间:2021/12/09
Downregulation of c-Myc expression confers sensitivity to CHK1 inhibitors in hematologic malignancies
期刊论文
OAI收割
ACTA PHARMACOLOGICA SINICA, 2021, 页码: 9
作者:
  |  
收藏
  |  
浏览/下载:48/0
  |  
提交时间:2021/05/24
CHK1 inhibitors
PY34
drug sensitivity
c-Myc
hematologic malignancies
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
  |  
收藏
  |  
浏览/下载:125/0
  |  
提交时间:2021/05/24
CHK1 inhibitor
diaminopyrimidine
DNA damage response
oral bioavailability