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科研机构
上海药物研究所 [8]
山东大学 [1]
上海生物化学与细胞生... [1]
内容类型
期刊论文 [10]
发表日期
2018 [4]
2017 [3]
2014 [1]
2012 [2]
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Rafoxanide, an organohalogen drug, triggers apoptosis and cell cycle arrest in multiple myeloma by enhancing DNA damage responses and suppressing the p38 MAPK pathway
期刊论文
Cancer letters, 2018, 卷号: 444, 页码: 45-59
作者:
Xiao, Wenqin
;
Xu, Zhijian
;
Chang, Shuaikang
;
Li, Bo
;
Yu, Dandan
收藏
  |  
浏览/下载:98/0
  |  
提交时间:2019/01/08
Identification of recurrent USP48 and BRAF mutations in Cushing's disease
期刊论文
NATURE COMMUNICATIONS, 2018, 卷号: 9
作者:
Chen, Jianhua
;
Jian, Xuemin
;
Deng, Siyu
;
Ma, Zengyi
;
Shou, Xuefei
收藏
  |  
浏览/下载:117/0
  |  
提交时间:2019/01/08
Identification of recurrent USP48 and BRAF mutations in Cushing's disease
期刊论文
NATURE COMMUNICATIONS, 2018, 卷号: 9, 期号: 1, 页码: 3171
作者:
Chen, Jianhua
;
Jian, Xuemin
;
Song, Zhijian
;
Li, Zhiqiang
;
Zhou, Juan
收藏
  |  
浏览/下载:75/0
  |  
提交时间:2019/04/28
Human Cancer
Proopiomelanocortin Gene
Deubiquitinating Enzyme
Pituitary-adenomas
Kappa-b
Transcription
Activation
Raf
Pathways
Genome
Design and discovery of thioether and nicotinamide containing sorafenib analogues as multikinase inhibitors targeting B-Raf, B-Raf(V600E) and VEGFR-2
期刊论文
BIOORGANIC & MEDICINAL CHEMISTRY, 2018, 卷号: 26, 期号: 9, 页码: 2381-2391
作者:
Sun, Shaofeng
;
He, Zuopeng
;
Huang, Mindong
;
Wang, Ningning
;
He, Zongzhong
收藏
  |  
浏览/下载:4/0
  |  
提交时间:2019/12/11
Nicotinamide
B-Raf
VEGFR-2
Kinase inhibitor
Antitumor
AKT is critically involved in the antagonism of BRAF inhibitor sorafenib against dabrafenib in colorectal cancer cells harboring both wild-type and mutant (V600E) BRAF genes
期刊论文
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 2017, 卷号: 489, 期号: 1, 页码: 14-20
作者:
Wang, Hongbin
;
Quan, Haitian
;
Lou, Liguang
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  |  
浏览/下载:24/0
  |  
提交时间:2019/01/08
Antagonism
AKT
BRAF
Dabrafenib
Sorafenib
Docking-based structural splicing and reassembly strategy to develop novel deazapurine derivatives as potent B-Raf(V600E) inhibitors
期刊论文
ACTA PHARMACOLOGICA SINICA, 2017, 卷号: 38, 期号: 7, 页码: 1059-1068
作者:
Wang, Gui-min
;
Wang, Xiang
;
Zhu, Jian-ming
;
Guo, Bin-bin
;
Yang, Zhuo
收藏
  |  
浏览/下载:17/0
  |  
提交时间:2019/01/08
B-Raf(V600E) inhibitor
anticancer
vemurafenib
deazapurine
fragment reassembly
molecular docking
structure-activity relationship
Docking-based structural splicing and reassembly strategy to develop novel deazapurine derivatives as potent B-Raf~(V600E) inhibitors
期刊论文
Acta Pharmacologica Sinica, 2017, 卷号: 38, 期号: 7, 页码: 1057-1068
作者:
Wang Guimin
;
Wang Xiang
;
Zhu Jianming
;
Guo Binbin
;
Yang Zhuo
收藏
  |  
浏览/下载:24/0
  |  
提交时间:2019/01/08
B-Raf~(V600E) inhibitor
anticancer
vemurafenib
deazapurine
fragment reassembly
molecular docking
structure-activity relationship
The B-Raf(V600E) inhibitor dabrafenib selectively inhibits RIP3 and alleviates acetaminophen-induced liver injury
期刊论文
CELL DEATH & DISEASE, 2014, 卷号: 5
作者:
Li, J-X
;
Feng, J-M
;
Wang, Y.
;
Li, X-H
;
Chen, X-X
收藏
  |  
浏览/下载:21/0
  |  
提交时间:2019/01/08
Combining pharmacophore, docking and substructure search approaches to identify and optimize novel B-Raf(V600E) inhibitors
期刊论文
BIOORGANIC & MEDICINAL CHEMISTRY LETTERS, 2012, 卷号: 22, 期号: 17, 页码: 5428-5437
作者:
Xu, Zhijian
;
Yan, Guirui
;
Wang, Gaihong
;
Li, Bo
;
Zhu, Jianming
收藏
  |  
浏览/下载:11/0
  |  
提交时间:2019/01/08
B-Raf(V600E) inhibitors
Pharmacophore
Docking
Substructure search
Development of a novel class of B-Raf(V600E)-selective inhibitors through virtual screening and hierarchical hit optimization
期刊论文
ORGANIC & BIOMOLECULAR CHEMISTRY, 2012, 卷号: 10, 期号: 36, 页码: 7402-7417
作者:
Kong, Xiangqian
;
Qin, Jie
;
Li, Zeng
;
Vultur, Adina
;
Tong, Linjiang
收藏
  |  
浏览/下载:17/0
  |  
提交时间:2019/01/08
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