中国科学院机构知识库网格
Chinese Academy of Sciences Institutional Repositories Grid
Discovery of Benzo[cd]indol-2(1H)-ones as Potent and Specific BET Bromodomain Inhibitors: Structure-Based Virtual Screening, Optimization, and Biological Evaluation

文献类型:期刊论文

作者Tu, Zhengchao; Zhou, Yulai; Ding, Ke; Xu, Yong; Xue, Xiaoqian; Zhang, Yan; Liu, Zhaoxuan; Song, Ming; Xing, Yanli; Xiang, Qiuping
刊名JOURNAL OF MEDICINAL CHEMISTRY
出版日期2016
卷号59期号:4页码:1565-1579
ISSN号0022-2623
学科主题Pharmacology & Pharmacy
语种英语
源URL[http://ir.foo.ac.cn/handle/2SETSVCV/10]  
专题中国科学院广州生物医药与健康研究院
推荐引用方式
GB/T 7714
Tu, Zhengchao,Zhou, Yulai,Ding, Ke,et al. Discovery of Benzo[cd]indol-2(1H)-ones as Potent and Specific BET Bromodomain Inhibitors: Structure-Based Virtual Screening, Optimization, and Biological Evaluation[J]. JOURNAL OF MEDICINAL CHEMISTRY,2016,59(4):1565-1579.
APA Tu, Zhengchao.,Zhou, Yulai.,Ding, Ke.,Xu, Yong.,Xue, Xiaoqian.,...&Wang, Zhen.(2016).Discovery of Benzo[cd]indol-2(1H)-ones as Potent and Specific BET Bromodomain Inhibitors: Structure-Based Virtual Screening, Optimization, and Biological Evaluation.JOURNAL OF MEDICINAL CHEMISTRY,59(4),1565-1579.
MLA Tu, Zhengchao,et al."Discovery of Benzo[cd]indol-2(1H)-ones as Potent and Specific BET Bromodomain Inhibitors: Structure-Based Virtual Screening, Optimization, and Biological Evaluation".JOURNAL OF MEDICINAL CHEMISTRY 59.4(2016):1565-1579.

入库方式: OAI收割

来源:广州生物医药与健康研究院

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