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	Fragment-Based Design, Synthesis, and Biological Evaluation of 1-Substituted-indole-2-carboxylic Acids as Selective Mcl-1 Inhibitors
	Wang, Ziqian; Xu, Wenjie; Song, Ting; Guo, Zongwei; Liu, Lu; Fan, Yudan; Wang, Anhui; Zhang, Zhichao
刊名	ARCHIV DER PHARMAZIE
	2017
卷号	350页码:-
关键词	Fragment-based drug design Ligand efficiency Mcl-1 inhibitor p1 pocket Selective
ISSN号	0365-6233
URL标识	查看原文
WOS记录号	[DB:DC_IDENTIFIER_WOSID]
内容类型	期刊论文
URI标识	http://www.corc.org.cn/handle/1471x/3281260
专题	大连理工大学
作者单位	1.Dalian Univ Technol, Sch Chem, State Key Lab Fine Chem, Dalian 116012, Peoples R China. 2.Dalian Univ Technol, Sch Life Sci & Technol, Dalian, Peoples R China.
推荐引用方式 GB/T 7714	Wang, Ziqian,Xu, Wenjie,Song, Ting,et al. Fragment-Based Design, Synthesis, and Biological Evaluation of 1-Substituted-indole-2-carboxylic Acids as Selective Mcl-1 Inhibitors[J]. ARCHIV DER PHARMAZIE,2017,350:-.
APA	Wang, Ziqian.,Xu, Wenjie.,Song, Ting.,Guo, Zongwei.,Liu, Lu.,...&Zhang, Zhichao.(2017).Fragment-Based Design, Synthesis, and Biological Evaluation of 1-Substituted-indole-2-carboxylic Acids as Selective Mcl-1 Inhibitors.ARCHIV DER PHARMAZIE,350,-.
MLA	Wang, Ziqian,et al."Fragment-Based Design, Synthesis, and Biological Evaluation of 1-Substituted-indole-2-carboxylic Acids as Selective Mcl-1 Inhibitors".ARCHIV DER PHARMAZIE 350(2017):-.

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