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	Design and synthesis of furyl/thineyl pyrroloquinolones based on natural alkaloid perlolyrine, lead to the discovery of potent and selective PDE5 inhibitors
	Zheng, Hongbo; Li, Lin; Sun, Bin; Gao, Yun; Song, Wei; Zhao, Xiaoyu; Gao, Yanhui; Xie, Zhiyu; Zhang, Nianzhao; Ji, Jianbo
刊名	EUROPEAN JOURNAL OF MEDICINAL CHEMISTRY
	2018
卷号	150页码:30-38
关键词	PDE5 inhibitors Pyrroloquinolones Bioavailability Male erectile dysfunction (MED)
DOI	10.1016/j.ejmech.2018.02.039
URL标识	查看原文
公开日期	[db:dc_date_available]
内容类型	期刊论文
URI标识	http://www.corc.org.cn/handle/1471x/4580010
专题	山东大学
作者单位	Shandong U
推荐引用方式 GB/T 7714	Zheng, Hongbo,Li, Lin,Sun, Bin,et al. Design and synthesis of furyl/thineyl pyrroloquinolones based on natural alkaloid perlolyrine, lead to the discovery of potent and selective PDE5 inhibitors[J]. EUROPEAN JOURNAL OF MEDICINAL CHEMISTRY,2018,150:30-38.
APA	Zheng, Hongbo.,Li, Lin.,Sun, Bin.,Gao, Yun.,Song, Wei.,...&Yuan, H 更多.(2018).Design and synthesis of furyl/thineyl pyrroloquinolones based on natural alkaloid perlolyrine, lead to the discovery of potent and selective PDE5 inhibitors.EUROPEAN JOURNAL OF MEDICINAL CHEMISTRY,150,30-38.
MLA	Zheng, Hongbo,et al."Design and synthesis of furyl/thineyl pyrroloquinolones based on natural alkaloid perlolyrine, lead to the discovery of potent and selective PDE5 inhibitors".EUROPEAN JOURNAL OF MEDICINAL CHEMISTRY 150(2018):30-38.

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