New Biscoumarin Derivatives: Synthesis, Crystal Structure, Theoretical Study and Antibacterial Activity against Staphylococcus aureus

被引:19
作者
Qu, Di [1 ]
Li, Jing [2 ]
Yang, Xiao-Hui [2 ]
Zhang, Zi-Dan [3 ]
Luo, Xiao-Xing [1 ]
Li, Ming-Kai [1 ]
Li, Xia [4 ]
机构
[1] Fourth Mil Med Univ, Sch Pharm, Dept Pharmacol, Xian 710032, Peoples R China
[2] Xian Univ, Sch Chem & Chem Engn, Xian 710065, Peoples R China
[3] Tianjin Univ, Sch Sci, Dept Phys, Tianjin 300072, Peoples R China
[4] Fourth Mil Med Univ, Xijing Hosp, Dept Neurosurg, Xian 710032, Peoples R China
关键词
biscoumarin; Staphylococcus aureus; minimum inhibitory concentration; 4-HYDROXYCOUMARIN; RESISTANCE;
D O I
10.3390/molecules191219868
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Five novel biscoumarins 1-5 were synthesized and characterized. In these compounds, two classical asymmetrical intramolecular O-H center dot center dot center dot O hydrogen bonds were used to stabilize the whole structures and the HB energies were performed with the density functional theory (DFT) [B3LYP/6-31G*] method. The five compounds were evaluated for their in vitro antibacterial activities against Staphylococcus aureus (S. aureus ATCC 29213), methicillin-resistant S. aureus (MRSA XJ 75302), vancomycin-intermediate S. aureus (Mu50 ATCC 700699), and USA 300 (Los Angeles County clone, LAC) by the means of minimum inhibitory concentration and time-kill curves.
引用
收藏
页码:19868 / 19879
页数:12
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