机构地区:[1]Department of Chemistry, COMSATS Institute of Information Technology, Abbottabad-22060, Pakistan [2]Dr. Panjwani Center for Molecular Medicine and Drug Research, International Center for Chemical and Biological Sciences, University of Karachi- 752 70, Pakistan [3]Department of Geology, University of Swabi Anbar-23430, KPK, Pakistan [4]Institute of Chemical Sciences, University of Peshawar, Peshawar 25120, Pakistan [5]Department of Pharmaceutical Chemistry, Faculty of Pharmacy, Federal Urdu University of Arts, Science and Technology, Karachi, Karachi 75300, Pakistan [6]Department of Environmental Sciences, COMSATS Institute of lnformation Technology, Abbottabad-22060, Pakistan
出 处:《Chinese Journal of Natural Medicines》2017年第12期944-949,共6页中国天然药物(英文版)
基 金:supported by Higher Education Commission(HEC)of Pakistan for financial support under NRPU programme(No.20-2003/NRPU);COMSATS Abbottabad for financial support
摘 要:Three new alkyl substituted anthraquinone derivatives, trivially named as symploquinones A-C(Compounds 1-3) were isolated from Symplocos racemosa. The structures of these compounds were determined on the basis of extensive spectroscopic analyses(UV, IR, Mass, ~1 H-and ^(13)C-NMR, and two-dimensional(2D) NMR techniques). The resulting data were also compared with the reported literature. These compounds were then subjected to antibacterial or antibiofilm testing. Compounds 1 and 3 exhibited good antibacterial activity in the concentration range of 160-83 μg·m L^(-1) against Streptococcus mutans, methicillin resistant Staphylococcus aureus and Proteus mirabilis. Both compounds were further screened for anti-biofilm activity, which revealed promising activities at sub-MIC concentrations. None of the compounds were found to be active against Klebsiella pneumoniae.Three new alkyl substituted anthraquinone derivatives, trivially named as symploquinones A-C(Compounds 1-3) were isolated from Symplocos racemosa. The structures of these compounds were determined on the basis of extensive spectroscopic analyses(UV, IR, Mass, ^1 H-and ^13C-NMR, and two-dimensional(2D) NMR techniques). The resulting data were also compared with the reported literature. These compounds were then subjected to antibacterial or antibiofilm testing. Compounds 1 and 3 exhibited good antibacterial activity in the concentration range of 160-83 μg·mL^-1 against Streptococcus mutans, methicillin resistant Staphylococcus aureus and Proteus mirabilis. Both compounds were further screened for anti-biofilm activity, which revealed promising activities at sub-MIC concentrations. None of the compounds were found to be active against Klebsiella pneumoniae.
关 键 词:SYMPLOCOS racemosa SUBSTITUTED ANTHRAQUINONE ANTIBIOFILM activity
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