Synthesis and antibacterial activity of four natural chalcones and their derivatives

被引:17
|
作者
Li, Yuanyuan [1 ]
Sun, Bingxia [1 ]
Zhai, Jiadai [2 ]
Fu, Lin [1 ]
Zhang, Shuxin [1 ]
Zhang, Jing [1 ]
Liu, Hongliang [1 ]
Xie, Wenhai [1 ]
Deng, Hongkuan [1 ]
Chen, Zhiwei [3 ]
Sang, Feng [1 ]
机构
[1] Shandong Univ Technol, Sch Life Sci, Zibo 255049, Peoples R China
[2] Tianjin Univ, Sch Pharmaceut Sci & Technol, Tianjin 300072, Peoples R China
[3] Shandong Univ Technol, Inst Food & Nutr Sci, Zibo 255049, Peoples R China
基金
中国博士后科学基金; 中国国家自然科学基金;
关键词
Hydroxyisoprenyl group; Chalcone; Natural product; Antibacterial activity; DORSTENIA-ANGUSTICORNIS; BIOLOGICAL EVALUATION; CONSTITUENTS; FLAVONOIDS; POTENT; TWIGS;
D O I
10.1016/j.tetlet.2019.151165
中图分类号
O62 [有机化学];
学科分类号
070303 ; 081704 ;
摘要
Four natural chalcones bearing hydroxyisoprenyl or prenyl groups, named Paratocarpin E (2), Xanthoangelol D (3), Angusticornin A (4) and Kanzonol C (5), were prepared by employing the Claisen-Schmidt condensation as the key step. In an attempt to investigate the effect of the hydroxyisoprenyl group on biological activity, two of their derivatives were also prepared for antibacterial activity research. The synthesized compounds were investigated for their expected antibacterial activities against Gram positive bacteria (Bacillus subtilis, Staphylococcus aureus) as well as Gram negative bacteria (Escherichia coli, Pseudomonas aeruginosa). Paratocarpin E (2) was found to be the most potent against two Gram positive bacteria while the majority of the remaining compounds showed promising activity as well. However, all of the compounds were inactive against both Gram-negative bacteria. (C) 2019 Elsevier Ltd. All rights reserved.
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页数:3
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