Synthesis and antimicrobial evaluation of pogostone and its analogues

被引:37
作者
Yi, Yu-Yang [1 ]
He, Jing-Jin [1 ]
Su, Jun-Quan [2 ]
Kong, Song-Zhi [1 ]
Su, Ji-Yan [1 ]
Li, Yu-Cui [1 ]
Huang, Si-Han [1 ]
Li, Chu-Wen [1 ]
Lai, Xiao-Ping [1 ,3 ]
Su, Zi-Ren [1 ,3 ]
机构
[1] Guangzhou Univ Chinese Med, Coll Chinese Med, Guangzhou, Guangdong, Peoples R China
[2] Shenzhen China Resource Gosun Pharmaceut Co Ltd, Shenzhen, Peoples R China
[3] Guangzhou Univ Chinese Med, Dongguan Math Engn Acad Chinese Med, Dongguan, Peoples R China
基金
中国国家自然科学基金;
关键词
Pogostone; Analogues; Synthesis; Antimicrobial activity; POGOSTEMON-CABLIN; ANTIFUNGAL AGENTS; CANDIDA-ALBICANS; MECHANISMS; OIL;
D O I
10.1016/j.fitote.2012.11.005
中图分类号
R914 [药物化学];
学科分类号
100701 ;
摘要
Pogostone (PO) is one of the secondary metabolites from Pogostemon cablin (Blanco) Benth. (Lamiaceae), serving as the effective component of the antimicrobial activity. In this study, PO and a series of its analogues were synthesized by the reaction of dehydroacetate and aldehydes in tetrahydrofuran under a nitrogen atmosphere. Their activities against Candida albicans, Gram positive bacteria and Gram negative bacteria were evaluated. The antifungal results demonstrated that PO (MIC ranged from 12 to 97 mu g/mL against all strains, MFC ranged from 49 to 97 mu g/mL against all strains) and A3 (MIC ranged from 12 to 49, MFC over 195 mu g/mL) showed a strong activity against Candida albicans. While A1 (MIC ranged from 49 to 97 mu g/mL) and A2 (MIC ranged from 24 to 49 mu g/mL) have only shown effect against Guangzhou clinical isolates, the antibacterial results demonstrated that PO and its analogues showed no effects against the tested bacteria strains. This study suggests that pogostone analogues, with the appropriated structure modification, represented a kind of promising antifungal agents. (c) 2012 Elsevier B.V. All rights reserved.
引用
收藏
页码:135 / 139
页数:5
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