化学
硫醚
多菌灵
百里香酚
乙酰胺
EC50型
立体化学
灰葡萄孢菌
最小抑制浓度
甲酰胺
核化学
体外
有机化学
抗菌剂
杀菌剂
生物化学
精油
植物
色谱法
生物
作者
Pei Li,Cong Chen,Rongxi Zhu,Guixia Yang,Min Xu,Guanghua Wan,Xiang Wang
标识
DOI:10.3389/fchem.2022.1036909
摘要
In this study, using the botanical active components of carvacrol, thymol, guaiacol, and sesamol as the lead structures, 19 novel botanical active component derivatives containing carboxamide and 1,3,4-thiadiazole thioether moieties ( 5a − 5s ) were synthesized and structurally characterized by 1 H NMR, 13 C NMR, and HRMS. The antibacterial bioassay results in vitro showed that compound 2-(2-methoxyphenoxy)-N-(5-(methylthio)-1,3,4-thiadiazol-2-yl)acetamide ( 5k ) revealed excellent inhibitory activities against Xanthomonas axonopodis pv. citri (Xac) and Xanthomonas oryzae pv. oryzicolaby (Xoc), with the median effective concentration (EC 50 ) values of 22 and 15 μg/ml, respectively, which were even better than those of thiodiazole copper and bismerthiazol. Meanwhile, all the target compounds revealed lower in vitro inhibitory effects on Mucor bainieri (M. bainieri), Mucor fragilis (M. fragilis), and Trichoderma atroviride (T. atroviride), than carbendazim.
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