化学
苯并噻唑
稻黄单胞菌
亚砜
体外
柠檬黄单胞菌
体内
抗菌活性
最小抑制浓度
组合化学
立体化学
有机化学
生物化学
细菌
生物
生物技术
基因
遗传学
作者
Jianhong Zhang,Chunle Wei,Shaoyuan Li,Deyu Hu,Baoan Song
标识
DOI:10.1016/j.pestbp.2020.104605
摘要
On the basis of the active substructure combination principle, 24 novel synthesis of novel bis-sulfoxide derivatives bearing acylhydrazone and benzothiazole moieties as potential antibacterial agents were designed and synthesized. The bioactivity assay results showed that many compounds had significant in vitro inhibitory effects against Xanthomonas oryzae pv. oryzae (Xoo) and Xanthomonas citri pv. citri (Xac). Notably, compound 4b had the best in vitro antibacterial activity against Xoo at an half-maximal effective concentration value of 11.4 μg/mL, which was superior to those of thiodiazole copper (TDC) and bismerthiazol (BMT). Compared with TDC and BMT, compound 4b was more effective in vivo controlling rice bacterial leaf blight with curative and protection activities of 42.5% and 40.3%, respectively. In addition, compound 4b can influence biofilm formation, inhibit extracellular polysaccharide production, and ultimately reduce the pathogenicity of Xoo. All the results indicated that bis-sulfoxide derivatives bearing acylhydrazone and benzothiazole moieties can be used for the development of small-molecule pesticides with high antibacterial activity.
科研通智能强力驱动
Strongly Powered by AbleSci AI