Design, synthesis and anti-bacterial evaluation of novel 1,3,4-thiadiazole derivatives bearing a semicarbazone moiety

Jin-Lin Wan, Yiyuan Gan, Wei-nan Hu, Jiao Meng, Kun Tian, Xiao-qin Li, Shou-Qun Wu, Yang Xu, Gui-ping Ouyang, Zhenchao Wang
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引用次数: 4

Abstract

GRAPHICAL ABSTRACT ABSTRACT Novel 1,3,4-thiadiazole derivatives bearing a semicarbazone moiety were prepared and evaluated for their anti-bacterial activities against Xanthomonas oryzae pv. oryzae (Xoo) and Xanthomonas axonopodis pv. citri (Xac) by performing a turbidimetre test. The products were structurally characterised by IR, 1H NMR, 13C NMR, 19F NMR and HRMS. Anti-bacterial testing showed that most of the evaluated compounds (6a-6s) exhibited excellent activity (≥74.19%) against Xoo at a concentration of 200 µg/mL, with 50% effective concentration (EC50) values ranging from 12.21 to 67.20 µg/mL, which were superior to the commercial antibacterial agent bismerthiazol (92.23 µg/mL). Among them, compound 2-((2-chloro-1H-indol-3-yl)methylene)-N-(5-((2-chlorobenzyl)thio)-1,3,4-thiadiazol-2-yl)hydrazine-1-carboxamide (6b) demonstrated good inhibitory activity against Xac (89.46% at 200 µg/mL) and Xoo (EC50 = 18.28 µg/mL); compound 2-((2-chloro-1H-indol-3-yl)methylene)-N-(5-((4-methoxybenzyl)thio)-1,3,4-thiadiazol-2-yl)hydrazine-1-carboxamide (6g) displayed excellent activity against Xoo with EC50 value of 12.21 µg/mL.
新型含氨基脲类1,3,4-噻二唑衍生物的设计、合成及抗菌评价
摘要本文制备了含有缩氨基脲基团的新型1,3,4-噻二唑衍生物,并对其抑菌活性进行了评价。稻瘟病菌(Xoo)和轴尾黄单胞菌(Xanthomonas axonopodis pv)。柠檬酸(Xac)进行浊度计试验。通过IR、1H NMR、13C NMR、19F NMR和HRMS对产物进行了结构表征。抑菌试验结果表明,大部分化合物(6a-6s)在200µg/mL的浓度下对Xoo具有良好的抑菌活性(≥74.19%),50%有效浓度(EC50)在12.21 ~ 67.20µg/mL之间,优于市售抗菌剂双硫噻唑(92.23µg/mL)。其中,化合物2-((2-氯- 1h -吲哚-3-基)亚甲基)- n -(5-(2-氯苯基)硫)-1,3,4-噻二唑-2-基)肼-1-羧酰胺(6b)对Xac和Xoo具有良好的抑制活性(200µg/mL时为89.46%)(EC50 = 18.28µg/mL);化合物2-((2-氯- 1h -吲哚-3-基)亚甲基)- n -(5-(4-甲氧基苄基)硫)-1,3,4-噻二唑-2-基)肼-1-羧酰胺(6g)对Xoo具有良好的抑菌活性,EC50值为12.21µg/mL。
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