Discovery of novel 3-(piperazin-1-yl)propan-2-ol decorated carbazole derivatives as new membrane- targeting antibacterial agents

被引:3
作者
Ding, Ying-Guo [1 ]
Chen, Ai-Qun [1 ]
Wang, Na [1 ]
Long, Zhou-Qing [1 ]
Liu, Hong-Wu [1 ]
Xie, Jiao [1 ]
Liu, Shi-Tao [1 ]
Qi, Pu-Ying [1 ]
Zhou, Xiang [1 ]
Liu, Li-Wei [1 ]
Yang, Song [1 ]
机构
[1] Guizhou Univ, Ctr R&D Fine Chem, Natl Key Lab Green Pesticide, Key Lab Green Pesticide & Agr Bioengn,Minist Educ, Guiyang 550025, Peoples R China
基金
中国国家自然科学基金;
关键词
Carbazole derivatives; Cell membrane; Toxicity; Microbial diseases; Drug discovery; PV.-ACTINIDIAE PSA; MOIETY DESIGN; KIWIFRUIT; BACTERIA; WATER;
D O I
10.1016/j.arabjc.2023.104991
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
The increasing resistance problems of pathogens have drastically reduced the efficiency of existing drugs and agricultural chemicals, increasing the difficulty of preventing and controlling bacterial diseases. To create effective bactericide alternatives, a series of novel 3-(piperazin-1-yl) propan-2-ol decorated carbazole derivatives was fabricated, and their bioactivities and drug-likeness properties were evaluated. The in vitro bioassays showed that target molecules had out-standing antibacterial activity against Xanthomonas oryzae pv. oryzae (Xoo), Xanthomonas axono-podis pv. citri (Xac), and Pseudomonas syringae pv. actinidiae (Psa), with optimal EC50 values of 6.80 lg/mL (A9), 6.37 lg/mL (A9), and 10.75 lg/mL (A10), respectively. Furthermore, a series of biochemical assays indicated that title molecules could negatively impact the function of bacteria by irreversibly damaging their cell membranes, resulting in cytoplasmic components leakage (nu-cleic acids and proteins). In addition, phytotoxicity test and in silico toxicity predictions suggested that compound A9 had low phytotoxicity, and possessed acceptable drug-like properties. Our results showed that carbazole derivatives containing an 3-(piperazin-1-yl)propan-2-ol moiety were promising skeletons to develop novel bactericides with low toxicity for controlling refractory micro-bial diseases by targeting cell membranes. (c) 2023 The Authors. Published by Elsevier B.V. on behalf of King Saud University. This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).
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页数:14
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