4.7 Article

Development of 1,3,4-Oxadiazole Derived Antifungal Agents and Their Application in Maize Diseases Control

期刊

FRONTIERS IN PLANT SCIENCE
卷 13, 期 -, 页码 -

出版社

FRONTIERS MEDIA SA
DOI: 10.3389/fpls.2022.912091

关键词

oxadiazole derivatives; antifungal pesticides; maize diseases; plant fungicides; crop protection; crop health

资金

  1. Special Scientific Research Program of Shaanxi Education Department [20JK0892]
  2. Natural Science Basic Research Project of Shaanxi Science and Technology Department [2022JM-492]
  3. Science and Technology Innovation Team of Xi'an Medical University [2021TD07]

向作者/读者索取更多资源

In this study, a series of 1,3,4-oxadiazole derivatives were designed and synthesized, and their antifungal activities against maize disease pathogens were evaluated. The synthesized derivatives showed strong antifungal activities, especially against E. turcicum. Some compounds induced significant shrinkage and collapse of E. turcicum hyphae. Furthermore, these compounds with antifungal activities exhibited almost no cytotoxicity to MCF-7 cells. The 1,3,4-oxadiazole derivatives have the potential to be used as antifungal agents for the control of maize diseases.
Maize is an important food crop and its fungal disease has become a limiting factor to improve the yield and quality of maize. In the control of plant pathogens, commercial fungicides have no obvious effect on corn diseases due to the emergence of drug resistance. Therefore, it is of great significance to develop new fungicides with novel structure, high efficiency, and low toxicity to control maize diseases. In this paper, a series of 1,3,4-oxadiazole derivatives were designed and synthesized from benzoyl hydrazine and aromatic aldehydes through condensation and oxidation cyclization reaction. The antifungal activity of oxadiazole derivatives against three maize disease pathogens, such as Rhizoctonia solani (R. solani), Gibberella zeae (G. zeae), and Exserohilum turcicum (E. turcicum), were evaluated by mycelium growth rate method in vitro. The results indicated that most of the synthesized derivatives exhibited positive antifungal activities. Especially against E. turcicum, several compounds demonstrated significant antifungal activities and their EC50 values were lower than positive control carbendazim. The EC50 values of compounds 4k, 5e, and 5k were 50.48, 47.56, 32.25 mu g/ml, respectively, and the carbendazim was 102.83 mu g/ml. The effects of active compounds on E. turcicum microstructure were observed by scanning electron microscopy (SEM). The results showed that compounds 4k, 5e, and 5k could induce the hyphae of E. turcicum to shrink and collapse obviously. In order to elucidate the preliminary mechanism of oxadiazole derivatives, the target compounds 5e and 5k were docked with the theoretical active site of succinate dehydrogenase (SDH). Compounds 5e and 5k could bind to amino acid residues through hydrophobic contact and hydrogen bonds, which explained the possible mechanism of binding between the inhibitor and target protein. In addition, the compounds with antifungal activities had almost no cytotoxicity to MCF-7. This study showed that 1,3,4-oxadiazole derivatives were worthy for further attention as potential antifungal agents for the control of maize diseases.

作者

我是这篇论文的作者
点击您的名字以认领此论文并将其添加到您的个人资料中。

评论

主要评分

4.7
评分不足

次要评分

新颖性
-
重要性
-
科学严谨性
-
评价这篇论文

推荐

暂无数据
暂无数据