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Natural Furan-Carboxylic Acid (HHCA) and Its Derivatives: Synthesis, Characterization, Bioevaluation, and Structure-Activity Relationships as Potential Fungicidal Agents

文献类型： 外文期刊

作者： Guo, Lirong 1 ; Wang, Hexiang 1 ; Zheng, Fuqiang 1 ; Xu, Shiyu 2 ; Liu, Fang 1 ; Huang, Wenbo 4 ; Zhang, Zhigang 1 ; Wang, Kaimei 1 ; Cao, Xiufang 2 ; Bao, Longzhu 1 ; Ke, Shaoyong 1 ;

作者机构： 1.Hubei Acad Agr Sci, Natl Biopesticide Engn Res Ctr, Hubei Biopesticide Engn Res Ctr, Key Lab Microbial Pesticides,Minist Agr & Rural Af, Wuhan 430064, Peoples R China

2.Huazhong Agr Univ, Coll Chem, Wuhan 430070, Peoples R China

3.Hubei Univ Technol, Sch Life & Hlth Sci, Wuhan 430068, Peoples R China

4.Hubei Three Gorges Lab, Yichang 443007, Hubei, Peoples R China

关键词： natural product; HHCA; structural diversity; antifungal activity; SARs

期刊名称：JOURNAL OF AGRICULTURAL AND FOOD CHEMISTRY （ 影响因子：6.2； 五年影响因子：6.4 ）

ISSN： 0021-8561

年卷期： 2025 年 73 卷 22 期

页码：

收录情况： SCI

摘要： The exploration of natural products as lead scaffolds continues to serve as a valuable strategy for the development of novel antifungal agents. In this investigation, we focused on the natural furanoid compound 2-heptyl-5-hexylfuran-3-carboxylic acid (HHCA) and designed and synthesized four distinct series of multisubstituted furan carboxylic acid derivatives. Comprehensive structural characterization and biological evaluation were performed for all 48 compounds. In vitro antifungal screening against eight prevalent plant pathogens revealed that some of these derivatives exhibited significant inhibitory effects against Botrytis cinerea and Sclerotinia sclerotiorum. Structure-activity relationship analysis demonstrated that peptide-containing derivatives showed superior antifungal potency compared with their hydrazide, amide, and ester counterparts. The most promising candidate compound 5g was further evaluated for its in vivo efficacy against two plant pathogens, S. sclerotiorum and B. cinerea, indicating potent antifungal activity with EC50 values of 17.14 mu g/mL and 19.63 mu g/mL, respectively. Notably, these values were significantly lower than those of the natural product HHCA with an enhanced antifungal potency. These findings highlight the practical potential of compound 5g as a novel antifungal agent for agricultural applications. Mechanistic investigations employing microscopic analysis, molecular docking simulations, and density functional theory (DFT) calculations provided insights into the putative mode of action of 5g, particularly regarding its interaction with succinate dehydrogenase (SDH). These findings establish a foundation for the rational development of HHCA-derived furan derivatives as novel SDH-targeting fungicidal agents.

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