Development and Biological Evaluation of New Diphenyl Ether Formylhydrazide Compounds as Potent Inhibitors of Succinate Dehydrogenase

• Published in: Journal of agricultural and food chemistry 2024-11, Vol.72 (47), p.26133-26141
• Main Authors: He, Bo, Chen, Wang, Fu, Lixiang, Hu, Mengxu, Xiong, Zhenxi, Luo, Xianghui, Hu, Yanhao, Mu, Yalin, He, Xu, Yan, Wei, Ye, Yonghao
• Format: Article
• Language: English
• Subjects: Agricultural and Environmental Chemistry; antifungal properties; benzene; biological assessment; boscalid; class; diphenyl ethers; enzyme inhibition; food chemistry; Fusarium graminearum; mycelium; pathogens; rapeseed; Sclerotinia sclerotiorum; structure-activity relationships; succinate dehydrogenase (quinone); succinic acid; ubiquinones; wheat
• ISSN: 0021-8561; 1520-5118; 1520-5118
• DOI: 10.1021/acs.jafc.4c07019

Succinate dehydrogenase (SDH), also recognized as succinate ubiquinone oxidoreductase (SQR), is considered one of the most promising targets for fungicide development, garnering significant international interest. We have focused on the development of highly effective, broad-spectrum-targeted SDH inhibitors. Using an active scaffold combining strategy, we designed and synthesized a series of novel diphenyl ether formylhydrazine derivatives, and most compounds have demonstrated broad-spectrum antifungal activity. Notably, compound M8 exhibited antifungal activity of more than 93% against four tested pathogen types at a concentration of 10 μg/mL, with an EC50 value below 0.3 μg/mL for each pathogen, outperforming boscalid. Additionally, compound M8 exhibited a control efficacy of 83% against Sclerotinia sclerotiorum on rapeseed leaves at a concentration of 200 μg/mL and demonstrated an 87% efficacy in controlling Fusarium graminearum on wheat ears when applied at 400 μg/mL. Structure–activity relationship research suggested that para-substituted benzene rings are more effective, offering stronger and more extensive antifungal potency. Further investigation, including enzyme inhibition assays, mycelial morphology observations, and molecular docking studies, suggests that the antifungal potency of M8 is due to the inhibition of its SDH activity. Therefore, our research positions compound M8 as a highly promising lead compound with broad-spectrum antifungal properties, potentially introducing a new class of fungicide.