Design, Synthesis, and Biological Evaluation of Novel Aryl Sulfonamide Derivatives as Potential Succinate Dehydrogenase Inhibitors Targeting Phytopathogenic Fungi

Abstract

In our pursuit of novel succinate dehydrogenase inhibitor (SDHI) fungicides for agriculture, we replaced the traditional amide structure with a sulfonamide framework and introduced various heterocyclic and aromatic rings at the sulfonamide’s termini. This strategy yielded 30 synthesized compounds, which were screened for antifungal activity against eight phytopathogenic fungi. The biological assay results demonstrated that several target compounds exhibited significant in vitro antifungal activity. Notably, compound 2f showed remarkable antifungal activity against Valsa mali with an EC₅₀ value of 0.56 mg/L, outperforming Boscalid (EC₅₀ = 1.79 mg/L). In vivo experiments revealed that compound 2f provided significant protection to apple fruits, comparable to Boscalid. SEM analysis of compounds 2f and 3e showed that compound 2f disrupted the structure and morphology of fungal hypha analysis, which suggested that the terminal polyhalogen-substituted pyridine moieties might be pivotal regions influencing their antifungal efficacy. Molecular docking analysis revealed that compound 2f and Boscalid exhibited a comparable binding mode to SDH. Furthermore, detailed SDH inhibition assays confirmed the potential of 2f (IC₅₀ = 2.51 μM) as prospective SDH inhibitors. RNA transcriptomic analysis indicated that the application of compound 2f could influence gene expression in fungi, thereby exerting a defensive effect against plant pathogenic fungi. Consequently, compound 2f shows promise for developing a novel and efficient agrochemical fungicide.