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  4. Synthesis and Anti-Plant Pathogenic Fungal Activity of Flavokawain-Derived Flavones and Related Flavones Against Rhizoctonia solani
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Synthesis and Anti-Plant Pathogenic Fungal Activity of Flavokawain-Derived Flavones and Related Flavones Against Rhizoctonia solani

Author(s)
Onnom, Panuwat
Chotpatiwetchkul, Warot
Meesin, Jatuporn
Thapanapongworakul, Pilunthana
Kittiwongwattana, Chokchai
Chotsaeng, Nawasit
Date Issued
January 3, 2024
Type
Article
DOI
10.55003/cast.2023.258374
Abstract
Flavones are organic compounds in the flavonoid family that have a diverse range of biological functions. In this research, many flavones with various substituents were designed and synthesized from flavokawains A, B, and C, and their chalcone derivatives via an iodinecatalyzed oxidative cyclization process. All synthetic flavones were investigated for antifungal activities against Rhizoctonia solani, a plant pathogenic fungus. At 400 µg, most of the substances did not inhibit the tested species and R. solani growth was inhibited by only obromoflavone (40) by 74.88±0.91%. This indicated that the detrimental effect of flavones depends on the type and position of substituent, with the ortho bromo group showing the most promise. The molecular docking study on the succinate dehydrogenase (SDH) enzyme revealed that the bromophenyl moiety (ring B) is a key molecular substructure of the flavone fungicide. The findings of this study will be used to develop novel plant pathogenic fungicides.
Citation
Current Applied Science and Technology, 24(2), 2024
Subjects

antifungal

flavokawains

flavones

phytopathogen

Rhizoctonia solani

SAR

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