Based on previous research, this study synthesized 24 compounds by splicing the substructures of the indolyl group and the isothiocyanate group. , , and were used to test the activity of the target compounds. At 100 μg/mL, compounds , , , and exhibited excellent inhibitory effects of more than 80% on , and . The EC values of compounds and were 0.64 and 2.08 μg/mL, respectively. Potted antifungal activity demonstrated that compounds and had a protective effect of around 80% against at 200 μg/mL. Further physiological and biochemical studies on revealed that compound 13 thickened cell walls and caused mitochondrial vacuolization. Moreover, theoretical calculations indicated that the charge distribution of indolyl isothiocyanate compounds played a crucial role in the observed fungicidal activity. In summary, this study provided fundamental reference data for the derivative synthesis of these indolyl isothiocyanate compounds.
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http://dx.doi.org/10.1021/acs.jafc.4c03033 | DOI Listing |
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