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.

Download full-text PDF

Source
http://dx.doi.org/10.1021/acs.jafc.4c03033DOI Listing

Publication Analysis

Top Keywords

indolyl isothiocyanate
12
synthesis indolyl
8
isothiocyanate compounds
8
compounds
7
isothiocyanate
4
isothiocyanate inhibitory
4
activity
4
inhibitory activity
4
activity fungi
4
fungi based
4

Similar Publications

Want AI Summaries of new PubMed Abstracts delivered to your In-box?

Enter search terms and have AI summaries delivered each week - change queries or unsubscribe any time!