Isolating Antipathogenic Fungal Coumarins from Coriaria nepalensis and Determining Their Primary Mechanism In Vitro

Abstract

Through bioassay-guided isolation, eight undescribed coumarins (1−8), along with six reported coumarins (9−14), were obtained from Coriaria nepalensis. The new structures were determined by using IR, UV, NMR, HRESIMS, and ECD calculations. The results of the biological activity assays showed that compound 9 exhibited broad spectrum antifungal activities against all tested fungi in vitro and a significant inhibitory effect on Phytophthora nicotianae with an EC 50 value of 3.00 μg/mL. Notably, compound 9 demonstrated greater curative and protective effects against tobacco balack shank than those of osthol in vivo. Thus, 9 was structurally modified to obtain new promising antifungal agents, and the novel derivatives (17b, 17j, and 17k) exhibited better effects on Sclerotinia sclerotiorum than did lead compound 9. Preliminary mechanistic exploration illustrated that 9 could enhance cell membrane permeability, destroy the morphology and ultrastructure of cells, and reduce the exopolysaccharide content of P. nicotianae mycelia. Furthermore, the cytotoxicity results revealed that compound 9 exhibited relatively low cytotoxicity against HEK293 cell lines with an inhibition rate of 33.54% at 30 μg/mL. This research is promising for the discovery of new fungicides from natural coumarins with satisfactory ecological compatibility.

Recent Advances and Outlook of Benzopyran Derivatives in the Discovery of Agricultural Chemicals

“…The two main isomers of benzopyran are benzo-α-pyran and benzo-γ-pyran, while benzodihydropyran, chroman-2-one, chroman-4-one, and 4 H -chromen-4-one contain variations in the scaffold structures of benzopyran (Figure ). In addition, some representative natural products containing a benzopyran structure have played an important role in the discovery of agricultural active compounds, − such as osthole and coumarin.…”