In order to investigate bioactive natural products derived from the endophytic fungus
Penicillium ochrochloron SWUKD4.1850, a comprehensive study focusing on secondary metabolites was conducted. This research led to the isolation of twenty distinct compounds, including a novel nortriterpenoid (compound
20), alongside nineteen
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In order to investigate bioactive natural products derived from the endophytic fungus
Penicillium ochrochloron SWUKD4.1850, a comprehensive study focusing on secondary metabolites was conducted. This research led to the isolation of twenty distinct compounds, including a novel nortriterpenoid (compound
20), alongside nineteen compounds that had been previously characterized (compounds
1–
19). The chemical structures of these compounds were elucidated using spectroscopic techniques and nuclear magnetic resonance (NMR) analyses. Compounds
1–
17 were isolated for the first time as metabolites of
P. ochrochloron. Except for compounds
1–
14, significant structural similarity was discerned between the metabolites of the endophytic fungus and those of the host plant. Compound
20 is noted as the inaugural instance of a naturally occurring 27-nor-3,4-secocycloartane schinortriterpenoid, while compound
17 was identified in fungi for the first time. An antifungal assay showed that compound
10 displayed a broader antifungal spectrum and a stronger inhibitory effect towards four important plant pathogens, at inhibitory rates of 74.9 to 85.3%. The in vitro radical scavenging activities of compounds
1,
3,
8,
15, and
16 showed higher antioxidant activity than vitamin C. Moreover, a cytotoxic assay revealed that compound
20 had moderate cytotoxicity against the HL-60, SMMC-7721, and MCF-7 cell lines (IC
50 6.5–17.8 μM). Collectively, these findings indicate that
P. ochrochloron has abundant secondary metabolite synthesis ability in microbial metabolism and that these metabolites have good biological activity and have the potential to enhance plant disease resistance.
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