is used as a medicinal fungus in Taiwan to treat fatigue, food intoxication, and enhance liver function. Here we identified fermented metabolic components from the mycelium of KH37 and explored their anti-hepatoma potentials with study models of human hepatoblastoma cell lines. Bioassay-guided fractionation of the solid fermentation powder of KH37 led to the isolation of one new quinonol, antroquinonol Z (), and nine known compounds (-). Treatment with 10 μM antrocamols LT1 () or LT3 () reduced cell viability of HepG2 and Huh-7 cells to about 60% in 48 hours. Antroquinonol Z () exhibited mild cytotoxicity against Huh-7 cells in 48 and 72 hours. Interestingly, two fractions showed cytotoxicity in HepG2 and Huh-7 cells, even better than compounds isolated from these fractions. The significant cytotoxicity of partially purified samples from KH37 exhibited a potential for developing alternative or complementary therapeutics against hepatoma.

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http://dx.doi.org/10.1080/14786419.2022.2076676DOI Listing

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