Heterocornols from the Sponge-Derived Fungus with Anti-Inflammatory Activity.

One strain-many compounds (OSMAC) manipulation of the sponge-derived fungus XWS03F09 resulted in the production of new secondary metabolites. The chemical study of the fermentation, cultivated on 3% artificial sea salt in the rice media, led to the isolation of twelve compounds, including eight new polyketide derivatives, heterocornols Q-X (-), one new ceramide (), and three known analogues (-). The structures and absolute configurations of the new compounds were elucidated by spectroscopic data and calculated ECD analysis. Heterocornols Q () and R () are novel 6/5/7/5 tetracyclic polyketide derivatives featuring dihydroisobenzofuran and benzo-fused dioxabicyclo [4.2.1] nonane system, which might be derived from the acetyl-CoA by epoxidation, polyene cyclization, and rearrangement to form the core skeleton. Compound showed moderate or weak antimicrobial activities against with MIC values ranging from 25 to 100 μg/mL. Heterocornols T and X ( and ) could inhibit the production of LPS-induced NO significantly, comparable to dexamethasone. Further Western blotting analysis showed and markedly suppressed the iNOS protein expression in LPS-induced RAW 264.7 cells in a dose-dependent manner. The result showed that and might serve as potential leads for development of anti-inflammatory activity.