There has been a tremendous increase in the rate of new terpenoids from marine-derived fungi being discovered, while new monoterpenes were rarely isolated from marine-derived fungi in the past two decades. Three new monoterpenes, diaporterpenes A–C (
1–
3), and one
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There has been a tremendous increase in the rate of new terpenoids from marine-derived fungi being discovered, while new monoterpenes were rarely isolated from marine-derived fungi in the past two decades. Three new monoterpenes, diaporterpenes A–C (
1–
3), and one new α-pyrones, diaporpyrone A (
6), along with nine known polyketides
4,
5, and
7–
13 were isolated from the ascidian-derived fungus
Diaporthe sp. SYSU-MS4722. Their planar structures were elucidated based on extensive spectroscopic analyses (1D and 2D NMR and HR-ESIMS). The absolute configurations of
1 and
3 were identified by an X-ray crystallographic diffraction experiment using Cu-Ka radiation, and those of compound
2 were assigned by calculating NMR chemical shifts and ECD spectra. It afforded an example of natural epimers with different physical properties, especially crystallization, due to the difference in intermolecular hydrogen bonding. Compounds
9,
10, and
13 showed moderate total antioxidant capacity (0.82 of
9; 0.70 of
10; 0.48 of
13) with Trolox (total antioxidant capacity: 1.0) as a positive control, and compounds
5 and
7 showed anti-inflammatory activity with IC
50 values of 35.4 and 40.8 µM, respectively (positive control indomethacin: IC
50 = 35.8 µM).
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