Abstract
Ergopolyketides A–D, presumably biosynthesized through Diels–Alder additions between
ergosterol and polyketides, along with two new andrastin-type meroterpenoids, isopenicins
D and E, were isolated from the co-culture of endophytic fungi Penicillium sp. sh18 and Pestalotiopsis sp. HS30, both, inhabiting Isodon species. The structures of these compounds were elucidated using spectroscopic analysis,
single-crystal X-ray diffraction, and quantum chemical calculations. Isopenicin D
and a known compound, peniandrastin D, exhibited moderate cytotoxic activities against
human cancer cell lines HL-60, A549, and SMMC-7721, with IC50 values ranging from 13.37 to 29.17 μM.
Key words
Isodon
- endophytic fungi - steroidal adducts - andrastin-type meroterpenoids - cytotoxic
activity - quantum chemical calculations - configuration determination