Phytochemical investigation on the extract of endophytic fungus Tolypocladium sp. SHJJ1 resulted in the identification of a pair of previously undescribed pyridoxatin atropisomers [1 (M/P)] and three new indole diterpenoids (3-5), together with a pair of known pyridoxatin atropisomers [2 (M/P)] and ten known indole diterpenoids (6-15). Their structures, including their absolute configurations were elucidated by extensive spectroscopic analysis, quantum chemical calculations, and X-ray diffraction. Among the undescribed natural products, [1 (M/P)] that two rapidly interconverting atropisomers are the third example to report in the pyridoxatin atropisomers. Except for compounds 1 (M/P) and 2 (M/P), all other compounds were tested for their cytotoxicity using HepG2, A549, and MCF-7 human cell lines. Compound 9 displayed moderate cytotoxicity against the HepG2, A549, and MCF-7 cell lines with IC50 values of 32.39 ± 1.48 μM, 26.06 ± 1.14 μM, and 31.44 ± 1.94 μM, respectively, which was similar to the positive drug cisplatin (with IC50 values of 32.55 ± 1.76 μM, 18.40 ± 1.43 μM, and 27.31 ± 1.22 μM, respectively).
Keywords: Cytotoxic activity; Endophytic fungus; Indole diterpenoid; Lindera glauca; Pyridoxatin atropisomers.
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