作者
Mengyi Deng,Enrui Zhang,Fang Qiu,Yingying Fei,Yuyan Liu,Lin Li,Ya Xiong,Xian‐Li Zhou
摘要
Penicinoid A (1), a previously undescribed sesterterpenoid, and ten known compounds, variculanol (2), citreoanthrasteroid A (3), ergosta-7,22E-diene-2β,3α,9α-triol (4), (22E,24R)-23-methylergosta-7,22-diene-3β,5α,6β,9α-tetrol (5), 9,11-dehydroergosterol peroxide (6), (22E,24R)-3β,5α,9α-trihydroxy-ergosta-7,22-dien-6-one (7), gymnasterone C (8), cyathisterol (9), demethylincisterol A3 (10), volemolide (11), were obtained from Aconitum carmichaelii endophytic fungus Penicillium herquei. Their structures were characterised by NMR, HRESIMS, ECD calculations and comparison with the reported literatures. All isolates were screened on their cytotoxicity against A549, Hepg2, HeLa, and HCT116 cells. Compounds 1-11 exhibited significant to weak cytotoxic effects (IC50 values: 1.5 ± 0.1-37.3 ± 3.0 μM). Additionally, their inhibitory activity on NO production in LPS stimulated RAW 264.7 macrophages were evaluated. Compounds 1-11 showed moderate to weak inhibitory activity (IC50 values: 10.9 ± 1.0-35.1 ± 3.1 μM). This is the first time that sesterterpenoids were found from the secondary metabolites of P. herquei.