| Literature DB >> 26324074 |
Han Wei1, Ya-ming Xu1, Patricia Espinosa-Artiles1, Manping X Liu1, Jiang-Guang Luo2, Jana M U'Ren3, A Elizabeth Arnold4, A A Leslie Gunatilaka5.
Abstract
Oxygenated guaiane-type sesquiterpenes, xylaguaianols A-D (1-4), an iso-cadinane-type sesquiterpene isocadinanol A (5), and an α-pyrone 9-hydroxyxylarone (6), together with five known sesquiterpenes (7-11), and four known cytochalasins (12-15) were isolated from a culture broth of Xylaria sp. NC1214, a fungal endophyte of the moss Hypnum sp. The structures of all compounds were elucidated by the analysis of their spectroscopic data and relative configurations of 1-5 were determined with the help of NMR NOESY experiments. Cytochalasins C (12), D (13), and Q (14) were investigated for their cytotoxic activity against five tumor cell lines. Cytochalasin D showed significant cytotoxicity against all five cell lines, with IC50s ranging from 0.22 to 1.44 μM, whereas cytochalasins C and Q exhibited moderate, but selective cytotoxicity.Entities:
Keywords: Cytochalasins; Fungal endophyte; Hypnum sp.; Sesquiterpenes; Xylaguaianols; Xylaria sp.; α-Pyrone
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Year: 2015 PMID: 26324074 PMCID: PMC4592834 DOI: 10.1016/j.phytochem.2015.08.010
Source DB: PubMed Journal: Phytochemistry ISSN: 0031-9422 Impact factor: 4.072