| Literature DB >> 23096258 |
Kai-Ze Shen1, Suo Gao, Yan-Xiu Gao, An-Ran Wang, Yao-Bo Xu, Rong Sun, Pei-Gen Hu, Guo-Fu Yang, Ai-Ji Li, Dan Zhong, Hai-Yang Liu, Jin-Yan Dong.
Abstract
Six new dibenzo[b,e]oxepinone metabolites, chaetones A-F (1-6), as well as three known compounds, 1-hydroxy-6-methyl-8-hydroxymethylxanthone (7), citreorosein (8), and emodin (9), were obtained from a freshwater-derived fungal strain Chaetomium sp. YMF 1.02105. Their structures were established on the basis of extensive spectroscopic data analysis and comparison with spectroscopic data reported. Compounds 1-6 are further additions to the small group of dibenzo[b,e]oxepinones represented by arugosins A-H. Compounds 1-7 were tested for their cytotoxic activities against A549, Raji, HepG2, MCF-7, and HL-60 cell lines. The results showed that compound 3 had significant cytotoxicity with IC50 values of 1.2, 1.8, 1.9, 2.3, and 1.6 µg/mL, respectively, against the five cancer cell lines. All compounds showed modest antimicrobial activity against Staphylococcus aureus (ATCC 6538) in standard disk assays. Georg Thieme Verlag KG Stuttgart · New York.Entities:
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Year: 2012 PMID: 23096258 DOI: 10.1055/s-0032-1327828
Source DB: PubMed Journal: Planta Med ISSN: 0032-0943 Impact factor: 3.352