| Literature DB >> 23954076 |
You-Min Ying1, Wei-Guang Shan, Li-Wen Zhang, Zha-Jun Zhan.
Abstract
Tremulane sesquiterpenes ceriponols A-K, together with three known ones tremulenediol A, 11,12-dihydroxy-1-tremulen-5-one and conocenol B, were isolated from the cultures of Ceriporia lacerate, a fungal endophyte residing in the stems of the medicinal plant Huperzia serrata. Among these isolates, ceriponol B possessed an unprecedent 12-nortremulane skeleton. The structures of all isolates were elucidated by spectroscopic methods, including MS and NMR (1D and 2D) spectroscopic techniques. The cytotoxic activities of ceriponols A-K were evaluated against three human tumor cell lines (HeLa, HepG2, and SGC 7901). Ceriponols F and K exhibited moderate cytotoxicity against all the tested human cancer cell lines with IC50 values ranging from 32.3 ± 0.4 to 173.2 ± 1.5 μM, while ceriponol G showed slightly better cytotoxicity against a HeLa cell line.Entities:
Keywords: Ceriporia lacerate; Endophytes; Huperzia serrata; Lycopodiopsida; Nor-sesquiterpenes; Polyporaceae; Sesquiterpenes; Tremulane
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Year: 2013 PMID: 23954076 DOI: 10.1016/j.phytochem.2013.07.025
Source DB: PubMed Journal: Phytochemistry ISSN: 0031-9422 Impact factor: 4.072