| Literature DB >> 27310249 |
Xue-Ming Zhou1, Cai-Juan Zheng1, Li-She Gan2, Guang-Ying Chen1, Xiao-Peng Zhang1, Xiao-Ping Song1, Gao-Nan Li1, Chong-Ge Sun3.
Abstract
A new enantiomeric pair of spirodiketones, (+)- and (-)-denobilone A (1 and 2), three new phenanthrene derivatives (3-5), and three new biphenanthrenes (22-24), along with 11 known phenanthrene derivatives (6-16), five known bibenzyl derivatives (17-21), and four known biphenanthrenes (25-28), were isolated from Dendrobium nobile. The structures of 1-5 and 22-24 were elucidated using comprehensive spectroscopic methods. (+)-Denobilone and (-)-denobilone A (1 and 2) were isolated as a pair of enantiomers by chiral HPLC. The absolute configurations of (+)- and (-)-denobilone A (1 and 2) were determined by comparing their experimental and calculated electronic circular dichroism spectra. The absolute configuration of denobilone B (3) was determined by X-ray crystallographic analysis. The inhibitory activities of all compounds against nine phytopathogenic fungi and three cancer cell lines were evaluated.Entities:
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Year: 2016 PMID: 27310249 DOI: 10.1021/acs.jnatprod.6b00252
Source DB: PubMed Journal: J Nat Prod ISSN: 0163-3864 Impact factor: 4.050