| Literature DB >> 29987893 |
Si-Yuan Ma1,2, Ling-Gao Shi1, Zheng-Bing Gu3, Yu-Lan Wu2, Liu-Bin Wei1, Qi-Qiu Wei1, Xing-Ling Gao1, Na Liao1.
Abstract
Five chromone glycosides were isolated from the water-soluble portions of 70% EtOH extract of the roots of Saposhnikovia divaricata, including two new chromone glycosides 1 and 2. The structures of the chromone glycosides were identified as (3'S)-3'-O-β-d-apiofuranosyl-(1 → 6)-β-d-glucopyranosylhamaudol (1), (2'S)-4'-O-β-d-apiofuranosyl-(1 → 6)-β-d-glucopyranosylvisamminol (2), 3'-O-glucopyranosylhamaudol (3), 4'-O-β-d-glucopyranosylvisamminol (4), and 4'-O-β-d-glucopyranosyl-5-O-methylvisamminol (5) on the basis of extensive spectroscopic methods, and the absolute configurations of the new compounds were elucidated by the electronic circular dichroism (ECD) calculation and acid hydrolysis. The cytotoxic activities of the glycosides 1 - 5 against three human cancer cell lines (PC-3, SK-OV-3, and H460) were evaluated. The result showed that compounds 1 - 5 had weak cytotoxic activities against the human cancer cell lines with IC50 values in the range of 48.54 ± 0.80 - 94.25 ± 1.45 μm.Entities:
Keywords: zzm321990Saposhnikovia divaricatazzm321990; ECD calculation; chromone; cytotoxic activities; glycoside
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Year: 2018 PMID: 29987893 DOI: 10.1002/cbdv.201800253
Source DB: PubMed Journal: Chem Biodivers ISSN: 1612-1872 Impact factor: 2.408