期刊
JOURNAL OF CHROMATOGRAPHY A
卷 1209, 期 1-2, 页码 145-152出版社
ELSEVIER
DOI: 10.1016/j.chroma.2008.09.004
关键词
Taraxacum mongolicum; Phenolic secondary metabolites; Antioxidant activity; HPLC-DAD-RSD-ESI-MS; NMR
资金
- National Scientific Foundation of China [20775092]
- Postdoctoral Science Foundation of Central South University [743410000]
Taraxacurn mongolicum was a traditional Chinese medicine for the treatment of inflammatory disorders and viral infectious diseases. Furthermore, fresh leaves of T mongolicum have been used by local people as vegetable food in Northern China. An on-line rapid screening method, high-performance liquid chromatography-diode array detection-radical-scavenging detection-electrospray ionization mass spectrometry (HPLC-DAD-RSD-ESI-MS) system, has been developed for the separation and identification of radical scavengers from the methanolic extract of T mongolicum. In addition, the detected antioxidants were isolated directly by preparative HPLC (PHPLC) and Sephadex LH-20, then the purified compounds were sampled to off-line nuclear magnetic resonance (NMR) spectrometer to acquire NMR spectra. The structure of the active compounds was elucidated by ultraviolet (UV), ESI-MS and NMR spectral data. Thirty-two radical-scavenging compounds including sixteen flavonoid derivatives, ten phenylpropanoid derivatives and six benzoic acid derivatives were screened, isolated and identified. Among them, seventeen compounds including three new compounds were first isolated from Taraxacurn genus by our group. Caffeic acid (6), isoetin-7-O-beta-D-glucopyranosyl-2'-O-alpha-L-arabinopyranoside (9), isoetin-7-O-beta-D-glucopyranosyl-2'-O-alpha-D-glucopyranoside (10) and isoetin-7-0-0-D-glucopyranosyl-2'0-p-D-Xyloypyranoside (12) were found to be the major metabolites in T mongolicum based on their relative peaks in the HPLC chromatogram. Antioxidant activity of three new compounds was assessed for their scavenging capacity on 2,2-diphenyl-1-picrylhydrazyl (DPPH) radical, and all of them showed potent activity. (C) 2008 Elsevier B.V. All rights reserved.
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