Quinic acid esters and sesquiterpenes from Sonchus arvensis |
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Authors: | Yang-Jun Xu Shao-Bo Sun Li-Mei Sun Dong-Feng Qiu Xiu-Jin Liu Zhi-Bo Jiang Cheng-Shan Yuan |
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Affiliation: | 1. State Key Laboratory of Applied Organic Chemistry, College of Chemistry and Chemical Engineering, Lanzhou University, Lanzhou 730000, PR China;2. Gansu College of Traditional Chinese Medicine, Lanzhou 730000, PR China |
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Abstract: | ![]() A phytochemical study on the whole plant of Sonchus arvensis and its antioxidant activity has been carried out. Three quinic acid derivatives (1–3), the rarely naturally occurring (p-hydroxyphenylacetyl) quinic acids, and two eudesmanolides (4 and 5) were newly found. Four known eudesmanolides (6–9) were isolated from the plant for the first time. Their structures were characterized by HRESIMS, IR, UV, 1D NMR, and 2D NMR. 1,1-Diphenyl-2-picrylhydrazyl (DPPH·)-scavenging activity was evaluated for each of the above 9 compounds (1–9) in comparison to standard antioxidants (caffeic acid and ascorbic acid). However, none proved to have a positive activity. The absence of antioxidant activity could be caused by the absence of ortho or para-diphenolic groups in all detected compounds, that are responsible of the activity against free radicals by an electron transfer reaction. |
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Keywords: | [α]D, specific optical rotation at sodium D line c, concentration calcd, calculated CC, column chromatography COSY, correlation spectroscopy 1D, 2D, one- or two-dimensional DEPT, distortionless enhancement by polarization transfer DPPH, 1,1-diphenyl-2-picrylhydrazyl ε, molar absorptivity HMBC, heteronuclear multiple-bond correlation HRESIMS, high resolution electron spray ionization mass spectrometry J, coupling constant MCI gel, MCI gel CHP20P high porous polymer (Mitsubishi Chemical Industries Co., Ltd., Japan) NOE, nuclear overhauser effect ppm, parts per million RP-18, reversed phase C18 TLC, thin-layer chromatography |
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