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논문 기본 정보

자료유형
학술저널
저자정보
Heejung Yang (Kangwon National University) Jeom Yong Kim (Greencrosshs, Suntech City) Sun Ok Kim (Greencrosshs, Suntech City) Young Hyo Yoo (Greencrosshs, Suntech City) Sang Hyun Sung (Seoul National University)
저널정보
고려인삼학회 Journal of Ginseng Research Journal of Ginseng Research Vol.38 No.3
발행연도
2014.7
수록면
194 - 202 (9page)

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초록· 키워드

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Background: Ginsenosides, the major ingredients of Panax ginseng, have been studied for many decades in Asian countries as a result of their wide range of pharmacological properties. The less polar ginsenosides, with one or two sugar residues, are not present in nature and are produced during manufacturing processes by methods such as heating, steaming, acid hydrolysis, and enzyme reactions. ¹H-NMR and <SUP>13</SUP>C-NMR spectroscopic data for the identification of the less polar ginsenosides are often unavailable or incomplete.
Methods: We isolated 21 compounds, including 10 pairs of 20(S) and 20(R) less polar ginsenosides (1-20), and an oleanane-type triterpene (21) from a processed ginseng preparation and obtained complete ¹H-NMR and <SUP>13</SUP>C-NMR spectroscopic data for the following compounds, referred to as compounds 1-21 for rapid identification: 20(S)-ginsenosides Rh2 (1), 20(R)-Rh2 (2), 20(S)-Rg3 (3), 20(R)-Rg3 (4), 6´-O-acetyl-20(S)-Rh2 [20(S)-AcetylRh2] (5), 20(R)-AcetylRh2 (6), 25-hydroxy-20(S)-Rh2 (7), 25-hydroxy-20(S)-Rh2 (8), 20(S)-Rh1 (9), 20(R)-Rh1 (10), 20(S)-Rg2 (11), 20(R)-Rg2 (12), 25-hydroxy-20(S)-Rh1 (13), 25-hydroxy-20(R)-Rh1 (14), 20(S)-AcetylRg2 (15), 20(R)-AcetylRg2 (16), Rh4 (17), Rg5 (18), Rk1 (19), 25-hydroxy-Rh4 (20), and oleanolic acid 28-O-β-D-glucopyranoside (21).

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abstract
1. Introduction
2. Materials and methods
3. Results and discussion
References

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