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Chiral LC-MS-guided isolation of angular-type pyranocoumarins from Peucedani Radix
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Yang YANG1, 2, Xing-cheng GONG1, 2, Peng-fei TU1, Wen-jing LIU3, *, Yue-lin SONG1, *
Acta Pharmaceutica Sinica | 2024, 59(8) : 2343 - 2349
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Acta Pharmaceutica Sinica | 2024, 59(8): 2343-2349
Chiral LC-MS-guided isolation of angular-type pyranocoumarins from Peucedani Radix
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Yang YANG1, 2, Xing-cheng GONG1, 2, Peng-fei TU1, Wen-jing LIU3, *, Yue-lin SONG1, *
Affiliations
  • 1. Modern Research Center for Traditional Chinese Medicine, Beijing Research Institute of Chinese Medicine, Beijing University of Chinese Medicine, Beijing 102400, China
  • 2. School of Chinese Materia Medica, Beijing University of Chinese Medicine, Beijing 102400, China
  • 3. School of Pharmacy, Henan University of Chinese Medicine, Zhengzhou 450046, China
Published: 2024-08-12 doi: 10.16438/j.0513-4870.2024-0085
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This study utilized a chiral liquid chromatography-mass spectrometry (LC-MS)-guided isolation strategy to accurately capture angular-type pyranocoumarins (APs) in Peucedani Radix (Chinese name: Qianhu). Sixteen APs were successfully purified from the ethyl acetate extract of Peucedani Radix through deploying various techniques such as silica gel, ODS, Sephadex LH-20, and achiral (chiral) semi-preparative liquid chromatography. After extensive structural measurements, such as 1H and 13C NMR spectroscopy, their structures were identified as (3′S)-3′-(2-methyl-butyroyl)-4′-oxo-3′, 4′-dihydroseselin (1A), (3′R)-3′-(2-methyl-butyroyl)-4′-oxo-3′, 4′-dihydroseselin (1B), (3′S)-3′-isovaleryl-4′-oxo-lomatin (2A), (3′R)-3′-isovaleryl-4′-oxo-lomatin (2B), (3′S)-3′-angeloyloxy-4′-oxo-3′, 4′-dihydroseselin (3A), (3′R)-3′-angeloyloxy-4′-oxo-3′, 4′-dihydroseselin (3B), (3′S, 4′S)-praeruptorin B (4A), (3′R, 4′R)-praeruptorin B (4B), (3′S, 4′S)-praeruptorin E (5A), (3′R, 4′R)-praeruptorin E (5B), 3′-isovaleryl-4′-angeloyl-cis-khellactone (6), 3′-angeloyl-4′-(2-methyl-butyroyl)-cis-khellactone (7), (3′S, 4′S)-praeruptorin A (8A), (3′R, 4′R)-praeruptorin A (8B), (3′S, 4′S)-khellactone (9A), and (3′R, 4′R)-khellactone (9B), respectively. Thereof, compounds 1A and 1B were new compounds, while compound 2A represents a new configuration for a known planar structure. Compounds 2A and 2B were isolated for the first time from Peucedani Radix. Above all, chiral LC-MS-guided isolation strategy is advantageous at rapid capturing new compounds from herbal medicines, providing an effective means for the separation of novel structures, especially new enantiomers.

Peucedani Radix  /  chemical component  /  angular-type pyranocoumarins  /  chiral LC-MS-guided isolation  /  enantiomer
Yang YANG, Xing-cheng GONG, Peng-fei TU, Wen-jing LIU, Yue-lin SONG. Chiral LC-MS-guided isolation of angular-type pyranocoumarins from Peucedani Radix[J]. Acta Pharmaceutica Sinica, 2024 , 59 (8) : 2343 -2349 . DOI: 10.16438/j.0513-4870.2024-0085
Year 2024 volume 59 Issue 8
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doi: 10.16438/j.0513-4870.2024-0085
  • Receive Date:2024-01-29
  • Online Date:2025-11-26
  • Published:2024-08-12
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History
  • Received:2024-01-29
  • Revised:2024-04-27
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Affiliations
    1. Modern Research Center for Traditional Chinese Medicine, Beijing Research Institute of Chinese Medicine, Beijing University of Chinese Medicine, Beijing 102400, China
    2. School of Chinese Materia Medica, Beijing University of Chinese Medicine, Beijing 102400, China
    3. School of Pharmacy, Henan University of Chinese Medicine, Zhengzhou 450046, China
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表12种不同金属材料的力学参数

Family
属数
Number of
genus
种数
Number of
species
占总种数比例
Percentage of
total species (%)

Genus
种数
Number of
species
占总种数比例
Percentage of total
species (%)
鹅膏菌科Amanitaceae 2 11 5.26 鹅膏菌属 Amanita 10 4.78
小菇科 Mycenaceae 2 12 5.74 丝盖伞属 Inocybe 5 2.39
多孔菌科 Polyporaceae 8 14 6.70 蜡蘑属 Laccaria 5 2.39
红菇科 Russulaceae 3 23 11.00 小皮伞属 Marasmius 6 2.87
小菇属 Mycena 11 5.26
光柄菇属 Pluteus 5 2.39
红菇属 Russula 17 8.13
栓菌属 Trametes 5 2.39
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