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Isolation and structural elucidation of oligosaccharides from Scutellaria baicalensis Georgi
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Yu-ting ZHANG1, 2, Juan SONG2, Si LIU2, Rui-zhe WANG1, 2, Xiao-juan CHEN2, Hai-zhen LIANG2, Bai-ping MA1, 2, *
Acta Pharmaceutica Sinica | 2026, 61(6) : 2230 - 2240
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Acta Pharmaceutica Sinica | 2026, 61(6): 2230-2240
• Original Articles •
Isolation and structural elucidation of oligosaccharides from Scutellaria baicalensis Georgi
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Yu-ting ZHANG1, 2, Juan SONG2, Si LIU2, Rui-zhe WANG1, 2, Xiao-juan CHEN2, Hai-zhen LIANG2, Bai-ping MA1, 2, *
Affiliations
  • 1Guangdong Pharmaceutical University, Guangzhou 510006, China
  • 2Academy of Military Medical Sciences, Academy of Military Sciences, Beijing 100850, China
Published: 2026-06-12 doi: 10.16438/j.0513-4870.2026-0183
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Thirteen oligosaccharides were isolated from the water-eluted fraction of Scutellaria baicalensis Georgi extract on macroporous adsorption resin, using techniques such as medium-pressure liquid chromatography, semi-preparative high performance liquid chromatography (HPLC), and a HPLC system equipped with a charged aerosol detector (CAD) as a trigger for fraction collector automatically. The structures of these compounds were identified by mass spectrometry (MS) and nuclear magnetic resonance spectroscopy (NMR) as α-D-galactopyranosyl-(1→6)-α-D-glucopyranosyl-(1→2)-β-D-fructofuranosyl-(6→1)-α-D-galactopyranosyl-(6→1)-α-D-galactopyranoside (1), α-D-galactopyranosyl-(1→6)-α-D-galactopyranosyl-(1→6)-α-D-glucopyranosyl-(1→2)-β-D-fructofuranosyl-(4→1)-α-D-galactopyranoside (2), and α-D-galactopyranosyl-(1→2)-α-D-galactopyranosyl-(1→6)-α-D-galactopyranosyl-(1→6)-α-D-glucopyranosyl-(1→2)-β-D-fructofuranoside (3), raffinose (4), stachyose (5), verbascose (6), ajugose (7), umbelliferose (8), erlose (9), loliose (10), α-D-galactopyranosyl-(1→6)-α-D-galactopyranosyl-(1→6)-α-D-glucopyranosyl-(1→2)-β-D-fructofuranosyl-(1→1)-α-D-galactopyranoside (11), rehmaglupentasaccharide E (12), and rehmaglupentasaccharide F (13). All oligosaccharides with degrees of polymerization ranging from 3 to 6 were isolated from Scutellaria baicalensis Georgi for the first time. Compounds 1-3 are new compounds belonging to the non-classical raffinose-family oligosaccharides. Furthermore, compounds 11-13 are non-classical raffinose-family oligosaccharides and compounds 4-7 are raffinose-family oligosaccharides.

Scutellaria baicalensis Georgi  /  oligosaccharide  /  isolation  /  structural elucidation  /  non-classical raffinose family oligosaccharide
张宇婷, 宋娟, 刘思, 王睿哲, 陈晓娟, 梁海珍, 马百平. 中药黄芩中寡糖的分离纯化与结构鉴定. 药学学报, 2026 , 61 (6) : 2230 -2240 . DOI: 10.16438/j.0513-4870.2026-0183
Yu-ting ZHANG, Juan SONG, Si LIU, Rui-zhe WANG, Xiao-juan CHEN, Hai-zhen LIANG, Bai-ping MA. Isolation and structural elucidation of oligosaccharides from Scutellaria baicalensis Georgi[J]. Acta Pharmaceutica Sinica, 2026 , 61 (6) : 2230 -2240 . DOI: 10.16438/j.0513-4870.2026-0183
Year 2026 volume 61 Issue 6
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doi: 10.16438/j.0513-4870.2026-0183
  • Receive Date:2026-02-10
  • Online Date:2026-09-21
  • Published:2026-06-12
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  • Received:2026-02-10
  • Revised:2026-03-20
Affiliations
    1Guangdong Pharmaceutical University, Guangzhou 510006, China
    2Academy of Military Medical Sciences, Academy of Military Sciences, Beijing 100850, China
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表12种不同金属材料的力学参数
科
Family
属数
Number of
genus
种数
Number of
species
占总种数比例
Percentage of
total species (%)
属
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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