Wei Feng, Ma Lin-Yun, Jin Wen-Tao, Ma Shuang-Cheng, Han Guo-Zhu, Khan Ikhlas Ahmad, Lin Rui-Chao
Division of Chinese Materia Medica and Natural Products, National Institute for the Control of Pharmaceutical and Biological Products, State Food and Drug Administration, Beijing, Peoples's Republic of China.
Chem Pharm Bull (Tokyo). 2004 Oct;52(10):1246-8. doi: 10.1248/cpb.52.1246.
Phytochemical study of the ethanol extract of the seeds of Aesculus chinensis led to the isolation of a new triterpenoid saponin (6), together with five known triterpenoid saponins (1-5). The structure of the new compound was elucidated on the basis of spectral data to be 21,28-di-O-acetylprotoaescigenin-3-O-[beta-D-glucopyranosyl(1-2)][beta-D-glucopyranosyl(1-4)]-beta-D-glucopyranosiduronic acid (aesculiside A, 6). The antiinflammatory activities of the four main saponins (1-4) were compared with those of total saponin extracts, and single saponins showed more potent activity than total saponin extracts in mice.
对七叶树种子乙醇提取物进行的植物化学研究,分离得到了一种新的三萜皂苷(6),以及五种已知的三萜皂苷(1 - 5)。基于光谱数据阐明该新化合物的结构为21,28 - 二 - O - 乙酰原七叶皂苷元 - 3 - O - [β - D - 吡喃葡萄糖基(1→2)][β - D - 吡喃葡萄糖基(1→4)]-β - D - 吡喃葡萄糖醛酸苷(七叶皂苷A,6)。比较了四种主要皂苷(1 - 4)与总皂苷提取物的抗炎活性,在小鼠中单一皂苷显示出比总皂苷提取物更强的活性。