A new hemiterpene glycoside from the ripe tomatoes

被引:3
|
作者
Ono, Masateru [1 ]
Yasuda, Shin [1 ]
Shiono, Yuki [1 ]
Furusawa, Chisato [1 ]
Inaba, Shinya [1 ]
Tanaka, Takayuki [1 ]
Ikeda, Tsuyoshi [2 ]
Nohara, Toshihiro [2 ]
机构
[1] Tokai Univ, Sch Agr, Kumamoto 8691404, Japan
[2] Sojo Univ, Fac Pharmaceut Sci, Nishi Ku, Kumamoto, Japan
基金
日本学术振兴会;
关键词
Lycopersicon esculentum; tomato; Solanaceae; hemiterpene glycoside; radical-scavenging effect; STEROIDAL ALKALOID GLYCOSIDES; CHERRY TOMATO; ESCULEOSIDE; FRUITS; CONSTITUENTS; SAPONIN; LEAVES; SHIFTS; PLANTS;
D O I
10.1080/14786419.2014.974053
中图分类号
O69 [应用化学];
学科分类号
081704 ;
摘要
[GRAPHICS] A new hemiterpene glycoside (1) was isolated from ripe tomatoes (the fruit of Lycopersicon esculentum, Solanaceae) along with eight known compounds. The chemical structure of 1 was determined to be 2-methylbutan-1-ol beta-d-glucopyranosyl-(1 -> 6)-beta-d-glucopyranoside, based on spectroscopic data as well as chemical evidence. In addition, the radical-scavenging activities of the isolated compounds on the free radical of 1,1-diphenyl-2-picrylhydrazyl were examined. Among the tested compounds, tryptophan, 4-O-beta-d-glucopyranosyl caffeic acid and dihydro-p-coumaryl alcohol gamma-O-beta-d-glucopyranoside demonstrated 42.0%, 50.1% and 76.0% scavenging activities, respectively, at a concentration of 0.5mM.
引用
收藏
页码:262 / 267
页数:6
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