| Literature DB >> 25421719 |
Masateru Ono1, Shin Yasuda, Yuki Shiono, Chisato Furusawa, Shinya Inaba, Takayuki Tanaka, Tsuyoshi Ikeda, Toshihiro Nohara.
Abstract
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 β-d-glucopyranosyl-(1 → 6)-β-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-β-d-glucopyranosyl caffeic acid and dihydro-p-coumaryl alcohol γ-O-β-d-glucopyranoside demonstrated 42.0%, 50.1% and 76.0% scavenging activities, respectively, at a concentration of 0.5 mM.Entities:
Keywords: Lycopersicon esculentum; Solanaceae; hemiterpene glycoside; radical-scavenging effect; tomato
Mesh:
Substances:
Year: 2014 PMID: 25421719 DOI: 10.1080/14786419.2014.974053
Source DB: PubMed Journal: Nat Prod Res ISSN: 1478-6419 Impact factor: 2.861