期刊
CHEMICAL & PHARMACEUTICAL BULLETIN
卷 64, 期 4, 页码 360-365出版社
PHARMACEUTICAL SOC JAPAN
DOI: 10.1248/cpb.c15-00830
关键词
Lumnitzera racemosa; Combretaceae; hepatoprotective; 1,1-dipheny1-2-picrylhydrazyl (DPPH)
资金
- JSPS KAKENHI [26460122, 00107385]
- Grants-in-Aid for Scientific Research [26460122] Funding Source: KAKEN
Phytochemical investigation of the n-BuOH fraction of the mangrove plant Lumnitzera racemosa WILLD. (Combretaceae) led to the isolation of one new flavonoid glycoside; myrcetin 3-0-methyl glucuronate (1), one new phenolic glycoside; lumniracemoside (2) and one new aliphatic alcohol glycoside; n-hexanol 1-0-rutinoside (3), in addition to seven known compounds (4-10). The structures of these compounds were determined by spectroscopic analyses (UV, IR, high resolution-electrospray ionization (HR-ESI)-MS, one-and two-dimensional (1D- and 2D)-NMR). Compound 7 showed the highest hepatoprotective activity against acetaminophen-induced hepatotoxicity using human HepG2 cells at protection % value of 34.2 +/- 3.1%, while compounds 1, 2, 3, 6, and 9 showed weak to moderate hepatoprotective activity (11.6-18.9%). Almost all of these compounds showed stronger 1,1-diphenyl-2-picrylhydrazyl (DPPH) radical scavenging activity compared with the standard Trolox. These results suggest the usefulness of this plant extract and the isolated compounds as promising hepatoprotective agents.
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