Dicaffeoylquinic acid derivatives and flavonoid glucosides from glasswort (Salicornia herbacea L.) and their antioxidative activity

被引:106
作者
Kim, Jin Young [1 ,2 ,3 ]
Cho, Jeong-Yong [1 ,2 ,5 ,6 ]
Ma, Young-Kyu [1 ,2 ]
Park, Keun Young [1 ,2 ]
Lee, Sang-Hyun [4 ]
Ham, Kyung-Sik [5 ,6 ]
Lee, Hyoung Jae [1 ,2 ]
Park, Keun-Hyung [1 ,2 ]
Moon, Jae-Hak [1 ,2 ]
机构
[1] Chonnam Natl Univ, Dept Food Sci & Technol, Kwangju 500757, South Korea
[2] Chonnam Natl Univ, Funct Food Res Ctr, Kwangju 500757, South Korea
[3] JeollaNamdo Inst Hlth & Environm, Kwangju 502810, South Korea
[4] Chonnam Natl Univ, Korea Pear Res Org, Kwangju 500757, South Korea
[5] Mokpo Natl Univ, Dept Food Engn, Muan 534729, Jeonnam, South Korea
[6] Mokpo Natl Univ, Solar Salt Biotechnol Res Ctr, Muan 534729, Jeonnam, South Korea
关键词
Salicornia herbacea L; Dicaffeoylquinic acid derivatives; Salicornate; Flavonoid glucosides; Antioxidant; CAFFEIC ACID; IDENTIFICATION; CONSTITUENTS; GLYCOSIDES;
D O I
10.1016/j.foodchem.2010.08.035
中图分类号
O69 [应用化学];
学科分类号
070301 [无机化学];
摘要
Two novel antioxidant compounds, isoquercitrin 6 ''-O-methyloxalate (6) and methyl 4-caffeoy1-3-dihydrocaffeoyl quinate (salicornate, 7), were isolated from Salicornia herbacea L. Six known compounds were also identified as 3,5-dicaffeoylquinic acid (1), quercetin 3-O-B-D-glucopyranoside (2), 3-caffeoyl-4-dihydrocaffeoylquinic acid (3), methyl 3,5-dicaffeoyl quinate (4), 3.4-dicaffeoylquinic acid (5), and isorhamnetin 3-O-beta-D-glucopyranoside (8). Their chemical structures were determined by spectroscopic data from ESI-MS and NMR. The isolated dicaffeoylquinic acid derivatives (1, 3, 4, 5, and 7) showed similar activities for scavenging 1,1-diphenyl-2-picrylhydrazyl radicals and inhibiting formation of cholesteryl ester hydroperoxide during copper ion-induced rat blood plasma oxidation. The two flavonol glucosides (2 and 6), which have no substitutions in the B ring of their aglycones, also had similar activity. However, compound 8, which has the same structure as 2 except for the presence of a methoxyl group in the C-3' position of the B ring, showed predominantly lower antioxidant activity than the other isolated compounds. (C) 2010 Elsevier Ltd. All rights reserved.
引用
收藏
页码:55 / 62
页数:8
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