Antioxidant and free-radical scavenging activity of constituents of the leaves of Tachigalia paniculata

被引:43
作者
Cioffi, G
D'Auria, M
Braca, A
Mendez, J
Castillo, A
Morelli, I
De Simone, F
De Tommasi, N
机构
[1] Univ Pisa, Dipartimento Chim Bioorgan & Biofarm, I-56126 Pisa, Italy
[2] Univ Salerno, Dipartimento Sci Farmaceut, I-84084 Fisciano, SA, Italy
[3] Cent Univ Venezuela, Fac Ciencias, Escuela Quim, Grp Prod Nat,Ctr Quim Organ, Caracas 1020A, Venezuela
来源
JOURNAL OF NATURAL PRODUCTS | 2002年 / 65卷 / 11期
关键词
D O I
10.1021/np0200764
中图分类号
Q94 [植物学];
学科分类号
071001 ;
摘要
Two new myricetin glycosides, myricetin 7-O-beta-D-glucopyranosyl-(1-->6)-beta-D-glucopyranoside (1) and myricetin 7-O-alpha-L-rhamnopyranosyl-(1-->6)-beta-D-glucopyranoside (2), together with the known compounds quercetin 3-O-beta-D-glucopyranoside (3), quercetin 3-O-alpha-L-rhamnopyranoside (4), quercetin 3-O-beta-D-galactopyranoside (5), methyl gallate (6), isovanillin (7), 4-hydroxymethylbenzoate (8), 3,4-dihydroxymethylbenzoate (9), and caffeoyl aldehyde (10) were isolated from the leaves of Tachigalia paniculata. The structures of these compounds were determined by spectroscopic methods, Their antioxidant activity was determined by measuring free-radical scavenging effects using three different assays, namely, the Trolox Equivalent Antioxidant Capacity (TEAC) assay, the coupled oxidation of beta-carotene and linoleic acid (autoxidation assay), and the inhibition of xanthine oxidase activity. Compounds 1, 2, and 6 showed activity in the TEAC test, compounds 5-7 and 10 were moderately active in the autoxidation assay, while compounds 1 and 2 were the most potent of the isolates in the xanthine oxidase test.
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页码:1526 / 1529
页数:4
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