New isoflavone glycosides from Iris spuria L. (Calizona) cultivated in Egypt

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作者
Salwa F. Farag
Yuka Kimura
Hideyuki Ito
Junko Takayasu
Harukuni Tokuda
Tsutomu Hatano
机构
[1] Assiut University,Pharmacognosy Department, Faculty of Pharmacy
[2] Okayama University Graduate School of Medicine,Division of Pharmaceutical Sciences
[3] Dentistry and Pharmaceutical Sciences,Department of Molecular Biochemistry
[4] Kyoto Prefectural University of Medicine,undefined
来源
Journal of Natural Medicines | 2009年 / 63卷
关键词
Auronol; Iridaceae; Isoflavone glycosides; Phenolic acid glycosides; Phenylpropanoid glycoside;
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摘要
Two new isoflavone glycosides, tectorigenin 7-O-β-d-glucopyranoside-4′-O-[β-d-glucopyranosyl-(1″″ → 6′′′)-β-d-glucopyranoside] (1) and iristectorigenin B 4′-O-[β-d-glucopyranosyl-(1′′′ → 6″)-β-d-glucopyranoside] (2), together with 11 known compounds, including six isoflavones, tectorigenin 7-O-β-d-glucopyranoside-4′-O-β-d-glucopyranoside (3), tectorigenin 4′-O-[β-d-glucopyranosyl-(1′′′ → 6″)-β-d-glucopyranoside] (4), tectorigenin 7-O-β-d-glucopyranoside (5), genistein 7-O-β-d-glucopyranoside (6), tectorigenin 4′-O-β-d-glucopyranoside (7), and tectorigenin (8); two phenolic acid glycosides, vanillic acid 4-O-β-d-glucopyranoside (9) and glucosyringic acid (10); a phenylpropanoid glycoside, E-coniferin (11); an auronol derivative, maesopsin 6-O-β-d-glucopyranoside (12); and a pyrrole derivative, 4-(2-formyl-5-hydroxymethylpyrrol-1-yl) butyric acid (13), were isolated from fresh Iris spuria (Calizona) rhizomes. The structures of these compounds were established on the basis of spectroscopic and chemical evidence. Inhibitory effects on the activation of Epstein–Barr virus early antigen were examined for compounds 1–8 and 12.
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