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篇名
Chemical constituents from a marine medicinal brown alga-derived Xylaria acuta SC1019   全文下載 全文下載
並列篇名
Chemical constituents from a marine medicinal brown alga-derived Xylaria acuta SC1019
英文摘要
In this study, a marine medicinal brown alga Sargassum cristaefolium-derived fungal strain Xylaria acuta SC1019 was isolated and identified. Column chromatography of the extracts from liquid- and solid-fermented products of the fungal strain was carried out, and led to the isolation of twenty-one compounds. Their structures were characterized by spectroscopic analysis, and the absolute configurations were further established by single X-ray diffraction analysis or modified Mosher's method as nine previously undescribed compounds, namely xylarilactones AeC (1e3), ent-gedebic acid 8-O-a-D-glucopyranoside (4), 5R-hydroxylmethylmellein 11-O-a-D-glucopyranoside (5), ent-hymatoxin E 16-O-a-Dmannopyranoside (6), 19,20-epoxycytochalasin S (7), 19,20-epoxycytochalasin T (8), and (2R)-butylitaconic acid (9), along with twelve known compounds 10e21. All the isolates were subjected to anti-inflammatory and anti-angiogenic assays. Compounds 1, 5, 7, 10, and 17 showed moderate nitric oxide production inhibitory activities in lipopolysaccharideactivated BV-2 microglial cells with IC50 values of 19.55±0.35, 16.10±0.57, 15.20±0.87, 11.76±0.49, and 11.30±0.32 mM, respectively, as compared to curcumin (IC50¼2.69±0.34 mM) without any significant cytotoxicity. Compounds 7, 8, and 21 displayed potent anti-angiogenic activities by suppressing the growth of human endothelial progenitor cells with IC50 values of 0.44±0.01, 0.47±0.03, and 0.53±0.01 mM, respectively, as compared to sorafenib (IC50¼5.50±1.50 mM).
起訖頁 155-167
關鍵詞 Anti-angiogenesisAnti-inflammationXylaria acutaXylariaceae
刊名 JOURNAL OF FOOD AND DRUG ANALYSIS  
期數 202406 (32:2期)
出版單位 衛生福利部食品藥物管理署
該期刊-上一篇 The role and mechanism of cinnamaldehyde in cancer
該期刊-下一篇 Comparative bioactivity assessment of bixin pigment and associated phytochemicals extracted from annatto seeds using conventional and green solvents
 

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