马尾藻中七种未曾描述过的 Meroterpenoids 及其对淀粉样蛋白 β 聚集的抑制活性。

IF 2.5 4区 医学 Q3 CHEMISTRY, MEDICINAL Journal of Natural Medicines Pub Date : 2024-10-15 DOI:10.1007/s11418-024-01847-6
Mitsuhiro Sekiguchi, Mafumi Horiuchi, Yuta Tozawa, Hideyuki Shigemori
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引用次数: 0

摘要

抑制淀粉样β(Aβ)聚集和降解Aβ聚集体是治疗和预防阿尔茨海默病的有效方法。在寻找 Aβ42 聚集抑制剂的过程中,我们从日本能登半岛采集的褐藻(Sargassum siliquastrum)中分离出了七种未曾描述过的美拉德萜类化合物--马尾藻内酯 A (1)-G (7)。我们利用光谱数据从结构上阐明了分离出的经萜类化合物,并利用硫黄素 T 试验和透射电子显微镜评估了它们的活性。在分离出的 7 个化合物中,马钱子内酯 B 的抑制活性最强。从结构和活性的比较来看,烯烃的几何异构性和异戊二烯侧链的长度对从褐藻中分离出的美拉皮内酯的活性非常重要。
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Seven undescribed meroterpenoids from Sargassum siliquastrum and their inhibitory activity against amyloid β aggregation.

The inhibition of amyloid β (Aβ) aggregation and degradation of Aβ aggregates are promising approaches for treating and preventing Alzheimer's disease. In our search for Aβ42 aggregation inhibitors, we isolated seven undescribed meroterpenoids, sargasilides A (1)‒G (7), from brown alga (Sargassum siliquastrum) collected at Noto Peninsula in Japan. We structurally elucidated the isolated meroterpenoids using spectroscopic data and evaluated their activities using Thioflavin T assay and transmission electron microscopy. Among the seven compounds isolated, sargasilide B had the strongest inhibitory activity. From the comparison of structure and activity, the geometric isomerism of olefins and length of isoprene side chains are important for the activity of meroterpenoids isolated from brown alga.

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来源期刊
CiteScore
6.90
自引率
3.00%
发文量
79
审稿时长
1.7 months
期刊介绍: The Journal of Natural Medicines is an international journal publishing original research in naturally occurring medicines and their related foods and cosmetics. It covers: -chemistry of natural products -biochemistry of medicinal plants -pharmacology of natural products and herbs, including Kampo formulas and traditional herbs -botanical anatomy -cultivation of medicinal plants. The journal accepts Original Papers, Notes, Rapid Communications and Natural Resource Letters. Reviews and Mini-Reviews are generally invited.
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