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来自长囊马尾藻的七种未描述的半萜及其对淀粉样β蛋白聚集的抑制活性。

Seven undescribed meroterpenoids from Sargassum siliquastrum and their inhibitory activity against amyloid β aggregation.

作者信息

Sekiguchi Mitsuhiro, Horiuchi Mafumi, Tozawa Yuta, Shigemori Hideyuki

机构信息

Graduate School of Bioresources and Environmental Science, Ishikawa Prefectural University, 1-308 Suematsu, Nonoichi, Ishikawa, 921-8836, Japan.

Graduate School of Science and Technology, University of Tsukuba, 1-1-1 Tennodai, Tsukuba, Ibaraki, 305-8572, Japan.

出版信息

J Nat Med. 2025 Jan;79(1):73-81. doi: 10.1007/s11418-024-01847-6. Epub 2024 Oct 15.

Abstract

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.

摘要

抑制淀粉样β蛋白(Aβ)聚集以及降解Aβ聚集体是治疗和预防阿尔茨海默病的有前景的方法。在我们寻找Aβ42聚集抑制剂的过程中,我们从采集于日本能登半岛的褐藻(海带)中分离出了七种未描述过的半萜类化合物,即海带内酯A(1)-G(7)。我们利用光谱数据对分离出的半萜类化合物进行了结构解析,并使用硫黄素T测定法和透射电子显微镜对它们的活性进行了评估。在分离出的七种化合物中,海带内酯B具有最强的抑制活性。通过结构与活性的比较,烯烃的几何异构和异戊二烯侧链的长度对从褐藻中分离出的半萜类化合物的活性很重要。

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