Isolation of three new meroterpenoids and seven known compounds from Albatrellus yasudae and their Aβ-aggregation inhibitory activity

被引:11
作者
Akiba, Megumi [1 ]
Kinoshita, Kaoru [1 ]
Kino, Yoshihiro [2 ]
Sato, Jun-ichi [2 ]
Koyama, Kiyotaka [1 ]
机构
[1] Meiji Pharmaceut Univ, Dept Pharmacognosy & Phytochem, 2-552-1 Noshio, Kiyose, Tokyo 2048588, Japan
[2] Meiji Pharmaceut Univ, Dept Bioinformat, 2-552-1 Noshio, Kiyose, Tokyo 2048588, Japan
关键词
Alzheimer's disease (AD); Amyloid beta aggregation; Thioflavin T; Mushroom; Albatrellus yasudae; Meroterpenoid; DERIVATIVES;
D O I
10.1016/j.bmcl.2019.126808
中图分类号
R914 [药物化学];
学科分类号
100701 ;
摘要
Alzheimer's disease is a serious neurologic disorder that cannot be cured completely. In this study, we targeted compounds that inhibit amyloid-beta (A beta) aggregation, based on the amyloid cascade hypothesis. Ten compounds (1-10) were isolated from CHCl3 extracts of the mushroom Albatrellus yasudae using A beta-aggregation inhibitory activity-guided separation. The structures of these compounds were elucidated from 1D and 2D NMR and MS spectral data. Compounds 1-3 were novel, whereas 4-10 were identified as the known compounds grifolin, grifolic acid, neogrifolin, confluentin, 2-hydroxyneogrifolin, daurichromenic acid, and a cerebroside derivative. Compounds 1-10 were tested for A beta-aggregation inhibitory activity. Compounds 1, 3, 5, 6, 8, and 9 have potential as A beta-aggregation inhibitory activity.
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页数:3
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