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Bioorg Med Chem Lett ; 30(2): 126808, 2020 01 15.
Article in English | MEDLINE | ID: mdl-31791817

ABSTRACT

Alzheimer's disease is a serious neurologic disorder that cannot be cured completely. In this study, we targeted compounds that inhibit amyloid-beta (Aß) aggregation, based on the amyloid cascade hypothesis. Ten compounds (1-10) were isolated from CHCl3 extracts of the mushroom Albatrellus yasudae using Aß-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 Aß-aggregation inhibitory activity. Compounds 1, 3, 5, 6, 8, and 9 have potential as Aß-aggregation inhibitory activity.


Subject(s)
Amyloid beta-Peptides/antagonists & inhibitors , Basidiomycota/chemistry , Resorcinols/chemistry , Terpenes/chemistry , Alzheimer Disease/metabolism , Alzheimer Disease/pathology , Amyloid beta-Peptides/metabolism , Basidiomycota/metabolism , Humans , Magnetic Resonance Spectroscopy , Mass Spectrometry , Molecular Conformation , Resorcinols/metabolism , Terpenes/metabolism
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