| Literature DB >> 31203103 |
Changxing Qi1, Qun Zhou1, Weixi Gao1, Mengting Liu1, Chunmei Chen1, Xiao-Nian Li2, Yongji Lai3, Yuan Zhou1, Dongyan Li4, Zhengxi Hu5, Hucheng Zhu6, Yonghui Zhang7.
Abstract
Spiroterreusnoids A-F, six undescribed spiro-dioxolane-containing adducts bearing 3,5-dimethylorsellinic acid-based meroterpenoid and 2,3-butanediol moieties were isolated from the endophytic fungus Aspergillus terreus Thom from Tripterygium wilfordii Hook. f. (Celastraceae). The structures of these adducts were established by spectroscopy, single-crystal X-ray diffraction, and experimental electronic circular dichroism (ECD) measurements. Spiroterreusnoids A-F represent the first examples of adducts composed of 3,5-dimethylorsellinic acid-based meroterpenoids. It is noteworthy that spiroterreusnoids A-F possessing a spiro-dioxolane moiety exhibited potential abilities in inhibiting BACE1 (IC50 values ranging from 5.86 to 27.16 μM) and AchE (IC50 values ranging from 22.18 to 32.51 μM), while the other analogues without this fragment displayed no such activities. Taken together, spiroterreusnoids A-F represent the first multitargeted natural adducts that could inhibit BACE1 and AchE, and might provide a new template for the development of new anti-Alzheimer's disease drugs.Entities:
Keywords: 3,5-Dimethylorsellinic acid-based meroterpenoid; Adducts; Alzheimer's disease; Aspergillus terreus Thom; endophytic fungus
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Year: 2019 PMID: 31203103 DOI: 10.1016/j.phytochem.2019.05.014
Source DB: PubMed Journal: Phytochemistry ISSN: 0031-9422 Impact factor: 4.072