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Nitric oxide inhibitory daphnane diterpenoids as potential anti-neuroinflammatory agents for AD from the twigs of Trigonostemon thyrsoideus

Authors
Liu, FengYang, XueyuanMa, JunYang, YulingXie, ChunfengTuerhong, MuhetaerJin, Da-QingXu, JingLee, DonghoOhizumi, YasushiGuo, Yuanqiang
Issue Date
11월-2017
Publisher
ACADEMIC PRESS INC ELSEVIER SCIENCE
Keywords
Anti-neuroinflammatory; NO inhibitors; Trigonostemon thyrsoideus; Daphnane diterpenoids; Molecular docking
Citation
BIOORGANIC CHEMISTRY, v.75, pp.149 - 156
Indexed
SCIE
SCOPUS
Journal Title
BIOORGANIC CHEMISTRY
Volume
75
Start Page
149
End Page
156
URI
https://scholar.korea.ac.kr/handle/2021.sw.korea/81778
DOI
10.1016/j.bioorg.2017.09.007
ISSN
0045-2068
Abstract
The extensive pathology studies revealed that Alzheimer's disease (AD) is closely related to neuroinflammation and anti-neuroinflammatory agents may be potentially useful for the treatment of AD. A continuous search for new nitric oxide (NO) inhibitory compounds as anti-neuroinflammatory agents for AD resulted in the isolation of four new (1 - 4) and eight known (5 - 12) daphnane diterpenoids from the twigs of Trigonostemon thyrsoideus. Their structures were elucidated on the basis of extensive nuclear magnetic resonance (NMR) spectroscopic data analysis and the time-dependent density functional theory (TDDFT) electronic circular dichroism (ECD) calculations. Compounds 1-4 represent new examples of daphnane diterpenoid orthoesters and 4 features a rare and complex macroring diterpenoid structure. The anti-neuroinflammatory effects were examined by inhibiting NO release in lipopolysaccharide (LPS)-induced murine microglial BV-2 cells. The possible mechanism of NO inhibition of some bioactive compounds was also investigated using molecular docking, which revealed the interactions of bioactive compounds with the inducible nitric oxide synthase (iNOS) protein. (C) 2017 Elsevier Inc. All rights reserved.
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