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NO inhibitory constituents as potential anti-neuroinflammatory agents for AD from Blumea balsamifera

Authors
Ma, JunRen, QuanhuiDong, BangjianShi, ZhaoyuZhang, JieJin, Da-QingXu, JingOhizumi, YasushiLee, DonghoGuo, Yuanqiang
Issue Date
Feb-2018
Publisher
ACADEMIC PRESS INC ELSEVIER SCIENCE
Keywords
Blumea balsamifera; Sesquiterpenoids; Diterpenoids; NO inhibitory activities; Molecular docking
Citation
BIOORGANIC CHEMISTRY, v.76, pp.449 - 457
Indexed
SCIE
SCOPUS
Journal Title
BIOORGANIC CHEMISTRY
Volume
76
Start Page
449
End Page
457
URI
https://scholar.korea.ac.kr/handle/2021.sw.korea/77426
DOI
10.1016/j.bioorg.2017.12.008
ISSN
0045-2068
Abstract
Our continuous search for new nitric oxide (NO) inhibitory substances as anti-neuroinflammatory agents for AD resulted in the isolation of one new labdane diterpenoid and three new guaiane sesquiterpenoids, as well as ten known compounds from Blumea balsamifera. Their structures were elucidated by NMR spectroscopic data analysis and the time-dependent density functional theory (TDDFT) electronic circular dichroism (ECD) calculations. The anti-neuroinflammatory effects were examined by inhibiting NO release in 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 iNOS protein. (C) 2017 Elsevier Inc. All rights reserved.
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