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Structural Characterization of Terpenoids from Abies holophylla Using Computational and Statistical Methods and Their Biological Activities

Authors
Kim, Chung SubOh, JoonseokSubedi, LalitaKim, Sun YeouChoi, Sang UnLee, Kang Ro
Issue Date
Aug-2018
Publisher
AMER CHEMICAL SOC
Citation
JOURNAL OF NATURAL PRODUCTS, v.81, no.8, pp.1795 - 1802
Journal Title
JOURNAL OF NATURAL PRODUCTS
Volume
81
Number
8
Start Page
1795
End Page
1802
URI
https://scholarworks.bwise.kr/gachon/handle/2020.sw.gachon/3536
DOI
10.1021/acs.jnatprod.8b00245
ISSN
0163-3864
Abstract
Three new diterpenoids (1-3) and three new triterpenoids (4-6) were isolated from the trunk of Abies holophylla together with 19 known terpenoids. The chemical structures of 1-6 were determined through NMR and MS data analyses. Also, the structural assignments of some of these compounds were verified and elucidated utilizing computational methods coupled with a statistical procedure (CP3, DP4, and DP4+). All the isolated compounds were evaluated for their cytotoxicity against four human cancer cell lines (A549, SK-OV-3, SK-MEL-2, and HCT-15). In addition, the compounds were tested for their anti-inflammatory effects in lipopolysaccharide-stimulated murine microglia BV2 cells by measuring nitric oxide levels, and for their neuroprotective activity in C6 cells through induction of nerve growth factor.
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