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Furanocoumarins from the Roots of Angelica dahurica with Inhibitory Activity against Intracellular Reactive Oxygen Species Accumulation

Authors
Kang, UnwooHan, Ah-ReumSo, YangkangJin, Chang HyunRyu, Seung MokLee, DonghoSeo, Eun Kyoung
Issue Date
Sep-2019
Publisher
AMER CHEMICAL SOC
Citation
JOURNAL OF NATURAL PRODUCTS, v.82, no.9, pp.2601 - 2607
Indexed
SCIE
SCOPUS
Journal Title
JOURNAL OF NATURAL PRODUCTS
Volume
82
Number
9
Start Page
2601
End Page
2607
URI
https://scholar.korea.ac.kr/handle/2021.sw.korea/63022
DOI
10.1021/acs.patprod.9b00547
ISSN
0163-3864
Abstract
Five new furanocoumarins, dahuribirin H (1), dahuribirin I (2), (2'S)-(+)-5-(2'-hydroxy-3'-methylbut-3'enyloxy)-8-(3 ''-methylbut-2 ''-enyloxy)psoralen (3), (2'R)(+)-5-(2',3'-epoxy-3'-methylbutoxy)-8-(3"-methylbut-2 ''- enyloxy)psoralen (4), and 5-methoxy-8((Z)-4'-(3 ''-methylbutanoate)-3'-methylbut-2'-enyloxy)psoralen (5), along with 15 known compounds (6-20), were isolated from the roots of Angelica dahurica. The structures of the new compounds were elucidated by spectroscopic analysis, along with electronic circular dichroism calculations and Mosher ester analysis. Compounds 3, 4, 11, 13, and 16 reduced H2O2-induced cell death in HepG2 cells and attenuated reactive oxygen species (ROS) formation without showing cytotoxicity, suggesting that these compounds might have cytoprotective effects against H2O2-induced oxidative damage via ROS scavenging activities.
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