TY - JOUR
T1 - Furanocoumarins from the Roots of Angelica dahurica with Inhibitory Activity against Intracellular Reactive Oxygen Species Accumulation
AU - Kang, Unwoo
AU - Han, Ah Reum
AU - So, Yangkang
AU - Jin, Chang Hyun
AU - Ryu, Seung Mok
AU - Lee, Dongho
AU - Seo, Eun Kyoung
N1 - Funding Information:
This research was supported by a grant (14272MFDS279) funded by the Ministry of Food and Drug Safety in 2014.*%blankline%*
Publisher Copyright:
Copyright © 2019 American Chemical Society and American Society of Pharmacognosy.
PY - 2019/9/27
Y1 - 2019/9/27
N2 - 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.
AB - 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.
UR - http://www.scopus.com/inward/record.url?scp=85072584967&partnerID=8YFLogxK
U2 - 10.1021/acs.jnatprod.9b00547
DO - 10.1021/acs.jnatprod.9b00547
M3 - Article
C2 - 31464439
AN - SCOPUS:85072584967
SN - 0163-3864
VL - 82
SP - 2601
EP - 2607
JO - Journal of Natural Products
JF - Journal of Natural Products
IS - 9
ER -