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Isolation of two new bioactive sesquiterpene lactone glycosides from the roots of Ixeris dentata

Authors
Park, SeonJuNguyen Xuan NhiemLee, Taek HwanKim, NanyoungKim, Sun YeouChae, Han-JungKim, Seung Hyun
Issue Date
15-Oct-2015
Publisher
PERGAMON-ELSEVIER SCIENCE LTD
Keywords
Ixeris dentata; Sesquiterpene lactone glycosides; Nitric oxide (NO); BV-2 cell; H-1 NMR; C-13 NMR
Citation
BIOORGANIC & MEDICINAL CHEMISTRY LETTERS, v.25, no.20, pp.4562 - 4566
Journal Title
BIOORGANIC & MEDICINAL CHEMISTRY LETTERS
Volume
25
Number
20
Start Page
4562
End Page
4566
URI
https://scholarworks.bwise.kr/gachon/handle/2020.sw.gachon/10032
DOI
10.1016/j.bmcl.2015.08.061
ISSN
0960-894X
Abstract
Two new sesquiterpene lactone glycosides, 3-O-beta-D-glucopyranosyl-8-hydroxy-(1,5,6,7,11)-guaia-3,10 (14)-dien-12,6-olide (1) and 3-O-beta-D-glucopyranosyl-8-(4-hydroxyphenylacetyloxy)-(1.5.6,7)-guaia-3,10(14), 11(13)-trien-12,6-olide (2), and 12 known sesquiterpene lactone derivatives (3-14) were isolated from the roots of Ixeris dentata. Their structures were determined by extensive spectroscopic methods including 1D and 2D NMR and MS spectra data. All compounds were tested for their ability to inhibit lipopolysaccharide (LPS)-induced nitric oxide (NO) production in BV-2 microglial cell. 3-O-bD- Glucopyranosyl-8-(4-hydroxyphenylacetyloxy)-(1.5.6,7)-guaia-3,10(14), 11(13)-trien-12,6-olide (2) showed the most potent inhibitory activity at a concentration of 20 mu M. (C) 2015 Elsevier Ltd. All rights reserved.
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