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Anti-Helicobacter pylori compounds from Maackia amurensis

Authors
Park, W.S.Bae, J.-Y.Kim, H.J.Kim, M.G.Lee, W.-K.Kang, H.-L.Baik, S.-C.Lim, K.M.Lee, M.K.Ahn, M.-J.
Issue Date
2015
Publisher
Korean Society of Pharmacognosy
Keywords
(?)-Medicarpin; Anti-Helicobacter pylori activity; Maackia amurensis; Tectorigenin
Citation
Natural Product Sciences, v.21, no.1, pp 49 - 53
Pages
5
Indexed
SCOPUS
KCI
Journal Title
Natural Product Sciences
Volume
21
Number
1
Start Page
49
End Page
53
URI
https://scholarworks.gnu.ac.kr/handle/sw.gnu/18383
ISSN
1226-3907
Abstract
Eight isoflavonoid compounds were isolated from the EtOAc fraction of Maackia amurensis which had shown the highest anti-Helicobacter pylori activity among the fractions, using medium pressure liquid chromatography and recrystallization. Based on the spectroscopic data including1H-NMR,13C-NMR, HMBC and MS data, the chemical structures of the isolates were determined to be (?)-medicarpin (1), afromosin (2), formononetin (3), tectorigenin (4), prunetin (5), wistin (6), tectoridin (7) and ononin (8). Anti-H. pylori activity of each compound was evaluated with broth dilution assay. As a result, (?)-medicarpin (1), tectorigenin (4) and wistin (6) showed anti-H. pylori activity. (?)-Medicarpin (1) exhibited the most potent growth inhibitory activity against H. pylori with the minimal inhibitory concentration (MIC)90 of 25 ?M, and tectorigenin (4) with MIC90 of 100 ?M ranked the second. This is the first study to show the anti-H. pylori activity of M. amurensis, and it is suggested that the stem bark of M. amurensis or the EtOAc fraction or the isolated compounds can be a new natural source for the treatment of H. pylori infection. ? 2015, Korean Society of Pharmacognosy. All rights reserved.
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