Eudesmane glycosides from Ambrosia artemisiifolia (common Ragweed) as potential neuroprotective agents

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dc.contributor.authorJ P An-
dc.contributor.authorT K Q Ha-
dc.contributor.authorH W Kim-
dc.contributor.authorB Ryu-
dc.contributor.authorJ Kim-
dc.contributor.authorJ Park-
dc.contributor.authorChul Ho Lee-
dc.contributor.authorW K Oh-
dc.date.accessioned2019-07-10T01:23:32Z-
dc.date.available2019-07-10T01:23:32Z-
dc.date.issued2019-
dc.identifier.issn0163-3864-
dc.identifier.uri10.1021/acs.jnatprod.8b00841ko
dc.identifier.urihttps://oak.kribb.re.kr/handle/201005/18805-
dc.description.abstractIn Alzheimer's disease, amyloid-β (Aβ) accumulation in the brain results in neuronal cell death and is one of the major causes of dementia. Because the current therapeutic agents are not yet sufficiently effective or safe, there have been attempts to find new neuroprotective chemicals against Aβ-induced cytotoxicity. A 70% EtOH extract of whole plants of Ambrosia artemisiifolia (common ragweed) was selected after the screening of a natural extract library. Seven new eudesmane-type glycosides (1-7) and seven known compounds (8-14) were obtained through bioactivity-guided fractionation from the aerial parts of this plant. Their structures were determined on the basis of their nuclear magnetic resonance spectra, high-resolution electrospray ionization mass spectrometry analysis, and electronic circular dichroism calculations. Among them, compounds 1, 2, 4-6, 8, 9, 11, 13, and 14 showed protective effects against Aβ-induced cytotoxicity in Aβ42-transfected HT22 cells. The most active compounds, 5 and 6, exhibited moderate protective activity dose-dependently (10, 20, and 40 μM).-
dc.publisherAmer Chem Soc-
dc.titleEudesmane glycosides from Ambrosia artemisiifolia (common Ragweed) as potential neuroprotective agents-
dc.title.alternativeEudesmane glycosides from Ambrosia artemisiifolia (common Ragweed) as potential neuroprotective agents-
dc.typeArticle-
dc.citation.titleJournal of Natural Products-
dc.citation.number5-
dc.citation.endPage1138-
dc.citation.startPage1128-
dc.citation.volume82-
dc.contributor.affiliatedAuthorChul Ho Lee-
dc.contributor.alternativeName안진표-
dc.contributor.alternativeNameHa-
dc.contributor.alternativeName김현우-
dc.contributor.alternativeName류별-
dc.contributor.alternativeName김진웅-
dc.contributor.alternativeName박준수-
dc.contributor.alternativeName이철호-
dc.contributor.alternativeName오원근-
dc.identifier.bibliographicCitationJournal of Natural Products, vol. 82, no. 5, pp. 1128-1138-
dc.identifier.doi10.1021/acs.jnatprod.8b00841-
dc.description.journalClassY-
Appears in Collections:
Ochang Branch Institute > Division of National Bio-Infrastructure > 1. Journal Articles
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