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dc.contributor.authorNguyen, Ngoc Hieu-
dc.contributor.authorHà, Thị Kim Quy-
dc.contributor.authorVu, Tien Chinh-
dc.contributor.authorTran, The Bach-
dc.contributor.authorLee, Chul Ho-
dc.contributor.authorEum, Sangmi-
dc.contributor.authorChoi, Sangho-
dc.contributor.authorOh, Won Keun-
dc.date.accessioned2018-11-20T03:39:06Z-
dc.date.available2018-11-20T03:39:06Z-
dc.date.issued2016-
dc.identifier.urihttp://localhost:8080//jspui/handle/123456789/4996-
dc.description.abstractFive acetophenones bearing spiroketal-hexofuranoside rings, one di-C-glycosidic acetophenone and two benzopyrans, along with 16 known compounds were isolated from the leaves of Melicope pteleifolia. Structures of all the isolates were elucidated using extensive spectroscopic methods, including 1D, 2DNMR and HRESIMS. All the isolates were also evaluated for their neuraminidase inhibitory activities against H1N1, H9N2, wild-type H1N1 and oseltamivir-resistant H1N1 (H274Y mutation) virus strains. Of the isolates, tamarixetin 3-robinobioside was found to exhibit the strongest enzymatic inhibition (IC50 24.93 ± 3.46, 23.19 ± 5.41, 26.67 ± 5.16 and 40.16 ± 4.50 µM, respectively). Selected candidates, kaempferol 3-robinobioside, kaempferol 3-O-β-D-glucopyranosyl (1/2)-α-D-xylopyranoside and tamarixetin 3-robinobioside, also showed moderate reductions in H1N1-induced cytopathic effects on MDCK cells.vi_VN
dc.language.isoenvi_VN
dc.relation.ispartofseriesPhytochemistry;130 .- p.291–300-
dc.subjectMelicope pteleifoliavi_VN
dc.subjectRutaceaevi_VN
dc.subjectSpiroketalvi_VN
dc.subjectNeuraminidasevi_VN
dc.subjectH1N1vi_VN
dc.titleChemical constituents from Melicope pteleifolia leavesvi_VN
dc.typeArticlevi_VN
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