Please use this identifier to cite or link to this item: https://dspace.ctu.edu.vn/jspui/handle/123456789/46369
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dc.contributor.authorNinh, Khac Ban-
dc.contributor.authorLuu, Hong Truong-
dc.contributor.authorTran, My Linh-
dc.contributor.authorNguyên, Chi Mai-
dc.contributor.authorDuong, Thi Hai Yen-
dc.contributor.authorVu, Van Doan-
dc.contributor.authorNguyên, Xuan Nhiem-
dc.contributor.authorBui, Huu Tai-
dc.contributor.authorPhan, Van Kiem-
dc.date.accessioned2021-03-11T01:09:13Z-
dc.date.available2021-03-11T01:09:13Z-
dc.date.issued2020-
dc.identifier.issn2525-2321-
dc.identifier.urihttps://dspace.ctu.edu.vn/jspui/handle/123456789/46369-
dc.description.abstractSeven phenolic compounds including (±)-erythro-1-(3',4',5'-trimethoxyphenyl)propane-l,2-diol (1), (±)-threo-1- (3',4',5'-trimethoxyphenyl) propane-l,2-diol (2), (R)-3-3-(3',4'-dimethoxyphenyl) propane-l,2-diol (3), (±)-3-(3',4',5'- trimethoxyphenyl) propane-1,2-diol (4), (+)-syringaresinol (5), (7S,8R,8'R)-5,5'-dimethoxylariciresinol (6), juniperoside (7) were isolated from the leaves of Trigonostemon honbaemis. Their chemical structures were determined using ESI-MS, 1D NMR, and 2D NMR spectra and in comparison with the reported literature. Compounds1- 7 were reported from Trigonoslemongemus for the first time. At concentration of 30 µM, compounds 1-7 exhibited weak cytotoxic activity with cell viability percentages as low as 73.3±0.87 % and 79.5±0.23 % on CAL-27 and MDA-MB231 cell lines, respectively.vi_VN
dc.language.isovivi_VN
dc.relation.ispartofseriesVietnam Journal of Chemistry;No.06, Vol.58 .- P.759-764-
dc.subjectTrigonostemon honbaensisvi_VN
dc.subjectPhenolicvi_VN
dc.subjectCytotoxic activityvi_VN
dc.titlePhenolic compounds from Trigonostemon honbaensis and their cytotoxic activityvi_VN
dc.typeArticlevi_VN
Appears in Collections:Vietnam Journal of Chemistry

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