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DC Field | Value | Language |
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dc.contributor.author | Chokchaisiri S. | |
dc.contributor.author | Apiratikul N. | |
dc.contributor.author | Rukachaisirikul T. | |
dc.date.accessioned | 2021-04-05T03:01:14Z | - |
dc.date.available | 2021-04-05T03:01:14Z | - |
dc.date.issued | 2020 | |
dc.identifier.issn | 14786419 | |
dc.identifier.other | 2-s2.0-85091316694 | |
dc.identifier.uri | https://ir.swu.ac.th/jspui/handle/123456789/11793 | - |
dc.identifier.uri | https://www.scopus.com/inward/record.uri?eid=2-s2.0-85091316694&doi=10.1080%2f14786419.2018.1540477&partnerID=40&md5=6ab9499e170493ef5f113ad781d21db8 | |
dc.description.abstract | A new ent-abietane lactone, 3-oxojolkinolide A (1), together with 16 known compounds, helioscopinolide E (2), helioscopinolide A (3), 3-methyl-9H-carbazole (4), carbalexin (5), carbalexin B (6), glycaborinine (7), arborinine (8), 1H-indole-3-carbaldehyde (9), glycoamide A (10), glycoamide B (11), 2-(N-methyl-2-phenylacetamido)benzoic acid (12), 2-(methylamine)-methylbenzoate (13), fraxidin (14), scopoletin (15), (-)-syringaresinol (16) and ferulic acid (17) were isolated from Glycosmis pentaphylla. The structures of these compounds were elucidated using spectroscopic techniques such as NMR and MS. Among them, compounds 1–3, 9 and 12-17 were isolated from the genus Glycosmis for the first time. © 2018 Informa UK Limited, trading as Taylor & Francis Group. | |
dc.rights | Srinakharinwirot University | |
dc.subject | ent abietane lactone | |
dc.subject | plant extract | |
dc.subject | unclassified drug | |
dc.subject | antineoplastic agent | |
dc.subject | coumaric acid | |
dc.subject | ferulic acid | |
dc.subject | indole derivative | |
dc.subject | indole-3-carbaldehyde | |
dc.subject | lactone | |
dc.subject | Article | |
dc.subject | cytotoxicity | |
dc.subject | drug identification | |
dc.subject | drug isolation | |
dc.subject | Glycosmis pentaphylla | |
dc.subject | human | |
dc.subject | human cell | |
dc.subject | IC50 | |
dc.subject | mass spectrometry | |
dc.subject | nuclear magnetic resonance | |
dc.subject | Rutaceae | |
dc.subject | spectroscopy | |
dc.subject | chemical structure | |
dc.subject | chemistry | |
dc.subject | drug screening | |
dc.subject | HeLa cell line | |
dc.subject | HT-29 cell line | |
dc.subject | isolation and purification | |
dc.subject | MCF-7 cell line | |
dc.subject | nuclear magnetic resonance spectroscopy | |
dc.subject | Abietanes | |
dc.subject | Antineoplastic Agents, Phytogenic | |
dc.subject | Coumaric Acids | |
dc.subject | Drug Screening Assays, Antitumor | |
dc.subject | HeLa Cells | |
dc.subject | HT29 Cells | |
dc.subject | Humans | |
dc.subject | Indoles | |
dc.subject | Lactones | |
dc.subject | Magnetic Resonance Spectroscopy | |
dc.subject | MCF-7 Cells | |
dc.subject | Molecular Structure | |
dc.subject | Rutaceae | |
dc.title | A new ent-abietane lactone from Glycosmis pentaphylla | |
dc.type | Article | |
dc.rights.holder | Scopus | |
dc.identifier.bibliograpycitation | Natural Product Research. Vol 34, No.21 (2020), p.3019-3026 | |
dc.identifier.doi | 10.1080/14786419.2018.1540477 | |
Appears in Collections: | Scopus 1983-2021 |
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