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DC Field | Value | Language |
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dc.contributor.author | Namdaung U. | |
dc.contributor.author | Aroonrerk N. | |
dc.contributor.author | Suksamrarn S. | |
dc.contributor.author | Danwisetkanjana K. | |
dc.contributor.author | Saenboonrueng J. | |
dc.contributor.author | Arjchomphu W. | |
dc.contributor.author | Suksamrarn A. | |
dc.date.accessioned | 2021-04-05T04:32:18Z | - |
dc.date.available | 2021-04-05T04:32:18Z | - |
dc.date.issued | 2006 | |
dc.identifier.issn | 92363 | |
dc.identifier.other | 2-s2.0-33749414443 | |
dc.identifier.uri | https://ir.swu.ac.th/jspui/handle/123456789/14996 | - |
dc.identifier.uri | https://www.scopus.com/inward/record.uri?eid=2-s2.0-33749414443&doi=10.1248%2fcpb.54.1433&partnerID=40&md5=1a38fadda1c1d8a2295eb34703c70a27 | |
dc.description.abstract | Investigation of the chemical constituents of the root bark of Artocarpus rigidus BLUME subsp. rigidus has led to the isolation of six, structurally diverse phenolic compounds. These included two new compounds with modified skeletons, the flavonoid 7-demethylartonol E (1) and the chromone artorigidusin (2), together with four known phenolic compounds, the xanthone artonol B (3), the flavonoid artonin F (4), the flavonoid cycloartobiloxanthone (5), and the xanthone artoindonesianin C (6). Compounds 1, 4, and 5 exhibited antiplasmodial activity against Plasmodium falciparum. All compounds showed antimycobacterial activity against Mycobacterium tuberculosis, with 4 being the most active compound (MIC 6.25 μg/ml). Compounds 5 and 6 were active against KB cells, whereas 2, 5, and 6 showed varying toxicity to BC cells. Compounds 1-3, 5, and 6 were active in the NCIH187 cytotoxicity assay, with 3 being the most active compound (IC50 1.26 μg/ml). © 2006 Pharmaceutical Society of Japan. | |
dc.subject | 7 demethylartonol e | |
dc.subject | Artocarpus rigidus extract | |
dc.subject | artoindonesianin c | |
dc.subject | artonin F | |
dc.subject | artonol B | |
dc.subject | chromone artorigidusin | |
dc.subject | cycloartobiloxanthone | |
dc.subject | flavanoid | |
dc.subject | phenol derivative | |
dc.subject | plant extract | |
dc.subject | unclassified drug | |
dc.subject | xanthone derivative | |
dc.subject | antimicrobial activity | |
dc.subject | article | |
dc.subject | bark | |
dc.subject | breadfruit | |
dc.subject | carbon nuclear magnetic resonance | |
dc.subject | concentration response | |
dc.subject | controlled study | |
dc.subject | cytotoxicity | |
dc.subject | drug structure | |
dc.subject | human | |
dc.subject | human cell | |
dc.subject | IC 50 | |
dc.subject | minimum inhibitory concentration | |
dc.subject | Mycobacterium tuberculosis | |
dc.subject | nonhuman | |
dc.subject | plant root | |
dc.subject | Plasmodium falciparum | |
dc.subject | proton nuclear magnetic resonance | |
dc.subject | structure activity relation | |
dc.subject | Animals | |
dc.subject | Artocarpus | |
dc.subject | Cell Line, Tumor | |
dc.subject | Cell Proliferation | |
dc.subject | Chromones | |
dc.subject | Drug Screening Assays, Antitumor | |
dc.subject | Flavonoids | |
dc.subject | Humans | |
dc.subject | Magnetic Resonance Spectroscopy | |
dc.subject | Microbial Sensitivity Tests | |
dc.subject | Molecular Structure | |
dc.subject | Mycobacterium tuberculosis | |
dc.subject | Phenols | |
dc.subject | Plant Bark | |
dc.subject | Plant Roots | |
dc.subject | Plasmodium falciparum | |
dc.subject | Reference Standards | |
dc.subject | Sensitivity and Specificity | |
dc.subject | Stereoisomerism | |
dc.subject | Structure-Activity Relationship | |
dc.subject | Xanthones | |
dc.title | Bioactive constituents of the root bark of Artocarpus rigidus subsp. rigidus | |
dc.type | Article | |
dc.rights.holder | Scopus | |
dc.identifier.bibliograpycitation | Chemical and Pharmaceutical Bulletin. Vol 54, No.10 (2006), p.1433-1436 | |
dc.identifier.doi | 10.1248/cpb.54.1433 | |
Appears in Collections: | Scopus 1983-2021 |
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