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ชื่อเรื่อง: | Bioactive constituents of the root bark of Artocarpus rigidus subsp. rigidus |
ผู้แต่ง: | Namdaung U. Aroonrerk N. Suksamrarn S. Danwisetkanjana K. Saenboonrueng J. Arjchomphu W. Suksamrarn A. |
Keywords: | 7 demethylartonol e Artocarpus rigidus extract artoindonesianin c artonin F artonol B chromone artorigidusin cycloartobiloxanthone flavanoid phenol derivative plant extract unclassified drug xanthone derivative antimicrobial activity article bark breadfruit carbon nuclear magnetic resonance concentration response controlled study cytotoxicity drug structure human human cell IC 50 minimum inhibitory concentration Mycobacterium tuberculosis nonhuman plant root Plasmodium falciparum proton nuclear magnetic resonance structure activity relation Animals Artocarpus Cell Line, Tumor Cell Proliferation Chromones Drug Screening Assays, Antitumor Flavonoids Humans Magnetic Resonance Spectroscopy Microbial Sensitivity Tests Molecular Structure Mycobacterium tuberculosis Phenols Plant Bark Plant Roots Plasmodium falciparum Reference Standards Sensitivity and Specificity Stereoisomerism Structure-Activity Relationship Xanthones |
วันที่เผยแพร่: | 2006 |
บทคัดย่อ: | 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. |
URI: | https://ir.swu.ac.th/jspui/handle/123456789/14996 https://www.scopus.com/inward/record.uri?eid=2-s2.0-33749414443&doi=10.1248%2fcpb.54.1433&partnerID=40&md5=1a38fadda1c1d8a2295eb34703c70a27 |
ISSN: | 92363 |
Appears in Collections: | Scopus 1983-2021 |
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