Please use this identifier to cite or link to this item: https://ir.swu.ac.th/jspui/handle/123456789/14996
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dc.contributor.authorNamdaung U.
dc.contributor.authorAroonrerk N.
dc.contributor.authorSuksamrarn S.
dc.contributor.authorDanwisetkanjana K.
dc.contributor.authorSaenboonrueng J.
dc.contributor.authorArjchomphu W.
dc.contributor.authorSuksamrarn A.
dc.date.accessioned2021-04-05T04:32:18Z-
dc.date.available2021-04-05T04:32:18Z-
dc.date.issued2006
dc.identifier.issn92363
dc.identifier.other2-s2.0-33749414443
dc.identifier.urihttps://ir.swu.ac.th/jspui/handle/123456789/14996-
dc.identifier.urihttps://www.scopus.com/inward/record.uri?eid=2-s2.0-33749414443&doi=10.1248%2fcpb.54.1433&partnerID=40&md5=1a38fadda1c1d8a2295eb34703c70a27
dc.description.abstractInvestigation 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.subject7 demethylartonol e
dc.subjectArtocarpus rigidus extract
dc.subjectartoindonesianin c
dc.subjectartonin F
dc.subjectartonol B
dc.subjectchromone artorigidusin
dc.subjectcycloartobiloxanthone
dc.subjectflavanoid
dc.subjectphenol derivative
dc.subjectplant extract
dc.subjectunclassified drug
dc.subjectxanthone derivative
dc.subjectantimicrobial activity
dc.subjectarticle
dc.subjectbark
dc.subjectbreadfruit
dc.subjectcarbon nuclear magnetic resonance
dc.subjectconcentration response
dc.subjectcontrolled study
dc.subjectcytotoxicity
dc.subjectdrug structure
dc.subjecthuman
dc.subjecthuman cell
dc.subjectIC 50
dc.subjectminimum inhibitory concentration
dc.subjectMycobacterium tuberculosis
dc.subjectnonhuman
dc.subjectplant root
dc.subjectPlasmodium falciparum
dc.subjectproton nuclear magnetic resonance
dc.subjectstructure activity relation
dc.subjectAnimals
dc.subjectArtocarpus
dc.subjectCell Line, Tumor
dc.subjectCell Proliferation
dc.subjectChromones
dc.subjectDrug Screening Assays, Antitumor
dc.subjectFlavonoids
dc.subjectHumans
dc.subjectMagnetic Resonance Spectroscopy
dc.subjectMicrobial Sensitivity Tests
dc.subjectMolecular Structure
dc.subjectMycobacterium tuberculosis
dc.subjectPhenols
dc.subjectPlant Bark
dc.subjectPlant Roots
dc.subjectPlasmodium falciparum
dc.subjectReference Standards
dc.subjectSensitivity and Specificity
dc.subjectStereoisomerism
dc.subjectStructure-Activity Relationship
dc.subjectXanthones
dc.titleBioactive constituents of the root bark of Artocarpus rigidus subsp. rigidus
dc.typeArticle
dc.rights.holderScopus
dc.identifier.bibliograpycitationChemical and Pharmaceutical Bulletin. Vol 54, No.10 (2006), p.1433-1436
dc.identifier.doi10.1248/cpb.54.1433
Appears in Collections:Scopus 1983-2021

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