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dc.contributor.authorMalyn Chulasirien_US
dc.contributor.authorNuntawan Bunyapraphatsaraen_US
dc.contributor.authorPrimchanien Moongkarndien_US
dc.contributor.otherMahidol Universityen_US
dc.date.accessioned2018-08-10T08:45:04Z-
dc.date.available2018-08-10T08:45:04Z-
dc.date.issued1992-01-01en_US
dc.identifier.citationEnvironmental and Molecular Mutagenesis. Vol.20, No.4 (1992), 307-312en_US
dc.identifier.issn10982280en_US
dc.identifier.issn08936692en_US
dc.identifier.other2-s2.0-0026480572en_US
dc.identifier.urihttps://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=0026480572&origin=inwarden_US
dc.identifier.urihttp://repository.li.mahidol.ac.th/dspace/handle/123456789/22288-
dc.description.abstractStudies of the mutagenicity and antimutagenicity of hispidulin and hortensin, the flavonoids from Millingtonia hortensis L. (Bignoniaceae), were performed using the liquid preincubation method of the Salmonella/microsome test. At the highest dose tested, 100 μg/plate, both compounds showed no mutagenicity and no cytotoxicity toward S. typhimurium strains TA98 and TA100 either in the presence or absence of S9 mix. However, these substances were antimutagens toward 2–aminoanthracene, aflatoxin Bl (in TA98), and dimethylnitrosamine (in TA100); but neither substance inhibited the direct mutagenic activity of 2‐(2‐furyl)‐3‐(5‐nitro‐2‐furyl) acrylamide nor that of sodium azide in strains TA98 and TA100, respectively. © 1992 Wiley‐Liss, Inc. Copyright © 1992 Wiley‐Liss, Inc., A Wiley Companyen_US
dc.rightsMahidol Universityen_US
dc.source.urihttps://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=0026480572&origin=inwarden_US
dc.subjectEnvironmental Scienceen_US
dc.subjectMedicineen_US
dc.titleMutagenicity and antimutagenicity of hispidulin and hortensin, the flavonoids from Millingtonia hortensis L.en_US
dc.typeArticleen_US
dc.rights.holderSCOPUSen_US
dc.identifier.doi10.1002/em.2850200409en_US
Appears in Collections:Scopus 1991-2000

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