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dc.contributor.authorChurdsak Jaikangen_US
dc.contributor.authorChaiyavat Chaiyasuten_US
dc.date.accessioned2018-09-04T04:41:19Z-
dc.date.available2018-09-04T04:41:19Z-
dc.date.issued2010-05-18en_US
dc.identifier.issn19960875en_US
dc.identifier.issn19960875en_US
dc.identifier.other2-s2.0-77954070002en_US
dc.identifier.urihttps://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=77954070002&origin=inwarden_US
dc.identifier.urihttp://cmuir.cmu.ac.th/jspui/handle/6653943832/50466-
dc.description.abstractEffect of 10, 50 and 100 μg/ml caffeic acid and its esters and amides derivatives on heme oxygenase 1 (HO-1) activity induction in Hep G2 cell line was studied. It was found that caffeic acid ester derivatives could induce HO-1 activity more than amide derivatives. The longer side chain and aromatic side chain affected HO-1 activity. At 10 μg/ml concentration, phenylmethyl 1-(3', 4'-dihydroxyphenyl) propenate (PMDP) had 2.1-fold more activity when compared with control. At 50 and 100 μg/ml concentrations, phenylethyl 1-(3', 4'-dihydroxyphenyl) propenate (PEDP) was the highest HO-1 inducer, whose activity was 2.1- and 2.3-fold greater, respectively, when compared with the control group. Caffeic acid and all derivatives induced HO-1 activity on a higher level than curcumin, positive control. This study implied that caffeic acid and its derivatives could be used to induce HO-1 to protect tissues against free radicals. © 2010 Academic Journals.en_US
dc.subjectAgricultural and Biological Sciencesen_US
dc.subjectMedicineen_US
dc.subjectPharmacology, Toxicology and Pharmaceuticsen_US
dc.titleCaffeic acid and its derivatives as heme oxygenase 1 inducer in Hep G2 cell lineen_US
dc.typeJournalen_US
article.title.sourcetitleJournal of Medicinal Plants Researchen_US
article.volume4en_US
article.stream.affiliationsChiang Mai Universityen_US
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