نمایش پرونده ساده آیتم

dc.contributor.authorFathiazad, F
dc.contributor.authorMazandarani, M
dc.contributor.authorHamedeyazdan, S
dc.date.accessioned2018-08-26T09:31:57Z
dc.date.available2018-08-26T09:31:57Z
dc.date.issued2011
dc.identifier.urihttp://dspace.tbzmed.ac.ir:8080/xmlui/handle/123456789/57216
dc.description.abstractIntroduction: Hyssopus officinalis (L) (Hyssop, Family: Lamiaceae), one of the endemic Iranian perennial herb with a long history of medicinal use, was studied to detect some biologically active chemical constituents of the plant. Methods: The flavonoids of the hydromethanolic extract of the aerial parts of Hyssopusofficinalis (L.) were studied by VLC and crystalisation of the major compound in subsequent fractions. Furthermore, the composition of its essential oil, total phenolic content and antioxidant activities were studied by GC-MS, Folin-Ciocalteau and DPPH reagents respectively. Results: Apigenin 7-O-?-D-glucuronide was isolated as the major flavonoid. All structural elucidation was performed by spectral means. A total of 20 compounds representing 99.97% of the oil have been identified. Myrtenylacetate, Camphor, Germacrene, Spathulenol were the main compounds The total phenol content of the n-butanol and ethylacetate extracts were determined spectrophotometrically according to the Folin-Ciocalteau procedure to be 246 mgGAE g-1 and 51 mgGAE g-1 in the aerial parts of Hyssopusofficinalis. The antioxidant activities of apigenin 7-O-?-D-glucuronide, ethylacetate and n-butanol extracts were also determined by DPPH radical scavenging assay with IC50 values of 116--10-3, 103--10-3, 25--10-3 mg mL-1 respectively. The purified flavonoid showed weak radical scavenging activity (IC50 = 116--10-3mg mL-1). N-butanol extract, because of the highest content of total phenolic compounds (246 mgGAE100-1g) had the best antioxidant activity (IC50 = 25mg mL-1). Conclusion: On the whole, the findings of the study revealed that Hyssop possesses valuable antioxidant properties for culinary and possible medicinal use. © 2011 by Tabriz University of Medical Sciences.
dc.language.isoEnglish
dc.relation.ispartofAdvanced Pharmaceutical Bulletin
dc.subject1,1 diphenyl 2 picrylhydrazyl
dc.subjectalpha cubebene
dc.subjectapigenin 7 beta dextro glucuronide
dc.subjectbornyl acetate
dc.subjectbourbonene
dc.subjectbutanol
dc.subjectcamphor
dc.subjectcaryophyllene
dc.subjectcaryophyllene oxide
dc.subjectcineole
dc.subjectcis sabinol
dc.subjectcubenol
dc.subjectdelta cadinene
dc.subjectelemol
dc.subjectessential oil
dc.subjectflavonoid
dc.subjectgermacrene
dc.subjectglucuronide
dc.subjecthumulene
dc.subjectHyssopus officinalis extract
dc.subjectlinalool
dc.subjectmyrtenyl acetate
dc.subjectnerodiol E
dc.subjectnerodiol Z
dc.subjectphenol
dc.subjectplant extract
dc.subjectplant medicinal product
dc.subjectquercetin
dc.subjectterpinen 4 ol
dc.subjectunclassified drug
dc.subjectantioxidant activity
dc.subjectarticle
dc.subjectconcentration response
dc.subjectcontrolled study
dc.subjectdrug determination
dc.subjectdrug isolation
dc.subjectdrug structure
dc.subjecthyssopus officinalis
dc.subjectIC 50
dc.subjectIran
dc.subjectLamiaceae
dc.subjectnonhuman
dc.subjectphytochemistry
dc.subjectstructure activity relation
dc.titlePhytochemical analysis and antioxidant activity of hyssopusofficinalis L. from iran
dc.typeReview
dc.citation.volume1
dc.citation.issue2
dc.citation.spage63
dc.citation.epage67
dc.citation.indexScopus
dc.identifier.DOIhttps://doi.org/10.5681/apb.2011.009


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