dc.contributor.author | Fathiazad, F | |
dc.contributor.author | Mazandarani, M | |
dc.contributor.author | Hamedeyazdan, S | |
dc.date.accessioned | 2018-08-26T09:31:57Z | |
dc.date.available | 2018-08-26T09:31:57Z | |
dc.date.issued | 2011 | |
dc.identifier.uri | http://dspace.tbzmed.ac.ir:8080/xmlui/handle/123456789/57216 | |
dc.description.abstract | Introduction: 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.iso | English | |
dc.relation.ispartof | Advanced Pharmaceutical Bulletin | |
dc.subject | 1,1 diphenyl 2 picrylhydrazyl | |
dc.subject | alpha cubebene | |
dc.subject | apigenin 7 beta dextro glucuronide | |
dc.subject | bornyl acetate | |
dc.subject | bourbonene | |
dc.subject | butanol | |
dc.subject | camphor | |
dc.subject | caryophyllene | |
dc.subject | caryophyllene oxide | |
dc.subject | cineole | |
dc.subject | cis sabinol | |
dc.subject | cubenol | |
dc.subject | delta cadinene | |
dc.subject | elemol | |
dc.subject | essential oil | |
dc.subject | flavonoid | |
dc.subject | germacrene | |
dc.subject | glucuronide | |
dc.subject | humulene | |
dc.subject | Hyssopus officinalis extract | |
dc.subject | linalool | |
dc.subject | myrtenyl acetate | |
dc.subject | nerodiol E | |
dc.subject | nerodiol Z | |
dc.subject | phenol | |
dc.subject | plant extract | |
dc.subject | plant medicinal product | |
dc.subject | quercetin | |
dc.subject | terpinen 4 ol | |
dc.subject | unclassified drug | |
dc.subject | antioxidant activity | |
dc.subject | article | |
dc.subject | concentration response | |
dc.subject | controlled study | |
dc.subject | drug determination | |
dc.subject | drug isolation | |
dc.subject | drug structure | |
dc.subject | hyssopus officinalis | |
dc.subject | IC 50 | |
dc.subject | Iran | |
dc.subject | Lamiaceae | |
dc.subject | nonhuman | |
dc.subject | phytochemistry | |
dc.subject | structure activity relation | |
dc.title | Phytochemical analysis and antioxidant activity of hyssopusofficinalis L. from iran | |
dc.type | Review | |
dc.citation.volume | 1 | |
dc.citation.issue | 2 | |
dc.citation.spage | 63 | |
dc.citation.epage | 67 | |
dc.citation.index | Scopus | |
dc.identifier.DOI | https://doi.org/10.5681/apb.2011.009 | |