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dc.contributor.authorNampoothiri, S V-
dc.contributor.authorRiya, M P-
dc.contributor.authorKankang, S-
dc.contributor.authorKiran, C R-
dc.contributor.authorMenon Nirmala, A-
dc.date.accessioned2016-06-21T06:13:10Z-
dc.date.available2016-06-21T06:13:10Z-
dc.date.issued2015-09-
dc.identifier.citationJournal of Essential Oil Bearing Plants 18(5):1051-1058,03-Sep,2015en_US
dc.identifier.urihttp://hdl.handle.net/123456789/2323-
dc.description.abstractCurcuma aromatica Salisb. is an aromatic medicinal plant belongs to the family Zingiberaceae. In the present study essential oil from the rhizome of C. aromatica analyzed by GC-MS. The major constituents in the oil were xanthorrhizol (26.3 %) followed by ar-curcumene (19.5 %) and di-epialpha- cedrene (16.5 %). The rhizome extracted sequentially with different solvents (hexane, dichloromethane and methanol) and evaluated its antioxidant activity. The dichloromethane extract showed maximum antioxidant potential and remarkable free radical quenching property. The solvent extracts were also screened for their antidiabetic activity via inhibition of α-amylase, and antiglycation assays. In α-amylase inhibition and antiglycation studies, dichloromethane extract got maximum activity with an IC50 value of 8.97±0.3 μg/ml and (561.37±2 μg/ml) respectively compared to other extracts. These significant activities of DCM were relevant parameters in the management of type 2 diabetes. The better activity of dichloromethane extract might be due to the high amount of phenolic compounds (10.9 %) and flavonoids (6.7 %) present in iten_US
dc.language.isoenen_US
dc.publisherTaylor&Francisen_US
dc.subjectCurcuma aromatica; GC-MS xanthorrhizol; α-amylase inhibition;antiglycationen_US
dc.titleEssential Oil Composition, Alpha-Amylase Inhibition and Antiglycation Potential of Curcuma Aromatica Salisben_US
dc.typeArticleen_US
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