SINTESIS DAN UJI AKTIVITAS ANTIBAKTERI SENYAWA KURKUMIN (3E,5E)-3,5-BIS(2’-HIDROKSIBENZILIDIN)-1-METILPIPERIDIN-4 -ON

dc.contributor.authorHasanah, U.
dc.contributor.authorZamri, A.
dc.contributor.authorBalatif, N.
dc.contributor.authorEryanti, Y.
dc.date.accessioned2014-03-27T07:09:01Z
dc.date.available2014-03-27T07:09:01Z
dc.date.issued2014-03-27
dc.description.abstractThe derivatives of curcumin are second ary metabolites belonging to the phenolic group. Some of them were reported to have biological activities such as anti -i nfl ammatory, anticancer and antioxidant activities. In this study, acurcumin of (3E,5E)-3,5bis(2’-hidroxybenzilidin)-1-metilpiperidin-4-one from 1-methyl-4-pi peridinone with 2-hydroxy benzaldehideh as been successfully synthesized using microwave irradiation method with NaOH (20 %) as catalyst . React ion was carried out for 1 minute at 180 watt . The compound resulted was in the form of yellow crystal withayield of 72 %. The compound was characterized by measuring its melting point, identifying by TLC, and elucidated by UV-Vis, FT- IR, MS, 1 H NMR, and 13 C NMR. Our result show edthatthecom pound had the target edmolecule structure. Ant i bacterial test was carried out using the agar di ffusion method against Staphylococcus aureus, Escherichia coli, Bacillus subtilis, and Salmonella enteritidis. Overall, inhibition zone ran ged from 6.5 t o 10 mm and showed avery weak activity.en_US
dc.description.sponsorshipZamri, A., Balatif, N., Eryanti, Yen_US
dc.identifier.otherRangga Dwijunanda Putra
dc.identifier.urihttp://repository.unri.ac.id/xmlui/handle/123456789/5953
dc.language.isootheren_US
dc.subject1-methyl-4-piperidinoneen_US
dc.subject2-hydroxy benzaldehideen_US
dc.subjectantbacterialen_US
dc.subjectcurcuminen_US
dc.titleSINTESIS DAN UJI AKTIVITAS ANTIBAKTERI SENYAWA KURKUMIN (3E,5E)-3,5-BIS(2’-HIDROKSIBENZILIDIN)-1-METILPIPERIDIN-4 -ONen_US
dc.typeOtheren_US

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