Please use this identifier to cite or link to this item: http://ir.lib.seu.ac.lk/handle/123456789/2098
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dc.contributor.authorJumani, ALF-
dc.contributor.authorSafeena, MIS-
dc.contributor.authorSenthilnithy, R-
dc.date.accessioned2017-01-13T06:22:30Z-
dc.date.available2017-01-13T06:22:30Z-
dc.date.issued2016-12-29-
dc.identifier.citationProceedings of Fifth Annual Science Research Sessions 2016 on "Enriching the Novel Scientific Research for the Development of the Nation" pp.217-224en_US
dc.identifier.isbn9789556271027-
dc.identifier.urihttp://ir.lib.seu.ac.lk/handle/123456789/2098-
dc.description.abstractSmall Gilligan molecules bind to DNA and artificially alter and/or inhibit the functioning of DNA. These small ligand molecules act as drug when alteration or inhibition of DNA function is required to cure or control a disease.The binding interaction of N-phenyllauroylhydroxamic acid with CTDNA was measured by four methods, (i) UV spectroscopic method, (ii) fluorescence spectroscopic method, (iii) viscosity Measurement and (iv) molecular docking. It showed that Nphenyllauroylhydroxamic acid-DNA complex has high absorption intensity than compound only and significant quenching of fluorescence intensity for the N-phenyllauroylhydroxamic-DNA complex. The values of binding constant, K, is 3.43x 10-2nd Stern Volmer constant Ksv is 4.8 x102 ng-1μl obtained by UV absorption and fluorescence spectral methods, respectively. The binding interaction is further confirmed by the increase in relative viscosity of CT-DNA. The molecular docking of N-phenyllauroylhydroxamic acid with the DNA confirmed to be a strong binder with DNA in the mode of groove.en_US
dc.language.isoen_USen_US
dc.publisherFaculty of Applied Sciences, South Eastern University of Sri lankaen_US
dc.subjectHydrodynamicen_US
dc.subjectCalf thymus DNA (ct-DNA)en_US
dc.subjectMolecular dockingen_US
dc.titleA Study on binding of hydroxamic acid derivative to DNA: experimental and computational approachen_US
dc.typeArticleen_US
Appears in Collections:ASRS - FAS 2016

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