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dc.contributor.authorDhanya, B P-
dc.contributor.authorGreeshma, G-
dc.contributor.authorReshmitha, T R-
dc.contributor.authorSaranya, J-
dc.contributor.authorSharathna, P-
dc.contributor.authorShibi, I G-
dc.contributor.authorNisha, P-
dc.contributor.authorRadhakrishnan, K V-
dc.date.accessioned2018-06-19T11:27:37Z-
dc.date.available2018-06-19T11:27:37Z-
dc.date.issued2017-05-26-
dc.identifier.citationNew Journal of Chemistry, 41(15):6960-6964en_US
dc.identifier.urihttp://10.10.100.66:8080/xmlui/handle/123456789/3111-
dc.description.abstractA series of zerumbone pendant derivatives were synthesized and evaluated for their a-glucosidase, a-amylase and glycation inhibition activities. In our study, some of the derivatives showed potent inhibitory activity in micromolar concentration. In addition, investigations were carried out to screen the cytotoxic effects of some selected derivatives against various cancer cell lines viz., A549, HCT116, HeLa, HT1080 and MDAMB231. Two of the derivatives showed potent activity towards HCT116 and HeLa cell lines.en_US
dc.language.isoenen_US
dc.publisherRoyal Society of Chemistryen_US
dc.titleSynthesis and In Vitro Evaluation of Zerumbone Pendant Derivatives: Potent Candidates for Anti-Diabetic and Anti-Proliferative Activitiesen_US
dc.typeArticleen_US
Appears in Collections:2017

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