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Please use this identifier to cite or link to this item: http://dspace.unitywomenscollege.ac.in/xmlui/handle/123456789/1925
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dc.contributor.authorMuhammed Basheer Ummathur-
dc.contributor.authorMalini Parakkulangara Thrithody-
dc.contributor.authorKrishnannair Krishnankutty-
dc.date.accessioned2024-10-14T11:02:37Z-
dc.date.available2024-10-14T11:02:37Z-
dc.date.issued2020-11-
dc.identifier.issn0976-3031-
dc.identifier.urihttp://dspace.unitywomenscollege.ac.in/xmlui/handle/123456789/1925-
dc.description.abstractThe antioxidant activity of eight curcuminoid analogues (HL1 to HL8 ) was studied by thiocyanate method. The results revealed that the antioxidant property depends on the nature of aryl substituents and the extent of conjugation present in the compounds. A comparison of the observed antioxidant and reported antitumour activities of these synthetic curcuminoids revealed that compounds having highest antitumour activity also exhibited maximum antioxidant activity.en_US
dc.language.isoenen_US
dc.publisherInternational Journal of Recent Scientific Researchen_US
dc.subjectAntioxidant studies, thiocyanate method, curcuminoid analogues and antitumour activity.en_US
dc.titleANTIOXIDANT STUDIES OF SOME SYNTHETIC CURCUMINOIDSen_US
dc.typeArticleen_US
Appears in Collections:Journal Articles

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