Please use this identifier to cite or link to this item: http://nopr.niscair.res.in/handle/123456789/55920
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dc.contributor.authorHariprasad, K Siva-
dc.contributor.authorHarikrishna, G-
dc.contributor.authorZehra, A-
dc.contributor.authorTiwari, A K-
dc.contributor.authorRaju, B China-
dc.date.accessioned2021-01-12T07:04:34Z-
dc.date.available2021-01-12T07:04:34Z-
dc.date.issued2021-01-
dc.identifier.issn0975-0983(Online); 0376-4699(Print)-
dc.identifier.urihttp://nopr.niscair.res.in/handle/123456789/55920-
dc.description111-116en_US
dc.description.abstract(E)-Methyl/ethyl-3-(2-hydroxyphenyl)acrylates 3a-x have been prepared by the reaction of salicylaldehydes 1a-l with Wittig reagents such as methyl (triphenylphosphoranylidene)acetate 2a and ethyl (triphenylphosphoranylidene)acetate 2b in dry DCM at room temperature. All the synthesized compounds have been evaluated for free-radical scavenging and α-glucosidase inhibitory activities. Compounds 3c and 3d display DPPH free radical scavenging activity. All the compounds have shown ABTS free radical scavenging activity except four compounds 3s-t and 3w-x. Compounds 3g, 3p and 3r display α-glucosidase inhibitory activity.en_US
dc.language.isoen_USen_US
dc.publisherNISCAIR-CSIR, Indiaen_US
dc.rights CC Attribution-Noncommercial-No Derivative Works 2.5 Indiaen_US
dc.sourceIJC-B Vol.60B(01) [January 2021]en_US
dc.subject(E)-Methyl/ethyl-3-(2-hydroxyphenyl)acrylatesen_US
dc.subjectSalicylaldehydesen_US
dc.subjectFree radical scavengingen_US
dc.subjectα-glucosidase inhibitory activityen_US
dc.titleFree radical scavenging and α-glucosidase inhibitory activity of (E)-methyl/ethyl-3-(2-hydroxyphenyl)acrylatesen_US
dc.typeArticleen_US
Appears in Collections:IJC-B Vol.60B(01) [January 2021]

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