Please use this identifier to cite or link to this item: http://nopr.niscpr.res.in/handle/123456789/59540
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dc.contributor.authorGaonkar, Sahili Ganesh-
dc.contributor.authorPhadte, Soniya-
dc.contributor.authorDesai, Shivlingrao Mamle-
dc.contributor.authorBiradar, Bheemanagouda-
dc.contributor.authorPorab, Nikita-
dc.date.accessioned2022-04-19T06:21:36Z-
dc.date.available2022-04-19T06:21:36Z-
dc.date.issued2022-04-
dc.identifier.issn2583-1321 (Online); 0019-5103 (Print)-
dc.identifier.urihttp://nopr.niscair.res.in/handle/123456789/59540-
dc.description431-437en_US
dc.description.abstractThe current research work involves in silico docking studies, synthesis, characterisation and study on hypoglycemicactivity of a series of N-(2-(4-methoxy-1-methyl/phenyl-2-oxo-1,2-dihydroquinolin-3-yl)-2-oxoethyl)-Nsubstitutedprimaryamino) -benzenesulfononamides [IVa/b (1-6)]. Compounds exhibit prominent anti-diabetic activity by glucose oxidase peroxidase (GOD-POD) method which involves measurement of average serum glucose levels in mg/dl as well as conserved hydrogen bonds with one or more amino acid residues in the active pocket of murine 11β-hydroxysteroid dehydrogenase domain. Among all the synthesized compounds, compound IVb2 shows prominent anti-diabetic activity and higher Moldock score as compared to standard drug Glibenclamide. Structural analysis of the synthesized compounds has been done by standard spectroscopic techniques.en_US
dc.language.isoenen_US
dc.publisherNIScPR-CSIR, Indiaen_US
dc.sourceIJC Vol.61(04) [April 2022]en_US
dc.subjectQuinolin-2-oneen_US
dc.subjectsulphonamidesen_US
dc.subjectmolecular dockingen_US
dc.subjectantidiabetic activityen_US
dc.subjectglucose oxidase-peroxidaseen_US
dc.titleDocking, synthesis and evaluation of N-(2-(4-methoxy-2-oxo-1-phenyl/methyl- 1,2-dihydroquinolin-3-yl)-2-oxoethyl)-N-substitutedphenylbenzenesulfonamide derivatives as hypoglycemic agentsen_US
dc.typeArticleen_US
Appears in Collections:IJC Vol.61(04) [April 2022]

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