Please use this identifier to cite or link to this item: http://nopr.niscpr.res.in/handle/123456789/65609
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dc.contributor.authorVerma, Shweta-
dc.contributor.authorSingh, Neeku-
dc.date.accessioned2025-03-28T08:46:16Z-
dc.date.available2025-03-28T08:46:16Z-
dc.date.issued2025-03-
dc.identifier.issnISSN: 2583-1321 (Online);ISSN: 0019-5103 (Print)-
dc.identifier.urihttp://nopr.niscpr.res.in/handle/123456789/65609-
dc.description328-338en_US
dc.description.abstractIn the present investigation, the docking of triphenyl imidazole derivatives have been done following which synthesis of the compounds have been carried out and the compounds have been characterized by TLC, IR, and 1H NMR. The compounds have been assessed in vivo for antianxiety activity by two different methods. Other parameters have also been assessed including similarity index and Log P values which is found to be in the range which indicate that drug penetration to CNS is good. Among the synthesized derivatives, the compounds NS-3 and NS-4 give remarkable anxiolytic activity. The studies of molecular docking studies display that the compounds appropriately docked into binding pocket of the GABAA receptor and bioavailability/drug-likeness has also been predicted to be satisfactory warranting forthcoming exploration. The further prospect is to optimize the synthesized derivatives to engender new moieties for treatment of anxiety.en_US
dc.language.isoenen_US
dc.publisherNIScPR-CSIR, Indiaen_US
dc.sourceIJC Vol.64(03) [March 2025]en_US
dc.subjectTriphenyl imidazole derivativesen_US
dc.subjectBenzilen_US
dc.subjectBenzaldehydeen_US
dc.subjectAntianxiety activityen_US
dc.subjectCNS agentsen_US
dc.subjectDocking scoreen_US
dc.titleSynthesis, molecular docking, and pharmacological evaluation of some new triphenyl imidazole derivatives as anxiolytic agentsen_US
dc.typeArticleen_US
dc.identifier.doihttps://doi.org/10.56042/ijc.v64i3.15347en_US
Appears in Collections:IJC Vol.64(03) [March 2025]

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