Please use this identifier to cite or link to this item: http://nopr.niscpr.res.in/handle/123456789/65614
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dc.contributor.authorRanganath, P L N-
dc.contributor.authorAnnapurna, K-
dc.contributor.authorAnil, T-
dc.contributor.authorNarsaiah, A Venkat-
dc.date.accessioned2025-03-28T09:06:26Z-
dc.date.available2025-03-28T09:06:26Z-
dc.date.issued2025-03-
dc.identifier.issnISSN: 2583-1321 (Online);ISSN: 0019-5103 (Print)-
dc.identifier.urihttp://nopr.niscpr.res.in/handle/123456789/65614-
dc.description285-290en_US
dc.description.abstract1,2,3-Triazole scaffolds are playing a vital role in various fields. These are not natural products but produced by synthetic chemists. Isafroxadin natural product and its 1,2,3-triazole derivatives have been synthesized using Click protocol. Thus, the newly generated scaffolds have been subjected to docking studies against inflammatory and tuberculosis activity.en_US
dc.language.isoenen_US
dc.publisherNIScPR-CSIR, Indiaen_US
dc.sourceIJC Vol.64(03) [March 2025]en_US
dc.subjectIsofroxadinen_US
dc.subjectTriazolesen_US
dc.subjectClick reactionen_US
dc.subjectInflammatoryen_US
dc.subjectTuberculosisen_US
dc.titleDesign and synthesis of novel triazole-isofroxadin molecules: Docking studies against inflammatory and tuberculosis targetsen_US
dc.typeArticleen_US
dc.identifier.doihttps://doi.org/10.56042/ijc.v64i3.16320en_US
Appears in Collections:IJC Vol.64(03) [March 2025]

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