Please use this identifier to cite or link to this item: http://nopr.niscpr.res.in/handle/123456789/66990
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dc.contributor.authorB Makane, Vitthal-
dc.contributor.authorU Sinde, Akash-
dc.contributor.authorAngayarkanni, B-
dc.contributor.authorMalik, Pradip-
dc.contributor.authorChopra, Sidharth-
dc.date.accessioned2025-12-24T05:35:42Z-
dc.date.available2025-12-24T05:35:42Z-
dc.date.issued2025-01-
dc.identifier.issn2583-1321 (Online); 0019-5103 (Print)-
dc.identifier.urihttp://nopr.niscpr.res.in/handle/123456789/66990-
dc.description1144-1155en_US
dc.description.abstractThe preparation and evaluation of α-aminoacyl amide derivatives against M. tuberculosis H37Rv is reported. The systematic modifications of hit compounds have been carried out. Compounds 19b and 19c are identified as potent and selective inhibitors of M. tuberculosis H37Rv with MIC 2.5 μM and 2.6 μM, respectively. Compounds 19b and 19c hold a promise for further development to discover new potent antituberculosis leads.en_US
dc.language.isoenen_US
dc.publisherNIScPR - CSIRen_US
dc.sourceIJC Vol.64(12) [December 2025]en_US
dc.subjectAntituberculosis agentsen_US
dc.subjectAmidesen_US
dc.subjectTuberculosisen_US
dc.subjectα-Aminoacyl amideen_US
dc.titleAntituberculosis activity of α-aminoacyl amide derivativesen_US
dc.identifier.doihttps://doi.org/10.56042/ijc.v64i12.19411en_US
Appears in Collections:IJC Vol.64(12) [December 2025]

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