Please use this identifier to cite or link to this item: http://nopr.niscpr.res.in/handle/123456789/66361
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dc.contributor.authorJoshi, K-
dc.contributor.authorMaheta, S-
dc.contributor.authorMahida, A-
dc.contributor.authorG Dubal, G-
dc.date.accessioned2025-08-25T09:45:14Z-
dc.date.available2025-08-25T09:45:14Z-
dc.date.issued2025-08-
dc.identifier.issn2583-1321 (Online);0019-5103 (Print)-
dc.identifier.urihttp://nopr.niscpr.res.in/handle/123456789/66361-
dc.description787-798en_US
dc.description.abstractA new series of substituted 2-[4-(3-oxo-[1,2,4]-triazolo-[4,3-a]pyridin-2-ylmethyl)-[1,2,3]triazol-1-yl]-N-(4-phenylthiazol- 2-yl)-acetamide compounds have been synthesized and evaluated for antimicrobial activity. Antibacterial activity has been performed against S. aureus and S. pyogenus (Gram-positive) and, E. coli and P. aeruginosa (Gram-negative) bacteria. Antifungal activity was performed against C. albicans, A. niger and A. clavatus. In the results, selected compounds exhibit significant antibacterial activity in comparison to others. MIC has been compared to currently marketed drugs also.en_US
dc.language.isoenen_US
dc.publisherNIScPR-CSIR, Indiaen_US
dc.sourceIJC Vol.64(08) [August 2025]en_US
dc.subject1,2,4-Triazoleen_US
dc.subjectAntimicrobialen_US
dc.subjectAntifungalen_US
dc.subjectMICen_US
dc.subjectMolecular dockingen_US
dc.titleSynthesis, in vitro antibacterial, antifungal biological activities along with in silico molecular docking studies of substituted 2-[4-(3-oxo-[1,2,4] triazolo [4,3-a]pyridin-2-ylmethyl)-[1,2,3]triazol-1-yl]-N-(4-phenyl-thiazol-2-yl)- acetamideen_US
dc.typeArticleen_US
dc.identifier.doihttps://doi.org/10.56042/ijc.v64i8.14374en_US
Appears in Collections:IJC Vol.64(08) [August 2025]

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