Please use this identifier to cite or link to this item:
http://nopr.niscpr.res.in/handle/123456789/65614| metadata.dc.identifier.doi: | https://doi.org/10.56042/ijc.v64i3.16320 |
| Title: | Design and synthesis of novel triazole-isofroxadin molecules: Docking studies against inflammatory and tuberculosis targets |
| Authors: | Ranganath, P L N Annapurna, K Anil, T Narsaiah, A Venkat |
| Keywords: | Isofroxadin;Triazoles;Click reaction;Inflammatory;Tuberculosis |
| Issue Date: | Mar-2025 |
| Publisher: | NIScPR-CSIR, India |
| Abstract: | 1,2,3-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. |
| Page(s): | 285-290 |
| ISSN: | ISSN: 2583-1321 (Online);ISSN: 0019-5103 (Print) |
| Appears in Collections: | IJC Vol.64(03) [March 2025] |
Files in This Item:
| File | Description | Size | Format | |
|---|---|---|---|---|
| IJC 64(3) 285-290.pdf | 4.9 MB | Adobe PDF | View/Open | |
| IJC 64(3) 285-290 Suppl. Data.pdf | 4.14 MB | Adobe PDF | View/Open |
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