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http://nopr.niscpr.res.in/handle/123456789/59543| Title: | Discovery of selective and potent anti-tubercular activity in arylpentane-1,4-diones |
| Authors: | Umarani, W A Sony, K P Hymavathi, K V Kumar, M Murali Krishna |
| Keywords: | Stetter reaction;1,4-diketones;antitubercular activity;MABA assay;docking |
| Issue Date: | Apr-2022 |
| Publisher: | NIScPR-CSIR, India |
| Abstract: | Anti-tubercular activity (MIC 50μg/mL against Mtb H37Rv) have been reported in hispolons, which possess α, β-unsaturated-1,3-diketone functional group. In the pursuit to optimize structure and bioactivity, various substituted arylpentane-1,4-diones S1-8 have been synthesised. Upon screening, the test compounds show negligible antimicrobial activity against the tested organisms at 100 μg/mL but show antitubercular activity against Mycobacterium tuberculosis H37Rv strain with an MIC 0.8 to 25μg/mL. Compounds having a halogen at the ortho position on the aromatic ring show highest potency (MIC 0.8μg/mL), implying a relation between the position of the halogen atom and anti-tubercular activity. |
| Page(s): | 411-415 |
| ISSN: | 2583-1321 (Online); 0019-5103 (Print) |
| Appears in Collections: | IJC Vol.61(04) [April 2022] |
Files in This Item:
| File | Description | Size | Format | |
|---|---|---|---|---|
| Indian J Chem, 61, 411-415 (Apr,2022).pdf | 648.47 kB | Adobe PDF | View/Open |
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