Please use this identifier to cite or link to this item: 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]

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