ArticleRSC advances2026
Vanillin-tethered quinazolin-2,4-dione analogues through five- and/or six-membered nitrogen-containing heterocycles as antibacterial agents: synthesis, biological evaluation and molecular docking study.
Article in RSC advances, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.
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Authors and funding
6 authors.
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Abstract
The escalating threat of drug-resistant bacteria confirms the urgent need to develop and identify new and potent antibacterial inhibitors. In the present research study, the molecular hybridization strategy involved the synthesis of vanillin linked to a quinazolin-2,4-dione skeleton through five- and/or six-membered nitrogen-containing heterocycles such as pyrazole, isoxazole and/or pyrimidine 1-15 and testing them for their
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