SYNTHESIS CHARACTERISATION AND BIOLOGICAL EVALUATION OF BIS-CHALCONES BASED ON RESORCINOL
DOI:
https://doi.org/10.47750/pnr.2022.13.04.083Keywords:
Bis-Chalcones. 2, 4-Diacetyl Resorcinol (DAR). Claisen-Schmidt Condensation. FT-IR. 1HNMR. 13CNMR. Biological activity.Abstract
The biogenetic antecedents of flavonoids and isoflavonoids, which are abundant in plants, are chalcones. They have antimitotic, antimutagenic, and antitumor-promoting properties, as well as antibacterial, antiviral, anti-inflammatory, and hepatoprotective properties.
Claisen condensation of 1:2 moles of 2,4-Diacetyl Resorcinol (DAR) and substituted aldehydes yielded novel bis-chalcones, which were characterized by 1HNMR, and 13C NMR. To determine whether these compounds have antibacterial activity, the disk diffusion method was performed. Microorganisms are Gram-positive and Gram-negative.
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2022-10-12
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SYNTHESIS CHARACTERISATION AND BIOLOGICAL EVALUATION OF BIS-CHALCONES BASED ON RESORCINOL. (2022). Journal of Pharmaceutical Negative Results, 13(4), 627-631. https://doi.org/10.47750/pnr.2022.13.04.083