Abstract

A series of novel chalcones 1a- 1l (12 compounds) has been synthesized by using commercially available apocynin and aromatic aldehydes. The newly synthesized chalcone derivatives were screened for their antibacterial activities against gram positive and gram negative bacteria at the concentrations 10 of μg/mL with reference to the standard antibacterial drug Gentamycin. The screening results revealed that among the tested analogs, compounds having the hetero rings such as benzo[b]furan, furan and pyridine (1j,1k and 1l) in the structure exhibited excellent antibacterial activity while the compounds bearing fluorine, 2-CF3, 4-CF3 and 4-OCF3 (1f, 1g, 1h and 1i) also exhibited good to excellent activity.

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