Open Access

ARTICLE

Bacteriostatic action of synthetic polyhydroxylated chalcones against Escherichia coli

MARÍA DE LOS ANGELES ALVAREZ, VALERIA E. P. ZARELLI, NORA B.PAPPANO, NORA B. DEBATTISTA

Laboratory of Physical-Chemistry, Department of Chemistry, National University of San Luis. Chacabuco 917. (5700) San Luis, Argentina.
Address correspondence to: Dra. Nora B. Pappano. Laboratory of Physical-Chemistry, Department of Chemistry, San Luis National University. Chacabuco 917, (5700) San Luis, ARGENTINA. Phone: (+54-2652) 424689 int. 122; Fax: (+543652) 422644; E-mail: npappano@unsl.edu.ar

BIOCELL 2004, 28(1), 31-34. https://doi.org/10.32604/biocell.2004.28.031

Abstract

In previous work the bacteriostatic action of trihydroxylated chalcones against Staphylococcus aureus ATCC 25 923 was investigated. In this work the action of 2´, 4´, 2-(OH)₃ -chalcone, 2´, 4´, 3-(OH)_3^- chalcone and 2´, 4´, 4-(OH)₃ –chalcone against Escherichia coli ATCC 25 922 was evaluated. Growth kinetic curves of E.coli were made in nutritive broth added with increasing drug concentrations. The specific growth rates of the microorganisms were calculated by a kinetic turbidimetric method, which was previously probed and the minimal inhibitory concentrations (MIC´s) were evaluated by a mechanism of action proposed. The MICs of 2´, 4´, 3-(OH)₃ -chalcone and 2´, 4´, 2-(OH)₃ -chalcone were 46 µg/ml and 122 µg/ml, respectively. The 2´, 4´, 4-(OH)₃ –chalcone was inactive. The MIC value of 2´, 4´, 3-(OH)₃-chalcone (46 µg/ml), more active than 2´, 3-(OH)₂-chalcone (72.2 µg/ml) may be due to the introduction of an electron donating group (-OH) at position 4´ in the aromatic A- ring, which activates the region that includes the 2´-hydroxyl neighbur group and the α,β- unsaturated carbonyl group.

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