Herein, we report the design, syntheses and in vitro anti-microbial activity of two series of rhodanines with chalcone moiety. Anti-microbial tests showed that some of the synthesized compounds exhibited good inhibition (MIC=1-8μg/mL) against multi-drug-resistant Gram-positive organisms, including methicillin resistant and quinolone-resistant Staphylococcus aureus, in which the compound 4g was found to be the most potent with minimum inhibitory concentration (MIC) value of 1μg/mL against two methicillin-resistant S. aureus.
CITATION STYLE
Song, M. X., Deng, X. Q., Li, Y. R., Zheng, C. J., Hong, L., & Piao, H. R. (2014). Synthesis and biological evaluation of (E)-1-(substituted)-3-phenylprop-2-en-1-ones bearing rhodanines as potent anti-microbial agents. Journal of Enzyme Inhibition and Medicinal Chemistry, 29(5), 647–653. https://doi.org/10.3109/14756366.2013.837899
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