Eco-friendly synthesis and in vitro antibacterial activities of some novel chalcones
Chalcone derivatives have been synthesized by reaction of 1-(2,5-dimethyl-furan-3-yl)-ethanone with corresponding active aldehyde in ethanolic NaOH in microwave oven. The structure of these compounds was established by elemental analysis, IR, 1 H NMR, 13 C NMR, and EI-MS spectral analysis. The anti-...
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Published in | Bioorganicheskaia khimiia Vol. 39; no. 3; pp. 312 - 317 |
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Main Authors | , , , , |
Format | Journal Article |
Language | English |
Published |
Dordrecht
SP MAIK Nauka/Interperiodica
01.05.2013
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Subjects | |
Online Access | Get full text |
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Summary: | Chalcone derivatives have been synthesized by reaction of 1-(2,5-dimethyl-furan-3-yl)-ethanone with corresponding active aldehyde in ethanolic NaOH in microwave oven. The structure of these compounds was established by elemental analysis, IR,
1
H NMR,
13
C NMR, and EI-MS spectral analysis. The anti-bacterial activity of these compounds was first tested in vitro by the disc diffusion assay against two Gram-positive and two Gram-negative bacteria, and then the minimum inhibitory concentration (MIC) was determined with the reference of standard drug chloramphenicol. The results showed that pyrazol containing chalcone (compound
8
) inhibited both types of bacteria (Gram-positive and Gram-negative) better than chloramphenicol. |
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Bibliography: | ObjectType-Article-1 SourceType-Scholarly Journals-1 ObjectType-Feature-2 content type line 23 |
ISSN: | 1068-1620 0132-3423 1608-330X |
DOI: | 10.1134/S1068162013030072 |