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-...

Full description

Saved in:
Bibliographic Details
Published inBioorganicheskaia khimiia Vol. 39; no. 3; pp. 312 - 317
Main Authors Khan, Salman A., Asiri, Abdullah M., Alamry, Khalid A., El-Daly, Samy A., Zayed, Mohie A. M.
Format Journal Article
LanguageEnglish
Published Dordrecht SP MAIK Nauka/Interperiodica 01.05.2013
Subjects
Online AccessGet full text

Cover

Loading…
More Information
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.
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