Please use this identifier to cite or link to this item:
|Title:||Antimicrobial and antioxidant activities of substituted halogenated coumarins||Authors:||Kasumbwe, K.
Venugopala, Katharigatta Narayanaswamy
|Keywords:||Coumarin;Antibacteria;Antifungal;Antioxidant||Issue Date:||3-Feb-2014||Publisher:||Academic Journals||Source:||Kasumbwe, K, Venugopala, K.N, Mohanlall, V. and Odhav, B. 2014. Antimicrobial and antioxidant activities of substituted halogenated coumarins. Journal of Medicinal Plants Research Vol.8(5), pp. 274-281.||Abstract:||Pathogens frequently display resistance to current drugs, which frequently lack selectivity/efficacy and have detrimental side effects. Thus, there is a constant need for novel therapeutic agents. Coumarins belong to the family of lactones, having a benzopyrone system that can be isolated from plants as well as total synthesis that can be carried out in the laboratory. To date, many chemical reactions have been established that can be used to synthesize coumarins. The synthesis of coumarins and their derivatives has attracted the attention of organic and medicinal chemists, as these are widely used as fragrances, pharmaceuticals and agrochemicals. In the present study, the antimicrobial and antioxidant activities of substituted coumarin analogue compounds have been screened. 3-(2-bromoacetyl)-2H-chromen-2-one (CMRN3) and 3-(2, 2-dibromoacetyl)-2H-chromen-2-one (CMRN6) showed bacterial growth inhibition for all the tested species except Klebsiella pneumonia and Bacillus stearothermophilus. CMRN4 and CMRN5 displayed moderate bacterial inhibition against Bacillus cereus, Micrococcus luteus, Staphylococcus aureus. CMRN3 and CMRN6 had a minimum inhibition concentration at 0.75 mg/ml against B. cereus, Bacillus coagulans, and Streptococcus faecalis. They displayed a minimum inhibitory concentration (MIC) of 1.5 mg/ml against Escherichia coli and S. aureus. (CMRN5) displayed an MIC at 0.75 mg/ml against M. luteus and 1.5 mg/ml against S. aureus. Compounds3-(2-bromoacetyl)-6-chloro-2H-chromen-2-one (CMRN4), 3-(2-aminothiazol-4-yl)-6-bromo-2H-chromen-2-one(CMRN7), 3-acetyl-6-bromo-2H-chromen-2-one (CMRN1) exhibited potent antioxidant activity at 85, 61 and 56%, respectively, as evaluated by the DPPH free radical method.||URI:||http://hdl.handle.net/10321/1076||ISSN:||1996-0875|
|Appears in Collections:||Research Publications (Health Sciences)|
Show full item record
Files in This Item:
|kasumbwe__venugopala_et_al_2014.pdf||491.21 kB||Adobe PDF|
Page view(s) 50402
checked on Feb 23, 2019
checked on Feb 23, 2019
Items in DSpace are protected by copyright, with all rights reserved, unless otherwise indicated.