Antibacterial Activity of Murrayaquinone A and 6-Methoxy-3,7-dimethyl-2,3-dihydro-1H-carbazole-1,4(9H)-dione
Author(s) -
Biswanath Chakraborty,
Suchandra Chakraborty,
Chandan Saha
Publication year - 2014
Publication title -
international journal of microbiology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.696
H-Index - 40
eISSN - 1687-9198
pISSN - 1687-918X
DOI - 10.1155/2014/540208
Subject(s) - staphylococcus aureus , bacillus subtilis , antibacterial activity , escherichia coli , carbazole , moiety , chemistry , minimum inhibitory concentration , bacteria , microbiology and biotechnology , quinone , stereochemistry , biology , antibiotics , organic chemistry , biochemistry , genetics , gene
The antibacterial activity of Murrayaquinone A ( 10 ), a naturally occurring carbazoloquinone alkaloid, and 6-methoxy-3,7-dimethyl-2,3-dihydro-1 H -carbazole-1,4(9 H )-dione ( 11 ), a synthetic carbazoloquinone, both obtained during the development of the synthesis of Carbazomycin G, having unique quinone moiety, was studied against Gram-positive ( Bacillus subtilis and Staphylococcus aureus ) and Gram-negative ( Escherichia coli and Pseudomonas sp.) bacteria. Compound 10 showed antibacterial activities against both of Escherichia coli and Staphylococcus aureus whereas compound 11 indicated the activity against Staphylococcus aureus only. Both compounds 10 and 11 exhibited minimum inhibitory concentration (MIC) of 50 μ g mL −1 against Staphylococcus aureus .
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