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- W2149185614 abstract "Despite being an ancient disease, tuberculosis (TB) remains the leading single-agent infectious disease killer in the world. The emerging serious problem of TB control and clinical management prompted us to synthesize a novel series of heterocyclic substituted diphenyl ether derivatives and determine their activity against the H37Rv strain of Mycobacterium. All ten compounds inhibited the growth of the H37Rv strain of Mycobacterium at concentrations of 1 μg/mL. This activity was found to be comparable to the reference drugs rifampicin and isoniazid at the same concentration. While the antimicrobial activity of other diphenyl ether analogues, such as triclosan, is associated with the inhibition of enoyl-ACP reductase (ENR), the synthesised substituted diphenyl ether derivatives did not affect this enzyme activity in spite of their structural similarity with triclosan. Therefore, these compounds appear to have a novel mechanism of action against M. tuberculosis, and their structural features should be studied further for their potential as new antitubercular drugs." @default.
- W2149185614 created "2016-06-24" @default.
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- W2149185614 date "2010-05-05" @default.
- W2149185614 modified "2023-09-27" @default.
- W2149185614 title "Synthesis and antitubercular activity of heterocycle substituted diphenyl ether derivatives" @default.
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- W2149185614 doi "https://doi.org/10.3109/14756361003671045" @default.
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