Abstract
In this study, a series of novel 3-(substituted phenyl)-6,7-dimethoxy-3a,4- dihydro-3H-indeno[1,2-c]isoxazole analogues were synthesized and evaluated for antimycobacterial activity against Mycobacterium tuberculosis (MTB) H 37Rv and isoniazid resistant M. tuberculosis (INHR-MTB). All the newly synthesized compounds were showing moderate to high inhibitory activities. The compound 6,7-dimethoxy-3-(4-chloro phenyl)-4H-indeno[1,2-c]isoxazole (4b) was found to be the most promising compound, active against MTB H 37Rv and INHR-MTB with minimum inhibitory concentrations of 0.22 and 0.34 μM. © 2011 Informa UK, Ltd.
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Ali, M. A., Ismail, R., Choon, T. S., Pandian, S., & Hassan Ansari, M. Z. (2011). Antimycobacterial activity: Synthesis of novel 3-(substituted phenyl)-6,7-dimethoxy-3a,4-dihydro-3H-indeno[1,2-c]isoxazole analogues. Journal of Enzyme Inhibition and Medicinal Chemistry, 26(4), 598–602. https://doi.org/10.3109/14756366.2010.529805
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