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Published on: June 23, 2019
Synthesis and antimycobacterial evaluation of various 6-substituted pyrazolo[3,4-d]pyrimidine derivatives
Amit Trivedi1, Shailesh Vaghasiya, Bipin Dholariya
1Department of Chemistry, Saurashtra University, Rajkot, India.
Abstract:
Various pyrazolo[3,4-d]pyrimidines carrying a variety of substituents in the 6-position have been synthesised and their ability to inhibit growth of Mycobacterium tuberculosis in vitro has been determined. Compounds 5a, 5b, 6c, 7a, 7b, 8d, 8e and 8f demonstrated a minimum inhibitory concentration (MIC) of <6.25 µg/mL and were found to be active against Mycobacterium tuberculosis strain H(37)RV. Compound 8d was found to be the most active compound in vitro with a MIC of <6.25 µg/mL and inhibitory concentration IC(90) of 1.53 µg/mL.
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