Bioorganic and Medicinal Chemistry p. 1462 - 1469 (2018)
Update date:2022-08-18
Topics:
Alluri, Kiran Kumar
Reshma, Rudraraju Srilakshmi
Suraparaju, Raghuram
Gottapu, Suryanarayana
Sriram, Dharmarajan
Need for new drugs to fight against tuberculosis (TB) is increasing day by day. In the present work we have taken a spiro compound (GSK 2200150A) reported by GSK as a lead and we modified the structure of the lead to study the antitubercular activity. For structure activity profiling twenty-one molecules have been synthesized, characterized and evaluated for their antimycobacterial potency against both active and dormant TB. Compound 06, 1-((4-methoxyphenyl)sulfonyl)-4′,5′-dihydrospiro[piperidine-4,7′-thieno[2,3-c]pyran] was found to be the most potent compound (MIC: 8.23 μM) in active TB and was less effective than the lead but more potent than standard first line drug ethambutol. It was also found to be more efficacious than Isoniazid and Rifampicin and equipotent as Moxifloxacin against dormant Mycobacterium tuberculosis (MTB). Compound 06 also showed good inhibitory potential against over expressed latent MTB enzyme lysine ε-amino transferase with an IC50 of 1.04 ± 0.32 μM. This compound is a good candidate for drug development owing to potential against both active and dormant stages of MTB.
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