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Novel quinoline and naphthalene derivatives as potent antimycobacterial agents

2010; Elsevier BV; Volume: 45; Issue: 5 Linguagem: Inglês

10.1016/j.ejmech.2010.01.024

1768-3254

Ram Shankar Upadhayaya, Jaya Kishore Vandavasi, Ramakant A. Kardile, Santosh Lahore, Shailesh S. Dixit, Hemantkumar Deokar, Popat D. Shinde, M.P. Sarmah, Jyoti Chattopadhyaya,

ATP Synthase and ATPases Research

We have designed and synthesized both the quinoline and naphthalene based molecules influenced by the unique structural make-up of mefloquine and TMC207, respectively. These compounds were evaluated for their anti-mycobacterial activity against drug sensitive Mycobacterium tuberculosis H37Rv in vitro at single-dose concentration (6.25 microg/mL). The compounds 22, 23, 26 and 27 inhibited the growth of M. tuberculosis H37Rv 99%, 90%, 98% and 91% respectively. Minimum inhibitory concentration of compounds 22, 23, 26 and 27 was found to be 6.25 microg/mL. Our molecular modeling and docking studies of designed compounds showed hydrogen bonding with Glu-61, Tyr-64 and Asn-190 amino acid residues at the putative binding site of ATP synthase, these interactions were coherent as shown by Mefloquine and TMC207, where hydrogen bonding was found with Tyr-64 and Glu-61 respectively. SAR analysis indicates importance of hydroxyl group and nature of substituents on piperazinyl-phenyl ring was critical in dictating the biological activity of newly synthesized compounds.