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Novel quinoline and naphthalene derivatives as potent antimycobacterial agents
Vise andre og tillknytning
2010 (engelsk)Inngår i: European Journal of Medicinal Chemistry, ISSN 0223-5234, E-ISSN 1768-3254, Vol. 45, nr 5, s. 1854-1867Artikkel i tidsskrift (Fagfellevurdert) Published
Abstract [en]

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 mu g/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 mu g/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. (C) 2010 Elsevier Masson SAS. All rights reserved.

sted, utgiver, år, opplag, sider
2010. Vol. 45, nr 5, s. 1854-1867
Emneord [en]
ATP synthase, Naphthalene, Quinoline, TMC207, Mefloquine, Anti-tuberculosis drugs
HSV kategori
Identifikatorer
URN: urn:nbn:se:uu:diva-136621DOI: 10.1016/j.ejmech.2010.01.024ISI: 000276695200021OAI: oai:DiVA.org:uu-136621DiVA, id: diva2:377165
Tilgjengelig fra: 2010-12-13 Laget: 2010-12-13 Sist oppdatert: 2018-01-12bibliografisk kontrollert

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