Fluoroquinolones (FQ) are an important family of synthetic antimicrobial agents being clinically used over the past thirty years. Currently some FQ are under investigation for the treatment of multidrug-resistant tuberculosis (MDRTB), defined as resistance to at least isoniazid and rifampicin, and are under investigation as first-line drugs. Their main biological target in Mycobacterium tuberculosis is the DNA gyrase, a topoisomerase II encoded by gyrA and gyrB that is essential to maintain the DNA supercoil. It has been demonstrated that mutations in short regions of DNA gyrase are associated with quinolone resistance or hypersusceptibility and take place in several MDR clinical isolates of M. tuberculosis. In this article we update§ our previous review (Carta et al. Anti-infective agents, 2008, 7, 134-147) about the anti mycobacterial properties, mode of action and structure activity relationship (SAR) studies of the known quinolone derivatives. Furthermore, we update the synthesis and activity of 3,9-disubstituted-6-oxo-6,9-dihydro-3H-[1,2,3]-triazolo[4,5- h,g]quinolone-carboxylic acids and their esters as a new class of potent and selective anti-mycobacterial agents, coupled with absence of cytotoxicity. Furthermore, particularly interesting is their activity against MDR M. tuberculosis.

SAR and Anti-Mycobacterial Activity of Quinolones and Triazoloquinolones: An Update / Briguglio, Irene; Piras, Sandra; Corona, Paola; Pirisi, Maria Antonietta; Jabes, D; Carta, Antonio. - In: ANTI-INFECTIVE AGENTS IN MEDICINAL CHEMISTRY. - ISSN 1871-5214. - 11:1(2013), pp. 75-89.

SAR and Anti-Mycobacterial Activity of Quinolones and Triazoloquinolones: An Update

BRIGUGLIO, Irene;PIRAS, Sandra;CORONA, Paola;PIRISI, Maria Antonietta;CARTA, Antonio
2013-01-01

Abstract

Fluoroquinolones (FQ) are an important family of synthetic antimicrobial agents being clinically used over the past thirty years. Currently some FQ are under investigation for the treatment of multidrug-resistant tuberculosis (MDRTB), defined as resistance to at least isoniazid and rifampicin, and are under investigation as first-line drugs. Their main biological target in Mycobacterium tuberculosis is the DNA gyrase, a topoisomerase II encoded by gyrA and gyrB that is essential to maintain the DNA supercoil. It has been demonstrated that mutations in short regions of DNA gyrase are associated with quinolone resistance or hypersusceptibility and take place in several MDR clinical isolates of M. tuberculosis. In this article we update§ our previous review (Carta et al. Anti-infective agents, 2008, 7, 134-147) about the anti mycobacterial properties, mode of action and structure activity relationship (SAR) studies of the known quinolone derivatives. Furthermore, we update the synthesis and activity of 3,9-disubstituted-6-oxo-6,9-dihydro-3H-[1,2,3]-triazolo[4,5- h,g]quinolone-carboxylic acids and their esters as a new class of potent and selective anti-mycobacterial agents, coupled with absence of cytotoxicity. Furthermore, particularly interesting is their activity against MDR M. tuberculosis.
2013
SAR and Anti-Mycobacterial Activity of Quinolones and Triazoloquinolones: An Update / Briguglio, Irene; Piras, Sandra; Corona, Paola; Pirisi, Maria Antonietta; Jabes, D; Carta, Antonio. - In: ANTI-INFECTIVE AGENTS IN MEDICINAL CHEMISTRY. - ISSN 1871-5214. - 11:1(2013), pp. 75-89.
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/11388/80713
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