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New trends in development of antimycobacterial compounds.
Biava, M; Porretta, G C; Deidda, D; Pompei, R.
  • Biava M; Dipartimento di Studi di Chimica e Tecnologia delle Sostanze Biologicamente Attive, Università "La Sapienza", P.le A Moro 5, 00185 Rome, Italy. Mariangela.Biava@uniroma1.it
Infect Disord Drug Targets ; 6(2): 159-72, 2006 Jun.
Article en En | MEDLINE | ID: mdl-16789877
ABSTRACT
The resurgence of tuberculosis and the surge of multidrug-resistant clinical isolates of Mycobacterium tuberculosis have reaffirmed tuberculosis as a primary public health concern. In this review we describe some new findings on the pharmacological status of fluoroquinolones derivatives (Gatifloxacin, Moxifloxacin and Sitafloxacin), new macrolides (Clarithromycin, Azithromycin and Roxithromycin), new rifamycin derivatives (Rifapentin, Rifabutin and Rifalazil) and new oxazolidinones (Linezolid and PNU 100480). We describe also other type of agents that are being developed as antimycobacterial drugs. Some of these are under clinical investigation, while others are considered to be promising candidates for future development. Among them, nitroimidazopyrans, new ketolides, Isoxyl (ISO), pyrroles derived from BM 212, Mefloquine and Diarylquinoline R207910 are discussed. We also describe the mechanism of drug resistance in mycobacteria, as well as new potential targets.
Asunto(s)
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Banco de datos: MEDLINE Asunto principal: Mycobacterium tuberculosis / Antituberculosos Límite: Humans Idioma: En Año: 2006 Tipo del documento: Article
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Banco de datos: MEDLINE Asunto principal: Mycobacterium tuberculosis / Antituberculosos Límite: Humans Idioma: En Año: 2006 Tipo del documento: Article