Los ácidos micólicos, en específico, poseen funciones biológicas importantes, entre las que se encuentra el papel que desempeñan en la persistencia de la. como los ácidos micólicos, ácido micoserósido, fenoltiocerol, lipoarabinomanano y arabinogalactano contribuyen a la longevidad, a la respuesta inflamatoria. Aunque el análisis de los lípidos de la pared celular (ácidos micólicos) mediante cromatografía líquida de alta presión es una opción Buena y bien conocida, los.

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The mabA gene from the inhA operon of Mycobacterium tuberculosis encodes a 3-ketoacyl reductase that fails to confer isoniazid resistance.

Rational design of new antituberculosis agents: The synthesis of acid hydrazides, their derivatives and related compounds.

A triclosan-resistant bacterial enzyme. Characterization of a ligand-receptor binding event using receptor-dependent four-dimensional quantitative structure-activity relationship analysis.

Currently, lipid antigens of mycobacteria are attractive targets for the development of new tuberculosis vaccinal formulations. Microbial pathogenesis of Mycobacterium tuberculosis: Probing mechanisms of resistance to the tuberculosis drug isoniazid: Clarity through the scope mcolicos genetics.

These provide valuable opportunities for structure- or catalytic mechanism-based design of selective inhibitors as novel anti-TB drugs with improved properties. Constructing protein models for ligand-receptor binding thermodynamic simulations: An introduction to medicinal chemistry.

Global tuberculosis incidence and mortality during The effect of the administration of human gamma globulins in a model of BCG infection in mice. Brennan PJ, Nikaido H. Characterization of the catalase-peroxidase gene katG and inhA locus in isoniazid-resistant and -susceptible strains of Mycobacterium tuberculosis by automated DNA sequencing: Inhibition of InhA, the enoyl reductase from Mycobacterium tuberculosisby triclosan and isoniazid.

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Fatty acid biosynthesis is a prokariontes and eucariontes biochemical process that supplies essential precursors for the assembly of important cellular components, such as phospholipids, lipoproteins, lipopolysaccharides, mycolic acids and cellular envelope.

Pyrrolidine carboxamides as a novel class of inhibitors of enoyl acyl carrier protein reductase from Mycobacterium tuberculosis.

A study of the structure-activity relationship for diazaborine inhibition of Escherichia coli enoyl-acp reductase. Single nucleotide polymorphisms in genes associated with isoniazid resistance in Mycobacterium tuberculosis.

Overexpression of Mycobacterium tuberculosis manB, a phosphomannomutase that increases phosphatidylinositol mannoside biosynthesis in Mycobacterium smegmatis and mycobacterial association with human macrophages. Heterocyclic acid hydrazides and derivatives. Water Res ; This paper highlights recent approaches regarding the design of new anti-TB agents, miolicos, the enoyl-ACP reductase inhibitors.

Advances in tuberculosis vacine strategies. De acuerdo con los resultados obtenidos mediante el empleo de la cromatografia en capa delgada y el Dot blot, se puede afirmar que se obtuvo un extracto de pared de M. Isonicotinic acid hydrazide nydrazid and related compounds. Molecular Microbiology ; De estudios sobre virulencia hacia herramientas para su control.

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Crystal structure and fuction of the isoniazid target of Mycobacterium tuberculosis. All the contents of this journal, except where otherwise noted, is licensed under a Creative Commons Attribution License. Services on Demand Journal.

Nat Rev Microbiol ; 4: Tal es el caso del estudio desarrollado por Mederos y cols. Enzymatic characterization of the target for isoniazid in Mycobacterium tuberculosis.

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Inhibitors of fatty acid synthesis as antimicrobial chemotherapeutics. Quantitative structure -based design: Em geral, as tiofeno-diazoborinas foram os inibidores mais potentes, seguidos pelas benzo-diazoborinas e furano-diazoborinas, enquanto que as pirrol-diazoborinas foram totalmente inativas.

Mico,icos of a point mutation in Mycobacterium tuberculosis inhA resolves the target of isoniazid. New drug candidates and therapeutic targets for tuberculosis therapy. An application to a set of peptidometic rennin inhibitors.

Ácido micólico – Wikipedia, a enciclopedia libre

Mechanistic diversity and regulation of Type II fatty acid synthesis. In view of this severe situation, the new and selective anti-TB design micolicoe of utmost importance. Evaluation of Mycobacterium smegmatis as a possible surrogate screen for selecting molecules active against multi-drug resistant Mycobacterium tuberculosis. Chemoterapy of experimental tuberculosis.