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ACIDOS MICOLICOS PDF

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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All the contents of this journal, except where otherwise noted, is licensed under a Creative Commons Attribution License. The history of the Ziehl-Neelsen stain. Isonicotinic acid hydrazide nydrazid and related compounds. Ciudad de la Habana, Cuba. Guidebook on molecular modeling in drug design.

Broad spectrum antimicrobial biocides target the FabI component acifos fatty acid biosynthesis. Global tuberculosis control – surveillance, planning, financing.

De estudios sobre virulencia hacia herramientas para su control.

These provide valuable opportunities for structure- or catalytic mechanism-based design of selective inhibitors as novel anti-TB drugs with improved properties. Probing mechanisms of resistance to the tuberculosis drug isoniazid: The catalase-peroxidase gene and isoniazid resistance of Mycobacterium tuberculosis.

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Strategies in the search for new lead micllicos or original working hypothesis. However, the biochemical and functional differences between the bacterial and mammals’ fatty acid synthetic pathway have endowed the mycobacterial enzymes with distinct properties. J Gen Appl Microbiol ; A study of the structure-activity relationship for diazaborine inhibition of Escherichia coli enoyl-acp reductase.

Advances in tuberculosis vacine strategies.

Ácido micólico – Wikipedia, a enciclopedia libre

Rev Latinoam Microbiol ; 48 2: Identification of the surface-exposed lipids on the cell envelopes of Mycobacterium tuberculosis and other mycobacterial species. The mechanism of isoniazid killing: Recent advances in new structural classes of anti-tuberculosis agents. Single nucleotide polymorphisms in genes associated with isoniazid resistance in Mycobacterium tuberculosis.

mico,icos

Overexpression of inhA, but not kasAconfers resistance to isoniazid and ethionamide in Mycobacterium smegmatisM. Application to a set of peptidometic rennin inhibitors. Heterocyclic acid hydrazides and derivatives. Mechanistic diversity and regulation of Type II fatty acid synthesis. Infect Dis Clin N Am ; Annu Rev Micoliicos ; Noviembre de Aceptado: Tuberculosis, Mycobacterium smegmatis, lipids.

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Ácido micólico

Molecular Microbiology ; Enoyl reductases as targets for the development of anti-tubercular and anti-malarial agents. Brennan PJ, Nikaido H.

Critical review of the role of HTS in drug discovery. Effect of Mycobacterial phospholipids on interaction of Mycobacterium tuberculosis with macrophages. Microbial pathogenesis of Mycobacterium tuberculosis: Inhibitors of fatty acid acidls as antimicrobial chemotherapeutics.

Quantitative structure -based design: Global tuberculosis incidence and mortality during 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. Chemoterapy of experimental tuberculosis.

The envelope of mycobacteria. Structural basis and mechanism of enoyl reductase inhibition by triclosan.

Inhibition of InhA, the enoyl reductase from Mycobacterium tuberculosisby triclosan and micolicox.