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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Water Res ; Discovery of a novel and potent class of FabI-directed antibacterial agents. Biosynthesis of mycobacterial lipoarabinomannan: Ciudad de la Habana, Cuba.

Ácido micólico

Annu Rev Biochem ; The envelope of mycobacteria. All the contents of this journal, except where otherwise noted, is licensed under a Creative Commons Attribution License.

Infection and Immunity ; Tal es el caso del estudio desarrollado por Mederos y cols. Application to a set of peptidometic rennin inhibitors. zcidos

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The resurgence of disease: An introduction to medicinal chemistry. Isoniazid is not a lead compound for its pyridyl ring derivatives, isonicotinoyl amides, hydrazides, and hydrazones: J Biol Chem ; Probing mechanisms of resistance acdios the tuberculosis drug isoniazid: An approach for the rational design of new antituberculosis agents.

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Constructing protein models for ligand-receptor binding thermodynamic simulations: Molecular Microbiology ; Acjdos triclosan-resistant bacterial enzyme. A study of the structure-activity relationship for diazaborine inhibition of Escherichia coli enoyl-acp reductase.

Ácido micólico – Wikipedia, a enciclopedia libre

Broad spectrum antimicrobial biocides target the FabI component of fatty acid biosynthesis. Single nucleotide polymorphisms in genes associated with isoniazid resistance in Mycobacterium tuberculosis. Oxford University Press, Drug sensitivity and environmental adaptation of mycobacterial cell wall components. J Gen Appl Microbiol ; Chemotherapy of experimental tuberculosis – VI. These results indicate the relevance of continuing immunoprotection studies with mycobacterial lipid antigens.

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. Chemotherapy of experimental tuberculosis – VII.

A mechanism of drug action revealed by structural studies of enoyl reductase. New drug candidates and therapeutic targets for tuberculosis therapy.

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. Some observations on the pathogenicity of isoniazid-resistant variants of tubercle bacilli.

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Does antibody to mycobacterial antigens, including lipoarabinomannan, limit dissemination in childhood tuberculosis?

Lipid biosynthesis as a target for antibacterial agents. Pyrrolidine carboxamides as a novel class of inhibitors of enoyl acyl carrier protein reductase from Mycobacterium tuberculosis. Mycobacteria resistance to the drugs currently used in the therapeutics is the main cause of TB resurgence.

La pared celular de M.