FARMACOS ANTIMICOBACTERIANOS PDF

antimicobacterianos la isioniazida rifampicina priazinamida, etambutol estreptomicina son los cinco fármacos de primera línea para el tratamiento de la. En determinadas situaciones debe añadirse un cuarto fármaco, etambutol en adultos y estreptomicina en niños, en quienes no puede Antimicobacterianos. Antibióticos beta-lactámicos y otros antibióticos de amplio espectro. Fármacos antimicobacterianos y antifúngicos. Fármacos antivirales.

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This paper highlights recent approaches regarding the design of new anti-TB agents, particularly, the enoyl-ACP reductase inhibitors. Inhibition of the Staphylococcus aureus NADPH-dependent enoyl-acyl carrier protein reductase by triclosan and hexachlorophene. It will also show you how to troubleshoot Drug Targetsv. Implications of multidrug resistance for the future of short-course chemotherapy of tuberculosis: The mechanism of isoniazid killing: Oxford University Press, Chemotherapy of experimental tuberculosis – VII.

Uso racional de los medicamentos en el manejo de la diarrea aguda Isonicotinic acid hydrazide nydrazid and related compounds.

Síntese e atividade antimicobacteriana de ésteres do ácido pirazinóico e quinolo

The growing burden of tuberculosis: In view of this severe situation, the new and selective anti-TB design is of utmost importance. Isoniazid is not a lead compound for its pyridyl ring derivatives, isonicotinoyl amides, hydrazides, and hydrazones: Reproduction for commercial use is forbidden.

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Chemoterapy of experimental tuberculosis. Characterization of a ligand-receptor binding event using receptor-dependent four-dimensional quantitative structure-activity relationship analysis.

Antimicobacterial agents Fluoroquinolones Prodrugs Pyrazinoic acid.

This wikiHow will teach you how to print them. Conformational changes caused by inhibition of InhA, the enoyl reductase from Mycobacterium tuberculosis.

Targeting tuberculosis and malaria through inhibition of enoyl reductase: The catalase-peroxidase gene and isoniazid resistance of Mycobacterium tuberculosis. The practice of medicinal chemistry.

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Pyrrolidine carboxamides as a novel class of inhibitors of enoyl acyl carrier protein reductase from Mycobacterium tuberculosis. All the contents of this journal, except where otherwise noted, is licensed under a Creative Commons Attribution License. Probing mechanisms of resistance to the tuberculosis drug isoniazid: Clarity through the scope of genetics.

Tuberculosis affects over than one billion people around the world. This document is only for private use for research and teaching activities.

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Crystal structure and fuction of the isoniazid target of Mycobacterium tuberculosis. Tripanosoma gambiense y T.

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This rights cover the whole data about this document as well as its contents. Overexpression of inhA, but not kasAconfers resistance to isoniazid farkacos ethionamide in Mycobacterium smegmatisM.

FÁRMACOS ANTIMICOBACTERIANOS by alejandro lopez lara on Prezi

Broad spectrum antimicrobial biocides target the FabI component of fatty acid biosynthesis. The mabA gene from the inhA operon of Mycobacterium tuberculosis encodes a 3-ketoacyl reductase that fails to confer isoniazid resistance. Will be grateful for any help! Preparation and antibacterial activities of new 1,2,3-diazaborine derivatives and analogues.

An application to a animicobacterianos of peptidometic rennin inhibitors. Em geral, as tiofeno-diazoborinas foram os inibidores mais potentes, seguidos faarmacos benzo-diazoborinas e furano-diazoborinas, enquanto que as pirrol-diazoborinas foram totalmente inativas. Gummerus Printing, Saarijarvi, Finland. Who could help me?