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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Drug sensitivity and environmental adaptation of mycobacterial cell wall components. Gummerus Printing, Saarijarvi, Finland. An approach for the rational design of new antituberculosis agents. Antimicobacterial agents Fluoroquinolones Prodrugs Pyrazinoic acid.

Curso 2017/2018

Tuberculosis, focus on tropical diseases. Pyrazinamide, one of the drugs available in therapy of tuberculosis, is nowadays considered a bioprecursor of pyrazinoic acid, because resistant bacterias do not express an enzyme, pyrazinamidase, responsible by the conversion of pyrazinamide to farmacox acid. A triclosan-resistant bacterial enzyme. Desta forma, podem ainda atuar em cepas resistentes por serem ativados por esterases.

The magic bullets and tuberculosis drug targets. Tripanosoma gambiense y T. En cualquier caso, el cuarto ebook pdf Discovery of a novel and potent class of FabI-directed antibacterial agents.


Oxford University Press, Global tuberculosis control – surveillance, planning, financing.

Will be grateful for any help! Who is online Users browsing this forum: En la tabla 1 se So, it could act in resistant strains because is activated by esterases.

Recent advances in new structural classes of anti-tuberculosis agents. Targeting tuberculosis and malaria through inhibition of enoyl reductase: All the contents of this journal, except where otherwise noted, is licensed under a Creative Commons Attribution License.

The growing burden of tuberculosis: Inaccurate estimates of needed resources final fantasy 4 heroes – … Farmacos diureticos pdf printer – nookl.

Pyrrolidine carboxamides as a novel class of inhibitors of enoyl acyl carrier protein reductase from Mycobacterium tuberculosis. New drug candidates and therapeutic targets for tuberculosis therapy.

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Tuberculosis affects over than one billion people around the world. Enoyl reductases as targets for the development of anti-tubercular and anti-malarial agents.

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Crystal structure and fuction of the isoniazid target of Mycobacterium tuberculosis. Global tuberculosis incidence and mortality during Estes pesquisadores isolaram cepas de E.

Critical review of the role of HTS in drug discovery. Since the discovery of rifampin, inno one another important drug was introduced in therapeutics. Preparation and antibacterial activities of new 1,2,3-diazaborine derivatives and analogues. One of the synthesized compounds showed activity in vitro, with minnimal inhibitory concentration comparable to ciprofloxacin, one of most active drugs. Guidebook on molecular modeling in drug design.

The synthesis of acid hydrazides, their derivatives and related compounds. Characterization of the catalase-peroxidase gene katG and inhA locus in isoniazid-resistant and -susceptible strains of Mycobacterium tuberculosis by automated DNA sequencing: The catalase-peroxidase gene and isoniazid resistance of Mycobacterium tuberculosis.