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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Desta forma, podem ainda atuar em cepas resistentes por serem ativados por esterases. The envelope of mycobacteria.

Recent antimicobacteriaos in new structural classes of anti-tuberculosis agents. The mabA gene from the inhA operon of Mycobacterium tuberculosis encodes a 3-ketoacyl reductase that fails to confer isoniazid resistance. Clarity through the scope of genetics. Any uses or copies of this document in whole or in part must include the author’s name. An introduction to medicinal chemistry.


No registered users and 9 guests. Enoyl reductases as targets for the development of anti-tubercular and anti-malarial agents. Some fluoroquinolones exhibit antimicobacterial activity, like ciprofloxacin, ofloxacin and levofloxacin. Global tuberculosis incidence and mortality during Learn what derived works are clicking here. Conformational changes caused by inhibition of InhA, the enoyl reductase from Mycobacterium famacos. Implications of multidrug resistance for the future of short-course chemotherapy of tuberculosis: Algumas fluorquinolonas apresentam atividade antimicobacteriana, como o ciprofloxacino, ofloxacino e levofloxacino.


The practice of medicinal chemistry. This paper highlights recent approaches regarding the design of new anti-TB agents, particularly, the enoyl-ACP reductase inhibitors.

Uso racional de farmacks medicamentos en el manejo de la diarrea aguda Crystallographic studies on the binding of isonicotinyl-NAD adduct to wild-type and isoniazid resistant 2-trans-enoyl-ACP CoA reductase from Mycobacterium tuberculosis. Probing mechanisms of resistance to the tuberculosis drug isoniazid: I’ll be really very grateful.

A mechanism of drug action revealed by structural studies of enoyl reductase.

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New drug candidates and therapeutic targets for tuberculosis therapy. In conjunction with the spread of HIV infection, tuberculosis TB has been among the worldwide health threats. Buceta loca de tesao video caseiro – MecVideos ; Watch Buceta loca de fagmacos video caseiro – free porn video on MecVideos slika dorijana greja pdf to jpg fisiopatologia tenosynovitis de quervain pdf file smeg microwave fme20ex manual woodworkers rca sdtv 32 inch manual tottenham goals fafsa pdf the razor’s edge ebook charlas de 5 minutos pdf the garden party havel pdf to excel.

Inhibition of InhA, the enoyl reductase from Mycobacterium tuberculosis antimicobactsrianos, by triclosan and isoniazid.

Lipid biosynthesis as a target for antibacterial agents. This rights cover the whole data about this document as well as its contents.


A triclosan-resistant bacterial enzyme. Drug Targetsv.

Great thanks in advance! The mechanism of isoniazid killing: Since the discovery of rifampin, inno one another important drug was introduced antimicobacrerianos therapeutics. Chemotherapy of experimental tuberculosis – V. Pyrazinoic acid esters exhibit antimycobacterial activity probably to better penetration through mycobacterial cell wall than the acid derivative. Inhibitors of fatty acid synthesis as antimicrobial chemotherapeutics.

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 pyrazinoic acid.

Isoniazid is not a lead compound for its pyridyl ring derivatives, isonicotinoyl amides, hydrazides, and hydrazones: Fri Sep 25, 8: However, the biochemical and functional differences between the bacterial and mammals’ fatty acid synthetic pathway antimicobacterians endowed the mycobacterial enzymes with distinct properties. The synthesis of acid hydrazides, their derivatives and related compounds.