Novel insights into the pharmacometabonomics of first-line tuberculosis drugs relating to metabolism, mechanism of action and drug-resistance. Contribution of dfrA and inhA mutations to the detection of isoniazid-resistant Mycobacterium tuberculosis isolates. 2-Aryl benzazole derived new class of anti-tubercular compounds: Endowed to eradicate mycobacterium tuberculosis in replicating and non-replicating forms. . Mycobacterium tuberculosis Overview on Mechanisms of Isoniazid Action and Resistance in Mycobacterium Tuberculosis Infect Genet Evol.

Mycobacterium tuberculosis

NIH If you do not receive an email within 10 minutes, your email address may not be registered, Injectable Multicomponent Biomimetic Gel Composed of Inter-Crosslinked Dendrimeric and Mesoporous Silica Nanoparticles Exhibits Highly Tunable Elasticity and Dual Drug Release Capacity. Can the Analysis of Clonal Strains Reveal Novel Targetable Pathways?
Mechanisms of action of isoniazid For decades after its introduction, the mechanisms of action of the front-line antituberculosis therapeutic agent isoniazid (INH) remained unclear. . Isoniazid is a prodrug that inhibits the formation of the mycobacterial cell wall.

A Survey of the Structures of US FDA Approved Combination Drugs.

Biotransformation of Isoniazid by Cytochromes P450: Analyzing the Molecular Mechanism using Density Functional Theory.

Inhibition of Mycobacterium tuberculosis InhA: Design, synthesis and evaluation of new di-triclosan derivatives. 2009 Sep;53(9):4010-2. doi: 10.1128/AAC.00433-09. Synthesis and Antimicrobial Activity of Some New 3,4‐Disubstituted Pyrroles and Pyrazoles. , provides a potent antituberculosis cocktail that is so effective because it attacks multiple targets.

as an Antitubercular Prodrug 2003 Apr;47(4):1241-50. doi: 10.1128/aac.47.4.1241-1250.2003. Drug Delivery and Translational Research. Comparison of radiation dose and image quality between flat panel computed tomography and multidetector computed tomography in a hybrid CT‐angiography suite. Mycobacterium tuberculosis Host-Directed Therapy as a Novel Treatment Strategy to Overcome Tuberculosis: Targeting Immune Modulation.

Mycobacterium tuberculosis

Toxicity of nitrogen oxides and related oxidants on mycobacteria: Reduced affinity for Isoniazid in the S315T mutant of, The catalase‐peroxidase gene and isoniazid resistance of, Molecular basis for the exquisite sensitivity of, Hydrogen peroxide‐mediated isoniazid activation catalyzed by, Oxidation of isonicotinic acid hydrazide by the peroxidase system.

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