Clinical isolates of Mycobacterium tuberculosis in four European hospitals are uniformly susceptible to benzothiazinones
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Structural Basis for Benzothiazinone-Mediated Killing of Mycobacterium tuberculosisStructural basis of inhibition of Mycobacterium tuberculosis DprE1 by benzothiazinone inhibitorsTowards a new combination therapy for tuberculosis with next generation benzothiazinonesDecaprenylphosphoryl-β-D-ribose 2'-epimerase, the target of benzothiazinones and dinitrobenzamides, is an essential enzyme in Mycobacterium smegmatis[Better search strategies, hopeful candidates. The search for new antimycobacterial drugs].Drug-resistant tuberculosis: emerging treatment options.Importance of the genetic diversity within the Mycobacterium tuberculosis complex for the development of novel antibiotics and diagnostic tests of drug resistanceTuberculosis drugs: new candidates and how to find more.Arabinogalactan and lipoarabinomannan biosynthesis: structure, biogenesis and their potential as drug targets.Antituberculars which target decaprenylphosphoryl-β-D-ribofuranose 2'-oxidase DprE1: state of art.Antituberculosis drug research: a critical overview.Resistance in tuberculosis: what do we know and where can we go?The DprE1 enzyme, one of the most vulnerable targets of Mycobacterium tuberculosis.Trends in discovery of new drugs for tuberculosis therapy.Synthetic investigational new drugs for the treatment of tuberculosis.Identification of Better Pharmacokinetic Benzothiazinone Derivatives as New Antitubercular Agents.Characterization of DprE1-Mediated Benzothiazinone Resistance in Mycobacterium tuberculosis.Drug Resistance Mechanisms in Mycobacterium tuberculosis.Azoreductases in drug metabolism.In vitro combination studies of benzothiazinone lead compound BTZ043 against Mycobacterium tuberculosisBenzothiazinones mediate killing of Corynebacterineae by blocking decaprenyl phosphate recycling involved in cell wall biosynthesis.Decaprenyl-phosphoryl-ribose 2'-epimerase (DprE1): challenging target for antitubercular drug discovery.
P2860
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P2860
Clinical isolates of Mycobacterium tuberculosis in four European hospitals are uniformly susceptible to benzothiazinones
description
2010 nî lūn-bûn
@nan
2010 թուականի Յունուարին հրատարակուած գիտական յօդուած
@hyw
2010 թվականի հունվարին հրատարակված գիտական հոդված
@hy
2010年の論文
@ja
2010年論文
@yue
2010年論文
@zh-hant
2010年論文
@zh-hk
2010年論文
@zh-mo
2010年論文
@zh-tw
2010年论文
@wuu
name
Clinical isolates of Mycobacte ...... usceptible to benzothiazinones
@ast
Clinical isolates of Mycobacte ...... usceptible to benzothiazinones
@en
type
label
Clinical isolates of Mycobacte ...... usceptible to benzothiazinones
@ast
Clinical isolates of Mycobacte ...... usceptible to benzothiazinones
@en
prefLabel
Clinical isolates of Mycobacte ...... usceptible to benzothiazinones
@ast
Clinical isolates of Mycobacte ...... usceptible to benzothiazinones
@en
P2093
P2860
P50
P356
P1476
Clinical isolates of Mycobacte ...... usceptible to benzothiazinones
@en
P2093
Ana Luisa de Jesus Lopes Ribeiro
Beate Heym
Giulia Degiacomi
Leopoldo Pucillo
Maurizio Mirrione
Panajota Troupioti
Patrizia De Mori
Roberto Brerra
Stewart T Cole
Vadim Makarov
P2860
P304
P356
10.1128/AAC.01676-09
P407
P577
2010-01-19T00:00:00Z