Syntheses and evaluation of substituted aromatic hydroxamates and hydroxamic acids that target mycobacterium tuberculosis

Lignende værker

• Syntheses and Biological Evaluations of Highly Functionalized Hydroxamate Containing and N-Methylthio Monobactams as Anti-Tuberculosis and β-Lactamase Inhibitory Agents
  af: Majewski, Mark W., et al.
  Udgivet: (2015)
• Design, syntheses, and anti-tuberculosis activities of conjugates of piperazino-1,3-benzothiazin-4-ones (pBTZs) with 2,7-dimethylimidazo [1,2-a]pyridine-3-carboxylic acids and 7-phenylacetyl cephalosporins
  af: Majewski, Mark W., et al.
  Udgivet: (2016)
• Syntheses of Mycobactin Analogs as Potent and Selective Inhibitors of Mycobacterium tuberculosis
  af: Juárez-Hernández, Raúl E., et al.
  Udgivet: (2012)
• Studies at the Ionizable Position of Cephalosporins and Penicillins: Hydroxamates as Substitutes for the Traditional Carboxylate Group
  af: Majewski, Mark W., et al.
  Udgivet: (2016)
• Design and Syntheses of Anti-Tuberculosis Agents Inspired by BTZ043 Using a Scaffold Simplification Strategy
  af: Tiwari, Rohit, et al.
  Udgivet: (2014)