Inhibition of S. aureus α-Hemolysin and B. anthracis Lethal Toxin by β-Cyclodextrin Derivatives

Eitemau Tebyg

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• Symmetry Requirements for Effective Blocking of Pore-Forming Toxins: Comparative Study with α-, β-, and γ-Cyclodextrin Derivatives
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• Kinetics and thermodynamics of binding reactions as exemplified by anthrax toxin channel blockage with a cationic cyclodextrin derivative
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• Blocking anthrax lethal toxin at the protective antigen channel by using structure-inspired drug design
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• In Vivo Efficacy of β-Cyclodextrin Derivatives against Anthrax Lethal Toxin
  gan: Moayeri, Mahtab, et al.
  Cyhoeddwyd: (2008)