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A prodrug approach toward the development of water soluble fluoroquinolones and structure--activity relationships of quinoline-3-carboxylic acids.

Abstract
A fluoroquinolone prodrug, PA2808, was prepared and shown to convert to the highly active parent drug PA2789. In vitro and in vivo activation of PA2808 by alkaline phosphatase was demonstrated using disk diffusion and rat lung infection models. The water solubility of PA2808 showed a marked increase compared to PA2789 over a pH range suitable for aerosol drug delivery. A total of 48 analogues based on PA2789 were prepared and screened against a panel of Gram-positive and Gram-negative pathogens. Incorporating a cyclopropane-fused pyrrolidine (amine) at C-7 resulted in some of the most active analogues.
AuthorsWilliam R Baker, Shaopei Cai, Martin Dimitroff, Liming Fang, Kay K Huh, David R Ryckman, Xiao Shang, Ribhi M Shawar, Joseph H Therrien
JournalJournal of medicinal chemistry (J Med Chem) Vol. 47 Issue 19 Pg. 4693-709 (Sep 09 2004) ISSN: 0022-2623 [Print] United States
PMID15341485 (Publication Type: Journal Article)
Chemical References
  • Anti-Bacterial Agents
  • Carboxylic Acids
  • Fluoroquinolones
  • Organophosphates
  • PA 2789
  • PA 2808
  • Piperazines
  • Prodrugs
  • Water
  • Nalidixic Acid
Topics
  • Animals
  • Anti-Bacterial Agents (chemical synthesis, chemistry, pharmacokinetics, pharmacology)
  • Bacteria (drug effects)
  • Carboxylic Acids (chemistry)
  • Fluoroquinolones (chemical synthesis, chemistry, pharmacokinetics, pharmacology)
  • Lung (metabolism)
  • Molecular Structure
  • Nalidixic Acid (analogs & derivatives, chemical synthesis, chemistry, metabolism, pharmacokinetics, pharmacology)
  • Organophosphates (chemical synthesis, chemistry, pharmacokinetics, pharmacology)
  • Piperazines (chemistry, metabolism, pharmacokinetics, pharmacology)
  • Prodrugs (chemical synthesis, chemistry, metabolism, pharmacokinetics)
  • Rats
  • Solubility
  • Structure-Activity Relationship
  • Water (chemistry)

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