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A Prodrug Approach toward the Development of Water Soluble Fluoroquinolones and Structure−Activity Relationships of Quinoline-3-carboxylic Acids

Authors :
Baker, W. R.
Cai, S.
Dimitroff, M.
Fang, L.
Huh, K. K.
Ryckman, D. R.
Shang, X.
Shawar, R. M.
Therrien, J. H.
Source :
Journal of Medicinal Chemistry; September 2004, Vol. 47 Issue: 19 p4693-4709, 17p
Publication Year :
2004

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 <BO>g</BO>) at C-7 resulted in some of the most active analogues.

Details

Language :
English
ISSN :
00222623 and 15204804
Volume :
47
Issue :
19
Database :
Supplemental Index
Journal :
Journal of Medicinal Chemistry
Publication Type :
Periodical
Accession number :
ejs6374407