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. 2012 Aug 9;3:226. doi: 10.3389/fmicb.2012.00226

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Copyright © 2012 Mackie, McKenney and van Hoek.

This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits use, distribution and reproduction in other forums, provided the original authors and source are credited and subject to any copyright notices concerning any third-party graphics etc.

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Structure of inhibitors used in this study. (1) Fosmidomycin (Fos, 3-[formyl(hydroxy) amino] propylphosphonic acid). (2) FR900098 (3-[acetyl(hydroxy)amino] propylphosphonic acid). (3) Compound 1: acyloxyalkyl ester prodrug derivative of FR900098 (Ortmann et al., 2003).