Abstract
We report the first total synthesis of 5-phenyl preacinetobactin and its characterization. The route was developed for the synthesis of preacinetobactin, the siderophore critical to the Gram-negative pathogen A. baumannii. It leverages a C5-substituted benzaldehyde as a key starting material and should enable the synthesis of similar analogs. 5-Phenyl preacinetobactin binds iron in a manner analogous to the natural siderophore, but it did not rescue growth in a strain of A. baumannii unable to produce preacinetobactin.
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Bray, J. M., Pierce, S., Angeles-Boza, A. M., & Peczuh, M. W. (2022). Synthesis and Characterization of Preacinetobactin and 5-Phenyl Preacinetobactin. Molecules, 27(12). https://doi.org/10.3390/molecules27123688
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