Antibiofilm Activity of a Diverse Oroidin Library Generated through Reductive Acylation

A diverse 20-compound library of analogues based on the marine alkaloid oroidin were synthesized via a reductive acylation strategy. The final target was then assayed for inhibition and dispersion activity against common proteobacteria known to form biofilms. This methodology represents a significan...

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Veröffentlicht in:Journal of organic chemistry 2009-02, Vol.74 (4), p.1755-1758
Hauptverfasser: Ballard, T. Eric, Richards, Justin J, Aquino, Arianexys, Reed, Catherine S, Melander, Christian
Format: Artikel
Sprache:eng
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Zusammenfassung:A diverse 20-compound library of analogues based on the marine alkaloid oroidin were synthesized via a reductive acylation strategy. The final target was then assayed for inhibition and dispersion activity against common proteobacteria known to form biofilms. This methodology represents a significant improvement over the generality of known methods to acylate substrates containing 2-aminoimidazoles and has the potential to have broad application to the synthesis of more advanced oroidin family members and their corresponding analogues.
ISSN:0022-3263
1520-6904
DOI:10.1021/jo802260t