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Cinnamide Derivatives of <sub>D</sub>-Mannose as Inhibitors of the Bacterial Virulence Factor LecB from Pseudomonas aeruginosa

Cinnamide Derivatives of D-Mannose as Inhibitors of the Bacterial Virulence Factor LecB from Pseudomonas aeruginosa

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SOMMER, Roman, Dirk HAUCK, Annabelle VARROT, Stefanie WAGNER, Aymeric AUDFRAY, Andreas PRESTEL, Heiko M. MÖLLER, Anne IMBERTY, Alexander TITZ, 2015. Cinnamide Derivatives of D-Mannose as Inhibitors of the Bacterial Virulence Factor LecB from Pseudomonas aeruginosa. In: ChemistryOpen. 4(6), pp. 756-767. ISSN 2191-1355. eISSN 2191-1363

@article{Sommer2015Cinna-33436, title={Cinnamide Derivatives of D-Mannose as Inhibitors of the Bacterial Virulence Factor LecB from Pseudomonas aeruginosa}, year={2015}, doi={10.1002/open.201500162}, number={6}, volume={4}, issn={2191-1355}, journal={ChemistryOpen}, pages={756--767}, author={Sommer, Roman and Hauck, Dirk and Varrot, Annabelle and Wagner, Stefanie and Audfray, Aymeric and Prestel, Andreas and Möller, Heiko M. and Imberty, Anne and Titz, Alexander} }

Prestel, Andreas Audfray, Aymeric Audfray, Aymeric Wagner, Stefanie Varrot, Annabelle Möller, Heiko M. Prestel, Andreas eng 2016-03-23T14:33:14Z Möller, Heiko M. Hauck, Dirk Pseudomonas aeruginosa is an opportunistic Gram-negative pathogen with high antibiotic resistance. Its lectin LecB was identified as a virulence factor and is relevant in bacterial adhesion and biofilm formation. Inhibition of LecB with carbohydrate-based ligands results in a decrease in toxicity and biofilm formation. We recently discovered two classes of potent drug-like glycomimetic inhibitors, that is, sulfonamides and cinnamides of d-mannose. Here, we describe the chemical synthesis and biochemical evaluation of more than 20 derivatives with increased potency compared to the unsubstituted cinnamide. The structure–activity relationship (SAR) obtained and the extended biophysical characterization allowed the experimental determination of the binding mode of these cinnamides with LecB. The established surface binding mode now allows future rational structure-based drug design. Importantly, all glycomimetics tested showed extended receptor residence times with half-lives in the 5–20 min range, a prerequisite for therapeutic application. Thus, the glycomimetics described here provide an excellent basis for future development of anti-infectives against this multidrug-resistant pathogen. Titz, Alexander 2016-03-23T14:33:14Z Sommer, Roman Cinnamide Derivatives of <sub>D</sub>-Mannose as Inhibitors of the Bacterial Virulence Factor LecB from Pseudomonas aeruginosa Varrot, Annabelle Sommer, Roman 2015 Imberty, Anne Imberty, Anne Wagner, Stefanie Titz, Alexander Hauck, Dirk

Dateiabrufe seit 23.03.2016 (Informationen über die Zugriffsstatistik)

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