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Martin Empting

Showing results (11-20 of 80) with videos related to

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Organic & Biomolecular Chemistry|June 10, 2014
From in vitro to in cellulo: structure-activity relationship of (2-nitrophenyl)methanol derivatives as inhibitors of PqsD in Pseudomonas aeruginosaMichael P Storz, Giuseppe Allegretta, Benjamin Kirsch, et al.
Mabs|December 20, 2014
Structural insights and biomedical potential of IgNAR scaffolds from sharksStefan Zielonka, Martin Empting, Julius Grzeschik, et al.
International Journal of Nanomedicine|May 6, 2024
Enzyme-Linked Lipid Nanocarriers for Coping Pseudomonal Pulmonary Infection. Would Nanocarriers Complement Biofilm Disruption or Pave Its Road?Noha Nafee, Dina M Gaber, Alaa Abouelfetouh, et al.
Biological Chemistry|January 19, 2019
Hit evaluation of an α-helical peptide: Ala-scan, truncation and sidechain-to-sidechain macrocyclization of an RNA polymerase InhibitorAhmed Ashraf Moustafa Kamal, Monica Habib, Joerg Haupenthal, et al.
Organic & Biomolecular Chemistry|October 2, 2009
Application of copper(I) catalyzed azide-alkyne [3+2] cycloaddition to the synthesis of template-assembled multivalent peptide conjugatesOlga Avrutina, Martin Empting, Sebastian Fabritz, et al.
European Journal of Medicinal Chemistry|June 16, 2014
Inhibition of 17β-HSD1: SAR of bicyclic substituted hydroxyphenylmethanones and discovery of new potent inhibitors with thioether linkerAhmed S Abdelsamie, Emmanuel Bey, Nina Hanke, et al.
Chembiochem : a European Journal of Chemical Biology|May 4, 2018
The Alkylquinolone Repertoire of Pseudomonas aeruginosa is Linked to Structural Flexibility of the FabH-like 2-Heptyl-3-hydroxy-4(1H)-quinolone (PQS) Biosynthesis Enzyme PqsBCFlorian Witzgall, Tobias Depke, Michael Hoffmann, et al.
Communications Chemistry|April 11, 2025
Domain adaptable language modeling of chemical compounds identifies potent pathoblockers for Pseudomonas aeruginosaGeorgios Kallergis, Ehsannedin Asgari, Martin Empting, et al.
Journal of Medicinal Chemistry|January 26, 2016
Novel Strategies for the Treatment of Pseudomonas aeruginosa InfectionsStefanie Wagner, Roman Sommer, Stefan Hinsberger, et al.
Chemmedchem|October 13, 2016
Structure-Activity Relationships of 2-Sufonylpyrimidines as Quorum-Sensing Inhibitors to Tackle Biofilm Formation and eDNA Release of Pseudomonas aeruginosaAndreas Thomann, Christian Brengel, Carsten Börger, et al.
Pageof 8

Showing results (11-20 of 80) with videos related to

Sort By:
Pageof 8
Organic & Biomolecular Chemistry|June 10, 2014
From in vitro to in cellulo: structure-activity relationship of (2-nitrophenyl)methanol derivatives as inhibitors of PqsD in Pseudomonas aeruginosaMichael P Storz, Giuseppe Allegretta, Benjamin Kirsch, et al.
Mabs|December 20, 2014
Structural insights and biomedical potential of IgNAR scaffolds from sharksStefan Zielonka, Martin Empting, Julius Grzeschik, et al.
International Journal of Nanomedicine|May 6, 2024
Enzyme-Linked Lipid Nanocarriers for Coping Pseudomonal Pulmonary Infection. Would Nanocarriers Complement Biofilm Disruption or Pave Its Road?Noha Nafee, Dina M Gaber, Alaa Abouelfetouh, et al.
Biological Chemistry|January 19, 2019
Hit evaluation of an α-helical peptide: Ala-scan, truncation and sidechain-to-sidechain macrocyclization of an RNA polymerase InhibitorAhmed Ashraf Moustafa Kamal, Monica Habib, Joerg Haupenthal, et al.
Organic & Biomolecular Chemistry|October 2, 2009
Application of copper(I) catalyzed azide-alkyne [3+2] cycloaddition to the synthesis of template-assembled multivalent peptide conjugatesOlga Avrutina, Martin Empting, Sebastian Fabritz, et al.
European Journal of Medicinal Chemistry|June 16, 2014
Inhibition of 17β-HSD1: SAR of bicyclic substituted hydroxyphenylmethanones and discovery of new potent inhibitors with thioether linkerAhmed S Abdelsamie, Emmanuel Bey, Nina Hanke, et al.
Chembiochem : a European Journal of Chemical Biology|May 4, 2018
The Alkylquinolone Repertoire of Pseudomonas aeruginosa is Linked to Structural Flexibility of the FabH-like 2-Heptyl-3-hydroxy-4(1H)-quinolone (PQS) Biosynthesis Enzyme PqsBCFlorian Witzgall, Tobias Depke, Michael Hoffmann, et al.
Communications Chemistry|April 11, 2025
Domain adaptable language modeling of chemical compounds identifies potent pathoblockers for Pseudomonas aeruginosaGeorgios Kallergis, Ehsannedin Asgari, Martin Empting, et al.
Journal of Medicinal Chemistry|January 26, 2016
Novel Strategies for the Treatment of Pseudomonas aeruginosa InfectionsStefanie Wagner, Roman Sommer, Stefan Hinsberger, et al.
Chemmedchem|October 13, 2016
Structure-Activity Relationships of 2-Sufonylpyrimidines as Quorum-Sensing Inhibitors to Tackle Biofilm Formation and eDNA Release of Pseudomonas aeruginosaAndreas Thomann, Christian Brengel, Carsten Börger, et al.
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