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Steffen Brunst

Showing results (11-20 of 21) with videos related to

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RSC Medicinal Chemistry|November 15, 2021
<i>N</i>-Aryl mercaptoacetamides as potential multi-target inhibitors of metallo-β-lactamases (MBLs) and the virulence factor LasB from <i>Pseudomonas aeruginosa</i>Samir Yahiaoui, Katrin Voos, Jörg Haupenthal, et al.
ACS Medicinal Chemistry Letters|July 21, 2022
Designing a Small Fluorescent Inhibitor to Investigate Soluble Epoxide Hydrolase Engagement in Living CellsSteffen Brunst, Julia Schönfeld, Peter Breunig, et al.
Chemmedchem|June 29, 2021
Rh<sup>II</sup> -Catalyzed De-symmetrization of Ethane-1,2-dithiol and Propane-1,3-dithiol Yields Metallo-β-lactamase InhibitorsMikhail Krasavin, Daniil Zhukovsky, Igor Solovyev, et al.
Biochemical Pharmacology|July 30, 2022
Compilation and evaluation of a fatty acid mimetics screening libraryJohanna H M Ehrler, Steffen Brunst, Amelie Tjaden, et al.
Journal of Medicinal Chemistry|February 21, 2022
<i>N</i>-Aryl Mercaptopropionamides as Broad-Spectrum Inhibitors of Metallo-β-LactamasesCansu Kaya, Jelena Konstantinović, Andreas M Kany, et al.
Journal of Medicinal Chemistry|August 15, 2025
Sustainable Joullié-Ugi and Continuous Flow Implementation Led to Novel Captopril-Inspired Broad-Spectrum Metallo-β-Lactamase InhibitorsAntonella Ilenia Alfano, Sveva Pelliccia, Simona Barone, et al.
Journal of Medicinal Chemistry|October 12, 2020
Design, Synthesis, and Structure-Activity Relationship Studies of Dual Inhibitors of Soluble Epoxide Hydrolase and 5-LipoxygenaseKerstin Hiesinger, Jan S Kramer, Sandra Beyer, et al.
Journal of Medicinal Chemistry|November 24, 2021
Structure-Based Design of Dual Partial Peroxisome Proliferator-Activated Receptor γ Agonists/Soluble Epoxide Hydrolase InhibitorsFelix F Lillich, Sabine Willems, Xiaomin Ni, et al.
Journal of Medicinal Chemistry|August 23, 2019
Discovery of the First in Vivo Active Inhibitors of the Soluble Epoxide Hydrolase Phosphatase DomainJan S Kramer, Stefano Woltersdorf, Thomas Duflot, et al.
Journal of Medicinal Chemistry|June 18, 2025
Structure-Based Design of PROTACS for the Degradation of Soluble Epoxide HydrolaseJulia Schönfeld, Steffen Brunst, Ludmila Ciomirtan, et al.
Pageof 3

Showing results (11-20 of 21) with videos related to

Sort By:
Pageof 3
RSC Medicinal Chemistry|November 15, 2021
<i>N</i>-Aryl mercaptoacetamides as potential multi-target inhibitors of metallo-β-lactamases (MBLs) and the virulence factor LasB from <i>Pseudomonas aeruginosa</i>Samir Yahiaoui, Katrin Voos, Jörg Haupenthal, et al.
ACS Medicinal Chemistry Letters|July 21, 2022
Designing a Small Fluorescent Inhibitor to Investigate Soluble Epoxide Hydrolase Engagement in Living CellsSteffen Brunst, Julia Schönfeld, Peter Breunig, et al.
Chemmedchem|June 29, 2021
Rh<sup>II</sup> -Catalyzed De-symmetrization of Ethane-1,2-dithiol and Propane-1,3-dithiol Yields Metallo-β-lactamase InhibitorsMikhail Krasavin, Daniil Zhukovsky, Igor Solovyev, et al.
Biochemical Pharmacology|July 30, 2022
Compilation and evaluation of a fatty acid mimetics screening libraryJohanna H M Ehrler, Steffen Brunst, Amelie Tjaden, et al.
Journal of Medicinal Chemistry|February 21, 2022
<i>N</i>-Aryl Mercaptopropionamides as Broad-Spectrum Inhibitors of Metallo-β-LactamasesCansu Kaya, Jelena Konstantinović, Andreas M Kany, et al.
Journal of Medicinal Chemistry|August 15, 2025
Sustainable Joullié-Ugi and Continuous Flow Implementation Led to Novel Captopril-Inspired Broad-Spectrum Metallo-β-Lactamase InhibitorsAntonella Ilenia Alfano, Sveva Pelliccia, Simona Barone, et al.
Journal of Medicinal Chemistry|October 12, 2020
Design, Synthesis, and Structure-Activity Relationship Studies of Dual Inhibitors of Soluble Epoxide Hydrolase and 5-LipoxygenaseKerstin Hiesinger, Jan S Kramer, Sandra Beyer, et al.
Journal of Medicinal Chemistry|November 24, 2021
Structure-Based Design of Dual Partial Peroxisome Proliferator-Activated Receptor γ Agonists/Soluble Epoxide Hydrolase InhibitorsFelix F Lillich, Sabine Willems, Xiaomin Ni, et al.
Journal of Medicinal Chemistry|August 23, 2019
Discovery of the First in Vivo Active Inhibitors of the Soluble Epoxide Hydrolase Phosphatase DomainJan S Kramer, Stefano Woltersdorf, Thomas Duflot, et al.
Journal of Medicinal Chemistry|June 18, 2025
Structure-Based Design of PROTACS for the Degradation of Soluble Epoxide HydrolaseJulia Schönfeld, Steffen Brunst, Ludmila Ciomirtan, et al.
Pageof 3