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Christopher J Schofield

Showing results (471-480 of 593) with videos related to

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Journal of Medicinal Chemistry|August 1, 2023
5-Substituted Pyridine-2,4-dicarboxylate Derivatives Have Potential for Selective Inhibition of Human Jumonji-C Domain-Containing Protein 5Lennart Brewitz, Yu Nakashima, Sonia K Piasecka, et al.
Journal of Medicinal Chemistry|December 23, 2017
In Silico Fragment-Based Design Identifies Subfamily B1 Metallo-β-lactamase InhibitorsRicky Cain, Jürgen Brem, David Zollman, et al.
Acta Crystallographica. Section D, Biological Crystallography|July 31, 2013
Structural and mechanistic studies of the orf12 gene product from the clavulanic acid biosynthesis pathwayKarin Valegård, Aman Iqbal, Nadia J Kershaw, et al.
Metabolites|February 23, 2019
A Noninvasive Comparison Study between Human Gliomas with IDH1 and IDH2 Mutations by MR SpectroscopyXin Shen, Natalie L Voets, Sarah J Larkin, et al.
Angewandte Chemie (International Ed. in English)|May 29, 2012
Dynamic combinatorial chemistry employing boronic acids/boronate esters leads to potent oxygenase inhibitorsMarina Demetriades, Ivanhoe K H Leung, Rasheduzzaman Chowdhury, et al.
Chemical Science|February 27, 2015
Studying the active-site loop movement of the São Paolo metallo-β-lactamase-1†Electronic supplementary information (ESI) available: Procedures for protein expression and purification, <sup>19</sup>F-labelling, crystallisation, data collection, and structure determination, table of crystallographic data, table of crystallographic parameters and refinement statistics, figures showing binding mode and distances, procedures for mass spectrometry measurements, differential scanning fluorimetry measurements, stopped-flow measurements and other kinetics measurements. See DOI: 10.1039/c4sc01752hClick here for additional data fileJürgen Brem, Weston B Struwe, Anna M Rydzik, et al.
RSC Medicinal Chemistry|September 10, 2025
Electrostatic interactions influence diazabicyclooctane inhibitor potency against OXA-48-like β-lactamasesJoseph F Hoff, Kirsty E Goudar, Karina Calvopiña, et al.
Chemical Communications (Cambridge, England)|May 5, 2017
Crystallographic analyses of isoquinoline complexes reveal a new mode of metallo-β-lactamase inhibitionGuo-Bo Li, Jürgen Brem, Robert Lesniak, et al.
Biomolecules|June 18, 2020
Bicyclic Boronates as Potent Inhibitors of AmpC, the Class C β-Lactamase from <i>Escherichia coli</i>Pauline A Lang, Anete Parkova, Thomas M Leissing, et al.
Journal of Medicinal Chemistry|August 28, 2019
Bicyclic Boronate VNRX-5133 Inhibits Metallo- and Serine-β-LactamasesAlen Krajnc, Jürgen Brem, Philip Hinchliffe, et al.
Pageof 60

Showing results (471-480 of 593) with videos related to

Sort By:
Pageof 60
Journal of Medicinal Chemistry|August 1, 2023
5-Substituted Pyridine-2,4-dicarboxylate Derivatives Have Potential for Selective Inhibition of Human Jumonji-C Domain-Containing Protein 5Lennart Brewitz, Yu Nakashima, Sonia K Piasecka, et al.
Journal of Medicinal Chemistry|December 23, 2017
In Silico Fragment-Based Design Identifies Subfamily B1 Metallo-β-lactamase InhibitorsRicky Cain, Jürgen Brem, David Zollman, et al.
Acta Crystallographica. Section D, Biological Crystallography|July 31, 2013
Structural and mechanistic studies of the orf12 gene product from the clavulanic acid biosynthesis pathwayKarin Valegård, Aman Iqbal, Nadia J Kershaw, et al.
Metabolites|February 23, 2019
A Noninvasive Comparison Study between Human Gliomas with IDH1 and IDH2 Mutations by MR SpectroscopyXin Shen, Natalie L Voets, Sarah J Larkin, et al.
Angewandte Chemie (International Ed. in English)|May 29, 2012
Dynamic combinatorial chemistry employing boronic acids/boronate esters leads to potent oxygenase inhibitorsMarina Demetriades, Ivanhoe K H Leung, Rasheduzzaman Chowdhury, et al.
Chemical Science|February 27, 2015
Studying the active-site loop movement of the São Paolo metallo-β-lactamase-1†Electronic supplementary information (ESI) available: Procedures for protein expression and purification, <sup>19</sup>F-labelling, crystallisation, data collection, and structure determination, table of crystallographic data, table of crystallographic parameters and refinement statistics, figures showing binding mode and distances, procedures for mass spectrometry measurements, differential scanning fluorimetry measurements, stopped-flow measurements and other kinetics measurements. See DOI: 10.1039/c4sc01752hClick here for additional data fileJürgen Brem, Weston B Struwe, Anna M Rydzik, et al.
RSC Medicinal Chemistry|September 10, 2025
Electrostatic interactions influence diazabicyclooctane inhibitor potency against OXA-48-like β-lactamasesJoseph F Hoff, Kirsty E Goudar, Karina Calvopiña, et al.
Chemical Communications (Cambridge, England)|May 5, 2017
Crystallographic analyses of isoquinoline complexes reveal a new mode of metallo-β-lactamase inhibitionGuo-Bo Li, Jürgen Brem, Robert Lesniak, et al.
Biomolecules|June 18, 2020
Bicyclic Boronates as Potent Inhibitors of AmpC, the Class C β-Lactamase from <i>Escherichia coli</i>Pauline A Lang, Anete Parkova, Thomas M Leissing, et al.
Journal of Medicinal Chemistry|August 28, 2019
Bicyclic Boronate VNRX-5133 Inhibits Metallo- and Serine-β-LactamasesAlen Krajnc, Jürgen Brem, Philip Hinchliffe, et al.
Pageof 60