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Nature Communications|August 9, 2016
Structural basis of metallo-β-lactamase, serine-β-lactamase and penicillin-binding protein inhibition by cyclic boronatesJürgen Brem, Ricky Cain, Samuel Cahill, et al.
Journal of Medicinal Chemistry|October 19, 2019
Structure-Guided Enhancement of Selectivity of Chemical Probe Inhibitors Targeting Bacterial Seryl-tRNA SynthetaseRicky Cain, Ramya Salimraj, Avinash S Punekar, et al.
ACS Medicinal Chemistry Letters|June 6, 2014
Structure guided development of potent reversibly binding penicillin binding protein inhibitorsEsther C Y Woon, Astrid Zervosen, Eric Sauvage, et al.
Molecular Microbiology|March 21, 2009
The nature of Staphylococcus aureus MurA and MurZ and approaches for detection of peptidoglycan biosynthesis inhibitorsKaty L Blake, Alex J O'Neill, Dominique Mengin-Lecreulx, et al.
Antimicrobial Agents and Chemotherapy|January 25, 2017
Cyclic Boronates Inhibit All Classes of β-LactamasesSamuel T Cahill, Ricky Cain, David Y Wang, et al.
Haematologica|May 2, 2020
Fibrinogen interaction with complement C3: a potential therapeutic target to reduce thrombosis riskRhodri J King, Katharina Schuett, Christian Tiede, 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.
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