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Journal of Applied Crystallography|April 9, 2021
Facilitated crystal handling using a simple device for evaporation reduction in microtiter platesTatjana Barthel, Franziska U Huschmann, Dirk Wallacher, et al.
Nucleic Acids Research|May 10, 2007
PDB2PQR: expanding and upgrading automated preparation of biomolecular structures for molecular simulationsTodd J Dolinsky, Paul Czodrowski, Hui Li, et al.
Acta Crystallographica. Section D, Biological Crystallography|September 4, 2013
High-affinity inhibitors of Zymomonas mobilis tRNA-guanine transglycosylase through convergent optimizationLuzi Jakob Barandun, Florian Immekus, Philipp C Kohler, et al.
Biomolecules|December 24, 2021
Which Properties Allow Ligands to Open and Bind to the Transient Binding Pocket of Human Aldose Reductase?Anna Sandner, Khang Ngo, Christoph P Sager, et al.
Angewandte Chemie (International Ed. in English)|February 18, 2014
Structure-based design of inhibitors of the aspartic protease endothiapepsin by exploiting dynamic combinatorial chemistryMilon Mondal, Nedyalka Radeva, Helene Köster, et al.
Structure (London, England : 1993)|May 16, 2020
F2X-Universal and F2X-Entry: Structurally Diverse Compound Libraries for Crystallographic Fragment ScreeningJan Wollenhaupt, Alexander Metz, Tatjana Barthel, et al.
Journal of Medicinal Chemistry|March 27, 2009
A structure-based approach to ligand discovery for 2C-methyl-D-erythritol-2,4-cyclodiphosphate synthase: a target for antimicrobial therapyNicola L Ramsden, Lori Buetow, Alice Dawson, et al.
Journal of Medicinal Chemistry|June 10, 2016
Optimization of Cyclic Plasmin Inhibitors: From Benzamidines to BenzylaminesStefan Hinkes, André Wuttke, Sebastian M Saupe, et al.
Journal of Medicinal Chemistry|October 14, 2005
Hydroxyethylene sulfones as a new scaffold to address aspartic proteases: design, synthesis, and structural characterizationEdgar Specker, Jark Böttcher, Andreas Heine, et al.
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