In silico fragment based design identifies subfamily B1 metallo-β-lactamase inhibitors
<p>Zinc ion dependent β-lactamases (MBLs) catalyze the hydrolysis of almost all β-lactam antibiotics and resist the action of clinically available β-lactamase inhibitors. We report how application of <i>in silico</i> fragment-based molecular design employing thiol-mediated metal a...
Κύριοι συγγραφείς: | Cain, R, Brem, J, Zollman, D, McDonough, M, Johnson, R, Spencer, J, Makena, A, Abboud, M, Cahill, S, Lee, S, McHugh, P, Schofield, C, Fishwick, C |
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Μορφή: | Journal article |
Γλώσσα: | English |
Έκδοση: |
American Chemical Society
2017
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Παρόμοια τεκμήρια
Παρόμοια τεκμήρια
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