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Structure-based optimization of Cephalothin-analogue boronic acids as β-lactamase inhibitors

Boronic acids have proved to be promising selective inhibitors of β-lactamases, acting as transition state analogues. Starting from a previously described nanomolar inhibitor of AmpC β-lactamase, three new inhibitors were designed to gain interactions with highly conserved residues, such as Asn343,...

תיאור מלא

שמור ב:
מידע ביבליוגרפי
Main Authors: Morandi, Stefania, Morandi, Federica, Caselli, Emilia, Shoichet, Brian K., Prati, Fabio
פורמט: Artigo
שפה:Inglês
יצא לאור: 2007
נושאים:
גישה מקוונת:https://ncbi.nlm.nih.gov/pmc/articles/PMC2396669/
https://ncbi.nlm.nih.gov/pubmed/17997318
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.bmc.2007.10.075
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