S-Aminosulfeniminopenicillins: Multimode β-Lactamase Inhibitors and Template Structures for Penicillin-Based β-Lactamase Substrates as Prodrugs
Author:
Affiliation:
1. Department of Chemical and Environmental Sciences, University of Limerick, National Technological Park, County Limerick, Ireland
Publisher
American Chemical Society (ACS)
Subject
Organic Chemistry
Link
https://pubs.acs.org/doi/pdf/10.1021/jo970737f
Reference67 articles.
1. Penem BRL 42715: An Effective Inactivator for .beta.-Lactamases
2. Design, Synthesis, and Evaluation of a Potent Mechanism-Based Inhibitor for the TEM .beta.-Lactamase with Implications for the Enzyme Mechanism
3. Mechanism of inactivation of TEM-1 β-lactamase by 6-acetylmethylenepenicillanic acid
4. Synthesis of a potent β-lactamase inhibitor- 1,1-dioxo-6-(2-pyridyl)methylenepenicillanic acid and its reaction with sodium methoxide
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