27 articles for thisTarget
The following articles (labelled with PubMed ID or TBD) are for your review
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Article Title
Organization
Novel mechanism of inhibiting beta-lactamases by sulfonylation using beta-sultams.
The University Of Huddersfield
Inhibitors of proteases and amide hydrolases that employ an alpha-ketoheterocycle as a key enabling functionality.
Johnson & Johnson Pharmaceutical Research & Development
4-Substituted trinems as broad spectrum beta-lactamase inhibitors: structure-based design, synthesis, and biological activity.
Lek Pharmaceuticals
Structure-based design of beta-lactamase inhibitors. 2. Synthesis and evaluation of bridged sulfactams and oxamazins.
F. Hoffmann-La Roche
Design, synthesis, and evaluation of 2 beta-alkenyl penam sulfone acids as inhibitors of beta-lactamases.
F. Hoffmann-La Roche
The inhibition of metallo-beta-lactamase by thioxo-cephalosporin derivatives.
University Of Huddersfield
The synthesis and SAR of rhodanines as novel class C beta-lactamase inhibitors.
The R. W. Johnson Pharmaceutical Research Institute
The synthesis and lactamase inhibitory activity of 6-(carboxymethylene)penicillins and 7-(carboxymethylene)cephalosporins
TBA
Thiophenyl oxime-derived phosphonates as nano-molar class C beta-lactamase inhibitors reducing MIC of imipenem against Pseudomonas aeruginosa and Acinetobacter baumannii.
Merck
Synthesis and SAR of novel benzoxaboroles as a new class of β-lactamase inhibitors.
Anacor Pharmaceuticals
Mechanistic studies of the inactivation of TEM-1 and P99 by NXL104, a novel non-beta-lactam beta-lactamase inhibitor.
Novexel
4,7-Dichloro benzothien-2-yl sulfonylaminomethyl boronic acid: first boronic acid-derived beta-lactamase inhibitor with class A, C, and D activity.
Merck
Mechanistic support for the stepwise process for inactivation of class A β-lactamases by clavulanate
TBA
Structure-activity relationship of 6-methylidene penems bearing 6,5 bicyclic heterocycles as broad-spectrum beta-lactamase inhibitors: evidence for 1,4-thiazepine intermediates with C7 R stereochemistry by computational methods.
Wyeth Research
Structure-activity relationship of 6-methylidene penems bearing tricyclic heterocycles as broad-spectrum beta-lactamase inhibitors: crystallographic structures show unexpected binding of 1,4-thiazepine intermediates.
Wyeth Research
Spirocyclopropyl beta-lactams as mechanism-based inhibitors of serine beta-lactamases. Synthesis by rhodium-catalyzed cyclopropanation of 6-diazopenicillanate sulfone.
Wyeth Research
Cephalosporin-derived inhibitors of beta-lactamase. Part 4: The C3 substituent.
Southern Methodist University
Specificity of extended O-aryloxycarbonyl hydroxamates as inhibitors of a class C ?-lactamase.
Wesleyan University
Synthesis and biological activities of an alpha-methyl and a beta-methyl carbapenem and the corresponding unsubstituted compound.
University Of Munich
SB-202742, a novel beta-lactamase inhibitor isolated from Spondias mombin.
Smithkline Beecham Pharmaceuticals