The following articles (labelled with PubMed ID or TBD) are for your review
PMID | Data | Article Title | Organization |
17353248 |
6 |
SCO-1, a novel plasmid-mediated class A beta-lactamase with carbenicillinase characteristics from Escherichia coli. |
Institut Pasteur Hellenique |
17665896 |
30 |
4-Substituted trinems as broad spectrum beta-lactamase inhibitors: structure-based design, synthesis, and biological activity. |
Lek Pharmaceuticals |
13678405 |
23 |
A specific mechanism of nonspecific inhibition. |
Northwestern University |
8809160 |
132 |
Design, synthesis, and evaluation of 2 beta-alkenyl penam sulfone acids as inhibitors of beta-lactamases. |
F. Hoffmann-La Roche |
11959006 |
10 |
Design, synthesis and bioactivity evaluation of tribactam beta lactamase inhibitors. |
Lek |
| 51 |
The synthesis and lactamase inhibitory activity of 6-(carboxymethylene)penicillins and 7-(carboxymethylene)cephalosporins |
TBA |
| 10 |
Synthesis and biological activity of novel penem sulfoxides and sulfones |
TBA |
| 22 |
Inhibition of the RTEM-1 β-lactamase by boronic acids |
TBA |
17709463 |
4 |
TEM-158 (CMT-9), a new member of the CMT-type extended-spectrum beta-lactamases. |
Chu Clermont-Ferrand |
17956081 |
24 |
Optimizing cell permeation of an antibiotic resistance inhibitor for improved efficacy. |
Università |
16854068 |
59 |
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 |
15588091 |
25 |
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 |
15214794 |
20 |
Mechanism of inactivation of beta-lactamases by novel 6-methylidene penems elucidated using electrospray ionization mass spectrometry. |
Wyeth Research |
14980686 |
50 |
Penicillin-derived inhibitors that simultaneously target both metallo- and serine-beta-lactamases. |
Southern Methodist University |
11327608 |
45 |
Allyl and propargyl substituted penam sulfones as versatile intermediates toward the syntheses of new beta-lactamase inhibitors. |
Wyeth-Ayerst Research |
10890171 |
6 |
Synthesis and biological activities of an alpha-methyl and a beta-methyl carbapenem and the corresponding unsubstituted compound. |
University Of Munich |
10230627 |
14 |
6-(1-Hydroxyalkyl))penam sulfone derivatives as inhibitors of class A and class C beta-lactamases II. |
Wyeth-Ayerst Research |
10230626 |
22 |
6-(1-Hydroxyalkyl)penam sulfone derivatives as inhibitors of class A and class C beta-lactamases I. |
Wyeth-Ayerst Research |
7699694 |
66 |
Synthesis and biological activity of 7-alkylidenecephems. |
Southern Methodist University |
3257523 |
13 |
N-aryl 3-halogenated azetidin-2-ones and benzocarbacephems, inhibitors of beta-lactamases. |
Cnrs-Cercoa |
3039137 |
20 |
Synthesis and beta-lactamase inhibitory properties of 2 beta-[(1,2,3-triazol-1-yl)methyl]-2 alpha-methylpenam-3 alpha-carboxylic acid 1,1-dioxide and related triazolyl derivatives. |
TBA |