Synthesis and kinetic testing of tetrahydropyrimidine-2-thione and pyrrole derivatives as inhibitors of the metallo-β-lactamase from Klebsiella pneumonia and Pseudomonas aeruginosa
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Authors
Hussein, Waleed M.
Fatahala, Samar
Mohamed, Zainab M.
McGeary, Ross Peter
Schenk, Gerhard
Ollis, David
Mohamed, Mosaad S.
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John Wiley & Sons Inc
Abstract
Metallo-β-lactamases (MBLs), produced by an increasing number of bacterial pathogens, facilitate the hydrolysis of many commonly used β-lactam antibiotics. There are no clinically useful antagonists against MBLs. Two sets of tetrahydropyrimidine-2-thion
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(1 benzyl 3 cyano 4,5 diphenyl 1h pyrrol 2 yl)carbonohydrazonoyl dicyanide, 1 (6 methyl 4 phenyl 2 thioxo 1,2,3,4 tetrahydropyrimidine 5 yl)ethanone, 1 (6 methyl 4 styryl 2 thioxo 1,2,3,4 tetrahydropyrimidine 5 yl)ethanone, 2 [(5 acetyl 6 methyl 4 styryl Inhibition assays, Metallo-ß-lactamases, Pyrrole, Tetrahydropyrimidine-2-thione
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Chemical Biology and Drug Design
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2037-12-31
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