Inhibitors of bacterial N-succinyl-l,l-diaminopimelic acid desuccinylase (DapE) and demonstration of in vitro antimicrobial activity |
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Authors: | Danuta Gillner Nicola Armoush Richard C. Holz Daniel P. Becker |
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Affiliation: | aDepartment of Chemistry, Loyola University, 6525 North Sheridan Road, Chicago, IL 60626, United States;bDepartment of Chemistry, Silesian University of Technology, Gliwice, Poland |
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Abstract: | The dapE-encoded N-succinyl-l,l-diaminopimelic acid desuccinylase (DapE) is a critical bacterial enzyme for the construction of the bacterial cell wall. A screen biased toward compounds containing zinc-binding groups (ZBG’s) including thiols, carboxylic acids, boronic acids, phosphonates and hydroxamates has delivered a number of micromolar inhibitors of DapE from Haemophilus influenzae, including the low micromolar inhibitor l-captopril (IC50 = 3.3 μM, Ki = 1.8 μM). In vitro antimicrobial activity was demonstrated for l-captopril against Escherichia coli. |
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Keywords: | Enzyme inhibition N-Succinyl- smCaps" >l, smCaps" >l-diaminopimelic acid desuccinylase DapE smCaps" >l-Captopril ZBG (zinc-binding group) Antimicrobial |
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