Abstract
3-(4-Hydroxypiperidine-1-yl) phthalic acid 1 shows potent inhibitory activity against metallo-β-lactamase, which is known to inactivate β-lactam antibiotics such as carbapenems. Here, the structure of co-crystals of the metallo-β-lactamase IMP-1 and 1 was first analyzed by X-ray crystallography, and then used for structure-based drug design. Four novel compounds bearing substituents at the 6-position were synthesized to produce 3,6-disubstituted phthalic acid derivatives, and their IMP-1 inhibitory activity and synergistic effect with the carbapenem biapenem (BIPM) were evaluated. 3,6-Disubstituted phthalic acid derivatives showed potent IMP-1 inhibitory activity. In particular, compound 13 showed 10-fold higher IMP-1 inhibitory activity as compared with the parent derivative 1.
Keywords:
IMP-1; Metallo-β-lactamase; Pseudomonas aeruginosa.
Copyright © 2014 Elsevier Ltd. All rights reserved.
MeSH terms
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Anti-Bacterial Agents / chemical synthesis
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Anti-Bacterial Agents / chemistry
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Anti-Bacterial Agents / pharmacology*
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Crystallography, X-Ray
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Dose-Response Relationship, Drug
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Drug Design*
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Drug Resistance, Multiple, Bacterial / drug effects
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Enzyme Inhibitors / chemical synthesis
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Enzyme Inhibitors / chemistry
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Enzyme Inhibitors / pharmacology*
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Models, Molecular
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Molecular Structure
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Phthalic Acids / chemical synthesis
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Phthalic Acids / chemistry
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Phthalic Acids / pharmacology*
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Piperidines / chemical synthesis
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Piperidines / chemistry
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Piperidines / pharmacology*
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Pseudomonas aeruginosa / drug effects*
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Pseudomonas aeruginosa / enzymology
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Pseudomonas aeruginosa / metabolism
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Structure-Activity Relationship
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beta-Lactamases / analysis*
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beta-Lactamases / chemistry
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beta-Lactamases / metabolism
Substances
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3-(4-hydroxypiperidine-1-yl)phthalic acid
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Anti-Bacterial Agents
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Enzyme Inhibitors
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Phthalic Acids
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Piperidines
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beta-lactamase IMP-1
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beta-Lactamases