Source:http://linkedlifedata.com/resource/pubmed/id/17892940
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Predicate | Object |
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rdf:type | |
lifeskim:mentions | |
pubmed:issue |
23
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pubmed:dateCreated |
2007-10-15
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pubmed:abstractText |
Bacterial enoyl-acyl carrier protein (ACP) reductases (FabI and FabK) catalyze the final step in each cycle of bacterial fatty acid biosynthesis and are attractive targets for the development of new antibacterial agents. Here, we report the development of novel FabK inhibitors with antibacterial activity against Streptococcus pneumoniae. Based on structure-activity relationship (SAR) studies of our screening hits, we have developed novel phenylimidazole derivatives as potent FabK inhibitors.
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pubmed:language |
eng
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pubmed:journal | |
pubmed:citationSubset |
IM
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pubmed:chemical | |
pubmed:status |
MEDLINE
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pubmed:month |
Dec
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pubmed:issn |
0968-0896
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pubmed:author | |
pubmed:issnType |
Print
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pubmed:day |
1
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pubmed:volume |
15
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
7325-36
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pubmed:meshHeading |
pubmed-meshheading:17892940-Enoyl-(Acyl-Carrier-Protein) Reductase (NADH),
pubmed-meshheading:17892940-Enzyme Inhibitors,
pubmed-meshheading:17892940-Escherichia coli,
pubmed-meshheading:17892940-Humans,
pubmed-meshheading:17892940-Imidazoles,
pubmed-meshheading:17892940-K562 Cells,
pubmed-meshheading:17892940-Microbial Sensitivity Tests,
pubmed-meshheading:17892940-Molecular Structure,
pubmed-meshheading:17892940-Stereoisomerism,
pubmed-meshheading:17892940-Streptococcus pneumoniae,
pubmed-meshheading:17892940-Structure-Activity Relationship,
pubmed-meshheading:17892940-Toxicity Tests
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pubmed:year |
2007
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pubmed:articleTitle |
Phenylimidazole derivatives as specific inhibitors of bacterial enoyl-acyl carrier protein reductase FabK.
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pubmed:affiliation |
Medicinal Chemistry Research Laboratories, Pharmaceutical Research Center, Meiji Seika Kaisha, Ltd, 760 Morooka-cho, Kohoku-ku, Yokohama 222-8567, Japan.
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pubmed:publicationType |
Journal Article
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