Source:http://linkedlifedata.com/resource/pubmed/id/21515052
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Predicate | Object |
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rdf:type | |
lifeskim:mentions | |
pubmed:issue |
11
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pubmed:dateCreated |
2011-5-20
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pubmed:abstractText |
We report herein the design and synthesis of novel 7-(4-alkoxyimino-3-aminomethylpiperidin-1-yl) fluoroquinolone derivatives. The antibacterial activity of the newly synthesized compounds was evaluated and compared with gemifloxacin, levofloxacin and ciprofloxacin. Results reveal that compounds 10, 16, and 17 have good activity against all of the tested gram-positive organisms including drug-resistance strains (MICs: 0.125-4 ?g/mL). In addition, compounds 16 and 17 (MICs: 4 ?g/mL) were 2- to 8-fold more potent than the reference drugs against Pseudomonas aeruginosa.
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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 |
Jun
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pubmed:issn |
1464-3405
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pubmed:author | |
pubmed:copyrightInfo |
Copyright © 2011 Elsevier Ltd. All rights reserved.
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pubmed:issnType |
Electronic
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pubmed:day |
1
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pubmed:volume |
21
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
3377-80
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pubmed:meshHeading |
pubmed-meshheading:21515052-Anti-Bacterial Agents,
pubmed-meshheading:21515052-Drug Design,
pubmed-meshheading:21515052-Fluoroquinolones,
pubmed-meshheading:21515052-Imino Pyranoses,
pubmed-meshheading:21515052-Microbial Sensitivity Tests,
pubmed-meshheading:21515052-Molecular Structure,
pubmed-meshheading:21515052-Pseudomonas aeruginosa
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pubmed:year |
2011
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pubmed:articleTitle |
Design, synthesis and in vitro antibacterial activity of 7-(4-alkoxyimino-3-aminomethylpiperidin-1-yl)fluoroquinolone derivatives.
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pubmed:affiliation |
Institute of Medical Biotechnology, Chinese Academy of Medical Sciences, Peking Union Medical College, Beijing 100050, China.
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pubmed:publicationType |
Journal Article
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