Source:http://linkedlifedata.com/resource/pubmed/id/15149646
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Predicate | Object |
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rdf:type | |
lifeskim:mentions | |
pubmed:issue |
12
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pubmed:dateCreated |
2004-5-19
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pubmed:abstractText |
A series of oxazolidinone antibacterial agents containing a 5-substituted isoxazol-3-yl moiety were synthesized via a nitrile oxide [3+2] dipolar cycloaddition reaction. These compounds were screened against a panel of susceptible and resistant Gram-positive organisms. Several analogs from this series were comparable to or more potent than linezolid in vitro.
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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 |
0960-894X
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pubmed:author | |
pubmed:issnType |
Print
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pubmed:day |
21
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pubmed:volume |
14
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
3069-72
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pubmed:meshHeading |
pubmed-meshheading:15149646-Animals,
pubmed-meshheading:15149646-Anti-Bacterial Agents,
pubmed-meshheading:15149646-Drug Evaluation, Preclinical,
pubmed-meshheading:15149646-Female,
pubmed-meshheading:15149646-Isoxazoles,
pubmed-meshheading:15149646-Mice,
pubmed-meshheading:15149646-Microbial Sensitivity Tests,
pubmed-meshheading:15149646-Oxazolidinones
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pubmed:year |
2004
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pubmed:articleTitle |
The synthesis and antimicrobial evaluation of a new series of isoxazolinyl oxazolidinones.
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pubmed:affiliation |
Antimicrobial Agents Research Team, Drug Discovery, Johnson & Johnson Pharmaceutical Research and Development, LL C, 1000 Route 202, Raritan, NJ 08869, USA.
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pubmed:publicationType |
Journal Article
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