Abstract
Combinatorial libraries of N-acylated 5-(S)-aminomethyloxazolidinone derivatives of S-oxide and S,S-dioxide tetrahydro-4(2H)-thiopyranyl and thiomorpholine phenyloxazolidinone series have been synthesized on a solid phase and evaluated for antimicrobial activity. Several novel potent leads have been identified, including orally active oxazolidinones with enhanced activity against respiratory tract infection pathogens Haemophilus influenzae and Moraxella catarrhalis.
MeSH terms
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Animals
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Anti-Bacterial Agents / administration & dosage
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Anti-Bacterial Agents / pharmacokinetics*
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Biological Availability
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Combinatorial Chemistry Techniques
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Haemophilus Infections / microbiology
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Haemophilus influenzae / drug effects*
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Lipid Metabolism
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Male
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Microbial Sensitivity Tests
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Moraxella catarrhalis / drug effects*
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Moraxellaceae Infections / microbiology
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Morpholines / chemistry*
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Oxazolidinones / administration & dosage
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Oxazolidinones / pharmacokinetics*
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Oxides / chemistry*
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Oxygen Compounds / pharmacokinetics*
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Rats
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Rats, Sprague-Dawley
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Structure-Activity Relationship
Substances
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Anti-Bacterial Agents
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Morpholines
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Oxazolidinones
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Oxides
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Oxygen Compounds
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thiamorpholine