Chemical and Pharmaceutical Bulletin
Online ISSN : 1347-5223
Print ISSN : 0009-2363
ISSN-L : 0009-2363
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Structure-Activity Relationship (SAR) Studies on Oxazolidinone Antibacterial Agents. 3.1) Synthesis and Evaluation of 5-Thiocarbamate Oxazolidinones
Ryukou TOKUYAMAYoshiei TAKAHASHIYayoi TOMITAMasatoshi TSUBOUCHINobuhiko IWASAKINoriyuki KADOEiichi OKEZAKIOsamu NAGATA
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2001 Volume 49 Issue 4 Pages 361-367

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Abstract

A series of 5-thiocarbamate oxazolidinones was prepared and tested for in vitro and in vivo antibacterial activities. The results of in vitro antibacterial activity indicated that the 5-thiocarbamate group was a suitable substituent for the activity by the 5-moderate hydrophilicity. The compounds within a favorable log P value range were found to have potent in vitro antibacterial activity against gram-positive bacteria including methicillin-resistant Staphylococcus aureus (MRSA) and vancomycin-resistant enterococci (VRE). Compounds 3a and 4h were superior to linezolid in both in vitro and in vivo potency and were considered to be hopeful compounds. We also discuss the pharmacokinetic properties of several compounds in mice.

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© 2001 The Pharmaceutical Society of Japan
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