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Structure-activity relationship (SAR) studies on oxazolidinone antibacterial agents. 3. Synthesis and evaluation of 5-thiocarbamate oxazolidinones.
Tokuyama, R; Takahashi, Y; Tomita, Y; Tsubouchi, M; Iwasaki, N; Kado, N; Okezaki, E; Nagata, O.
Afiliación
  • Tokuyama R; Research and Development Division, Hokuriku Seiyaku Co., Ltd., Katsuyama, Fukui, Japan. organ-hs@mitene.or.jp
Chem Pharm Bull (Tokyo) ; 49(4): 361-7, 2001 Apr.
Article en En | MEDLINE | ID: mdl-11310658
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 logP 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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Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Oxazoles / Antibacterianos Idioma: En Revista: Chem Pharm Bull (Tokyo) Año: 2001 Tipo del documento: Article País de afiliación: Japón
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Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Oxazoles / Antibacterianos Idioma: En Revista: Chem Pharm Bull (Tokyo) Año: 2001 Tipo del documento: Article País de afiliación: Japón