Synthesis and in vitro activity of new oxazolidinone antibacterial agents having substituted isoxazoles

Bioorganic & Medicinal Chemistry Letters
1999.0

Abstract

Two series of oxazolidinone derivatives having substituted isoxazoles were synthesized and tested for antibacterial activities against several Gram-positive strains including the resistant strains of Staphylococcus and Enterococcus, such as MRSA, CRSA, MSSA and VRE. Some of them showed in vitro activities (MIC) comparable or superior to the reference compound vancomycin.

Knowledge Graph

Similar Paper

Synthesis and in vitro activity of new oxazolidinone antibacterial agents having substituted isoxazoles
Bioorganic & Medicinal Chemistry Letters 1999.0
Synthesis and in vitro activity of novel isoxazolyl tetrahydropyridinyl oxazolidinone antibacterial agents
Bioorganic & Medicinal Chemistry Letters 2003.0
Synthesis and in vitro activity of new methylenepiperidinyl and methylenepyrrolidinyl oxazolidinone antibacterial agents
Bioorganic & Medicinal Chemistry Letters 2003.0
Synthesis and antibacterial activity of arylpiperazinyl oxazolidinones with diversification of the N-substituents
Bioorganic & Medicinal Chemistry Letters 2004.0
Synthesis and antibacterial activity of some aryloxy/thioaryloxy oxazolidinone derivatives
Bioorganic & Medicinal Chemistry Letters 2004.0
Synthesis and antibacterial evaluation of isoxazolinyl oxazolidinones: Search for potent antibacterial
Bioorganic & Medicinal Chemistry Letters 2009.0
Design, synthesis and antibacterial evaluation of novel oxazolidinone derivatives nitrogen-containing fused heterocyclic moiety
Bioorganic & Medicinal Chemistry Letters 2021.0
Synthesis and antibacterial activity of novel (un)substituted benzotriazolyl oxazolidinone derivatives
Bioorganic & Medicinal Chemistry Letters 2005.0
Synthesis and antibacterial activity of oxazolidinones containing triazolyl group
European Journal of Medicinal Chemistry 2007.0
Synthesis and antibacterial evaluation of novel oxazolidinone derivatives containing a piperidinyl moiety
Bioorganic & Medicinal Chemistry Letters 2019.0