Title of article :
Synthesis of novel oxazolidinone antimicrobial agents Original Research Article
Author/Authors :
David C. Ebner، نويسنده , , Jeffrey C. Culhane، نويسنده , , Tyler N. Winkelman، نويسنده , , Mitchell D. Haustein، نويسنده , , Jayna L. Ditty، نويسنده , , J. Thomas Ippoliti، نويسنده ,
Issue Information :
روزنامه با شماره پیاپی سال 2008
Pages :
6
From page :
2651
To page :
2656
Abstract :
The oxazolidinone class of antimicrobials represents a promising advance in the fight against resistant Gram-positive bacterial infections. Four novel oxazolidinone antimicrobial compounds, each containing a benzodioxin ring system, have been prepared. The general synthesis of each compound begins with the construction of a benzodioxin ring system containing a nitro substituent that ultimately becomes the nitrogen of the oxazolidinone ring. Three of the compounds utilize high yielding ‘click chemistry’ in their final step. The antimicrobial activities of the new oxazolidinones have been measured and the MIC against Staphylococcus aureus for one of the antimicrobials was determined to be 2–3 μg/mL, which is comparable to the well-known oxazolidinone, linezolid.
Keywords :
HbS , Lignin , LTR , NF-?B , TNF-? , HIV-1
Journal title :
Bioorganic and Medicinal Chemistry
Serial Year :
2008
Journal title :
Bioorganic and Medicinal Chemistry
Record number :
1304101
Link To Document :
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