| Title |
Synthesis of novel oxazolidinone antimicrobial agents
|
|---|---|
| Published in |
Bioorganic & Medicinal Chemistry, November 2007
|
| DOI | 10.1016/j.bmc.2007.11.040 |
| Pubmed ID | |
| Authors |
David C. Ebner, Jeffrey C. Culhane, Tyler N. Winkelman, Mitchell D. Haustein, Jayna L. Ditty, J. Thomas Ippoliti |
| 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 microg/mL, which is comparable to the well-known oxazolidinone, linezolid. |
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Mendeley demographics
Geographical breakdown
| Country | Count | As % |
|---|---|---|
| United States | 1 | 3% |
| Faroe Islands | 1 | 3% |
| Unknown | 28 | 93% |
Demographic breakdown
| Readers by professional status | Count | As % |
|---|---|---|
| Student > Ph. D. Student | 10 | 33% |
| Researcher | 4 | 13% |
| Lecturer | 2 | 7% |
| Student > Master | 2 | 7% |
| Professor > Associate Professor | 2 | 7% |
| Other | 5 | 17% |
| Unknown | 5 | 17% |
| Readers by discipline | Count | As % |
|---|---|---|
| Chemistry | 12 | 40% |
| Agricultural and Biological Sciences | 4 | 13% |
| Pharmacology, Toxicology and Pharmaceutical Science | 2 | 7% |
| Biochemistry, Genetics and Molecular Biology | 2 | 7% |
| Medicine and Dentistry | 2 | 7% |
| Other | 4 | 13% |
| Unknown | 4 | 13% |