Compound ID | 804
VIC-106841
Class: Oxazolidinone
| Agent Type: | Synthetic; Small molecule; Direct acting; |
| Spectrum of activity: | Gram-positive |
| Mechanism of action: | Protein synthesis inhibitor |
| Target Pathogen: | Active against Staphylococcus aureus and Streptococcus pneumoniae |
| Description: | Renslo AR, Gao H, Blais J, et al. Structure-activity studies of the C-ring nitrogen substituent in a new class of azabicyclo[3.1.0]hexylphenyl oxazolidinone analogs. 45th-Intersci-Conf-Antimicrob-Agents-Chemother 2005;202 |
| Institute where first reported: | Vicuron Pharmaceuticals (Durata Pharmaceuticals, USA) |
| Year first mentioned: | 2005 |
| Development status: | Experimental |
| External links: |
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