Compound ID | 806
VIC-106922
Class: Oxazolidinone
| Agent Type: | Synthetic; Small molecule; Direct acting; |
| Spectrum of activity: | Gram-positive & Gram-negative |
| Mechanism of action: | Protein synthesis inhibitor |
| Target Pathogen: | Active against Staphylococcus aureus, Streptococcus pneumoniae, and Haemophilus influenzae |
| Description: | Renslo AR, Jaishankar P, Gao H, et al. Structure-activity studies of the C-5 substituent in a new class of bicyclo[3.1.0]hexylphenyl oxazolidinone analogs. 45th-Intersci-Conf-Antimicrob-Agents-Chemother 2005;200 |
| Institute where first reported: | Vicuron Pharmaceuticals (Durata Pharmaceuticals, USA) |
| Year first mentioned: | 2005 |
| Development status: | Experimental |
| External links: |
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