Compound ID | 165
Class: Oxazolidinone
Spectrum of activity: | Gram-positive |
Details of activity: | MRSA (methicillin resistant Staphylococcus aureus) and VRE (vancomycin resistant Enterococcus sp.) ABSSI infections. |
Institute where first reported: | MicuRx Pharmaceuticals, USA |
Year first mentioned: | 2014 |
Highest developmental phase: | Phase 3 (NCT06081361) |
Development status: | Active (as of 2024) |
Chemical structure(s): | |
Canonical SMILES: | C1=CN(CCC1=O)C2=C(C=C(C(=C2F)F)N3C[C@H](CNC4=NOC=C4)OC3=O)F |
Isomeric SMILES: | C1CN(C=CC1=O)C2=C(C=C(C(=C2F)F)N3C[C@@H](OC3=O)CNC4=NOC=C4)F |
InChI: | InChI=1S/C18H15F3N4O4/c19-12-7-13(15(20)16(21)17(12)24-4-1-10(26)2-5-24)25-9-11(29-18(25)27)8-22-14-3-6-28-23-14/h1,3-4,6-7,11H,2,5,8-9H2,(H,22,23)/t11-/m0/s1 |
InChI Key: | SULYVXZZUMRQAX-NSHDSACASA-N |
Structure link: | https://pubchem.ncbi.nlm.nih.gov/compound/25184541 |
External links: | |
Guide to Pharmacology: | contezolid |
Main Source: | https://www.newtbdrugs.org/pipeline/compound/contezolid-mrx-4mrx-1 |
Citation: | http://aac.asm.org/content/58/4/2418.full |