Structure via PubChem · Public domain (PubChem)
eperezolid
Sign in to saveEperezolid is an oxazolidinone antibiotic.
Chemical data
- Formula
- C18H23FN4O5
- Molecular weight
- 394.4 g/mol
- IUPAC name
- N-[[(5S)-3-[3-fluoro-4-[4-(2-hydroxyacetyl)piperazin-1-yl]phenyl]-2-oxo-1,3-oxazolidin-5-yl]methyl]acetamide
- SMILES
- CC(=O)NC[C@H]1CN(C(=O)O1)C2=CC(=C(C=C2)N3CCN(CC3)C(=O)CO)F
- InChIKey
- SIMWTRCFFSTNMG-AWEZNQCLSA-N
- XLogP
- -0.3
- Polar surface area
- 102 Ų
- H-bond donors
- 2
- H-bond acceptors
- 7
- Formal charge
- 0
via PubChem
Drug data · ChEMBL
- Max clinical phase
- Phase 2
- Molecule type
- Small molecule
via ChEMBL · EBI
Research
61 papers- Oxazolidinones: a review.Drugs · 2000
- In vitro activity of linezolid and eperezolid, two novel oxazolidinone antimicrobial agents, against anaerobic bacteria.Anaerobe · 1997
- Linezolid compared with eperezolid, vancomycin, and gentamicin in an in vitro model of antimicrobial lock therapy for Staphylococcus epidermidis central venous catheter-related biofilm infections.Antimicrobial agents and chemotherapy · 2003
- The oxazolidinone eperezolid binds to the 50S ribosomal subunit and competes with binding of chloramphenicol and lincomycin.Antimicrobial agents and chemotherapy · 1997
- Mechanism of action of oxazolidinones: effects of linezolid and eperezolid on translation reactions.Antimicrobial agents and chemotherapy · 1997
via PubMed
Wikidata facts
- Subclass of
- chemical compound
- Mass
- 394.165
Show 4 more facts
- chemical formula
- C₁₈H₂₃FN₄O₅
- isomeric SMILES
- CC(=O)NC[C@H]1CN(C(=O)O1)C2=CC(=C(C=C2)N3CCN(CC3)C(=O)CO)F
- canonical SMILES
- CC(=O)NCC1CN(C(=O)O1)C2=CC(=C(C=C2)N3CCN(CC3)C(=O)CO)F
- Commons category
- Eperezolid
Sources (2)
via Wikidata · CC0
~1 min read
Encyclopedic overview
3 sectionsContents
- Synthesis
- See also
- References
Eperezolid is an oxazolidinone antibiotic.
==Synthesis== thumb|center|600px|class=skin-invert-image|Eperezolid synthesis
Excerpted from Wikipedia’s “eperezolid” article, available under the CC BY-SA 4.0 licence.